Photos From our 2024 AGM & Conference
See some of the photos from our 2024 AGM & Conference.
Representing people living with haemophilia, von Willebrand’s and other inherited bleeding disorders
Representing people living with haemophilia, von Willebrand’s and other inherited bleeding disorders
Latest news & updates from the I.H.S.
See some of the photos from our 2024 AGM & Conference.
The Long Acting Factor 9 (LAF9) study is being carried out in the National Coagulation Centre to assess the impact of switching from Benefix to Alprolix treatment for adults with
The Irish Haemophilia Society would like to get your feedback and opinions or support and services during the pandemic. We\’ve compiled a short survey looking at Outreach, Publications, Social Media
Continuing with our series of Webinars and Q&A Sessions, we have further meetings coming up on; Wednesday, November 11 @ 6PM: \’Covid-19 & Haemophilia\’ with Dr. Cedric Hermans This webinar
We’ve been uploading recordings from our ongoing series of webinars so you catch up on the ones you’ve missed at your convenience. The latest of which is An Update on
Thanks to everyone who applied for an educational grant from the I.H.S. This year we received a lot of applications once again this year, which is brilliant! The I.H.S. educational
We have received an update from the National Coagulation Centre, you can read below in full: We would like to thank everyone in the patient community for their continued support
Comprehensive Care services at St. James’s Hospital The Covid-19 pandemic has had a significant impact on the infrastructure for treatment of haemophilia and other inherited bleeding disorders in St. James
We’ve been uploading recordings from our ongoing series of webinars so you catch up on the ones you’ve missed at your convenience. The latest of which is the Exercise &
The I.H.S. is delighted to announce a new, updated information booklet on von Willebrand Disorder (vWD) and we would like thank Dr Michelle Lavin & Declan Noone for their contribution