I have two friends who have MS and they go to centers that do physical therapy and hydrotherapy and oxygen therapy and more. We as fibro sufferers could benefit from all of this. I see all that they do and honestly say I am jealous because all kinds of alternative therapies are offered there
Unfortunately we really don't' have a category yet ... and even though symptoms may be similar it is not the same and is treated in a different way.
We of us that don't have MS are very lucky. I hope someday we will have a center for us and I would believe that we have so many people with FM that our center will not be able to help someone with a different diagnoses, not being FM.
There have been studies and prof of MS... how ever with FM ... studies are being done but nothing conclusive yet.
XXOO
Yeah I guess, but I am going to look into this center and see if they won't let me go as well. I understand that carers and support people can also use these facilities and I am one of these friends care coordinator and they know me at the center she goes to. I have talked with many of them about her care and taken her there myself a few time and met some of them. I am hoping they will let me use some of there services there but all people with fibro should be included or we should have our own center.
I do not think all Dr. Know about fibro then selves some think it is in our heads.you just have to wait on the medical field to catch up
I have been saying this I think its totally unfair we need help too