Acabar con la soledad de los enfermos en todo el mundo
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Nuestras páginas están dirigidas a todos los afectados por esta enfermedad genética rara, Cutis Laxa:
a enfermos y a familias de enfermos, pero también a profesionales de salud y a cualquier persona sensibilizada a las problemáticas de las enfermedades raras.
No aceptamos publicidad y no recibimos fondos de la publicidad.
¿Es usted enfermo, familiar de un enfermo, médico o investigador? ¿Quiere entrar en contacto con otros enfermos?
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