Alice Eaves Bush
Alice Eaves Bush has been closed because of the threat of kauri dieback. Unfortunately pests ignore the signs and still have to be dealt with in the Park. A group of volunteers has been trained to work in the bush where there is kauri dieback. Training involves attending a course and passing a test. Once qualified volunteers are issued with distinctive labelled vests for identification. Working among kauris where there is the risk of spreading kauri dieback involves observing the highest possible standard of cleanliness of equipment, especially footwear. This disease can be spread by microscopic fungal spores. Boots and equipment have to be cleaned and disinfected frequently with a special disinfectant, sterigene.
Workers have to keep well clear of the root systems of kauri trees. The infection spreads into the trees through damaged roots. Stands of kauri have interlocking root systems so it can be quite challenging working in a stand. Boots and equipment has to be cleaned when moving from one stand to another. It is to be hoped a prevention and a cure can soon be found for this horrible kauri affliction.
Volunteers working with rangers are illustrated.
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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