Hi friends!

I’m thrilled to announce I will be running the NYC Marathon with Team ALS in memory of my dad, who passed away from ALS in 2021. Throughout his illness, my sister and I cared for him alongside our partners, and the ALS Association was an invaluable resource for our family. They were compassionate, easy to communicate with, and provided guidance and access to critical resources that helped us navigate the challenges of his care.

I am running with Team ALS to support those affected by ALS, spread awareness of the disease, and fight for a cure. By partnering with ALS United Greater New York, all the funds I raise will go toward where it’s needed most: vital research, community support, and patient services.

Amyotrophic lateral sclerosis (ALS), often referred to as “Lou Gehrig’s Disease,” is a progressive disease of the nervous system that affects cells in the brain and spinal cord. Currently, there is no known cure.

Every ninety minutes, someone is diagnosed with ALS, and someone passes away from it.

• 90% of cases occur without any known family history or genetic cause, while the remaining 10% are inherited through a known genetic mutation.

• The average age of onset is 55, with most diagnoses occurring between ages 40 and 70, though it can also affect people in their twenties and thirties.

• ALS is about 20% more common in men than women, though this gap narrows with age.

• Military veterans are twice as likely to be diagnosed as the general public, for reasons that are still unknown.

I joined Team ALS to push my physical limits for those who can’t anymore. I want to bring hope, raise awareness, and make an impact – and you can help me! Please donate because every contribution brings us closer to better treatments, stronger support for families, and ultimately, a cure for ALS.

Together, we end ALS!