Jimmy  Darts

SB Mowing

Pattie Gonia

Little Miss Flint

Kalina Silverman / @makebigtalk on Instagram

Samuel Weidenhofer

Patriotic Kenny Foundation

Ben Saunders - Flawless Cleaning

The Dogist

Peter Bond

Amy Jandrisevits

Ask Uncle Jack

That Good News Girl

Tess Bohne

FowlMouthFarmer

Latonja and Taylor Richardson

Officer Richard Craig

Flavor Flav

John Wolfe

Khloe

<div>This year Jo Parish turns 80! Ever since I can remember, mum has talked about Sweden...their healthcare, their architecture, design, public policy...you name it, she loves it! She worked in Sweden as a young nurse and has not been back since. And so it came to be that we decided we would go there together (mum, Tim and I) so she could enjoy Sweden all over again and show us what her dreams are made of. 
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<div>With this Go Fund Me page, I'd like to raise money for mum to fly to Sweden. It was supposed to be Stockholm 2020 but it will have to be 2022 instead! Mum is up for it, we're up for it and raising money for a ticket to Scandinavian heaven would be extremely helpful. 
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<div>We plan to present this money to her on her birthday with a card including everyone's well wishes. If you can chip in a little or a lot, we would be most grateful. 
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<div>Helen and Tim. 
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<div>xo xo 
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Jo Parish - Stockholm 2022!

<p><strong><img src="https://d2g8igdw686xgo.cloudfront.net/44738310_1654166346421572_r.jpeg" width="100%" media_type="3" alt="44738310_1654166346421572_r.jpeg" />Filmed over 7 years in Northeast Arnhem Land, Luku Ngarra - The Law of the Land is a powerful  and intimate journey into the world of the Yolngu First Nations of Australia.</strong><br /><br />At its centre is a remarkable man, Rev. Dr Djiniyini Gondarra, who has been a tireless beacon for freedom and justice for Indigenous <br />Australians for the last 40 years, as well as a highly respected clan leader, traditional lawman and spiritual leader. <br /><br />The film will deeply challenge audiences' understanding of traditional Yolngu Law, the crisis currently facing remote Aboriginal <br />communities today, and offer a better way forward that upholds the dignity, respect and sovereignty of the oldest living culture in the<br />world.<br /><br />It offers viewers a fascinating exploration of traditional Yolngu culture and law, and how it is completely at odds with the dominant <br />mainstream paradigm. By opening big questions that require a humanitarian response, audiences will be compelled to question their <br />own world and the views that come with it. <br /><br />The film is a timely vehicle of wisdom from one of Australia's most respected Indigenous Elders, that addresses the challenges of our times with soul and compassion.<br /><br />Its director, Sinem Saban (<a href="http://www.ourgenerationmedia.org" target="_blank" rel="noreferrer noopener">Our Generation Media</a> ), has been closely interwoven with the Yolngu of Northeast Arnhem Land for more than 20 years, and directed the award-winning and groundbreaking documentary on Aboriginal rights - Our Generation (2010). <br /><br />The Luku Ngarra project is entirely independent, and is now at post-production stage, for which it is seeking funds for completion.<br /><br />Once the sufficient funds have been raised, the film will be passed onto the award-winning editor Tania Nehme (<em>10 Canoes, Charlies <br />Country, My Name is Gulpilil</em>) for the fine cut edit, and then color grade and sound master.<br /><br />We welcome any contribution you can make to this important film.<br /><br />We also accept tax deductible donations through Documentary Australia Foundation.<br /><a href="https://documentaryaustralia.com.au/project/luku-ngarra/"><a href="https://documentaryaustralia.com.au/project/luku-ngarra/" target="_blank" class="" rel="nofollow noopener noreferrer">https://documentaryaustralia.com.au/project/luku-ngarra/</a></a><br /><br />If you feel moved, please share this fundraising campaign far and wide.<br /><br />If all goes well, we will have a September 2022 launch at the Darwin Festival and then start screenings across the country.<br /><br />With our sincere gratitude for your support,<br /><br />Sinem Saban, Director /  Producer and<br />Rev Dr Djiniyini Gondarra, Producer<br /><br /><strong>'Dr Gondarra gently places audiences in their heart space, and without divisiveness, has an incredible way of shedding light on things that are gravely unjust, not only for Indigenous Australians, but all humanity.'  - Director Sinem Saban</strong><br /><br /><strong>THESE FUNDS WILL BE USED TO:</strong> <br /><br />1. Fine Cut edit with Tania Nehme <br /><br />2. Color Grade<br /><br />3. Sound Master,<br /><br />5. Licensing of Music and Archives,<br /><br />5. Education Package (made free for all teachers to use the film in schools)<br /><br />To find out more about the film, please visit the website:<br /><br /><a href="http://www.luku">www.lukungarrafilm.com</a><br /><br />
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Luku Ngarra: Documentary Post Production

