Thank you for visiting my fundraising page for the Myasthenia Gravis Association (MGA). The support that the MGA provides to improve the lives of those with myasthenia gravis is important to me because they are able to offer their services 100% free of charge to anybody who needs them.
Myasthenia gravis is a rare autoimmune, neuromuscular disease which impacts 36,000-60,000 in the US. The most common symptoms are difficultly with breathing, swallowing, speech, double vision and muscle fatigue. There is currently no cure.
The MGA works to support the lives of those impacted by myasthenia gravis and their communities through support groups, clinics, 1-1 consultations, new patient packets, research, education and awareness events. Your support ensures that the MGA can continue to provide these tools to support patients along their journey with myasthenia gravis.
My journey with MG began in 2018 and it has been a time of change for me, my wife, and our family. God has blessed this journey with His constant presence during the good days and the ones that were a true challenge. Because there is still so much to learn about MG and because each of us that are diagnosed with it travels our own personal path in the unknown, every step along the research that is being done is so very important to our future. Thank you for considering a donation toward the research and assistance that is made available to those who truly need that help.
For more information go to www.mgakc.org
