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Organización Sin Fin de Lucro
ALS Association
Misión
In the quest to create a world without ALS, our vision is to care for and support all people living with Lou Gehrig's disease as we leave no stone unturned in our relentless search for a cure.
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The ALS Association is a non-profit organization addressing the needs of persons with Amyotrophic Lateral Sclerosis (ALS) (more commonly known as "Lou Gehrig's Disease").
The following programs and services are provided through our organization:
- ALS patients and families are provided information and resources about ALS as requested.
- Support Groups have been established and maintained providing peer and family support in all three states.
- Adaptive devices and equipment can be provided at no cost through our loan closets, located in the three states.
- Increased public awareness in our communities about ALS through educational talks by knowledgeable staff.
- Supporting ALS advocacy efforts.
- Informing patients and families about clinical trial opportunities.
Áreas de Impacto incluyen
- Salud & Medicina
- Derechos Humanos & Libertades Civiles
Información y Contacto
- 8022062825
- 1300 Wilson Blvd, Suite 600, Arlington, Virginia, US
Suite 600
Avisos recientes
| Virtual Volunteering - Events and Fundraising | En cualquier lugar(A Distancia) | ... |
| The ALS Association Volunteering | Massachusetts, US | ... |
Descubre Tu Vocación
Encuentra oportunidades para cambiar el mundo con las últimas oportunidades de empleo, pasantías/prácticas y voluntariado con impacto social. Además, podrás explorar recursos para generar impacto positivo en tu comunidad.
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