Heart Space Copa is a Central Coast Yoga Studio & Art Gallery.
Our Mission; To Raise the Vibration of our Community. Through Mindful Movement, Heart-Centered Healing & Art.
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HEART Gallery
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ARTIST SPOTLIGHT I JUL
‘Lillian’s Journey’
MICK BROWN X HEART SPACE.
A FUNDRAISER FOR LILLIAN + EXHIBITION OF MICK’S WORK.
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FUNDRAISER EVENT + OPEN EVE I 16. 07. 2026
THURSDAY 16th JULY - SUN 26th JULY
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‘ALL SEEING EYES’ - By Mick Brown.
‘MANDALA STARS’ - By Mick Brown.
‘OCEAN EYES’ - By Mick Brown.
‘LAND EYES’ - By Mick Brown.
‘FOREST EYES’ - By Mick Brown.
This is a very special Exhibition.
Lillian (6) is in desperate need of craniotomy brain surgery to remove a tumour on her pineal gland, in the centre of her brain. Unfortunately, this life changing major surgery cannot be undertaken in Australia and she needs to travel to China.
Mick Brown (known as 'Browny Baby') is an Internationally recognised Artist, and proud Noongar man from Perth, living on the Central Coast. His art has attracted much recognition. In conjunction with this year's NAIDOC week 2026 (‘50 years of Deadly’), he would like to Donate his Acrylic Dot Painting on Canvas; ‘All Seeing Eyes’ in honour of Lillian’s Journey. Together - he joins us at Heart Space Copa to raise money to assist Lillian’s cause.
A $10 entry will allow you to go into the draw to win this painting! You can enter as many times as you like.
The winner will be announced Monday 27th July.
You are also invited to see Mick’s amazing work, (including this piece) on display at The Heart Gallery between Thu 16th & Sun 26th July.
Come along also to the Open Evening on Thu 16th July
(7-9pm) at The Heart Gallery I Heart Space Copa, to enjoy his work, Meet the Artist & learn more about this special cause.
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A Message from Lillian's Family:
"At around 18 months old, our daughter Lillian was diagnosed with what we were told was a “pineal cyst with solid components” on her pineal gland after we noticed difficulty with her upward eye gaze and being referred further by her ophthalmologist. The pineal gland itself is located in the centre of your brain.
We were relieved when it was confirmed that it was benign, and we trusted the health system when they told us there was “no change” and to simply return for yearly MRIs and follow ups. Year after year, we were met with the same response: “It’s just a cyst with no growth, it’s asymptomatic, we can’t determine what the solid lesions are, we will keep monitoring annually with MRIs'. Basically - See you next year, for 5 years so far. But as parents, we knew something wasn’t right.
Lillian continued struggling with symptoms that were seemingly dismissed — daily nausea, headaches, mood swings, eye issues, pain and discomfort and neurological symptoms, assured there was nothing to worry about with the ‘cyst’ and over the years we tried gut health, supplements, allergy testing, diet changes, etc. trying to find something to ease the symptoms she was experiencing with no real luck.
So I did what any mother would do.
I researched, obsessively.
Medical journals, support groups, stories from other families and people with the same diagnosis, contacting other Neurosurgeons privately (unwilling to assist), podcasts - the lot. I’m not a doctor — I’m just a mum trying to help her child and connecting the dots. That research eventually led us to Prof. Charles Teo who willingly took Lillian on as his patient and reviewed her annual scans. After reviewing her scans and history, he confirmed that this is not just a harmless asymptomatic cyst. It is multiple cysts and a suspected pineocytoma that has changed/grown over time and can be directly linked to her upward gaze palsy and very likely explains nausea, headaches and neurological symptoms.
Hearing those words was devastating, but also validating. For years we felt dismissed but now we had some better clarity and understanding.
Now we are faced with the main challenge.
Unfortunately access to treatment for pineal region masses is very limited and as a result many people in Australia are left without help. This likely is why we have gone so long without clear answers. The surgery she needs is not available to us in Australia with Prof. Teo involved, despite him giving hope and options to so many families when others won’t. Charlie is one of very few who are experienced enough to operate on pineal region cysts and tumours. Because of this, we are now looking at the opportunity of travelling to China for life-changing brain surgery within the next few months.
The estimated cost of surgery/post op care in China is between $70,000-$80,000 AUD, none covered by Medicare.
This does not include travel, accommodation, time off school and work to care for Lillian and also looking after our other two children during this process.
Anyone who knows us knows that we don’t ask for help (especially me!) but now we are hoping for help to give Lillian the chance she deserves at some relief, healing and a future without pain or potential long term issues.
A chance to remove the tumour in the hands of one of the best. As hard as this journey has been, if we had continued accepting “wait and see,” the long-term outcome for our daughter could have been far worse as she grows older, with little to no chance of having the tumour removed.
A donation, a message and prayer or a simple share of this fundraiser means more to our family than words can express. Times are tough for all families at the moment but even a small donation of a morning coffee will make a big difference for us and won’t go unnoticed.
Thank you for standing beside us in the hardest chapter of our lives."
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More about Mick Brown:
Mick Brown (also known as 'Browny Baby') is an Internationally recognised artist, a proud Noongar man from Perth, living on the central Coast. His art has attracted much recognition. Mick has been drawing and painting since he was ten years old, using creativity as a way to make sense of the world long before he ever knew it would become his life’s passion.
For Mick, every piece begins as emotion.
Sometimes he dreams his art before he paints it. Sometimes it arrives as a feeling he can’t ignore. Every brushstroke carries a story, of culture, memory, healing, and heart.
His work has travelled far beyond Australia, but Mick himself remains grounded, humble, and deeply connected to community. He has donated countless artworks to charity over the years, always stepping forward when someone needs help. Giving is part of who he is. His art is his way of taking care of people.
That’s why this fundraising event is so special.
This isn’t just a painting. It’s a piece of Mick - his emotion, his culture, his generosity, offered to support little Lilian and her journey.
When you buy a ticket entry, you’re not just entering a draw. You’re standing with a family, with a child, with a community that believes in lifting each other up.