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Dainere's Rainbow Brain Tumour Research Fund

By Dainere's Rainbow Team

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Childhood Cancer Awareness Month - Turn September Golden

Today is the first day of Childhood Cancer Awareness Month.
These are inspiring and selfless words shared by Dainere:
"In our lives we often underestimate the true power of a smile, a touch, a kind word, a listening ear, an honest compliment and the act of just simply caring. These all have the potential to turn a life around; tomorrow and everyday take the time to reach out and change a life".
We would like to invite you to be part of working towards a more prominent and widespread Golden September 2023 for Childhood Cancer by continuing to elevate awareness about Childhood Cancer and especially brain cancer within the Community each and every day.
This is a very special project that Dainere requested and one that we hope will reach far and wide and beyond all expectations....... 'Pot of Gold' for Childhood Cancer.
At the end of every rainbow is a pot of gold and from today you can be a rainbow of hope in the lives of children diagnosed with cancer...... start saving gold coins and collect them in your 'Pot of Gold' all the way through this month until 30th September 2023 and then make an online donation.

Your 'Pot of Gold' will go a very long way in working towards the most precious gift in this world.....the reality of a cure!

Raising Awareness Needs To Be Done Every Day

It is essential to raise awareness 365 days a year, as children are each day being diagnosed, are fighting brain cancer, the treatments and effects and tragically many are losing their lives.
These are Dainere's words, she was continually determined, dedicated and extremely selfless in her passionate and tireless efforts to make a difference, we hope that many in the Community will follow her advocacy and work to see the eradication of childhood brain tumours.
"My life goal is to do as much as I can to make a difference. A cure will not be found in my lifetime but my wish is that others will continue my lead to ensure that no children in the future will have to suffer as many others and myself have had to.
In a world where there is so much advancement, my heart breaks to know that there is no screening tests for early detection for a brain tumour, there are very few advancements in treatments, the treatments themselves are harsh and cause life long cruel side effects, funding is minimal for the impact of this disease and there is no cure. This is just so very wrong".

24th June - Ten Years Since Dainere's Final Breath

Saturday is a day of most unimaginable, deep heartache and loss for our family, for it was on Monday 24th June in 2013 that our most truly divine, precious, adored and beautiful Dainere had her young life cruelly stolen by brain cancer.

She inspired so many and we know that she left lasting footprints on so many hearts and lives and continues to do so every day.

We so love and miss our beautiful and beloved Dainere endlessly and so, so desperately wish she was still here with us. Brain Tumours are such a horrid, cruel, vicious and insipid disease. 

Young children like Dainere, who so randomly are inflicted by this disease through no fault of their own don't deserve to have to suffer. Families should not have to face a second, a minute, a day, a week, a year, a life without their child or sibling.

A cure must to be found for this disease. We will for an eternity work as tirelessly, selflessly, devotedly and passionately as Dainere did to one day see a cure found.

We would also like to honour and remember on this day all the children who too have lost their battles, those that continue to battle and those who will receive the devastating news of a brain tumour diagnosis in the future.

You can help us to continue Dainere's incredibly selfless and inspiring legacy to give hope and create change for others by doing any of the following:

1. Sharing Dainere's story and the work of Dainere's Rainbow with others to help us to elevate significant awareness in the Community and beyond.

2. Encourage family, friends and work colleagues to visit the Dainere's Rainbow website or like the Dainere's Rainbow Facebook or Instagram Page.

3. We know that during these continued difficult times, this is a massive ask, but if you are in a position to make a small donation of ten cents or $10 (a cent or dollar for each year since Dainere had her life stolen) it would be so humbly and sincerely appreciated as 100% of all that is donated or raised by Dainere's Rainbow goes directly to vital and desperately needed research projects and programs.

The Unimaginable

The 24th of March......a date that will forever remain imprinted in our lives; a turbulent, devastating and life changing day.

On this particular day in 2009, after a visit to the paediatrician, then being rushed to the Canberra Hospital for an emergency MRI and to witness a sea of worried faces behind a glass screen.

Then the serious and poignant words from the medical staff…..”we need to talk”……

We walked slowly, shakily, and anxiously down a long, long corridor and into a room, where three solemn and worried faces of the medical team ushered us in and beckoned us to sit. They all looked at each other and before speaking took a long, slow, deep breath.

Our attention was drawn to a round coffee table and on the middle of the table there was a single box of tissues, nothing else, just the tissue box.......this image has remained embedded so clearly in our minds, it remains so vivid even still today.

Then with empathy, we were informed that our most adored and beloved youngest daughter and sister had a brain tumour.

