Jake is celebrating his tenth birthday. That’s a remarkable feat, because at birth he was given only three years to live. Miriam Edelson is his mother, a dedicated fighter for Jake and families in similar situations. Edelson poses some tough questions: How do parents cope with a child who has special needs? Are we failing, as a society, to care for children with disabilities? Whatever happened to the federal government’s promise of a “Children’s Agenda”? My Journey with Jake works on two levels. It’s a poignant memoir by a devoted mother, and a hard-hitting, well-researched look at health care for Canada’s children.
Miriam Edelson, and the story of her son Jake, have appeared across Canada in newspapers and magazines, and on television and CBC Radio. She works as a trade-union and disability-rights activist.
“With an unflinching honesty, Edelson recalls the sorrow, bouts of near despair and the painful divorce that followed Jake’s diagnosis-as well as her love and acceptance of her son. The book is also a tough-minded account of the battles Edelson has fought on behalf of Jake against the medical establishment and government funding cuts.”
“A remarkable story. On her journey, Edelson travels roads, and achieves levels of awaresness, depths of fear, anger, love, that many of us will never know.”
“Miriam Edelson cuts through our natural distancing on this subject by taking readers on a surprising voyage of discovery. My Journey with Jake deftly draws you into an intense, private world of a couple’s expectations, momentary joy at their firstborn and devastation as they realize their baby is not normal…This book provides such powerful revelations of the raw emotions of having a child with extraordinary needs that it seductively draws you into the larger political issues.”