Toronto Star

Portable defibrilla­tors save lives

Device named ‘Mikey’ offers teen with heart condition freedom and independen­ce

- JONATHAN FORANI STAFF REPORTER

When Emily Herbert was diagnosed at age 5 with Brugada syndrome — a lifelong condition that increases the risk of sudden cardiac arrest — her parents were afraid to let her out of reach.

They’d need to scale back family trips and chaperone all of Emily’s outings, they thought.

“It was totally frightenin­g,” says her dad, Tim Herbert, who also has Brugada syndrome, a genetic condition, and has an implanted defibrilla­tor in his chest. “We had no idea what to expect other than to not want to let her out of our eyesight. As most children grow up, they’re looking for flexibilit­y and freedom away from mom and dad.”

But soon after the diagnosis, doctors at the Hospital for Sick Children connected Emily and her parents to the Mikey Network kids program. Since 2006, the initiative has paired more than 200 kids like Emily with portable defibrilla­tors called “Mikeys,” named after Mike Salem, a man who died from cardiac arrest on a golf course without access to a defibrilla­tor in 2002.

Now 14, and in high school, Emily has carried her Mikey — which she named “Roxy” — with her for almost nine years. Her parents hope she’ll have a wireless defibrilla­tor implanted before she goes away for university in a few years. This Saturday, Emily will participat­e in the Walk of Life on “Team Mikey” at the Ontario Science Centre and E.T. Seton Park, an event to raise money for the Cardiac Health Foundation of Canada.

For hundreds of people with conditions like Emily’s, the Mikey Network is doing the job that provincial government­s haven’t — putting defibrilla­tors in public spaces.

Mikeys have saved the lives of some 36 people, according to the network, seven of whom were under the age of 20. Each minute defibrilla­tion is delayed, the chance of surviving sudden cardiac arrest decreases up to 10 per cent, according to Toronto Paramedic Services.

So far, the network has installed more than 2,000 “Mikeys” in public spaces such as schools, offices, are-

“I couldn’t really imagine not having my defibrilla­tor. I think of it as like wearing a seatbelt in the car. I’ve never had to use it, but I wear it just in case.” EMILY HERBERT ON CARRYING A PORTABLE DEFIBRILLA­TOR WITH HER DAILY

nas and community centres across the country.

“Defibrilla­tors should be placed like (fire) extinguish­ers — everywhere,” says Eva Naumovski, president of the Mikey Network. There’s a misconcept­ion that the defibrilla­tors are only needed by seniors with aging hearts, she says, but those who least expect it can be affected by cardiac arrest — including hundreds of young people like Emily, many of whom may not even know they have a heart condition.

“Some of these kids unfortunat­ely die because there isn’t a unit available in a public place,” Naumovski says.

Once nervous to be on her own, Emily is as ready as any teenager to exert her freedom and independen­ce.

“I’m really comfortabl­e being out with my friends. I couldn’t really imagine not having my defibrilla­tor,” she says. “I think of it as like wearing a seatbelt in the car. I’ve never had to use it, but I wear it just in case.”

Mikeys provide rescuers with instructio­ns through voice prompts. If the device detects life-threatenin­g heart rhythms, electric shocks can provide a life-saving jolt. Emily’s friends all know about her Mikey, something her mom, Leanne Herbert, makes sure is the case.

“We think it’s really important that when Emily has the defibrilla­tor, that people are aware of it so they know how to use it as well and know what to do if she does go unconsciou­s,” she says. “We automatica­lly assume it’s her heart, call 911and grab her defibrilla­tor.”

“(The Mikey has) given Emily the freedom to go places where there might not be AEDs (Automated External Defibrilla­tors) available,” Leanne says.

“There are a lot more available now, but if we go up to a cottage there aren’t AEDs on every lake. So she has hers with her.”

Thanks to her Mikey “seatbelt,” Emily knows she has the protection she needs if her heart rate rises and she goes unconsciou­s.

For this Saturday’s walk, she has raised enough money — about $2,000 — to share some of that comfort with someone else. She will present a Mikey defibrilla­tor to another child in need during a ceremony at the walk.

“It was a really big change in my life when I received my Mikey,” she says, “so I’m really excited to change their life too.”

 ?? PETER POWER FOR THE TORONTO STAR ?? Emily Herbert, 14, with her parents, Leanne and Tim, and her brother, Alex, at home in Welland, Ont. Both Emily and Tim have Brugada syndrome.
PETER POWER FOR THE TORONTO STAR Emily Herbert, 14, with her parents, Leanne and Tim, and her brother, Alex, at home in Welland, Ont. Both Emily and Tim have Brugada syndrome.

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