AMYOTROPHIC LATERAL SCLEROSIS ASSOCIATION
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About this organization
To lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig's disease and their families to live fuller lives by providing them with compassionate care and support.
Interesting data from their 2020 990 filing
The filing clearly states the mission of the non-profit as “Leading the fight to treat and cure als through global research and nationwide advocacy while empowering people with lou gehrigs disease to live fuller lives.”.
When outlining its functions, they were explained as: “Leading the fight to treat and cure als through global research and nationwide advocacy while empowering people with lou gehrigs disease to live fuller lives.”.
- In compliance with legal regulations, the non-profit has reported their state of operation as LA.
- As of 2020, the non-profit's form reports a total of 8 employees.
- Does not operate a hospital.
- Does not operate a school.
- Does not collect art.
- Does not provide credit counseling.
- Does not have foreign activities.
- Is not a donor advised fund.
- Is not a private foundation.
- Expenses are between $500,000 and $1,000,000+.
- Revenue is between $500,000 and $1,000,000+.
- Revenue less expenses is -$8,499.
- The CEO's salary plan within the organization is subject to review and endorsement by an independent body.
- The organization has 10 independent voting members.
- The organization was formed in 2005.
- The organization has a written policy that addresses conflicts of interest.
- The organization is required to file Schedule B.
- The organization is required to file Schedule O.
- The organization pays $378,994 in salary, compensation, and benefits to its employees.
- The organization pays $194,768 in fundraising expenses.
- The organization provides Form 990 to its governing body.
- The organization has minutes of its meetings.
- The organization has fundraising events.
- The organization's financial statements were reviewed by an accountant.
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