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EURORDIS-Rare Diseases Europe competitors & alternatives
The 12 closest competitors and alternatives to EURORDIS-Rare Diseases Europe among non-profit & advocacy companies — ranked by similarity to what EURORDIS-Rare Diseases Europe actually does, not by market-cap band.
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About EURORDIS-Rare Diseases Europe
EURORDIS-Rare Diseases Europe is a non-governmental patient-driven alliance that advocates for people living with rare diseases in Europe.
EURORDIS-Rare Diseases Europe at a glance
EURORDIS-Rare Diseases Europe is a non-profit & advocacy company headquartered in France. Xcout tracks 10 named people at EURORDIS-Rare Diseases Europe, including Avril Daly (President).
EURORDIS-Rare Diseases Europe leadership
- Avril DalyPresident
- Dorica DanVice President
- Alexandre MéjatBoard Member
- Anna ArellanesováGeneral Secretary
- Graham SlaterDeputy General Secretary
- Johan De GraafTreasurer
4 more named people on record for EURORDIS-Rare Diseases Europe, with roles, board committees and tenure — see the full roster →
Top 12 EURORDIS-Rare Diseases Europe competitors
Ranked by semantic similarity — how close each company is to EURORDIS-Rare Diseases Europe by what it does, using Xcout's live company graph. Click any company for its full profile, or its competitor set.
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 & Civil Rights Organization
European Digital Rights is an association of civil and human rights organizations defending rights and freedoms in the digital environment across Europe.
Nonprofit Organization
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.
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 organization
Suomen Migreeniyhdistys is a national patient and advocacy organization that provides information, support, and advocacy for people with migraines and headache disorders.
Similar non-profit & advocacy company
TGEU is an international non-profit organization advocating for the rights, health, and wellbeing of transgender people across Europe and Central Asia.
Non-profit
The European AIDS Treatment Group is a patient-led non-governmental organization founded in 1992. Headquartered in Brussels, Belgium, the group focuses on European HIV activism, treatment access, and health advocacy.
Non-profit
AGE Platform Europe is a European network of non-profit organizations representing older people. It advocates for the rights, social inclusion, and equality of older adults by influencing European Union policies on ageing, employment, and anti-poverty strategies.
Non-profit organization
The Danish Rheumatism Association provides support, knowledge, and counseling for people with arthritis while funding research and advocating for patients' rights.
Non-profit
The BHD Foundation is a non-profit organization that provides resources, advice, and a patient registry for individuals affected by Birt-Hogg-Dubé (BHD) syndrome, a rare genetic condition. It serves patients, families, and researchers by raising awareness, connecting the global BHD community, and supporting research initiatives.
Non-profit organization
CERMI is the representative platform for people with disabilities in Spain, advocating for their rights and social inclusion.
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.
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