“Ask what can you do instead of thinking about what you can’t” Profile: Clive Smith
21 dic 2018
INFORMAZIONI SU QUESTO ARTICOLO
Categoria dell'articolo: Community Focus
Pubblicato online: 21 dic 2018
Pagine: 152 - 155
DOI: https://doi.org/10.17225/jhp00114
Parole chiave
© 2018 Steve Chaplin, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Few would disagree that haemophilia presents challenges for everyone who lives with it. Perhaps the greatest of these is being denied the opportunities available to other people through fear of bleeding and joint damage. The regular infusions and clinic appointments that characterise treatment are certainly burdensome, and sometimes traumatic for children and parents alike; but being told ‘People with haemophilia can’t do this…’ is damning in its finality. It is enough to make you demand, ‘Why not?’ - which is exactly what Clive Smith and a growing number of people in the haemophilia community are asking.