Thank you for joining me for this week’s Friday Quote.

Melinda
Thank you for joining me for this week’s Friday Quote.

Melinda
Thank you for joining me for this week’s Friday Quote.

Melinda
Customer Service has become a relic term, not even common courtesy is extended today.
Medical doctor’s offices claim to be the top in the field with all these awards including ones for customer service. Why is it that I can’t get a critical question answered by my doctor through the portal?
I had to wait an hour on the phone until the receptionist could find a live person to talk with me, I didn’t have anything better to to do. Maybe it’s time we start charging for the hours we spend trying to get answers. It took me from 10/22/24 to 11/6/24 to get someone on the phone and schedule my surgery.
Today I had an appointment with my new pharmacist since I’m changing pharmacies. We scheduled last week to meet today at 2:00 pm, at 2:30 pm I called to say I had other things to do and when she was ready she could call to reschedule. I got a message back saying one of the pharmacists had a meeting that ran long. Why can’t you text me the minute you knew there was a conflict? Again where the hell is the communication. It’s like the medical community has decided it’s no longer their issue. I disagree!
Why did the powers that be allow text spam? Who’s making money here? Or is it that big business has so much power over the FTC that allowed this to happen?
Who is selling my email information? I get a 10-15 spam emails a day. It is impossible to track down because I will not click on any links. Be sure to read the Privacy Information for companies you sign up with to see what they do with your data.
All the issues I was having with Bots were because WordPress shares your information with its so-called partners. I had to search a bit but found a hidden sentence that if clicked allows WordPress to share information with their AI partners for training AI. Ok, I switch it off thinking that mess is over. Not so quick. I went three days without Bots and now they are back with a vengeance. I don’t have a complete problem with AI but I want to know how my content is used and how I get credit for the content. It also screws up the views, it can get so complicated that it’s not worth it. I will say that FaceBook/Meta is the AI bot that attacks my archives daily.
I realize not every town has these problems, that’s great for you. I hope it remains that way for a long time.
I’m observing that most businesses are pushing you to their portals so they don’t have to talk with you. How far down do we go from here? Will we have to make an appointment just to have a question answered?
I don’t care for this lack of human connection one bit, it will only spill over to the rest of our lives. Scary!
What bothers you today about the lack of communication?
Melinda
Thank you for joining me for this week’s Friday Quote.

Melinda
Thank you for joining me for this week’s Friday Quote.

