We are excited to share that the poster abstracts from the 2026 TANGO2 Family Conference have been published in Therapeutic Advances in Rare Disease.
View the publication at https://t.co/wRCKqrjN0t
#TANGO2ResearchFoundation#TANGO2FamilyConference
We’re thrilled to share that several TANGO2 Research Foundation (T2RF) leaders have been selected as mentors in national rare disease initiatives — helping empower other organizations and strengthen the global rare disease community.
#TANGO2ResearchFoundation
Congratulations and Thank to Ann Geffen on her 5-Year Anniversary with the TANGO2 Research Foundation!!
🔗 Read the new blog post here: https://t.co/u98yQnbsKH
#TANGO2ResearchFoundation
Forgot to post this last week, but it's a cool story worth sharing. TANGO2 deficiency disorder in a 61-year-old! The story continues... @TANGO2Research
https://t.co/Fn9DZmPA5Z
We're leaving the #RareAsOne Network 2025 Meeting energized by powerful conversations + new connections! Participants shared examples of patient-led #RareDisease collaborations that are moving us closer to treatments and cures across diseases. Thanks to all who joined! #Patients
It’s been an incredible week at the @ChanZuckerberg Rare As One Network Science in Society Meeting. Inspiring and invigorating to say the least! Looking forward to reaching greater heights and making more progress for rare disease families.
A banana duct-taped to a wall — a conceptual artwork by Maurizio Cattelan titled "Comedian" — sold to a crypto entrepreneur for $6.2 million with fees at Sotheby's contemporary art auction on Wednesday. https://t.co/bSewDkCv72
🌟 Meet Heloisa, a courageous 6-year-old TANGO2 Warrior from São Paulo, Brazil! 🌟
Heloisa’s joy for life shines brightest when she's in the water, swimming her heart out at the club pool. When she's not in the water, you'll find her dancing up a storm or whipping up sweet t ...
How cool was it to see I AM ALS represented on stage last night at the DNC? We’re so proud of the work this community is doing together. In case you missed it, you can watch Brian and Sandra’s remarks in full: https://t.co/pf7aDSGwD1
Brian and Sandra are the epitome of hope.
When Brian was diagnosed with ALS, he turned tragedy into action by launching @iamalsorg and leading a movement to find a cure.
I’m inspired by these two—and after you hear their story at the @DemConvention, you will be, too.
Just finished up an amazing @TANGO2Research family conference. When patient families, researchers, clinicians, and caregivers collaborate, we move mountains.