Hi, I have FMS as well. Not only B-vitamins, but "Omega 3's" help with the brain fog / farts.
As for exercise with FMS, I used to bike for an hour and a half every day, and it didn't prevent me from getting fibro, so I have to ask how on earth it's expected to cure me. Although it's a "point to ponder", I do have to say that exercise is beneficial - we are going to hurt anyway, so may as well have strong muscles that hurt instead of weak ones.
Hope you have a pain-free day!
I would certainly call the pain variable. And while there are activities that are sure to make it worse, at other times it may decide to flare up even without a known stimulus. As you know from experience, at its most severe the pain is a major distraction and hindrance to normal activities.
I find that I feel better when I am warm enough, as opposed to when I am chilled. But extra heat in the form of a heat pack or hot water bottle doesn't seem to help (me, at least).
You may have noticed that regular anti-inflammatories (either over-the-counter or a prescription like Celebrex) don't do much for the severe pain that makes you limp. That's a clue that it isn't true tendonitis, like tennis elbow or something. Medication for nerve pain should be more effective.
I hope whatever treatment you choose works well for you!
Let me ask you this... Did your knee feel really stiff and painful sometimes and then others not so ??? My ankle can feel pretty calm (I still baby it by not using much range of motion with it) and then I sit down or something and go to walk and it hurts so bad that I have to limp to get anywhere. Then after a period of time(varies), I can walk with only sl. pain. Sound familiar??? Also the hip on that side is so tight and less flexible. Did heat help you? I'm looking into meds. thanks
You might consider waiting on the surgery until you try the Elavil or Neurontin for a while (a year, say). Calming the nerve symptoms actually relieves some of the stiffness over a long time. I walked with a very stiff knee for 2 years due to severe tendon/muscle pain that might be like your ankle situation. This made my hip tight also, and began to reshape the bones.
With the Neurontin (1 year), continued exercise, and a healthy diet, I have gradually gained range of motion in that knee and have started to be able to strenthen some of the muscles that weren't used for a long time. I'm not totally symmetric in terms of flexibility and function, but it's a lot better.
Studies have shown that fibro patients have more pain and for longer duration after surgery. It may not be easy to rehabilitate. I had arthroscopic knee surgery before we knew I had fibro, and it was a much bigger deal for me than for most young athletes. In fact, it would have been preferable not to have it.
But you are not me! It might be different for you. I just wanted to share what I know from experience. As for your attainable level of activity... everything with fibro is "until further notice." Maybe, maybe not. Enjoy each day!
Thanks for the info. I have met others with fibro that take Elavil at night and they say it helps. Will look into it. I hate to hear that you have had to modify your exercise so much. I keep hoping to run/jog again. I loved to go on a run and I miss that so much. The pain on my inside left ankle (dx as post-tibial tendonitis by ortho) is so bad even when I try to walk. I walk with a stiff ankle to relieve the pain. I'm considering surgery on it now. The modifications in my gait are hurting my knee and hip so I have to do something. Sending healing prayers your way. God Bless
Hello, hope you're feeling well today. I got on some more sites and read alot about B-12 (and its different forms). Lots of people with fibromyalgia report numbness and tingling like feelings and I saw where the B vitamins have helped them. I used to take alot of vitamins but as I began other programs I limitted what I took so that my clinical picture was more clear. I also read where most people have a normal blood level of B-12 and folate but the vitamin, whether oral, or sl or inj. really helped. I knda figured whether my levels were normal or abnormal, the B-12 couldn't hurt since it's water sol. Anyhow, I had called my gp about 3 weeks ago for a lyme test and I have never heard back. Just wanted to get a jump on healing. I understand your point. When my gp schedules me, I'll hold off on all my vit. before I go. I believe you hit the nail on the head with the B-12 problem. Thanks!!!!!!!