Menu

Post image 1
Post image 2
Post image 3
Post image 4
Post image 5
Post image 6
Post image 7
Post image 8
Post image 9
Post image 10
Post image 11
Post image 12
Post image 13
Post image 14
Post image 15
Post image 16
Post image 17
Post image 18
1 / 18
0

Families organize amid government funding cuts into rare disease research - The World from PRX

Science & Technology Archives - The World from PRX·Deepa Fernandes·3 days ago
#Nq4la3N8
Reading 0:00
15s threshold

Public radio’s longest-running daily global news program. About Contact Donate Meet the Team Privacy Terms of use ©2026 The World from PRX PRX is a 501(c)(3) organization recognized by the IRS: #263347402. Families organize amid government funding cuts into rare disease research Dramatic cuts to science research grants have particularly affected rare disease research. But some of the people most affected, including those with Nicolaides-Baraitser syndrome, are now organizing their own global research collaborations. Dr. Paola Nicolaides visiting the home in Palaichori, Cyrpus, where her family fled in 1974 to escape the Turkish invasion of their city of Nicosia. Deepa Fernandes/The World Some 25 million Americans live with rare genetic diseases — that’s nearly 1 in 13. More than half are children. The path to discovering what the condition is and finding treatments can take years. But for children who are medical mysteries, getting a diagnosis can be life-changing. Dr.…

Continue reading — create a free account

Join HashtagPLUS to read full articles, follow hashtags, vote, and join the conversation.

Read More