Mike Heslin

Mike Heslin, a 56-year-old man from New York, was diagnosed with ALS in 2015. ALS, also known as Lou Gehrig's disease, is a fatal neurodegenerative disorder that affects the motor neurons in the brain and spinal cord. In most cases, ALS leads to paralysis and eventually death within a matter of years.

Heslin was initially devastated by his diagnosis, but he quickly decided to make the most of his remaining time. He began working with ALS organizations to raise awareness of the disease and to help others who were living with it.

In 2017, Heslin and his wife, Amy, founded the Mike Heslin Fund for ALS Research. The fund has raised over $1 million to support ALS research and to provide financial assistance to ALS patients and their families.

Heslin has also become a vocal advocate for ALS awareness. He has spoken at numerous events and has been featured in several media outlets. He has used his platform to share his story and to urge others to learn more about ALS and to support research efforts.

Heslin's story is one of hope and resilience. He has shown that even in the face of a devastating diagnosis, it is possible to live a full and meaningful life.

Heslin's work has made a difference in the lives of many people. He has helped to raise awareness of ALS and to provide financial assistance to ALS patients and their families. He has also given hope to others who are living with the disease.

Heslin is an inspiration to all who know him. He is a reminder that even in the face of adversity, it is possible to make a positive difference in the world.