65_RedRoses: Lawn Summer Nights 2026

Hosted by

Cool.World

Film Access
July 17, 2026 12:00 am

September 1, 2026 11:59 pm
Event info
Watch the film this summer and support CF Canada
Price

Sliding Scale, starting at $5

Days
Hours
Minutes
In honour of the annual Canada-wide lawn bowling tournament and fundraiser established in tribute to Eva Markvoort (aka 65_RedRoses), watch the powerful film about her life this summer and we’ll donate half of the proceeds to Cystic Fibrosis Canada.

Event Details

Lawn Summer Nights

Warm Nights. Great people. Good vibes for an important cause. These are the key ingredients of Lawn Summer Nights, the national lawn bowling tournament and fundraiser for Cystic Fibrosis Canada, inspired by Eva Markvoort, aka 65_RedRoses.

In honour of Eva’s association with this fun event taking place across Canada, we are making the award-winning film available at a sliding scale from $5 with half of the profits donated to Cystic Fibrosis Canada until the end of summer.

Play for fun. Play #4Eva.

Join the thousands of bowlers across Canada helping to improve and lengthen the lives of those living with cystic fibrosis. Gather at least 4 friends together to register a team and hit the greens, all while wearing fun uniforms and enjoying delicious food and drinks. Since its launch in 2009, Lawn Summer Nights has raised over $5 million through the participation of more than 6,000 Canadians across the country!

Register and find out more at: www.lawnsummernights.com

Watch the Film & Support Eva’s Legacy

When Eva Markvoort agreed to open up her life through the documentary 65_RedRoses, the result was a powerful message of life, love, and hope. By doing so, she started a global campaign to find a cure for cystic fibrosis and encourage organ donation.

While waiting for a second transplant on March 27, 2010, at the age of 25, Eva’s breath ran out. But her vision did not die. To date, the award-winning film has screened at numerous international festivals and been televised in a dozen countries. It was chosen for OWN Documentary Club in the US. Eva believed that after seeing her film and witnessing her struggle with cystic fibrosis, people would finally understand the importance of supporting CF research and awareness, as well as be inspired to become an organ donor.

Learn more at: 65redroses.com

Buy the DVD in Canada & USA

Want your own copy of the film? We have a limited number of Special Edition DVDs, the deluxe collector’s version housed in gorgeous, eco-friendly packaging and featuring a commemorative picture book with quotes from Eva’s blog.

 

Film Access

July 17, 2026 12:00 am

September 1, 2026 11:59 pm
After purchasing a ticket, you will have access to a viewing page where you can watch the film at any time during the access window.

About the Host

Cool.World are the Canadian distributors of the film and our mission is to spread Eva’s campaign for cystic fibrosis awareness and organ donation far and wide.

EVENT HOST

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