Celebrate Life · Chronic Illness · Family · Health and Wellbeing · Medical · Men & Womens Health · Mental Health

NAMI September Newsletter-Suicide Prevention

Note from NAMI National:

“September is Suicide Prevention Month, when we work to raise awareness about this urgent crisis. Like mental health conditions, suicidal thoughts can affect anyone regardless of age, gender, or background. But suicidal thoughts should not be considered normal and often indicate more serious issues.”

Fast Facts:

Individual Impact

  • 79% of all people who die by suicide are male.
  • Although more women than men attempt suicide, men are 4x more likely to die by suicide.
  • In the U.S., suicide is the second leading cause of death among people aged 10-14, the 3rd leading cause of death among those aged 15-24, and the 12th leading cause of death overall.
  • 46% of people who die by suicide had a diagnosed mental health condition — but research suggests that 90% may have experienced symptoms of a mental health condition.

Community Impact:

Annual prevalence of serious thoughts of suicide, by U.S. demographic group:

  • 8% of all adults
  • 4% Native Hawaiian/other Pacific Islander
  • 2% Mixed/Multiracial
  • 5% American Indian/Alaska Native
  • 13% of young adults aged 18-25
  • 22% of high school students
  • 41% of lesbian, gay, bisexual, transgender, and queer youth
  • The highest rates of suicide in the U.S. are among American Indian/Alaskan Natives, followed by non-Hispanic white people.
  • Lesbian, gay, and bisexual youth are 4x more likely to attempt suicide than straight youth.
  • Transgender adults are nearly 9x more likely to attempt suicide at some point in their life compared to their peers.
  • Suicide is the leading cause of death for people held in local jails.

This Suicide Prevention Month, check in on your loved ones. Knowing the risk factors and warning signs can assist you in finding help for yourself, a loved one, or a friend. You can learn more about this here.

With gratitude,

The NAMI Texas Public Policy Team

Melinda

 

Celebrate Life · Chronic Illness · Family · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Moving Forward · Survivor

October Awareness Months

For the complete list of Awareness Months click on the link under references. Below are the issues that are most important to me or ones I have a personal connection to for which there are several.

ADHD Awareness Month
AIDS Awareness Month

National Breast Cancer Awareness Month

National Depression Education and Awareness Month
National Depression and Mental Health Screening Month
Sober October
Pregnancy & Infant Loss Awareness Month
National Bullying Prevention Month
Domestic Violence Awareness Month
Dyslexia Awareness Month
LGBTQ+ History Month

Melinda

Reference:

https://www.goodgoodgood.co/articles/october-awareness-days-months

Celebrate Life · Chronic Illness · Health and Wellbeing · Infectious Diease · Medical · Men & Womens Health · Moving Forward

Dr. Dave Martz overcame an ALS death sentence with Lyme treatment

As Dave Martz lay dying, an idea serpentined around his mind and would not loosen its grip: Despite the absolute diagnosis and the insistence of the doctors, including a world expert, that he was dying of ALS, despite his own vow to face things head-on and reject the lure of denial, Martz couldn’t shake the notion that possibly, just maybe, he actually had Lyme disease. (from Cure Unknown: Inside the Lyme Epidemic by Pamela Weintraub.)

One of the earliest Lyme conferences I ever attended featured Dr. Dave Martz and the story of his remarkable recovery from what had been diagnosed as ALS–a fatal condition.

I would later write this about him in my blog:

Kind of a rock star

Dr. David Martz is kind of a rock star in the Lyme world. You may have read about him in Pam Weintraub’s Cure Unknown and seen footage of him in the documentary Under Our Skin.

His story is riveting. He had a lifetime of good health and a successful career as a physician practicing internal medicine-hematology-oncology for 30 years. Then, in 2003, Martz suddenly started experiencing strange symptoms. First deep fatigue, then profound muscle aches and body-wide pain. Soon he was too weak to get out of bed. As his condition rapidly deteriorated, his physicians gave him a devastating diagnosis: ALS (aka Lou Gehrig’s Disease). They said nothing could stem his physical decline and he would likely be dead within two years.

But events went in a different direction. As his health spiraled downward, Martz connected with a Lyme disease specialist who prescribed hard-hitting, long-term antibiotics. The gamble paid off. By the end of 2004, Martz was a new man. In fact, the doctor who had diagnosed him so definitively with ALS, now pronounced that condition completely gone.

Martz devoted the next two and a half years to a project that gave extended antibiotics to about 90 ALS patients and demonstrated objective improvements in 15% of them. He has also treated more than 800 chronic Lyme patients, with good response and minimal side effects.

A message of hope

In 2010, I helped organize a Lyme patient education conference in the San Francisco Bay Area and we had Dr. Martz as our keynote speaker. He was a kind, thoughtful man who offered a message of hope to an audience which sorely needed it.

This week, I learned that Dr. Martz passed away last month at the age of 83. Rest in peace, Dr. Martz, rest in peace.

TOUCHED BY LYME is written by Dorothy Kupcha Leland, President of LymeDisease.org. She is co-author of Finding Resilience: A Teen’s Journey Through Lyme Disease and of When Your Child Has Lyme Disease: A Parent’s Survival Guide. Contact her at dleland@lymedisease.org.

Very interesting read! So glad he had an open mind and thought to seek out a Lyme Literate Doctor, it saved his life.

Melinda

Chronic Illness · Health and Wellbeing · Medical · Men & Womens Health · Self-Care

Numb the Pain by Navigating Chronic Discomfort with Style

Life with chronic discomfort can feel like living out an endless drama, yet its protagonist (that would be you), deserves smoother scenes. Luckily, there are multiple techniques to alleviate persistent pain, providing pockets of relief from daily struggle into a manageable storyline. 

Photo by Gizem Nikomedi on Unsplash

Embrace the Power of Movement

Exercise may make your spine shudder, but physical activity is an excellent way to manage chronic pain. Engaging in low-impact activities such as swimming, yoga, or tai chi can improve circulation, and flexibility and release endorphins. Natural painkillers are made available without an expectation of compensation.

Endorphins Are Like Comedians

Your body’s endorphins act like the stand-up comedians of its own world, helping lighten the mood and make things bearable. Movement produces endorphins which in turn reduce perceptions of pain. So whether it’s taking a daily stroll around your neighborhood or doing some light stretching exercises, find something that makes you want to move, even if that means dancing awkwardly without anyone watching.

Mind Over Matter: Mental Techniques for Relief 

Your mind can be used as an effective weapon, all it needs to be properly deployed. Practices such as mindfulness meditation, cognitive behavioral therapy (CBT), and guided imagery can have profound effects on pain perception while changing our relationship to discomfort.

Mindfulness Magic: Transforming Present into Peace

Engaging in mindful practice means staying present to each moment without judgment, helping to ease stress and anxiety that exacerbate pain. Apps or online resources designed to guide this process could prove invaluable, and your mind and body will thank you.

Harnessing Nature for Alternative Therapies

Incorporating natural methods can often provide what is needed for living with chronic pain. Acupuncture, chiropractic care, and herbal remedies may complement other pain management approaches by offering more holistic approaches.

Pricking Away the Pain: An Acupuncture Adventure 

While Acupuncture may seem strangely offbeat for television dramas, its roots lie deep within traditional Chinese medicine. By strategically placing needles along nerve pathways to reduce pain and promote healing.

Medical Marijuana as a Natural Alternative 

Medical marijuana has emerged as an attractive solution for chronic pain sufferers, thanks to cannabinoids found within cannabis which interact with our bodies’ endocannabinoid system and modulate pain and inflammation. While legal challenges have historically limited medical marijuana’s use, studies show its efficacy for various forms of pain such as neuropathic and arthritis pain relief. Patients often find medical cannabis helps them decrease reliance on traditional painkillers while potentially decreasing adverse side effects. You must consult your healthcare professionals regarding appropriate usage as soon as possible before beginning.

Becoming a Master Chef: Nutritional Tweaks

No one’s suggesting an appearance on a cooking show, rather, what you eat has more power to affect pain levels than you realize. An anti-inflammatory diet may work wonders. Try including foods rich in omega-3 fatty acids like fish, flax seeds, and walnuts in your daily meal plans to reduce inflammation and pain levels. Remember: balance doesn’t mean balancing pizza slices between both hands.

Spice It Up: The Turmeric Tale

Turmeric is one of the greatest spices imaginable, boasting powerful anti-inflammatory effects and rich with curcumin. Add turmeric to dishes, smoothies, or teas for an intoxicating flavor and potential pain relief. But be careful not to mistake it for its competitor, saffron. They both love taking center stage but serve distinct functions.

Conclusion

Chronic pain may be a constant part of life, but exploring different strategies may provide relief. Pain management becomes less exhausting with laughter as your guide and professionalism as your shield. Embrace these tips as creative tools to write a narrative that features discomfort less prominently in it.

This is a collaborative post.

Melinda

Chronic Illness · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Self-Care

Blood Cancer Awareness Month 

My husband was diagnosed last year with Leukemia and it was a total shock to the system. He’s been healthy our entire 22-year marriage only having a cold a few times, this diagnosis rocked me hard. One blessing is that he has a team of doctors who he sees regularly and so far his cancer is growing very slowly. Skin Cancer can also pop up with Leukemia and he has been diagnosed with that as well. He goes every three months and usually has a new spot removed or scrapped and burned. Sunscreen is more important than ever but he hasn’t bought into that yet.

As scary as it was in the beginning, after educating ourselves and him seeing a doctor every three months we are more comfortable about where his health is at.

This Is Blood Cancer

Blood Cancer Awareness Month is a global event helping to raise awareness of one of the world’s most prevalent and dangerous cancers: blood cancer.

September turns red each year as the spotlight is put firmly on blood cancer and the impact it has on our communities and the urgent need for more action.

Raising awareness of blood cancer, its signs and symptoms, and its impact, will help to improve early diagnosis, encourage policymakers to prioritize the disease, as well as help everyone with blood cancer feel connected and heard.

 

Tricia Hernandez with the Leukemia Lymphoma Society says many blood cancers are treatable through chemotherapy, stem cell transplants, and surgery.

She says in Maine, nearly 900 people have been diagnosed with blood cancer this year.

“A person is diagnosed with a blood cancer approximately every three minutes. So, it’s quite a large number although a rare disease than other cancers. There are hundreds of thousands of people affected by this,” said Hernandez.

Major Types of Leukemia

The four major types of leukemia are:

CLL is one of the most common types of leukemia in adults. ALL is the most common type of leukemia in children.

Types of Lymphoma

Lymphomas begin in cells of the lymph system, which is a part of the immune system. Lymph tissue is found throughout the body. As a result, lymphoma can begin almost anywhere. The disease occurs in two types: Hodgkin and non-Hodgkin lymphomas.

Both types can occur in adults and children. An estimated 80,620 people in the United States will develop non-Hodgkin lymphoma in 2024, according to the NCI. Approximately 20,140 people will die from non-Hodgkin lymphoma. For Hodgkin lymphoma, 8,570 new cases and 910 deaths are estimated for 2024, according to the NCI.

FOR MORE INFORMATION

There are many different types of leukemia and lymphoma in adults and children. For more information on these different diseases, please see:

References:

https://bloodcancermonth.org

https://www.msn.com/en-us/health/other/nearly-2-million-americans-live-with-blood-cancer-september-marks-awareness-month/ar-AA1qPvUH?ocid=BingNewsSerp

September is Leukemia and Lymphoma Awareness Month

Celebrate Life · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Self-Care

Healthy Aging Month

What a great awareness month, we all age so why not age healthy. Below are tips you can apply to your life today for better physical and mental health Here’s to our future.

———-

It’s time to celebrate September Healthy Aging® Month, the annual observance month designed to focus national attention on the positive aspects of growing older.

What is September is Healthy Aging Month All About?

The observance month began more than 30 years ago as part of our National Healthy Aging® Campaign to continue to draw attention to healthy, active lifestyles at any age.

Carolyn Worthington, president of Healthy Aging®, the official multi-media platform promoting the month, created it in 1992.

“Our goal in creating the month was to draw attention to the positive sides of growing older. We felt there needed to be a second time during the year in addition to May is Older Americans Month. September was chosen because so many people felt they could “get started” more easily at that time. Maybe the back-to-school routine never really goes away.”

Now, after more than thirty years, Worthington sees the national interest in continuing healthy lifestyles well into old age as never been stronger.

“We were pleased to announce that the U.S. Senate unanimously passed the resolution marking September as National Healthy Aging Month in 2021,” Worthington said. Numerous governors before that proclaimed the national observance month for their states as well.

“We are proud of our efforts to continue to build awareness for healthy lifestyles. Since we kicked off the observance month, the myths of aging have been chipping away,” Worthington said. “We are also proud to say the month we started is now on most national health observance calendars.”

“Of course, there are still stereotypes about older adults,” Worthington said. Perhaps the baby boomers embracing aging like no other generation started turning the tide. Seeing people in their 80s and 90s doing spectacular things today is not unusual.”

10 Tips for Healthy Aging®

The four main components of a healthy lifestyle fall into four main categories: physical, social, mental, and financial wellness.

  1. Move more, sit less. Why? Physical activity is your weapon to help control blood pressure, help prevent heart disease and stroke, and possibly lower your risk for depression, anxiety, and conditions like certain cancers and type 2 diabetes. What to do? Choose something fun so you can keep at it, like cycling, walking, dancing, swimming, or aerobics.
  2. How much do you need to do? Current national recommendations are 150 minutes of moderate-intensity physical activity per week and two days of muscle-strengthening training. That’s only 20 minutes a day, 7 days a week, or around an hour a day if you do three days a week.
  3. Get motivated with free websites and apps like All Trails to find parks and trails around the world; American Heart Association with ideas on how to join a walking club, or The CDC with ideas for individuals with a disability 
  4.  Get Those Annual Check-Ups. Make this month the time to set up your annual physical and other health screenings. Go to the appointments, and then, hopefully, you can stop worrying about ailments for a while.
  5. Volunteer. ..Being of service is an excellent way to bring happiness into your life and not focus on yourself. Refocus on others and volunteer your time and expertise. United Way, the American Red CrossVolunteerMatch,  and AmeriCorps are all helpful resources.
  6. Beat back loneliness. Don’t wait for the phone to ring. Be proactive and call someone for a lunch date. Set up a calendar of lunch dates and challenge yourself to have at least two lunch dates per month (once a week is even better!) It doesn’t have to be expensive … pack a picnic, and head to a park. Try to mix up your get-togethers with old friends and new acquaintances.
  7. Rekindle or follow a new passion. Take a hard look at what you like to do rather than what other people tell you to do to meet new people. Pick some activities where you might meet new friends.
  8. Get a dog. If you don’t have one, get one and walk. You will be amazed how many people you will meet through your dog. Can’t have one? Check your local humane society to see if they need dog walkers
  9. Be realistic about what you can accomplish. Learn to say no …, and don’t overwhelm yourself with a to-do list. The non-profit Mental Health America offers more tips for reducing or controlling stress.
  10. Plan for your next passage. Capitalize on your career experience and start a new one. Yes, enjoy a brief “retirement.” Travel, and spend more time with family and friends. Develop new hobbies. Redefining your purpose to maintain a sense of identity and purpose is essential to a healthy lifestyle.

