Sharonika finds resilience through Graeme Dingle Foundation
Teen Sharonika Prasad used to be scared, of life, of opportunity. She lacked self-confidence. ‘‘I had a negative mind set in which I had beliefs that I would never be successful at anything, with a very low self-esteem. ‘‘I made excuses because I had no motivation and little confidence and I let life pass me by even if it was a wonderful opportunity because I was so afraid of the unknown.’’
Not anymore! Prasad, 18, and the youngest in a family of five, is now working as a caregiver while studying a foundation course at NZMA for occupational therapy and has realised she ‘‘could do anything’’. She is the first in her family to go to university. The South Auckland teen has found her potential with the help of our Foundation that aims to transform young Kiwi lives.
Read more abour Sharonika's story here: bit.ly...
Show your support for Sharonika and other young people by joining our Supporters Group here: bit.ly...
Neighbourhood Challenge: Who Can Crack This One? ⛓️💥❔
What has a head but no brain?
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Some Choice News!
Many New Zealand gardens aren’t seeing as many monarch butterflies fluttering around their swan plants and flower beds these days — the hungry Asian paper wasp has been taking its toll.
Thanks to people like Alan Baldick, who’s made it his mission to protect the monarch, his neighbours still get to enjoy these beautiful butterflies in their own backyards.
Thinking about planting something to invite more butterflies, bees, and birds into your garden?
Thanks for your mahi, Alan! We hope this brings a smile!
You are never alone
This year, I was given news that took the wind right out of this solo mum’s stomach: I was diagnosed with two types of curable breast cancer. Even writing those words still feels surreal.
I’ve recently completed five rounds of radiation, and while that chapter has closed, my journey is far from over. I now take daily medication — which, if I’m honest, comes with its own wild rollercoaster of highs and lows — along with monthly injections and six-monthly IV infusions.
All of this while raising two incredible, energetic tween boys who are full of wonder, life, and light. They have been my anchors on the darkest days and my reason to keep putting one foot in front of the other.
I’m sharing this because, in the New Year, I want to create a support group for anyone walking this path — no matter where you are on your journey. Whether you’re newly diagnosed, in treatment, finished treatment, or supporting someone you love.
Let’s build a village.
A place to lean, to cry, to laugh, to talk openly, and to remind each other that none of us have to do this alone.
Because the story doesn’t end when they tell you you’re “in the clear.”
In many ways, it’s just the beginning. 🌻
If this story touches your heart, and you’re on this journey too, feel free to message me. Even a quiet “me too” is enough...
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