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arthritis
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cancer
colitis
crohn's disease
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dementia
depression
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down syndrome
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flu
heart health
hepatitis
hiv/aids
hpv
kidney disease
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what it feels like
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a papilloma led this woman to choose a mastectomy
after finding three benign lumps, deirdre naughton had her breast removed. she is wondering if anyone else shares her experience.
emma jones
what it feels like
jul 05, 2021
adenosine deaminase and the search for a stem cell donor
'until he gets the stem cell transplant, you are pretty much just buying time with your kid.'
emma jones
what it feels like
jun 23, 2021
sideroblastic anemia: 28 days post-transplant and waiting
"they told us the plan and the official transplant date. that was surreal. i couldn't believe what i was hearing."
emma jones
what it feels like
jun 14, 2021
juvenile myelomonocytic leukemia highlights need for more diversity in stem cell donors
xavier pesito was just three years old when his frequent fevers and eye infections were diagnosed as a rare form of blood cancer.
emma jones
what it feels like
jun 08, 2021
infertility: the struggle to conceive
'my husband and i didn't really tell anyone, family or friends, when we first went to the fertility clinic.'
emma jones
what it feels like
may 25, 2021
lupus: what it feels like
at 23, marisa zeppieri was hit by a drunk driver and admitted to hospital. it was then that she received another diagnosis: lupus.
emma jones
what it feels like
may 07, 2021
young-onset parkinsonism: what it feels like
many young people that will hide their parkinson's symptoms because they're ashamed to talk about it.
emma jones
what it feels like
apr 28, 2021
anorexia: what it feels like
thirty-nine year old anne lost her children because of an eating disorder. here's what she wants you to know.
vanessa hrvatin
mental health
apr 14, 2021
a papilloma led this woman to choose a mastectomy
after finding three benign lumps, deirdre naughton had her breast removed. she is wondering if anyone else shares her experience.
emma jones
what it feels like
jul 05, 2021
adenosine deaminase and the search for a stem cell donor
'until he gets the stem cell transplant, you are pretty much just buying time with your kid.'
emma jones
what it feels like
jun 23, 2021
sideroblastic anemia: 28 days post-transplant and waiting
"they told us the plan and the official transplant date. that was surreal. i couldn't believe what i was hearing."
emma jones
what it feels like
jun 14, 2021
juvenile myelomonocytic leukemia highlights need for more diversity in stem cell donors
xavier pesito was just three years old when his frequent fevers and eye infections were diagnosed as a rare form of blood cancer.
emma jones
what it feels like
jun 08, 2021
verified voice
sponsored by:
wellspring cancer support
going back to work after cancer: how support programs can guide the way
harnessing the power of cancer support programs to cope with the emotional scars
listening is often enough when having difficult conversations about cancer: 'people want to feel heard and validated'
teddy bears and team bonding: how wellspring supported rachel swiednicki and her son through cancer
jim turner: wellspring is the reason i am still alive today
three simple techniques to combat cancer brain fog
franco viudez: wellspring improved my mental and physical state
david johnston: wellspring’s exercise program transforms prostate cancer patient’s blood results
infertility: the struggle to conceive
'my husband and i didn't really tell anyone, family or friends, when we first went to the fertility clinic.'
emma jones
what it feels like
may 25, 2021
lupus: what it feels like
at 23, marisa zeppieri was hit by a drunk driver and admitted to hospital. it was then that she received another diagnosis: lupus.
emma jones
what it feels like
may 07, 2021
young-onset parkinsonism: what it feels like
many young people that will hide their parkinson's symptoms because they're ashamed to talk about it.
emma jones
what it feels like
apr 28, 2021
anorexia: what it feels like
thirty-nine year old anne lost her children because of an eating disorder. here's what she wants you to know.
vanessa hrvatin
mental health
apr 14, 2021
verified voice
sponsored by:
als society of canada (als canada)
the harsh reality of als: facing the unknown takes determination and community support
how i care for als: a lonely journey through anticipatory grief
diagnosed with als: managing stages, treatments and support
caregiving for a person with a rare disease is about accepting 'without any expectations'
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