APS Type 1 Foundation

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

[APS Type 1 Foundation @APSType1]

In case you missed it, video recordings of the 5th International Symposium on APS Type 1 are now available! Watch now: https://t.co/xigUu3RLmZ

[APS Type 1 Foundation @APSType1]

Sustained increases' reported in flu nationwide, as RSV hits kids hard https://t.co/krJujQzGvG

[APS Type 1 Foundation @APSType1]

Many clinicians are unfamiliar with APS Type 1, and misdiagnoses are common. That's why we've created essential clinician resources! Explore here: 📚🩺

https://t.co/kx7OvpC0Iz

[APS Type 1 Foundation @APSType1]

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. https://t.co/AeHfAvN3wb

[APS Type 1 Foundation @APSType1]

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: https://t.co/ockJ4GIgPf

[APS Type 1 Foundation @APSType1]

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! 🎟️🤝
https://t.co/W6VzN4cQ6J

[APS Type 1 Foundation @APSType1]

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: https://t.co/svAgq2l3Y1

[APS Type 1 Foundation @APSType1]

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: https://t.co/q8zsJD66nX

[APS Type 1 Foundation @APSType1]

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. https://t.co/W6VzN4cQ6J

[APS Type 1 Foundation @APSType1]

From Harvard Health -- "How much sleep do you actually need?" https://t.co/FSyVSjesPV

[APS Type 1 Foundation @APSType1]

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: https://t.co/q8zsJD66nX

[APS Type 1 Foundation @APSType1]

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. https://t.co/ZMy9dD9rI6

[APS Type 1 Foundation @APSType1]

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: https://t.co/ZmIikkgGxB

[APS Type 1 Foundation @APSType1]

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: https://t.co/ZmIikkgGxB

[APS Type 1 Foundation @APSType1]

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! https://t.co/ZmIikkgGxB

[APS Type 1 Foundation @APSType1]

"The Privilege of Access to Care" -- this blog post from NORD sheds light on the need for more equitable access to care and diagnosis. https://t.co/v0WTphXIWU

[APS Type 1 Foundation @APSType1]

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. https://t.co/nsswi7sLhg

[APS Type 1 Foundation @APSType1]

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.

[APS Type 1 Foundation @APSType1]

The latest from the NIH, "Genetics Experts Support Adding Hundreds of Treatable Rare Diseases to Newborn Screening." Read the full blog post now: https://t.co/w06rh5Zgds

[APS Type 1 Foundation @APSType1]

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. https://t.co/ZmIikkgGxB

[APS Type 1 Foundation @APSType1]

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!

https://t.co/PArPswd8FW