This a great reference it’s given me many ideas on how I can improve my life.

Melinda

Reference:

September is Healthy Aging® Month 2024

Celebrate Life · Chronic Illness · Family · Fun · Health and Wellbeing · Medical · Men & Womens Health · Music

#Weekend Music Share-Eddie Van Halen & Sammy “Love Walks In” (Bridge School Benefit 1993)

My husband sent me this video and the first thing I said was, “Who knew Eddie could play the piano?” I don’t buy into aliens but I like the song played this way, I didn’t listen to the original version because I wanted to remember this special occasion. You can tell they were having fun and really enjoyed each other’s company. I still love Sammy’s voice, his club in Cabo, not so much.

A tidbit about the Bridge School Benefit.

The Bridge School Benefit was an annual charity concert usually held in Mountain View, California, every October at the Shoreline Amphitheatre from 1986 until 2016 with the exception of 1987. The concerts lasted the entire weekend and were organized by musicians Neil Young and Pegi Young. An annual Bay Area highlight, the concerts were billed online as the primary means of funding for  The Bridge School; over both days, the reserved seats alone brought in well over a million dollars every year.

Organized by musicians Neil Young and Pegi Young, the Bridge School Benefit Concert is an annual, all acoustic, non-profit charity event held every October at Shoreline Amphitheatre in Mountain View, California. All proceeds directly benefit the operations of The Bridge School.

Our Mission

The Bridge School is a non-profit organization whose mission is to ensure that individuals with severe speech and physical impairments achieve full participation in their communities through the use of augmentative & alternative means of communication (AAC) and assistive technology (AT) applications and through the development, implementation and dissemination of innovative life-long educational strategies. The Bridge School is an internationally recognized leader in the education of children who use augmentative and alternative communication and has developed unique programs and trained highly skilled professionals in the use of state of the art assistive technology.

References at the bottom of the post.

It’s the weekend!!!!!!

 I’m glad you joined me this week for another edition of Weekend Music Share.

Have a great weekend!

Melinda

Welcome back to Weekend Music Share, the place where everyone can share their favorite music.

Feel free to use the Weekend Music Share banner in your post, and use the hashtag #WeekendMusicShare on social media so other participants can find your post.

Reference:

https://en.wikipedia.org/wiki/Bridge_School_Benefit

https://www.bridgeschool.org

Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Moving Forward

Just Pondering

Hi, I’m glad you stopped by and I look forward to seeing you soon. 

If you had to make a decision in life that would change the quality of life in your future and potentially wipe out your savings, how would you approach it?

I’m praying and waiting for answers.

Melinda

 

Celebrate Life · Communicating · Health and Wellbeing · Medical · Mental Health · Self-Care

Unboxing Menopause: Why fear shouldn’t dictate our health choices

America’s leading menopause advocates lead the way for changing the way we speak about menopause.

The black box warning labels on local estrogen products are costing menopausal women their wellbeing, and their money, and HELLO’s not-for-profit partner, Let’s Talk Menopause is on a mission to remove them. 

Along with the Menopause Advocacy Working Group, Let’s Talk Menopause is calling for the removal of the outdated FDA-mandated boxed warning from local vaginal estrogen products used to treat Genitourinary Syndrome of Menopause (GSM).

GSM is a condition that affects up to 84% of menopausal women, manifesting in symptoms such as vaginal dryness, urinary urgency, and recurrent urinary tract infections, aka UTIs. Despite the proven effectiveness of local vaginal estrogen in treating GSM, an outdated boxed warning prevents many women from accessing this essential treatment.

The black box warning labels on local estrogen products are costing menopausal women their wellbeing, and their money, and HELLO’s not-for-profit partner, Let’s Talk Menopause is on a mission to remove them. 

Along with the Menopause Advocacy Working Group, Let’s Talk Menopause is calling for the removal of the outdated FDA-mandated boxed warning from local vaginal estrogen products used to treat Genitourinary Syndrome of Menopause (GSM).

GSM is a condition that affects up to 84% of menopausal women, manifesting in symptoms such as vaginal dryness, urinary urgency, and recurrent urinary tract infections, aka UTIs. Despite the proven effectiveness of local vaginal estrogen in treating GSM, an outdated boxed warning prevents many women from accessing this essential treatment.

Get involved and learn more by visiting the Unboxing Menopause campaign website and sign the consumer advocacy letter to the FDA.

The Real Cost of the Boxed Warning

The boxed warning on local vaginal estrogen has caused unnecessary fear and confusion for millions of women suffering from GSM. This barrier to treatment has led to higher healthcare costs, multiple doctor visits, and prolonged discomfort. 

“The boxed warning poses a massive economic burden on women — and on society,” said Jen Weiss-WolfLet’s Talk Menopause Board Member, author, and Executive Director at Birnbaum Women’s Leadership Center. “Untreated GSM leads to higher healthcare costs, lost productivity, and unnecessary suffering.”

Advocating for Change

Let’s Talk Menopause and the Menopause Advocacy Working Group are calling on women and healthcare providers to join their campaign to demand the FDA remove the boxed warning from local vaginal estrogen products.

“Vaginal estrogen is the gold standard treatment for GSM,” Dr. Robin Noble, an OBGYN and Let’s Talk Menopause’s Chief Medical Advisor tells HELLO! “It targets the problem at the source, helping women regain their comfort, their sexual function, and their quality of life with minimal risk.”

“Fear shouldn’t dictate our health choices,” explains Tamsen Fadalauthor, journalist, filmmaker, and Let’s Talk Menopause board member. “The black box warning is costing us our well-being and our money.”

Join the Campaign

Let’s Talk Menopause and the Menopause Advocacy Working Group urge women and healthcare providers to advocate for removing the outdated boxed warning, making local vaginal estrogen more accessible. For more information on how to get involved or to learn more about GSM and local vaginal estrogen, visit the Unboxing Menopause campaign website and sign the consumer advocacy letter to the FDA.

Women have the right to know how Box Warnings are decided upon by the FDA. There have been several occasions that I’m aware of where the data has been misapplied and it can take many years before the correct information comes to light.

Melinda

Reference:

https://www.hellomagazine.com/healthandbeauty/health-and-fitness/718793/unboxing-menopause-why-fear-shouldnt-dictate-our-health-choices/

Celebrate Life · Chronic Illness · Health and Wellbeing · Medical · Men & Womens Health · Mental Illness · Moving Forward

6 Rap Artists Who Have Opened Up About Their Bipolar Disorder

By Tanya Hvilivitzky 

Last Updated: 16 Sep 2024

These rappers have shared their struggles with bipolar disorder, bringing awareness to their experiences within the rap community and beyond.

In recent years, it has become more common for celebrities to talk openly about their mental health, and several well-known rappers have significantly contributed to this conversation over the years. Despite facing controversies and navigating the complexities of the public eye, these artists shared their own stories about living with bipolar disorder. Their honesty helps others feel less alone and sparks more conversations about mental health.

Whether discussing their experiences in interviews or incorporating them into their lyrics, these rappers contribute to a more extensive dialogue about mental health. They’re helping to shift perceptions and encourage a more accepting and informed conversation around bipolar disorder. Here are six rappers who are part of this critical conversation:

1. Krizz Kaliko

Samuel William Christopher Watson, who performs under the stage name Krizz Kaliko, is an American rapper, singer, and songwriter. He has made significant contributions to the music industry as a longtime collaborator with Tech N9ne, another artist from his hometown. Initially signed to Strange Music, the label co-owned by Tech N9ne, Kaliko established his own label, Ear House Inc., in 2021.

Diagnosed with bipolar disorder, Kaliko has openly addressed his mental health struggles in his music. Specifically, in his album Genius, he delves deep into his experiences on the track titled “Bipolar,” where he raps and sings about the challenges of living with the condition.

Beyond his music, Kaliko has spoken candidly about his use of psychotherapy and anti-anxiety medications as part of his ongoing effort to maintain emotional and mental stability. His openness about his struggles inspires and supports others facing similar battles.

2. Ye

Kanye West, now known as Ye, has been vocal about his bipolar disorder, referring to it as his “superpower.” He first revealed his diagnosis around the release of his 2018 album Ye, where he used his music and public statements to address the complexities of living with the condition. The album’s cover features the phrase, “I Hate Being Bipolar; it’s Awesome,” reflecting his struggle with the extremes of the disorder.

Ye has continued to discuss the impact of bipolar disorder on his life, comparing it to having a “sprained brain” and emphasizing the importance of proper care, even though he has openly struggled with staying on medication consistently.

In recent years, Ye has also opened up about the paranoia and erratic behavior that accompanies his manic episodes. He has criticized how people with mental health conditions are often mistreated, both by healthcare systems and society at large, contributing to the stigma around mental illness.

3. Charles Hamilton 

Charles Eddie-Lee Hamilton, Jr., a Harlem, New York City native, is a recognized figure in the hip-hop community as a recording artist and record producer. His album The Pink Lavalamphas been hailed as one of the standout underground hip-hop releases of its time.

In a candid interview with Billboard, Hamilton discussed the personal struggles he faced due to his undiagnosed bipolar disorder. He described a period of intense isolation, where distrust of others led him to confine himself to his home, dedicating his time solely to music production as a way to combat his depression. “I just didn’t trust anybody,” he admitted. “I didn’t leave my house; I just made music all the time. I was fighting depression — I shut myself in.”

Over the years, Hamilton has been open about his mental health journey, using his platform to raise awareness about bipolar disorder and the importance of mental health care. His career has seen various ups and downs, including a brief retirement in 2016 followed by a return to music with new projects that reflect his ongoing battle with mental health and his resilience in the face of adversity. His candidness about his struggles has not only helped to destigmatize mental health issues among musicians and fans but also resonated with audiences worldwide.

4. DMX (Dark Man X)

Earl Simmons, known professionally as DMX, was a prominent figure in the music and acting industries, rising to fame in the late 1990s. His raw and emotional lyrical content often reflected the personal pain and struggles associated with bipolar disorder, which was especially evident in his groundbreaking album, It’s Dark and Hell Is Hot.

DMX’s bold and unique contributions significantly shaped the music landscape, particularly as the only artist to debut his first two albums at number one in the same year.

His music not only captivated fans but also offered a visceral insight into his battles with mental health. Until his passing in 2021, DMX’s powerful voice in music and film left a lasting impact, celebrating the profound expressiveness of his work.

RELATED: 20 Musicians You May Not Know Have Battled Bipolar Disorder

5. Adam Steven Deacon

Adam Steven Deacon, an English talent celebrated as a film actor, rapper, writer, and director, shot to fame with his performance in the British film Kidulthood and his directorial debut, Anuvahood. In an interview with the BBC, Deacon discussed his initial fears that his bipolar disorder might derail his career. He described the condition’s impact, saying, “Bipolar life has two speeds: One minute, it’s all too fast. The next, everything becomes so slow that I can’t cope.”

This candid account of his daily struggles sheds light on the complexities of living with this brain-based disorder. Deacon has since learned to embrace and manage his conditioneffectively. His story of resilience and adaptability provides hope and insight, encouraging others to navigate similar challenges.

6. Yo Yo Honey Singh

Yo Yo Honey Singh, also known as Honey Singh, is a prominent Indian rapper, music producer, and film actor renowned for his contributions to Bollywood music. He rose to fame as one of the highest-paid music producers in Bollywood. But in late 2014, Singh took a sudden hiatus from the public eye, sparking concern among his fans. After a quiet return to the music scene in 2015, he maintained a low profile with the media. It was not until March 2016 that Singh revealed the reason for his 18-month absence: he had been battling bipolar disorder.

Since disclosing his diagnosis, Singh has gradually resumed his music career and has been involved in several new projects, adapting his workload to manage his health effectively. His openness about his mental health struggles has been instrumental in raising awareness and reducing the stigma associated with mental health issues in the entertainment industry and beyond.

Tanya Hvilivitzky

Tanya Hvilivitzky has spent more than 30 years in the communications field — a career that has included stints as an investigative journalist, managing editor for a lifestyle and wellness magazine, corporate communications director, and researcher/writer. She has been with bpHope (and bp Magazine) since 2016, serving in roles such as features editor, interim editor, and, currently, senior editor. She has been devoted to mental health awareness since she was the editor of Schizophrenia Digest in her early days, and now with a particular focus on highlighting the complexities of bipolar disorder through compassionate, service-based journalism. As an award-winning writer/editor, Tanya received the Beyond Borders Media Award for her 2012 investigative exposé about human trafficking for Niagara Magazine. Her work on this critical topic also earned the Media Freedom Award “Honouring Canada’s Heroes” from the Joy Smith Foundation to Stop Human Trafficking.

Melinda

Celebrate Life · Chronic Illness · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Moving Forward

Mini Me Health Update

I recently wrote about how the new medication Trintellex for my Bipolar Disorder made me feel better than I had in years. It still has that effect on my life but it’s marred with new and ongoing health issues. Some have popped up in the past few weeks. It’s a woop on the head trying to understand what is happening to my body and messing up my ability to live my best life. 

I’m very happy to report that The Mayo has accepted me as a patient and I will be flying to Rochester, MN in a few weeks. I trust them with my life and I am confident they will find what or what several issues are affecting my health. The first day will start with an Internal Medicine Doctor for an evaluation, later that day I pick up a Pulse Oximeter to wear overnight. 

The second day starts early with a load of blood tests, the test appears to focus on my blood. Later that afternoon, there is a consultation with a Hematologist to discuss the lab results. Probably additional information as well. At this time my schedule is free on the third day and on Friday I return back to Internal Medicine for a readout. 

The last time I went for my heart there were so many tests that we ran from one appointment to the next, sometimes without a breath. This trip is very different and I’m so glad due to the way I’m feeling. They did want me to come back in November for a Fibromyalgia and Chronic Fatigue evaluation but I don’t see the need. I was diagnosed with both many years ago and I don’t need to fly up there for a day of testing and education. I canceled that appointment. The Mayo did send a video on Fibro & Chronic Fatigue I will watch as a fresher but I’m not flying up to get evaluated for something I already know. Unless they can give me a reason I can make logic out of, I’m not spending the money for a one-day trip. 

I met with an Orthopedic Surgeon who specializes in hands and was not surprised to hear I had Carpal Tunnel in both hands, as well as arthritis but the diagnosis of Osteoarthritis in both thumbs was a shock. He is ordering a Nerve Conduction Study since I do have nerve issues in my hands. I thought a barnacle was growing on my wrist only to find out it was caused by the wrist plate put in when I broke my wrist years ago. When he does the carpal tunnel surgery on the left hand he will remove the wrist brace and I will have the right hand surgery after the left heals. The great news is that technology has improved so much that Carpal Tunnel surgery can be done with a very small incision, ultrasound is used and only a band ade is required after the surgery. It is said that most a back to full range of motion in three days. Boy, what a difference in the right hand Carpal Tunnel surgery I had years ago. It won’t be as easy on my left hand with the removal of the wrist plate but I have no doubt that surgery has improved in that area as well. I’m currently wearing a painful thrumb support that hurts other areas of my hand and it’s impossible to wear except when on the computer. I’ve asked for another option. 

