3 rods and a cane: Why disability doesn’t have to define your outdoor adventure

SETTING THE HOOK

Three days earlier, our floatplane had touched down on the glassy surface of French Lake, about 30 minutes by air from Cochrane, Ontario. In many ways, this wasn’t my typical fishing adventure, but that was by design. Usually when I plan outpost trips, I assemble a group of serious fishing types, often including my close friend Wes Nelson.

But this time, Wes and I had decided on something different. Instead of adding another hardcore angler, we invited Pete Kloppenburg. The three of us have been close friends since university in the early 1990s, but Pete had virtually zero fishing experience. He’s a long-time cottage owner in Ontario’s Muskoka region, and loves spending time outside, but he hadn’t picked up a rod in many years.

“Are you guys sure about this?” he asked more than once as we planned our adventure. “I know you love these trips, and I really don’t want to slow you down.”

There was more to that question than his fishing inexperience. Pete has multiple sclerosis, an autoimmune disease that significantly affects his mobility and stamina. It’s a quiet, stubborn disability, the kind that people don’t always see right away. But it’s there, with every step. Almost 15 years after his diagnosis, Pete now uses a cane or walker to get around, and he tires easily. None of that mattered to us.

“That’s the whole point of an outpost. We make our own schedule. The fish will be there when we’re ready,” I assured him.

“Think about it,” Wes added. “No cell service. No neighbours. Just three old friends, a cabin in the wilderness, and more pike and walleye than you’ve ever caught.”

Pete’s expression turned pensive. “Will there be beer?”

Multiple sclerosis (MS) is a chronic autoimmune disease in which the body’s immune system mistakenly attacks the protective covering of nerve fibres, disrupting communication between the brain and body. The resulting damage can lead to a wide range of symptoms, including fatigue, numbness, difficulty walking, vision problems and cognitive changes. MS often appears when people are between the ages of 20 and 40, just as they’re building careers and raising families. Canada has one of the highest rates of MS in the world, with approximately 90,000 people living with the condition. The challenges of MS remain significant, but treatments continue to advance, offering hope for the future. You can help by supporting the MS Society of Canada through donations or volunteering, as well as by advocating for better healthcare policies and helping to reduce stigma through education. At a personal level, small gestures—offering a ride to an appointment, for example, or lending a hand with daily tasks—can have a lasting positive impact. Learn more at www.mscanada.ca.