I think a support group is a great idea, I'm game. But any ideas on strumming up others. I try not to inform people of my fibro or ibs b/c it raises eyebrows if the person knows about it like I have lepracy (sp?) or something and if they don't know then they want an explanation. I don't know which is worse. And us fibromites look normal even though we feel like we have 90 year old bodies. So I don't know how to find fibromites in our area. You can't spot'em and they are probably not gonna tell ya. I know JenX is from the baltimore area and she has fibro also but I think she has been really busy lately as I haven't seen much activity on the Maryland IBS Support Board which she moderates.
We could kidnap Ruchie from Arizona and Linz from the UK and Laura Sue from ...I can't remember where she is from right now. Darn Fibro Fog!! Anyway then we would have an awesome group.
We could try to set up a meeting and try to get JenX to come too and go from there.
Let me know, Christie
-------------------- Christie
~Hoping and Praying for Sleep!~