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

Resisting the Lure of Toxic Positivity While Chronically Ill

by Hannah Shewan Stevens

Medically Reviewed by:

Francis Kuehnle, MSN, RN-BC

Chronic illness is hard to live with, but coping by responding with excessive positivity can suppress our real feelings.

Those who live with chronic illnesses know all too well how frequently people shower you with meaningless platitudes like “just be positive” and “mind over matter.”

Of course, how we feel mentally affects our physical health, but being chronically ill also sucks sometimes. It’s OK to acknowledge that reality. But often, when we do, we’re told we’re being overdramatic or to force ourselves to “think our way back to being healthy.”

It’s time to reject toxic positivity and find coping mechanisms that actually work for you instead of methodologies that punish you for having “negative feelings.”

What is toxic positivity?

Toxic positivity is an expectation that no matter how serious a situation or diagnosis is, a person should maintain an ongoing optimistic and positive outlook and attitude regardless of how serious the circumstances are,” said Chicago-based clinical social worker Iris Waichler, MSW, LCSW.

This invasive method of communication shows up in countless ways, often slipping out of people’s mouths without them even noticing. Sometimes, it comes from the inside, led by an internal battle to just “get over it,” but it typically arises when people place their life view onto others.

“Toxic positivity often looks like someone giving you a motivational quote instead of actually listening, helping, or being there for you,” said Kitty Underhill, a body and self-acceptance coach from London, England. “For example, you could be struggling and communicating that to a friend, and they shut down the conversation with a statement like ‘good vibes only’ or dismissing it as being ‘low frequency.’

“Toxic positivity also looks like using buzzphrases like ‘what doesn’t kill you makes you stronger’ and telling you that you need to have a more positive attitude rather than hearing you out — it’s an emotional cop-out,” she added.

The impact of toxic positivity is wide-ranging and pervasive, sometimes hiding beneath the surface for years before we’re able to recognize that it’s prevented us from feeling the full spectrum of human emotion without feeling guilty for not being cheerful enough for those around us.

“Toxic positivity may cause people to believe their feelings are not worthwhile, create self-doubt and shame, and make them believe their feelings are invalid,” said Waichler. “The unintended consequences may be enhanced insecurity, which lessens self-confidence and self-worth.”

How can it show up in our lives with chronic illness?

The effects may largely be the same, but chronically ill people deal with another poisonous layer when facing toxic positivity: disbelief.

Too often, disabled and chronically ill people are encouraged to “think themselves well” because it’s “mind over matter,” but this neglects reality. A positive outlook can improve someone’s overall well-being. However, it’s not a magical cure for incurable illness.

“A healthy person may not have a real understanding of the physical, medical, and psychological ramifications that chronic illness has on an individual,” Waichler said. “A healthy person’s attempt to “cheer them up” or be unrealistically positive can create feelings of alienation, resentment, and anger for the person on the receiving end.”

Toxic positivity is dismissive because it discards their feelings, insisting that they be processed on the other person’s terms. Unsurprisingly, this is a common occurrence between people with and without chronic illnesses, as it’s easily assumed that we’re being overdramatic or exaggerating our symptoms.

Faced with an onslaught of forced cheerfulness and disbelief, submitting to toxic positivity sometimes feels like the only option, but chronically ill and disabled people deserve to be heard.

“It can be easy to fall for toxic positivity, especially when a lot of ableism depends on disabled folks not speaking up about what they are experiencing and overriding their own comfort and pain levels to make abled folks feel more comfortable,” said Underhill.

“We must remember that toxic positivity is another way of shutting down unpalatable emotions and that our emotions still deserve to be heard and expressed,” she added.

Understanding the difference between toxic positivity and genuine positivity 

“Genuine positivity makes space for the negative and doesn’t try to write it off or bat it away,” said Underhill. “Genuine positivity helps you to see things from different angles and perspectives, which can be helpful if we’re getting tunnel vision from feeling hopeless, angry, or upset from experiencing chronic pain issues.”

Where genuine positivity leaves spaces for pain while searching for light, comparatively, toxic positivity shuts down the conversation and obliterates the beautiful spectrum of our emotions.

Resisting the seductive pull of toxic positivity is exhausting, and sometimes, we fall under its spell before it’s possible to throw up a shield.

“If you’ve succumbed to toxic positivity, consider taking a step back to evaluate why you acquiesced,” said Carissa Hodgson, LCSW, OSW-C, director of programs and community outreach at Bright Spot Network and a clinical social worker. “Is it because you don’t have anyone who can authentically support you? Are you struggling with accepting your feelings about an experience? What is it that you need?”

