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The final part of our mini-series featuring Terence O'Rourke, in which he reflects on living with severe haemophilia A.
In this episode, Terence discusses his approach to making decisions about treatment, and the importance of teamwork in both his working life and in relation to his haemophilia care.
CREDITS:
Speaker: Terence O’Rourke
Interviewer: Dr Meila Roy
Producer: Chris Caton
Music: Once Again Royalty Free Music by Benjamin Tissot via bensound.com
In part 5 of Terence O'Rourke's story, he again reflects on his working life and how this was impacted by both his haemophilia and its treatment.
He discusses his approach to and choices about treatment and managing his haemophilia, and about eventually overcoming hepatitis C.
Terence continues to be driven by determination and confidence in his own problem-solving ability throughout.
CREDITS:
Speaker: Terence O’Rourke
Interviewer: Dr Meila Roy
Producer: Chris Caton
Music: Once Again Royalty Free Music by Benjamin Tissot via bensound.com
In part 4 of our mini-series in conversation with Terence O'Rourke, he reflects on changes in treatment for haemophilia and the arrival of Factor VIII.
Terence describes some of the prejudice he experienced as a person with haemophilia, and the faith his wife had in him. He also discusses the progression of his career, and how it shifted and changed around his haemophilia.
CREDITS:
Speaker: Terence O’Rourke
Interviewer: Dr Meila Roy
Producer: Chris Caton
Music: Once Again Royalty Free Music by Benjamin Tissot via bensound.com
In the third part of our conversation, Terence O’Rourke looks back on his young adulthood in the late 1950s and early 1960s, starting work in an architect’s office and becoming a student.
This was an important time for Terence. He was studying with his peers for the first time and embarking on the early stages of what would become a very successful career.
Terence also reflects on how his haemophilia was treated during this time – and how he questioned the accepted methods of treating bleeds at a time when most people accepted that doctors knew best.
CREDITS:
Speaker: Terence O’Rourke
Interviewer: Dr Meila Roy
Producer: Chris Caton
Music: Once Again Royalty Free Music by Benjamin Tissot via bensound.com
We rejoin Terence O'Rourke to as he reflects on growing up with haemophilia, not being able to go to school, his education, and the impact of this on his life.
Now in his 80s, Terence also looks back on his career aspirations and goals. What comes through is his determination to pursue these despite the obstacles he faced as a young person with haemophilia and limited access to treatment.
Credits:
Speaker: Terence O'Rourke
Interviewer: Dr Meila Roy
Producer: Chris Caton
Music: Once Again Royalty Free Music by Benjamin Tissot via bensound.com
In the first part of a six-part mini-series, Terence O’Rourke looks back on his childhood memories of living with severe haemophilia, including his education and experience of treatment.
Terence, who is now in his 80s, has an exceptional mind and has enjoyed a successful career. Over the course of this series he reflects on how his relationship with haemophilia has both impacted and shaped his approach to life, from childhood through adulthood.
Credits:
Speaker: Terence O’Rourke
Interviewer: Dr Meila Roy
Producer: Chris Caton
Music: Once Again Royalty Free Music by Benjamin Tissot via bensound.com
In this episode of Haemcast, we speak to our very own Dr Kate Khair following her Lifetime Achievement award at EAHAD 2024.
Tune in to hear about Kate's journet into nursing, the first patient she met with a bleeding disorder and how they influenced her career, and the many years dedicated to researching the lived experience of those with haemophilia and bleeding disorders. You don't want to miss out on hearing from one of the undisputed legends of the bleeding disorders community.
Be sure to follow us on Twitter & LinkedIn, and you can support Haemcast by sharing this episode on your social media platforms.
In this episode, host Luke Pembroke (Director of Community Engagement, Haemnet) sat down with Len Valentino (P2C Chief Executive Officer; and NBDF President & CEO) and Teri Willey (P2C Managing Director) to hear more about the Pathway to Cures; a venture philanthropy fund created specifically to accelerate the development of cures across all inheritable blood and bleeding disorders.
In this episode we commemorate World AIDS Day 2023. Host, Dr Kate Khair is joined by contaminated blood scandal campaigner and The Haemophilia Society UK's LGBT Ambassador to discuss the impact HIV and AIDS has had on the bleeding disorders community. Mark generously shares his personal experience growing up with haemophilia from receiving no treatment, to then receiving contaminated blood products.
After taking to the skies to pursue his dream of working in the air travel sector, Mark hung up his cabin crew uniform to become one of the leading community advocates, campaigning for justice of those affected by contaminated blood and serving as the worlds first recognised LGBT Ambassador in the hemophilia and bleeding disorders world.
More about Mark Ward - https://haemophilia.org.uk/who-we-are/people/mark-ward/
More about World AIDS Day - https://worldaidsday.org/
In this episode, Director of Community Engagement, Luke Pembroke, and Director of Research, Kate Khair spoke with community advocates Sunny Maini and Hannah Yarnalll.
Sunny and Hannah share their experiences of living with von Willebrand Disorder (VWD), their journey in to the world of advocacy and tell us about their latest venture establishing the VWD working group through The Haemophilia Society UK.
For more information about the VWD working group and their upcoming event in Sheffield on 26th August, you can contact Sunny via email: [email protected]
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