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This section is a place to share stories about Coping With Myasthenia Gravis
Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation.
You may also Help others by sharing your story.
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the unknown disease
by: deedee
on Wed, Mar 19 2008
Why do most people,including doctors suddenly become defensive to the word MG? When I try to explain it,people act like I am crazy or because they haven’t heard of it then it must not exist.The neurologist tells me to avoid stress, but how can I when I am treated like a druggy or an acoholic? To beat all, S.S. told me to get out and work because it is all make believe.I have worked at the same job for 30 years and am treated like I am lazy or trying to get something for nothing.It is very stressful.
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Thu, Mar 27 2008
When I got sick in the late 80's. I had been working 12 hours minimum a day & driving 2 hours a day. Then I got sick, had surgery & just kept ...Read
March 2008
- 18 and full of life - by Jess - (Thu, Mar 20 2008)
I was diagnosed with MG in February 2007. I was 17 years old. As a younger teenager I had always had some weakness but doctors told me it was because I was growing and was put on iron tablets more than once.
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- the unknown disease - by deedee - (Wed, Mar 19 2008)
Why do most people,including doctors suddenly become defensive to the word MG? When I try to explain it,people act like I am crazy or because they haven’t heard of it then it must not exist.
[more..]
- My Story - by Sarah - (Wed, Mar 12 2008)
I initially had leg weakness off and on, nothing I was alarmed about. January 2004, 33 years old, I started having double vision, so I went to the eye doctor. Since then, I’ve had to wear glasses with prism lenses, so my eyes don’t fatigue as quickly.
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- Myasthenic Falls at Officers feet … - by MaryAnn - (Sun, Mar 02 2008)
(I had been gradually worsening due to stress …. felt extreme weakness and had fallen)….
It terrifies me to live in a world where I may fall, shake, be extremely weak, unable to speak, swallow, have double vision, or worse … all because of my disease, Myasthenia Gravis and though I explain it, my symptoms may be perceived as “crazy” or “drunk” and I may be denied care. Anyone with a rare disability could die as a result of such ignorance!
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