Building your defenses

“To get rid of toxic positivity, it’s worth asking yourself the question, ‘Why do I feel like I cannot hold space for harder emotions?’” said Underhill.

“It’s also worth remembering that no emotion has a moral value. Emotions are not ‘good’ or ‘bad,’” she added. “Emotions are information that we can learn from and take into account.”

Allow yourself to feel everything you need to feel by granting yourself the gift of patience. There is no better defense against toxic positivity than the freedom to feel your emotions without judging them or suffocating them.

Confronting the toxic positivity around us

Try to practice patience when dealing with toxically positive people. It’s hard when you’re so regularly bombarded with it, but know that they are probably trying to empathize. It’s human instinct to jump straight to suggesting solutions. We all do it, even when it’s unwanted.

“Understand that the person is trying to be helpful,” said Waichler. “Help them to then understand how what they said makes you feel.

“Tell a well-meaning loved one with toxic positivity that you appreciate that they are trying to be supportive and positive about your medical condition,” she continued.

Developing healthier coping mechanisms

It’s crucial to develop additional coping mechanisms that manage the mental impact of chronic illness to resist the lure of toxic positivity long term.

“Educate yourselves about the medical condition and how it will progress so your expectations are realistic,” advised Waichler. “It will help you prepare for changes that will evolve in the future.”

Broaden your circle of friends to ensure that your support network is full of people who will understand your experiences with chronic illness. Your loved ones will support you, but unless they also have a chronic illness, they will struggle to understand. Fellow chronically ill people may be better suited to supporting you without relying on toxic positivity to do so.

However, be wary, too. Even the most well-developed support groups can fall prey to toxic positive influences.

“Toxic positivity is often a trojan horse found in online support groups and discussion boards — seemingly helpful and cheery but completely dismissive of the real struggles people are having,” said Hodgson.

As an additional shield, she suggests that people “Create an empowering mantra that entitles you to your feelings, such as ‘My feelings are real’ or ‘I have a right to feel how I want to feel,’ so when you see a dismissive statement, you can repeat your mantra to yourself and keep on reading.”

Medically reviewed on April 20, 2024

I can see how someone chronically ill can fall deep into the positivity route, it feels good at first but over time it overshadows the reality of being chronically ill. As mentioned in the post, many days suck and we can’t just cover them up as if they don’t exist. I’m all for positive energy but if someone just wants to change your thoughts and act like everything is ok, they are not doing you any favor.

Melinda

Reference:

Celebrate Life · Family · Health and Wellbeing · Holiday · Men & Womens Health

Celebrate Diwali On November 1st

I hope your year is filled with love and light.

  Melinda

Celebrate Life · Fun · Health and Wellbeing · Men & Womens Health · Travel

Sending A Special Thank You To-Cook Islands, Finland, Faroe Islands, Bangladesh, And Luxembourg

Thank you for visiting my blog. I truly appreciate you stopping by. I hope you found a post or two you could relate to and will return soon. I have not been to your home countries, but they are all on my bucket list.

I’m sending you and your family well wishes for health and happiness.

Take good care. :)

Melinda

Celebrate Life · Fun · Health and Wellbeing · Mental Health

Wordless Wednesday-Purple

I’m glad you joined me on Wordless Wednesday and I hope to see you soon.

 

 

Have a great day.

Melinda

Chronic Illness · Health and Wellbeing · Infectious Diease · Lyme Disease · Medical · Men & Womens Health · Mental Health · Moving Forward · Self-Care · Tick Borne Illnesses

Understanding and supporting invisible disabilities, including Lyme disease

Lonnie Marcum

OCT 24, 2024

Invisible disabilities are physical, mental, or neurological conditions that are not immediately apparent to others. Despite being “invisible,” these conditions can significantly impact a person’s life and require special accommodations and ongoing support.

Unlike conditions that other people can see, such as those requiring the use of a wheelchair, invisible disabilities often go unnoticed, leading to misconceptions about a person’s needs.

