HyperIgM

Exciting news! 🎉 The @HyperIgM Foundation proudly presents their latest Podcast series, "Patient Voices," led by their very own 15-year-old #HyperIgM patient, Ezra Fineman. Dive into the inaugural episode on YouTube here: youtu.be/_jmXWluYNos?si…

@RareDiseases Thank you for sharing this!

Did you know April is Primary Immunodeficiency Awareness Month? To help spread the word, we’re giving away two $25 Starbucks gift cards along with a Hyper IgM Foundation mug. #hyperigm #PIAwareness

Don't miss three days of connection, learning, and networking with the primary immunodeficiency (PI) community. Featuring the most up-to-date information from world-renowned healthcare professionals, this will be an experience you won't want to miss! bit.ly/3TU743j

Check out our President and Founder on the podcast of @OsmosisMed.

@AK_The_Great @rarediseaseuk Hi Alan, are we already in touch with you? We have a support group for Hyper IgM patients, not as many Type 2, but some.

@rarediseaseuk Im one of the #1in17 as I have Hyper IgM syndrome type 2. Today is also coincidentally my birthday, sending love and support to all of those with a #RareCondition and those supporting us.

Having a #RareCondition isn't that #rare! 3.5 million in the UK are affected by a rare condition, that's #1in17 of us. RT if you're part of the #RareCommunity. #RareDiseaseDay2022 #RareDiseaseDay #RareDisease

@Miyahoka @Boondockfinds @raddik17 @JoeBiden Sorry to hear about your grandson. Are we already in touch and connected to his parents?

Just posted a photo instagram.com/p/Ca2LtAEuCMp/…

Just posted a photo instagram.com/p/CahnQaLObtC/…

ESID is pleased to announce an excellent grant funding opportunity. Researchers with interest in advancing a cure for Hyper IgM Syndrome - the Hyper IgM Foundation is calling you to apply! hyperigm.org/hyper-igm-foun…

Heartwarming story of 11 year old #HyperIgM patient, Adam, from Australia. We are so glad to see how well Adam is doing after his bone marrow transplant. Looking forward to seeing him grow and thrive and maybe one day command a battalion! makeawish.org.au/wishes/wish-st…

Thank you @ESIDsociety for getting the word out! #hyperigm

New blog entry - #HeadOfTheHerd w/ Akiva Zablocki, President, @HyperIgM! "In the end I am an optimist, because there is no other way to approach the #raredisease world we are in besides optimism." Read more: bit.ly/2TXbYN5

Hyper IgM Families already spend their daily lives avoiding germs and illnesses like the common cold or flu. Hyper IgM Foundation President, Akiva Zablocki, shares his secrets to staying safe when germs are all around us. #coronavirus #hyperigm #TheMighty yahoo.com/lifestyle/5-ti…

Akiva Zablocki, President of the Hyper IgM Foundation, shares his family's secrets to avoiding germs in hopes of curtailing the spread of the coronavirus. #coronavirus #hyperigm #RareDiseaseDay

We wanted to share with you some touching words from a partner of one of our rare adult patients. This year the Foundation allocated grant funds to support Dr. Caroline Kuo’s Gene Editing research at UCLA. We were… instagram.com/p/B5yu4H3gF2j/…

Congratulations to Dr. Caroline Kuo from UCLA, and BIG news for Hyper IgM!! Dr. Kuo just received a $4.9 million award from the California Institute for Regenerative Medicine (CIRM) in support of her development of… instagram.com/p/B4U0VlyAOtq/…

The Hyper IgM Foundation is proud to announce that it joins the Primary Immune Deficiency Treatment Consortium (PIDTC) as one of its Patient Advocacy Group (PAG) partners. The PIDTC consists of 42 centers in North… instagram.com/p/B4AmDVAgryn/…

Big thank you to Lisa Boyer and her wonderful team at Wells Fargo!! Through their efforts during the annual Wells Fargo Community Support Campaign, they raised $500 for the Hyper IgM Foundation. We love the size of… instagram.com/p/B2zdgX_gbyS/…

Board member and Co-Founder of the Hyper IgM Foundation, Amanda Zablocki, share insights into how to gain gender parity in the workforce.