Raising awareness for the ALS community on Lou Gehrig Day June 2, 2022
Jon ‘Boog’ Sciambi on Project Main St.
Amyotrophic lateral sclerosis (ALS), sometimes called Lou Gehrig’s disease, is a rapidly progressive, invariably fatal neurological disease that attacks the nerve cells (neurons) responsible for controlling voluntary muscles. No cure has yet been found for ALS. About 10 percent of those individuals with ALS survive for 10 or more years.
Project Main St. provides support for individuals afflicted with Amyotrophic Lateral Sclerosis (ALS) and their families, by reducing the financial burden associated with the disease. Click The button below to help support this foundation.
Project Main St. strives to improve the quality of life for people afflicted with ALS. The organization helps both low income and middle income individuals and families. Project Main St. is committed to helping those who are experiencing financial challenges as a direct result of ALS (Lou Gehrig’s Disease).
How To Help
Project Main St. is a non-profit, volunteer organization that relies on private donations to enable us to help those in need. Project Main St. is a 501(c)(3) non-profit organization and all donations are tax-deductible.
Request Help
Are you or someone you know under financial burden as a result of ALS? Project Main St. may be able to help. Contact them today in order find out the next steps.