Just another interesting week in my life but I’m thankful I have a life and it’s great outside of the health conditions. 

Melinda

Celebrate Life · Chronic Illness · Health and Wellbeing · Infectious Diease · Medical · Men & Womens Health · Tick Borne Illnesses

IGeneX Lyme ImmunoBlot test receives FDA clearance

Important Read

SEP 5, 2024

This is a huge win for Lyme patients and may diagnose Lyme faster and save patients the cost and pain of long-term treatment. The key point is that the tests are only available from labs that perform Lyme testing and do not meet the CDC standards which means that insurance companies will not pay for the cost. I would encourage you to seek out a lab for the test regardless of insurance pay, IGeneX has led the way in Lyme testing for years and is the gold standard. Paying for the test is worth every penny because you are testing for even possible antigens out there and you won’t receive that from your doctor. This test could make a huge difference in your treatment by pinpointing the virus versus a cross-the-board method.

The Lyme ImmunoBlot test first introduced by IGeneX in 2017 has now been converted to a test kit–and has received FDA clearance.

The name of the test is iDart™ Lyme IgG ImmunoBlot Kit.

It’s a stand-alone test for the detection of IgG antibodies against Borrelia-causing Lyme disease.

The iDart ImmunoBlot Kit features 31 Lyme antigen bands, which are more antigen bands than any other Lyme immunoblot test on the market.

Moreover, it is the only immunoblot that includes Osp A (P31) and Osp B (P34). (Note: those are the two bands removed from other Lyme tests in the 1990s because of their use in the development of Lyme vaccines.)

The inclusion of 31 antigens improves the sensitivity of the detection of Lyme-specific IgG antibodies, which in turn will improve the sensitivity of the diagnosis of Lyme disease in suspected patients without sacrificing specificity.

“We are delighted to have received FDA clearance for our Lyme ImmunoBlot Kit,” said Dr. Jyotsna Shah, Ph.D., President and Director of IGeneX Labs.

These kits are not available for sale to consumers, but only to labs that perform Lyme diagnostic testing.

Key features of the iDart Lyme IgG ImmunoBlot kit

  • Results interpretation is based upon new criteria and not CDC criteria.
  • The bands are grouped according to their antigen groups. The test is considered positive if the Lyme Screen Antigen (LSA) band and one or more bands from at least two other groups are present on the ImmunoBlot.
  • Bands 31 and 34 are included, making this the only FDA-cleared Lyme serological test that includes these bands.

SOURCE: IGeneX, Inc.

Melinda

Reference:

https://www.lymedisease.org/lyme-immunoblot-fda-clearance/

 

Celebrate Life · Fun · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Moving Forward · Self-Care

How to Be Happy: 27 Habits to Add to Your Routine

Medically reviewed by Lori Lawrenz, PsyD — Written by Ann Pietrangelo — Updated on March 10, 2023

Regardless of your version of true happiness, living a happier, more satisfied life is within reach. A few tweaks to your regular habits like getting more sleep and exercise can help you get there.

Habits matter. If you’ve ever tried breaking a bad habit, you know all too well how engrained they are.

Well, good habits are deeply engrained, too. Why not work on making positive habits part of your routine?

Below, you’ll find suggestions for daily, monthly, and yearly habits to help kickstart your quest. Just remember that everyone’s version of happiness is a little different, and so is their path to achieving it.

If some of these habits create added stress or just don’t fit your lifestyle, ditch them. With a little time and practice, you’ll figure out what does and doesn’t work for you.

Daily habits

The following daily habits may help you achieve more happiness in your life.

1. Smile

You tend to smile when you’re happy. But it’s actually a two-way street.

We smile because we’re happy, and smiling causes the brain to release dopamine, which makes us happier.

While not completely foolproof, researchers have found that the link between smiling and happiness could be attributed to the “facial feedback hypothesis,” where facial expressions may have a modest influence on emotions. 

That does not mean you have to go around with a fake smile plastered on your face all the time. But the next time you find yourself feeling low, crack a smile and see what happens. Or try starting each morning by smiling at yourself in the mirror.

2. Exercise

Exercise isn’t just for your body. Regular exercise can help reduce stress, feelings of anxiety, and symptoms of depression while boosting self-esteem and happiness.

Even a small amount of physical activity can make a difference. You don’t have to train for a triathlon or scale a cliff — unless that’s what makes you happy, of course.

The trick is to not overexert yourself. If you suddenly throw yourself into a strenuous routine, you may just end up frustrated (and sore).

Consider these exercise starters:

  • Take a walk around the block every night after dinner.
  • Sign up for a beginner’s class in yoga or tai chi.
  • Start your day with 5 minutes of stretching.

Remind yourself of any fun activities you once enjoyed but that have fallen by the wayside. Or you could consider starting activities you always wanted to try, such as golf, bowling, or dancing.

3. Get plenty of sleep

Most adults need at least 7 hoursTrusted Source of sleep every night. If you find yourself fighting the urge to nap during the day or just generally feel like you’re in a fog, your body may be telling you it needs more rest.

No matter how much our modern society steers us toward less sleep, we know that adequate sleep is vitalTrusted Source to good health, brain function, and emotional well-being. Getting enough sleep also reduces your riskTrusted Source of developing certain chronic illnesses, such as heart diseasedepression, and diabetes.

Here are a few tips to help you build a better sleep routine:

  • Write down how many hours of sleep you get each night and how rested you feel. After a week, you should have a better idea how you’re doing. You can also try using an app to track your sleep.
  • Go to bed and wake up at the same time every day, including on weekends.
  • Reserve the hour before bed as quiet time. Take a bath, read, or do something relaxing. Avoid heavy eating and drinking.
  • Keep your bedroom dark, cool, and quiet.
  • Invest in some good bedding.
  • If you have to take a nap, try limiting it to 20 minutes.

If you consistently have problems sleeping, consider talking with a doctor. You may have a sleep disorder that requires treatment.

4. Eat with mood in mind

You may already know that your food choices have an impact on your overall physical health. But some foods can also affect your state of mind.Trusted Source

For example:

  • Carbohydrates release serotonin, a “feel good” hormone. Just keep simple carbs — foods high in sugar and starch — to a minimum because that energy surge is short and you’ll crash. Choosing complex carbs, such as vegetables, beans, and whole grains, can help you avoid a crash while still providing serotonin.
  • Lean meat, poultry, legumes, and dairy are high in protein. Protein-rich foods release dopamine and norepinephrine, which boost energy and concentration.
  • Omega-3 fatty acids, such as those found in fatty fish, have been found to have anti-inflammatory effectsTrusted Source that extend to your overall brain health. If you don’t eat fish, you might consider talking with a doctor about possible supplementation. 
  • Highly processed or deep-fried foods tend to leave you feeling down and so will skipping meals.

If you want to eat with your mood in mind, consider starting with making one food choice for your mood each day.

For example, swap a big, sweet breakfast pastry for some Greek yogurt with fruit. You’ll still satisfy your sweet tooth, and the protein will help you avoid a midmorning energy crash. Consider adding in a new food swap each week.

5. Practice gratitude 

Simply being grateful can give your mood a big boost, among other benefits. For example, a two-part study found that practicing gratitude can have a significant impact on feelings of hope and happiness.

You might try starting each day by acknowledging one thing you’re grateful for. You can do this while you’re brushing your teeth or just waiting for that snoozed alarm to go off.

As you go about your day, consider keeping an eye out for pleasant things in your life. They can be big things, such as knowing that someone loves you or getting a well-deserved promotion.

But they can also be little things, such as a co-worker who offered you a cup of coffee or the neighbor who waved to you. Maybe it could even just be the warmth of the sun on your skin.

With a little practice, you may even become more aware of all the positive things around you.

6. Give a compliment

Research shows that performing acts of kindness may also help promote your overall well-being. 

Giving a sincere compliment is a quick, easy way to brighten someone’s day while giving your own happiness a boost.

Catch the person’s eye and say it with a smile so they know you mean it. You might be surprised by how good it makes you feel.

If you want to offer someone a compliment on their physical appearance, make sure to do it in a respectful way.

7. Breathe deeply

You’re tense, your shoulders are tight, and you feel as though you just might “lose it.” We all know that feeling.

Instinct may tell you to take a long, deep breath to calm yourself down.

Turns out, that instinct is a good one. ResearchTrusted Source supports the fact that slow breathing and deep breathing exercises can help reduce stress.

The next time you feel stressed or are at your wit’s end, work through these steps:

  1. Close your eyes. Try to envision a happy memory or beautiful place.
  2. Take a slow, deep breath in through your nose.
  3. Slowly breathe out through your mouth or nose.
  4. Repeat this process several times until you start to feel yourself calm down.

If you’re having a hard time taking slow, deliberate breaths, try counting to 5 in your head with each inhale and exhale.

8. Acknowledge the unhappy moments

positive attitude is generally a good thing, but bad things happen to everyone. It’s just part of life.

If you get some bad news, make a mistake, or just feel like you’re in a funk, don’t try to pretend you’re happy.

Acknowledge the feeling of unhappiness, letting yourself experience it for a moment. Then shift your focus toward what made you feel this way and what it might take to recover.

Would a deep breathing exercise help? A long walk outside? Talking it over with someone?

Let the moment pass and take care of yourself. Remember, no one’s happy all the time.

9. Keep a journal

A journal is a good way to organize your thoughts, analyze your feelings, and make plans. And you don’t have to be a literary genius or write volumes to benefit.

It can be as simple as jotting down a few thoughts before you go to bed. If putting certain things in writing makes you nervous, you can always shred it when you’ve finished. It’s the process that counts.

Not sure what to do with all the feelings that end up on the page? Our guide to organizing your feelings may help.

10. Face stress head-on

Life is full of stressors, and it’s impossible to avoid all of them.

There’s no need to. Stress isn’t always harmful, and we can even change our attitudes about stress. Sometimes, there’s an upside to stress.

For those stressors you can’t avoid, remind yourself that everyone has stress — there’s no reason to think it’s all on you. And chances are, you’re stronger than you might think you are.

Instead of letting yourself get overwhelmed, try to address the stressor head-on. This might mean initiating an uncomfortable conversation or putting in some extra work, but the sooner you confront it, the sooner the pit in your stomach may start to shrink.

11. Avoid comparing yourself to others

Whether it happens on social media, at work, or even at a yoga class, it’s easy to fall into a place where you’re comparing yourself to others. The result? You may experienceTrusted Source more discontent, lower self-esteem, and even depression and anxiety.

It can take practice to stop comparing yourself to others, but it’s worth it for the benefit of having your inner peace and happiness. 

You can start with some of the other tips on this list that can help draw your attention inward to yourself, such as deep breathing and journaling. You may also consider talking with a therapist for perspective.

Melinda

Reference:

Celebrate Life · Chronic Illness · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Self-Care

What’s the Difference Between Chronic and Acute Stress?

Medically reviewed by Francis Kuehnle, MSN, RN-BC — Written by S. Srakocic on December 12, 2023

Acute stress is a part of life, but when it turns into chronic stress, it can cause serious health concerns both mentally and physically. 

Acute stress is the stress you feel as the direct result of a specific situation or event. For instance, it’s acute stress when you’re running late for an appointment and begin to feel symptoms of stress such as anxiety and difficulty focusing. 

Chronic stress is the result of stress that builds up from repeated exposure to stressful situations and the hormones your body releases during each stressful episode. Many things can lead to chronic stress, including factors such as difficult relationships, job demands, and financial concerns.

Acute vs. chronic stress: Symptoms

Acute and chronic stress share some overlapping symptoms. However, the symptoms of chronic stress are longer-lasting and can be harder to manage.

Symptoms of acute stress include:

Symptoms of chronic stress include:

Over time, chronic stress can lead to additional complications. These include:

Acute vs. chronic stress: Causes 

Stress is a reaction that happens when something activates your body’s fight-or-flight response. It gets your heart racing and puts you on high alert. A wide range of things can cause acute stress. 

Generally, acute stress is a reaction to situations that are challenging to manage but that are temporary, such as:

  • car accidents
  • medical emergencies
  • work deadlines
  • unexpected expenses
  • upcoming events
  • traffic
  • weather
  • travel

On the other hand, chronic stress is a reaction to long-term stressors. These long-term stressors keep your body on high alert for an extended time. Examples of situations that can lead to chronic stress include:

Acute vs. chronic stress: Treatment options

Treatment options for stress depend on the severity and how the stress is affecting your life. Acute stress doesn’t typically need treatment unless it’s making daily activities difficult. 

If you’re experiencing episodes of acute stress frequently, your primary healthcare professional might recommend lifestyle treatments such as:

  • Increasing your physical activity: Exercise and an active lifestyle can help your body release stress-reducing hormones.
  • Cutting back on caffeine: Caffeine can increase the symptoms of stress. For some people, cutting back can help reduce episodes of acute stress.
  • Making time to relax: Taking time for self-care and relaxation through steps like hot showers and baths, yoga or meditation practice, and spending time with friends can reduce stress levels.
  • Avoiding stress triggers: If you’re able to avoid specific stressful situations, it can help lower your overall stress levels.
  • Lowering your sugar intake: Eating a healthy diet and reducing the amount of sugar you take in can help manage your body’s reaction to stress. 
  • Disconnecting from phones and other devices: Cutting back on the amount of time you spend engaged with social media and news sources can help reduce stress levels.

Treatment options for chronic stress can be more complex. You might receive treatment to help you manage your stress and treatment to help alleviate your symptoms. Options can include:

  • Cognitive behavioral therapy (CBT): CBT is a therapy method that helps you identify your thought patterns and discover how they contribute to your stress levels. It can give you the tools you need to lower stress and cope with the difficulties in your life.
  • Mindfulness-based stress reduction (MBSR): MBSR is a treatment that teaches mindfulness techniques to help manage responses to stress.
  • Medication: Sometimes, prescription medications for anxiety or depression can help with the symptoms of chronic stress. The right ones for you will depend on your symptoms and on factors such as any other medications you already take.
  • Symptom-specific treatment: Your doctor might prescribe medications for any complications and symptoms connected to your chronic stress. For instance, your treatment could include medications to help with insomnia or IBS.

Takeaway

Acute stress is the stress that results from a specific, temporary situation or event. It can cause symptoms such as anxiety and insomnia. 

Chronic stress is stress that is the result of an ongoing situation such as a demanding job or chronic illness. It can lead to long lasting physical health compilations and sometimes needs treatments such as therapy and medication.

