ashley hickey lives with cvid, a rare disease, and knows all too well how important to rare disease strategy in the country is for herself and people like her.

shaping the future of rare disease care in canada: new report outlines key considerations for fund allocation
a new report created by takeda pharmaceutical company highlights six key areas of unmet needs, offering an outline of how policymakers can go about making rare disease drug access and care better in canada.
angelica bottaro, aug 22 2024
leaders in health: dr. sean wharton and compassion in obesity medicine
ashley hickey lives with cvid, a rare disease, and knows all too well how important to rare disease strategy in the country is for herself and people like her.
karen hawthorne
spinal muscular atrophy screening expanded to all infants in canada: 'early diagnosis and effective treatment are critical'
ashley hickey lives with cvid, a rare disease, and knows all too well how important to rare disease strategy in the country is for herself and people like her.
angelica bottaro
diagnosed with leukemia: managing support, resources and your care team
ashley hickey lives with cvid, a rare disease, and knows all too well how important to rare disease strategy in the country is for herself and people like her.
karen hawthorne
diagnosed with melanoma: managing treatments, surveillance, and support 
ashley hickey lives with cvid, a rare disease, and knows all too well how important to rare disease strategy in the country is for herself and people like her.
angelica bottaro
coulter: what is it like for a parent whose child is struggling?
ashley hickey lives with cvid, a rare disease, and knows all too well how important to rare disease strategy in the country is for herself and people like her.
chris coulter