Emily’s fundraising efforts reach dizzying heights
Some people do fundraising runs, walks and cycles, others bake cakes. Emily is hurling herself…
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Blow for new extended half-life product
We’re extremely disappointed to learn that a new extended half-life product for haemophilia A will…
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Dental care – what’s your experience?
We’re launching a survey to find out more about dental care for people with a…
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New medical advisory group launched
We have changed the way we review medical and scientific information by widening the range…
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Welcome to our new trustees
We’re thrilled to introduce two new trustees who will help to shape and provide strategic…
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Volunteers needed to assess centres
Could you help improve treatment and care for people with bleeding disorders? Next year, 31…
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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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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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