Overview
What is Amyotrophic Lateral Sclerosis Assn?
The Amyotrophic Lateral Sclerosis Association, also known as The ALS Association, is a nonprofit organization headquartered at 1300 Wilson Blvd 600, Arlington, VA, 22209. With a workforce of 547 employees, the Association is dedicated to providing comprehensive, consistent programs and services for individuals with Amyotrophic Lateral Sclerosis (ALS), their families, caregivers, and professionals across the United States. Their initiatives are shaped by key stakeholders, and their activities cater to both current needs and future services. The Association leads the fight to cure and treat ALS through research, advocacy, and care services. Their offerings include clinical and professional education programs, certified care center certification and recertification, strategies to deliver care through other means, and current information, resources, and referrals for the communities they serve. Additionally, they provide compassionate care and support to empower people with ALS and their families to live fuller lives.
Official website here: www.als.org
Is Amyotrophic Lateral Sclerosis Assn legitimate?
Amyotrophic Lateral Sclerosis Assn is a legitimate nonprofit organization registered as a 501(c)(3) entity. Amyotrophic Lateral Sclerosis Assn submitted a form 990, which is a tax form used by tax-exempt organizations in the U.S., indicating its operational transparency and adherence to regulatory requirements. Donations to this organization are tax deductible.
Here are some key statistics you may want to consider:
Executive Compensation: $2,009,534
Professional Fundraising Fees: $648,986
Other Salaries and Wages: $27,608,816
For more financial information, click here
Official website here: www.als.org
What is the mission statement of Amyotrophic Lateral Sclerosis Assn?
The Amyotrophic Lateral Sclerosis Association is dedicated to leading the charge in treating and curing Amyotrophic Lateral Sclerosis (ALS) through innovative, global research and providing compassionate care and support to those afflicted by the disease. Their mission is to empower individuals with ALS and their families to live fuller lives and make a significant impact in the fight against this debilitating condition. The organization's efforts focus on funding research to advance understanding and treatment of ALS while offering essential services and resources to enhance the quality of life for those living with the disease.
Official website here: www.als.org
Who is the CEO of Amyotrophic Lateral Sclerosis Assn?
Calaneet Balas is the President And Ceo of Amyotrophic Lateral Sclerosis Assn. The CEO's salary of Amyotrophic Lateral Sclerosis Assn is $456,666 and their total compensation is $497,765.
Official website here: www.als.org
What is the revenue of Amyotrophic Lateral Sclerosis Assn?
Amyotrophic Lateral Sclerosis Assn's revenue in 2023 was $55,567,608.
Official website here: www.als.org
Who are the executives of Amyotrophic Lateral Sclerosis Assn and what are their salaries?
The average compensation at Amyotrophic Lateral Sclerosis Assn during 2023 was $54,147. There are 547 employees and 31 volunteers at Amyotrophic Lateral Sclerosis Assn.
