European Conference Discusses Better Support For Women
The weekend of 21 and 22 May 2022 saw the second ever European conference dedicated to…
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Cell and Gene Collective calls for more political leadership to ensure patient access to gene therapies
The Haemophilia Society is part of a group of rare disease charities called the Cell…
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Thank you for your support of Ukraine!
We’ve been overwhelmed by your generous support of our Ukraine emergency appeal to help people…
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Government needs to publish study on Compensation Framework for people affected by contaminated blood products
The Haemophilia Society, MPs and other campaigners have written to the Government demanding they publish…
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Advances in inhibitor knowledge and treatment
Inhibitors are a complication of haemophilia treatment, in which the patient’s body begins to produce…
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Success at Talking Red Live
Talking Red Live in York in early March brought together women with bleeding disorders from…
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New Treatment Options for Glanzmann’s on the Horizon
Last month clinicians and researchers from across the world gathered virtually at EAHAD, a congress…
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Reporting from EAHAD, which met virtually for its 2022 Congress on Bleeding Disorder Treatment and Care
In February, the European Association for Haemophilia and Allied Disorders had their annual meeting. We…
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A Life Inhabited
Thanks to advances in the treatments made available in the last few years, developing inhibitors…
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New Health and Care Bill will reorganise the NHS
The Health and Care Bill, which is currently being debated in parliament, has the potential…
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NHS Innovative Medicines Fund provides route to new treatments for bleeding disorders
Last year the Government announced plans for a new fund to allow people with rare diseases in…
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Launch of New women’s bleeding symptom checker
We’re proud to have launched an easy-to-use online symptom checker to help women and girls with heavy periods find out if…
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