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APS Type 1 Foundation

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The APS Type 1 Foundation was started by a group of dedicated parents who were determined to ensure that their children received the best care possible and that no one should have to wait for a diagnosis or treatment for APS Type 1.Our Mission is to unite and empowers a global community to drive awareness, education, and groundbreaking research for APS Type 1, transforming lives affected by this rare autoimmune disorder.

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