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-   -   MG with Thymoma (https://www.neurotalk.org/new-member-introductions/87817-mg-thymoma.html)

kimp 09-05-2010 07:34 PM

thymoma with mg
 
hello
[QUOTE=Nicknerd;514935]Hello everyone,

I just wanted to tell you that I understand what you are going through because 4yr ago I was diagnosed with thymoma and had to have it removed. I didn't know that I had mg at the time until I started having odd symptoms like you with the mg and still they tell me that there is no pain with mg but the docs don't always listen to us. The second thymoma was diagnosed 2/2010 and then the mg was horrible. I had vision problems, double and blurred. It was horrible and very painful. I do understand what you are going through if you need anything let me know and I will try to help. I have been looking for someone like me because we are so very hard to find. We are like zebra's very special ones we have a reason why we have this. I try reaching out to all kind of people and talking to everyone I can.

I am undergoing chemo right know for the thymoma. The chemo is rough and I will have it until Dec 2010 hopefully it will be gone and I can live the rest of my life w/o any recurrences.


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