Melinda
Loneliness is more prevalent than ever — especially for people with chronic or invisible illnesses. Even when it feels difficult or impossible, here’s how you can stay socially connected.
If you live with a chronic illness, you likely know that loneliness is often an unexpected side effect. A chronic illness is a long lasting or permanent condition that requires ongoing medical treatment or limits activities of daily living. Examples include Crohn’s disease, endometriosis, fibromyalgia, and many other conditions.
And when your days are filled with attending doctor’s appointments, feeling too crummy to socialize, and constantly explaining your condition when you do make it out, it’s really no surprise that loneliness and chronic illness go hand in hand.
But now, this problem is becoming more prevalent than ever. The United States Surgeon General released an advisory in May 2023 calling attention to “the public health crisis of loneliness, isolation, and lack of connection in our country.”
If you’re living with a chronic illness, it can be helpful to create your own strategy for staying connected with others and preventing loneliness as much as possible. Take a look at why this is so important, as well as some accessible ideas to try.
People who live with chronic illness often feel the impact of isolation more than those without a chronic condition. Illness-related factors that can contribute to loneliness include:
If your illness is mostly or entirely invisible, this can lead to even more feelings of isolation as you try to explain what’s going on in your body. And since the onset of the COVID-19 pandemic, many people with chronic illnesses have found that their loneliness has gotten even worse as they have continued to be conscientious about keeping their already-fragile bodies safe.
Even when you’re feeling relatively well, it can be hard to socialize. Chronic illness is often unpredictable, and our society isn’t set up to accommodate it. Fear of stigma or ableism might keep you at home. Or you may find that every ounce of your limited energy goes into school or work, with nothing left over for a social life.
Long-term loneliness can be a serious issue. The report from the Surgeon General stated that for older adults especially, the physical health consequences of a lack of connection include:
A lack of social connection also increases the risk of premature death by more than 60%. And loneliness and isolation increase the risk of mental health conditions such as depression, creating a vicious cycle.
When symptoms and appointments dictate your life, it can feel nearly impossible to increase your social connection. But doing so is crucial for your mental and emotional health. Here are a few accessible ideas to try.
If the thought of ramping up your social life feels overwhelming, it’s OK to start small and take off the pressure, thinking in terms of acquaintances instead of best friends. Even “micro-interactions,” such as waving at your mailman or thanking a cashier, can give you a boost of connection.
Send someone a message on social media instead of passively scrolling, or go to a coffee shop on your next low-symptom day so you can be around people even if you aren’t directly speaking with them. These simple actions can have a bigger impact than you might think.
Connecting with people who also live with chronic illness can stave off loneliness by reminding you that you aren’t the only one. Look for a support group run by a hospital or nonprofit — your doctor may have ideas. Or search online for a community similar to Bezzy. You’ll find countless social media groups, forums, and Zoom events created for people who live with certain conditions or chronic illness in general (including those who don’t have a diagnosis).
As you spend time with people who have similar experiences, it will become easier to articulate and explain your condition to people who aren’t sick.
Animals can help reduce stress and loneliness, and pet ownership is associated with lower levels of social isolation in adults. A pet is great company and can help you feel loved and needed.
If you can, consider adopting a pet. If you can’t put a lot of effort into caring for a pet due to your physical symptoms, look into a low-maintenance pet such as an adult cat. Or see if you can do any of the following from time to time:
A therapist, counselor, or other mental health professional can help you navigate the mental and emotional side of chronic illness, including thoughts like “My illness makes me unworthy of friendship” and “Connection isn’t worth it.”
Look for a therapist who specifically focuses on clients with chronic illness. Ask your doctor for suggestions or search online. If you cannot pay for therapy, look into sliding-scale options or services offered by a nonprofit or community center.
Remember, your social connections don’t always have to be big. If you can make it out for a night on the town, great! But if not, make sure you’re still doing something to stay in touch with the people you love.
Use email, social media platforms, phone calls, texting, or whatever communication method works for you. Planning video calls ahead of time might work best for one chronically ill person’s symptoms and schedule, while answering text messages on their own time could be better for somebody else.
Think about the options that are most accessible to you, and tell your family and friends that you want to intentionally catch up with them on a regular basis. Connecting with others as best you can will help you feel less isolated, even during flare-ups.
People are important. We need each other. We can’t live without each other. And even when it feels difficult or impossible, fighting for social connection is worth it.
Use these ideas to work around your chronic illness as you prioritize connection over isolation. Your body and mind will thank you.
Melinda
Reference:
Thank you for joining me for this week’s Friday Quote.

