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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Introducing our new identity
Today, at our Annual General Meeting, CEO Kate Burt unveiled a new look for the Haemophilia Society (THS), after…
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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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Opportunity To Take Part In Our Survey On The Compensation Framework Study
If you or any members of your family has been affected by contaminated blood, we…
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Alex Dowsett to attempt the Hour Record on 3 November in Mexico
We are beyond excited that British professional cyclist and Haemophilia Society member Alex Dowsett will attempt to…
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Useful new mobile app on rare bleeding disorders & novel therapies
The European Haemophilia Consortium (EHC) has launched a really useful mobile app as an information…
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Conservative Party Conference 2021
Our Policy and Public Affairs Manager Jeff Courtney was at the Conservative party conference this…
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Health Policy at Labour Party Conference
The Labour Party met down in sunny Brighton this week for their annual conference. There…
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Meeting in the East Midlands
If you’d like to meet other people in the East Midlands affected by bleeding disorders,…
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Family places available for Over The Wall ‘Camp in the Cloud’
We’re super excited to offer 10 lucky Haemophilia Society member families the chance to enjoy…
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Why taking part in research really matters
William McKeown, a doctor in Northern Ireland – who also has severe haemophilia A – has recently…
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