Melinda

Reference:

Celebrate Life · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Mental Illness · Moving Forward

Accepting Your Bipolar Disorder Diagnosis

By Donna Jackel 

Medically Reviewed by Allison Young, MD

Last Updated: 10 May 2024

Accepting a bipolar diagnosis can be immediate, offering clarity on past experiences, or it may be a gradual process of coming to terms with a lifelong condition.

At age 29, Julie C. seemed to be at an enviable place in life. She had good friends. She had come out as a lesbian and was comfortable with her sexuality. And she had a fulfilling job that took her to far-off places: She was coordinator of a Toronto-based foundation.

That life began to slip away from her in 2007, when she was beset by money and relationship problems. Julie was hospitalized twice, and treated for depression. But her psychologist knew another side of the young woman — the high-energy, high achiever who could sometimes work at a furious pace with little sleep. In 2008, the psychologist told Julie that she believed she had bipolar disorder.

Fearing the Unexpected, a Diagnosis of Bipolar

“I was terrified at first,” Julie recalls months later. “I had this dropping feeling in my gut. All the stereotypes I had about bipolar came flooding into my head. I have a friend who has bipolar, and she has been almost homeless a couple of times, and in and out of the hospital. I thought, ‘Oh my God — is this what my life is going to be?’”

Julie has since accepted her diagnosis. She is stable and feels much better than in the past. She takes her medication daily, maintains a regular sleep schedule, works out, and has improved her eating habits. She still works for the foundation, but is planning to move back to her hometown and work long-distance.

For others, the road to acceptance can be long and circuitous. Peggy M. of Wisconsin has experienced highs and lows since her teens. Although Peggy was diagnosed with bipolar in 2002, acceptance did not come until six years later when she had her first negative work evaluation.

Peggy received a poor rating in several areas; the comment that hurt most was “poor communication skills.” “I have a master’s degree in communications. [The review] was a direct contradiction to what I knew about myself,” Peggy says. “That’s when I finally had to admit it was the bipolar affecting my work.”

Your Journey to Acceptance of Bipolar Is Unique to You

Many factors influence how well a person is able to adapt to bipolar. These include the severity of the illness, level of self-awareness, one’s attitude about mental illness, availability of a support system, and access to quality health care.

Some are able to accept their illness after one or two manic episodes. Others remain in denial for years, burning through relationships, jobs, and money until they hit rock bottom.

“Bipolar is one of the illnesses people have the hardest time accepting,” says Sagar V. Parikh, MD, deputy psychiatrist-in-chief at the University Health Network in Toronto and professor of psychiatry at the University of Toronto.

“Maybe one-third accept the diagnosis right away. At least a third totally reject it, and a third believe it, but when they are better for a while, begin to doubt it again,” explains Dr. Parikh.

“It’s common for acceptance to take years,” agrees Evette J. Ludman, PhD, a clinical psychologist and researcher at Group Health Cooperative in Seattle and coauthor of Overcoming Bipolar Disorder: A Comprehensive Workbook for Managing Your Symptoms and Achieving Your Life Goals.

Fully accepting the diagnosis is “almost like joining the priesthood,” Parikh says. “The commitment to treatment is a major one that involves going to the doctor regularly and paying a lot of effort to regulating one’s lifestyle. It’s not just a commitment to medication, but a way of life.”

In his research, Parikh found that people living with bipolar 2 have greater difficulty acknowledging the diagnosis than do those with bipolar 1, which is typically characterized by clear-cut episodes of mania and depression.

The symptoms of bipolar 2 are more subtle, he explains, making it difficult to perceive the hypomania as a symptom of the mental health condition, rather than part of one’s identity. 

“Your highs are mild, your brain is working faster, you have more confidence and energy, you need less sleep — it’s the ideal human condition,” says Parikh. Because hypomania is less obvious than mania, “it is difficult to conceptualize it as an illness,” he adds.

Personal Research, Reflection, and Ultimate Acceptance of the Diagnosis

In his 20 years as a Methodist minister, Ron M. encountered people with bipolar disorder — there was the female parishioner who had threatened him with a knife, and the wild young man who had stripped off all his clothes. Because Ron associated the illness with such extreme behavior, he missed his own symptoms when they began in early 2003. He attributed his racing thoughts, restlessness, and crying jags to depression.

His behavior resulted in Ron being placed on disability leave by his denomination; he began seeing a psychiatrist and a therapist and started taking an antidepressant. Eight months later, Ron was diagnosed with bipolar 2 and prescribed a mood stabilizer.

He continued to tell himself he was “only” suffering from depression, however.

“I was convinced that if I could tough it out, I’d be fine,” he says. “I told myself, ‘There is no way I’m bipolar.’”

During this period, his marriage of 20 years ended. Looking back, Ron says it was this denial that prevented him from getting adequate treatment. Despite his skepticism, Ron began reading about bipolar disorder and keeping a mood chart.

By the summer of 2004, he had accepted his diagnosis. “The research indicated that my moods and cycling were pretty consistent with the disease,” he says.

Since this breakthrough, life has “gotten a lot easier,” Ron says. He is more open-minded about taking medication. And by continuing to chart his moods, he can predict the ups and downs

“I will have five to seven good days and then I will crash and have about seven to 10 dark days,” he says. “You can almost set your watch by my cycling.”

Meanwhile, a series of changes have enriched Ron’s life. He moved from St. Louis to Tucson to be near family and friends; medication adjustments have brought him greater wellness, and he fell in love and remarried.

“When I grieve for how my life used to be, I remind myself that if it was like it used to be, I would never have met her,” he says of his wife.

Because of his rapid-cycling, Ron, now in his fifties, does not believe he will be able to lead a congregation again. However, he finds great fulfillment in helping others as president of the Tucson chapter of Depression and Bipolar Support Alliance (DBSA).

“I force myself to go to meetings when I’m not feeling good,” he says, “And when I am feeling good, I need to go so I can share with someone to help them in their time of struggle.”

Stigma, Discrimination, and Denial of Bipolar

Indeed, the stigma and discrimination associated with mental illness is a huge barrier to coming to terms with bipolar, consumers and experts agree. It is because there are so many misconceptions and preconceptions about mental illness that Dr. Ludman hesitates using phrases like “accepting the diagnosis.”

“I’m not very fond of labels,” she explains. “Everyone has their own story of what ‘accepting’ [the illness] means. It may mean ‘I’m crazy,’ or ‘No one loves me.’”

Jo R., an executive assistant for an Atlanta-based optometry association, resisted her 1997 diagnosis for eight years. To her, bipolar disorder meant that she could no longer trust her own mind.

“After 36 years of living, I couldn’t think my thoughts were incorrect,” says Jo, who grew up in poverty in the small hamlet of Jasper, Florida. “I was intelligent and had accomplished a lot, so I couldn’t be ‘crazy.’”

Jo told herself that her sleeplessness and psychoses were side effects of her antidepressant. Denial cost her deeply: She lost two jobs, resulting in bankruptcy and the loss of her home. But it was not until she spent a week in a state mental hospital that the reality of her situation fully hit.

“There was a beautiful woman there who yelled and barked like a dog; there was another girl who urinated on herself,” she says. “The people there were ‘crazy,’ and I was among them, so I was one of them. I told the doctor, ‘I’m ready to do whatever I need to do to manage this.’ That’s when I accepted the diagnosis.”

Jo made good on her promise, learning all she could about bipolar and what she needed to do to stay well. Today, she works full-time and has her own apartment. She keeps a mood chart and a journal, exercises, takes her medication, and avoids “toxic” people.

Indeed, Jo is so vigilant about maintaining her downtime and getting enough sleep that friends and family know not to call her after 9 p.m. She carefully tracks her spending, keeping to a strict budget, and recording all her purchases.

“The bipolar diagnosis has been a true blessing,” Jo now will tell you. “Having bipolar forces you to change to be the best you can be … to live a good life.”

Moving Toward Accepting and Embracing Your Bipolar

The first step following a diagnosis of bipolar — even before medication — should be learning about your illness, says Parikh. “It is the single most effective remedy aiding acceptance. You’re not going to follow any treatment plan unless it makes sense to you.”

Mental health experts generally agree that accepting the diagnosis makes it easier to follow a treatment plan. Yet disagreement exists as to how to best approach patients who are in denial. Gary S. Sachs, MD, founder and director of the Bipolar Clinic and Research Program at Massachusetts General Hospital and an associate professor of psychiatry at Harvard Medical School, doesn’t “push acceptance as a requirement.”

“Many patients will be willing to accept some form of intervention if I don’t require that they accept the label as well,” he says.

“Ambivalence about treatment is kind of the norm,” agrees Mark S. Bauer, MD, professor of psychiatry at Harvard Medical School, director of the Harvard South Shore Psychiatry Residency Training Program, and a coauthor of Overcoming Bipolar Disorder.

“Studies show that only 20 percent [of consumers] come to treatment fully on board,” says Dr. Bauer.

Rather than try to convince skeptical patients, Bauer teaches them how to recognize their mood swings, understand how episodes have affected their quality of life, and how to control these patterns. He also helps people “develop a detailed plan for living a full life, based on their values and core goals.”

But others believe that accepting the diagnosis is integral to treating the mental health condition effectively. “By accepting what the problem is and informing yourself about the disease and treatment, you are empowering yourself to control the disease,” says Francis M. Mondimore, MD, assistant professor at Johns Hopkins University School of Medicine’s Department of Psychiatry and Behavioral Sciences and author of Bipolar Disorder: A Guide for Patients and Families.

“My message to people is that we know a lot about how to treat this problem and manage the symptoms,” says Dr. Mondimore. “You need to know all the options so you can make an informed healthcare decision. Once you’ve named something, you’ve got some control over it.”

Lise, of Vermont, grew up around mental illness. Her father died when she was 17, and her late sister dealt with a mental health condition.

“I was always in fear of being like my sister,” Lise admits. A librarian at Norwich University in Northfield, and the mother of three teenage boys, Lise had for years been treated sporadically for depression. Then a 2003 car accident — a drunk driver totaled the car she and her family were riding in — heightened her depression.

Her family doctor switched her antidepressant, and before long, Lise became manic. She left her husband and sons and moved into an apartment. Hospitalization and a diagnosis of bipolar 2 followed.

“At first, I was just dealing with the ramifications of what I had done, and was kind of in shock — how could I lose sight of my kids and my family?”

Then, Lise had to learn to live with a new diagnosis. Instead of the more socially acceptable label of depression, she had a severe, chronic mood disorder. “It was scary, and it made me sad,” she recalls.

In fact, people often “get very caught up in whether symptoms indicate depression or bipolar,” says Mondimore. “What we’re learning about mood disorders is there is a lot of overlap.” 

Although sometimes there are discrete manic or depressive episodes, people can also experience mixed episodes, which have symptoms of both.

As time goes on, we probably won’t even have separate categories for depression and bipolar. Instead, there will be a classification for mood disorders.”

Lise found that her family history actually strengthened her resolve to reclaim her life. “I lost my father … and I will not do that to my kids, no matter how hard it is,” she says. “I go get help as soon as I feel those thoughts coming.”

Medication Can Make a Difference in Bipolar Mood Management

Medication adherence is the biggest roadblock to fully accepting bipolar disorder, according to Mondimore. “That is the hardest thing — admitting that you are not always able to control your emotional life,” he says.

But these feelings subside with the support of loved ones and by undergoing psychotherapy, he adds.

Side effects are a more tangible reason people refuse, or go off, psychotropic medication. For example, Jo had to learn to live with a 100-pound weight gain and hand tremors.

For her part, Julie initially refused to take lithium because it was so heavily associated with bipolar disorder. “I had talked myself into thinking I had bipolar-lite — that I had a very mild version of what other people had,” she says wryly. “Friends also told me not to take it — that I could manage without it.”

But then Julie began cycling more noticeably. “One week I would be excited and the next, I would think the world was ending,” she says. “My therapist said lithium would help that.”

It can also be deeply frustrating to accept that medications can only manage, not cure bipolar, Ludman points out.

The notion of having to take pills every day for the rest of her life intimidated Wendy L., of Owensboro, Kentucky, who has “trouble doing anything routinely.” But there was a more basic reason Wendy at first resisted medication: “I liked my manic highs — I felt very productive. I didn’t want them taken away,” she says.

After discussions with her husband, however, Wendy decided that, for his sake, she needed to stabilize her moods. “We’d been married for 30 years and I put my husband through hell those 30 years,” she says.

Diagnosed at age 50, Wendy has gradually learned to live with “flat” moods. “I was used to flying high and feeling all these ranges of emotions, and that wasn’t there anymore.”

Missing the soaring highs and bursts of energy leads many to stop their medication and land back in the hospital. “It’s very common for patients to stop taking mood-stabilizing medication when they begin to feel better,” Ludman says.

Social Support to Stay on Track With Bipolar Treatment

Dr. Sachs believes that having someone in your life to help you stay on track is so crucial for individuals with bipolar that he helps those who don’t have an existing support system to develop one. “Mood disorders include periods when your perceptions are distorted, so the most important thing to include in your treatment plan is a care partner,” he says.

Those fortunate enough to have a loved one willing to join them on the road to recovery travel a less lonely path. “My husband educated himself. We sat down, talked about the symptoms, signs, and different triggers that had happened over years,” says Wendy. “He was willing to work through the changes. He was so accepting of it that it helped me accept it.”

You don’t have to be in a romantic relationship to find support — an understanding boss who lets you come to work a bit later because a new medication is making you sleepy; family and friends who visit you in the hospital; or a relative with bipolar who shares what worked for him — all can contribute to your wellness.

Julie, who was living in a small town when she came out as a lesbian, believes society is more accepting of homosexuality than mental health conditions. “In my office, I don’t care if people know I’m gay,” she says. “The few co-workers who do know about my bipolar will be like, ‘So are your meds working now?’ as if I’ll get on some meds, and then I’ll be ‘normal.’ That’s not going to be it — I’ll have to manage my bipolar — even when I’m well.”

When Julie told her boss she had bipolar, the woman, who is also a good friend, responded: “You are still the same person. Nothing has changed, except that you know something about yourself that can make you feel better.”


UPDATED: Printed as “Accepting The Diagnosis,” Summer 2009

Donna Jackel

Donna Jackel specializes in mental health, animal welfare and social justice issues. She earned a bachelors degree in journalism at the S.I. Newhouse School of Public Communications at Syracuse University. For 15 years, Donna was a staff reporter at the Democrat and Chronicle, a daily newspaper in Rochester, NY, where she still lives. As a freelancer, in addition to contributing to bp Magazine and esperanza, Donna’s work has appeared in ReWireThe ProgressiveLilithTexas MonthlyYes! MagazineThe Chicago TribuneBark MagazineCityLab, Leap Magazine and other national publications. A story Donna wrote about her mother’s (Marie Rogers) service in the British Air Force during World War II was included in the anthology, Before They Were Our Mothers: Voices of Women Board Before Rosie Started Riveting (copyright 2017). In 2019, Donna won an honorable mention in health writing from the American Society of Journalists & Authors for a feature story she wrote for The Progressive about college students who were denied transgender hormone therapy. When Donna isn’t working, she can be found hanging out with her Lab, Bear, horseback riding or catching a movie at the Little Theatre. Her work can be seen at donnajackel.com.

