February is #BlackHistoryMonth, the annual celebration of the achievements and contributions of African Americans in the US! Black Americans face additional barriers to proper healthcare. By honoring the struggles of the past, we can work together for equitable care for all.

When you donate to the Immune Deficiency Foundation, you change lives. Here's how.

And finally it has arrived. Thank you so much, waomeo Ch. ワオメオ🍊| Commission Open It's sooooo cute. I love it so much

Health insurance companies require prior authorization for certain medical care related to primary immunodeficiency (PI). Work with your healthcare provider to ensure they submit the necessary documentation. bit.ly/3MfpJWn

Three days where you don't have to explain yourself. Where someone else finally gets it. Join us in San Antonio, TX, June 25-27! bit.ly/4rq1xQe

!! EMERGENCY COMMISSIONS !! theyre gonna cut me damn internet off !! (retweets appreciated uwu)

Everyone else: 'Just a cold, I'll be fine by Monday.' You: Week 3 of recovery. Sound familiar? Take our self-assessment to find out if your symptoms could point to a primary immunodeficiency: #ImmuneHealth bit.ly/4pZWp3T

With several #measles outbreaks gaining steam, check out our article on a study showing that immunoglobulin (Ig) replacement therapy offers protection in patients with #PrimaryImmunodeficiency. bit.ly/3OuI0j4

Here's why getting your flu vaccine is important.

Follow Follow Like It Like It 🩷🧡 We have a gift for you this Valentine's Day. Let's create the perfect virtual husbando. A song collab by Mikan ♨️🍊 Capybara Vtuber and ChocoCoTV. We sang Fake Heart - Kira X Asteroid. Premiering this coming Valentine's! ❤️and RTs are appreciated!

#ValentinesDay is almost here and this reminds us how amazing it is to see the outpouring of love and support for immunocompromised individuals at walks and other events. Thank you to the friends, family, caregivers and more who show their love and support for the community. ❤️

We're excited to attend the American Academy of Allergy, Asthma & Immunology conference, February 27- March 2, to connect with providers across the U.S. to discuss primary immunodeficiency (PI) diagnosis, research, and treatment! Stop by booth 1509 to learn more and say hi.

Show some love! 🍕💕 Now through March 31, when you order from Little Caesars Fundraising, a portion of the proceeds will support the Call of Duty Endowment. Learn more: bit.ly/4ch5cva

Show some love! 🍕💕 Now through March 31, when you order from Little Caesars Fundraising, a portion of the proceeds will support the Call of Duty Endowment. Follow LCF: linkedin.com/company/little… Learn more: bit.ly/4ch5cva

We will return to office tomorrow, Tuesday February 17.

Chris Simpson, diagnosed with CD40 ligand (CD40L) deficiency, also known as X-linked hyper IgM syndrome, received gene therapy that uses both base-edited stem cells and base-edited T cells in a clinical trial at the National Institutes of Health (NIH). bit.ly/4rMxW3m

We’re excited to announce an exclusive charity signing with the cast of Aphmau on Streamily for Rare Disease Day! Prints purchased will help support our vision to create a healthier day, every day, for every person with immune deficiency. Tune in on 2/28 at 7pm EST 💙

Meet our new medical director, Dr. Paula Henao! Dr. Henao is an associate professor of allergy, asthma, and immunology at Penn State Health Milton S. Hershey Medical Center. Read more: bit.ly/4ryaFTa

On February 22, 1984, the world lost David Vetter, who was known as the "Boy in the Bubble." His story and protected environment brought global awareness to primary immunodeficiency (PI). Honor his legacy and support our work through a tribute gift today: bit.ly/4qMNy74

Sadly I have to announce this: I'm quitting Twitch and social media in general. To make it clear: I'm sad for no longer supporting the wonderful people I met but it's time for me to move on. I wish you all the best