Discussion of MG related matters. The only criteria here is that you have an interest in Myasthenia Gravis. Do you have Myasthenia Gravis? Do you think you have Myasthenia Gravis? Do you know someone with MG (Myasthenia Gravis)or that thinks they have MG (Myasthenia Gravis)?
Did you know we have members that have not been diagnosed with Myasthenia Gravis after years of displaying what they believe are symptoms synonymous with the disease? How can this occur? What makes this disease so difficult to diagnose? Is there a definitive diagnostic tool?
Join us and seek answers to these questions from people that have experienced MG and that have had similar instances in their life.
Myasthenia Gravis IS NOT a death sentence, it is merely a condition that we must learn to cope with. And remarkbly most people lead a near normal life once they have learnt to cope with their medication regime etc. Obviously we are all different. That's what makes us interesting! :-)
Hi Y'all I like to do a world survey call "The prevalence of MG". For that I like to receive information from every country in the world that gets this
Hi Doug, I was refused the tablets . GP said the side effects were too risky. Meanwhile I get worse and worse waiting for a dx. Last night I had another bad
Jane, I have heard the same thing too. That is why I am going to push to try the medication. If it doesn't work at least I haven't lost anything, but I want
Hi Doug, I have been told that there isn't a test for MG that can prove you DON'T have it. Only tests to prove you have it.... There are people in UK and USA
Hi Donna, I have no MG dx but have all the symptoms and 2 GPs that think it probably is MG. But my blood tests are negative. I have just had a MuSK test come