advertisement

what it feels like

treatment-resistant depression: what it feels like

"when you have depression you feel like you're the only person out there," says bruce ross, who lives with depression that hasn't responded to medication or therapies.
emma jones
mar 31, 2022

what it feels like: 'i can conquer anything' living with epilepsy

although epilepsy is highly treatable with medication, 30 per cent of people with the disease, like 37-year-old erin mcdonald, rely on brain surgery to keep it in check.
karen hawthorne
mar 25, 2022

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 01, 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 09, 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 02, 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
powered by
diabetes canada
powered by
obesity matters
powered by
canadian centre for caregiving excellence

treatment-resistant depression: what it feels like

"when you have depression you feel like you're the only person out there," says bruce ross, who lives with depression that hasn't responded to medication or therapies.
emma jones
mar 31, 2022

what it feels like: 'i can conquer anything' living with epilepsy

although epilepsy is highly treatable with medication, 30 per cent of people with the disease, like 37-year-old erin mcdonald, rely on brain surgery to keep it in check.
karen hawthorne
mar 25, 2022

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 01, 2022
powered by
diabetes canada

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 09, 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 02, 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
powered by
obesity matters
advertisement

advertisement