Here are 47 key members and their salaries (Amyotrophic Lateral Sclerosis Assn's CEO's salary is $456,666 and their total compensation is $497,765):
- Calaneet Balas (President And Ceo)
- Tina Zeff (Chief Operations Officer)
- Greg Mitchell (Chief Financial Officer)
- Neil Thakur (Chief Mission Officer)
- Kuldip Dave (Senior Vice President Research)
- Lance Slaughter (Svp Strategic Alliances And Governance)
- Monica Santa Cruz (Chief People Officer)
- Dean Feener (Chief Information And Marketing Officer)
- Keith Gary (Vice President Mission Acceleration)
- Vickie Lobello (Senior Vice President Organizational Change)
- Brian Frederick (Senior Vice President Strategic Communications)
- Scott Kauffman (Chair) [Trustee/Director]
- Fred M Degrandis (Vice-Chair) [Trustee/Director]
- Sue Gorman (Immediate Past Chair) [Trustee/Director]
- Connie Houston (Treasurer) [Trustee/Director]
- Sandra Piersol (Secretary) [Trustee/Director]
- Jinsy Andrews (Trustee)
- Eugene Brandon Phd (Trustee)
- David Van De Riet (Trustee)
- Clifton Gooch Md (Trustee (Thru 02/22))
- Christi L Kolarcik Phd (Trustee)
- Charlie Robinson D Sc Pe (Trustee)
- J Thomas May (Trustee)
- John P Krave Jd (Trustee)
- John Robinson (Trustee (Thru 02/22))
- Judy Pratt Dmd (Trustee)
- Kenneth Menkhaus (Trustee)
- Kevin Spinella (Trustee (Thru 12/22))
- Larry Falivena (Trustee)
- Lou Libby Md (Trustee)
- Mark Calmes (Trustee)
- Mark Stancil (Trustee)
- Millie Arnold (Trustee)
- Nancy Leamond (Trustee)
- Paul Ingholt (Trustee)
- Tobin M Kucharski (Trustee (Thru 02/22))
- Tom Carroll (Trustee)
- Warren Nelson (Trustee)
- Wendy J Schriber (Trustee)
- Ken Baltes (Trustee (Thru 09/22))
- Michael Benatar (Trustee)
- Kathleen Boyce (Trustee)
- Amy Brachio (Trustee)
- John Rocky Dallum (Trustee)
- Peter Mckown (Trustee)
- Rebecca Moss (Trustee)
- Kenton Van Harten (Trustee)
Official website here: www.als.org
Where can I find the form 990 for Amyotrophic Lateral Sclerosis Assn?
The Amyotrophic Lateral Sclerosis Assn’s most recent form 990 was submitted in 2023 and can be accessed here
Official website here: www.als.org
Learn more at the official website: www.als.org
Mission Statement of Amyotrophic Lateral Sclerosis Assn
The Amyotrophic Lateral Sclerosis Association, commonly known as ALS Association, is a leading force in the battle to cure and treat Amyotrophic Lateral Sclerosis (ALS), also referred to as Lou Gehrig's disease. This nonprofit organization is dedicated to making a significant impact on people's lives who are affected by ALS and their families. Through global, state-of-the-art research, the ALS Association strives to find innovative treatments and ultimately, a cure for this debilitating disease.
The mission of the Amyotrophic Lateral Sclerosis Association is multifaceted, encompassing not only research but also advocacy and care services. By leading the charge in research, the ALS Association aims to uncover the mysteries behind ALS and develop effective therapies to treat and cure the condition. Simultaneously, the organization empowers those living with ALS and their families by providing them with compassionate care and support, enabling them to live fuller lives.
In their relentless pursuit to make a difference, the ALS Association fosters a collaborative research environment, bringing together renowned scientists, researchers, and clinicians to pool their knowledge and expertise. This global approach to research not only accelerates progress but also ensures that the most promising discoveries are translated from the lab to the clinic as efficiently as possible. Ultimately, the ALS Association's mission is to bring hope and support to those affected by ALS, guiding them through their journey with compassion, respect, and understanding.
Impact
This information is meant to be a general summary of Amyotrophic Lateral Sclerosis Assn. Please take the time to review official sources before making any decisions based upon the content provided here.
Thursday, August 15, 2024
Amyotrophic Lateral Sclerosis Association's impact is significant in leading the fight to cure and treat ALS through research, advocacy, and care services. The association is committed to providing fully developed, managed, and evaluated programs and services to people living with ALS, their families, caregivers, and professionals across the United States. This includes developing and implementing clinical and professional education programs, certifying care centers, providing information, resources, and referrals, and offering comprehensive programs and services tailored to individual, family, and caregiver needs. Their mission is to empower individuals with ALS and their families to live fuller lives through compassionate care and support, while also advancing cutting-edge research globally to treat and cure ALS.
Financials
This financial information is from Propublica.
Other financial information:
This information is from the most recently submitted tax form from this organization, which was in 2023.
- Assets and Liabilities:
Organization Details
Founding Year
1985
Phone
(202) 407-8580
Principal Officer
Calaneet Balas
Main Address
1300 WILSON BLVD 600, ARLINGTON, VA, 22209
Website
www.als.org
NTEE Category
Code: G50 - Disease
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