The Barossa Mag Summer 2019 | Page 32

32 | T HE B A R O SSA M A G Megan’s message of hope WORDS ALICIA LÜDI-SCHUTZ PHOTOGRAPHY PETE THORNTON > Don’t ever tell Megan McLoughlin she can’t do something, she’ll prove you wrong. To say this Tanunda mother of two is tough, resilient and inspirational seems an understatement, for this woman’s courage and sheer grit is something few can muster. And muster is the key word. This big-hearted farmer’s daughter with a wicked sense of humour is a master of “bringing the herd together”- not just cattle in the paddock, but also like-minded people with a passion for their communities. Megan will tell you humanity is a herd and everything meaningful she does in life is about “having one’s back”, offering hope and caring for the wellbeing others. “People think I’m strong, but I don’t see it as strength,” Megan says. “I see it as just wanting to be normal. I crave normality and in order to do that, I seem to do really unusual, extraordinary things in the hope that I can fit into society.” Despite her best intentions, Megan is far from fitting into that box. She’s a double transplant recipient and legally blind, not that you would know when meeting her for the first time. Diagnosed with Type I diabetes at the age of 8, Megan quickly discovered an inner toughness. “Being a young kid that rode horses and did sport and a lot of outside activities, it was a bit of a shock. All of a sudden they are telling me I can’t do anything. My parents were completely against that, so I kept riding my horse, kept playing my sport and kept doing everything.” At the age of 12, the medical profession painted a very bleak future. Megan won’t use a cane, even though she admits the scars on her legs say she probably should and there’s been many a time she’s been speaking to a pot plant or wheelie bin and wondered why it hasn’t answered. “I had a doctor say to me, you are going to lose your legs, your eyesight, your kidneys and you are going to die before you are 30 because that’s what diabetes does to you…it’s a daunting thing to be told. “A disability should not define who you are, it’s just something that happens,” says Megan. “I decided to ride my horses from Melrose in the Flinders Ranges where we were living, to Adelaide to raise awareness for Juvenile Diabetes. “We raised $25,000 and a lot of awareness... I road through King William Street, down Sir Donald Bradman Drive to the diabetes headquarters. It was an amazing thing - don’t tell me that I can’t do something when I am quite able bodied!” A keen horse sportswoman, she excelled at barrel racing and went on to win seven state titles, five national titles and a scholarship to a university in Georgia, America to compete as part of the college’s horse team. “I studied animal science, so pre-vet, large animal husbandry. Returned home and got a job with an animal health company, living in Sydney and loving life!” Work led her back to South Australia until one day, she ended up in hospital after getting “a bit of a headache”. D sh bl “T th at ce pe pe “A re of m fu aft th st an Sh sh “a “I