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The Journal of Haemophilia Practice
Volume 7 (2020): Numero 1 (January 2020)
Accesso libero
“He's a normal kid now”: an ethnographic study of challenges and possibilities in a new era of haemophilia care
Thomas Hughes
Thomas Hughes
,
Mikkel Brok-Kristensen
Mikkel Brok-Kristensen
,
Yosha Gargeya
Yosha Gargeya
,
Anne Mette Worsøe Lottrup
Anne Mette Worsøe Lottrup
,
Ask Bo Larsen
Ask Bo Larsen
,
Ana Torres-Ortuño
Ana Torres-Ortuño
,
Nicki Mackett
Nicki Mackett
e
John Stevens
John Stevens
| 17 dic 2020
The Journal of Haemophilia Practice
Volume 7 (2020): Numero 1 (January 2020)
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CONDIVIDI
Article Category:
Community Focus
Pubblicato online:
17 dic 2020
Pagine:
150 - 157
DOI:
https://doi.org/10.17225/jhp00167
Parole chiave
haemophilia
,
community
,
embodied knowledge
,
embodied sense of the disease
,
normality
,
chronic illness
,
new era of care
© 2020 Thomas Hughes et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
While advances in treatment mean that young people with haemophilia can now expect to lead a much more ‘normal’ life than previous generations, it is essential that the discourse around ‘normality’ in haemophilia does not obscure the remaining and new challenges they experience in their everyday lives.
Engaging in physical activity is one way in which PwH are living more ‘normal’ lives, and is important for joint health and wellness. Paradoxically, advances in in haemophilia care mean that younger PwH may be less aware of their condition, lacking embodied awareness and intuitive understanding of their limitations.