We did not know what type it was. All we were told was that it was life threatening, it was extremely large, it had deposited several metastasis spread to other areas in her brain and it was blocking the cerebrospinal fluid from flowing around her spinal cord and brain. It was not good and they urgently had to get her to Sydney or we could lose her that night.

On this day we stepped from a life filled with normal routines, happiness, hopes and dreams into the most unimaginable, terrifying nightmare that any family could experience. It what was not only devastating, soul destroying and heartbreaking, it was in many ways so surreal, a total blur.

Dainere needed to get to Sydney Children’s Hospital as soon as possible for emergency brain surgery............ Life would never, ever be the same again and we were thrown into a world that no family should ever be.

Since Dainere's diagnosis more children each year are being diagnosed with brain cancer and we have been told this is in line with population growth.

Also, tragically despite the devoted work of many researchers and families who do not want any other family to have to face the shear pain of losing a child to this disease there is still, every year in excess of an entire classroom of precious and innocent children that have their lives and futures stolen by what remains the number one disease killer of children in Australia. This is not well known, it is confronting, it is terrifying but it is something that needs people to raise their voices about in the Community.

Dainere worked so tirelessly, selflessly and devotedly to raise an awareness of childhood brain tumours. Her words of "My little voice can only make a small difference, but together many voices could create change" are a plea for many to unite together to take action, give hope and create change.

You each and every day can shine a rainbow of hope by adding your voice and help to be an advocate to elevate much needed awareness of childhood brain tumours within the Community; in memory of every single child that has battled, lost their life, continues to battle or who will be diagnosed in the future.

Give The Gift of Hope For What Should Have Been Dainere's 25th Birthday

Tomorrow, 8th February is our most beloved, inspiring and selfless Dainere's Birthday. Dainere should have been turning 25, however our beautiful angel remains forever 15, having her young life stolen by what is the most horrendous and indiscriminate disease; brain cancer.
Forever our hearts are broken and the pain we feel each and every day is truly indescribable. We have the most treasured and special memories and she remains in our hearts, thoughts and actions every moment of every day.
Brain cancer took away her chance to live life, to do and be all she dreamed of, to grow up and experience many wondrous things, to continue to make an enormous difference in the world or get to experience the joy of love, being an Aunty, meeting that someone special, marriage or motherhood.
Dainere always put others before herself, when she was in pain and when her disease caused her so much suffering and loss of quality of life, she would become more and more determined to fight to selflessly make a difference for others.
In honour of her Birthday we would like to ask others to consider giving a gift: that is to continue her fight, to elevate awareness of this insidious disease by sharing a fact with as many people as you possibly can.
Brain Cancer kills more children than any other disease in Australia.
Children in Canberra diagnosed with brain cancer have to travel to Sydney for surgery, treatment and other procedures and being away from family and friends.
Brain cancer has the highest total burden of disease for children and adolescents in Australia.
Alarmingly there have been significantly increasing trends in the incidence of Medulloblastoma, a shocking 58% increase over a thirty-five year period.
The needs of children with brain cancer in treatment, rehabilitation and end of life care are very different and particularly acute.
If anyone would like to make a donation for Dainere's Birthday perhaps $2.50 or $25 to continue her selfless, inspiring and tireless work you can do so here.
100% of all funds raised by Dainere's Rainbow goes directly to research projects and programs set up in memory of and as a legacy to Dainere that are specifically for better outcomes for children with brain tumours.
We express our deepest gratitude to each and every person who is helping to take action, give hope and create change.

Giving for 2023

'Giving' - Dainere continually opened her heart in the act of giving to others.
So our mission into 2023 is to 'give' to others, to give a knowledge of the disease that does not discriminate, the disease that takes the lives of young babies, children, teenagers, young adults, adults in the prime of their lives and older people.
By 'giving' a knowledge of brain cancer we hope that it will then have people sharing and talking about a disease that needs to receive an elevation of attention to create change.
1. When a child dies from brain cancer, each death means the loss of what should be their entire lifetime.
2. If a child survives brain cancer they face serious medical complications, secondary cancers, cognitive impairments, debilitating disabilities and shortened lifespans.
3. There are paediatric brain tumours, like DIPG that are terminal upon diagnosis. Recurrent Medulloblastoma has long been considered universally fatal.
4. It can be difficult to treat paediatric brain cancer with chemotherapy drugs because the brain is protected by the blood brain barrier. This is a natural filter within the body. It only allows certain substances through from the blood to the brain tissues. So this limits the options of the type of chemotherapy that can be used or it means that the chemotherapy has to be delivered at shockingly high dose which cause devastating side effects.
Dainere gave so much to help others, we continue her inspirational legacy, she said that her little voice could only make a small difference but together many voices could create change.
Many voices are needed so that the facts presented above will indeed change.
We wish to express our heartfelt gratitude to those who are helping to shine a light out of the darkness by sharing, talking and giving knowledge to others about paediatric brain cancer and to those who donate or raise vital funds.

