ALS Treatment Fund

My dad was diagnosed with amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, when I was about 7 years old. The doctors said he would have about 3 more years before the diseased consumed his life.

In just a few months, I will turn 21 and celebrate it with my family, my friends, and most importantly, my dad. Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurlogical disease that attacks the nerve cells responsible for controlling voluntary muscles. There are currently no known cures for ALS but science keeps advancing and developing new treatments. 

My name is Gianni Achoy and the whole purpose of this campaign is to help my dad get involved with new treatments and possibly the chance to see something more than the four walls he is enclosed in. All money received will go directly towards his medical and travel expensives. As much as I would like to help alone, there's only so much I can do while pushing through my college expenses.

It would mean more than the world to us if we could receive just a little help. My dad is the type of person that captures everyone's heart when they meet him. He is sweet, humble, and caring. His will power has kept him alive for many more years than he was given, and we hope to see many more.

No donation is too small and we would love it if you'd share our story. Thank you!