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08-02-2024 - Fondation Maladies Rares and Algodystrophie France Launch Joint Call on Complex Regional Pain Syndrome (CRPS)
Fondation Maladies Rares (FMR - Foundation for Rare Diseases) is an umbrella organisation created within the framework of France's second National Rare Diseases Plan. It promotes scientific cooperation in all aspects of research on rare diseases. The Foundation provides funding and access to innovative technologies and specialised technological platforms. Association Algodystrophie France is a French association established in 2018 with the objectives of supporting people affected by complex regional pain syndrome (CRPS)/algodystrophy. The Association provides support for CRPS patients, their families and those recovering from the condition.
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