Melinda

Celebrate Life · Chronic Illness · Health and Wellbeing · Medical · Men & Womens Health · Self-Care

Barometric Pressure May Affect Fibromyalgia Symptoms


Medically reviewed
 by Angelica Balingit, MD — Written by Alysa Hulletton August 19, 2024

Lower barometric pressure is associated with higher self-reported pain scores in fibromyalgia patients, but more research is needed to determine causation. 

People with fibromyalgia often report that the weather, particularly the barometric pressure, affects their symptoms. 

Also called atmospheric pressure, barometric pressure is the amount of air pressure in the atmosphere. It is higher when oxygen molecules are more concentrated and is basically a measure of the heaviness of the air at a given time.

The thinking behind this theory is that when barometric pressure drops, the “lighter” air may make joints, tendons, and muscles swell to compensate, causing pain.

While there’s evidence to support the idea that air pressure does indeed affect conditions like arthritisheadaches, and generalized chronic pain, so far, the research on the link between barometric pressure and fibromyalgia is limited. Here’s what to know.

In a 2019 studyTrusted Source of 48 patients with fibromyalgia, researchers compared self-reported pain scores over a 30-day period with local weather data. They found lower barometric pressure to be strongly correlated with higher pain scores in the majority of patients studied. The breakdown was as follows:

  • 40 out of 48 patients reported more pain on lower barometric pressure days. 
  • 8 out of 48 patients reported more pain on higher barometric pressure days. 

Researchers noted that the second subgroup had lower baseline anxiety levels than the control group. Lower barometric pressure was also linked to higher stress levels. As a result, scientists speculated that there may be a mental-emotional component to pain levels in those with fibromyalgia, though it’s not yet well understood. 

Other key findings include the following:

  • Higher humidity was associated with higher pain scores.
  • Colder temperatures were associated with higher pain scores.

In a 2021 studyTrusted Source, researchers found that 58% of 64 patients with fibromyalgia said weather-related factors aggravate their symptoms. Here are some other key findings:

  • Researchers used a self-reported quality-of-life measure where 1 is perfect health and 0 is many health difficulties. On average, fibromyalgia patients reported a score of 0.55.
  • Researchers found that the 37 people with weather sensitivity had worse quality of life scores (by an average of 0.16 points) than those who didn’t report weather sensitivity. They also reported an average of 1.5 more pain points on a scale of 0 to 10.

Keep in mind that these sample sizes are small and that there are few studies on the link between barometric pressure and fibromyalgia in particular. Although there appears to be a strong association, scientists have not conclusively shown that barometric pressure causes increased pain.

However, in a 2020 study of 10,584 patients with chronic pain, researchers also found a strong association between lower barometric pressure and higher pain scores over the course of 15 months. About 26% of those surveyed had fibromyalgia, while the rest had other health issues, including various forms of arthritis, neuropathic pain, headaches, and migraine episodes.

Based on the (somewhat limited) data, the best weather for those with fibromyalgia appears to be

  • higher barometric pressure
  • lower humidity
  • less rain
  • calmer winds
  • warmer temperatures

Keep in mind that fibromyalgia flare-ups tend to be individualized, with some patients reporting increased pain on higher barometric pressure days, for instance. Many people with fibromyalgia also don’t report experiencing weather-related sensitivity at all.

As noted above, fibromyalgia symptoms tend to be highly individualized, so it’s challenging to pinpoint the optimal climate for those with fibromyalgia.

However, since many people with fibromyalgia report improved symptoms with warmer weather, less rain, and less humidity, desert regions may offer the most relief. In fact, there are many anecdotal reports of people living with fibromyalgia experiencing pain reduction after moving to these areas.

In the United States, this includes regions like:

  • The Mojave Desert, which covers parts of southeastern California, southern Nevada, southwestern Utah, and northwestern Arizona. This includes areas around Las Vegas and Death Valley.
  • The Sonoran Desert, spanning parts of southern Arizona and southeastern California, including areas around Phoenix and Tucson.
  • The Chihuahuan Desert, which covers parts of southern New Mexico and west Texas, including areas around El Paso.
  • The Colorado Plateau, including parts of southeastern Utah, northern Arizona, northwestern New Mexico, and southwestern Colorado. While this region can have cooler temperatures at higher elevations, lower areas often meet the criteria.
  • The Great Basin, including parts of Nevada, western Utah, and southeastern Oregon. Some areas, particularly at lower elevations (such as Reno), meet most of the criteria.
  • The Southern California Interior, including inland areas of southern California such as the Coachella Valley (where Palm Springs is located) and Imperial Valley.

Will climate change affect fibromyalgia symptoms?

So far, there’s no evidence that climate change will affect fibromyalgia symptoms. However, since climate change is associated with moisture evaporation that worsens severe rainfall, increased rain and humidity may affect people negatively in some regions.

Meanwhile, hotter temperatures shouldn’t negatively affect those with fibromyalgia and may even improve symptoms for some. On the other hand, climate change is also associated with more frequent and more severe storms, so those experiencing pain during times of shifting barometric pressure may be negatively affected. 

Potential strategies for managing weather-related fibromyalgia pain include the following:

  • Monitor your symptoms and local weather patterns to identify your unique triggers. A symptom journal may be helpful with this. 
  • Use climate control support in your home, including dehumidifiers, to reduce moisture in the air.
    • You may also want to keep your home at a slightly higher temperature or use a heating unit (e.g., by your desk or bed) to reduce symptoms. Heated blankets may also help lend relief at nighttime or while lounging on the couch. 
  • Talk with your doctor about your symptoms and discuss adjustments to your pain medications. 

Remember, treating fibromyalgia typically requires an individualized, multifaceted approach. Learn more about general treatments for fibromyalgia.

While research into the relationship between weather and fibromyalgia pain is ongoing, evidence increasingly supports a connection between lower barometric pressure and higher pain scores in fibromyalgia patients.

Keep in mind that everyone with fibromyalgia is different, with many people saying that they don’t experience any weather-related sensitivities at all. Ultimately, understanding your personal triggers can help you better manage your symptoms and improve your day-to-day quality of life.

Melinda

Celebrate Life · Chronic Illness · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Moving Forward

Health Update September 2024

Over the past six months, my health has gone haywire, and the past two have been the worst. I’ve been working closely with multiple specialists including keeping them up to date with the ongoing symptoms. None are concerned about my quality of life and I hit a wall this week. I contacted The Mayo Clinic, one of the top hospitals in America, and now have an appointment for next month.

The greatest thing about going to The Mayo is they have a team of specialists working on your case, giving them a bigger picture of what is happening. I’ll be there for at least seven days and they will be full of tests, blood work, and meetings with specialists. Your days are full from when you arrive until they have an answer. It’s exhausting but you get what you came for which will improve your health.

I stayed at The Mayo for a week in 2010 so I have an idea of what I can look forward to. At the time I had been having issues with my heart for two years, I had worked with two cardiologists and had been through multiple catheterizations but no answers. I was experiencing what I now know is Supra Ventricular Tachycardia, it’s just like having a heart attack but you’re not. These events were happening every day and sometimes multiple times. It was so painful and you never knew when they would happen. I had Nitro for when they started but it often didn’t work.

After a week of intensive tests including a catheterization, I had the answers. Luckily nothing major was wrong with my heart, several small things were causing the arrhythmia. I took medication for a short time and have only had issues when my potassium is low.

I am looking forward to the day when my health has improved, my quality of life has improved and I have answers.

Melinda

Chronic Illness · Communicating · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Mental Illness · Moving Forward

How to Tell Others About Your Bipolar Disorder

By

Julia Métraux

Medically Reviewed

by

Allison Young, MD

Published on September 26, 2023

While some people may not struggle to tell friends, family members, or an employer about their bipolar disorder, for others it can feel very nerve-racking. These 7 tips can help.

At age 31, Julie A. Fast — now a bipolar disorder expert and researcher — was diagnosed with the condition. Later on, she was diagnosed with schizoaffective disorder, bipolar type (a psychotic disorder involving symptoms of both schizophrenia and bipolar disorder).

Bipolar disorder wasn’t entirely new to Fast, now 59, when she was diagnosed. Her partner at the time was diagnosed with the condition in 1994, just one year before.

Still, in her social circles, she found that most people did not know or understand her condition. “I’d go to a party, and maybe two or three people would say, ‘I know of bipolar disorder,’” says Fast, who coauthored the book Take Charge of Bipolar Disorder with John Preston, PsyD. 

Because awareness of bipolar disorder and its symptoms is increasing, many people with the condition, like Fast, feel more comfortable sharing their diagnosis with others. “I can deal with whatever happens when I disclose my illness to others,” Fast says. “It will show who can help me and who can’t.” 

But some people with bipolar disorder may still feel hesitant to share their diagnosis, in part because of stigma and fear about how others will respond, experts say.

Why Sharing a Bipolar Disorder Diagnosis Can Feel Challenging

Factors like shame, embarrassment, or stigma — negative and often untrue beliefs society holds about someone or something — make some people with bipolar disorder feel hesitant to talk about their condition, research shows.

Many people with bipolar disorder experience a form of stigma called “public stigma,” which is related to how other people view and act toward people with bipolar disorder, according to research published in February 2022 in the Australian & New Zealand Journal of Psychiatry. Public stigma is linked to more anxiety symptoms, worsened ability to function, and problems at work, per the same research.

Although public stigma can come from anyone around them, many people with bipolar disorder experience it from people close to them — family, friends, or even their healthcare providers, per the same report.

Fear of how others may respond as a result of stigma is another potential barrier. “They may worry that disclosure could negatively affect their relationships with friends, family, or romantic partners,” says Leanne Quigley, PhD, an assistant professor in clinical psychology at Yeshiva University in New York City.

Public stigma and how others view bipolar disorder can lead many people with the condition to feel negatively about themselves, according to the aforementioned report.

“[They] may also experience internalized stigmas where they report low self-esteem, low quality of life, and limited engagement in their communities,” says Adrian Jacques H. Ambrose, MD, MPH, the medical director of the psychiatry faculty practice organization at Columbia University in New York City, who treats people with bipolar disorder. This is what’s known as “self-stigma,” per the aforementioned report.

RELATED: A Therapist Speaks: What Is Bipolar Disorder Stigma, and How Can We End It?

When to Tell Someone About Your Bipolar Disorder Diagnosis

The decision about when to share your diagnosis with someone else is very personal. It can depend on the type of relationship you have with the other person and whether they seem to have some sort of understanding of conditions like bipolar disorder.

When It Comes to Your Significant Other or Someone You’re Dating …

For romantic relationships, Fast recommends sharing a bipolar diagnosis as soon as possible. “I don’t really support the idea of getting in a relationship with somebody unless you have fully discussed the impact of bipolar on the relationship,” Fast says.

That’s important because the symptoms can affect the way someone with bipolar disorder thinks, feels, acts, and communicates with their partner, according to the United Brain Association. For instance, during a manic episode, someone with bipolar disorder may experience intense irritability toward their partner or may have a higher chance of engaging in risky behaviors like unprotected sex or heavy spending, which could lead to tension or mistrust in a relationship, per the United Brain Association. 

If you haven’t talked about your condition with your partner, it can be difficult for them to know what to say or do to help.

When It Comes to New Healthcare Providers …

It’s also crucial to be up-front about your diagnosis with any new healthcare providers you see, Fast Adds. They need to know about your health history and any medications you take. Research shows that certain medications, such as corticosteroids like prednisone, can trigger mania and psychosis in people with bipolar disorder.

That’s why Fast told her doctors before a recent minor surgery that she was not comfortable being prescribed steroids, which are sometimes used to help reduce inflammation. “When they suggest steroids, and so many doctors use steroids, I explain why I can’t use them,” she says, adding that her doctors were receptive to her needs.

Some antidepressants, such as fluoxetine (Prozac),  also trigger mania in people with bipolar disorder.

When It Comes to Your Friends and Family …

When it comes to telling friends and family, it might take you some time to feel comfortable doing so — and that’s okay. Prioritize telling close friends and family members that you interact with frequently and who you feel understand you well — rather than people you rarely interact with, Fast advises.

Before sharing your diagnosis with friends or family, Dr. Ambrose recommends asking yourself the following questions:

  • Do you feel ready to share?
  • Is there anything pressing or urgent happening that makes it important to tell them sooner rather than later, such as the onset of a mood episode?

When It Comes to Your Employer …

When it comes to your work environment, it’s important to weigh the possibility of discrimination, says Ambrose. You could look to see if the company has in recent years tried to reduce mental health stigma, which research suggests could make the workplacemore welcoming for workers with mental health conditions. 

And if you don’t feel comfortable revealing your specific diagnosis, that’s okay. You can still bring a note from your healthcare provider asking for accommodations based on how your mental health condition impacts your functioning, according to the U.S. Equal Employment Opportunity Commission.

7 Tips for Talking About a Bipolar Disorder Diagnosis

If you feel ready to share your diagnosis with someone else, here are seven expert tips to get the conversation started.

1. Prepare Yourself for All Sorts of Reactions

Just as people diagnosed with bipolar disorder may have a range of reactions to their diagnosis, reactions from others can vary, too. “We can allow the other person to ask whatever questions they want, have any type of response that they want,” says Fast.

Although some people may react positively to hearing about your diagnosis, others may react in a negative way. “Remember that your self-worth is not determined by a diagnosis of bipolar disorder or others’ reactions to your disclosure of a diagnosis,” Dr. Quigley says.

2. Talk About How Your Bipolar Symptoms May Affect Others

During a manic episode, some people with bipolar disorder may be more prone to engaging in risky or hurtful behaviors, such as cheating or lying. This can be common for people who are undiagnosed, Fast adds.

Whether you’ve just gotten your bipolar disorder diagnosis or you’ve received treatment for a new mood episode, it could help to reach out to people who may have been harmed by your words and actions during the episode. It could be a message like, “I’d love to talk to you about my diagnosis because I know my behavior impacted you,” says Fast.

But it’s important to recognize that not everyone will want to engage in this conversation, especially if they feel really hurt by actions like cheating or stealing, for instance, Fast adds.

If behavior related to a bipolar diagnosis hasn’t yet come up in your relationship with someone else, the person you’re telling may have questions about how it could affect the relationship in the future. Be prepared to discuss how any episodes could manifest.

3. Have a Summary on Hand

After sharing a bipolar disorder diagnosis, some people may have follow-up questions about your symptoms or, in the case of work, any accommodations you might need. “In certain situations, your loved ones [or employer] may know very little about mental health conditions, so it may be helpful to prepare a short summary about the condition,” Ambrose says.

The summary could be either written or verbal (or both), depending on what you’re most comfortable with.

