News

THS representatives at 2023 party political conferences

We are at the major party political conferences this year to highlight the treatment and…
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First steps towards self-treatment

Learning to self-infuse is a milestone moment for anyone who relies on intravenous treatment to…
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New chapter for cycling hero 

Although Alex Dowsett spent 12 years at the top of professional cycling and is the…
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Three lads, one 130-mile commute

Three friends are taking commuting to the next level by walking 160 miles between two…
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Haemtrack’s web app launched  

Haemtrack’s new website app goes live today [20 September], replacing its phone app.  The new…
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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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