Guest guest Posted September 30, 2005 Report Share Posted September 30, 2005 Hi Jeanne--welcome Blessings to you! I can't tell you what a lifesaver this group has been for me. I'm one of those people with a wad of symptoms from the fibro arena and another wad from RA with normal labs all around. I've been to a dozen docs and my current rheum. says " fibro " but my neurologist says " RA " . I get better when they treat it like RA so the rheum is going along with it for now, but he really thinks I'm just nuts. This group is a place where we all believe you when you say, " I'm not a wimp " because we know how hard it is to just get out of bed in the morning sometimes. I've gotten lifesaving advice, warmth and a lot of laughs here. I'd love to hear more about you. Your job must be very interesting because people really open when they're getting a massage. I bet you're wise beyond your years from hearing people pour their hearts out to you while you work. As for where to begin, you really want to get into a rheumatologist a.s.a.p., I guess, because they are the ones in a position to prescribe the meds you really need. Don't be surprised, though, if you leave the office more confused than when you arrived. I've been to four different ones and the information I've gotten from one often completely contradicts the information I got from the others. My rheumatologist even admitted that there's a saying that if you have two rheumatologists in the same room you have three different opinions. Still, the other specialists are too chicken to deal with drugs like prednisone and methotrexate. Remember, though, this is only one person's viewpoint. Your experience might be totally different. Best wishes, laura jeanne <oceangypsey@...> wrote: Hi ALL i HAVE BEEN LURKING for awhile...just wanted to make sure i fit in here...i have thyroid disease,and my current doc is convinced i also have RA or lupus, was told i had fibro myalgia a number of years ago...do not know where to start...my endo told me to see a rheumy...but , i have not done it yet....i am in chronic pain all the time...have the swollen joints(two )in my finger...also have joint and bone pain thru out my body...i am not a wimp,(as i am sure none of you are either)i have been a marthon runner for many years, and a mountain biker....so, you see this hitting home for me too...i am a licensed massage therapist by profession,and my job so far has not been affected,(i have just figured out ways to adjust)--i have been on vioxx,bextra,relafen,celebrex,etc...none of them even took the edge off really,try really hard not to take narcotics very often,but sometimes i have to in order to sleep at all.--oh, and i had iriditis this summer too,anyone had that yet?--please tell me where to begin...thanx, jeanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2006 Report Share Posted May 11, 2006 I've been dealing with a number of autoimmune issues all my life (hoshimotos, raynauds, Rhematoid) and quite a bit recently. A few weeks ago I was hospitalized and diagnosed with ITP, idopathic thrompocytopenia Purpura, " Idiopathic " means that the cause is unknown. " Thrombocytopenic " means the blood doesn't have enough platelets. " Purpura " means a person has excessive bruising. In people with ITP, all of the blood cells are normal except for the blood platelets. Platelets are the tiny cells that seal minor cuts and wounds and form blood clots. A person with too few platelets bruises easily and bleeds for a long time after being injured. And now they think i amy also have Antiphospholipid Antibody Syndrome is a very rare blood disorder characterized by recurring blood clots. In the Antiphospholipid antibody syndrome, the body recognizes phospholipids, (part of a cell's membrane), as foreign and produces antibodies against them. In young women, it may be associated with spontaneous abortions for no apparent reason. I have started a webpage www.miseryandmirth.com where i discuss my autoimmune problems, treatments options and such. I would greatly appreciate people looking it over, sharing it with others and leaving me comments/feed back. The page is in reveres chronological order with newest entry on the top, so not to get too confused, scroll down to the entry titled ITP and reading up would be wise. THANK YOU, Angel Quote Link to comment Share on other sites More sharing options...
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