APS Type 1 Foundation

Support Groups — Raregivers

HUDDLE with the APS Type 1 community - APS Type 1 Foundation, Inc.

Donate - APS Type 1 Foundation, Inc.

NORD® Webinar: Open Enrollment Essentials for Rare Disease Families - APS Type 1 Foundation, Inc.

Welcome Amy Coan, our New Director of Community Relations - APS Type 1 Foundation, Inc.

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Nutrition and Autoimmunity: NIH NOURISH Challenge

Myth-Busting + Common Misconceptions - GivingTuesday

RARE Advocacy Exchange - Global Genes

HPA - Youth Advocacy Program Survey

DAVE’S RESEARCH CORNER: BACK TO SCHOOL - APS Type 1 Foundation, Inc.

Commitment to Privacy

www.science.org

Dating with a Disease!

World's First Patient Treated with Personalized CRISPR Gene Editing Therapy at Children’s Hospital of Philadelphia

Advocacy Opportunity: Big Beautiful Bill - APS Type 1 Foundation, Inc.

Progress on Insurance Prior Authorizations: What the New Industry Pledge Means for Patients - APS Type 1 Foundation, Inc.

President John F Kennedy's medical history: coeliac disease and autoimmune polyglandular syndrome type 2 - PubMed

RARE Disease Siblings Resource Guide

Words of Encouragement from Emily O'Brian as She Completes NIH Clinical Trial - APS Type 1 Foundation, Inc.

Symposium - APS Type 1 Foundation, Inc.

Welcome! You are invited to join a webinar: Navigating Your Path: Living and Working with Chronic Autoimmune Disease . After registering, you will receive a confirmation email about joining the webinar.

Microsoft Forms

Global Genes Guide to Medical Gaslighting

Symposium - APS Type 1 Foundation, Inc.

9 Summer Camps and Programs for Medically Complex Kids | Gus Gear

Online EventOnline Event

'I don't know where to start.' Parents and caregivers are burned out. Who's most at risk?

PETITION TO CONGRESS!