Jimmy  Darts

SB Mowing

Pattie Gonia

Little Miss Flint

Kalina Silverman / @makebigtalk on Instagram

The Dogist

Samuel Weidenhofer

Patriotic Kenny Foundation

Peter Bond

That Good News Girl

Ben Saunders - Flawless Cleaning

Flavor Flav

Ask Uncle Jack

Amy Jandrisevits

FowlMouthFarmer

Tess Bohne

Latonja and Taylor Richardson

Officer Richard Craig

John Wolfe

Khloe

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 This fundraiser has been created by myself, Mary, on behalf of my closest friend Madison Noble following her stage 2 breast cancer diagnosis. All funds raised are for Madison and will be used for financial support during her treatment, surgery and recovery.
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 On the 4th of August, Maddie's life was turned upside down when she received the news of her cancer diagnosis.
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 Triple negative breast cancer is not rare, however it is widely considered aggressive, so the decision to start treatment immediately was made. The treatment plan currently in place is 6 months of chemotherapy, followed by surgery and radiation.
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 Unfortunately, this has meant Maddie has had to step back from her newly established business and start weekly treatment.
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 There are no words that can truly prepare you for news like this, especially with two young children. Maddie is an amazing mother, daughter, sister and friend. She has always been the person anyone could go to for advice and support, and chances are she's given you the biggest belly laugh and smile at least once in your life. The world is cruel, and she doesn't deserve this.
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 Since sharing Maddie's diagnosis, we've been overwhelmed with love, support and messages from people wanting to help. Creating this GoFundMe felt like the simplest way to bring everyone's generosity together in one place and ease her financial pressure while she continues her treatment journey.
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 Our hope is that Maddie can focus on this journey and have the time to do it properly, without the stress of everything else life throws at her. She deserves that, and so much more.
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 Every donation, no matter the amount, will make a meaningful difference and we appreciate any donation so much we know how tough it is out there right now ❤️
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A Mum’s Fight Against Breast Cancer

Mallacoota is in the heart of the devastating bushfire region of the Gippsland region of Victoria Australia. This region, as with multiple parts of rural Australia has been struck by raging bushfires and these continue to threaten communities, families, the town, residents, tourists and of course animals and wildlife. We are raising money for the Mallacoota Wildlife Shelter who are currently working to assist and support wildlife in the area. Monies raised will be used for: - Emergency relief and support of animals in the Mallacoota region - Continued support and rehabilitation of animals at the shelter 100% of all money raised will be donated directly to the Mallacoota Wildlife Shelter. 100% of all money raised will be used for the emergency relief and ongoing support of the animals at the Mallacoota Wildlife Shelter. Photographic updates will be provided. Direct commentary will be provided. Confirmation of donation from founders of Mallacoota Wildlife Shelter and Local Government Representatives will be provided. Please support the shelter in any way you can. If you cannot donate please visit the shelter’s page and leave a “like” and comment of support. <a href="https://m.facebook.com/Mallacoota-Wildlife-Shelter-183833965703647/" target="_blank" rel="noreferrer noopener">Mallacoota Wildlife Shelter</a> ——— This Gofundme page is being organised by Leon and Silke Hayes, Directors of Melbourne based technology company Smartsensor Technologies Pty Ltd. <a href="https://www.facebook.com/solarbins/" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.facebook.com/solarbins/</a> The relief page will be co-contributed by the founders of Mallacoota Wildlife Shelter as soon as they are available.  The shelter has been contacted with complete identification and information provided. An initial donation has been made by the organisers of this page. Organisers can be contacted on 0408 060 827. Photo credit Mallacoota Wildlife Shelter

