O TYM PODKAŚCIE 🔗
Welcome to the Haemcast, where we talk about all things haemophilia and bleeding disorders. Join us as we speak with leading experts in the field to tackle and address the latest news, hot topics and research.
Prowadzący:
Częstotliwość aktualizacji:
monthly
Średnia długość dźwięku:
31 minutes
Wywiady gościnne
Język angielski
Stany Zjednoczone
45 odcinków
od 19 stycznia 2021
episodic
NAJNOWSZY ODCINEK 🔗
Haemcast’s special series in collaboration with Local families with bleeding disorders continues with a reflection on what makes the parents of children with haemophilia feel supported.
Mums Melissa and Alex both acknowledge the importance of the ongoing support they have from their sons’ haemoph…
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POPRZEDNIE ODCINKI 🔗
In this episode of Haemcast’s special series in collaboration with Local families with bleeding disorders, we look at some of the challenges that can arise when treating a child with haemophilia.
Getting used to administering treatment can be challenging, particularly in the early days. Until recen…
In this episode of Haemcast’s special series in collaboration with Local families with bleeding disorders, we look at some of the challenges that can arise when treating a child with haemophilia.
Getting used to administering treatment can be challenging, particularly in the early days. Until recen…
The next in our special collaboration between Haemcast and Local families with bleeding disorders focuses on the partners of people who live with haemophilia and von Willebrand disease.
Anya, Emma and Tom agree that while bleeding disorders are significant in their lives, they don’t define their …
When making choices about treatment for a bleeding disorder, for a child or for yourself, what matters most?
In this episode of Haemcast’s special series in collaboration with Local families with bleeding disorders, we speak with parents about the considerations that come into play when making dec…
When it comes to managing family life with a child who has a bleeding disorder, parents aren’t just caregivers – they’re organisers, advocates and educators. Alongside managing their child’s condition, they have to help them understand it too.
In this episode of Haemcast’s special series in collabo…
The first in a special Haemcast series in collaboration with Local families with bleeding disorders, exploring aspects of family life.
In this episode, members of Local families with bleeding disorders discuss the online workshops that helped them explore their experiences and express their hopes,…
Morris Okello lives in Northern Uganda. In this episode of Haemcast, he tells Dr Kate about the childhood experiences that eventually led to him being diagnosed with haemophilia B.
As well as describing his own journey towards becoming an advocate for people with haemophilia in Uganda, Morris hig…
Dance teacher and Haemophilia Society trustee Helen Tate talks with Haemnet's Dr Kate Khair about living with Factor V deficiency, a rare bleeding disorder that affects around one in a million people.
Helen leads an active life despite her condition and is a passionate advocate for the rare bleedi…
Following our six-part mini-series 'Reflections on a life with severe haemophilia', with Terence O'Rourke, Haemnet's Dr Kate Khair considers some of the things that have changed in haemophilia care during Terence's lifetime – and some of the things that perhaps haven't.
Kate discusses the importa…
Zastrzeżenie: Podcast i grafika osadzone na tej stronie pochodzą z Haemnet, który jest własnością jego właściciela i nie jest powiązany ani wspierany przez Listen Notes, Inc.
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