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A day in the life
A day in the life
A day in the life: a glimpse into my life living with scleroderma
By CONTRIBUTOR
15 September 2023
RARE News
Uncommon knowledge
By admin
13 September 2023
Patient voice
The physical, mental, and emotional toll of Charcot-Marie-Tooth disease: Joe Hogan’s story
By CONTRIBUTOR
13 September 2023
RARE News
W. David Arnold, MD joins CMT Research Foundation Advisory Board
By admin
7 September 2023
Medical
Transitioning successfully from paediatric to adult care in Duchenne muscular dystrophy
By CONTRIBUTOR
6 September 2023
RARE News
Sickle Cell Disease Association recognises Sickle Cell Awareness Month
By admin
5 September 2023
RARE News
Dyne Therapeutics and CureDuchenne partner to give the gift of mobility to two local families
By admin
30 August 2023
Turning the tide for rare disease
Alpha-1: best practices for testing for this and other late-onset genetic diseases
By CONTRIBUTOR
30 August 2023
RARE News
Million Dollar Bike Ride pilot grant program request for applications
By admin
24 August 2023
Turning the tide for rare disease
Life in the slow lane: finding strength after ataxia diagnosis
By CONTRIBUTOR
23 August 2023
RARE News
NHL All-Star Ryan Getzlaf returns to the links for the 12th annual Getzlaf Golf Shootout on September 9 benefiting CureDuchenne
By admin
16 August 2023
Science & tech
Marie Curie: the inspiring legacy of a great woman of science and our RARE inspiration
By CONTRIBUTOR
16 August 2023
RARE News
IGA issues position statement on non-comparable medicines
By admin
15 August 2023
RARE News
Double dose of suffering: how the war in Ukraine has affected patients with rare diseases
By admin
14 August 2023
RARE Ramblings
Richard’s RARE Ramblings: accommodating for rare conditions
By CONTRIBUTOR
9 August 2023
RARE News
Landmarks illuminate pink and purple for National Eosinophilic Week
By admin
4 August 2023
Charity & advocacy
Creld1 Warriors—bringing the scientific and parent community together
By CONTRIBUTOR
2 August 2023
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