Eleanor began her treatment for Stage Four High Risk Neuroblastoma in Jan 2018 after a large tumour was discovered on her right adrenal gland. Eleanor along with her mum and dad, Jacqui and Rob, had to uproot their lives in Tasmania and move to Melbourne immediately to receive treatment at The Royal Children’s Hospital. Approximately forty children are diagnosed with Neuroblastoma each year in Australia. This extensive treatment regime was scheduled to last between 18 months to two years. <br /><br />Eleanor’s frontline treatment included chemotherapy, surgery to remove tumours and her right kidney, a stem cell transplant with high dose chemotherapy, radiotherapy, and immunotherapy. Eleanor had an incredibly tough treatment journey. Her main complication came after her stem cell transplant which affected her lungs so badly she had to be placed on breathing life support for nearly a week and her life was very much in the balance.<br /><br />After overcoming hurdles and showing immense resilience, Eleanor had received clear scans in April this year showing she had no evidence of disease. To keep disease away we enrolled Eleanor in the clinical drug trial, Difluoromethylornithine (DFMO) a cancer pathway inhibitor. This is designed to increase long term survival for children with Neuroblastoma. We were enrolled in the DFMO clinical drug trial from April to July this year. <br /><br /><strong>Unfortunately two weeks ago at Eleanor’s three month post treatment follow up scan, a new tumour was discovered in Eleanor’s right frontal lobe on her brain.</strong> She has now been diagnosed with a central nervous system neuroblastoma relapse. Our world has been turned upside down again. Our beautiful daughter has once again fallen victim to this relentless disease. Prior to her scan she was doing so well. She had just enjoyed her third birthday surrounded by her beloved family in Hobart. She was loving being back home in Hobart with her new baby brother George.<br /><br />A week after the tumour was discovered, Eleanor had major brain surgery to resect it. The surgery was successful but the frightening reality is that some neuroblastoma cells remain in the central nervous system and require therapy to stabilise and hopefully prevent further spread. The treatment starts this week and includes chemotherapy and radiotherapy. Eleanor will need a new central drug line and nasogastric feeding tube as she will be unable to eat. This treatment will occur in Melbourne.<br /><br />The all familiar nightmare has returned. We have again had to uproot our lives to live in Melbourne indefinitely. We have had to leave our jobs once again to focus on Eleanor. But this time it feels so much worse that our original diagnosis in January 2018. Back then we were naive and filled with hope of following a treatment path that most children respond to. Hearing horrendous stories of the unlucky children who would relapse was a reality, but we chose to focus more on being positive and thinking that would not be Eleanor. This nightmare now becomes the most sobering reality. Generally, children who relapse have an extremely low chance of surviving, let alone with an extremely rare relapse to the brain. Our hearts are filled with deep sadness.<br /><br />If Eleanor’s disease remains stable she will be eligible for a clinical drug trial of 8H9 antibody that targets and attacks neuroblastoma cells in the central nervous system. The antibody therapy is the only hope to cure Eleanor’s relapsed neuroblastoma. Central nervous system relapse is incredibly rare and traditional chemotherapy and radiotherapy is used as palliative treatment. We want to cure Eleanor and give her the best chance of living a full and happy life. The 8H9 protocol is deemed the best, and possibly only chance to achieve this. The 8H9 protocol is not available in Australia, only in hospitals in the US and Barcelona, Spain.<br /><br /><strong>Please support Eleanor in reaching her goal to receive the 8h9 antibody. This treatment is available at three hospitals in America and we desperately need to raise the funds to get her there. For an entire neuroblastoma central nervous system relapse protocol in New York, we have been quoted $2,200,000. Yes that’s correct, two point two million dollars! Completely unattainable. We have found two other hospitals that are more affordable. We need to raise $300,000 to get Eleanor this life saving treatment. We are unable to work and really need your support to help us reach our goal. We are begging everyone to please help our Eleanor fight for her life.</strong><br /><br />Note: We are awaiting a final quote and decision on funding from the drug company and hospitals that are running the trial, we are hoping that some of the costs may be covered by the drug company. Until we know that, we have chosen the lower of the two quote amounts to fundraise for as we can't wait till the end of this round of Australian treatment to find out if Eleanor will get into the trial to then suddenly raise money.  Any money not needed directly for this 8H9 protocol trial will be used to cover the time off work, travel and other expenses that the family is going to need over this period.  If there is any leftover money that isn't needed we will donate to children’s cancer research to try and help other families embarking on this terrifying journey.<br /><br />This fundraiser was set up by Stuart Gillies on behalf of Robert, Jacqui, Eleanor and George Oakley. All fund are being sent directly to their account.

