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>Hi all, 
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<div>I’m setting this up to try to raise some funds for my brother Nathan Wilson.
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<div> He is extremely hard working and as decent as they come. He has recently been diagnosed with a malignant melanoma and is currently undergoing immunotherapy treatment
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<div>to try to smack it on the head. This however is rendering him unable to work  so
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<div>funds as we know especially at this time are hard to come by. 
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<div>More so when you can’t work to support your family. I’m asking for everyone’s generosity to reach in and see
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<div>if they may be able to help support Nathan while he chips away and kicks this crap
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<div>in the arse. Any help will be much appreciated. And I thank you dearly for any assistance.
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<div>Cheers,
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<div>Simon Wilson
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Help a brother out

<div>Anybody who knew Steve 'Scoobs' Biggs is feeling shocked and saddened by his sudden passing on Saturday 30th May.
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<div>Steve was one of those people you could always count on, Mr. Dependable. A devoted husband to Mel, a proud and loving dad to Kaili, Montana and Thomas, a much loved son in law to John and Brenda, and a loyal friend to many.
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<div>He was the sort of bloke who showed up when you needed him, asked for little in return, and left a lasting impression on everyone fortunate enough to know him.
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<div>The support shown to Steve’s family and the way his friends have rallied together is a reflection of the respect and affection we all had for him. In the aftermath of Steve’s passing, a lot of people have wondered how they can help.
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<div>To ensure those wishing to contribute something can, in a simple and meaningful way, this single fundraising page has been established on behalf of Mel, Kaili, Montana and Thomas.
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<div>Funds raised through this page will go directly to Steve’s family to be used in whatever way they feel is most meaningful and beneficial in the months and years ahead.
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<div>Whether that’s creating special memories together, taking a family holiday, supporting future opportunities for the kids, or simply giving them some breathing room as they navigate life without Steve.
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<div>Thank you for keeping Steve’s family in your thoughts during this incredibly difficult time.
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Supporting Mel, Kaili, Montana and Thomas.

<div>As many of you know, our dear friend Renee is about to begin the most challenging chapter of her health journey yet. To access the life-saving care she needs, Renee will soon leave her husband, Brad, and their four children in Mildura to undergo 33 sessions of radiation treatment in Melbourne.
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<div>This is a battle Renee has fought before. After facing cancer three years ago, she is now dealing with a rare head and neck cancer. This news is a heavy blow for a young family who have already given so much to the recovery process. Furthermore, Renee carries the profound emotional weight of having lost both of her parents to cancer. We want to ensure she feels held by a community that refuses to let her face this history or this recurrence alone.
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<div><strong>Managing Complex Care at Home</strong>
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<div>Adding to the family’s daily challenges, Renee and Brad’s youngest daughter, Brigitte, lives with Type 1 Diabetes. Managing T1D in a toddler involves constant monitoring and high-stakes medical complexity.
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<div>With Renee in Melbourne and Brad solo-parenting while working, the need for stability is paramount. Part of this fund will go toward ensuring Brigitte can access consistent daycare. This provides her with a vital routine and, most importantly, puts her in the care of medically trained educators who can manage her T1D needs during the day. This support will provide Renee with the peace of mind she needs to focus on her own survival, knowing her youngest is safe and stable.
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<div><strong>Renee’s work</strong>
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<div>Renee is also a dedicated nurse. This’ a role that brings her great purpose and is a significant part of her weekly life and income. During treatment, she will need to step away from nursing, something she loves deeply, while also losing her ability to earn during this period. This is another layer of pressure the family is navigating alongside treatment.
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<div><strong>A Collaborative Circle of Care</strong>
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<div>Because Renee’s friends and loved ones are geographically spread across many different areas, providing traditional “hands-on” support is a challenge. Our goal is to create a coordinated, collaborative circle of care. By centralizing our efforts through this fund, we can provide the high-level support Renee needs from afar, bridging the distance between us all and the family home in Mildura.
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<div><strong>Where Your Heartfelt Donations Go</strong>
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<div>We are asking for any contribution you have the capacity for. Every dollar reduces the immense mental and physical load on Renee and Brad.
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<div>While Renee is in treatment (6.5 weeks):
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<div>• Specialized Support for Brigitte: Assisting with the costs of daycare to ensure Brigitte has a medically safe, routine-filled environment while Brad is working and keeping the family at home afloat.
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<div>• Nutritionally Dense Meals: Fresh, premade meals for Renee in Melbourne to ensure she stays nourished when she is too fatigued to cook.
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<div>• Safe Daily Transport: Uber credits for her daily trips to the hospital, sparing her the exhaustion of public transport.
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<div>• Support for the Kids: Weekly grocery deliveries to the family home in Mildura.
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<div>• Maintaining the Home: A regular cleaner in Mildura to help Brad manage a household of four children and the complexities of T1D management.
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<div>Through the Recovery Phase:
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<div>The journey doesn’t end with the final treatment. We want to continue food and cleaning support for several weeks once Renee returns, giving her the grace to recover in a peaceful, supported environment.
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<div><strong>Every Bit Counts</strong>
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<div>Renee is always the first to step up for others; now, it’s our turn to carry her. If you aren’t in a position to donate, a simple share of this page is an incredible way to help.
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<div>Thank you for your kindness, your prayers, and for showing this family that they are not walking this long road alone.
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<div>Love Kate and Kirby 
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Supporting Renee: Strength for a Mother of Four

