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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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#1 | ||
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Member
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I've been on Disability since 2006... approved in 2009 and will probably be up for review next year.
How many are disabled due to MG? And how long have you been on SSDI? Just curious |
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#2 | ||
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Senior Member
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Not me, because I timed my MG very carefully
![]() If I had a full-time job outside the home, I don't see how I could do it. Abby |
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#3 | ||
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Member
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It's great that you have quite a bit of help since you have teenagers Stellatum
![]() ![]() I tried my best to keep working with MG. Worked for 10 years after diagnosis but finally realized that I just couldn't do it anymore. I always said that Social Security couldn't say that I didn't try! I went from Full-time in the office to reduced full-time in office to part-time in office to reduced full-time at home to part-time at home! Finally I accepted the fact that I just couldn't work at all and filed for SSDI. I mean if you can't work part-time from home, what's left? |
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#4 | ||
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Junior Member
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Me. I fought and fought it. Mainly to keep the healthcare. The state disability did physical/mental reviews annually and couldn't understand why SSI kept denying me.
applied in 2006. Got denied and applied for benefits from the state. I didn't get approved until 2010 either. After my 2nd ALJ hearing (with the same judge) to award a BENCH decision. Can you believe that? One word in one of my eye Dr's note changed his mind. I originally started with Ocular MG then to Generalized. Now it's Ocular still. |
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#5 | |||
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Member
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Diagnosed in 2000 and retired on disability in 2010. I have applied for SSDI and still waiting for a decision. However, my employer had great STD/LTD policies and I was approved without any delay. I'll let you know how it goes once I get a SSDI decision.
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