Eleanor's Fight

Molly Shorthouse

<div>We are reaching out to share the story of Max, a beloved friend to many, who is facing an incredibly difficult journey. Max was recently involved in a serious road accident in Bali, leaving him with multiple serious injuries.
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<div>Thank you to the doctors in Bali who saved Max’s life.
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<div>Max's mother, Astrid, a solo parent with no relatives, has been by his side every step of the way. However, this situation has placed immense pressure her. As the sole caregiver for Max, Astrid is now unable to work, leaving her without the financial means to support their daily needs. To make matters worse, the insurance company has stopped covering Max's medical expenses, even though his treatments and rehabilitation are far from over.
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<div>Right now, Max is facing medical bills and multiple therapies to help with his recovery. 
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<div>Max is enrolled at the Green School in Bali, where he has been thriving. He is loved by his teen friends, teachers, and parents, and his gentle and kind spirit touches everyone he meets. His beautiful mum, Astrid, is equally adored for her devotion, humor, and determination.
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<div>Green School is a nurturing and safe place for Max and remaining in his home is an essential part of his brain injury recovery. They only live a few footsteps away from the school and The Green School community has become their extended family. However, the school fees are an additional financial burden, and without the means to pay, they may have no choice but to be home-schooled. This isolation would be a worst-case scenario for Max’s healing journey.
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<div>This is where we ask for your help. We are hoping to raise funds to cover the following:
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<div>●	Ongoing medical costs and treatments for Max’s recovery.
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<div>●	Daily living expenses for Max and his mother, as Astrid cannot work while caring for him.
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<div>●	Green School tuition fees, so Max can continue his education at the best school in the world.
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<div>Every little bit helps, and no donation is too small. Your support will go directly to ensuring Max receives the care he needs and that Astrid can continue to care for him without the added stress of financial worry.
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<div>Thank you from the bottom of our hearts for helping Max and Astrid during this incredibly challenging time.
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<div>With love and gratitude,
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<div>Friends of Max&amp; Astrid
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Please Help Teenager Max after Serious Road Accident in Bali

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Molly Shorthouse

Molly Shorthouse

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Please Help Teenager Max after Serious Road Accident in Bali

Jo Parish - Stockholm 2022!

Luku Ngarra: Documentary Post Production

Eleanor's Fight

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