Mallacoota Wildlife Shelter Fire Relief Fund

Lisa has been given the prognosis that anyone would never want to hear, being, that her condition is now TERMINAL. Her life expectancy is a matter of months. The Cancer has spread substantially and aggressively throughout her lungs and skull. Anyone that has had the privilege to have this Lisa in their lives is nothing short of blessed. I don’t remember my life before Lisa and I sure as hell do not want a life without her, and I am confident in saying most of you would feel the same. We are not going to accept this prognosis, which is why we need your help. Lisa was diagnosed at 22 years of age, she is now 26. Never once has she ever complained or looked for sympathy even when she was devastatingly faced with loss of eyesight, had her drivers licence suspended, suffered memory loss, learned to walk again, suffer difficulty with speech and cognitive functions, to only name a few. She hid all this from the world with the people only closest to her knowing what she was dealing with. Through every grim diagnosis and only weeks after each surgery she turned up to work every day personality with a positive attitude, always looking to make others smile. This is why it is now time for the community to get behind Lisa and help save her life. Lisa’s Timeline of events: Diagnosed July 2015 – Brain Cancer Brain Operation - July 2015 Radiation - September 2015 Chemo - September 2015 to May 2016 Cancer Relapse – December 2016 Brain Operation - December 2016 Cancer Relapse - September 2018 Brain Operation - September 2018 Radiation - September 2018 Cancer spread to Lungs – July 2019 New treatment commenced – August 2019 (unsuccessful) Cancer spread to Skull – October 2019 7 x Lung tumours continue to grow despite treatment– October 2019 Terminal Diagnosis – October 2019 Current day: We are now at a stage where we are looking at all available options to save Lisa’s life. What we know, is the next form of treatment is going to be a costly exercise. This involves sending Lisa overseas to a medical treatment facility in Mexico. How can you help? The only way to access the treatment needed is to pay for it. There is no government assistance or anyway of subsidising this cost. This is why we are asking people to help in the form of donating funds. This is not a cheap option, but our only one. We need a minimum of $150K for this treatment which will cover intensive therapy, future supplementation and medication to save her life. This is how this campaign was born. It’s called the '150K FOR LIFE CAMPAIGN'. As you can understand, Cancer does not work to a timeline. This is why we need these funds immediately as every day we wait, Lisa’s cancer progresses. Time is of the essence. We are reaching out to anyone who can help us save Lisa's life!

TERMINAL I HELP US SAVE LISA I 150K FOR LIFE

This is the hardest post I have ever had to do my world has been rocked tonight I said good bye to my best friend and soul mate taken from me way to soon it’s a very tough moment so rather than fielding phone calls and message I’m putting it up so all my friends and family can see Jacinta foulds my beautiful wife lost her fight as she was extremely sick with influenza a as a result she caught a secondary infection as well as pneumonia and it was to much for body to handle she fought hard all the way to the end as expected from the Jacinta we all know sorry if I don’t reply to message I’m really struggling and am trying to hold it together for my 3 kids Jacinta Foulds taken to soon and forever in my heart and soul rip my true love

Dan and the children will need all of our help.

