{"id":311,"date":"2014-03-26T22:44:22","date_gmt":"2014-03-26T21:44:22","guid":{"rendered":"http:\/\/s519078666.onlinehome.fr\/?page_id=311"},"modified":"2015-04-08T15:31:07","modified_gmt":"2015-04-08T14:31:07","slug":"join-us","status":"publish","type":"page","link":"https:\/\/www.stargardt.fr\/en\/join-us\/","title":{"rendered":"Join us"},"content":{"rendered":"
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You are concerned by Stargardt disease and are a carrier of the mutating\u00a0 ABCA4 gene. Come and join us\u00a0!<\/strong><\/h2>\n

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Stargardt Foundation supports research on Stargardt disease.<\/strong><\/h3>\n

It aims to create an active interaction between patients and the world of medical research, in order to stop the disease and restore vision.<\/p>\n

\u00a0<\/strong>The aim of the Stargardt Foundation is to federate patients with the desease or carriers of the ABCA4 gene.<\/p>\n

In joining us as carriers of the mutating ABCA4 gene, you\u00a0:<\/p>\n

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  • \u00a0take part in setting up a community of\u00a0 people with Stargardt desease, carriers of the mutating ABCA4 gene, involved in finding a treatment.<\/li>\n
  • \u00a0will follow via the Stargardt Foundation, the development of clinical trials set up by teams of world-reknown researchers (ophtalmology, biology in gene and cellular therapy \u2026) and also of hospital services (private and public).<\/li>\n
  • \u00a0receive every 6 months the latest information on Stargardt desease research.<\/li>\n<\/ul>\n

     <\/p>\n

    To help\u00a0 research, accompany the Stargardt Foundation.<\/strong><\/h3>\n

    \u00a0<\/strong>Join the community \u00ab Research for Stargardt desease\u00a0\u00bb by filling in the following form\u00a0:<\/strong><\/p>\n

    We need your contact details to add you to our community database.<\/p>\n

    The law on Information Systems and Personal Freedoms give you access to modify or erase any personal data. Just get in contact with the Stargardt Foundation.<\/p>\n

     <\/p>\n

    Please fill in the following form.<\/h2>\n