The Gift of Hope for Christmas 2022

These are Dainere's wise and powerful words to inspire you this December.

"The lead up to Christmas is a busy time, a time where we sometimes forget the important things in life in the rush to shop and party. If we stop for a while, remember to smile, to be considerate, patient, tolerant , respectful and caring then we can make a person's day bright. If we can take the time to reach out to give to others rather than expecting to receive then our hearts are set alight with love, hope and joy" ~ Dainere Anthoney 1998-2013

We know there have been two difficult and uncertain years for so many, so please know that any small donation brings a mountain of hope for children diagnosed with a brain tumour.

Bringing Hope For Christmas

These are Dainere's wise and powerful words to inspire you this December.
"The lead up to Christmas is a busy time, a time where we sometimes forget the important things in life in the rush to shop and party. If we stop for a while, remember to smile, to be considerate, patient, tolerant , respectful and caring then we can make a persons day bright. If we can take the time to reach out to give to others rather than expecting to receive then our hearts are set alight with love, hope and joy" ~ Dainere Anthoney 1998-2013

We know it has been such a difficult and uncertain year for so many, so please know that any small donation brings a mountain of hope for children diagnosed with a brain tumour.

Many Voices Can Help To Create Change

Dainere continually opened her heart in the act of giving to others.
So our mission today is to 'give' to others, to give a knowledge of the disease that does not discriminate, the disease that takes the lives of young babies, children, teenagers, young adults, adults in the prime of their lives and older people.
By 'giving' a knowledge of brain cancer we hope that it will then have people sharing and talking about a disease that needs to receive an elevation of attention to create change.
1. When a child dies from brain cancer, each death means the loss of what should be their entire lifetime.
2. If a child survives brain cancer they face serious medical complications, secondary cancers, cognitive impairments, debilitating disabilities and shortened lifespans.
3. There are paediatric brain tumours, like DIPG that are terminal upon diagnosis. Recurrent Medulloblastoma has also long been considered universally fatal.
4. It can be difficult to treat paediatric brain cancer with chemotherapy drugs because the brain is protected by the blood brain barrier. This is a natural filter within the body. It only allows certain substances through from the blood to the brain tissues. So this limits the options of the type of chemotherapy that can be used or it means that the chemotherapy has to be delivered at shockingly high dose which cause devastating side effects.
Dainere gave so much to help others, we continue her inspirational legacy, she said that her little voice could only make a small difference but together many voices could create change.
Many voices are needed so that the facts presented above will indeed change.
We wish to express our heartfelt gratitude to those who are helping to shine a light out of the darkness by sharing, talking and giving knowledge to others about paediatric brain cancer and to those who donate or raise vital funds.

September is Childhood Cancer Awareness Month

Today is the first day of Childhood Cancer Awareness Month.
These are inspiring and selfless words shared by Dainere:
"In our lives we often underestimate the true power of a smile, a touch, a kind word, a listening ear, an honest compliment and the act of just simply caring. These all have the potential to turn a life around; tomorrow and everyday take the time to reach out and change a life".
We would like to invite you to be part of working towards a more prominent and widespread Golden September 2022 for Childhood Cancer by continuing to elevate awareness about Childhood Cancer and especially brain cancer within the Community each and every day.
This is a very special project that Dainere requested and one that we hope will reach far and wide and beyond all expectations....... 'Pot of Gold' for Childhood Cancer.
At the end of every rainbow is a pot of gold and from today you can be a rainbow of hope in the lives of children diagnosed with cancer...... start saving gold coins and collect them in your 'Pot of Gold' all the way through until 30th September 2022.
We encourage you and would absolutely love you to share throughout the year to this page how your collection is going.
Your 'Pot of Gold' will go a very long way in working towards the most precious gift in this world.....the reality of a cure!

"I Don't Want Other Children To Have To Suffer As I Have" - Dainere Anthoney 1998-2013

Dainere was so selfless and passionate in her quest to elevate significant awareness of her disease, in fact just a month prior to her passing she was out in the Community advocating that her little voice could only make a small difference but many voices could create change.

