News

Thank you for supporting our winter appeal!

We’re excited to tell you that our winter fundraising appeal has raised an incredible £47,000. …
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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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World AIDS Day: Mark Ward

Mark Ward is the Haemophilia Society’s LGBT Ambassador. He has spent all his adult life…
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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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Living with von Willebrand disorder, part 2

Carly, 32, lives with her husband Nick in Devon. They have a busy house; with…
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Can you help further research into pain and pain memories?

Anna Wells has worked as a physiotherapist within bleeding disorders services for the past 15…
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