Examples of common invisible disabilities

  • Dysautonomia, also known as autonomic dysfunction, refers to a condition in which the autonomic nervous system (ANS) does not function properly. The ANS controls many crucial bodily functions, such as heart rate, blood pressure, digestion, temperature regulation, and respiratory rate. When the ANS is impaired, these processes can become dysregulated, leading to a wide range of symptoms.
  • Post-exertional malaise (PEM) where even minor physical or mental exertion can result in severe symptom exacerbation, often lasting days or weeks.
  • Chronic fatigue syndrome (CFS): Fatigue lasting six months or more, and PEM
  • POTS (Postural Orthostatic Tachycardia Syndrome) is a condition characterized by a significant increase in heart rate when a person stands up from a lying down position. It is a form of dysautonomia. People with POTS experience an abnormal response when they move to an upright position, leading to symptoms that can be disabling.
  • Myalgic Encephalomyelitis (ME): Causes widespread neuro-immune related symptoms including: neuroinflammation, immune dysfunction, muscle pain, headaches, cognitive dysfunction (often described as “brain fog”), dysautonomia, PEM, CFS and POTS.

Patients with Lyme and tick-borne disease are often left with persistent symptoms following treatment. In MyLymeData, now with over 18,000 participants, the three most frequently reported worst symptoms include neurological-associated symptoms (84%), fatigue (62%), and musculoskeletal-associated symptoms (57%).

POTS is the most common manifestation of dysautonomia reported to occur in patients with persistent symptoms of Lyme disease.

Infection-associated chronic conditions

For years, ILADS conferences have been the only place I heard clinicians and researchers expressing an understanding and a desire to help patients with complex, infection-associated chronic conditions (IACC).

In 2021, I reviewed a paper entitled “Recent Progress in Lyme Disease and Remaining Challenges,” co-authored by 31 researchers from 19 separate institutions. That paper felt like a real tipping point to me.

Last week, I watched the final meeting of the CDC/HHS funded “Infection-Associated Chronic Conditions – Understanding and Engagement” (ICUE) project. During that meeting, LymeDisease.org’s Lorraine Johnson, represented and gave voice to the millions of patients living with chronic symptoms following infection with Lyme and/or other tick-borne diseases. (Read her summary of that meeting here)

With all the new collaborations coming out of the National Academies of Science, Engineering and Medicine (NASEM) workshop on “Lyme infection-associated chronic illness or “Lyme IACC,”  I have high hopes for continued progress—not just for patients with chronic Lyme and co-infections, but so many other marginalized illnesses like long-COVID, ME/CFS, and dysautonomia.

Last year, I wrote about the real symptoms suffered by patients with invisible illness.Recently I offered suggestions on how patients can track those symptoms and share them with their doctors  to aid in better diagnosis and treatment.

For everyone out there suffering from an invisible illness: I just want to say that I see you, I hear you, and I believe you.

LymeSci is written by Lonnie Marcum, a physical therapist and mother of a daughter with Lyme. She served two terms on a subcommittee of the federal Tick-Borne Disease Working Group. Follow her on Twitter: @LonnieRhea Email her at: lmarcum@lymedisease.org.

Melinda

Reference:

https://www.lymedisease.org/invisible-disabilities-lyme-disease/

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

Announcing NO MORE Week 2025

I’m excited to share that NO MORE Week 2025 has been set for March 2nd through March 8th, the annual time when thousands of survivors, allies, employers, organizations, colleges, and communities around the world unite for the cause of ending domestic and sexual violence. 

This year, our theme is NO MORE Silence. Every time we break the silence, we destigmatize conversations around domestic and sexual violence and help survivors find support. And, we help to prevent abuse by educating more people about healthy relationships and by creating a culture where abuse is not tolerated.

Now is the time to plan how you can be a part of NO MORE Week 2025. Here are some simple ways to get started:

Join the NO MORE Week Challenge:

Sign up for the NO MORE Week Challenge, a virtual Walk/Run that allows you to choose your distance—5K, 10K, or a half marathon—and complete it at your own pace in March. This year, every dollar raised will go to support victims/survivors of abuse. Rally your friends and family to sponsor your efforts, or form a team to amplify your impact.

Join the Challenge

Attend the NO MORE Week Tech Summit

Save Tuesday, March 4th to attend the 2025 NO MORE Week Tech Summit, “Empowering or Endangering? Tech’s Impact on Domestic and Sexual Violence.”During this free, online conference, global experts will discuss cutting-edge research, policy shifts and product development, providing a wealth of insights and opportunities for action. Early registration is now open! 

Sign Up Now

Use Your Own Platform to Raise Awareness

Create an event – online or in person – to raise awareness on your campus, at work, or in your community. Whether it’s hosting a coffee or happy hour; holding a workplace conversation; or engaging friends on social media, every action will get more people to join the movement. Let us know what you’re planning so we can help amplify your efforts! 

