Craftypisces
Greenlighter
- Joined
- May 5, 2010
- Messages
- 36
I would like to say something about Fibromyalgia. Now, I experience pain daily in every part of my body. It drastically decreases my quality of life and makes me really miserable. It would be easy to diagnose myself with Fibromyalgia and I have gone to the doctors and said thats what I think is wrong with me.
The thing is, I just dont think any more that it is a real illness. Yes, the symptoms are real but I think they are the physical symptoms of psychological problems such as depression due to dissatisfaction in life. Actually, I think the symptoms are a normal reaction to the crazy pressures of modern life and all the stuff we have to deal with that we are not really evolved to do.
I thinks that realising the symptoms are psychological is the first step to recovery. If you give yourself a label like 'Fibromyalgia' then you are creating a belief that you have some kind of disease and you are stuck with it since there is no cure.
I think that, in fact, that you have to sort out the problems in your life, improving your psychological health, in order to recover.
However, this is easier said than done.
LS, I would like to say that I respectfully disagree

I am in my mid 20's and when Fibro struck me, it was during the happiest time of my life. I went to the gym daily, I went out with friends, and had just gotten married and landed a job at a company I was dying to work for. BUT when I was diagnosed with Fibro I will say that I thought it was a load of horse s#!t. I honestly thought the same thing you did. So much that I quit taking Lyrica and just let myself be in pain for 3 years following that diagnosis. That being said, those years were so hard for me. My husband and i desperately searched for answers and even chronicled my symptoms with photos and journals. Did I become a little anxious and depressed, yes, but I also would pull out of it as soon as I possibly could. I was still working and able to do some things. In January, I could not possibly have been in more pain and I was living on adderrall and lortab. I was ingesting more pills than food because I couldn't take the pain. My family and doctor urged me to go to Mayo Clinic in Rochester, MN. I was called to come for an appointment and my father and I flew up there. I saw three neurologists and they did seperate testing. The day after i had the classic "tender point test" I was so sore I could barely get out of bed. My father and I watched the doctor hit these spots on my body and I would literally almost climb the walls in pain. Not until then, confronted with proof from 5 days of intense testing and 9 doctors telling me this, did I believe in Fibro. Now I am home and take Lyrica as well as do physical therapy. It is working and I feel better than I have in 3 years.
Don't dismiss Fibromyalgia though. It's actually not a disease --it is a syndrome (collection of symptoms).
If you think you may have something like Fibro, go see a doctor and get the proper diagnosis. Not everyone uses FMS as a crutch or an excuse to be sad and lazy. I will post pictures of my worst symptoms. Maybe if they look familiar you could relate. I hope this didn't come across as angry or rude. I just wanted to post my experience with FMS and Lyrica. It's a good one.
3 years ago I trashed my Lyrica and swore it off, now it works like magic.
