If you are reading this, THANK YOU!!
I met Hannah about 15 years ago when we worked together at M&T Bank. Hannah was always kind, compassionate, positive, supportive, and encouraging. About one year ago her baby boy Austin, at only 5 months old, was diagnosed with a rare and fatal form of muscular dystrophy, L-CMD. Despite the daily challenges and heartbreak Hannah and her family now face every day, Hannah is still the beautiful, positive, and supportive person I have come to know even more over the last couple of years.
Hannah and her husband Mark have started the L-CMD Research Foundation to urgently advance medicine that will establish treatments and a cure. Their goal is to raise $2 Million by Austin’s second birthday to fund gene therapy research for L-CMD. On behalf of Hannah and her family, and others who may be faced with this rare and fatal disease, please consider a donation. This is an opportunity to be part of something truly amazing, with the potential to transform the life of a beautiful boy. There is currently no cure, but with your help, we can make the necessary research a reality! Please help if you can. I know we can make this happen. Let’s be a part of this miracle together!!!