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The Canadian Pulmonary Fibrosis Foundation, the Robinson family, and fellow Islanders are proud to host the first CPFF Walk for Pulmonary Fibrosis on October 4, 2025, on the beautiful shores of PEI. Bring your friends, bring your family, and bring your big Island heart. Together, we’ll make every step count.

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Victoria Park, Kiwanis Field (10:00 AM ADT)

50 Victoria Park Roadway, Charlottetown, PEI C1A 2R4

• Registration is FREE
• 10:00 am ADT | Check-in & children's activities
• 10:45 am ADT | Welcome message & opening stretch
• 11:00 am ADT | Walk starts
• 12:00 pm ADT | FREE lunch, more children's activities
  

**If you'd like to cover the cost of your lunch, you may do so by making a donation

**Same day registrants will receive lunch with a $20 donation.

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Come walk with us—or cheer from the sidelines—as we gather in true east coast spirit to raise awareness, funds, and hope for people living with PF. After the walk, stick around for good food, warm company, and heartfelt conversation.

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Despite the challenges, John lived life fully. He enjoyed support groups, coffee with friends, and organizing family pizza nights. He faced his illness with humor and grace, welcoming caregivers. Both John and Hazel attended a monthly PF support group and John looked forward to his Tuesday afternoon CPFF Zoom sessions with people from all across Canada. John passed away in November 2023, five years after his diagnosis.

Now, the Robinson family’s hope is for a medication that can halt the spread of fibrosis, especially given its potential familial nature. They walk to support people living with pulmonary fibrosis and remember John, Eric, and Jim.