Check out our NO MORE Week 2025 Guide you can use to get more information and ideas. We’re looking forward to uniting once again on March 2nd because we know that we are louder, stronger and more impactful together! Thank you for your continued support.

Get Involved

I’ve signed up for the No More Week Tech Summit, no doubt registration will go fast. I’ll follow up with a post specific to the Tech Summit.

Melinda

Reference:

https://www.nomore.org/email/f68b3e4b-5f24-4b32-9063-7776875bf364/?ref=no-more-newsletter

Celebrate Life · Health and Wellbeing · Men & Womens Health · Mental Health · Photography

Blogger Highlight-Peerless Cynic

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 the blog of Peerless Cynic. I have followed Charlie for some time now and thoroughly enjoy his posts. I’m not usually one for poetry but his is short, makes total sense, is seamless, and not to mention the photos he adds photos that are a perfect fit. 

Peerless Cynic

Where derision meets concision.

From the serious to the satirical, modest musings on topics ranging from politics to culture to nature, with a side dish of photography. Or, an ill-defined adventure destined for great pings.  In any case, how can we avoid being cynical?

My name is Charlie and I hail from Nova Scotia, Canada.  I’m a semi-retired IT consultant who has traveled throughout the U.S. and Canada and also a nature photography, a hobby I started PeerlessCynic mostly as a way to express political commentary and satire, always with a good dose of humor.  While I still write about those topics the blog itself increasingly became mostly about nature.  Over time my love of nature photography expanded to include little vignettes or stories about the pictures themselves, a kind of attempt, for better or worse, to capture that peaceful sensibility of the woods.
 
My hobbies include playing guitar, reading and hiking.  I am most definitely a hobby writer rather than a published writer, but I do enjoy it and hope from time-to-time others do as well. 
 
All my photos are from my travels around Nova Scotia, the many lakes and hidden gems. I have so many favorites and each one has its own story.  But a few stand out for sure.  One photo under the title of ‘Faraway Woods’ is special, as that trip was one of the last I took with my father before he passed.  As I took the shot, he was nearby enjoying that beautiful vista.  Fishing and being in the woods were his favorite things, and I guess some of that rubbed off on me. 
 
 
Another is under the title ‘Woven in the Sun’, a lovely sunset on a lake near the Musquodoboit valley in Nova Scotia.  Of all the lakes I’ve visited this one stands out as the finest one for sunsets, a very inspiring place indeed.
 
 
And probably one of the most visited spots for me is a well travelled place called Triplet Lake,  one in a series of lakes not too far outside Halifax, which inspired the poem ‘By the Lake’, a piece that in a way sums up my love of the woods.
 

I asked Charlie a couple of questions that you will find interesting.

M.  How and when did you get into writing poetry?

C.  I’ve always had a special affinity to nature even when I was very young, in fact as far back as I can remember.  When I began the nature photography, I just suddenly had all these ideas in my mind that I had to get down on paper, which began probably around 2013.  I was imaging the forest and the rivers and so on in conversation with each other, the connectivity of the natural world.  So I suddenly created an interesting outlet for myself with the poetry to try and express those connections, as well as the harmony of nature.  The results are mixed as you can see, but I do enjoy the challenge of creating these little stories, of recreating that feeling of peace that I’ve always had while in nature.  

M.  Your photography skills are breathtaking, when did you pick up photography?

C.  I’ve always had a fascination with expression mainly through writing but also nature photography, a hobby I developed rather late in life. 

Here is a recent post I truly enjoyed.

The Autumn Light

The words of the poem and the photo are symbiotic, I love how the beautiful colors unfold around me.

Stop by Charlie’s blog, say hello, pull up a chair, and stay a while. You’ll be so glad you did. 

Melinda

Looking for the Light

 

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

AIDS Awareness Month & History

How My Lyme Doctor diagnosed the first HIV/Aids patient in North Carolina

A second-generation physician from Illinois, curious about medical mysteries (“It’s just like detective work!”), young Dr. Joe Jemsek became an infectious diseases fellow in 1977. In 1979, Jemsek and his young family resettled in Charlotte, North Carolina, where he began a promising infectious disease practice at the renowned Nalle Clinic. Intrigued by reports of a “gay cancer,” Joe’s “detective” instincts led him to diagnose North Carolina’s first case of what would soon be known as HIV/AIDS. As the years went by, he grew absorbed by the AIDS epidemic, bearing witness to some of its most dire casualties — losing patient after patient to opportunistic infections — as well as to the first signs of hope with the advent of life-saving drugs in 1995.

