Shared decision making in an evolving treatment landscape for haemophilia and bleeding disorders ft. Dr Len Valentino, CEO National Hemophilia Foundation
Haemcast20 Helmi 2023

Shared decision making in an evolving treatment landscape for haemophilia and bleeding disorders ft. Dr Len Valentino, CEO National Hemophilia Foundation

"Shared decision making" has quickly become the new phrase bandied about at event and conferences within the haemophilia community. But what does shared decision making in haemophilia and bleeding disorders really look like? In this episode, our host Dr Kate Khair deep dives in to this topic with Dr Len Valentino, CEO at the National Hemophilia Foundation (USA), exploring what shared decision making really means in this community and why, in this evolving treatment landscape, this is drawing so much focus and attention. There is a need to shift away from the paternalistic healthcare professional and patient relationship, and to engage patients in a dialogue about their treatment, care and goals. This is at the heart of shared decision making.

If you enjoyed this episode, please do share it with your peers and colleagues, and consider leaving a rating or review wherever you listen to your podcasts.

You can also connect with us on Twitter! We'd like to hear your thoughts around the topic of shared decision making.

Check out NHF's Blue Sky Vision: Community Conversation here.

Tämä jakso on lisätty Podme-palveluun avoimen RSS-syötteen kautta eikä se ole Podmen omaa tuotantoa. Siksi jakso saattaa sisältää mainontaa.

Jaksot(42)

Ports, pressure and panic — Coping with haemophilia treatment challenges

Ports, pressure and panic — Coping with haemophilia treatment challenges

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.Getti...

25 Kesä 31min

"I'm the worrier in our relationship" — Being the partner of a person with a bleeding disorder

"I'm the worrier in our relationship" — Being the partner of a person with a bleeding disorder

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...

27 Touko 29min

"Everything's new with haemophilia" — Treatment choices and changes

"Everything's new with haemophilia" — Treatment choices and changes

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 blee...

30 Huhti 29min

Sticky blood, teddies and teens — Talking to children about their bleeding disorder

Sticky blood, teddies and teens — Talking to children about their bleeding disorder

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...

31 Maalis 34min

Veins, verse and voices: How poetry helped Local families with bleeding disorders be heard

Veins, verse and voices: How poetry helped Local families with bleeding disorders be heard

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...

5 Maalis 34min

Banana sap, mangos and factor IX — a Ugandan haemophilia B journey

Banana sap, mangos and factor IX — a Ugandan haemophilia B journey

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 describi...

9 Loka 202525min

Quality of life in the balance: Helen Tate on living with Factor V deficiency

Quality of life in the balance: Helen Tate on living with Factor V deficiency

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....

21 Elo 202522min

Looking back on Terence's life: Haemophilia then and now, with Kate Khair

Looking back on Terence's life: Haemophilia then and now, with Kate Khair

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 du...

30 Heinä 202518min

Suosittua kategoriassa Terveys ja hyvinvointi

unicast
tiedenaiset-podcast
rss-pitaisko-erota
psykopodiaa-podcast
vakeva-elama-viisaampi-mieli-vahvempi-keho
meditaatiot-suomeksi
voi-hyvin-meditaatiot-2
rss-seksicast
rss-uplevel-by-sonja-hannus
rss-kuumilla-aalloilla
terapiassa
selviytyjat-tarinoita-elamasta
rss-sanelunpurku-podcast
traumapodi
rss-pt-paahtio
rss-rentoudu-podcast-rentoutumiseen-hanna-viljanmaa
fitnesskulmapodcast
paritellen
rss-eropodi
rss-nautinto