Welcome to haemophilia.ie
Representing people living with haemophilia, von willebrand’s and other inherited bleeding disorders
The Irish Haemophilia Society represents the interests of people with haemophilia, von Willebrand’s disease and other inherited bleeding disorders. We provide information, education, publications, outreach and support, advocacy, hospital and home visits and conferences and events for people with bleeding disorders and their families. We aim to assist people with bleeding disorders to be positive and proactive with their health and to maximise their quality of life.
For a full list of treatment centres in Ireland, please click here.
Newsfeed
I.H.S. Autumn Magazine Out Now!
Our Autumn Magazine is out now and comes packed with lots of interesting articles from members and staff, news and updates, reports and more. We, like you are looking forward to the return of life to some semblance of normality Read more >
Routine follow up in the National Coagulation Centre for people with Mild Bleeding Disorders
People with mild bleeding disorders (including Low Von Willebrand factor, mild factor deficiencies, Bleeding Disorders of Unknown Aetiology and platelet disorders) are registered at the National Coagulation Centre (NCC). In general, people with these mild bleeding disorders will have regular Read more >
EHC Educational App EHCucate goes live
The new educational app from the EHC, EHCucate, has gone live and you can download it to your device from the iOS App Store and Android Google Play. With the sheer volume of information on rare bleeding disorders and novel Read more >
Fiction Through Image – Art workshops for teenagers
Do you know a teenager living with a long term health condition who would benefit from exploring their creativity, having fun and building friendships in a safe and stimulating environment? CREATE YOUR OWN STORIES THROUGH IMAGE-MAKING – Join Helium Arts Read more >
2021 Educational Grants: Deadline Extended
The deadline for applications for this year’s I.H.S. educational grants has been extended by one week to Friday, October 1. The Society offers educational grants each year to people with haemophilia or related bleeding disorders, and/or their immediate family members Read more >
