Subscribe Now

By entering these details you are signing up to receive our newsletter.

Medical

What can we learn from European rare disease policies to future-proof our health systems?

By CONTRIBUTOR
4 April 2022

Patient voice

MNGIE: Verity Grainger’s mission to raise funds for a life-saving therapy

By CONTRIBUTOR
30 March 2022

Turning the tide for rare disease

Time for action

By CONTRIBUTOR
28 March 2022

Turning the tide for rare disease

The Global Genes Rare Disease Equity, Diversity and Inclusion Report: the glimmers of hope

By CONTRIBUTOR
23 March 2022

Turning the tide for rare disease

Libmeldy gene therapy offers a lifeline to children with leukodystrophy and gives hope to the rare disease community

By CONTRIBUTOR
23 March 2022

Turning the tide for rare disease

Turning the tide for adult polyglucosan body disease (APBD)

By CONTRIBUTOR
16 March 2022

Turning the tide for rare disease

The Global Genes Rare Disease Diversity, Equity and Inclusion Report: the challenges

By CONTRIBUTOR
16 March 2022

Turning the tide for rare disease

The healing power of storytelling

By CONTRIBUTOR
14 March 2022

Turning the tide for rare disease

Gillian Jackson: bringing positive energy and information to the online BBS community

By CONTRIBUTOR
11 March 2022

Charity & advocacy

The Vascular Birthmarks Foundation, Dr. Giacomo Colletti, Laserplast, and Candela collaborate to provide pro bono laser treatments

By CONTRIBUTOR
10 March 2022

Turning the tide for rare disease

How 10,000 people living with disability could end the foster care crisis

By CONTRIBUTOR
7 March 2022

Turning the tide for rare disease

Brace! Brace! Brace… for burnout!

By CONTRIBUTOR
2 March 2022

Turning the tide for rare disease

Turning the tide for rare disease

By CONTRIBUTOR
28 February 2022

Industry Insights

Living with Gaucher disease: challenging encounters along the patient journey

By CONTRIBUTOR
17 February 2022

Patient voice

Cavernomas—a patient’s efforts to understand the possible systemic implications of a defect in the KRIT1 (CCM1) gene

By CONTRIBUTOR
14 February 2022

Patient voice

The global disability community and the DE&I discussion: a match that needs to be made

By CONTRIBUTOR
9 February 2022

Patient voice

Everyone, on the bus!

By CONTRIBUTOR
28 January 2022
Skip to content