4. Work With Your Therapist on a Plan to Tell Others

If you feel nervous or worried about sharing your diagnosis with others, your doctor or therapist could help you come up with the best strategy for you for sharing your diagnosis, says Fast. “Share most of your concern and your worries with your healthcare professionals because they’re trained to handle it,” Fast says.

5. Understand Your ADA Rights (and Note That They Vary by State)

While the Americans with Disabilities Act (ADA), which prohibits discrimination against people with disabilities at work and all other areas of life, is a federal law in the United States, some states offer more protections than others when it comes to employment laws related to disability discrimination, says Ambrose.

“Given the complexity of work-related rights, you should learn more about your specific state’s legal statutes,” Ambrose says.

If you’re in an area with less protection, it might be worth talking to a third party, for example your state labor office, about the best approaches for disclosing a bipolar diagnosis at work. State government offices belonging to the U.S. Department of Labor can help you better understand your rights as a worker in the state you live in. The Department of Labor has a directory of state labor offices.

6. Offer Different Information in Different Situations

If you’re only comfortable disclosing the entirety of your diagnosis to some people and not others, that is perfectly fine. “You may choose to discuss certain parts of your experience with bipolar disorder and not others,” Quigley says. “It is okay to maintain boundaries and not share everything.”

7. Give Yourself Grace

It can be difficult to figure out how to tell others about your diagnosis. It’s important to take care of yourself during this time. “It’s even more important to cultivate a sense of empathy and grace for yourself during the process,” Ambrose says.

Julia Métraux

Author

Julia Métraux is a journalist whose work touches on disability, mental health, and chronic illness. She went to the University of California in Berkeley Graduate School of Journalism. Métraux lives with vasculitis, a traumatic brain injury, and hearing loss.

See full bio

————

I know how hard telling others about your mental illness can be, especially family members. Many family members looked at me differently because they were from a different generation that did not believe in mental illnesses. I did not tell friends or my employers because it wasn’t their business. One of my employers fired me from a high-level job because they found out I had a mental illness, yes I could have sued the billion-dollar company but why go down that multi-year road through the rabbit hole. I caution everyone to think hard before telling your employer, it can be held against you and they can find a way to fire you.

Melinda

Celebrate Life · Fun · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Moving Forward

The Paralypmics Is Coming To An End On the 8th

The Paralympics is a great joy for me to watch, it’s a world stage showcasing people who are disabled performing a sport they have achieved great talent in. The athletes don’t get special treatment, what you see is the pure grit of each athlete competing with another disabled athlete for the top honors. Each of the athletes has endured setbacks in life and on the field. I admire the commitment they have made to the sport and then go on to push themselves to make the Paralympic team. This in itself tells you so much about the people competing in the Paralympics. They are all winners in my book, everyone who participates is a winner and needs to take tremendous pride in returning to their home country.

Paralympics 2024: Know Facts, Figures, Venues, List of Sports - Edudwar

If you would like to participate in the closing ceremony it is happening on Sept. 8, 2024, at  13:30. The opening and closing ceremonies are thrilling to watch.

Melinda

Celebrate Life · Health and Wellbeing · Medical · Mental Health · Self-Care

What’s Your Mood Today?

 I’m feeling a bit down today, fighting my health issues makes me tired. I want someone to comfort me and tell me it will get better.

I hope this post finds you happy and healthy.

 Melinda

Celebrate Life · Chronic Illness · Communicating · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Mental Illness

12 Celebrity Quotes That Perfectly Describe Life With Bipolar Disorder

By Tanya Hvilivitzky 

When famous people share their personal battles with bipolar disorder, it serves as a reminder that no one is isolated in this struggle. After all, bipolar disorder is indifferent to wealth, fame, or success.

It’s easy to believe that celebrities — actors, musicians, or comedians — enjoy lives of perfection. However, what is publicly seen represents just a fraction of their actual lives. The truth is, bipolar disorder doesn’t discriminate. It makes no distinction between a person’s age, gender, race, or bank account size.

So, when stars living with bipolar disorder share their own struggles, it signals to others that they are not navigating the complexities of this brain-based disorder alone, reinforcing the message that, together, managing it is within reach.

Here are personal and powerful quotes from 12 such celebrities:

1. Taylor Tomlinson

It took a little while for comedian Taylor Tomlinson to accept her bipolar diagnosis. She explains to E! News her reaction upon learning about her mood disorder. “I was surprised that I felt embarrassed when I first found out. Because I think I’m very open-minded. I have friends who have bipolar. And you never judge your friends. You never felt like that was a big deal. But then when it’s you, you somehow realize you have all this deeper stuff from when you were a kid.”

2. Cameron Esposito

After telling her fans earlier this year of her bipolar diagnosis, Cameron Esposito, standup comic, actor, and writer, took to her Instagram channel on her birthday in October 2023 to reflect on the year: “… you know what? I’m lucky. I’m lucky that I figured it out. I’m lucky that I had a place to go. I’m lucky that I was enough in my faculties that I was extremely persistent with following up after that experience, and getting my meds and finding a psychiatrist. All that s&*t is impossible and so expensive. I have healthcare coverage; I have insurance. I just want to say to anybody who’s had to navigate this [mental health care] system … you are a hero! Look at you! Look at what you’ve been able to do!

3. Alan Ritchson

Actor Alan Ritchson, star of Prime Video’s Reacher, was diagnosed with bipolar at age 36. In a February 2024 interview with CBC Radio’s “Q” program, Ritchson explains why he’s been sharing his story to help others: “As much as I would like to ignore that I’m a suicide survivor, if I didn’t share what I’ve learned I feel like my life would be meaningless,” he says. “I’ve always been a happy-go-lucky guy, but once you experience the grip [of depression] — the talons it can sink into you — you realize how sinister this thing is and how out of control the biology can really be for somebody in the midst of it.”

4. Carrie Fisher

“In my opinion, living with manic depression takes a tremendous amount of balls. Not unlike a tour of Afghanistan (though the bombs and bullets, in this case, come from the inside). At times, being bipolar can be an all-consuming challenge, requiring a lot of stamina and even more courage, so if you’re living with this illness and functioning at all, it’s something to be proud of, not ashamed of. They should issue medals along with the steady stream of medication.” — Carrie FisherWishful Drinking, 2008

5. Ye (Kanye West)

As a guest in 2019 on David Letterman’s Netflix series, My Next Guest Needs No IntroductionYe (Kanye West) uses the term “ramping up” to convey the process of entering a hypomanic or manic bipolar mood episode: “When you ramp up, it expresses your personality more. You can become almost adolescent in your expression. … When you don’t take medication every day to keep you at a certain state, you have the potential to ramp up … and even end up in the hospital.”

6. A.J. Mendez

In an interview with bp Magazine, former pro wrestler A.J. Mendez (AJ Lee) says, “I see bipolar disorder as the gift of extraordinary emotions. It makes me bold, brave, loud, and capable of withstanding whatever obstacles the world throws at me. It has made me empathetic. It has given me a lofty imagination, a belief in the impossible, and has made me confident beyond reason. I was 90 pounds and five feet tall and believed I could succeed in the world of giants … because I didn’t have that voice of doubt holding me back.”

7. Richard Dreyfuss

Richard Dreyfuss has starred in blockbusters like JawsAmerican GraffitiClose Encounters of the Third Kind, and The Goodbye Girl (which earned him an Academy Award for Best Actor). Of his bipolar diagnosis, he says, “No matter what you call it, this is an illness no different from, say, diabetes or asthma — and like those conditions, [it] should be neither ignored nor stigmatized. Feeling ashamed would mean surrendering to someone else’s judgment — an ignorant judgment at that.”

8. Linda Hamilton

The Terminator actress Linda Hamilton uses a holistic health plan to help her stability, with a structured and balanced lifestyle, exercise, and medication. “Exercise is an incredible key to feeling well. But for people with mental illness, taking care of the body is not an automatic thing. The mind is in such chaos, it’s hard to come up with a plan. So, to people like us, it’s more important than ever to follow a regimen.”

9. Maurice Benard

Daytime actor Maurice Benard — who plays Michael “Sonny” Corinthos Jr. on General Hospital — talked with bp Magazine on life with bipolar“I’ve lived a productive life having bipolar. I’ve talked to people who don’t want to talk about [having bipolar] because it’s embarrassing. I’m proud of it because I know it’s made me the actor I am and the person I am. It’s given me strength. If I can go through being in a mental hospital, and that kind of pain, and that kind of fear, I can do anything.”

10. Maria Bamford

In an interview with bp Magazine’s Melody Moezzi, the comedian Maria Bamford talked about being diagnosed: “I was surprised how prejudiced I was against myself. They tell you it’s the brain chemistry also working its magic, but I was really surprised at how resistant I was to going on a mood stabilizer, taking any time off of work, acknowledging that I needed to be hospitalized. I was just so angry. I didn’t want to go on the meds. It wasn’t until it got bad enough to where I was starting to feel unsafe by myself that I reconsidered.”

11. Stephen Fry

In an interview with bp MagazineStephen Fry said of creativity, “It is not a coincidence, it can’t be, that so many comedians suffer from depression. As for whether the hypomanic side of bp can be said to help creativity, I hesitate to say yes because of all those out there living with the disorder who are not in creative industries. … But certainly, the energy, self-belief, exuberance, tirelessness, optimism, and, yes, grandiosity that mark out hypomania can really help one achieve much in terms of writing and creation.”

12. Mariah Carey

In 2018, during an interview with People magazine, Maria Carey spoke about the confusing ups and downs of bipolar disorder: “For a long time I thought I had a severe sleep disorder, but it wasn’t normal insomnia. … I was working and working and working. … I was irritable and in constant fear of letting people down. It turns out that I was experiencing a form of mania. Eventually, I would just hit a wall. I guess my depressive episodes were characterized by having very low energy. I would feel so lonely and sad, even guilt that I wasn’t doing what I needed to be doing for my career.”

UPDATED: Originally posted June 19, 2020

Tanya Hvilivitzky

Tanya Hvilivitzky has spent more than 30 years in the communications field — a career that has included stints as an investigative journalist, managing editor for a lifestyle and wellness magazine, corporate communications director, and researcher/writer. She has been with bpHope (and bp Magazine) since 2016, serving in roles such as features editor, interim editor, and, currently, senior editor. She has been devoted to mental health awareness since she was the editor of Schizophrenia Digest in her early days, and now with a particular focus on highlighting the complexities of bipolar disorder through compassionate, service-based journalism. As an award-winning writer/editor, Tanya received the Beyond Borders Media Award for her 2012 investigative exposé about human trafficking for Niagara Magazine. Her work on this critical topic also earned the Media Freedom Award “Honouring Canada’s Heroes” from the Joy Smith Foundation to Stop Human Trafficking.

I dislike what Carrie Fisher had to say. It’s not appropriate to compare an illness to those who fought in Afghanistan and I do not think people with Bipolar Disorder deserve a medal and more medication. My thoughts about her have remained the same, she used her Bipolar Disorder as an excuse for her bad behavior and to make money. My opinion. 

Melinda

Celebrate Life · Chronic Illness · Health and Wellbeing · Medical · Men & Womens Health · Mental Illness · Moving Forward

Denial in Bipolar Disorder: The Manic Fallacy of Wellness

By June Rawlston 

Last Updated: 7 Aug 2024

During my first manic episode, I was convinced I’d finally recovered from my chronic depression. But my therapist saw symptoms of bipolar disorder.

I’m a doctor by training, so you’d think I would have guessed I had bipolar disorder, for heaven’s sake. I certainly manifested every symptom of mania in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), from boundless energy and soaring spirits to severe insomnia.

I should have known something was up when I treated myself to a $4,000 antique French buffet table. (The credit card company considered shutting down my account, but I convinced them that my finances were under control.)

I subscribed to delusions of grandeur, scouring my home for a spot to exhibit the writing award I was guaranteed to win. My sexual appetite spiked to new heights, too (no complaints from my guy on this point).

Friends and Loved Ones Were Baffled by My Behavior

Certainly, my friends and loved ones noticed a bizarre new me bursting onto the scene. One friend, irritated by my self-absorption, said she felt I had come across “like a bomb exploding in my face.”

My boyfriend raised his voice at me for the first time in our friction-free relationship, because I was passionately scrubbing his bathroom at 3 a.m.

A fellow choir member, flabbergasted at what I took to be my brilliant plans to eradicate mental health conditions in the world, shot me a disbelieving look and said, “I’ve never seen you like this.” I wasn’t sure whether he was worried or jealous.

RELATED: Do You Know These Symptoms of Bipolar Mania?

Delusions of Wellness

To me, it just seemed like I had reached a pinnacle in my life after years of chronic depression. I couldn’t wait to thank my psychiatrist for his contribution to my greatness. I wrote him a card saying I had completed my arduous journey to wellness and would no longer be requiring his services.

Instead of clapping and stomping his feet for me, my doctor became more and more appalled as I tried to convince him of my freedom from the frenzy. I, in turn, became furious at the party pooper for raining on my parade.

It wasn’t until he called my sister and begged her to come watch over me that I began to entertain a sliver of doubt.

My sister, a family physician, hopped on the next plane and flew down to Toronto to babysit me and dispense copious amounts of medication and advice. If anyone can convince me of anything, it’s my sister. (She persuaded me that I was adopted when I was 12 — it took my parents months to undo the damage.)

Bit by bit, her certainty that I was experiencing a psychotic episode superseded my insistence that everything was great.

Before 24 hours had passed, I was loaded up on heavy-duty doses of antipsychotics. I actually slept through the night.

By the end of the week, I had come down to earth.

Lack of Insight and 20/20 Hindsight

Looking back on my current (and carefully managed) stability, I’m still blown away by the depths of my denial. After all, I had been exhibiting a textbook case of mania. Why hadn’t I used my medical judgment to uncover my self-evident diagnosis?

I was so certain that I was just happy, at last, and I was furious at those who wanted to pathologize my well-earned contentment.

My sister reminded me of something I already knew: My lack of insight was not my fault; my delusion of wellness was part of the symptom package of mania.

I shudder to think what might have happened if my mania had continued unchecked. My psychiatrist told me I was hours away from requiring urgent hospitalization. I’m lucky that he and my sister prevailed on me to accept that I was unwell instead of special.

I’m also fortunate that my first manic episode led to a diagnosis of bipolar. With my new drug regimen (including a mood stabilizer) and lifestyle changes (regular running, a balanced diet, and mindfulness meditation), I feel a sense of peace I’ve never experienced before. For the first time in my life, I have faith that I will be okay.

UPDATED: Printed as “On My Mind: Queen of Denial,” Summer 2013

June Rawlston

June Rawlston is a pseudonym for a Toronto physician who is forging a new career as a writer.

————-

When you’re manic you think you are on top of the world, magnified creativity, and know better than others, rarely listen to logic when it comes to your behavior, quite simply you don’t want the high to end. The truth is it always ends and the higher you go the further you fall. When you fall you may find yourself disoriented, or not knowing where you are, It’s extremely frightening.

