Close
×
Subscribe Now
By entering these details you are signing up to receive our newsletter.
First Name
Last Name
Your Email
Type of visitor?
Individuals with a rare condition
Caregiver/family member
Industry/biotech/pharma
Healthcare professionals
Charity/advocate
General interest
Newsletters
RAREBite Newsletter Subscribers (Twice Weekly)
Magazine and RARE Round-Up Weekly Newsletter
Latest Edition
Subscribe Now
Home
Meet the team
Magazine
RARE INSIGHTS
A day in the life
Charity & advocacy
Industry insights
Letters
Medical
News
Patient voice
RARE caregiving
RARE ramblings
RARE REV-inar
Reviews
Science & tech
Sunday sessions
Turning the tide for rare disease
THE PEOPLE OF RARE
Digital Spotlight
RARE Reports
Resources
Charity Partners
WORK WITH US
Rare Revolutionaries
Community Gallery
Rare Youth
SHOP
Latest Edition
Subscribe Now
To use more accessibility options, please use a different browser such as Chrome or Firefox.
RARE News
RARE News
CureDuchenne Welcomes Patricia Brown as Senior Director of Community Engagement
By admin
23 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
RARE News
IGA celebrates 30th anniversary in 2024
By admin
9 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 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
RARE News
CureDuchenne raises more than $1.3 million at ninth annual Napa in Newport to help find a cure for Duchenne muscular dystrophy
By admin
16 November 2023
RARE News
Exciting news: $100,000 in funding for Myhre syndrome research projects
By admin
7 November 2023
RARE News
Rare Stories initiative illuminates lives in Northern Ireland rare disease community
By admin
2 November 2023
RARE News
Pilbara Rare Care Centre to open in remote Western Australia
By admin
31 October 2023
RARE News
CureDuchenne welcomes new executive director, vice president of medical affairs, and board members
By admin
25 October 2023
RARE News
Arthur Suckow, former co-founder and chief executive officer of DTx Pharma, joins CMT Research Foundation board of directors
By admin
5 October 2023
RARE News
NHL all-star Ryan Getzlaf and CureDuchenne raise more than $500,000 at 12th Annual Getzlaf Golf Shootout
By admin
29 September 2023
« Previous
1
…
4
5
6
7
8
…
15
Next »
Skip to content
Open toolbar
Accessibility Tools
Accessibility Tools
Increase Text
Increase Text
Decrease Text
Decrease Text
Grayscale
Grayscale
High Contrast
High Contrast
Negative Contrast
Negative Contrast
Light Background
Light Background
Links Underline
Links Underline
Readable Font
Readable Font
Reset
Reset