Lupus Support Group
Lupus is an auto-immune disease in which the immune system cannot distinguish between threats (like viruses and bacteria), and healthy cells and tissue. As a result, the body produces antibodies that inflict cell damage, most commonly targeting joints, skin, kidneys and the nervous system. Join the group and find support for coping with lupus.
I have been diagnoised with idiopathic prca since may 2006. the doctors i see have tried cellcept, atg, treatments for parvo virus, higher doses of predisone, they have tried stopping all the meds they dare stop, switch my meds from prograf to cyclosporin and finially back to prograf, and stopped plaquniel.
They don't know what caused prca. I continue to think its sle causing this new crisis in my body.
I am transfusion dependent now, I recieve 2 pints of red blood cells every two weeks and will continue to do so for as long as i live. I've also had two bone biopseys.
They don't know what caused prca. I continue to think its sle causing this new crisis in my body.
I am transfusion dependent now, I recieve 2 pints of red blood cells every two weeks and will continue to do so for as long as i live. I've also had two bone biopseys.
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This isn't really bipolar related but there is never anyone on the parenting groups, this is the most active group I've been in.My 6yr old son has really bad seasonal allergies and they're in full force right now. He gets a terrible cough; he coughs all day and all night, making it hard for him to sleep, and his nose runs.I've tried every allergy medicine, OTC and RX, and none of them affect his...
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Is anyone here allergic to Sulfa that is currently taking Diamox? I have been diagnosed with IH now for almost 2 years. I am allergic to Sulfa drugs meaning that my throat will swell up so my Neurologist put me on Topamax. I was suffering from major loud whoosing noises and the topamax helped that but everyday I still hear those mainly between 6 - 12 pm. I am at my wits end and have not went...
I've discovered from my research about lupus-related anemia that 10 percent of lupus patients develop AIHA (autoimmune hemolytic anemia), and there are rare cases (in which you may be one), circulating plasma factors tell the bone marrow to turn off the production of red blood cells. The end result of this slow-down or shut-down of the bone marrow, termed hypoplasia or aplasia. This usually reflects active disease, and corticosteroids or cytotoxic drugs are necessary. A careful drug history should be taken, since many prescription drugs can occasionally cause aplasia. I don't think the last sentence applies to you, but it does seem as if sle and prca may be related in some way. I hope this information helps you out...