The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd
The Les Turner ALS Foundation is a 501(c)(3) nonprofit founded in 1977 that delivers free ALS support services, education, and equipment loans to patients and families, while funding ALS research through the Les Turner ALS Center at Northwestern Medicine. It sustains operations via donations, events, and corporate partnerships.
- Company typePrivate
- Founded1977
- HeadquartersSkokie, United States
- Headcount11–50
- GTM typeB2C
- OfferingServices
What The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd does
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd is a 501(c)(3) nonprofit organization founded in 1977 and headquartered at 5550 W Touhy Avenue, Suite 302, Skokie, Illinois. It is one of the longest-serving ALS organizations in the United States, operating under the tagline "Care, Community, Cure." The foundation delivers a coordinated suite of free services to people living with ALS and their families, including individualized care coordination, online and in-person support groups, needs-based financial grants, equipment loans, and a portfolio of educational resources spanning 15+ topic areas (breathing, nutrition, mobility, genetics, caregiving, etc.). It also operates digital tools including the My ALS Decision Tool, which reached 7,590 users in 2025, and the ALS Learning Series webinar program, alongside signature events such as the ALS Walk for Life at Soldier Field, the Hope Through Caring Gala, Team Race for ALS, and the All in for ALS Casino Night.
The foundation sustains scientific research through its core partnership with Northwestern Medicine and Northwestern University's Feinberg School of Medicine, funding and operating the Les Turner ALS Center and the Lois Insolia ALS Clinic. In 2025, the foundation funded over $1 million in ALS research grants and clinic/endowment support — the highest level in its history — and provided a $500,000 emergency gift to the center during a federal research funding freeze. It is a participating site in the Healey ALS ACE Initiative and the Healey MyMatch early-phase research program, and it co-advocates federally with peer organizations for legislation such as ACT for ALS Reauthorization (H.R.8205).
The business model is donations and event-based fundraising: all patient services are provided free of charge, and revenue is generated from individual donors, corporate partners, legacy giving, and event fundraising. The foundation holds BBB accreditation, Candid's Platinum Seal of Transparency, and a Charity Navigator 4-star rating. It is governed by an independent Board of Directors, has no parent company, and is not venture-backed. Geographic scope is regional for clinical care (Chicago metropolitan area) and effectively global for digital and educational resources, which reached 177,000+ users across 184 countries in 2025.
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd firmographics
Firmographics- Name
- The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd
- Legal name
- Les Turner Amyotrophic Lateral Sclerosis Foundation, Ltd.
- Website
- https://lesturnerals.org
- Company type
- Private
- Founded year
- 1977
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- The Les Turner ALS Foundation is a 501(c)(3) nonprofit founded in 1977 that delivers free ALS support services, education, and equipment loans to patients and families, while funding ALS research through the Les Turner ALS Center at Northwestern Medicine. It sustains operations via donations, events, and corporate partnerships.
- Ownership category
- akta.pro rank
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd industry classification
Industry- Product category
- ALS Nonprofit Patient Support Services
- NAICS
- Voluntary Health Organizations (813212), Other Individual and Family Services (624190)
- SIC
- Services-Misc Health & Allied Services, Nec (8090), Services-Membership Organizations (8600)
- akta.pro primary industry
- Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS) (BPAGACAA)
- akta.pro secondary industries
- Disability Services & Independent Living Support (BPAGACAG), Special Education, Disability Support & Inclusive Education Nonprofits (BPAGADAH)
Keywords
Where The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd is headquartered
LocationHeadquarters
- HQ city
- Skokie
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd business model
Business model- GTM type
- B2C
- Offering type
- Services
- Cost components
- Personnel, Operations, Marketing or Sales, Technology or R&D, Infrastructure, Supply Chain
Revenue model
- Donations and Fundraising: The foundation raises funds from individual donors, corporate partners, and event participants. Revenue is generated through direct donations, event fundraising (ALS Walk for Life, Hope Through Caring Gala, Team Race for ALS, All in for ALS Casino Night), corporate partnerships, and legacy giving. The foundation is a 501(c)(3) nonprofit organization.