So today we are sharing just a small portion of information that Dainere worked so tirelessly on to try to give the community knowledge of the disease that stole her young life and the lives of way too many other children and leaves any children that do survive with devastating side effects.

"My tumour is cancerous, it is called Medulloblastoma. Did you know that Medulloblastoma is the most common brain tumour of childhood, representing about 20% of all paediatric brain tumours.

They are most common in children between 4 and 10 and are slightly more common in boys than girls.

These tumours typically arise in the middle of the cerebellum, interfering with the flow of cerebrospinal fluid and causing hydrocephalus. Medulloblastoma is highly malignant and aggressive and can spread to other parts of the brain and spine through the cerebrospinal fluid.

Common symptoms of Medulloblastoma include:

Persistent or recurrent vomiting with or without nausea and most often in the morning after waking

Headaches

Dizziness

Wobbly or gaited walk, poor balance and co-ordination

Difficulty with tasks like handwriting

Frequent flu like symptoms

Seizures

Abnormal head position like a head tilt or stiff neck

Gradual decline in school performance (impaired attention)

Unusual sleepiness or change in energy level

Abnormal Eye movements, blurred or double vision

Loss of bowel or bladder control

Change in personality or behaviour

Unexplained weight loss or weight gain

Reduced consciousness

It is so important that people in our Community are aware of this disease, how totally horrific it is and what the symptoms are, please help me to make a difference for other children, I don't want any children in the future to have to suffer as I have. I thank you with all my heart"

Light Your Hearts and Bring Hope

This year is flying by, July already. We continue to face unprecedented and uncertain times. We thought sharing Dainere's words from the year she learnt her cancer had spread and all treatment options had been exhausted, her time was limited. We hope that her outlook may assist others.
Dainere's reflection on her year in 2012 and her hope for 2013 to make a difference.....
"This year I have also continued with what is so dear to my heart and my greatest wish and vision and that is to contribute through advocacy, awareness and fundraising to helping find improved treatment options and the reality of a cure for paediatric brain tumours.
I so passionately believe that no children in the future should have to suffer as myself and many others have with this absolutely, terrifying, painful, incurable, cruel, malicious and hideous disease.
Next year in the time I have remaining, I will continue to tirelessly and passionately work to significantly increase desperately required awareness and fundraising: using every breath, every heartbeat and every ounce of strength.
I hope that I can give knowledge and educate the Community, so that they feel inspired, determined and motivated to help me in my endeavor to bring hope and create change.
Every one talking about brain cancer and every dollar really does count and I know that it is so deeply appreciated by those doing the research. Helping others gives you a sense of worth, hope, courage, love and lights your heart."

Dainere's Angelversary 24th June 2023

Friday is a day of most unimaginable, deep heartache and loss for our family, for it was on Monday 24th June in 2013 that our most truly divine, precious, adored and beautiful Dainere had her young life cruelly stolen by brain cancer.
She inspired so many and we know that she left lasting footprints on so many hearts and lives and continues to do so every day.
We so love and miss our beautiful and beloved Dainere endlessly and so, so desperately wish she was still here with us.
Brain Tumours are such a horrid, cruel, vicious and insipid disease. Young children like Dainere, who so randomly are inflicted by this disease through no fault of their own don't deserve to have to suffer. Families should not have to face a second, a minute, a day, a week, a year, a life without their child or sibling. A cure must to be found for this disease. We will for an eternity work as tirelessly, selflessly, devotedly and passionately as Dainere did to one day see a cure found.
We would also like to honour and remember on this day all the children who too have lost their battles, those that continue to battle and those who will receive the devastating news of a brain tumour diagnosis in the future.
You can help us to continue Dainere's incredibly selfless and inspiring legacy to give hope and create change for others by doing any of the following:
1. Sharing Dainere's story and the work of Dainere's Rainbow with others to help us to elevate significant awareness in the Community and beyond.
2. Encourage family, friends and work colleagues to visit the Dainere's Rainbow website or like the Dainere's Rainbow Facebook or Instagram Page.
3. We know that during these continued unprecedented and difficult times, this is a massive ask, but if you are in a position to make a small donation of nine cents or $9 (a cent or dollar for each year since Dainere had her life stolen) it would be so humbly and sincerely appreciated as 100% of all that is donated or raised by Dainere's Rainbow goes directly to vital and desperately needed research projects and programs.

A Tribute From Dainere

This was written by Dainere as a tribute to her doctors who give everything they have to try to treat or in some cases cure children with cancer.  As brain cancer kills more children than any disease in Australia, the heartbreak the doctors must carry with them when they lose precious patients is unimaginable.  This is often what drives them to a lifetime commitment to finding better treatments with less side effects and the hope one day of a cure for all children's cancer.