Melinda
Bullying is an issue that people of all ages deal with especially if they are on Social Media, bullying is not just for kids and teens anymore. Bullying when I was growing up was calling people names, starting rumors about you, and a few fist fights but nothing as life-altering as today. The worst that happened to me was I was hit in the back of the head with a coke bottle over someone starting a rumor that I was making fun of my best friend and neighbor about her cleft palate. Of course, the rumor wasn’t true but she took it personally, it wasn’t her that hit me in the back of the head with the Coke bottle it was one for her friends looking for trouble.
Nowadays are bullied at a very young age about everything from the clothes they wear, who their friends are, to whether or not they have a phone or an email, It can go as far as what car their parents drive, where they work and on and on, it there’s a hater out there, there is a bully. One of the biggest challenges is that kids and teens don’t often tell their parents before things get out of control. Nor do they talk to the school about it even if they know who is doing it. It’s the same pressure that’s always been there, being a tattle tale. We have to know how to stand up for ourselves and teach our children to do the same.
On Social Media, it is so much worse and more vicious, if they troll you they also troll your friends and their friends, start outrageous rumors, makeup conversations that never happened, manufacture photos that don’t exist, and send them to everyone you know even your employer. Some trolls make it their life obsession to ruin your life before they move on to the next person. They can make it look like a message comes from someone and not from that person.
One of the reasons I closed all my social accounts was the negativity. If you write about an accomplishment or good health news you can get bombarded with messages like “You aren’t sick”, “You’re Lying”, You just want sympathy” and the negative comments go on and on. The other issue I had is, that I only followed a short list but would still see all of Elon’s tweets about his views, overpopulating the world with children and other views I never asked to see, like him talking about sex or showing him grabbing a woman’s but. I’m no prude by any stretch of the imagination but that isn’t why I joined back in 2015. I also grew tired of the pushing of other sites I might want to follow, some may find that helpful but not me.
Of course, there is a more sinister side of Social Media but that’s for another post. What will say to parents is to monitor how much time their kids spend on Social Media, what they are looking at, who they are following, and check their Direct Messages. Teens have to earn the right to have a phone and to access these sites. They also need your guidance to know that they don’t know who is on the other end no matter what they think or what the other heart is telling them.
A scary way young adults and adults alike can be bullied is by a troll gathering info posted and piecing together your life, your photos, where you hang out, and even where you work. Now think of what a troll can do with that information and believe me this happens every day. Remember all the stories of kids being ostracized because their parents were Only Fans members?
October is National Bullying Awareness Month, a timely reminder for organizations to take action at the local level to foster safe and supportive environments. Workplace bullying—whether through hostile comments, discriminatory actions, or other forms of intimidation—should never be tolerated.
By promoting kindness, inclusivity, and respect, we can contribute to creating workplaces where everyone feels valued and respected. Together, we have the power to make bullying a thing of the past and build a better, more compassionate world.
The reason, I only included this information is everything I read was focused on kids and that’s not reality anymore.
I don’t see bullying going away but we can control it with protective measures and education.
Melinda
This is some very serious news for ALL WordPress bloggers! Educate yourself and BE SURE to back up all your data. Be sure to read the link in Daniels’s post, all the facts and details are spelled out there. So many concerns.
Is WordPress on the verge of Destruction?
I recently discovered that the WordPress project owned by Automattik is in a complicated battle with its Hosting company WP. The integrated aspect of WordPress with Automattik and WP is complex and currently under threat. WordPress represents about 40% of all websites on the Internet and a punitive legal battle could drastically affect the Internet … Continue reading
To think for one moment about what Christopher Columbus accomplished is mind-blowing. He shaped our world, taught us about countries we didn’t know existed, and built solid teams committed to the cause. I would love to feel what Christopher felt when he landed in America, what was the emotion?
Christopher Columbus (born between August 26 and October 31?, 1451, Genoa [Italy]—died May 20, 1506, Valladolid, Spain) was a master navigator and admiral whose four transatlantic voyages (1492–93, 1493–96, 1498–1500, and 1502–04) opened the way for European exploration, exploitation, and colonization of the Americas. He has long been called the “discoverer” of the New World, although Vikings such as Leif Eriksson had visited North America five centuries earlier. Columbus made his transatlantic voyages under the sponsorship of Ferdinand II and Isabella I, the Catholic Monarchs of Aragon, Castile, and Leon in Spain. He was at first full of hope and ambition, an ambition partly gratified by his title “Admiral of the Ocean Sea,” awarded to him in April 1492, and by the grants enrolled in the Book of Privileges (a record of his titles and claims). However, he died a disappointed man.
Christopher’s world travels lived on with many new discoveries including the Mayflower heading to America.
Melinda
References:
https://www.britannica.com/biography/Christopher-Columbus
The memorial is very nice, it was opened in 1996 and Rochester is very proud of the soldiers who gave all.
The day was extremely windy so I was not able to get many photographs but I’m thrilled with the ones I did, The images itched into the granite are breathtakingly real.






Melinda
We landed last night with just enough light to find our car and head to Trader Joe’s for some goodies. We grabbed some dinner there so all we had to do was bring half a ton of luggage into the room and eat. My husband was happy because a college football game was on. After watching for a few minutes, I laid down to rest after an exhausting day at airports, walking and pulling luggage.
It’s very chilly here compared to home so I’m glad I brought my extra warm clothes. We’ve slept in this morning and plan to head out to see a few sites. I don’t know everywhere we’re going but I have the Vietnam Veterans Memorial at the top of my list. I like to pay my respect when I travel, that’s the very least I can do.
Tomorrow is Columbus Day and a holiday for many, I will write a post about it this afternoon. We have free days until Tuesday and then it’s off to The Mayo for meetings with doctors, getting blood work, testing, and leaving with a diagnosis.
Have a great day.
Melinda
Thank you for joining me for this week’s Friday Quote.

Melinda
This awareness month is critical for all ages, even the youngest of children can feel depression and even though you may think they should blow it off, it’s not that easy and you can alienate them from talking to you again. Today life is so hard on kids, from an early age they are judged for the way they look, and who their friends are, for any reason because there are so many who don’t know who to communicate with and are haters. Kids also mimic their parents, if your child is having problems, look at your own behavior.
Young girls are fed to believe that these so-called influencers are real perfect-looking people who are pumping the greatest products they have to have. It never crosses their mind that the person is not an influencer, they are made up to look like the girls want to be and they are selling a product they make money on. They don’t get it or don’t want to. They are bullied for being a certain weight or not looking like someone else’s unrealistic standards.
Mix in real life as they get older and a deeper depression may present itself, it could be short-term term or it could be from unresolved issues, one you may not even know about. The key is to get your children the help they need at every step. As they age, professional help may be the answer. Don’t let stigma keep your child from getting the help they need.
As for adults, life can get messy, people can hurt you deeply, someone you trusted can betray you and family can hurt the worst. Some people may be more predisposed to depression whereas others may be situational driven. Adults have their own stigma and don’t seek out help, some men don’t think they need help and some just don’t know where to turn because the answer is not their parents. This is where a therapist comes in, therapy can be short-term just to get over a hump or more long-term because you have many buried issues that need to be addressed.
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October is recognized as Depression Awareness Month each year. The purpose is to increase understanding, decrease stereotypes, and help educate on how depression and other mental health issues impact people.
Awareness months give people affected by a specific condition a chance to share their stories. The goal is to help increase the overall understanding of depression or other conditions and help overcome stereotypes.
Depression is a common mental health concern in America and throughout the world. Far more than just “feeling sad,” depression negatively impacts how a person feels, thinks, and acts. It can cause disruption to school, work, and personal interests.
Misconceptions and misunderstandings of depression contribute to continuing stigmas about people living with the condition, the reasons it occurs, and their willingness to seek care.
In a 2018 study, researchers conducted a survey to assess the public’s knowledge of depression and the severity of the stigma surrounding it. Key findings included:
Depression can wear you out at the exact time you need all of your strength to fight. Trying to cope is extremely tiring — and it’s often difficult to know when others are suffering. That’s why, during October, we observe National Depression Education & Awareness Month. This important holiday helps teach us about the signs, symptoms, and treatment options for depression. It also lets all of us know that seeking help — either from a counselor, a trusted friend, or your community — is a sign of hope and strength.
References:
https://www.medicalnewstoday.com/articles/depression-awareness-month
The newsletter talks about how to vote, the players in Texas who are up for election, and additional resources. Sometimes these newsletters publish a link, not sure why I can see the content but WordPress turns it to a link. Please click on the link or copy in paste on your computer to read. This message is important to all Texans.
October 2024
We are less than one month out from General Election Day! It is critical that Texans get out and vote as policymakers elected in 2024 will make major decisions regarding individuals and families affected by mental health conditions. Furthermore, exercising your right to vote ensures representation, the individuals we elect will be our voice at the local, state, and federal levels. When you participate in elections, we hold our elected officials accountable for their actions and decisions. Additionally, voting has the ability to drive social change as voters have the opportunity to advocate for policy reform and issues that are important to us. Finally, voting promotes equality, providing an opportunity for all citizens to have a say in the decision-making process. Important Dates: General Election Day: Tuesday, November 5th, 2024 Early Voting: Monday, October 21st-Friday, November 1st, 2024 Last day counties can receive mail-in ballot requests: Friday, October 25th, 2024 Find out what’s on your personalized ballot by checking out Vote411. Get involved & encourage others to do so too! The NAMI Texas team encourages you to check out NAMI National’s #Vote4MentalHealth campaign webpage where you can pledge to vote for mental health, learn more about why mental health is more than a single policy issue and several ways to get engaged. Furthermore, the campaign provides resources like finding your voting options, requesting an absentee ballot, and planning to vote. #Vote4MentalHealth Videos Check out this video that highlights the importance of voting in all elections, from those at the White House to local school board elections. Additionally, watch this educational video on how votes for education, economy, and healthcare all impact mental health! Please note: #Vote4MentalHealth is nonpartisan – the NAMI Alliance will never tell people what party or candidate to vote for; instead, it focuses on understanding how every person’s vote impacts mental health. NAMI Texas Voter Guide: Additionally, check out NAMI Texas’ General Election 2024 Voter Guides! The Policy Team has collected information from Texas candidates on various mental health topics. This guide can be used to help you gather information regarding where candidates stand on various mental health systems and what they hope to improve upon if they are elected. Please note, that all candidates were contacted and only those who responded are in the guides. Texas House of Representatives General Election Voter Guide Texas Senate General Election Voter Guide |
Let’s get out and vote!!!!!!! Our voice needs to be louder than ever if policy changes are going to happen.
Melinda

