
DADA2 Foundation
@dada2foundation
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We're a nonprofit looking for innovative ways to accelerate research into the rare inflammatory disease DADA2.
Joined September 2016
Partnering w/ @TNFPharma to launch compassionate use study of #Isomyosamine for #DADA2 patients when the disease can become life-threatening. Hope for families, progress for patients. 💙🔗 #RareDisease #CompassionateUse #DADA2Foundation #PediatricResearch.
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Review/download our physicians brochure - printable and digital versions to take with you to summer conferences and medical rounds. #CME #physicianconference #rheumatology #ERMedicine #InternalMedicine #Immunology #Dermatology #Neurology #Hematology
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RT @DavidFajgenbaum: Deadly hyperinflammatory disease finds curative treatment from a repurposed drug!. DADA2, a rare hyperinflammatory con….
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It's an honor to call @DavidFajgenbaum a friend of the Foundation. He brings attention to an important issue for consideration in rare diseases. Repurposing! #RareDisease.
Deadly hyperinflammatory disease finds curative treatment from a repurposed drug!. DADA2, a rare hyperinflammatory condition, tragically forces children to endure strokes at a young age, often leading to premature death in their teenage years. Without a single clinical trial,
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Thank you, @JAMANetworkOpen for selecting the DADA2 Consensus Statement paper as a CME-credit eligible paper for one credit. This is an important way to continue to share awareness of DADA2 among doctors.
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Andy's story is classic for #raredisease. Decades of questions. But today? Andy is THRIVING - a testament to collaboration. Best wishes to Andy & his family on #RareDiseaseDay2024 - & our deepest gratitude to all researchers & docs working to cure DADA2.
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. and while we're on the topic of more knowledge this #RareDiseaseDay2024 . Take 3 min to learn more about DADA2.
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Latest newsletter is out & we're celebrating collaboration, that irreplaceable phenomenon that happens when people choose a shared purpose. This #RareDiseaseDay2024, we don't take for granted the dedicated of clinicians & researchers on the case of DADA2.
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Honoring #rarediseaseday2024? We have a few ways you can help - whether you are a patient or family, doctor or researcher. Check out our toolkit and help us spread awareness in 2024!
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Newsletter alert! How can our website help build a care team? And more. Take a look and retweet! Who else needs to learn more about DADA2? #RareDisease
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We are on the VERGE OF DISCOVERY - so much to do in 2024! Invest in our new Patient Registry, collaboration among dedicated researchers & doctors, and the lives of DADA2 patients this #givingTuesday. Here's how your gift TODAY can make a difference:
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