Recovering from a manic episode depends on how hard you hit the ground and what happened while you were manic. The recovery time could take months possibly even longer. It’s a long climb up. This is why I keep a close look each day to see if my mood is elevated, it can go from joy to sheer madness very quickly. The key is to track your moods, be aware that your mood is escalating and reach out for help if you continue to escalate.

I spent close to 10 years hypo manic or manic before I fell down the rabbit hole. Crawling out was not pleasant and I spent several weeks in a Psychiatric Hospital to recover.

Stay aware and don’t be tempted by the escalated state, it will bite back.

Melinda

Chronic Illness · Health and Wellbeing · Infectious Diease · Medical · Men & Womens Health · Tick Borne Illnesses

Fighting to save our lifeline of Glutathione, B12, and more

by Crystal A. Frost

AUG 23, 2024

The daily life of a Lyme warrior can be unpredictable and terrifying—whether it’s managing debilitating symptoms or navigating a healthcare system that rarely understands our needs.

So when my doctor told me in June, “Your Lyme treatments could be outlawed soon,” I knew another fight was on the horizon.

This time though, it wasn’t just about my health. It was about standing up for every patient in California who relies on glutathione therapy, NAD+, and methylcobalamin.

The California State Board of Pharmacy (BOP) is trying to take dozens of natural compounds away from us. But they’ve messed with the wrong Lyme patient, and I’m fighting back.

The master antioxidant

For those of us with neurological Lyme disease, treatments like glutathione and NAD+ aren’t just beneficial—they’re our lifeline. Glutathione, the master antioxidant, is depleted by many illnesses including Lyme, which is why replenishing it through infusions is effective for so many.

This compound protects immune cells and helps clear out harmful toxins, reducing oxidative stress. NAD+ supports cellular repair, giving us a fighting chance against relentless fatigue and brain fog. Methylcobalamin, the active form of vitamin B12, is crucial for nerve repair and cognitive function. These treatments are not luxuries. They’re essential.

The BOP’s proposed regulations would severely limit—and, in many cases, end—access to legal Category 1 sterile compounds on the FDA 503A bulks list. If these regulations pass, Lyme patients across California could lose access to treatments that make life bearable. The worst part? The BOP has not provided a single legal, scientific, or safety-based reason why California patients should be treated differently than those in the rest of the United States.

The moment that sparked the fight

When I first heard the news from my doctor, it knocked the wind out of me. I’m no stranger to fighting, but this is different; this is a fight with no explanation. The compounds on Category 1 have an excellent safety track record, which is why they have the green light from the FDA.

In fact, patients like me often turn to these alternative medicines when standard drug therapy fails. Why does California want to supersede the FDA and deprive sick patients of treatments that work? This regulatory board exists to protect us but is instead threatening our access to the very treatments that keep us alive.

Teaming up: the birth of “Stop The BOP”

I’m not alone in this fight. At the June 18 public hearing, I learned that Jacqui Jorgeson, founder of the Volunteer Fire Foundation in Sonoma, is facing a similar battle. Jacqui’s foundation co-administers a detoxification pilot program for firefighters who face severe toxic exposure in the line of duty.

Like many of us with Lyme, California firefighters under major oxidative stress have found incredible relief in nebulized and intravenous glutathione therapy. In fact, the results from Round 2 of the pilot study showed an 85.1% reduction in environmental toxins—a true testament to the effectiveness of glutathione therapy.

When Jacqui and I connected after hearing each other’s testimonies, it was clear we were fighting the same enemy: Board of Pharmacy overreach.

Together, we launched Stop The BOP, a movement to protect patient access to these vital treatments. We started with a petition in July, and it quickly gained traction, reaching 2,000 signatures in the first month.

As of August 22, our petition has over 2,600 signatures, and our movement is publicly backed by organizations like LymeDisease.org, the Center for Lyme Action and the California Naturopathic Doctors Association.

Why this fight is personal

Before falling ill in 2020, I was a recent PhD graduate, composing music and writing articles for the GRAMMYs. I was happily engaged to my now-husband, Bram.

But when Lyme disease took over my body, it sent us off course onto an unexpectedly dark path. My brain inflammation became so severe that I was paralyzed in my left leg and arm, barely able to walk for months. The brain fog was so thick I would forget my own phone number and my friends’ names. I experienced daily anaphylaxis and constant vertigo, and for a while, I thought this was the end.

But through it all, treatments with glutathione therapy, NAD+, and B12 have been my lifeline, allowing me to reclaim pieces of my life.

If these treatments are taken away, what happens to the thousands of patients just like me? What happens if the BOP succeeds in making California the only state where these compounds are inaccessible?

For many of us, losing access to these treatments would mean a return to those darkest days—days when hope felt like a distant memory.

The broader impact: beyond Lyme disease

It’s not just Lyme patients and firefighters who will be affected. Imagine you suffer from ME/CFS and that NAD+ has finally given you the energy required to return to work. Imagine you have pernicious anemia and methylcobalamin therapy has finally restored you to healthy B12 levels. Now imagine that relief being snatched away by a regulatory board that doesn’t seem to understand—or care—about the consequences.

That’s the reality we face. It’s why Jacqui and I are so determined to fight back. It’s why we’re asking the Lyme community to stand with us. This isn’t just about a few compounds—it’s about our right to access the treatments we need to live our lives.

What you can do

We’re not giving up, and we need your help. Here’s how you can join the fight:

Sign and share the petition: If you haven’t already, please add your name to our petition. Every signature counts.

Contact Your Representatives: We’ve made it easy with templates on our website. Your voice can make a difference.

Spread the Word: Share this blog post, tell your friends and family, and help us get the word out. The more people who know about this, the stronger our movement becomes.

Voice your opposition at the 9/12 board meeting: Anyone is welcome to join the September 12 meeting online via webex or in person in Sacramento. Information and access links will be available on stopthebop.com/actnow.

Join the movement: Sign up, learn more, or donate to the cause at stopthebop.com.

Stay Informed: Follow @stop.thebop and @volunteerfirefoundation on Instagram for updates on our progress and ways you can get involved.

The strength to fight

You don’t know how strong you are until being strong is the only choice you have. For those of us with Lyme disease, that strength is something we’ve had to find over and over again. The California Board of Pharmacy might think they can push these regulations through without a fight, but they underestimate us. They underestimate the power of a community that knows what it means to fight for every ounce of health.

Together, we’re going to stop the BOP.

Follow us on Instagram @stop.thebop and @volunteerfirefoundation.

Crystal A. Frost is Southern California leader of Stop The BOP.

————n

This is indicative of what Lyme patients deal with on an ongoing basis. If a doctor can enhance your chances of recovery they don’t need an association board standing in their way. In this case, the add-ons aren’t expensive in the big scheme of things and can make all the difference for patients.

This happens because of the bias against Chronic Lyme Disease. The more doctors who deny that Chronic Lyme exists the government and insurance companies will refuse to pay for treatment. I don’t see this changing shortly because it’s all about money.

Melinda

Celebrate Life · Chronic Illness · Health and Wellbeing · Medical · Men & Womens Health · Moving Forward

September Awareness Months And Days

The main days and months you should know about for September are:

National Suicide Prevention Awareness Month September 1
Blood Cancer Awareness Month  September 1
National Food Bank Day 1st Friday
International Literacy Day September 8
R U OK Day September 9
World Suicide Prevention Day September 10
Hispanic Heritage Month September 15
International Day of Peace September 21
International Day of Sign Language September 2

National Public Lands Day                                                                                                 Saturday 4th

Achalasia Awareness Month

Alopecia Awareness Month

Animal Pain Awareness Month

Blood Cancer Awareness Month

Childhood Cancer Awareness Month

Craniofacial Awareness Month

Falls Prevention Month

Gynecologic Cancer Awareness Month

Healthy Aging Month

Hispanic Heritage Month

 

We have so much to educate ourselves on and to advocate for to make a better future. I apologize for the inconsistent graph, that is the way it was copied. 

Melinda

Communicating · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Trauma

89% Of Blind Riders Are Being Denied A Ride By Lyft And Uber

I could not believe it when I heard on the national news that 89% of blind riders were being denied a ride by Lift and Uber. This looks like a driver issue with the service dogs and not wanting them in the vehicle. This behavior is against the law not to mention the company’s policies. The riders have a way to report a driver but those interviewed said nothing happened. One woman even recorded a driver refusing her a ride after she had already reported this behavior to Lyft. Rideshare companies are condoning this behavior and are accountable for the driver’s decisions. I’m sure there is a loophole in there that needs closing.

This type of behavior and failure to accommodate the blind is a Class Action lawsuit that is way overdue. I’m shocked no one has sued the companies for breaking the law and doing nothing when its customers report a driver. Don’t get me wrong, I’m not one to say jump on a lawsuit, quite the opposite but this is not a frivolous issue. If the ride-share companies refuse blind riders they need to lose any government contracts they may have and if cities have a choice to allow the rideshare company to do business in the city, they need to reverse the approval.

I know a few people who are blind and life is challenging enough and for their transportation to refuse them a ride is shameful. Apparently, it’s been happening for years but it’s not been in the media which is typical for the media, just feed us the same day after day instead of pressing the important issues.

I feel so strongly about the issue that I created a Change.org petition that I hope you will support by going to https://www.change.org/p/require-rideshare-services-to-accept-blind-riders-with-guide-dogs/share_for_starters?just_created=true and signing.

Copy of Petition

This petition is deeply personal because it strikes at the heart of disability discrimination, a struggle that blind individuals face daily. It’s both shocking and disheartening when a company that provides a critical service like transportation discriminates against individuals with disabilities, specifically those who rely on guide dogs. According to the American Foundation for the Blind, millions of people in the US are experiencing vision loss. And many of them, depend on guide dogs to navigate and live independently.

However, troubling instances have surfaced where these individuals are refused service by rideshare companies simply because of their guide dogs. This is not only inconvenient but also unlawful – the Americans with Disabilities Act (ADA) prohibits discrimination against individuals with disabilities in all areas of public life, and that includes transportation.

Apart from being illegal, such practices are inhumane and show a complete disregard for the rights and dignity of people living with disabilities. Furthermore, it contradicts the spirit of rideshare services which aim to provide convenient and accessible transportation for everyone. All this considered, it’s high time for all rideshare companies to commit to full accommodation for blind riders with guide dogs.

We cannot allow this blatant discrimination to continue. Together, we can change this. Please sign this petition to send a strong message across: Require Rideshare Services to Accept Blind Riders with Guide Dogs.

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My husband told me that once he signed the petition Change.org asked for a donation, a donation is not required. Change.org is a global organization that is free and as such they solicit donations. This is common but you are never required to donate or I would not work with them.

Melinda

Chronic Illness · Communicating · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Mental Illness · Moving Forward

When a Loved One Denies Their Bipolar Diagnosis

By Julie A. Fast 

Medically Reviewed by Allison Young, MD

Last Updated: 21 Aug 2024

Although it’s incredibly frustrating when someone is in denial of having bipolar disorder, it’s important to remember that acceptance cannot be forced.

It can be upsetting, stressful, and downright incomprehensible when someone with a diagnosis of bipolar disorder denies the mental health condition and refuses treatment. You may find yourself watching helplessly as behaviors tied to untreated bipolar lead to family distress, broken relationships, problems at school and work, money woes, and alcohol and drug abuse.

If you try to help someone in denial, you will probably be accused of interfering if you even mention the word “bipolar.” This is confusing, because it’s very easy for you to see what’s wrong, and naturally you want to point out the problem in hopes that the person will then get help. Often, however, your attempt just makes things worse.

RELATED: 8 Essential Things to Know When First Diagnosed With Bipolar Disorder

It hurts when a person in denial shuts you out, but, sadly, it’s common.

What’s even more confusing is that you can have an honest conversation about bipolar when your loved one is stablereviving your hopes that the person will enter or stick with treatment. Then … boom! Here comes the denial again.

Learning to Accept That Your Loved One Is in Denial About Their Bipolar Diagnosis

It may be cold comfort to learn that it is very typical behavior for people with bipolar disorder to deny they are “sick” and to avoid treatment, even if they have been in the hospital or taken medications for bipolar in the past.

Also, it’s important to remember that people in denial are usually miserable, in a great deal of internal pain, and can’t see a way out. It’s easy to believe they really can’t see what’s going on. But unless denial is a result of a mood swing — such as strong mania or paranoia — the affected individuals usually know what is happening. They respond to your concern with aggression, because they are trying to protect their decision to deny the brain-based disorder.

It hurts when a person in denial shuts you out, but it’s common. The person prefers to be around others who don’t mention bipolar, and will paint you as the “bad guy” because you are the one who is stating the truth.

RELATED: 10 Ways to Support Someone Who Has Bipolar

There is good news, however. I’ve talked with hundreds of people who moved through denialto eventually admitting that bipolar is at the root of their problems and they needed help. Over and over again, I’ve been told how, despite their relentless inner pain and confusion, they refused help and pushed away the people who cared about them.

It’s when someone realizes they no longer want a life controlled by bipolar disorder that they begin to listen to loving advice instead of fighting back.

Steps to Take When a Loved One Is in Denial About Their Bipolar Diagnosis

If your loved one continues to be in denial of their bipolar diagnosis, here are a few things to keep in mind.

  • Find the sweet spot: Are there periods when your loved one is more open to discussion? Oftentimes, people are more receptive during a mild depressive episode. Once you see a pattern in your loved one’s moods, you’ll have a better sense of when to gently start a conversation.
  • Set expectations: If a loved one with bipolar is living with you, you have the right to set expectations for behaviors, such as drug use, drinking, yelling, staying in bed all day, staying out all hours, and yes, refusing treatment. You are always in control of what works best for you. It’s not always about the person with the mental health condition. It will be up to you to decide the consequences — and set and reinforce boundaries — if your expectations aren’t met.
  • Understand the challenges: Always remember that bipolar is a mental health condition. No one chooses to have bipolar disorder. People in denial can be very unpleasant, and it’s easy to walk away from them, but don’t forget they are suffering. It’s okay to address this directly. Go ahead and say you understand that it must be hard to have someone tell you what to do. Say that you can tell they feel misunderstood. People in denial may get angry or refuse to reply, but they have heard you. Many times, when they get better, they will tell you they heard you.
  • Hold onto hope: I’ve known many people who accepted treatment after years of being in denial, often when loved ones learned simple strategies and got them help at the right time. It isn’t easy to hang on until then. Nothing with bipolar disorder is easy! But bipolar is treatable, even for those who currently refuse to admit they are unwell and need help.


