People living with muscular dystrophy, ALS and other related neuromuscular diseases, are robbed of the strength that most of us take for granted every day the power to walk, talk, laugh, hug, even breathe.
I’m participating in the MDA Muscle Walk to give strength to the MDA so that they can continue to fund breakthrough research and provide comprehensive, compassionate care to kids and adults.
I hold the MDA in the highest regards and close to my heart. My beautiful princess bride was diagnosed in 2016 with Myasthenia gravis (MG - for short). MG is a long-term neuromuscular disease, who’s symptoms are muscle weakness, difficulty breathing, difficulty swallow, trouble talking, and difficulty walking. Onset can be sudden and often resulting in a visit to the ICU. Currently, there’s only management treatments and medication but no cure. The MDA is working diligently to find the cures but needs our help through awareness and donations to continue the research.
Please make your tax-deductible donation to support the MDA and their mission to transform the lives of people living with neuromuscular disease. 100% of donations go directly to the MDA for their research.
If you are not in the position to do so, it is an even bigger act of charity and compassion to spread the word... please share this post. Help is never reached if people never know...