RARE News

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

A day in the life

#JosiahStrong: Living with familial cold autoinflammatory syndrome—one year on

By CONTRIBUTOR

14 August 2024

RARE News

Introducing the Vascular Voice Network

By admin

12 August 2024

RARE News

PSP Association increases support to families

By admin

12 August 2024

RARE News

Nod to Naz art exhibit opens in California

By admin

9 August 2024

Letters

A troubling development in access to treatment for people living with primary biliary cholangitis (PBC)

By CONTRIBUTOR

7 August 2024

RARE News

Timothy Syndrome Alliance (TSA) looks to recruit Trustee

By admin

2 August 2024

RARE News

CMT Research Foundation invests in project at nationwide children’s hospital to develop improved gene therapy delivery systems for several types of CMT

By admin

1 August 2024

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