Lori Oberholtzer

Aug 10, 2024

We are praying for a cure in our lifetime! Justin was 35 when he was diagnosed with ALS, just two months before our second child was born. What started as weakness in his hands has progressed to all over the body weakness, muscle loss, fasciculations, voice changes...

Michael G. Pierson

Aug 10, 2024

We quickly came to realize that battling ALS takes a village – and ours is strong, dedicated, and unrelenting in their pursuit of and hope for a cure. On July 26, 2018, my beloved father, Mike Pierson, was diagnosed with ALS. From that awful day, to his last day...

Lindsey Heiser

Aug 10, 2024

I remember my sister and brother coming up to me and asking what my father was like when he was healthy. My father has had ALS for 15 years. Growing up I was fortunate enough to see my father in his “healthy” stage. I remember my sister and brother coming up to me and...

Cassandra Haddad

Aug 10, 2024

We have lost at least 33 family members to ALS including my mother on Aug 30 2022. We have lost at least 33 family members to ALS including my mother on Aug 30 2022. I am a genetic carrier of SOD1 A5V an aggressive form of ALS. I fight in memory of my family, for my...

David Travis

Aug 10, 2024

I have lost my ability to speak and can eat very few foods. Served 27 years in the US NAVY. Retired 2019, and was diagnosed with ALS may 2021. First symptoms showed up January of 2021. Bulbar ALS. I have lost my ability to speak and can eat very few foods. I normally...