
The Haemophilia Society
The Haemophilia Society is a UK-wide charity supporting people affected by bleeding disorders, including haemophilia and von Willebrand disorder.
Check if this group covers your diagnosis
Hematological Disorders
- Hemophilia A (Factor VIII Deficiency)
- Hemophilia B (Factor IX Deficiency)
- Von Willebrand Disease
- Acquired Hemophilia
Mission
Through our community, we find the freedom, opportunity and fun in life after diagnosis., At THS we want to empower everyone affected by a bleeding disorder to live life to the full, whatever stage you are at.
How they can help
It offers help and support for people who are newly diagnosed and for those living with a bleeding disorder., The site also points people to support and information, including global support and support for women with bleeding disorders., The organization offers support group, Peer support, Financial support, and education including Support groups, Https, Annual report 2010, and Trusts and foundations are grant., The researcher identified 12 named programs or services in total., The society offers free member events, a local group network, and online communities to share advice and experiences., a local group network, and online communities to share advice and experiences., It also provides up-to-date information and resources on issues such as visas, immigration, It also provides up-to-date information and resources to help with questions about visas, immigration, and access to healthcare in the UK., and access to healthcare in the UK., and gaining access to healthcare in the UK.
The organization offers event, The organization offers information service, event, The organization offers webinar, event, information service, and financial assistance including Written updates and webinar reporting on grant progress, Buggins Family Camp, Newly Diagnosed Families Weekend, Newly Diagnosed Weekend, Youth Camp, and Inhibitor Information and Support., and financial assistance including Written updates and webinar reporting on grant progress, Buggins Family Camp, Newly Diagnosed Families Weekend, Newly Diagnosed Weekend, Youth Camp, and Inhibitor Information and Support., and support group including Written updates every four months, grant, and information service including Family Camp, Voluntary Financial Guidance, The Haemophilia Society receives one-year government grant, Hemlibra administration kit needle information, 2025 THS Superstar Awards, and Global Support., These services are aimed at Families, People seeking financial guidance, and The Haemophilia Society., The researcher identified 29 named programs or services in total., The organization offers support group, Peer support, Financial support, and education including Support groups, Https, Annual report 2010, and Trusts and foundations are grant., The researcher identified 12 named programs or services in total., and grant including Written updates and webinar reporting on grant progress, These services are aimed at Members and officials at the DHSC, These services are aimed at members, families affected by haemophilia, and Newly diagnosed families affected by a bleeding disorder., and Newly diagnosed families affected by a bleeding disorder., The researcher identified 32 named programs or services in total., The researcher identified 37 named programs or services in total., The researcher identified 38 named programs or services in total.
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