Immune Deficiency Foundation

Immune Deficiency Foundation

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Improving the diagnosis, treatment, and quality of life of people affected by primary immunodeficiency. We are Rare and we are powerful.

The Immune Deficiency Foundation improves the diagnosis, treatment, and quality of life of people affected by primary immunodeficiency through fostering a community empowered by advocacy, education, and research. Like the stripes of a zebra, no two people are the same. At IDF, we celebrate this uniqueness every day. An inclusive, diverse, and fair workplace makes our community more powerful. As a

05/28/2026

Chronic illness affects more than your body—it impacts your mental wellbeing too. The uncertainty of unexplained symptoms can be exhausting. Knowledge is your strongest medicine. When you understand your symptoms, you become your best health advocate. Start your wellness journey here. https://bit.ly/4blrKZK.

05/26/2026

People with primary immunodeficiency (PI) often experience anxiety, depression, and other mental health symptoms. Don't suffer in silence. https://bit.ly/4un1S81

05/25/2026

We're closed today, Monday, May 25, in honor of Memorial Day. We'll be back tomorrow, Tuesday, May 26!

Rheumatologist to discuss autoimmunity at National Conference | Immune Deficiency Foundation 05/22/2026

Learn the importance of seeing a rheumatologist to determine if you have autoimmunity along with your primary immunodeficiency (PI) diagnosis during a presentation by Dr. Daniella Schwartz at the Immune Deficiency Foundation's 2026 National Conference, June 25-27, in San Antonio, Texas. https://bit.ly/3QRDQmQ

Rheumatologist to discuss autoimmunity at National Conference | Immune Deficiency Foundation Dr. Daniella Schwartz will discuss immune dysregulation in people with primary immunodeficiency (PI), including autoimmunity and autoinflammation, and the importance of seeing a rheumatologist.

05/21/2026

Together, we're a Mosaic. 🎨✨Register now for the 2026 National Conference in San Antonio! Join us for a transformative experience where every story, voice, and journey creates something extraordinary.

From cutting-edge insights with world-renowned experts to the 9-acre water park, it’s the perfect setting to learn, connect, and thrive. Whether you’re newly diagnosed or a long-time advocate, your presence strengthens our community.

https://bit.ly/4859fI7

05/20/2026

Walk & Community Days 2026 is officially here! Registration is now open, and this year's walk cities are Milwaukee, Philadelphia, Boston, Seattle, Tampa, San Antonio, and a virtual Coast to Coast event. Make a difference with every step and sign up today: https://bit.ly/3Pe1mde

Spring 2026 IDF ADVOCATE newsletter | Immune Deficiency Foundation 05/19/2026

Have you read the Spring 2026 ADVOCATE newsletter yet?🤔 There's something for everyone!

• What the MIRACLE study hopes to learn about fertility, pregnancy, & PI.
• A Kids Korner explainer on Ig replacement therapy.
• How a family supports their son with ataxia-telangiectasia.

Check it out: https://bit.ly/42xIby0.

Spring 2026 IDF ADVOCATE newsletter | Immune Deficiency Foundation This edition of the IDF ADVOCATE features articles on a Wiskott-Aldrich carrier study, appealing health insurance denials, and state advocacy priorities.

Photos from Immune Deficiency Foundation's post 05/18/2026

Many people with primary immunodeficiency (and other conditions) rely on plasma for lifesaving treatment. Learn more about how plasma saves lives!

Protecting access to immunoglobulin therapy | Immune Deficiency Foundation 05/15/2026

Thanks to the efforts of our Advocacy Day participants 🙌🏽, & joined & to sponsor H.R. 8528, the PI Post Acute Access Act 🎉 It addresses barriers to receiving immunoglobulin replacement therapy in skilled nursing facilities: https://bit.ly/42xDzId

Protecting access to immunoglobulin therapy | Immune Deficiency Foundation IDF advocates with policymakers and payers for insurance coverage of immunoglobulin (Ig) replacement therapy for those with PI, including access to specific Ig products, modes of administration, and sites of care.

Teen with A-T explores passion for adventure | Immune Deficiency Foundation 05/14/2026

Alex Olive, diagnosed with ataxia-telangiectasia (A-T), a primary immunodeficiency (PI) and neurodegenerative condition that requires him to use a wheelchair, is an outdoor enthusiast who has hiked with his family through Canadian mountains and the Grand Canyon. https://bit.ly/4nqiHwe

Teen with A-T explores passion for adventure | Immune Deficiency Foundation Alex Olive, who lives with ataxia-telangiectasia (A-T), a neurodegenerative condition that causes loss of muscle control and primary immunodeficiency (PI), enjoys traveling to new places and outdoor activities.

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Telephone

Address


7550 Teague Road, Ste 220
Hanover, MD
21076

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm