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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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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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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A Week In The Life: Jessica
As part of a series featuring staff at the Haemophilia Society, Jessica Bomford, our Public…
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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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Gene Therapy for Haemophilia B to be licensed next year
A gene therapy for haemophilia B has moved a step closer to being licensed for…
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Living with von Willebrand disorder, part 6
Carly, 32, lives with her husband Nick in Devon. They have a busy house; with…
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Living with von Willebrand disorder, part 5
Carly, 32, lives with her husband Nick in Devon. They have a busy house; with…
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Remembering Nigel Pegram
We were very sorry to hear of the recent death of Nigel Pegram, a long…
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CRG PPV application process now open
Would you like to take on a role which can really influence what care should…
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Living with von Willebrand disorder, part 4
Carly, 32, lives with her husband Nick in Devon. They have a busy house; with…
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Living with von Willebrand disorder, part 3
Carly, 32, lives with her husband Nick in Devon. They have a busy house; with…
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