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ALSE ALL SCHOOL DUKE

Founded in 1985 and headquartered in Washington, D.C, The ALS Association is an American nonprofit organization that raises money for research and patient services, promotes awareness about and advocates in state and federal government on issues related to amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease.
Country/AreaUnited States
Company Emailinfo@als.org
IndustryCharitable Organizations & FoundationsOrganizations
Company website
Company phone(202) 464-8869
Established1986
Company Revenue$37,032,000
Number of employees113
SIC Code83839
NAICS Code81813
Main ProductsVolunteerDonateBecome an advocateUnderstanding ALSNavigating ALS
http://www.linkedin.com/company/aircraft-leasing-servicehttp://www.twitter.com/notosaltcabbagehttp://www.facebook.com/alsltdhttps://www.youtube.com/user/thealsassociationhttps://www.instagram.com/als/

Company News

Kerry & Gary Challenge to Defeat ALS: Alabama Rivalry at the Heart of Second Annual Fundraising Challenge
Rivalry meets compassion as Auburn and Alabama unite to battle ALS in annual showdown BIRMINGHAM, ALABAMA, USA, October 17, 2023 /⁨EINPresswire.com⁩/ -- Former Auburn basketball player, Gary Godfrey, and former Alabama running back, Kerry Goode, are …
New $400,000 Grant Supports EverythingALS.org and Mass General Hospital (MGH) to Develop NeuroLens, a Digital Diagnostics technology initiative for early detection of Amyotrophic Lateral Sclerosis (ALS)
SEATTLE--(BUSINESS WIRE)--EverythingALS today announced it has received $400,000 from ALS Finding a Cure® and The ALS Association to support studies for the identification of early digital diagnostic markers of ALS. The NeuroLens digital diagnostics program is a unique partnership with diverse and multidisciplinary research teams formed between - EverythingALS, a citizen led nonprofit research organization dedicated to changing the paradigm for ALS through AI/ML, digital monitoring and open inn
ALS Finding a Cure, The ALS Association Partner to Reduce Time to Initial ALS Diagnosis
Organizations Commit $2 million toward New International ALS Diagnostics Effort BOSTON and BOYNTON BEACH, Fla., Aug. 17, 2023 /PRNewswire/ -- ALS Finding a Cure® (ALSFAC) and The ALS Association announced today seven new grants worth a total of $2 million to support the development of...
dateAug 17, 2023
7th annual CEO Soak benefits ALS Association | TribLIVE.com - Tribune-Review
CEOs don’t wait for things to happen — they make things happen. That’s what more than 50 executives, along with local business and community leaders, did on Thursday at CEO Soak, the seventh annual ALS Association Western Pennsylvania Chapter’s fundraiser to support the fight against the disease. Amyotrophic lateral sclerosis
dateAug 11, 2023
Sandra Bullock Helps Raise Donations For ALS Association After Partner's Death
Sandra Bullock helps raise donations for the ALS Association after her partner dies from the illness. - www.tmz.com

Web Summary

Q1: What is the physical address of the ALS Association's national office?
A1: The physical address of the ALS Association's national office is 1300 Wilson Boulevard, Suite 600, Arlington, VA 22209.

Q2: What is the phone number for general inquiries and providing non-medical information and referral resources?
A2: The phone number for general inquiries and providing non-medical information and referral resources is 800-782-4747.

Q3: How can one reach a local team in their state for support and guidance?
A3: To reach a local team directly, visit the state listing page via the link provided on the ALS Association website.

Q4: What is the email address for general inquiries and non-medical information and referral resources?
A4: The email address for general inquiries and non-medical information and referral resources is not explicitly stated in the text, but it can be obtained by visiting the ALS Association's website and filling out a contact form.

Q5: What is the phone number for donations to support ALS research and services?
A5: The phone number for donations is 888-949-2577.

Q6: How can one get involved with the ALS Association through volunteering or sponsorship opportunities?
A6: While not explicitly stated in the text, the ALS Association website provides information on how to get involved through various programs and initiatives, including research grants, national signature events, and sponsorship opportunities.

Q7: What is the purpose of the ETRAN Communicator developed by Rob's father and his friend?
A7: The ETRAN Communicator was a groundbreaking tool that allowed individuals with ALS to communicate using only their eye movements, specifically enabling the selection of the most frequently used letters with a single glance.

Q8: How did Rob Eichler first learn about ALS at the age of 13?
A8: Rob Eichler learned about ALS when he visited his friend who was living with the disease and saw the impact it had on his father, an engineer.
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