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.
Author:
CONTRIBUTOR
Charity & advocacy
GACI Global: circulating hope for families affected by a rare genetic disease that primarily affects the circulatory system
By CONTRIBUTOR
17 May 2023
Patient voice
Generalised arterial calcification of infancy (GACI): Ruben’s story
By CONTRIBUTOR
17 May 2023
Turning the tide for rare disease
Changing the landscape for the differently-abled community one smile at a time. Dr Sai Kaustuv is our RARE Inspiration
By CONTRIBUTOR
10 May 2023
Industry Insights
COVID: Three years on—what has changed?
By CONTRIBUTOR
3 May 2023
A day in the life
A day in the life with hypokalemic periodic paralysis: Ralph Berthiaume
By CONTRIBUTOR
1 May 2023
Turning the tide for rare disease
Arianna’s Magic Boots: stamping out a taboo in children’s books
By CONTRIBUTOR
26 April 2023
Patient voice
Raymond: A “ray of sunshine” living with VAMP2
By CONTRIBUTOR
21 April 2023
Science & tech
Engaging patients to shape the research of the future
By CONTRIBUTOR
21 April 2023
Charity & advocacy
Ableism can hurt your confidence. Learn to use your voice to regain your personal power!
By CONTRIBUTOR
19 April 2023
Turning the tide for rare disease
FOP Friends: celebrating a decade of support for the fibrodysplasia ossificans progressiva community
By CONTRIBUTOR
19 April 2023
Medical
The GLISTEN trial
By CONTRIBUTOR
14 April 2023
Charity & advocacy
An advocate’s fight across the finish line: learning to live with multiple rare conditions and the trauma of the Boston Marathon bombing
By CONTRIBUTOR
12 April 2023
RARE Ramblings
Richard’s RARE Ramblings: Why?
By CONTRIBUTOR
12 April 2023
Patient voice
Going great lengths: a mother and son’s journey with fibular hemimelia
By CONTRIBUTOR
5 April 2023
A day in the life
A day in the life with Behcet’s disease: Pamela Price
By CONTRIBUTOR
29 March 2023
Charity & advocacy
The incalculable costs of rare diseases for individuals, families and society
By CONTRIBUTOR
29 March 2023
Turning the tide for rare disease
Lea Jabre: helping to lift the voice of the stiff person community
By CONTRIBUTOR
22 March 2023
Posts navigation
Older posts
Newer posts
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