I am glad that we are all finding each other here, this syndrome/disease (whatever they want to call it today) can be very difficult to deal with and although I would never wish this on anyone, it is great to be able to talk to others who know what I am going through and can also give advice on what works for them. I know since I was DX'd in 2004 my meds have been changed a few times to get them "fine tuned" to work for me. I know of only one other person with FM and that is my cousin who lives in another state, so again, I appreciate talking to each of you here. Gentle hugs to you all and thanks for sharing.
__________________ Jasmine's, Prissy's and Maggie Mae's Mommy  |