We are 3 days away from this walk, you still have time to register, join my team or just make a donation if you are not able to attend.
This is very personal to me as my husband got this crappy disease 4 years ago and overnight our lives changed forever. There is no cure but can be controlled with the right combination of treatments and meds IF that even works. This is rare so many times it gets misdiagnosed and the symptoms mirror many other diseases. The main issue is your muscles or the lack of I should say, it causes double vision, droopy eyelids, trouble swallowing, chewing, and the worst of all is breathing. There is extreme fatigue, and I could just go on and on, as my husband has said he would not wish this on his own worst enemy. So we are asking for any donation to help with this research to find a cure. He may not see it in his lifetime but I hope that someday they do find a cure and nobody will ever have to live with this disease.
Thank you for visiting my "MG Walk" personal fundraising page!
I am excited to be supporting the Myasthenia Gravis Foundation of America (MGFA) through the MG Walk. The MGFA is the only national volunteer health agency in the United States dedicated solely to the fight against myasthenia gravis.
MGFA is committed to finding a cure for myasthenia gravis and closely related disorders, improving treatment options, and providing information and support to people with myasthenia gravis through research, education, community programs, and advocacy.
Together We Can Make A Difference!