Recent family and friends of mine have been diagnosed with ALS, and far too late. These diagnosis' alerted me how little is known of ALS, especially compared to other neurodegenerative diseases like Alzheimer’s and Parkinson’s disease. As a scientist, I stand for research that improves survival and ability to thrive with a quality of life- an ALS diagnosis quickly diminishes both. 

Not only will my run, but every mile dedicated to train for the 2026 NYC Marathon symbolize the fight against ALS.

This run is dedicated to David Bader and Ken Mercer, who are bravely fighting ALS now.

I am running with Team ALS to also support others affected by ALS, spread awareness of our cause, 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.

Here is some information on ALS:

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. Presently, there is no known cure for ALS.

• Every ninety minutes, someone is diagnosed with the disease, and someone passes away from it.
• 90% of ALS cases occur without any known family history or genetic cause. The remaining 10% of ALS cases are inherited through a mutated gene with a known connection to the disease.
• 55 is the average age of onset with most people who develop ALS between the ages of 40 and 70. However, cases of the disease do occur in people in their twenties and thirties.
• ALS is 20% more common in men than women. However, with increasing age, the incidence of ALS is more equal between men and women.
• Military veterans are twice as likely to be diagnosed with the disease than the general public for yet unknown reasons.

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 -

Together, We End ALS!