Go-to-market motion1 record
Distribution channels5 records
Marketing channels7 records
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd product offering
Product offeringCore offering
The Les Turner ALS Foundation delivers free ALS support services, care coordination, support groups, needs-based grants, and equipment loans to people living with ALS and their families, and operates educational programs including the ALS Learning Series and My ALS Decision Tool. It sustains the Les Turner ALS Center and Lois Insolia ALS Clinic at Northwestern Medicine through research grants, endowment support, and operational funding, and drives awareness and fundraising through signature events such as the ALS Walk for Life.
Product overview
The Les Turner ALS Foundation is a nonprofit healthcare organization (not a technology company) offering a coordinated suite of ALS care and support services. The foundation operates as a single integrated service portfolio centered on three pillars: (1) individualized patient care through its Support Services Team and ALS Support Groups, (2) financial and equipment assistance via Grant Programs & Equipment Loans, and (3) scientific research funding through the Les Turner ALS Center at Northwestern Medicine and Lois Insolia ALS Clinic. Educational resources including My ALS Decision Tool and the ALS Learning Series help patients and families navigate care decisions. Community engagement programs like the ALS Walk for Life, Team Race for ALS, and Hope Through Caring Gala drive fundraising and awareness. The foundation does not offer technology products, APIs, or AI-powered solutions.
Differentiator
Problem solved
Functional benefit
Products and services
- ALS Support Services Team
- ALS Support Groups
- Grant Programs and Equipment Loans
- My ALS Decision Tool
- ALS Learning Series
- Les Turner ALS Center at Northwestern Medicine
- Lois Insolia ALS Clinic
- ALS Communication Passport
- ALS Guides and Educational Webinars
Quantifiable outcome
- 4,684 care coordination meetings conducted in 2025
- +6 more outcomes
Companies that use The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd
Customer profileNamed customers3 records
Segments4 records
Ideal customer profiles4 records
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd partnerships and signals
Strategic signalPartnerships
Nine partnerships are on record, tiered core, flagship and minor.
- Northwestern Medicine / Northwestern University Feinberg School of MedicinecoreThe foundation's most significant partnership is with Northwestern Medicine and Northwestern University's Feinberg School of Medicine. The foundation funds and sustains the Les Turner ALS Center and the Lois Insolia ALS Clinic at Northwestern Medicine, which serves as the primary site for ALS clinical care and research. Foundation-funded scientists and clinicians at the center conduct groundbreaking research into the causes and treatments of ALS.
- Sean M. Healey & AMG Center for ALS at Massachusetts General HospitalflagshipThe foundation partners with the Healey ALS Center on the Acceleration Centers of Enrollment (ACE) Initiative, which strengthens ALS research infrastructure and accelerates clinical trial enrollment. Since its inception in 2024, enrollment has more than doubled across three sites. The Les Turner ALS Center was also selected as one of only four sites to participate in the Healey ALS MyMatch early-phase research program.
- International Alliance of ALS/MND AssociationscoreThe foundation is a member of the International Alliance of ALS/MND Associations, a global network of national ALS/MND organizations that collaborate on advocacy, research, and awareness efforts.
- Illinois Public Health Association and HAP FoundationminorThe foundation partners with the Illinois Public Health Association and the HAP Foundation to train community health workers across Illinois, particularly in rural and underserved communities, to help people connect to multidisciplinary ALS care and support sooner.
- ALS AssociationcoreThe foundation co-signed a letter with the ALS Association and other leading ALS organizations calling on Congress to swiftly pass the ACT for ALS Reauthorization Act (H.R.8205).
- ALS NetworkcoreThe foundation co-signed a letter with the ALS Network and other leading ALS organizations calling on Congress to swiftly pass the ACT for ALS Reauthorization Act.
- ALS UnitedcoreThe foundation co-signed a letter with ALS United and other leading ALS organizations calling on Congress to swiftly pass the ACT for ALS Reauthorization Act.
- I AM ALScoreThe foundation co-signed a letter with I AM ALS and other leading ALS organizations calling on Congress to swiftly pass the ACT for ALS Reauthorization Act.
