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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board

Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index

I'd bet you can find better info on the net than from me. Auto-immunes run in my family, so I only know a little about FMS. There is a definate test that can be done now to determine your diagnosis of FMS. As for what I know, it's a simple blood test that has to be sent to a special lab (your doc should be able to get info as well) somewhere and they will run genetic testing (DNA) and let you know in a couple of weeks if you have the genetic malformation that causes FMS. I would try looking at some of the popular FMS websites, am sure they'd have information on it as well, just do a websearch and see what it comes up with. I also used to go to a local FMS support group (because RSD is close in symptoms and I needed someone to talk with) and they had tons and tons of information for me as well. You might want to look into your local hospitals and see if they have any programs for people with Fibro. They are the best resource for information because they hear everything directly from the hospital. Hope that helps you. - Jessica
PS If i'm remembering correctly the test has been out since 99 or 00??

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