<div>My name is Bo and I’m raising money to help Simon get his radiator fixed so he can get back on the road for his delivery job!
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<div>Simon was diagnosed with cerebral palsy at the age of 4 months old. He receives only $400pw via the disability pension and earns a living through delivering for Uber Eats.
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<div>Recently, Simon has had major car issues and after spending thousands at numerous mechanics, they still can’t fix his radiator.
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<div>Lets raise $1k to replace his radiator, fill up his car and get him back earning an income! 
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Help Simon Get Back On The Road

<div>Whilst Miss Independent Katie is not going to be comfortable with this, we feel this is the best (only) way we can help.
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<div>Poor Koben has had serious ongoing medical issues and after a painfully long wait, he has finally received his liver transplant this month.
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<div>Everything was going really well but unfortunately another hurdle including a collapsed lung and further tests etc.
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<div>With the tireless stays and trips back and forwards to the Royal Children’s Hospital, plus needing to take so many days off work, we thought a helping hand to cover some costs could ease the burden for Katie, Koben &amp; Ayla.
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<div>If you can spare a couple of dollars, please donate, every little bit counts.
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Koben’s liver transplant and ongoing care

<div>My name is Mark skinner, I’ve set up this go fund me page to help Shimmy and Liz Neylon from longlea in vic,to help them continue their well deserved trip around Australia. Their 4wd caught fire . The car and all belongings were desecrated to ashes within minutes . Cameras ,laptops ,fridge ,phones, clothing . Not to mention the much loved 4wd . This tragic event has left them with that hollow lost feeling we all know. Every dollar will help lift spirits and enable them to continue. As we all know they are earthy forward payers who wouldn’t ask for anything. The farm they operate is a fantastic nucleus to all friends and relatives. Please reach into pocket to help on this odd occasion. Much appreciated in advance and Thankyou all very much .❤️let’s make their life long trip a wholesome one to remember and be completed. All donations go to our account to be transferred to them as they have lost all devices .
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Shambala and Liz’s fire destroyed car fund

