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.
A day in the life
A day in the life
Don’t let your condition define you! David’s journey with stiff person syndrome
By CONTRIBUTOR
14 February 2024
Industry Insights
Rare Disease Day 2024: Sheela Upadhyaya previews some of the events taking place across the world
By CONTRIBUTOR
14 February 2024
Industry Insights
The UK Rare Diseases Framework: Sheela Upadhyaya reflects on recent progress across the UK
By CONTRIBUTOR
12 February 2024
Patient voice
Love isn’t rare—Ken To’s journey with Huntington’s disease
By CONTRIBUTOR
11 February 2024
RARE News
MEF2C Foundation & MUSC launch program to develop MEF2C therapeutics
By admin
9 February 2024
Turning the tide for rare disease
Congenital muscular dystrophy: Kelly and Avery’s mission to challenge perceptions of disability
By CONTRIBUTOR
7 February 2024
RARE News
National Tay-Sachs & Allied Diseases Association hosts first of its kind drug development meeting for GM2
By admin
2 February 2024
RARE News
Get Ready to #ShowYourStripes for Rare Disease Day 2024 29th February: the rarest day of the year!
By admin
1 February 2024
Patient voice
If you want to make God laugh, tell him about your plans
By CONTRIBUTOR
31 January 2024
RARE News
CureDuchenne announces educational events for families and caregivers of individuals with Duchenne or Becker muscular dystrophy
By admin
31 January 2024
RARE News
Sickle Cell Disease Association of America Inc. appoints two to board
By admin
29 January 2024
RARE News
American Kidney Fund announces April 30 as the first annual APOL1-mediated kidney disease (AMKD) awareness day
By admin
26 January 2024
Science & tech
Faster diagnosis for patients with rare diseases
By CONTRIBUTOR
24 January 2024
RARE News
REGISTER NOW for M4RD’s ANNUAL SYMPOSIUM
By admin
23 January 2024
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
« Previous
1
…
8
9
10
11
12
…
33
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