"TRIBUTE TO A SPECIAL DOCTOR
My doctor is an extraordinary human being.
With a heart of gold and a touch of love,
he has been a guardian angel, always there for me.
His studies never seem to conclude as he seeks and searches.
Continually looking for superior and successful treatments
He always desires the very best of care for his patient.
Late hours and long days are his plight.
To meet the heavy demands that may fall in his path.
In my battle he has been my unsung hero giving me hope.
He has helped me to believe in brighter days.
Given me comfort and courage when I fall.
He’s taught me that the future belongs to those who dream.
Compassion, love and healing are his life.
He remains dedicated to each individual circumstance.
Constantly placing the welfare of others before his own.
He has traveled through the many storms with me.
His goal is to help me find that precious rainbow.
I am forever grateful to you, my magnificent doctor."
Written especially for you by Dainere Anthoney

Dainere's Selflessness

Just a few weeks before Dainere tragically lost her battle with her disease, she wrote this:
"This week I have mostly slept, I have not been able to attend school for normal lessons at all. I have done a little work from home though when I can manage to keep my weary eyes open.
On Tuesday however I was determined to go for a special presentation that had been planned from last Term. Jarrett, Nalani and I were doing a special presentation to Senior School on Brain Cancer.
We began with an introduction and then showed an exceptional movie that Jarrett had made on paediatric cancer and he also investigated my cancer as part of it. We then showed a power point containing important and startling facts about Brain Cancer, we even had music to accompany it to make it more effective.
Nalani read some passages from my first book, followed by some information about my treatment and side effects. We then spoke about the awareness and fundraising that I am so extremely passionate about.
Nalani reminded people that it is through raising awareness and funds that other cancers no longer have the high fatality rates they used to. She emphasised that if more awareness and funds are raised about Brain Cancer, then perhaps the same results could be achieved.
Jarrett and I also shared about our very special and meaningful City2Surf initiative which we hope to raise a phenomenal amount of funds and awareness through. Every dollar and every time someone talks to others about childhood brain cancer can make an enormous impact and difference.
I know that a cure will not be found in my lifetime, but I hoped that through the presentation that people would go out in the community and continue to raise awareness and funds so that one day my greatest wish of a cure being found will actually become a reality and no children will have to face the same battle, excruciating pain and suffering that I have".
Dainere was in excruciating pain despite being on morphine and other medications at this stage, she could not sit up very well, her speech was beginning to slur and she was terribly weak and fragile.
The fact that she found an inner strength to advocate to raise awareness on that day is a testimony to her courage, selflessness, tireless and passionate efforts to raise awareness and her desire to make a difference, this day she was truly inspiring.

The Beginning of our Brain Cancer Journey - 24th March 2009

The 24th of March......a date that will forever remain imprinted in our lives; a turbulent, devastating and life changing day.
On this particular day in 2009, after a visit to the paediatrician, then being rushed to the Canberra Hospital for an emergency MRI and to witness a sea of worried faces behind a glass screen. Then the serious and poignant words from the medical staff…..”we need to talk”……
We walked slowly, shakily, and anxiously down a long, long corridor and into a room, where three solemn and worried faces of the medical team ushered us in and beckoned us to sit. They all looked at each other and before speaking took a long, slow, deep breath.
Our attention was drawn to a round coffee table and on the middle of the table there was a single box of tissues, nothing else, just the tissue box.......this image has remained embedded so clearly in our minds, it remains so vivid even still today.
Then with empathy, we were informed that our most adored and beloved youngest daughter and sister had a brain tumour.
We did not know what type it was. All we were told was that it was life threatening, it was extremely large, it had deposited several metastasis spread to other areas in her brain and it was blocking the cerebrospinal fluid from flowing around her spinal cord and brain. It was not good and they urgently had to get her to Sydney or we could lose her that night.
On this day we stepped from a life filled with normal routines, happiness, hopes and dreams into the most unimaginable, terrifying nightmare that any family could experience.
It what was not only devastating, soul destroying and heartbreaking, it was in many ways so surreal, a total blur.
Dainere needed to get to Sydney Children’s Hospital as soon as possible for emergency brain surgery............ Life would never, ever be the same again and we were thrown into a world that no family should ever be.
This day is also 3195 days since our most inspiring, courageous, selfless, sweet, precious loving, gentle and extraordinary Dainere lost her battle with this truly insidious, cruel and indiscriminate disease.

