Representing people living with haemophilia, von Willebrand’s and all other inherited bleeding disorders
The I.H.S. pride ourselves on the close relationships we build with our members. We do so by maintaining close contact, keeping them up-to-date on the latest treatment developments through educational events and conferences and publishing educational publications to help members manage their bleeding disorders.
New research reveals that more than half of people have experienced an unusual bleeding symptom, as campaign launches to improve diagnosis Finding Von Willebrand shares
Around 4,900 people are affected by VWD in Ireland, yet only a third have received a diagnosis.
Find out the recipients of this year’s educational grants.
We aim to ensure that people haemophilia & related bleeding disorders & their families get the best possible treatment, care & support.
UPDATE: Our Parents Conference is now taking place the 14th-16th of July. Make sure to put it in you...
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RT @HaemophiliaIRL: Our AGM and Conference will take place on the 3rd-5th of March. This will take p...
Read More » Our #vWD Information Day took place last Saturday. Members and non-members came together to discuss ...
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