Ed’s rowing for gold
Rower Ed Fuller has set his sights on a gold medal at the 2024 Paralympics…
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VWD awareness day in Sheffield
More than 50 adults with von Willebrand disorder (VWD) got together for a day of…
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Von Willebrand what?… Disease? Disorder? Dismissed?
Sunny Maini and Hannah Yarnall from the Haemophilia Society’s von Willebrand Disorder (VWD) Working Group…
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Travelling with haemophilia: Josh’s trip to Thailand
Josh Taylor-Rose, our Youth Ambassador and member of the newly-formed Youth Board, has just spent…
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First licensed gene therapy for haemophilia B not recommended for use in the NHS
The first attempt to get a gene therapy for haemophilia B commissioned in the UK…
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My physio and I are a team
Regular access to specialist physiotherapy has helped Tom stay active and develop his love of…
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Paul missed out on 20 years of physio services
Although Paul received physiotherapy as a child for his severe haemophilia, he did not access…
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Raise money for us at work
Hannah was so happy with the support her family received from the Haemophilia Society (THS)…
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Empowering the next generation
We’re proud to announce the launch of our first Youth Board which will support, empower…
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Take pride in who you are
Mark Ward has been the Haemophilia Society’s LGBT Ambassador since 2019 and works within our community…
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Letter from Kate Burt, Chief Executive of the Haemophilia Society
Kate Burt, Chief Executive at the Haemophilia Society, shares her response to The Spectator’s article…
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The challenge is on!
Join our 36 Challenge and get active to raise money. Working at your own pace,…
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