OUR ALS FAMILY
All of the board and committee members are volunteers and receive no money for their time and dedication.
- Maneuver a diagnosis of ALS
- To inspire them to believe that their life does not have to be over, just different than planned.
- Assurances that technology and nutrition can help to live longer, fulfilling lives.
- Provide skills by which families and friends can raise money for PALS
- Along with knowing that no one will embark on this journey alone
What is ALS?
ALS (Amyotrophic Lateral Sclerosis) is also known as Lou Gehrig’s disease. ALS is a fatal disease that attacks the nerve cells (motor neurons) in the brain and spinal cord that control voluntary muscle movement and muscle power, eventually leaving the patient completely paralyzed. As the muscles waste away, a person with ALS loses their ability to walk, speak, swallow, and eventually breathe. Yet in most patients their mind remains unaffected.
ALS is not a rare disease. A little over 5,600 people in the U.S. are diagnosed with ALS each year, every 90 minutes someone dies of ALS. ALS can strike anyone, at any age, without regard to race or ethnic background. Approximately 80% of cases begin between 40-70 years of age.
ALS board of directors
Sherry DePerno, Board President & Executive Director
Yvonne Buehler, Secretary/Treasurer
Sue Giglio, Patient Advocate
Advisory Board: Dr. Joanne Joseph