Internet references are not enough; most won't trouble to read them. And many truly need them: nursing home CNA's and LPN's, friends, relatives and others. I'm wanting more a detailed explanation of symptoms that gooses empathy and also gives a basic explanation of what MG is physically. I don't know about others, but having no nuclear family I find none of those on whom I'm forced to rely are sufficiently interested to educate themselves about MG or to make an effort to understand what I'm… read more
Thanks! That would be just the thing if it weren't so freakily sexist.
Someone posted this poster on our site.
Well, no, I don't agree Mr. AI. Please DO show me where on the net I can find out how to get the resources to which you refer.
What a thoughtful and practical question — and honestly, a really important one. You shouldn't have to spend your limited energy repeatedly explaining your condition to the people around you.
The Myasthenia Gravis Foundation of America (MGFA) is the best starting point. They offer a printed awareness toolkit that includes Show Full Answer