Some people with Myasthenia Gravis have shared their stories with the hope that others will feel they are not alone battling the disease. If you have a story to share, please contact us.
My name is Christine. I have MG and I will share my thymectomy experience with you, but remember, we are all different. For me, it got worse before it got better.
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My name is Jan and I am 66 years old. I was diagnosed with myasthenia gravis when I was 58.
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My name is Brad and in late August 2015 I was diagnosed with MG. I am 67 years old and a fifth generation Tejano (South Texas native).
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Hi, my name is Donna. I’ve never wanted to talk about my disability. Now I realize how important it is for others to know about this life-changing disease.
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I’m Jack and I am 68 years old I was first diagnosed with MG in 2007. At first I was having trouble with double vision and droopy eyelids.
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Hi…..My name is Charles (Chuck) Duffy . I am a retired USAF CMSGT living with my wife of 50 years plus (Darlene) in San Antonio, Texas.
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My name is Andrea; I was diagnosed with Myasthenia Gravis and underwent a thymectomy prior to my 30th birthday.
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My name is Stephanie, I’m 26 years old, and I was recently diagnosed with Myasthenia Gravis.
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Hi, My name is Zayna and I am 22 years of age. Just about 6 months ago or so I have been seeing double.
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Hi, my name is Elroy and I live in San Antonio, Texas. I have a rare, often misdiagnosed disease called Myasthenia Gravis, known also as MG.
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Myasthenia Gravis 