Thank you for joining me for this week’s Friday Quote.

Melinda
Ahead of the upcoming US presidential election, NO MORE is committed to helping survivors of domestic violence and stalking participate safely in the democratic process. This month we launched a new State Voting Guide for Survivors, outlining key options to help survivors protect their privacy and security while making their voices heard.

By consolidating this critical information in one place, the guide simplifies the voting process every step of the way. NO MORE will continue to provide information for survivors, as well as for their friends, employers, and communities to help support them.
Thank you, No More for supporting and thinking of how to protect us in each situation.
Melinda

Thank you for all the great feedback on the Blogger Highlight series, I’ve enjoyed meeting each blogger and sharing their site with you. This week we highlight John Malone and his blog. We haven’t followed each other long but we have become fast friends and I feel like a kindred spirit to him. John has brought my sense of creativity alive, he’s whip-smart, funny, and knows how to express himself through words. I could sit and talk with John for hours and would still have more questions, he’s interesting.
‘This then I can say about my life:
I have two cats, a dog.
three children
and a wife’
except I no longer have a wife or pets, except a cat called Rosco, but have accrued numerous grandchildren and yes, I still whistle while I walk 🙂
I have five books of poetry published, two of which have been self published and many , many poems anthologized. Between 2000 and 2012 I had over 170 childrens’ poems published in major magazines, in the North America, NZ and here in Oz, some of which are still earning royalties from being republished.
I also have three educational titles with major publishers, guides to creative writing in classrooms which schools use, written during the same period.
I sometimes think I should write children’s poems again but I wrote them for/with my grandchildren while they grew up in my presence.
To dig deeper into John’s career accomplishments click here.
What was your first job and what did you learn from it?
A secondary English teacher; learnt how to ;handle’ teenagers, not always successfully; learnt how to impart my love of literature and get them to write poetry themselves: we were a vibrant writing community.
What is your greatest career accomplishment?
My first book of poems by a major publisher was a thrill. Also between 2001 and 2013 I had over 70 children’s poems published in literary magazines for children in Australia, the Us and NZ. The three poems I’m proudest of are ‘Fork’, ‘Fearless’ and ‘The Mothering Tree’
Did you have a goal for your blog and have you achieved it?
As for the blog I just wanted to get my stuff out there and get immediate feedback instead of going through the delayed process of magazine submissions. I’ve built a lively following and feel part of a vibrant ever evolving literary community: a tribe !
John’s post New Direction was a surprise and a day to rejoice. We had been talking about his accomplishments which I greatly admire and later this post arrived. I’m thrilled John gave me some credit but most importantly, he wrote a new short story after taking many years off from writing. I’m counting the days until it’s published so we can read it on his blog. I look forward to new stories as John has his mojo back.
This post makes me think of all the journals and notebooks I carried around for years, starting as a child, they included writings, drawings, goals, and daydreams. They were my calm, my comfort, they knew my inner thoughts and they never betrayed me. John’s notebook was no doubt just as special, holding his thoughts, stories, and many ideas. The cover is fitting with its lived-in look and who would want to change that?
One of John’s favorite tunes:
I set a goal in 5th or 6th grade to become a Journalist for Life Magazine, but that isn’t where my career took me for multiple reasons. John’s career accomplishments are not directly related to my goal but I can imagine that being published gives you the same high and sense of accomplishment. I admire his accomplishments but what’s more important is that John is humble, no boasting, there are no airs about him and I admire him for that.
Be sure to stop by and say hello to John and while there browse through his extensive archives. You will not be disappointed and you may find yourself following John as well.
Melinda
Thank you for joining me for this week’s Friday Quote.