I’m so proud of Dr. Jemsek, he took his knowledge as an Infectious Disease doctor and made history. Due to his commitment more research has been done and the lives on people with HIV/AIDS have improved.

What is HIV?

The human immunodeficiency virus, or HIV, is a virus that attacks the immune system, specifically CD4 cells (or T cells).

The virus is transmitted through bodily fluids such as blood, semen, vaginal fluids, anal fluids, and breast milk. Historically, HIV has most often been spread through unprotected sex, the sharing of needles for drug use, and through birth.

Over time, HIV can destroy so many CD4 cells that the body can’t fight infections and diseases, eventually leading to the most severe form of an HIV infection: acquired immunodeficiency syndrome, or AIDS. A person with AIDS is very vulnerable to cancer and to life-threatening infections, such as pneumonia.

Though there is no cure for HIV or AIDS, a person with HIV who receives treatment early can live nearly as long as someone without the virus. And a study in 2019 in the medical journal, Lancet, showed that an anti-viral treatment effectively halted the spread of HIV.

In September of 1982, the CDC used the term AIDS to describe the disease for the first time. By the end of the year, AIDS cases were also reported in a number of European countries.

Where Did AIDS Come From?

Scientists have traced the origin of HIV back to chimpanzees and simian immunodeficiency virus (SIV), an HIV-like virus that attacks the immune system of monkeys and apes.

In 1999, researchers identified a strain of chimpanzee SIV called SIVcpz, which was nearly identical to HIV. Chimps, the scientist later discovered, hunt and eat two smaller species of monkeys—red-capped mangabeys and greater spot-nosed monkeys—that carry and infect the chimps with two strains of SIV. These two strains likely combined to form SIVcpz, which can spread between chimpanzees and humans.

SIVcpz likely jumped to humans when hunters in Africa ate infected chimps, or the chimps’ infected blood got into the cuts or wounds of hunters. Researchers believe the first transmission of SIV to HIV in humans that then led to the global pandemic occurred in 1920 in Kinshasa, the capital and largest city in the Democratic Republic of Congo.

The virus spread may have spread from Kinshasa along infrastructure routes (roads, railways, and rivers) via migrants and the sex trade.

In the 1960s, HIV spread from Africa to Haiti and the Caribbean when Haitian professionals in the colonial Democratic Republic of Congo returned home. The virus then moved from the Caribbean to New York City around 1970 and then to San Francisco later in the decade.

International travel from the United States helped the virus spread across the rest of the globe.

Advances in Treatment options

DOVATO

Cabenuva

Lenacapavir

islatravir. close to FDA approval

There are older medications that may work for you, talk to your doctor about and come up with a plan that works for you.

Melinda

References:

https://www.history.com/topics/1980s/history-of-aids

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

November Awareness Months And Days

October was full of informative awareness months, and November will also be. The list is extensive, if you want to read about all the awareness months and days, click here.

Awareness Months

Native American Heritage Month

Movember

National Homeless Youth Awareness Month

COPD Awareness Month

Diabetes Awareness Month

Epilepsy Awareness Month

Lung Cancer Awareness Month

Pancreatic Cancer Awareness Month

Awareness Days

International Stress Awareness Day – November 2

World Adoption Day – November 9

Veterans Day – November 11th

Humane Society Anniversary Day – November 22

National Recycling Day – November 15

International Day for Tolerance – November 16

International Transgender Day of Remembrance – November 20

International Survivors of Suicide Loss Day – 1st Saturday before Thanksgiving

Melinda

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

What Are the Signs and Symptoms of Depression in Men?

Men, women, and people of all gender identities may experience depression at some point in their lives. Depression is a serious condition that affects how a person thinks, feels, and acts.

According to the Centers for Disease Control and Prevention (CDC), women seem to experience depression at a higher rate than men. However, it’s thought that men may be underrepresented in these numbers. 

This may be due to mix of social and biological factors that make it more challenging to notice and diagnose depression in men. They may also feel culturally pressured to act “manly” by hiding their emotions.

Because of this, it’s more common for men to have depression with symptoms that are different and sometimes harder to identify. 

If you think that you or someone you love may be struggling with depression, read on to learn about the signs and symptoms that men may experience and what you can do next.

