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The Ehlers-Danlos Society competitors & alternatives
The 12 closest competitors and alternatives to The Ehlers-Danlos Society among nonprofit organization companies — ranked by similarity to what The Ehlers-Danlos Society actually does, not by market-cap band.
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About The Ehlers-Danlos Society
The Ehlers-Danlos Society is a global organization dedicated to saving lives and improving the quality of life for individuals affected by the Ehlers-Danlos syndromes, hypermobility spectrum disorders, and related connective tissue conditions.
The Ehlers-Danlos Society at a glance
The Ehlers-Danlos Society is a nonprofit organization company headquartered in United States. Its most recent funding round, Grant, raised $6.7M in December 2023. Xcout tracks 6 named people at The Ehlers-Danlos Society, including Lara Bloom (President and CEO).
The Ehlers-Danlos Society leadership
- Lara BloomPresident and CEO
- Eric AlleyChief Financial Officer
- Dr. Dacre KnightChief Medical Officer
- Dr. Maggie Linn Bartlett, PhDChief Scientific Officer
- Erin SimonsChief Marketing Officer
- Sinead WaughChief Operations Officer
The Ehlers-Danlos Society funding rounds
Every round on record:
| Date | Round | Amount | Investors |
|---|---|---|---|
| Grant | $6.7M | 1 named |
Who invested in each round, lead investors, valuations and the co-investor graph — open the full funding history →
Top 12 The Ehlers-Danlos Society competitors
Ranked by semantic similarity — how close each company is to The Ehlers-Danlos Society by what it does, using Xcout's live company graph. Click any company for its full profile, or its competitor set.
Non-profit Organization
The National Down Syndrome Society is an advocacy and support organization dedicated to empowering individuals with Down syndrome and creating a world where they can thrive.
Non-profit Organization Management
The National Organization for Rare Disorders (NORD) is a patient advocacy organization dedicated to identifying, treating, and curing rare disorders through programs of education, advocacy, research, and patient services.
Non-profit Organization
The Celiac Disease Foundation is a non-profit organization dedicated to driving research, education, and advocacy for celiac disease.
Non-Profit & Advocacy
EURORDIS-Rare Diseases Europe is a non-governmental patient-driven alliance that advocates for people living with rare diseases in Europe.
Nonprofit & Advocacy
The Invisible Disabilities Association provides support, education, and resources for individuals living with invisible illnesses, pain, and injuries, as well as their families and caregivers. The organization offers online support communities, advocacy initiatives such as National Disability ID cards, educational publications, and consulting services to raise awareness and foster understanding.
Non-profit Organization
The Lupus Foundation of America is a national non-profit organization dedicated to solving the mystery of lupus, supporting those affected, and advancing research for a cure.
Nonprofit
Rowe's Research Runners is a volunteer-driven nonprofit organization that raises funds and awareness to support research on ME/CFS, dysautonomia, and related chronic illnesses. The organization aims to foster hope, connection, and progress for patients and families worldwide who are affected by these conditions.
Similar nonprofit organization company
The Christopher Dana Reeve Foundation is a nonprofit organization dedicated to curing spinal cord injury and improving the quality of life for individuals and families impacted by paralysis.
Similar nonprofit organization company
The International OCD Foundation is a nonprofit organization dedicated to helping people with obsessive-compulsive disorder and related disorders live full and productive lives.
Nonprofit & Advocacy
The International Dyslexia Association is a nonprofit organization that provides advocacy, resources, and services for individuals, families, and professionals impacted by dyslexia.
Nonprofit & Patient Advocacy
Cure HHT is a patient advocacy organization that supports individuals affected by hereditary hemorrhagic telangiectasia (HHT) and their families. The organization provides educational resources, connects patients with specialized care centers, and supports clinical research aimed at finding a cure for the genetic disorder.
Non-Profit & Patient Advocacy
The Sjögren's Foundation serves as a resource and advocacy organization for individuals affected by Sjögren's disease, providing information on research, treatments, and patient support. It offers educational materials, community networks, and guidance for patients, caregivers, and healthcare professionals.
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