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atak spain

ATAK

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  • Diseases: Takayasu
Spain

ATAK was founded to stand up for people living with Takayasu’s arteritis and their families — fighting for their rights, their access to care, and their quality of life.

The association runs on values like commitment, solidarity, mutual support and open dialogue. Practical values, not just words on paper.

What ATAK works toward: reaching everyone affected by Takayasu’s arteritis and offering them companionship, advice and information; building visibility within the medical community; having a seat at the table where policy decisions are made; and actively contributing to research and therapeutic innovation. Their broader goal is simple — to be a connecting force between patients, healthcare providers, and both public and private institutions, all in the service of better health.

Contacts

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Ana Ruiz Díaz

Ana Ruiz Díaz

Presidenta

  • Email: info@arteritistakayasu.com
  • Work: +34655899607

ATAK nació para defender a las personas que viven con arteritis de Takayasu y a sus familias — luchando por sus derechos, su acceso a la atención médica y su calidad de vida.

La asociación se basa en valores como el compromiso, la solidaridad, la ayuda mutua y el diálogo abierto. Valores prácticos, no solo palabras sobre el papel.

Lo que ATAK persigue: llegar a todas las personas afectadas por la arteritis de Takayasu y ofrecerles acompañamiento, asesoramiento e información; ganar visibilidad en el ámbito sanitario; tener voz donde se toman las decisiones; y contribuir activamente a la investigación y la innovación terapéutica. Su objetivo más amplio es sencillo — ser un puente entre pacientes, profesionales de la salud e instituciones públicas y privadas, todo al servicio de una mejor salud.

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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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