Myasthenia Gravis Support Group
Myasthenia gravis (MG) is a neuromuscular disease leading to fluctuating muscle weakness and fatiguability. The hallmark of myasthenia gravis is muscle weakness that increases during periods of activity and improves after periods of rest. Although myasthenia gravis may affect any voluntary muscle, muscles that control eye and eyelid movement, facial expression, and...
OK, I went to a UCLA MG specialist today. He likes Cellcept over Prednisone. I guess Prednisone is a short-term treatment, but what makes Cellcept better.
Cellcept is for transplant patients while Prednisone is for autoimmune patients. My doctor said the Cellcept will take 6 months to take effect while Prednesone a matter of weeks (maybe even a week).
Maybe cellcept is better if you get an infection /virus? But because it take so long to take effect, wouldn't take for ever to get it out your system?
Anyway, he is keeping my Prednisone at just 40 mg / day and starting me at 500mg of Cellcept. He also ordered some IVIG treatments until the Cellcept kicks in (every two weeks as long as the insurance pays - but with Obamacare my insurance program is likely to change at the end of the year - or maybe the individual policy will be eliminated - we will see).
I bet Cellcept has some long-term side effects too.
Cellcept is for transplant patients while Prednisone is for autoimmune patients. My doctor said the Cellcept will take 6 months to take effect while Prednesone a matter of weeks (maybe even a week).
Maybe cellcept is better if you get an infection /virus? But because it take so long to take effect, wouldn't take for ever to get it out your system?
Anyway, he is keeping my Prednisone at just 40 mg / day and starting me at 500mg of Cellcept. He also ordered some IVIG treatments until the Cellcept kicks in (every two weeks as long as the insurance pays - but with Obamacare my insurance program is likely to change at the end of the year - or maybe the individual policy will be eliminated - we will see).
I bet Cellcept has some long-term side effects too.
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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...
But what if it doesn't work? The doctor also put me on Cellcept just in case. AT LEAST THIS IS WHAT IT SEEMS. But since that takes longer they might as well start me on it now.