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amyotrophic lateral sclerosis (als)

how i care for als: a lonely journey through anticipatory grief

anticipatory grief is the experience of the emotions associated with grief before an expected loss happens. for jennifer hutton, it's an unshakeable reality.
andrew robichaud
sep 25, 2023

als: new therapies offer hope in treating a mysterious deadly disease

als expert dr. agessandro abrahao and his team conducted a world-first study using mri-guided ultrasound to open the blood-brain barrier so drugs can directly target the brain regions affected by amyotrophic lateral sclerosis.
robin roberts
apr 04, 2023

family of börje salming expressed frustration with swedish health-care system before hockey legend's passing

sweden-based salming had travelled to canada for treatment, but his medication was not approved for use in his home country.
karen hawthorne and emma jones
nov 25, 2022

als has stolen roberta flack's ability to sing

the multi-award winning singer of "killing me softly with his song" was diagnosed with lou gehrig's disease in august.
maija kappler
nov 16, 2022

als claims b.c. trailblazer, but his crusade for a cure lives on

greg gowe worked hard to get research going in b.c., now it's up to others to continue that fight
lori culbert
nov 07, 2022

'i am tired of screaming for help': a local family's struggle to care for a loved one with als at home

adam rodney's care is considered complex, meaning he can’t go to a long-term care home for a period of respite, only to a facility capable of providing the level of care he needs. but his family have been unable to find any facility that can take him
elizabeth payne
sep 26, 2022

diagnosed at age 44 with als, this mom and advocate left this world swinging

the magic and determination of taya jones had us all believing that she would be the one to beat the impossible odds of als.
lisa machado
sep 06, 2022

'als will be a treatable chronic disease': new treatment slows disease progression and increases life expectancy

mcgill university's dr. angela genge is optimistic about what the future holds for amyotrophic lateral sclerosis care: "every step gives our patients more time, better function for longer, better care every year."
maja begovic
jul 08, 2022
powered by
canadian centre for caregiving excellence
powered by
pancreatic cancer canada
powered by
canadian coalition for seniors’ mental health (ccsmh)

how i care for als: a lonely journey through anticipatory grief

anticipatory grief is the experience of the emotions associated with grief before an expected loss happens. for jennifer hutton, it's an unshakeable reality.
andrew robichaud
sep 25, 2023

als: new therapies offer hope in treating a mysterious deadly disease

als expert dr. agessandro abrahao and his team conducted a world-first study using mri-guided ultrasound to open the blood-brain barrier so drugs can directly target the brain regions affected by amyotrophic lateral sclerosis.
robin roberts
apr 04, 2023

family of börje salming expressed frustration with swedish health-care system before hockey legend's passing

sweden-based salming had travelled to canada for treatment, but his medication was not approved for use in his home country.
karen hawthorne and emma jones
nov 25, 2022

als has stolen roberta flack's ability to sing

the multi-award winning singer of "killing me softly with his song" was diagnosed with lou gehrig's disease in august.
maija kappler
nov 16, 2022
powered by
canadian centre for caregiving excellence

als claims b.c. trailblazer, but his crusade for a cure lives on

greg gowe worked hard to get research going in b.c., now it's up to others to continue that fight
lori culbert
nov 07, 2022

'i am tired of screaming for help': a local family's struggle to care for a loved one with als at home

adam rodney's care is considered complex, meaning he can’t go to a long-term care home for a period of respite, only to a facility capable of providing the level of care he needs. but his family have been unable to find any facility that can take him
elizabeth payne
sep 26, 2022

diagnosed at age 44 with als, this mom and advocate left this world swinging

the magic and determination of taya jones had us all believing that she would be the one to beat the impossible odds of als.
lisa machado
sep 06, 2022

'als will be a treatable chronic disease': new treatment slows disease progression and increases life expectancy

mcgill university's dr. angela genge is optimistic about what the future holds for amyotrophic lateral sclerosis care: "every step gives our patients more time, better function for longer, better care every year."
maja begovic
jul 08, 2022
powered by
pancreatic cancer canada
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