UPDATED: Printed as “Fast Talk: The Denial Factor,” Summer 2011

Julie A. Fast

Julie A. Fast is the author of the bestselling mental health books Take Charge of Bipolar DisorderLoving Someone with Bipolar Disorder: Understanding and Helping Your PartnerGetting It Done When You’re DepressedOMG, That’s Me! (vol. 2), and The Health Cards Treatment System for Bipolar Disorder. She is a longtime bp Magazine writer and the top blog contributor, with over 5 million blog views. Julie is also a researcher and educator who focuses on bipolar disorder prevention and ways to recognize mood swings from the beginning—before they go too far and take over a person’s life. She works as a parent and partner coach and regularly trains health care professionals, including psychiatric residents, pharmacists, general practitioners, therapists, and social workers, on bipolar disorder and psychotic disorder management. She has a Facebook group for parents, The Stable Table, and for partners, The Stable Bed. Julie is the recipient of the Mental Health America excellence in journalism award and was the original consultant for Claire Danes’s character on the TV show Homeland. Julie had the first bipolar disorder blog and was instrumental in teaching the world about bipolar disorder triggers, the importance of circadian rhythm sleep, and the physical signs of bipolar disorder, such as recognizing mania in the eyes. Julie lives with bipolar disorder, a psychotic disorder, anxiety, and ADD.

Melinda

Health and Wellbeing · Infectious Diease · Medical · Men & Womens Health · Mental Health

West Nile Is Now A Global Crisis

There is a global crisis warning about the West Nile Virus and the areas it effects are growing by the day. West Nile is new to many countries and we have to take notice.

What is West Nile?

West Nile virus (WNV) is a single-stranded RNA virus that causes West Nile fever. It is a member of the family Flaviviridae, from the genus Flavivirus, which also contains the Zika virus, dengue virus, and yellow fever virus. The virus is primarily transmitted by mosquitoes, mostly species of Culex. The primary hosts of WNV are birds, so that the virus remains within a “bird–mosquito–bird” transmission cycle.[1] The virus is genetically related to the Japanese encephalitis family of viruses. Humans and horses both exhibit disease symptoms from the virus, and symptoms rarely occur in other animals.

Contrary to popular belief, West Nile virus was not named directly after the Nile River, but rather, after the West Nile district of Uganda where the virus was first isolated in 1937.[2]However, the names are indirectly connected since that district of Uganda is named after the Albert Nile, a tributary of the Nile River in this region. After its original discovery there, it was found in many other parts of the world. Most likely, it spread from the original West Nile district.

What are the symptoms of West Nile?

West Nile virus (WNV) is usually spread by mosquitoes that become infected when they feed on infected birds, which often carry the disease.[53] Rarely the virus is spread through blood transfusions, organ transplants, or from mother to baby during pregnancy, delivery, or breastfeeding,[53] but it otherwise does not spread directly between people.[55] Risks for severe disease include being over 60 years old and having other health problems.[53] Diagnosis is typically based on symptoms and blood tests.[53]

What time of year is West Nile most active?

According to the Center for Disease Control, infection with West Nile Virus is seasonal in temperate zones. Climates that are temperate, such as those in the United States and Europe, see peak season from July to October. Peak season changes depending on geographic region and warmer and humid climates can see longer peak seasons.[58] All ages are equally likely to be infected but there is a higher amount of death and neuroinvasive West Nile Virus in people 60–89 years old.[58] People of older age are more likely to have adverse effects.[citation needed]

There are several modes of transmission, but the most common cause of infection in humans is by being bitten by an infected mosquito. Other modes of transmission include blood transfusion, organ transplantation, breast-feeding, transplacental transmission, and laboratory acquisition. These alternative modes of transmission are extremely rare.[59]

Prevention

Prevention efforts against WNV mainly focus on preventing human contact with and being bitten by infected mosquitoes. This is twofold, first by personal protective actions and second by mosquito-control actions. When a person is in an area that has WNV, it is important to avoid outdoor activity, and if they go outside they should use a mosquito repellent with DEET.[59] A person can also wear clothing that covers more skin, such as long sleeves and pants. Mosquito control can be done at the community level and include surveillance programs and control programs including pesticides and reducing mosquito habitats. This includes draining standing water. Surveillance systems in birds is particularly useful.[60] If dead birds are found in a neighborhood, the event should be reported to local authorities. This may help health departments do surveillance and determine if the birds are infected with West Nile Virus.[61]

This is all important information to know and to know and how to prevent. The outcome of getting the virus is serious even life-threatening.

Melinda

References:

https://en.wikipedia.org/wiki/West_Nile_virus#Humans

 

Celebrate Life · Chronic Illness · Communicating · Health and Wellbeing · Medical · Men & Womens Health · Mental Health · Mental Illness · Moving Forward

13 Celebrities Who Embrace Their Bipolar Disorder

 

These 13 celebs accept their bipolar and are using their platforms to break the stigma and push for acceptance of brain-based conditions.

By Jade Zora Scibilia

Whether you love them or “love to hate them,” celebrities can make a real difference, especially when they take a stand for something positive. The following stars with bipolar disorder use their fame (and occasional notoriety) to draw our attention to what really matters, start meaningful conversations among loved ones and policymakers, break the silencing effect of social stigma, and enhance both awareness and acceptance of this brain-based disorder. These celebrities — among others — have had a life-affirming, morale-boosting impact. Whether through a “tell-all” interview or memoir, a powerful pop song, or a moving on-screen performance, these stars continue to rally people with bipolar — and their supporters — to power through and find the hope of a new day.
1. Faye DunawayIn the HBO documentary Faye, the iconic Faye Dunaway, now 83, talks about her lifelong battle with mental health, including her bipolar disorder diagnosis.“Emotion is a strength, not a weakness,” she shared with The Independentat the documentary’s premiere in Cannes in May 2024. Dunaway reflects on how her intense emotions fueled her performances but also contributed to her reputation for being difficult on set — earning her the nickname “the dreaded Dunaway” (and “Dread” for short) from Jack Nicholson during Chinatown. In the documentary, Dunaway candidly discusses how she’s worked with doctors and taken medication to manage her mood swings. She acknowledges it’s been difficult, but “it’s something I’ve had to deal with and overcome and understand. It’s part of who I am.” 
2. Alan RitchsonYou may know Alan Ritchson as the star of Prime Video’s Reacher, but did you know he also lives with bipolar disorder? Diagnosed at 36, the now 41-year-old actor has been open about his struggles.“As much as I would like to ignore that I’m a suicide survivor, if I didn’t share what I’ve learned, I feel like my life would be meaningless,” Ritchson told CBC Radio’s “Q” program. “I’ve always been a happy-go-lucky guy, but once you experience the grip [of depression] — the talons it can sink into you — you realize how sinister this thing is and how out of control the biology can really be.”

Click to Read More

Jade Zora Scibilia is a former editor at bpHope, bp Magazine and Esperanza. She was formerly the managing editor at Prometheus Booksand the senior editor of Seventh Street Books and Pyr. She is also the author of two nonfiction children’s books.


I applaud anyone who steps out and embraces their mental illness, there is still a stigma, and those who are public about it are brave and very strong.

Melinda

References:
https://www.bphope.com/bipolar-buzz/celebrities-who-embrace-their-bipolar-disorder/?utm_source=iContact&utm_medium=email&utm_campaign=bphope&utm_content=BUZZ+-+Aug25+-+Celebrities

Health and Wellbeing · Medical · Men & Womens Health

Unexpected Bruising On My Face

I sleep on only one side and over the years I have woken up with redness or a faint bruise right under my eye, it wasn’t concerning at the time. On Thursday I had a doctor’s appointment and my husband went with me. He didn’t say anything at the time but later that evening he asked me to turn my face towards him. He said your face is all bruised on one side, I was shocked and headed for the mirror.

Sure enough, my face was lightly bruised alongside my eye, in the hairline, and all down my cheek close to my nose. He then said my face was bruised earlier that morning and was darker. I was surprised the doctor didn’t say anything.

I sat and thought about my day from the time I woke up and could find no reason for the bruising. I know that bruises don’t fade that quickly so I went to copilot to see what answer it gave. It was what I already knew. Bruising is caused by hitting something and that bruising takes 1-3 days to go away. Still perplexed.

The next morning I woke up with light bruising as well, not as bad as Thursday but still bruised. The only answer I could come up with was my pillow. I had slept on a goosedown pillow for years and several years ago changed to a harder pillow for more neck support. I ordered another goosedown and it’s scheduled to arrive today.

This morning I woke up to redness all around my eye and a small bruise. The bruising started three days ago and makes no sense. I’ll see if the new pillow makes a difference, if not I’m not sure what type of doctor to see.

Have you ever had this happen?

Melinda

Chronic Illness · Health and Wellbeing · Infectious Diease · Medical · Men & Womens Health · Tick Borne Illnesses

Treating Neurologic Lyme Disease with Hyperbaric Oxygen

Important Read

By Fred Diamond

Many listeners of my Love, Hope, Lyme podcast ask me to go deeper on some treatment topics that I mention in my book “Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know.” One such topic is hyperbaric oxygen treatment (HBOT).

On today’s Love, Hope, Lyme podcast, Dr. Mo Elamir of the Aviv Clinics in Florida clarifies what HBOT is and how it may benefit those with persistent Lyme disease.

Breathing new life into Lyme treatment

Amidst the search for effective treatments, HBOT has emerged as a compelling approach, possibly offering new hope for those battling the persistent effects of chronic Lyme disease.

HBOT involves breathing pure oxygen in a pressurized environment. This method significantly increases the amount of oxygen in the blood, facilitating the body’s natural healing processes.

Dr. Elamir, a leading physician at Aviv Clinics, explains the transformative impact of HBOT on Lyme disease patients: “By increasing the oxygen levels in the body under pressure, HBOT can break through the biofilm that protects Lyme bacteria, which are often anaerobic and thrive in low-oxygen environments. This process can destroy the bacteria and lead to significant improvements in neurological function.”

The specific HBOT protocol used at Aviv Clinics involves fluctuating oxygen levels, a technique designed to trigger the body into a state of healing. This healing process includes the growth of new stem cells and blood vessels, improved mitochondrial function, and the repair of damaged brain tissue.

“Our approach is highly individualized, focusing on each patient’s unique needs and the specific ways Lyme has affected their neurological health,” says Dr. Elamir.

How Lyme impacts the brain

Lyme disease affects an estimated 60 million people worldwide in its chronic stage. The disease can invade various parts of the body, including the brain, where it causes a range of neurological symptoms.

These symptoms can be particularly challenging to diagnose and treat, often leaving patients in a state of cognitive fog, battling memory loss, and struggling with anxiety and depression.

Dr. Elamir provides critical insights into how Lyme disease can affect the brain. “The bacteria that cause Lyme disease, Borrelia burgdorferi, are spirochetes that can invade the brain, leading to symptoms such as brain fog, memory problems, anxiety, depression, and even issues with movement, coordination, and balance,” he explains.

“These symptoms can vary greatly from person to person, depending on how the disease affects their nervous system.”

One of the most challenging aspects of chronic Lyme disease is that its neurological effects are often dismissed or misdiagnosed.

“Standard tests like MRIs and nerve conduction studies may not reveal the subtle dysfunctions caused by Lyme,” Dr. Elamir points out. “As a result, many patients are told that their symptoms are ‘all in their head,’ leading to frustration and a sense of isolation.”

Stress: a catalyst for symptom reactivation

Stress plays a significant role in the reactivation of Lyme symptoms. Dr. Elamir explains that various stressors—whether physical, emotional, or even as minor as a common cold—can trigger the dormant spirochetes in the brain to become active again.

“Stress can cause these bacteria, which might have been lying dormant in the brain, to reemerge, leading to a resurgence of neurological symptoms,” he notes. This makes stress management a critical component of care for Lyme survivors.

The spirochetes’ ability to remain dormant and reemerge under stress is one of the reasons why Lyme disease can be so difficult to treat. Even after successful treatment with antibiotics, the bacteria can remain hidden in the body, waiting for an opportunity to resurface.

Comprehensive assessment and tailored treatment

At Aviv Clinics, treatment begins with a comprehensive assessment that spans three to five days. This in-depth evaluation includes structural and functional imaging of the brain, neurocognitive testing, and a thorough medical evaluation. One of the key tools used in this assessment is SPECT (Single Photon Emission Computed Tomography) scanning.

“SPECT scans allow us to see the metabolic function or dysfunction within the brain,” Dr. Elamir explains. “This is crucial because standard MRIs primarily show the structure of the brain, but SPECT scans give us a clearer picture of how Lyme disease has affected the patient’s neurological health.”

Based on the assessment, the clinic develops a personalized treatment plan that includes HBOT as a cornerstone therapy. But HBOT is just one component of a broader treatment protocol that also includes neurocognitive training, physical therapy, vestibular therapy (for balance issues), and psychotherapy.

Healing the mind alongside the body

Psychotherapy plays a crucial role in the recovery process for many Lyme survivors. As the brain begins to heal, patients may experience a resurfacing of traumatic memories or new psychological challenges. The clinic’s psychotherapists work closely with patients to help them navigate these changes and provide them with the tools they need to cope.

Cognitive Behavioral Therapy (CBT) is one of the most common forms of psychotherapy used at Aviv Clinics.

“CBT helps patients understand their symptoms, process their emotions, and develop strategies for managing anxiety, depression, and other psychological challenges,” says Dr. Elamir. Group therapy sessions are also offered, allowing patients to connect with others who are going through similar experiences.

The role of diet in neurological health

Diet is another critical aspect of treatment at Aviv Clinics. Dr. Elamir emphasizes the importance of following a diet that supports neurological health.

“One of the most effective diets for this purpose is the ketogenic diet, which has shown significant benefits for people with neurological conditions,” he says.

Originally developed for children with epilepsy, the ketogenic diet involves consuming high-fat, low-carbohydrate foods that induce a state of ketosis, where the body burns fat for fuel instead of carbohydrates. This can lead to improvements in brain function and a reduction in neurological symptoms.

Intermittent fasting is another dietary approach that can be beneficial for Lyme survivors.

“Intermittent fasting has been shown to improve metabolic processes and reduce inflammation, which can support the healing process in Lyme disease,” notes Dr. Elamir. This involves eating all meals within a specific window of time each day, such as an eight-hour period, and fasting for the remaining 16 hours.

Dr. Elamir also advises patients to reduce their intake of processed sugars, which can exacerbate inflammation and contribute to chronic health issues. “Minimizing sugar intake is essential in managing Lyme disease because it is characterized by chronic inflammation,” he explains.

Addressing co-infections

Co-infections are a common complication of Lyme disease. These are other infections transmitted by the same tick that carries Lyme disease, such as Bartonella and Babesia. These co-infections can cause their own set of symptoms and make the treatment of Lyme disease more complex.

“HBOT can also be effective in treating these co-infections,” says Dr. Elamir. “The increased oxygen levels can help destroy the bacteria responsible for these infections, while the overall treatment protocol supports the repair of any damage caused by the body’s immune response to the infection.”

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Learn more about the Aviv Clinics here.

Fred Diamond is based in Fairfax, Virginia and can be contacted via Facebook. His popular book, “Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know” is available on Amazon. The e-version of the book is always free to Lyme survivors. PM Fred on Facebook for your copy.

Melinda