Als in San Diego, CA is a self-funded organization that aims to raise awareness about Amyotrophic Lateral Sclerosis (ALS), also known as motor neuron disease or Lou Gehrig's disease. Founded in 1996, their website provides information on ALS symptoms, diagnosis, treatments, and resources for caregivers. The organization is dedicated to supporting individuals living with ALS and advocating for research towards finding a cure.
Debbie Tope, who has been living with ALS for 15 years, shares her personal story on the website and invites visitors to sign the guest book. The organization also encourages participation in fundraising events, such as the Tope's Hope walk team, to support ALS chapters. With a positive attitude and a focus on hope, Als in San Diego strives to empower individuals affected by ALS and promote a better understanding of the disease.
Generated from the website