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RARE News
RARE News
New research puts the spotlight on tube feeding
By admin
23 January 2024
RARE News
CureDuchenne Welcomes Patricia Brown as Senior Director of Community Engagement
By admin
23 January 2024
Rare insights
Rare Disease Summit, March 19-21 in Philadelphia, PA, United States
By admin
22 January 2024
RARE News
Project CASK Grant Program now accepting applications
By admin
18 January 2024
RARE News
International Kawasaki Disease Awareness Day: Special Podcast to Illuminate the Importance of Awareness
By admin
17 January 2024
RARE News
Benchmarking report published on “Early and Expanded Access Pathways in Ukraine, Poland, & the Baltic States”
By admin
10 January 2024
RARE News
UK charity PSPA raising awareness in news-style programme
By admin
10 January 2024
Industry Insights
UK report calls for more government input to make cell and gene therapies a true health system priority
By CONTRIBUTOR
9 January 2024
RARE News
IGA celebrates 30th anniversary in 2024
By admin
9 January 2024
Charity & advocacy
Davis Out of the Unknown: a family’s life with Koolen-de Vries Syndrome and their search for treatment
By CONTRIBUTOR
3 January 2024
RARE News
Sickle cell disease is not a joke
By admin
19 December 2023
RARE News
Sickle Cell Disease Association of America Inc. statement about gene therapy approval
By admin
15 December 2023
RARE Ramblings
Richard’s RARE Ramblings: Winter is coming… and I am ecstatic!
By CONTRIBUTOR
13 December 2023
RARE News
PSPA celebrates after receiving £164,000 National Lottery funding to help people living with PSP & CBD
By admin
13 December 2023
RARE News
Worthing couple take part in cooking challenge supported by celebrity chefs to raise funds for Muscular Dystrophy
By admin
8 December 2023
Science & tech
The Undiagnosed Diseases Network’s mission to eradicate the diagnostic odyssey: an interview with Sarah Marshall
By CONTRIBUTOR
6 December 2023
A day in the life
A day in the life: a medically complex condition that is as unpredictable as the weather
By CONTRIBUTOR
29 November 2023
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