Lawn bowling charity keeps cystic fibrosis research rolling

MoreIslanders are taking the opportunity to get active and raise money for cystic fibrosis research this July.

Every Thursday this month means Lawn Summer Nights for bowlers. It's a charity eventcentredaround lawn bowling, toraise money and awareness for cystic fibrosis (CF) research.

CF is a genetic disease that causes persistent lung infections and limits theability to breathe over time it also affects the pancreas and other organs.

There are 18 events in cities across Canada participatingin Lawn Summer Nights this year, including Charlottetown.

This year the city had its highest participation in the event since it started on P.E.I. in 2017,saidSarah Riehl, Charlottetown city lead for Lawn Summer Nights. It now has 17 teams, up from the usual 14.

"With those 17 teams we also have some people who come over just to be social as well," she said.

Growing support

Lawn Summer Nights only has space for 18 teams of four and this year Riehl said she was happy to see support increase.

But,"we have one more space left and they can snag it if they want," she added.

The Charlottetown events take place at the Sherwood Lawn Bowling Club on Juniper Drive, and go from 6-9 p.m. Riehlsaid people in the area are always curious about the event.

"The residents of that community they can hear us having fun, singing along, laughing and they are interested in what is going on because typically lawn bowling is a quieter event," she said.

The bowling events are "spiced up" a little, she said, and drawa younger crowd.

"We have food and live music. There's washer tossand that is all included with the lawn bowling," Riehlsaid, adding the event is for those legal drinking age and over.

How it all started

Riehlsaid Lawn Summer Nights started in 2009 as a way to honour and remember Eva Markvoortof British Columbia. Shespent her life with cystic fibrosis and was committed tofinding a cure.

She used lawn bowlingas a way to get out, be social and see friends while battling her disorder.

She died in 2010 at the age of 25but Lawn Summer Nights continues to raise money and awareness for cystic fibrosis research.

Since the first Lawn Summer Nights in 2009 the events have raised $3,400,000.

For more information on Lawn Summer Nightsvisit the organization's website.

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