Since Dainere's diagnosis more children each year are being diagnosed with brain cancer and we have been told this is in line with population growth.
Also, tragically despite the devoted work of many researchers and families who do not want any other family to have to face the shear pain of losing a child to this disease there is still, every year in excess of an entire classroom of precious and innocent children that have their lives and futures stolen by what remains the number one disease killer of children in Australia. This is not well known, it is confronting, it is terrifying but it is something that needs people to raise their voices about in the Community.
Dainere worked so tirelessly, selflessly and devotedly to raise an awareness of childhood brain tumours. Her words of "My little voice can only make a small difference, but together many voices could create change" are a plea for many to unite together to take action, give hope and create change.
You each and every day can shine a rainbow of hope by adding your voice and help to be an advocate to elevate much needed awareness of childhood brain tumours within the Community; in memory of every single child that has battled, lost their life, continues to battle or who will be diagnosed in the future.

Giving - Many Voices Could Create Change

'Giving' - Dainere continually opened her heart in the act of giving to others.
So our mission today is to 'give' to others, to give a knowledge of the disease that does not discriminate, the disease that takes the lives of young babies, children, teenagers, young adults, adults in the prime of their lives and older people.
By 'giving' a knowledge of brain cancer we hope that it will then have people sharing and talking about a disease that needs to receive an elevation of attention to create change.
1. When a child dies from brain cancer, each death means the loss of what should be their entire lifetime.
2. If a child survives brain cancer they face serious medical complications, secondary cancers, cognitive impairments, debilitating disabilities and shortened lifespans.
3. There are paediatric brain tumours, like DIPG that are terminal upon diagnosis. Recurrent Medulloblastoma has long been considered universally fatal.
4. It can be difficult to treat paediatric brain cancer with chemotherapy drugs because the brain is protected by the blood brain barrier. This is a natural filter within the body. It only allows certain substances through from the blood to the brain tissues. So this limits the options of the type of chemotherapy that can be used or it means that the chemotherapy has to be delivered at shockingly high dose which cause devastating side effects.
Dainere gave so much to help others, we continue her inspirational legacy, she said that her little voice could only make a small difference but together many voices could create change.
Many voices are needed so that the facts presented above will indeed change.
We wish to express our heartfelt gratitude to those who are helping to shine a light out of the darkness by sharing, talking and giving knowledge to others about paediatric brain cancer and to those who donate or raise vital funds.

A New Year

As a New Year begins we wanted express our always heartfelt and humble gratitude to all those extraordinary people who have so kindly supported Dainere's Rainbow throughout the unprecedented and difficult year of 2021.
For 2022, we would like to let Dainere's always inspiring, beautiful and wise words to provide you with hope and inspiration.
"May the gift of love, the gift of peace and the gift of happiness not only live in your heart during the Festive Season but throughout the coming year. In the New Year may the good times and treasures of the present become the golden memories of tomorrow and may your year ahead sparkle with moments of love, laughter, contentment, joy, hope and goodwill towards others.
I believe with all my heart that everyone should go out and make the absolute most of every single day of their lives; because you don't know what is around the corner or how much time you have on this Earth, so please don't waste a single precious moment of it.
This year I have continued with what is so dear to my heart and my greatest dream and that is to contribute to helping finding a cure for paediatric brain tumours, I so passionately believe that no children in the future should have to suffer as myself and so many others have with this absolutely hideous and atrocious disease.
Be true to your dreams, and keep them alive, never let anyone try change your mind about what you feel you can achieve. Always and forever believe in yourself.
I know that tragically a cure for this most cruel and devastating disease will not be found in my lifetime and my time is rapidly running out. When I am no longer here I encourage and hope that many people will raise their voices in the community to significantly elevate desperately needed awareness of this truly painful, debilitating, lethal and cruel disease. Raising awareness is vital to then raising funds, which are so critically needed and then one day my greatest wish of greater awareness, new and improved treatment options, increased funding, no more children suffering and a cure will become a reality.
Look for me in rainbows shining in the sky, wish me to be near you and I'll be by your side."

This December Give the Gift of Hope

These are Dainere's wise and powerful words to inspire you this December.
"The lead up to Christmas is a busy time, a time where we sometimes forget the important things in life in the rush to shop and party. If we stop for a while, remember to smile, to be considerate, patient, tolerant , respectful and caring then we can make a persons day bright. If we can take the time to reach out to give to others rather than expecting to receive then our hearts are set alight with love, hope and joy" ~ Dainere Anthoney 1998-2013

We know it has been such a difficult and uncertain year for so many, so please know that any small donation brings a mountain of hope for children diagnosed with a brain tumour.

