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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Empowering the next generation
We’re proud to announce the launch of our first Youth Board which will support, empower…
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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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‘I made the choice to take my life back.’
For Ros Cooper, finding support for her mental wellbeing has been challenging, but it is…
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How to double your fundraising results
Having a sympathetic employer can really boost your fundraising, as Emma discovered when her firm…
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Ross’s tips on staying fit and active
Ross Bennett, one of our youth ambassadors, has recently been interviewed by the European Haemophilia…
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Tegen teaches school friends about haemophilia
We are so impressed by 7-year-old Tegen, from Wiltshire, who gave a talk to her…
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A Week In The Life: Jeff
As part of a series featuring staff at the Haemophilia Society, Jeff Courtney, our Policy…
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Contaminated blood scandal: Update on compensation and redress following meeting with Jeremy Quin MP
Yesterday, 7 March, the All Party Parliamentary Group (APPG) on Haemophilia and Contaminated Blood had…
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Our request to Sir Keir Starmer MP
Today, 1 March, we have written to Sir Keir Starmer MP, to ask that he…
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Show your support on Rare Disease Day on 28 February
In the UK there are over 36,000 people with a rare genetic bleeding disorder such…
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Christina’s Story
“Nobody in my family knew anything about bleeding disorders, when I was born,” says Christina,…
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