WELCOME! If you’ve found this site, either you or someone you know or love has been recently diagnosed with a rare disease called Autoimmune Polyglandular Syndrome Type 1 (APS Type 1) also known as (APECED) Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.

We have established a 501C3 Foundation called the APS Type 1 Foundation to support the following areas…Education, Awareness, and Fundraising.

Provide a centralized registry that will unify all those that have the disease so that we can find and communicate with one another.
Help educate those that have been recently diagnosed, and their families, about this rare disease.
To raise money for research that hopefully will find a cure for those who suffer from this disease.

We hope you will take the time to visit our research section, ask a leading authority on this disease a question or two, and register with us so we can get you in contact with those that have gone before you in dealing with the challenges of APS Type 1/APECED. The best advise you receive many times will come from those that have gone before you.

Please take time to visit the great links to the ailment sites like Hypoparathyroidism and Addison’s Disease. These diseases, as stand alone conditions, have great people supporting them through these sites and are a wealth of excellent information for those of us that have to manage multiple conditions.

Finally, if your financial means allows, please donate to our Restricted Grant that we have set up with NORD (National Organization of Rare Diseases). By channeling funding into research we can ultimately find ways to take what researches already know about the AIRE gene and find a cure.

Our story about Gaby’s 6 years of missed diagnosis, and how you can prevent this from happening.

Read Gaby’s Full Story