Tāmaki Herenga Waka Festival is on tonight!
The story of Tāmaki Makaurau Auckland and the waka that sailed here will take centre stage in January 2020 when the region celebrates its Māori heritage through the Tāmaki Herenga Waka Festival.
For the first time since its inaugural year in 2016, the Festival will feature both land and water performances that will go on into the night, as well as storytelling that captures the region’s rich waka history which shaped the Tāmaki Makaurau we know and love today.
Highlights include:
• Gates open 5.30pm
• Waka showcase
• A marketplace of kai and toi (art)
• A land stage for performances and storytelling (6pm – 9.30pm)
• A water stage for performances and storytelling (9.30pm – 11pm)
• Kapa haka
• Contemporary Māori dance
• Music
• Vector Lights on the Auckland Harbour Bridge
Check out the full festival line-up on aucklandnz.com/tamakifest
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!
Neighbourhood Challenge: Who Can Crack This One? ⛓️💥❔
What has a head but no brain?
Do you think you know the answer? Simply 'Like' this post if you know the answer and the big reveal will be posted in the comments at 2pm on the day!
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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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