June is Myasthenia Gravis Awareness Month. I have had MG for over 5 years now. This is a rare neuromuscular disease which is also an autoimnune disease. Please check out The Myasthenia Gravis Foundation of America for more information.
Also the Muscular Dystropy Association - MDA - has information and opens their clinics to people [...]

I’m a realist. I like to be prepared for the worst and expect the best. When I travel I take along extra medications just in case something happens that we need to stay longer. I have my Advance Directives in place as well as a will. Some consider me over cautious but with all of [...]

Please check out Fighting Fatigue, not only because of my guest blogging post there about Sjogren’s Syndrome but because this is an excellent health blog.
I’m thankful for the opportunity to share my knowledge and my experience with an invisible chronic illness in the hopes that it could assist someone searching for answers or needing [...]