On January 21st 2017 our lives changed forever.  My husband Peter was rushed to hospital failing to walk or talk, suffering pain throughout his entire body.  After enduring 7 long weeks in 2 hospitals and 7 different specialist wards, he underwent countless scans, biopsies, infusions and drugs, finally establishing, the diagnosis of a rare double auto immune disease called Sarcoid like Myositis. Already diagnosed with lupus, fibromyalgia, haemachromatosis and bipolar, the auto-immune disease diagnosis result has left Peter and my family in a catastrophic situation. <img class="not-resizable" src="https://d2g8igdw686xgo.cloudfront.net/24399070_1509329222.276_funddescription.jpg" alt="" width="100%" /> Sarcoid like Myositis is an incurable and debilitating, rare, double auto-immune disease. Myositis alone, presents itself in the form of inflammation of the muscle tissue, which the body's immune system is attacking and destroying the muscle cells. The mere presence of inflammation causes weakness, which initially, being a tiler by trade, the disease went unidentified for months leading up to his total immobility and race to the hospital. Muscles such as the heart, lungs, swallowing, hands, fingers and lower legs (causing foot drop) were highly affected in Peter's case resulting in total inability to work. His extreme case included his vital muscles, the heart and lungs, ensuring his condition to be fatal. Sarcoidosis is the abnormal collections of inflammatory cells which form lumps, known as granulomas. With the disease beginning in the lungs, skin and lymph nodes, followed up with all organs potentially being affected, Peter was covered in a rash with extreme bruising and blood clottting under his skin. He suffered with shortness of breath, wheezing and chest pain. The rare, double auto-immune disease left Peter and our family frightened for his life, fighting the unknown and undetected disease prior to diagnosis. <img class="not-resizable" src="https://d2g8igdw686xgo.cloudfront.net/24399070_1509329254.8852_funddescription.jpg" alt="" width="100%" /> 9 months later we have exhausted all our savings, superannuation funds and none of our insurances have covered us, due to rare illness clauses in our policies fine print. Centrelink refused Disability Payments, even though Peter can NEVER work again as rare illness and experimental drugs did not tick the appropriate boxes for our application.  Medical Certificates from over 6 doctors, specialists, GP's and psychiatrists did not count either, exhausting all ability to stay afloat. Our only chance to keep our home and pay the bills was to house students which just provides enough to scrape by. Our lives have turned into chaos from 5am in the morning to 9pm at night, we take care of 2 Japanese tennis students amid countless specialist appointments throughout the days. However, this brief income is only just enough to keep the banks off our backs and selling our home is the inevitable in the New Year which will leave us homeless and unable to house students for income. We are currently on our last experimental drug which causes liver and renal failure and his fatigue keeps him in bed most days.  We attend weekly specialist outpatient appointments along with further Petscans and Bone densomitry scans as the meds are eating his organs and weakening his bones. Prognosis is terminal. <img class="not-resizable" src="https://d2g8igdw686xgo.cloudfront.net/24399070_1509421743.8539_funddescription.jpg" alt="" width="100%" /> His medications (12) different ones keep giving him various side effects and make him feel sick constantly.  With no answer in sight, we are asking for some help for us to keep our home as we would have no where to go.  We are hoping for a review with Disability which can take up to 6-8 months on appeal. Then the tribunal, but in the meantime our situation is URGENT! I don't have any gruesome pictures as whilst they were trying to diagnose  Peter we were all so distraught we did not think to photograph his situation. We have tried to keep this as private as possible, for as long as possible, but, have now reached our whits end. PLEASE HELP US It will take a miracle to overcome this, with no posssibity of survival and a sure, painful death, we pray that the loving and generous people in our community can find it in their hearts to help us make it through.

Help Me Save My Husband and My Home

On September 30,2016 Courtney was burned in a horrific camp fire accident involving gasoline.  Courtney spent 51 days in ICU Burn Unit and has undergone Many surgeries and skin grafts. The doctor estimates around 12 more surgeries in the next 2 years.  Two weeks after her release from the hospital, her husband abandoned Courtney and her four year old daughter.  This left Courtney with no income and with the severe injuries to her hands, it is uncertain that she will ever return to work.  Courtney is being forced to leave her home because of financial difficulties along with her mounting medical bills.  A small group of loving people are desperatly trying to build Courtney and Caroline a small home on her family's land. We are in very desperate need of funding forher huge pile of medical bills that keep rolling in as well as cosmetic surgery in the future to restore mouth, ear and nose to a more normal appearance.  As well as providing finances for her and Caroline a future considering their difficult situation.  You can follow Courtney's road to recovery at FB. COURTNEYS COMEBACK    Any help would be so greatly appreciated! Private donations can also be mailed to Courtney Waldon . Addess is PO Box 905 Tallapoosa, Georgia 30176

Burn Victim Courtney Cosper Waldon

Isobel John Dwyer

Isobel John Dwyer

Isobel John Dwyer

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