Discussion in 'Fibromyalgia Main Forum' started by craftycats6, Jan 2, 2003.
Does anyone know of a FMS support group in New Orleans,La?
I lived in New Orleans for 3 years (99-2001) and the only one around had been defunct for awhile. The climate was really hard on my soft california constitution.
Dr. Lawrence Giambelluca in Belle Chase treats a lot of CFIDS/FM people and he was a great dr, if you are looking. His office might be able to tell you about a group out there.
Let me know if you turn up anything. Are you a native or a transplant?
Thanks for the info.I will deffinitly call the office and see if they may know of a group.So far I havnt had any luck in finding one,other than on the web.Yea,Im a transplant from Oklahoma,Florida,Georgia,Kentucky.LOL
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