Melinda
Thank you for joining me for this week’s Friday Quote.

Melinda
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 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-Wolf, Let’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.”

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 Fadal, author, journalist, filmmaker, and Let’s Talk Menopause board member. “The black box warning is costing us our well-being and our money.”
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:
Thank you for joining me for this week’s Friday Quote.

Melinda
So many celebrities and wanna-be are plastic it’s refreshing to hear the raw truth, “Nothing Is Perfect”. I read one UK celebrity magazine/trash mag and sometimes it inspires me. Today, it was a story about Nicole Kidman and Keith Urban
“There’s no perfect anything,”
“Anything that’s presented as perfect… forget it,”
“We don’t want to be a pin-up couple,”
“We just want to be a couple that has a great life together.”
“Everyone has the right to their own relationship. We are just very protective of our little bubble. What works for us is what works for us.”
“I have no advice for anybody,”
“You guys figure out whatever works for you…We’re figuring it out. You figure it out. Everybody’s different. There’s no one size fits all.”
I live for this type of honesty which is reality! Not all the other plastic lives.
Melinda
Thank you for visiting my blog and allowing me into your life. I have not been to any of your countries but they are on my bucket list and all are so inviting. My travel fix comes from you as I often do a search on each country to learn more about it.
I hope you found a post or two that caught your attention and that you will return soon.
Melinda
By
Medically Reviewed
by
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.
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?
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.
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.
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 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:
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.
If you feel ready to share your diagnosis with someone else, here are seven expert tips to get the conversation started.
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.
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.
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.
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.
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.
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.”
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 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.
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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
Mukta has been a regular Guest Blogger on Looking for the Light because she writes about complex topics in a style all can understand and her writing is smooth. I have followed her for a long time and always find her posts enlightening. Be sure to stop by and say hello, pull up a chair, and read through her archives, no doubt there are many posts you will relate to.
Learn how mindful inputs can transform your mental and emotional health. “When you are mentally and emotionally strong, you are able to handle your thoughts skillfully and regulate your emotions in healthy and helpful ways.” This seemingly simple sentence holds a profound truth about the essence of our mental and emotional well-being. Our thoughts, which … Continue reading
Thank you for joining me for this week’s Friday Quote.
Winston Churchill was a great leader and his quotes are so on point. I read them and do not question what he is saying. Must be a respect thing.

Melinda
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:
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.”
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!“
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.”
“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 Fisher, Wishful Drinking, 2008
As a guest in 2019 on David Letterman’s Netflix series, My Next Guest Needs No Introduction, Ye (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.”
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.”
Richard Dreyfuss has starred in blockbusters like Jaws, American Graffiti, Close 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.”
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.”
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.”
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.”
In an interview with bp Magazine, Stephen 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.”
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 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
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Melinda
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I have known for some time that the statistics provided by WordPress are not accurate and today it was cemented in my mind. When you publish a post it goes to each follower including those who subscribe to receive the post via email. The catch is that WordPress counts all of your posts as email which is the opposite of what the explanation of what the statistics are.
I have around 20-25 followers who receive my posts via email yet today I looked at a post from a few days ago and it showed 917 received my posts along with the number of email opens and unique opens, whatever that means. If you take the numbers at face value that means that out of close to 4K followers only 917 received the posts and that even fewer read the posts and fewer are commenting.
Commenting I understand, I don’t comment on every post I read but I have a hard time swallowing that the community has turned off receiving my posts. Maybe this is naive of me but when I see the level of long-time followers, new followers, comments, and the level of conversations I’m having with many people the number isn’t consistent.
This is no surprise, I have a long-time follower friend whose husband is a Statistical Engineer and he stated that the statistics on WordPress are inaccurate. This is not a rant, just an explanation for others who are perplexed with their statistics.
I’ve been blogging on WordPress for 24 years and have spent countless hours frustrated working with the Happiness Engineers to understand the issue I was having. Many, many years ago asking for help became futile and I gave up on contacting them. I did recently contact WordPress to let them know about the Bots that were enjoying my archives but as usual, I received no response. When I have a question now, I ask the community or go to Copilot for an explanation. Copilot has helped me understand what the statistics mean at a high level however the answers don’t apply to WordPress.
I hope this information helps others make sense out of what doesn’t make sense. :)
Melinda