{"id":17851,"date":"2022-03-30T00:00:00","date_gmt":"2022-03-30T00:00:00","guid":{"rendered":"https:\/\/fundaciolaninetadelsulls.org\/som-part-de-feder-la-federacio-espanyola-de-malalties-rares-3\/"},"modified":"2025-07-07T12:28:49","modified_gmt":"2025-07-07T12:28:49","slug":"som-part-de-feder-la-federacio-espanyola-de-malalties-rares-3","status":"publish","type":"post","link":"https:\/\/fundaciolaninetadelsulls.org\/en\/som-part-de-feder-la-federacio-espanyola-de-malalties-rares-3\/","title":{"rendered":"We are part of FEDER, the Spanish Federation for Rare Diseases"},"content":{"rendered":"<p>From today, the Fundaci\u00f3 La Nineta dels Ulls, becomes part of FEDER, the <a href=\"https:\/\/www.enfermedades-raras.org\/\">Spanish Federation of Rare Diseases<\/a>.<\/p>\n<p>FEDER&#8217;s mission is to represent and defend the rights of people with RD and suspected diagnosis, favouring their inclusion and generating strategies that contribute to improving their quality of life.<\/p>\n<p>We are proud to join this great organisation that represents and defends the rights of people with rare diseases.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>From today, the Fundaci\u00f3 La Nineta dels Ulls, becomes part of FEDER, the Spanish Federation of Rare Diseases. 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