Barry and Lorraine Young, with Nick at October’s Garden Fete.
Among those who wandered through the Amanda’s Garden Fete in Southern River earlier this month was a meningococcal survivor, Nick Peters.
Nick first met Barry and Lorraine Young in 2002, shortly after contracting meningococcal disease. “They came to visit me when I was first admitted,” he said. “They introduced themselves and offered me support, letting me know about the foundation and that they were there for me.”
More than 20 years later, Nick said the Amanda Young Foundation has changed his life. “They’ve helped me immensely, both financially and emotionally,” he said.
Hundreds turned out to enjoy the colour and calm of Amanda’s Garden Fete, supporting Amanda Young Foundation’s ongoing work in meningococcal research and awareness.
“They even helped me buy a new rugby chair after my old one was destroyed. Playing wheelchair rugby helped me get back into life and gain confidence after losing my limbs.”
Now a dad to two young children, Nick said the foundation recently helped him replace his modified car so he could continue caring for his family. “Without them, I don’t know where I’d be,” he said.
He said the Youngs’ dedication continues to inspire him. “Barry and Lorraine put in blood, sweat and tears to make life better for people like me,” he said. “Their passion and generosity are beyond words.”
Nick hopes the community keep supporting the Amanda Young Foundation. “If they can save even one person from going through what I did, it’s worth it,” he said.
He had this to say to those recently diagnosed with meningococcal disease: “Life doesn’t end after the disease. It might be different and not what you envisioned, but it can still be beautiful and meaningful; there’s hope.”
The Amanda’s Garden Fete, held on October 12, was a success with over 1,500 visitors in attendance.
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