Fibromyalgie France
About
be the spokesperson for chronic fibromyalgic pain to the public authorities, the national media (generalists and specialists) or to any other external physical or legal person involved in the knowledge, recognition, management or treatment of fibromyalgia and chronic pain; contribute to the dissemination of quality medical, institutional, scientific or social information on fibromyalgia and chronic pain, first to the members of the association, but also to patients in general, families, health professionals and the general public; carry out training and awareness-raising activities, as well as advocacy for people with fibromyalgia and chronic pain for the improvement or maintenance of the quality of life and in the employment of chronic fibromyalgic pain patients; continue the dynamics of association in partnerships with …
être le porte-parole des douloureux chroniques fibromyalgiques auprès des pouvoirs publics, des médias nationaux (généralistes et spécialisés) ou devant toute autre personne physique ou morale extérieure, impliquée dans la connaissance, la reconnaissance, la prise en charge ou le traitement des fibromyalgies et des douleurs chroniques ; contribuer a la diffusion d'éléments d'information de qualité de type médical, institutionnel, scientifique ou social sur la fibromyalgie et des douleurs chroniques, d'abord auprès des membres de l'association, mais également auprès des patients en général, des familles, des professionnels de santé et du grand public ; mener des actions de formation et de sensibilisation, ainsi que des actions de plaidoyer au profit des personnes atteintes de fibromyalgie et de douleurs chroniques pour une amélioration …
Focus & reach
Verification & registration
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Integrity assessment
A score from 0 to 100 for how openly a charity shares public information across five areas: registration, financial disclosure, governance, contact details, and data recency. It does not measure programme impact. document.querySelector('#data-knowledge') && document.querySelector('#data-knowledge').scrollIntoView({behavior:'smooth', block:'start'}))" class="gr-link" style="color:#0E827A;font-weight:700;text-decoration:none;cursor:pointer">See exactly what we do and do not have →
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GiveRadar Analysis
GiveRadar's verified records show Fibromyalgie France with a partial profile.
- Established in 2001, it predates 79% of the health charities in France GiveRadar has a founding year for. View this cohort
- GiveRadar has not yet verified financial records for this organization, nor for only 2% of health charities in France - a gap in GiveRadar's dataset for the region, not a feature of this charity. Explore France data
- It is one of the better-documented health charities in France GiveRadar currently tracks, because GiveRadar has verified its registration and its contact details. View this cohort
- government registration
- a website
- a contact email
- a donation page
Analysis based on GiveRadar's benchmark dataset of 2026-09-07. It describes what GiveRadar has verified, not a judgment of the organization itself.
See 5 years of revenue, expense breakdowns, and balance sheet.
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Whether a gift to Fibromyalgie France lowers your own taxes depends on where you pay them. Choose your country to see the rule that applies.
French donations to associations d'intérêt général or associations reconnues d'utilité publique are deductible (66% crédit d'impôt for individuals up to a cap).
Fibromyalgie France is in France, a TGE (Transnational Giving Europe) member country. Dutch donors can route gifts via Stichting Transnational Giving Europe to receive Dutch ANBI-equivalent deductibility, subject to TGE's 5% pass-through fee.
Fibromyalgie France is registered in France. US donors generally cannot deduct gifts to non-US charities directly. To claim a deduction, route the gift through a US 'Friends of' fiscal sponsor or a donor-advised fund that performs equivalency determination (IRS Rev. Proc. 92-94).
This is general guidance, not tax advice. Confirm treatment with the charity or your tax advisor before donating.
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In the news
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#893 of 132,826 health charities in France on integrity score
50/100 puts it in the top 2% of the cohort, tied with 3,900 others. Positions are competition ranks: ties share a position. Cohorts are the tightest local peer set with at least 30 comparable organizations; a metric is left out where the cohort is too small or nearly uniform.
Bars show the share of the cohort this charity outranks. Ranks describe how much is publicly disclosed, not how good the charity is.
How it stacks up against peers
Compared with 8 similar health charities in France.
Cause areas in France
Charities working in each area, this charity's highlighted.
Sources and verification
What we know and don't know
Every data point we track for this charity, and whether we have found it. Disclosure only, never a judgment of the charity's work.
Data freshness
How current this profile is, and when we last checked it against the official source.
Methodology
GiveRadar builds each profile primarily from official government charity registries, supplemented where available by third-party nonprofit databases and news archives, and combines it into a single 0-100 integrity assessment. The exact sources for this charity are listed above. We don't take a cut of any donation, ever.
Read full methodologyIf you represent this organization and want to correct or update its data, you can claim this listing to edit details yourself, or email info@giveradar.com with the correct information. We review every request and respond within 30 days.
Frequently asked questions about Fibromyalgie France
Fibromyalgie France is a registered health nonprofit based in Paris, France. It is registered with the Repertoire National des Associations (RNA). It was founded in 2001 and has been operating for 25 years. Its registration number is W751190228. GiveRadar's Integrity Assessment for the organization is 50/100, which reflects how much public information is available, not whether the charity is legitimate.
be the spokesperson for chronic fibromyalgic pain to the public authorities, the national media (generalists and specialists) or to any other external physical or legal person involved in the knowledge, recognition, management or treatment of fibromyalgia and chronic pain; contribute to the dissemination of quality medical, institutional, scientific or social information on fibromyalgia and chronic pain, first to the members of the association, but also to patients in general, families, health professionals and the general public; carry out training and awareness-raising activities, as well as advocacy for people with fibromyalgia and chronic pain for the improvement or maintenance of the quality of life and in the employment of chronic fibromyalgic... Fibromyalgie France is classified as a health organization registered in France. The organization was founded in 2001.
Fibromyalgie France is a French association under simple declaration (declaration simple) - the most common legal form for nonprofits in France, governed by the Loi du 1er juillet 1901. It is created by at least two persons and registered with the prefecture. It is registered in the Repertoire National des Associations (RNA), maintained by the French Ministry of the Interior, under RNA number W751190228.
Fibromyalgie France's official registration number is W751190228, as recorded in the national registry of France.
Fibromyalgie France is located in Paris, France. The organization was established in 2001 and has been active for 25 years. Its registered address is 32 RUE de Laghouat, 75018, France.
Fibromyalgie France is based in Paris. France is divided into 101 departements across 18 regions (13 in metropolitan France plus 5 overseas). French associations can operate nationally regardless of where they are registered - the RNA registration is done at the prefecture of the registered address but does not limit the geographic scope of activities.
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Quick facts about Fibromyalgie France
- What is Fibromyalgie France?
- Fibromyalgie France is a health registered association based in Paris, France. be the spokesperson for chronic fibromyalgic pain to the public authorities, the national media (generalists and specialists) or to any other external physical or legal person involved in the knowledge, recognition, management or treatment of fibromyalgia and chronic pain; contribute to the dissemination of quality medical, institutional, scientific or social information on fibromyalgia and chronic pain, first to the members of the association, but also to patients in general, families, health professionals and the general public; carry out training and awareness-raising activities, as well as advocacy for people with fibromyalgia and chronic pain for the improvement or maintenance of the quality of life and in the employment of chronic fibromyalgic pain patients; continue the dynamics of association in partnerships with the medical body, institutions, etc., as well as representation of the members of the association in the various bodies of health democracy, in an advocacy approach, not only in the interest of persons with fibromyalgic pain, and in the interest of persons with fibromyalgic pain, and in the context of the research for the various forms of the disease, and in the context of the research for the research for the various forms of the interests of the health, in order of the disease, and in order to improve the in order of the in order of the in order of the in order of the in order of the prevention of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in order of the in of the in the in the in the in the in of the in of the in of the in of the in of the in the in the in the in the in the in the in the in of the in the in the in of the in of the in of the in of the in of the in of the in of the in of the in of the in of the in of the in of the the in of the in of the in of the in of the
- When was Fibromyalgie France founded?
- Fibromyalgie France was founded in 2001.
- Where is Fibromyalgie France located?
- Headquartered in Paris, France.
- Is Fibromyalgie France trustworthy?
- Fibromyalgie France has a GiveRadar Integrity Assessment of 50 out of 100 (Partial transparency). The score reflects public-data transparency: registration, financial disclosure, governance, contact details, and how recently data was refreshed. It does not measure program impact.
- What is Fibromyalgie France's registration number?
- Registration: W751190228 (France).
- What is Fibromyalgie France's website?
- http://www.fibromyalgie-france.org
- Are donations to Fibromyalgie France tax-deductible?
- Donations may be tax-deductible for residents of France under local rules. US donors should check whether the charity has an equivalency-determination letter or a US-based fiscal sponsor before claiming a deduction.
