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.

Memories & Condolences

 

 
 
 
 
 
Fields marked with * are required.
Your E-mail address won't be published.
We reserve the right to edit, delete, or not publish entries.
Deb Discenza
I remember when Karen reached out to me years ago via LinkedIN. I run the NICU Pros list, Early Intervention Pros list and more and she knew instantly that we needed to talk as she prepared to publish her book "The Boy Who Could Run But Not Walk." We talked by phone and there was an instant connection. I was excited to hear about her background, her work and her book. We worked on ways to help get it out there and we did. At the time I quietly noted to Karen my former 30-week preemie, then 11 years old had always had some issues with running and with walking and that I had always quietly asked doctors if this wasn't more than just low muscle tone and later more than gross motor delays and still later more than just Developmental Motor Coordination Disorder. Little did I know that I would be needing Karen's help when Becky was diagnosed officially at 13.5 years old. My frustration was audible to Karen as we talked by phone that winter. This rebel, this "difficult" person in the field of CP and baby brain science was nothing but straightforward, understanding and respectful as I poured out my rage at the establishment in this field and how people didn't seem to truly get that this was a catastrophic mess in my mind. She helped me understand how things had played out medically and where the mistakes likely happened. She also confirmed and connected the dots with me that my daughter's "slight curvature in the spine" as told me months early by the baffled pediatrician was consistent with the CP. She gave me some ideas of where to start. After 6 months of typical PT, appointments and other interventions that burnt out my daughter and myself, we stopped everything and took account of where we were. And this was only in the first year of diagnosis so I could only imagine what other families before us had done to keep their minds straight and focused. After the new year I contacted Karen again noting that we were definitely struggling with this and wondered if she had other thoughts. We talked, she said it was time to go see Pia Stampe in New York and get a CP Intensive. A short time afterward we spent a long weekend in New York and Pia was truly phenomenal. Becky came away walking better, running better and with a confidence and excitement that floored my husband and myself. She looked at me and said, "Thank you." Yes, my TEENAGER! Prior to leaving Pia that last day, she took a video of Becky and myself to send to Karen who was by now very sick. To hear my daughter speak to Karen with such awe and gratitude was amazing. In a few days she got the theory, she understood what Karen had been trying to teach medical and therapeutic professionals for a long time. And she was living proof that it worked. I finally got to meet Karen a month ago in Toronto. I got to give her a hug, say thank you in person. I also handed her a note . . . from my Becky. It totally moved her. It was then that we discussed the impending foundation. While I know Karen would have loved to see this come together, I know she left this in very, very capable hands. She will be missed but she will always be remembered, always be thanked for being "difficult" for being that rebel. For every infant, child, teen and adult that has received help from her over the years is now her ongoing living legacy alongside her own family. We carry it forward for her. Thank you, Karen. Thank you on behalf of the thousands of families you have helped over the years including mine. With Love & Gratitude, Deb Discenza PreemieWorld
Please wait...