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Dear Friends and Family,
I am reaching out to share the story of my uncle, John Silvia, who has recently been diagnosed with ALS (Amyotrophic Lateral Sclerosis). ALS is a progressive neurodegenerative disease that affects the nerve cells in the brain and spinal cord. It leads to the degeneration and death of motor neurons, which are responsible for controlling voluntary muscle movements. As these neurons deteriorate, individuals with ALS experience increasing muscle weakness, loss of coordination, and eventually paralysis.
Symptoms often begin with subtle changes, such as difficulty speaking or walking, and can progress to challenges in swallowing and breathing. There is currently no cure for ALS, and treatment focuses on managing symptoms and improving quality of life.
Living with ALS presents significant challenges, both for patients and their families, as they navigate the physical, emotional, and financial impacts of the disease.
This diagnosis has changed John’s life and the lives of those who love him, as he requires extensive care and assistance that is not covered by insurance.
John has always been a source of joy in our lives, inspiring us with his kindness, humor, and resilience. Now, it’s our turn to support him during this challenging time. The funds raised through this campaign will go directly toward his medical care, therapies, and the essential support he needs to maintain his quality of life.
Every contribution, no matter how small, will make a difference. We are grateful for your support and encourage you to share this campaign with others who may want to help. Together, we can provide John with the care he deserves as he faces this battle.
Thank you for your generosity and support.
Organizer
Julia Feldman
Organizer
Dartmouth, MA