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what it feels like

thrombotic thrombocytopenic purpura: what it feels like

bruce morton has been treated five times for the rare, and potentially fatal, disease.
emma jones
mar 21 2022

graves' disease: what it feels like

"i was given a liquid that was basically a cup of water. it tasted like nothing. [the healthcare workers who were wearing] hazmat suits told me to exit the hospital as quickly as possible," says jenika hamilton.
emma jones
mar 1 2022

sporadic inclusion body myositis: what it feels like

“we don't have any treatment and we sure don't have any cure for it,” doctors told tom wood after he was diagnosed with sporadic inclusion body myositis.
emma jones
feb 9 2022

how a stem cell transplant cured multiple sclerosis

a chance meeting with a man in a wheelchair led brooke robinson to a clinical trial that was using stem cells to treat multiple sclerosis: 'he saved my life.'
emma jones
feb 2 2022

gist: what it feels like

maureen went from feeling completely healthy to hearing a doctor tell her that she had gastrointestinal stromal tumours, a rare cancer that affects 1 in 100,000 people.
emma jones
jan 25 2022

amyloidosis: what it feels like

when anne marie carr was diagnosed in 2015, she was told most patients only survive three years. six years later, she's the founder and executive director of hereditary amyloidosis canada.
emma jones
jan 18 2022

what it feels like: 'i went from healthy to not' with rheumatoid arthritis

rheumatoid arthritis doesn't just happen to elderly people: sharmila sriram was diagnosed with the condition at just 29.
emma jones
jan 4 2022

a six-month-old, an artist, and a teacher: just 3 of the remarkable people who shared their stories of resilience and courage in 2021

the one common thread that runs through every story is the ability to keep moving forward — no matter what.
emma jones
dec 27 2021
powered by
obesity canada
powered by
canadian digestive health foundation
powered by
movember canada

thrombotic thrombocytopenic purpura: what it feels like

bruce morton has been treated five times for the rare, and potentially fatal, disease.
emma jones
mar 21 2022

graves' disease: what it feels like

"i was given a liquid that was basically a cup of water. it tasted like nothing. [the healthcare workers who were wearing] hazmat suits told me to exit the hospital as quickly as possible," says jenika hamilton.
emma jones
mar 1 2022

sporadic inclusion body myositis: what it feels like

“we don't have any treatment and we sure don't have any cure for it,” doctors told tom wood after he was diagnosed with sporadic inclusion body myositis.
emma jones
feb 9 2022

how a stem cell transplant cured multiple sclerosis

a chance meeting with a man in a wheelchair led brooke robinson to a clinical trial that was using stem cells to treat multiple sclerosis: 'he saved my life.'
emma jones
feb 2 2022
powered by
obesity canada

gist: what it feels like

maureen went from feeling completely healthy to hearing a doctor tell her that she had gastrointestinal stromal tumours, a rare cancer that affects 1 in 100,000 people.
emma jones
jan 25 2022

amyloidosis: what it feels like

when anne marie carr was diagnosed in 2015, she was told most patients only survive three years. six years later, she's the founder and executive director of hereditary amyloidosis canada.
emma jones
jan 18 2022

what it feels like: 'i went from healthy to not' with rheumatoid arthritis

rheumatoid arthritis doesn't just happen to elderly people: sharmila sriram was diagnosed with the condition at just 29.
emma jones
jan 4 2022

a six-month-old, an artist, and a teacher: just 3 of the remarkable people who shared their stories of resilience and courage in 2021

the one common thread that runs through every story is the ability to keep moving forward — no matter what.
emma jones
dec 27 2021
powered by
canadian digestive health foundation

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