The mission of the ALS Association is to find the cause of, and a cure for, Amyotrophic Lateral Sclerosis and improve the quality of life for people living with ALS, their friends, families, and caregivers.

Chapter Goals

• Address the needs of ALS patients and the ALS community.
• Encourage and fund worldwide ALS research.
• Manage resources necessary to support the programs of ALSA and The Keith Worthington Chapter.
• Promote awareness and understanding of ALS and the work of ALSA and The Keith Worthington Chapter.
• Advocate for public policy in support of ALS research and ALS-related health care issues.

It is the policy of the Keith Worthington Chapter that staff may provide information regarding self-determination and end of life issues (advanced directives, living wills, do not resuscitate orders, etc.) but will not influence or coerce persons living with ALS or their families in the decision-making process.

Chapter Funding
The Chapter is funded solely by contributions from individuals, corporations, and foundations. It receives no funding from local, state or federal entities; it receives no funding from The Jerry Lewis Telethon or local, state or federal entities. Approximately two thirds of the revenues comes from special events and one third from grants, planned gifts, and memorials.