Le parcours de Rob Garbutt avec la fibrose pulmonaire

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The Canadian Pulmonary Fibrosis Foundation

The Canadian Pulmonary Fibrosis Foundation

Күн бұрын

Rob Garbutt de Winnipeg, au Manitoba, au Canada vit avec la fibrose pulmonaire idiopathique ou FPI (l'un des types les plus courants de fibrose pulmonaire, dont la cause est inconnue). Avant son diagnostic de fibrose pulmonaire (FP), Rob était très actif physiquement et appréciait le ski, le ski nautique et le vélo de montagne. Après une grippe il y a 11 ans, Rob s'est rendu compte que quelque chose n'allait pas alors qu'il n'arrivait pas à se remettre comme d'habitude.
Rob a d'abord reçu un diagnostic de maladie pulmonaire obstructive chronique (MPOC), puis plus tard de FPI. Pendant environ huit ans, il a pu continuer ses activités jusqu'à qu'en 2019, il fût « très durement frappé » par une exacerbation et hospitalisé pendant une semaine. Sa FP s'est depuis aggravée avec le temps.
Rob essaie toujours de rester aussi actif que possible - avec un tricycle couché tiré par sa chienne Maggie, sa « meilleure amie », ou en se connectant à sa bonbonne d'oxygène portable sur son quai au chalet. « Je ne suis pas du genre à être arrêté », dit-il.
Rob est soutenu par sa femme et sa chienne Maggie. Il est frustré par les changements dans ses capacités, mais appartenir à un groupe de soutien l'aide. En attendant, il attend l'appel pour une transplantation pulmonaire.
Nous célébrons Rob pour son courage et le remercions d'avoir partagé son parcours de fibrose pulmonaire. Si vous ou quelqu'un que vous aimez rencontrez des difficultés respiratoires, parlez-en à votre médecin. Pour en savoir plus sur la fibrose pulmonaire ou pour aider à amasser des fonds pour trouver un remède, visitez cpff.ca/.
** Nouvelles de février 2023 ** C'est avec grande tristesse que nous annonçons le décès de Rob Garbutt le 4 février 2023. Rob était une inspiration pour nous tous, et nous offrons nos plus sincères condoléances à sa famille et aux membres de notre communauté. Nous continuons de partager son histoire pour conscientiser la population au sujet de cette maladie dévastatrice.
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Rob Garbutt of Winnipeg, Manitoba, Canada lived with idiopathic pulmonary fibrosis (IPF) for a remarkable 12 years, before receiving a lung transplant on July 21, 2022. This is his story pre-transplantation.
Before his pulmonary fibrosis (PF) diagnosis, Rob was very physically active and enjoyed skiing, waterskiing, and mountain biking. After a bout of flu 11 years ago, Rob realized something was not right when he couldn't seem to recover as usual.
Rob was first diagnosed with chronic obstructive pulmonary disease (COPD) and then later with IPF. For about eight years he was able to continue with his activities until in 2019, he was “hit really hard” with an exacerbation and hospitalized for a week. His PF has since worsened over time.
Even with this condition, Rob still tried to remain as active as possible - with an incumbent bike pulled by his dog Maggie, his “best friend,” or by hooking up to his portable oxygen tank on his dock at the cottage. “I’m not one to be stopped,” he says.
Rob is supported by his wife and dog Maggie. He sometimes got frustrated by the changes in his abilities, but belonging to a support group did help.
*Post Lung Transplantation Update*
Rob worked hard to stay as fit as possible, with medication, exercise, and oxygen therapy, while he waited for the call for a lung transplant. That day came in July, 2022. Supported by his wife Beth (and dog Maggie), Rob was hopeful about his future post-transplant.
Rob’s case is exceptional. Not all of the 30,000 Canadians living with PF are eligible for a lung transplant, even if there were enough organs available. A lung transplant is the only long-term treatment for this chronic, incurable disease, but comes with its own set of health challenges.
We celebrate Rob for his courage and thank him for sharing his pulmonary fibrosis journey. If you or someone you love is experiencing breathing difficulties talk to your doctor.
To learn more about pulmonary fibrosis or to help raise funds to find a cure, visit cpff.ca/.
** Update February 2023 ** It is with great sadness that we announce the passing of Rob Garbutt on February 4, 2023. Rob was an inspiration to us all and we offer our deepest condolences to their families and our community. We continue to share his story to build awareness around this devastating condition.

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