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what it feels like

living with acromegaly: the story of a former canadian athlete

this ottawa resident shares his acromegaly journey
sophie ash, postmedia content works
mar 12, 2021

ehlers-danlos syndrome: what it feels like

'i would get sick and it would throw me for a loop, but then i'd get better and just keep going, until my body said no more.'
emma jones
mar 05, 2021

crohn’s patient endures long journey to health

sandra zelinsky can barely remember a time when she was not living with crohn’s disease.
lisa machado
feb 27, 2021

joubert syndrome: what it feels like

it wasn't until scott was in his 20s that a doctor asked if he had heard of the rare genetic syndrome.
emma jones
feb 18, 2021

huntington disease runs in my family

'genetic discrimination is a real thing that exists in canada.'
emma jones
feb 05, 2021

what it feels like: 'always felt like i was swimming against the current' with bipolar disorder

"i could see my behaviour starting to affect my family and the other people around me. there were days when i would have a burst of energy that you couldn't keep up with. then the next day, i couldn't get motivated."
emma jones
jan 11, 2021

what it feels like: darin diehl embraced life, despite living with lung cancer

"the only control you have, really, is to try and understand it better."
emma jones
dec 29, 2020

ulcerative colitis: what it feels like

adam polak describes 'the most horrific moment of his life'
emma jones
dec 18, 2020
powered by
the leukemia & lymphoma society of canada (llsc)
powered by
movember canada
powered by
obesity canada

living with acromegaly: the story of a former canadian athlete

this ottawa resident shares his acromegaly journey
sophie ash, postmedia content works
mar 12, 2021

ehlers-danlos syndrome: what it feels like

'i would get sick and it would throw me for a loop, but then i'd get better and just keep going, until my body said no more.'
emma jones
mar 05, 2021

crohn’s patient endures long journey to health

sandra zelinsky can barely remember a time when she was not living with crohn’s disease.
lisa machado
feb 27, 2021

joubert syndrome: what it feels like

it wasn't until scott was in his 20s that a doctor asked if he had heard of the rare genetic syndrome.
emma jones
feb 18, 2021
powered by
the leukemia & lymphoma society of canada (llsc)

huntington disease runs in my family

'genetic discrimination is a real thing that exists in canada.'
emma jones
feb 05, 2021

what it feels like: 'always felt like i was swimming against the current' with bipolar disorder

"i could see my behaviour starting to affect my family and the other people around me. there were days when i would have a burst of energy that you couldn't keep up with. then the next day, i couldn't get motivated."
emma jones
jan 11, 2021

what it feels like: darin diehl embraced life, despite living with lung cancer

"the only control you have, really, is to try and understand it better."
emma jones
dec 29, 2020

ulcerative colitis: what it feels like

adam polak describes 'the most horrific moment of his life'
emma jones
dec 18, 2020
powered by
movember canada
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