rheumatology departmemt at king George been messing me around. I was also on mild was on hydrocloqiune (wrong spelling but get jist) with steroids and caluim tablets. The hydro was affecting my eye sight and opticians wrote to my Gp. Was told to stop medication havent been on anything since august and the doctor cancelled my dec appointment cause she was ill. And im chasing up 4 my next appointmemt not taking me serously talking about july 13th kmt so Im gna go A&E 2mo cause this is a joke now havent beem seen by doc since july august. Will keep you all posted.
I fatigue always i getbtired alot can fall asleep standing up.
Will keep u posed
In Jan. I told my rhemy that I was waking up to horrific arthritic pain in my arms, hands and legs. Now I just emailed I'm on week three of pins and needle feeling all over my body at night when I lay down. According to message boards I'm reading online this is related to my MCTD - why is she saying that according to my bloodwork my disease is quiet so it can't be the MCTD???? Do I need to find a...
Hi everyone, I am a new for this forum . I woul like to learn from everyone.I have been diagnosed MCTD last May. I have got pain left hand, dry eyes , mouth , sore throat , tingling togue, white mucuss on the togue. Stuffed nose , allergic rhinitis, reflux, lost appetite and lost a lot weight. Very bad insomia , stress etc.I am on plaquenil 200/300 alterntive and pred 5mg daily. Hand joints pain...