- Muscular Dystrophy AssociationcoreThe foundation co-signed a letter with the Muscular Dystrophy Association and other leading ALS organizations calling on Congress to swiftly pass the ACT for ALS Reauthorization Act.
Scale indicators9 records
Recent moves6 records
Expansion highlights6 records
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd competitors and assessment
Company assessmentDirect peers
- Project ALS: A nonprofit funding ALS research and treatment development, with a focus on preclinical and translational science. Comparable as a peer ALS research-funding nonprofit.
- I AM ALS: A patient-led ALS nonprofit focused on advocacy, awareness, and accelerating treatments. Comparable as a fellow ALS mission-driven organization co-signing ACT for ALS advocacy letters.
- ALS Therapy Development Institute (ALS TDI): A nonprofit biotechnology institute focused on ALS research and drug discovery. Comparable as a peer ALS organization investing in translational research and clinical-trial acceleration.
- The Robert Packard Center for ALS Research at Johns Hopkins: An academic ALS research center funded by philanthropy that brings together leading ALS scientists. Comparable as a peer ALS research organization embedded in a major U.S. academic medical institution.
- The ALS Association: The largest national ALS-focused nonprofit in the U.S., providing care services, advocacy, and research funding. Directly comparable as a fellow ALS patient-services and research-funding organization co-advocating on ACT for ALS.
- ALS United: A national federation of independent ALS organizations providing care services and funding research. Highly comparable as a peer ALS nonprofit engaged in joint advocacy and patient support.
- ALS Network: A regional ALS nonprofit (formerly the Golden West Chapter) providing care services, equipment loans, and research funding in the western U.S. Operates the same patient-support and advocacy model as Les Turner.
- Answer ALS: A research consortium and program generating the largest ALS multi-omic dataset and supporting clinical trial acceleration. Comparable as a peer ALS infrastructure initiative tied to research advancement.
Broad incumbents
- Muscular Dystrophy Association (MDA): A large national neuromuscular disease nonprofit that funds ALS research among many other conditions. Comparable as a peer advocacy and research-funding partner on ACT for ALS and overlapping care services.
Others
- International Alliance of ALS/MND Associations: A global umbrella organization of which Les Turner is a member, coordinating international ALS advocacy and research collaboration. Comparable as a peer network partner rather than a direct competitor.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks6 records
Key highlights7 records
Customer concentration
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd social profiles
Digital presenceThe Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd financial estimates
Financial estimateRevenue estimate
Valuation estimate
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd leadership team
Management profileNumber of profiles
Profiles5 records
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd
What does The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd do?
The Les Turner ALS Foundation delivers free ALS support services, care coordination, support groups, needs-based grants, and equipment loans to people living with ALS and their families, and operates educational programs including the ALS Learning Series and My ALS Decision Tool. It sustains the Les Turner ALS Center and Lois Insolia ALS Clinic at Northwestern Medicine through research grants, endowment support, and operational funding, and drives awareness and fundraising through signature events such as the ALS Walk for Life.
Is The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd a public or private company?
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd is a private company. It is classified as nonprofit foundation owned and is currently operating.
When was The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd founded?
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd was founded in 1977. It employs 11 to 50 people.
Where is The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd based?
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd is headquartered in Skokie, United States, in the North America region.
How does The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd make money?
One revenue line is on record: donations and Fundraising.
Who are The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd's main competitors?
Direct peers on record are Project ALS, I AM ALS, ALS Therapy Development Institute (ALS TDI), The Robert Packard Center for ALS Research at Johns Hopkins, The ALS Association, ALS United, ALS Network and Answer ALS. Muscular Dystrophy Association (MDA) is listed as a broad incumbent. International Alliance of ALS/MND Associations is listed as an others.
Does The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd have an API?
No public API is recorded for The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd.
What industry is The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd in?
The Les Turner Amyotrophic Lateral Sclerosis Foundation Ltd's product category is ALS Nonprofit Patient Support Services. Its primary akta.pro industry code is BPAGACAA, Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS), with a secondary code of BPAGACAG, Disability Services & Independent Living Support. Its NAICS code is 813212 and its SIC code is 8090.