Advocates say Canada needs national pain strategy to provide care, lower costs
VANCOUVER — When Jeanine McDonald heard a pop in her low back as she bent down to pick up a lid from a box, she had no idea she’d ruptured a disc and would wait three months for surgery. Then a second disc ruptured and left her in more debilitating chronic pain, the kind that millions of Canadians live with daily.
In McDonald’s case, a condition called cauda equina syndrome, involving a bundle of spinal-cord nerves, causes severe neuropathic pain in her lower legs and feet, forcing her to wear leg braces and forearm crutches so she can walk.
Her neurosurgeon told her there’s no known reason why the two discs ruptured three years apart, in 2005 and 2008, leaving her able to work only one day a week for a non-profit organization helping families of special-needs kids.
“There’s super sharp pins-and-needles type of pain and what I call fire feet, which is a burning type of pain that happens,” McDonald said. “And there’s what I refer to as Charlie horses on steroids. You have to find humour in it or you just lose your mind.”


