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You are here: Home / Conditions / Fibromyalgia / Why are so few men diagnosed with Fibromyalgia? (guest post)

Why are so few men diagnosed with Fibromyalgia? (guest post)

Last Updated: June 15, 2015

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

Why are so few men diagnosed with Fibromyalgia?

During my recent interview with @Fibro_boy (aka Leo) he brought up the rarity of guys being diagnosed with Fibro, and his thoughts were so insightful (again I’m amazed at how wise this guy is for his age) that I wanted to share them as a separate post.

Why are so few men diagnosed with fibromyalgia?Image by Pexels from Pixabay
 

Why are so few men diagnosed with Fibromyalgia?
by Leo Cristea

guys with Fibro aren’t actually that rare Share on X
Consider the fact that guys with Fibro aren’t actually that rare! This is a misconception for two reasons, that are nevertheless, intricately linked:

Men are expected to weather pain. It’s something we are simply expected to do. Men are the strong; women are the weak. Of course, it’s utter tosh. People are absolutely equal. But everyday sexism is ingrained deeply into peoples’ mindsets and therefore, as with many things that men do or say unwittingly to offend women, the same will inevitably happen with men. Imagine wives telling husbands to stop being babies, making jokes about Man Flu if their husband happens to have the Fibro symptoms that mimic those of colds and flu, every day. And, in the same way that women often body-shame other women, or cast doubt on accounts of assault, etc, other men will also add fuel: it will be laddish and meant harmlessly, but it isn’t.

It really isn’t harmless. They will eventually be told to “man up”. So, out of embarrassment or shame or irritation, they remain quiet and eventually begin to think that everyone else is right: that they do need to man up. Sexism hurts men just as much as it attacks women. It runs both ways. And that’s why I identify heavily as a Feminist. Men, women—anyone can and should identify as a Feminist. Maybe if men weren’t too afraid of the ridicule of being weak and sick—let alone with a women’s disease, gods forbid!—the stats on men with Fibro would be more accurate.

Furthermore, consider the above in relation to men with any kind of chronic illness or pain. Maybe they never even read into such things because they’ve convinced themselves it’s “nothing”. Or that it really is all in their heads. But what about the smart guys who have a pretty good hunch that it is Fibro? Those guys might still remain silent because, well—who has the spoons for the stress of potentially having to convince a doctor it might be Fibro? That’s going to be one fear: that they will be flat-out dismissed. And yes, this happens. Heck, it happens with other diseases, like Lyme disease, where some doctors still refuse to accept it as a real illness. So how many guys really have illnesses like Fibro or CFS and trudge on with ultimately difficult and unhappy lives, just because we live in a sexist society? It sucks, doesn’t it?

Men often keep their pain quiet out of fear of being dismissed. Share on X

I do think that, yes, as with many conditions and diseases, women suffer more commonly. But the key word there is: more. Not entirely. Not totally. Just more. And yet if you start looking at stats that actually care to dig deeper, you find that much of the myth is just lazy research and assumption. The last paper I saw on “Men with Fibro” was from 2012. We’re now in 2015—tell me that there wouldn’t be more men diagnosed if the condition was treated like any other?

I remember reading a statistic somewhere that for every four or six (I don’t remember entirely) people who have Fibro, one of them is male. That’s, if we go with the higher number, still one in six. One sixth of all people with fibro are guys. Translate that into numbers, into actual men with fibro. It’s a smaller number than the female side of the chart, but it is by no means an insignificant number. One in six is a lot. Never mind if it was actually one in four!

 

Related Posts:

  • Guys with Fibromyalgia: @JohnnyTribs
  • Fibro Warrior : Gary of @FibroGuys
  • Fibro Warrior : Guys with Fibro – Richard Gerome
  • Fibro Warrior: Andy – Running With Fibromyalgia

 

3 Comments Filed Under: Fibromyalgia, relationships Tagged With: Guys with Fibro

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. mj says

    March 17, 2023 at 1:26 am

    Kent…was it difficult for you to get diagnosed?

    Reply
  2. Mike Montbriand says

    June 23, 2015 at 10:56 pm

    I think there is good evidence why women are at risk for Fibromyalgia (FM)
    1) Hormonal – transexual study – men becoming women: 30% developed pain. Women becoming men – 5/11 lessened their pain on testosterone. http://www.ncbi.nlm.nih.gov/pubmed/17379410
    2) Sleep – sleep disordered breathing is common in menopause. http://www.ncbi.nlm.nih.gov/pubmed/12615621
    sleep disordered breathing linked in big way to FM – http://www.ncbi.nlm.nih.gov/pubmed/15164899
    3) Celiac – undiagnosed dumbed- down version of celiac called gluten intolerance very common in FM with irritable bowel http://painmuse.org/?p=4330
    Celiac is diagnosed twice as common in women. http://celiacdisease.about.com/od/diagnosingceliacdisease/f/GenderDiff.htm
    4) Bipolar: 1 out of every 4 FM cases are bipolar:http://www.ncbi.nlm.nih.gov/pubmed/20712752.
    Some bipolar disease is a mitochondrial disease. FM has been found to have mitochondrial deficits: http://painmuse.org/?p=4468. I suspect low testosterone adversely effects mitochondrial metabolism. BTW I have never seen a women with FM have any testosterone at all. There is an interplay of mood and FM that multiplies the severity of each illness.Those with transmittible mood disorders will have kids with same and that will break their heart..
    5) Smaller frame more susceptible to whiplash injury
    6) Polycystic ovary victims – near 5 times the FM rate
    7) Etc – lower muscle mass, effects of pregnancy on nutrition, SI joints.
    8) Higher rates of women smoking now
    9) autoimmunity – more common in women – http://www.sciencedirect.com/science/article/pii/S0091302214000466
    Thyroid autoimmune antibodies almost twice is common in FM: http://www.ncbi.nlm.nih.gov/pubmed/16541203
    Women can’t win re FM.

    Reply
    • Kent says

      November 25, 2015 at 8:04 am

      Man here with fibromyalgia!

      Reply

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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