NEWS AND EVENTS
Blog
Groupama Foundation - Innovation Award 2016
The Groupama Health Foundation launches its call for projects for the 2016 Social Innovation Award.
DIU 'Rare diseases: from research to treatment'.
The 2016-2017 session of the IUD "Rare diseases: from research to treatment" is opened in partnership with 5 Universities.
Fronto-Temporal Lobar Degeneration Day
The second edition of the World Day of Fronto-Temporal Degeneration in France, organized by the association France-DFT and the Center of...
The Foundation publishes its 2015 activity report
The Foundation publishes its activity report for the year 2015.
Announcement of a 3rd rare disease plan
After Marisol Touraine's announcement, the Plateforme Maladies Rares reminds us of the two essential conditions for the success of this plan.
The new Filnemus website
[The new website of the neuromuscular network, Filnemus, is online.
The Rare Disease Foundation will be present today at the 2nd Annual Rare Immuno-Hematological Disease Day
European Conference on Rare Diseases and Orphan Products
[:en]The Rare Diseases Foundation is at the European Conference on Rare Diseases and Orphan Products...
The Line POMARET-DELALANDE Prize
[:en] The Medical Research Foundation is pleased to inform you of the launch of its new 2016 call for projects: The Line Prize...
Call for applications for the Rare Diseases Research Award
The Groupama Health Foundation has launched its call for applications for the Rare Diseases Research Prize.
"RespirH@cktion" and the Rare Disease Foundation
[The Foundation is a partner of the first European Hakathon dedicated to respiratory pathologies "RespirH@cktion"[:]
The solidarity walk In the Footsteps of SO for the benefit of the Rare Disease Foundation
[:fr]The 1st stage on Saturday organized in the Cotentin by our volunteer ambassador Sophie Champaux. 22 kms between Port-en-Bessin Huppain and...