TNPO2 Foundation
TNPO2 FOUNDATION WORKED TO ACCELERATE ACCESS TO A CURE FOR ANY "N-OF-1" PATIENT. INCLUDING THE DEVELOPMENT OF NEW TREATMENTS FOR PATIENTS DIAGNOSED WITH TRANSPORTIN-2 ("TNPO") MUTATION AND SIMILARLY RARE MONOGENIC DISEASES.
Founded
2022
Web
tnpo2.org
Address
Sacramento
Home | tnpo2 Home TNPO2 Patients News Project Baby Lion About Us Donate More A Courageous Future for Ultrarare Children About Us We39re reshaping ultrarare care to support all children and the families who love them starting with those who need it most. Forging New Pathways for Precision Medicine In the U. S. alone millions of children live with an ultrarare disease.
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Discussions
Odpovědí v diskuzi
1
What innovative strategies could TNPO2 Foundation implement to better connect families of children with ultrarare diseases to necessary resources and support services?
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Brooklyn Simmons
2 days ago
Odpovědí v diskuzi
1
How can we raise awareness among healthcare providers about the unique challenges faced by families navigating the complexities of ultrarare diseases to ensure timely and effective care?
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Brooklyn Simmons
2 days ago
Latest reviews
Together, we can make a real impact in communities around the world. Help us bring hope and support.
What an incredible initiative! Every child deserves a chance at a healthier future, and TNPO2 Foundation is doing just that. Let’s support their mission to bring hope and healing to ultrarare children! 💖🌟
Brooklyn Simmons
Product Manager
So proud of the work TNPO2 Foundation is doing for families facing these challenges! Together, we can pave the way for precision medicine and transform lives. Let’s spread the word and help raise awareness! 🙌💜
Brooklyn Simmons
Product Manager
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