Bringing Hope

This year is flying by, November already. It has been a truly difficult, uncertain and unimaginable year for many. We thought sharing Dainere's words from the year she learnt her cancer had spread and all treatment options had been exhausted, her time was limited. We hope that her outlook may assist others.

Dainere's reflection on her year in 2012 and her hope for 2013 to make a difference.....

"This year I have also continued with what is so dear to my heart and my greatest wish and vision and that is to contribute through advocacy, awareness and fundraising to helping find improved treatment options and the reality of a cure for paediatric brain tumours.

I so passionately believe that no children in the future should have to suffer as myself and many others have with this absolutely, terrifying, painful, incurable, cruel, malicious and hideous disease.

Next year in the time I have remaining, I will continue to tirelessly and passionately work to significantly increase desperately required awareness and fundraising: using every breath, every heartbeat and every ounce of strength.

I hope that I can give knowledge and educate the Community, so that they feel inspired, determined and motivated to help me in my endeavor to bring hope and create change.

Every one talking about brain cancer and every dollar really does count and I know that it is so deeply appreciated by those doing the research. Helping others gives you a sense of worth, hope, courage, love and lights your heart."

I’ve chosen to raise much needed funds for Sydney Children's Hospitals Foundation

Sydney Children's Hospital, Randwick provides a safe and friendly healing environment for children from NSW and beyond.
The Hospital's expert medical staff care for more than 61,500 critically ill and injured children every year. Thank you for your support!

Thank you to my Supporters

$501.22k

Anonymous

$65.44k

Offline Fundraising 2023

$6.62k

City2surf 2022

Thanks to Jarrett, Mark and Nicole!

$2.02k

Karen Anderson

Given with love for our two beautiful, brave and spirited children - Mitchell and Dainere

$1.02k

Tricia Moore

Dainere and her family are an inspiration to us all. Let's keep up the fight!

$1.01k

Jerrabomberra Public School

Money raised from holding a Rainbow Day at school.

$1,000

Leanne Kilduff

$1,000

Leanne Kilduff

$520

Callum Woods

$520

E And J Ingster

Given with lots of love xoxo

$515

Kylie, Steve, Harrison, Jasmyn, Charlie, Hayden, Ashlee, Zali, Abby And Super Dog Roxy.

Beautiful Anthoney family, you are all extra amazing and it is an honour to be part of Dainere's Rainbow. Much love to you all. xxx

$500

Anonymous

Jett Arentz

$401

Noelle Pocknall

Happy Halloween from Noelle and Amy

$400

Anonymous

$375

Mel S Massage

September fundraising efforts to date 18/9/2022

$350

Lex Anderson

$300

Carlo

A special donation in lieu of the Canape Mingle and helping you to make a difference.

$269.35

Laura - Arentz Cards

$263.75

Phil Spedding Consulting Pty Ltd

$250

Canberra Metro Operations

$245

Mels Massage

September donation 19th-30th

$214.02

Bron Collins

From the staff at Black Mountain School and Campbell High School.

$209

Patricia Arentz

$200

Kylie, Steve And Family

Helping make a difference through our Garage Sale. So happy to support and bring hope. xoxoxoxoxo

$177.48

Bron Collins

From the lovely Black Mountain School community who bought face masks.

$150

Bill And Jenny Brodie

In Lieu of attending the Canape Mingle and thanking you for all you do for children with brain cancer.

$150

Monique And Mark

In lieu of the cancelled Canape Mingle and in memory of Dainere xoxoxoxoxo

$132

Laura L Martiniello

$131.88

Arentz Card Sales

$125.44

Maggie Coy

Thankyou for all the wonderful work you do!

$121.10

Jerrabomberra Public School

Money raised from hosting a Rainbow day at school.

$105.50

Monica Johns

$105.50

Ellen Newhouse

In loving memory of my beautiful granddaughter whose birthday falls on 8 February.. Taken far too soon with incurable cancer. Always in my heart.

$105.50

Anonymous

I can still see young Dainere's face sitting around the table at mealtime at RMH each parent wondering what was going to be the fate of their child

$105.50

Crystal, Peter, Braxton, Jett & Cruz Arentz

Anthoney family, Thinking of you on the 9 year anniversary of the loss of your beautiful girl, Dainere. Thank you for all that you do to elevate awareness for brain tumours in children. Sending much love.

$105.50

Wayne, Carole And Heather Boreham

In memory of Dainere and in recognition of the wonderful work you do to help find a cure for children’s brain cancer.

