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Living with Fibromyalgia

This section is a place to share stories about Living with Fibromyalgia.

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by: Janelle on Wed, Aug 01 2007

I, like so many went undiagnosed for many years. I knew something was terribly wrong around 1992, as I was having new symptoms and my migraines were becoming more frequent and severe. I had been married for 21 years and it was a good marriage, with 2 wonderful children. I had the wonderful family I had always prayed for. My parents were both deceased, so all the other family I had was a brother and sister.

I became very depressed, as no-one seemed to know what was wrong. My husband left me for a coworker 15 years younger and in perfect health, leaving me to care for our 2 children. And that was only the beginning. Within a period of just over a year he divorced me, forced me to file bankruptcy, I lost my only brother to cancer, lost my home, both children went into deep depressions, one suicidal and there were many other things. Too many to mention. He took me to court many times to drain me of any financial means that I had. Because of major errors, he was able to stop all support so I became destitute with nowhere to go, as my sister was too busy with her own life.

I had a wonderful physician who became my touchstone, my lifeline and I was finally diagnosed with severe Fibromyalgia in 1996. Due to the overwhelming stressors in my life my symptoms were off the charts! And I was basically on my own. I had wonderful friends who did their best, but were so overwhelmed they slowly faded into the distance. I had never felt so abandoned and alone in my life to the point that I contemplated suicide. But couldn’t do that to my children since I was all that they had.

What I want to share is through all of this I had to come to some realizations of this disease. Since it is invisible to most people and not known or understood especially by the majority of the medical profession it becomes a crazy-making disease that can cause many to go into isolation and lose all hope. We are looked at as drug seekers, addicts, etc. And that is why the suicide rate is so high.

Unfortunately, we must find a way to become our own support and more importantly our own advocates! Which can be so difficult when you can hardly function most of the time. I knew one woman who could not get any pain medication from her physician and was contemplating suicide. Then she was diagnosed with “cancer.” And her physician began giving her all types of pain meds. The irony in this is her pain had not changed only the label! It is very difficult to understand why people with terminal illnesses receive so much support and pain meds, but those of us with chronic pain that can go on for years and years with no relief are left to suffer. It is nothing less than inhumane. I hope that in the near future there will be more knowledge of Fibromyalgia to both the medical profession and the public and we will get the pain medication and support that we, as humans deserve. My prayers are with you all.

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August 2007

  • fibromyalgia - by c.s - (Tue, Aug 28 2007)
    i read about this in the news paper one day and i talke to my mum about it and she said that what she has soi started to recurch and every thing i have are the symyoms. this site really helped me to understand what it is. [more..]
  • fibromyalgia - by jeri - (Mon, Aug 20 2007)
    i started experiencing pain 2 to 3 years ago. last year i got to the point where i started falling. i have been thro so many tests, with no diagnosis i put all my symptoms in the computer and it always comes up ms lubus [lupus], rheumatoid arthritis, or fibromyalgia. [more..]
  • fibro - by lesley - (Thu, Aug 16 2007)
    hi. i was ill for 8 months my doctor keep saying it was flu but i knew that something was wrong. had all test done and they came back ok. he still was saying it was flu so i changed doctors. [more..]
  • For Cassandra from a mom w/ FMS - by FMS Mom - (Tue, Aug 07 2007)
    I am a mom w/ severe FMS [Fibromyalgia]. Have had it at least 10 years. I have two young children. Cassandra your story touched me so much because I really saw my disease from a child’s perspective. I wanted to offer my support to you. You are right - your Dad’s guilt and sorrow over not being the father he wants to be to you is likely his biggest sorrow - far surpassing the physical pain of the disease. [more..]
  • Fibromyalgia - by Audrey - (Tue, Aug 07 2007)
    I’ve had it for years but it was never diagnosed. Then I had a lot of stress and since then I’ve had just about every ache and pain that is in your fibromyalgia article. I’ve been under the care of several doctors and have had much physical therapy [more..]
  • I have never been this sick - by Sandra - (Mon, Aug 06 2007)
    Hello my name is Sandra. Back in late March 2007 I woke up and I could not move, I felt like I had the flu high Temp 103, I was in bed for 1 week lost 20 lbs. I went to the doctor and was told I had Hepatitis A. It is now 4 months later I am still off work and in so much pain. [more..]
  • hope for children with fibromyalgia - by P C - (Mon, Aug 06 2007)
    When my son was in second grade he got up one morning and could not stand for me to brush his hair. He said it hurt real bad. He could not stand for us to touch his head. We went to our family doctor and he referred him to a doctor in Memphis Tennessee. He took a look at him and took one blood test and told us he had fibromyalgia. [more..]
  • My dad and fibromyalgia - by Cassandra J - (Mon, Aug 06 2007)
    I dont have Fibromyalgia but my dad does…. I watch him go through every day in pain…. I know that he always depressed…. I notice alot that he feels because of this my dad feels that hes not a good father to me…. i tell him he is all the time but he never listens… hes had this disease for 5 years and i would do anything to make this go away… my dad has had many surgeries and none of them seem to help…. [more..]
  • Living with narcolepsy, fibromyalgia, and others - by Cat - (Wed, Aug 01 2007)
    Where did I GO? I have Narcalepsy [narcolepsy], Cataplexy, Fibromyalgia, Myofascial pain & a few more problems. I was top in my field of work, making $80,000.00 a year. I started passing out, stayed in such severe pain in my back,neck, lower back,legs,etc. Then I couldn’t manage the computer, I would forget everything, [more..]
  • We need support too - by Janelle - (Wed, Aug 01 2007)
    I, like so many went undiagnosed for many years. I knew something was terribly wrong around 1992, as I was having new symptoms and my migraines were becoming more frequent and severe. I had been married for 21 years and it was a good marriage, with 2 wonderful children. [more..]
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