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APS Type 1 Foundation @APSType1

The APS Type 1 Foundation supports education, awareness, and fundraising for Autoimmune Polyglandular Syndrome Type 1, also known as APECED.

Joined February 2019
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APS Type 1 Foundation@APSType1
22 Sep 2023
In case you missed it, video recordings of the 5th International Symposium on APS Type 1 are now available! Watch now: youtube.com/playlist?list=PL…

2023 - 5th International Symposium on APS Type 1

youtube.com
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Sustained increases' reported in flu nationwide, as RSV hits kids hard nbcnews.com/health/health-ne…
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Many clinicians are unfamiliar with APS Type 1, and misdiagnoses are common. That's why we've created essential clinician resources! Explore here: 📚🩺 ow.ly/JlLU50Qix3x

Clinician Information - APS Type 1 Foundation, Inc.

If you are treating someone with APS Type 1, thank you for your commitment to helping your patient and our community. We can pool our resources to make an impact on patient care.

apstype1.org
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The Immune Deficiency Foundation’s 2024 PI Conference in Chicago, IL, will bring together the primary immunodeficiency (PI) community for three days of connection, learning, and networking. web.cvent.com/event/5cc2fa51…
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Help us bring joy to rare disease patients and caregivers spending their holidays in the hospital. NORD will deliver care packages to NORD Rare Disease Centers of Excellence in CT, MA, and DC. 🌟 Help make a difference! 💙 Donate: rarediseases.org/2023-holida…

Help NORD Spread Cheer This Holiday Season!  - National Organization for Rare Disorders

The holiday season is almost here! To bring seasonal cheer and remind one another that no one in the rare community fights alone, NORD will be creating and

rarediseases.org
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Let’s make Brent’s 50th birthday unforgettable! Every contribution funds critical research, empowers patient support initiatives, and accelerates the journey toward a cure. 🌟 Buy tickets, become a sponsor, or make a donation today! 🎟️🤝 apstype1.org/get-involved/fo…
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Want to learn more about APS Type 1? We’ve curated a list of research articles with short summaries and key quotes. Visit our website: apstype1.org/research/resear…
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Mutations in the AIRE gene predominantly cause APS Type 1. AIRE provides instructions for making a protein called the autoimmune regulator (AIRE), which helps control when other genes are expressed. For more info, visit our website: apstype1.org/education/what-…
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Join us on February 17 to celebrate Brent’s 50th birthday with the iconic sounds of Surreal Neil and Super Diamond. 🎉 Your presence will contribute to finding a cure for APS Type 1. Get your tickets now or become a sponsor. apstype1.org/get-involved/fo…
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From Harvard Health -- "How much sleep do you actually need?" health.harvard.edu/blog/how-…
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APS Type 1 is a rare genetic disorder caused by mutations of the AIRE gene. Mutations in AIRE lead to multi-organ system autoimmunity typified by three classic manifestations. Visit our website for more info: apstype1.org/education/what-…
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The countdown to Rare Disease Day 2024 begins now! This isn’t just a date on the calendar; it’s the start of a global movement, a collective voice championing the cause of the 300 million people living with rare diseases. rarediseaseday.org/news/join…

Join the Countdown: Rare Disease Day 2024 Starts Now

With 100 days to go, the countdown to Rare Disease Day 2024 begins today. This isn’t just a date on the calendar; it’s the start… Continue reading Join the Countdown: Rare Disease Day 2024 Starts Now

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The APS Type 1 Foundation is grateful for the support we received this #GivingTuesday! Thank you for your generosity. Explore our website to discover the impact your kindness will have on our goals for 2024: apstype1.org/get-involved/gi…
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TODAY is #GivingTuesday!!! Every dollar you donate is a step towards achieving our critical objectives for the upcoming year. Here’s a glimpse into what your generosity can help us accomplish in 2024. Click here to donate: apstype1.org/get-involved/gi…
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Tomorrow is #GivingTuesday, let's show our compassion by coming together to help the APS Type 1 Foundation. Your donation can change lives and bring us closer to finding a cure. 💖 Together, we can make a difference! apstype1.org/get-involved/gi…
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"The Privilege of Access to Care" -- this blog post from NORD sheds light on the need for more equitable access to care and diagnosis. rarediseases.org/jennifer-b-…

The Privilege of Access to Care: Jennifer B.’s Story in Honor of Rare Cancer Day - National...

NORD is proud to share this patient story in recognition of Rare Cancer Day 2023. Learn about Rare Cancer Day here. 

rarediseases.org
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On November 30th at 7AM ET, join the conversation! The Economist will convene a panel of experts to discuss case studies from different countries and ways to achieve a more equitable future for people with rare diseases. events.economist.com/custom-…

Leaving no one behind: implementing the UN resolution on rare diseases - Webinar Registration

This webinar will discuss the crucial next steps governments, healthcare professionals and research companies must take on the road to change.

events.economistenterprise.com
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We thank you for your continued support of our foundation and the patient community we serve. We wish you a wonderful Thanksgiving and holiday season with your families.
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The latest from the NIH, "Genetics Experts Support Adding Hundreds of Treatable Rare Diseases to Newborn Screening." Read the full blog post now: ncats.nih.gov/news-events/ne…
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On #GivingTuesday, let's create a ripple of kindness and generosity! Share this post and help us support the APS Type 1 Foundation. Your donation can provide hope and support to those living with APS Type 1. apstype1.org/get-involved/gi…
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On Giving Tuesday, please support our work by helping us reach our fundraising goal of $25,000. Your donation is a link that joins the people and resources necessary for our community to thrive. From our family to yours - THANK YOU! ow.ly/FytV50Q8oQO
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