$105.50

David And Anne

$105.50

Ellen Newhouse

For my beautiful Granddaughter Dainere who was taken far too young with brain tumour. Never forgotten always loved.

$105.50

Gail Mcculloch

Remembering Sweet Pea on this 10 year anniversary. Loved beyond measure, always in my heart 🌈💗

$104.40

Usha Naidu

Thank you for raising funds to find a cure for brain cancer.

$53.75

Zaeem Khan

$52.75

Zachary, Annalise And Lily Rowswell

$52.75

Madeline Goland

♥️

$52.75

Sandie Moore

$52.75

Adam And Zareen Coenraads

We came across your place during Xmas 2022, and your story so moved us we felt compelled to donate straight away. Thank you for sharing your daughters story with us (and our dog). We hope you have a Merry Christmas

$52.75

Jenni And Jurek

We always like to support Dainere's Rainbow Jenni and Jurek

$52.75

Catherine Brimage

our sincere apologies for missing event on 4 December.

$52.75

Anna Hayes

It is a pleasure to Support Dainere's Rainbow.

$52.75

Jennifer Cantlon

$52.40

Bruce Humphries

From selling steel to help make a difference.

$52.25

Kim Crosby

Jett Arentz

$52.20

Emindally

$52.20

Merilyn Hancock

$52.20

Threse Tranter

Worthy cause Dainere. Great masks for fundraising I love it.

$52.20

Jasmine Sharma

$51

Emma Calvert

$50

Mukesh Bharania

$50

Monique, Mark, Annie

As we were unable to hold our Gala Dinner to raise funds this year.

$41.20

Alba Agius

From Christmas Craft and Coins to help make a difference.

$40.55

Ellen Newhouse

Silver Coin Collection in memory of my precious Granddaughter, Dainere xoxoxoxo

$31.65

Helga Visser

For your anniversary. Condolences to all. Let’s safe some children in your name.

$31.65

Mrs Tammy Brown

Jett Arentz

$31.65

Helga Visser

Happy Birthday to your beautiful spirit.

$31.32

Robynn Munier

$31.32

Grace Edwards

$31.32

Jessica Eustace

$31.32

Helga Visser

$31.32

Kate Taylor

Amazing fundraising for an amazing cause :)

$31.32

Helga Visser

Let progress be made in Dainere’s name.

$31.32

Helga Visser

$30

Anonymous

Sending lots of love xo

$30

Corinne Hedditch

For Charlotte, as always... 💞🩷💞

$26.38

Helga Visser

$26.38

Michael

$26.38

Rebecca Minty

So sorry for the loss of your beautiful girl. Sending wishes to your family.

$26.38

Jennifer Hutchison

$26.10

Madelyn Love

$26.10

Deb Little

What wonderful work you do ❤️

$26.10

Letitia Hobday

$26.10

Scott Cass-dunbar

$26.10

Steph Boxall

thanks for the masks!

$25

Nat Gastineau

$25

Bryan Parsons - Arentz Cards

$20.88

Helena Williams

$20.88

Ninetta Mccauley

$20.88

Jasmine Webb

$20.88

Rhonda Miller

Good luck with your fundraising

$20

Jarrett Anthoney

From my book Anthony Christmas Bear to bring hope and create change just as Dainere wished xoxo

$16.70

Morgan Galbraith-hamilton

$15.66

Lexi Hayward

$15.66

Anonymous

$15

Callaghan

$10.44

Morgan Galbraith-hamilton

$10.44

Lizabeth Lipscombe

$10.44

Chelsea Williamson

$10.44

Anonymous

$10.44

Nicole Croker

$10.44

Caitlin Horan

$10.44

Danielle Harrison

$10.44

Adam George

$10.44

Tom Griffith

$10.44

Jimmy Mackenzie

Thanks Bron Collins!

$10.44

Andrea Kemp

$10.44

Carrie Andersen

Carrie – Arentz Cards

$10.44

Sylvia Mezei

$10

Tomas Rodriguez Lovibond

Thanks for the lovely mask!

$10

Clare Melvin

$8.35

Sophie Cazabon

$8.35

Beverly Clark

$8.35

Anonymous

$8

Guthrie

$5.28

Anonymous

$5.22

Kiahna Kosseck

$5.22

Sarah Hubbard

$5.22

Anonymous

$5.22

Beverly Clark

$5.22

Mateo

$5

Grace Guthrie

$5

Corinne Hedditch

For Charlotte... 💗 🩵 💗

$2.64

Anonymous