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
World Orphan Drug Congress 2022 – Europe’s most exciting orphan drug event
By admin
10 October 2022
RARE News
World Duchenne Organization announces Accredited Duchenne Centers Programme
By admin
7 October 2022
RARE News
Sickle Cell Disease Association holds 50th annual national convention virtually
By admin
5 October 2022
Turning the tide for rare disease
CMTC-OVM: improving the lives of people with blood vessel abnormalities (vascular malformations)
By CONTRIBUTOR
3 October 2022
Medical
Sanius Health’s mission to personalise care for people with sickle cell disease—using advanced wearable technology
By CONTRIBUTOR
29 September 2022
Charity & advocacy
Governing with Purpose: How to lead a brilliant board – a guide for charity trustees
By CONTRIBUTOR
29 September 2022
RARE News
American Kidney Fund’s Unknown Causes of Kidney Disease Coalition set to advance policies on rare kidney diseases
By admin
26 September 2022
Science & tech
Merging the metaverse and the rare disease community: join the conversation
By CONTRIBUTOR
22 September 2022
RARE News
The Dash Alliance and RARE Revolution Magazine – levelling up for RARE
By admin
21 September 2022
Medical
The RAPSODI study: an online study to understand the association between the Gaucher-causing gene and Parkinson’s
By CONTRIBUTOR
14 September 2022
Turning the tide for rare disease
Being a strong father does not mean staying silent in times of trauma
By CONTRIBUTOR
14 September 2022
Turning the tide for rare disease
A ‘bullhorn in stilettoes’: Tisha Foster’s unique approach to raising awareness of hidden disabilities
By CONTRIBUTOR
12 September 2022
Patient voice
Passing on a rare disease: a RARE mother’s journey from ‘blameless guilt’ to joy
By CONTRIBUTOR
5 September 2022
RARE News
The 2022 Jeans For Genes grant programme is now open and inviting applications
By admin
1 September 2022
RARE News
Sickle Cell Disease Association celebrates National Sickle Cell Awareness Month
By admin
31 August 2022
Turning the tide for rare disease
Ms Colorado America 2022: two-time aneurysm survivor and a champion for cardiovascular disease prevention
By CONTRIBUTOR
31 August 2022
Turning the tide for rare disease
Jeans for Genes: raising awareness and funds to help people living with life-altering genetic conditions
By CONTRIBUTOR
29 August 2022
« Previous
1
…
19
20
21
22
23
…
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