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Senior Member
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Join Date: Jul 2008
Location: San Antonio
Posts: 1,471
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Senior Member
Join Date: Jul 2008
Location: San Antonio
Posts: 1,471
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Hi Pippi!
Hello and welcome to Neurotalk! You are gonna love it here! There are so many amazing, wonderful, supportive people here with tons of info!
MG is a RARE disease - that's prolly why you haven't found that many people with it where you live - lucky us, huh?
But the GOOD thing is that you have been dx'ed - now we just need to get you WELL! You are not letting your family down - you are SICK! YOU need help, not scorn. Sadly, few people know anything about MG and how it effects us - feel great one minute and down on our backs the next.
Take a deep breath and make sure your neuro knows that you are still weak----there are lots of options for us now! IV IG, plasma exchange, pred, imuran, etc......You just don't want to over do it and pay the price! I speak from experience on this one!
Stress makes MG worse - sad but true. You need to stop beating yourself up and start taking care of yourself! It sounds like you need a support group - well you've got one now! We are all here for YOU! If you need to vent, vent away! 
I'd love to hear from you when you have the time/energy!
Erin
I was given Paxil by my neuro - he said a lot of people with MG suffer from bouts of depression as well!
Quote:
Originally Posted by Pippi
Hey All. I was diagnosed August of last year with Myasthenia Gravis after going to 2 emergency rooms, 2 general practitioners, and eye doctor, and 2 Neurologist. I had droopy eyes,shortness of breath, could not swallow(Did not eat solid food for 45 days) and severe weakness/fatigue. I am a diabetic, so my Neuro has me on Mestinon and Cellcept. Progress has been very slow. In November I was climbing steps.fell backward and was knocked unconcious and airlifted to an Intensive care trauma unit. I have not been able to work since Nov. as I cannot climb stairs, still slur speac, and has a great deal of fatigue after writing/typing/walking for 10-15 minutes. I have found no support groups in East Tennessee and have not found any other males in this area with the disease. I am 58 years old and have applied to Social Security for disability benefits and have been denied once.(They keep sending me PAIN questionaires to fill out and I can't seem to get them to understand the disease, I was turned down the first time and have now appealed. When reading about the disease, I really thought I would be doing much better by now, but inability to work, being months behind on bills, etc. am under so much pressure I feel like a failure to my family and don't understand or know what to do. Found this site referenced by a support group I found on Facebook.
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Erin .
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