A Week In The Life: Jeff
As part of a series featuring staff at the Haemophilia Society, Jeff Courtney, our Policy…Read more
News
Read more
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…Read more
Matthew’s Story
Matthew is aiming to complete an astonishing eight endurance events this year to raise thousands…Read more
Our request to Sir Keir Starmer MP
Today, 1 March, we have written to Sir Keir Starmer MP, to ask that he…Read more
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…Read more
A Week In The Life: Jessica
As part of a series featuring staff at the Haemophilia Society, Jessica Bomford, our Public…Read more
Thank you for supporting our winter appeal!
We’re excited to tell you that our winter fundraising appeal has raised an incredible £47,000. …Read more
Christina’s Story
“Nobody in my family knew anything about bleeding disorders, when I was born,” says Christina,…Read more
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…Read more
Living with von Willebrand disorder, part 6
Carly, 32, lives with her husband Nick in Devon. They have a busy house; with…Read more
Living with von Willebrand disorder, part 5
Carly, 32, lives with her husband Nick in Devon. They have a busy house; with…Read more
Remembering Nigel Pegram
We were very sorry to hear of the recent death of Nigel Pegram, a long…Read more