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.
Medical
Medical
Goal Attainment Scaling: delivering patient-centred clinical trials using personalised outcome measures
By Geoff Case
11 September 2024
Industry Insights
NICE’s key developments in 2024 in summary
By CONTRIBUTOR
11 September 2024
Charity & advocacy
Hope on the horizon: celebrating two years of Hereditary Brain Aneurysm Support and a bright future ahead
By CONTRIBUTOR
10 September 2024
Turning the tide for rare disease
Sickle cell disease: The urgent need for better care, increased research funding and better treatment options
By CONTRIBUTOR
8 September 2024
Patient voice
Find the power in you
By CONTRIBUTOR
4 September 2024
RARE News
UK LSD Collaborative set to release new short—‘Hadid and I’
By admin
2 September 2024
RARE News
Make your voice heard: Participate in the Rare Barometer Survey on the impact of living with a rare diseases on everyday life
By admin
2 September 2024
RARE News
Sickle Cell Disease Association recognises Sickle Cell Awareness Month
By admin
2 September 2024
Charity & advocacy
SMA Europe unites international voices in the new documentary ‘One Community. Shared Dreams’
By CONTRIBUTOR
31 August 2024
Industry Insights
How ‘do’ we versus how ‘should’ we think about disease awareness activities?
By CONTRIBUTOR
30 August 2024
RARE News
Exercise is medicine for people living with PSP & CBD
By admin
28 August 2024
Patient voice
Rare cancers: Sarcoma and your mental health
By CONTRIBUTOR
28 August 2024
Turning the tide for rare disease
Rare Patient Voice: Helping patients and caregivers share their voices
By CONTRIBUTOR
28 August 2024
RARE News
CureDuchenne expands global initiatives andspreads awareness for World Duchenne Day 2024
By admin
23 August 2024
Patient voice
Finding Joy and Keeping Joy: Morven-May MacCallum’s 17-year battle with Lyme disease
By CONTRIBUTOR
21 August 2024
Patient voice
Looking for the positives during hard times: visual snow syndrome
By CONTRIBUTOR
21 August 2024
RARE News
Ladies Luncheon Newport Beach to debut at Shady Canyon Golf Club on October 15 benefiting CureDuchenne
By admin
20 August 2024
« Previous
1
2
3
4
5
…
32
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