Help Brad McGarry and Family with ALS expenses

Many of us know Brad McGarry for his work with autism, Angelman syndrome and mental health. He is selfless in his efforts to help others and inspires everyone he meets. Brad has dedicated his life to making a difference in the world. All of us are truly grateful and blessed to know him.

 

What everyone does not know is that Brad has been diagnosed with amyotrophic lateral sclerosis (ALS) also known as Lou Gehrig's disease. ALS is a degerative nervous system disease that weakens muscles and impacts physical function. Although there are treatments to help, this disease cannot be cured. Brad's progression is rapid and he is doing everything to slow it down. His goal is to spend as much time as possible with his family and friends.

 

 

The cost of medical treatments, assistive technology, accommodations and general daily living expenses has already accumulated a large amount of debt that will only continue to grow. Brad McGarry and his family need our help!

 

We, Liana Hicks and Amanda Mulder, are trying to raise money to offset whatever financial hardships Brad and his family are facing now and in the future. Any amount of money you can give is greatly appreciated. We will make sure the family gets all of the proceeds after fees and taxes.

 

Brad has given us all so much. Now, it is our time to give back to him.