Karen Elaine Magee Pape

Karen passed away peacefully at home on Saturday June 2, 2018. Daughter of the late Brian and Elaine Magee. Mother of Sarah, Aaron (Lisa Richardson), and loving Nana to Daniela and Jack. Much-loved sister of Brian (Susan) Magee, Ivan Magee and the late Judy (Normand) Baril. Beloved former spouse of Paul Pape. Proud aunt of Brendan, Diana & Charles. Karen was a pillar of strength for her family with an enormous heart.

A graduate of Havergal College, McGill University and the University of Toronto Medical School, Karen was a neonatologist at The Hospital for Sick Children, the Director of the Neonatal Follow - Up Program and the President of the Medical Staff. Widely published, she was instrumental in the development of neonatal ultra sound brain scanning now used in intensive care units around the world. After leaving HSC, Karen became a pioneer in the field of neuroplasticity in children with early brain and nerve injuries. She was a tireless advocate for a revolution in the treatment for children with cerebral palsy. Karen captured this work in her recently published book, The Boy Who Could Run But Not Walk.

She was a rebel with a cause who took no prisoners nor suffered fools. Karen took the road less travelled by and that made all the difference to thousands of her patients and their families. To the end, Karen was still thinking of ways to advocate for improving the treatments available for children with early brain and nerve injuries. She did not go gentle into that good night. In the weeks before her death, Karen endowed a foundation to provide funds to continue her work in this field.

Her family would like to thank Wing Lam and Pia Stampe for their support.
There will be a celebration of Karen’s life on Tuesday June 12, 2018 at The Rosedale Golf Club from 4 to 7pm. In lieu of flowers, the family asks you to consider a donation to Karen’s foundation.

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Merryn Straker
Watching a TedX talk of Karen on 8th November 2015 singularly changed our lives forever. Our son Oscar, then an 8 year old with Ataxic Cerebral Palsy on the other side of the world in New Zealand had no idea what I was about to get him into! I contacted Karen the next day who put me in touch with Pia and we took an 9 year old on tour to spend two weeks with Pia's team. What astounded me and was so unexpected was Karen's integral involvement - pouring over all his past specialist reports, requesting videos of him doing this and that, telling us to do it again as it wasn't good enough 🙂 Making no bones about incompetent assessments in some areas with Pia and Karen we got the full picture of our son's issues - fine/gross motor, speech, vision. She set us on a journey that I believed to the right course but one that I seemed to be a lone crusader in view on. I cannot thank her enough for the life changing input she had and I have certainly spread her message as far and wide as I can. Her book is what every family with a CP kid should read. Driven, passionate and relentless sums her up to me with a constant need to question what we were seeing and how else we might tackle it. Such a selfless need to see better options for our CP kids and adults and with such care and dedication. The world is truly a lesser place without her shining light. Much love to her family and friends. In New Zealand we have a Maori proverb "Whāia te iti kahurangi ki te tūohu koe me he maunga teitei" which means "Seek the treasure you value most dearly: if you bow your head, let it be to a lofty mountain". I truly bow my head to Karen, such for respect for all she has given.
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