Physical symptoms of depression in men

Men with depression may first notice its physical effects. While depression is thought of as a mental health disorder, it can also manifest in the body. 

Many men are more likely to visit their doctors for physical issues than for emotional issues.

Some common physical signs of depression in men include:

Mental symptoms of depression in men

Mental symptoms of depression may present differently in men than they do in people of other genders, which can make depression harder to detect. 

These symptoms may interfere with the way a person thinks and processes information, affecting behavior and emotions.

Some of the most common mental symptoms of depression in men include: 

  • inability to concentrate
  • memory problems
  • obsessive-compulsive thought patterns
  • racing thoughts
  • sleep issues, usually difficulty falling asleep or staying asleep
  • suicidal thoughts

Emotional symptoms of depression in men

When most people hear the word “depression,” they think of a person who seems very sad. However, sadness is just one of many possible emotions depression can cause. 

In addition to sadness, men may experience the following emotional symptoms of depression: 

  • agitation
  • aggression
  • anger
  • emotional withdrawal from friends, family, and colleagues
  • hopelessness
  • lack of interest in family, community, hobbies, and work
  • lack of libido
  • restlessness

Behavioral signs of depression in men

The mental, physical, and emotional symptoms of depression in men can also affect behavior. Because some men resist discussing their emotions, it’s often their behavioral symptoms of depression that are most apparent to others. 

In men, the behavioral symptoms of depression most commonly include:

  • difficulty meeting work, family, and other personal responsibilities
  • drug misuse
  • drinking alcohol in excess
  • engaging in risky activities, such as driving recklessly or having unprotected sex
  • social isolation
  • suicide attempts

Why can depression go undiagnosed in men?

While discussions around mental health seem to be expanding in reach and compassion, there’s still some cultural and social stigma around depression— particularly among men. 

Generally, men are socialized by society to hold in their emotions, though we know doing so isn’t healthy. In their efforts to maintain these social norms, many men may be compromising their emotional, physical, and mental well-being. 

In addition, many men are never taught to recognize the less typical signs of depression that they’re more likely than others to experience.

Some men never seek help for their depression because they never recognize the signs. On the other hand, some men who do recognize the signs may struggle to discuss their experience because they fear the judgment of others. 

As a result, when many men experience the signs of depression, they begin to work long hours or otherwise fill their time to stay busy, instead of addressing the depression itself. 

Diagnosing depression and seeking treatment can help save lives. Suicide rates are high among men, especially those who have served or currently serve in the military. Additionally, men are three to four times more likely than women to complete suicide.

In continuing to open up the conversation, we can help men with depression recognize the signs. By seeking treatment, men with depression can live their fullest possible lives.

What are the current treatment options?

Depression is most often treated with talk therapy, medications, or both of these things together. A healthcare professional can help create a personalized treatment plan that works best for you. 

Many men begin treatment for moderate cases of depression by scheduling an appointment with a talk therapist (psychotherapist). From there, the therapist might suggest specific types of care, such as: 

From there, medication may be added, if needed.

However, for more severe cases, medication might be prescribed right away to help alleviate some of the physical, mental, emotional, and behavioral symptoms of depression. This may be the case for someone with suicidal thoughts or who has attempted suicide.

Antidepressants such as paroxetine (Paxil) or sertraline (Zoloft) are commonly used to treat depression. However, a mental healthcare professional may also suggest other medications. 

Be aware that these medications often take several weeks to months or begin making a noticeable difference in the way you feel. Be patient and stick closely to the treatment plan. 

When to seek help

If you’re experiencing one or more of the above symptoms of depression to the point that it interferes with your daily life, consider scheduling an appointment to meet with a mental health counselor. 

Most insurance plans provide coverage for such counseling, and receiving care is discreet and confidential.

If you’re experiencing suicidal thoughts, plan to attempt, or have attempted suicide, call the National Suicide Prevention Lifeline at 800-273-8255, or dial 911.

The takeaway

While recent conversations around mental health have become more candid and inclusive, many men still find it difficult to talk about their emotions in a society that upholds traditional views about men. 

It can also be challenging to identify the symptoms of depression in men, which are influenced by those same social factors as well as male biology.

By sharing knowledge about the symptoms of depression in men, we can help clear a pathway toward better, more inclusive mental healthcare.

With talk therapy, medication, or a combination of these two things, depression becomes a much more manageable part of the human experience.

Melinda

Reference: