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Association Takayasu France

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  • Diseases: Takayasu
France

OUR MISSIONS

The mission of the Takayasu France association is to provide information, guidance and links between patients. The association provides support and reassurance. We provide moral and technical support to Takayasu patients and their families. We participate in research through our actions. The association gathers and disseminates information. We liaise with doctors and researchers. We work with other associations, such as France Vascularites.

We raise public awareness of the disease.

Contacts

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Christine Nicollet

présidente

  • Email: contact@association-takayasu-france.org
  • Work: +31 6 36 17 20 70

NOS MISSIONS

L’association Takayasu France s’est donnée pour mission d’informer, orienter, et faire le lien entre patients. L’association accompagne et rassure. Nous apportons soutien moral et technique aux malades du Takayasu et à leurs proches. Nous participons à recherche par nos actions. L’association collecte des informations et les diffuse. Nous sommes le relais avec les médecins et les chercheurs. Nous contribuons à l’amélioration de la prise en charge et nous travaillons avec d’autres associations, telle que France Vascularites, par exemple.

Nous faisons connaître la maladie au grand public.

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  • We encourage and support Vasculitis Patient Advocacy Groups (VPAGs) to collaborate and grow stronger.
  • If there is no existing VPAG in a particular country we can  help to create one.
  • We collaborate with any institution willing to help us in achieving these goals.

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