Details What Has Happened To Steve Gleason?

Steve Gleason was diagnosed with ALS (amyotrophic lateral sclerosis), also known as Lou Gehrig’s disease, in 2011.

Despite this diagnosis, Steve Gleason has remained incredibly active and has become a powerful advocate for people living with ALS. He’s established the Team Gleason foundation, which provides resources and support to those with ALS. This foundation has developed innovative technology to help people with ALS maintain their independence and quality of life. Steve Gleason’s work has also brought attention to the need for more research into treatments and cures for ALS.

ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. It causes muscle weakness and atrophy, leading to difficulty with speaking, swallowing, breathing, and mobility. There is currently no cure for ALS, but treatments can help manage symptoms and slow the progression of the disease.

While ALS presents a significant challenge, Steve Gleason’s story is one of courage, resilience, and hope. He continues to inspire countless people with his determination and commitment to making a difference in the lives of others living with ALS.