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<div><strong>HELP US HELP JASON</strong>
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<div>On Saturday May 6th, Jason Lindhorst experienced a tragedy that would change his life forever. Driving home from a fish fry at his step-brother Steve’s land, Jason and his mother were hit head-on by a speeding three-quarter ton truck. It darted across the median and catapulted into his front driver’s side, completely demolishing Jason's one-ton dually. Even though he was driving with reduced speed due to a storm that night, Jason never saw it coming. An off-duty police officer that was following the other truck witnessed the accident and was able to quickly circle back and call for help. Tragically, Jason's mom, Elizabeth McWhorter, did not survive the impact.
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<div><strong>WE ARE RAISING MONEY TO HELP JASON WHILE HE HEALS</strong>
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<div>The left side of the truck collapsed on Jason, crushing his body and causing life-threatening injuries. Jason was trapped in his truck for 45 minutes before first responders were able to get the jaws of life and cut through the steel rubble to free him. He was taken to John Peter Smith Hospital, a nationally ranked Level One trauma hospital in downtown Fort Worth. Jason arrived at their trauma center around 90 minutes after the initial impact. Once doctors were able to stabilize his urgent injuries, they started working on his broken body.
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<div><strong>OVER 35 FRACTURED BONES</strong>
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<div>Doctors were unsure if they would be able to save Jason's left arm or leg. He had a severe compound break just above the left wrist. He shattered his left shoulder socket, broke his left hip, and four ribs. His left ankle was crushed and both bones in his lower leg had also torn through the skin.
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<div>In addition, Jason broke two vertebrae, both kneecaps and had compound breaks to both his right arm and right lower leg. He had multiple cuts to his head and face that required many stitches. He sustained a concussion, ruptured his spleen, and had an airbag burn on the left side of his face.
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<div>Jason had seven surgeries in that first week. He has had five more surgeries since then. The JPS doctors and nurses from his first admission came to check on Jason in the days to follow and said they had never seen someone with so much trauma survive.
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<div>After the initial life-saving surgeries, the outstanding surgeons at JPS moved on to trying to save Jason's arm. They had to remove muscle from his right thigh and transplant it to his left forearm in hopes that his fingers will be functional. They grafted skin from his left thigh to cover the wounded area. Jason's most recent surgery was to replace his shattered shoulder.
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<div><strong>$250,000 GOAL</strong>
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<div>The driver of the other truck had minimum insurance coverage. Jason's health coverage through his employer will cover the majority of the hospital bills, but he was only able to take paid time off through June 2nd. Health insurance will continue to be paid through July 28th, at which time he will need to pay COBRA for up to 18 months until he can find another job.
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<div>Jason is going to need extensive physical rehab that is anticipated to last at least a year. The loss of his mother and the change in his mobility are going to take a heavy toll on him, not only physically, but also mentally. He is going to need time and support to process what has happened. We are hoping to generate funds to help cover physical therapy, medical and living expenses that insurance is not going to cover. Our goal is $250,000 to help him bridge this shortfall in coverage.
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<div><strong>PRAY FOR JASON</strong>
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<div>Let this be a reminder to us all that every day is a gift. Join us in praying for Jason's full recovery and remember to live each day to the fullest, hug the ones you love, and help those that are less fortunate along the way.
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<div><strong>DOCTOR'S NOTES</strong>
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<div>Injuries/Repairs In The Order They Occurred
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Jason Lindhorst Medical Fundraiser

<div>Update from the Caldwell family. Saturday 26th August 2023.
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<div>Hello good people! We’ve been trying to put together this update for weeks, sorry! 
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<div>Many of you have mentioned you’ve been waiting for it.  We’re approaching 4-months in Harriet’s SCI journey. 
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<div>Oh, we can’t tell you how good it is for us to all be back home together again! It’s all those creature comforts; our beds, our fireplace, our shower, the fresh country air, our own coffee, our pets, and the familiar faces in our community! 
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<div>It’s wonderful to catch up with family and friends and we hope to see a few more good folks as things sort themselves out in time.
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<div>All the caring conversations, check-in’s and general banter is a real feel-good for us! 
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<div>We truly feel the support and enjoy sharing Harriet’s updates with you beautiful souls. 
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<div>Day by day, we continue to find and settle in to our new normal, juggling a return to business, alongside Harriet’s very busy schedule of Physio, strength training through Exercise Physiology, Hydrotherapy sessions, and a gradual return to school which she had been pretty nervous and uneasy about, but it’s another box ticked now! 
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<div>Aside from the obvious big emotions at times, Harriet’s in great spirits, always smiling, and working hard. Her progress continues to improve, however maybe slightly at a slower rate in recent weeks. All along, we have had to remind her how well she is doing and that the process to walking shall be a slow process.
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<div>As parents, we want the best for our kids and would do anything for them, but it’s a hard reality when you can’t just fix this one for her. 
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<div>And then, at times, we have to listen to our own advice, reminding ourselves that it’s just one day at a time on this long road to recovery. 
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<div>So it’s that rollercoaster ride we are on - You can get pretty down when you allow yourself to think that maybe this is as good as it gets, after no real obvious improvement for a few weeks and that maybe a positive attitude can only get you so far…. And then, that rollercoaster goes back up! 
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<div>Harriet had a freak day a week or so ago, where for the first time she managed to ride the exercise bike without holding on, which proves that her core strength is activating! 
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<div>Then after a week of trying, she stood up out of a chair by herself!! There was pure grit and determination all over her face, all while laughing at the same time! She was so proud of herself! 
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<div>We have a couple of trips back to the Royal Children’s Hospital over the next couple of weeks for a follow up MRI, tests and a Neurology review, so fingers crossed the location of the stroke in her spinal cord will show less trauma now. Time will tell. 
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<div>It’ll be great to catch up with our Physio team down there! 
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<div>Sending love - Team Caldwell! X
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<div>Update from the Caldwell family. Saturday 8th July 2023;
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<div>Greetings! Well, we’ve just clocked over the 9-week mark in Harriet’s Spinal Cord Injury (SCI) Journey here at the Royal Children’s Hospital.
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<div>Harriet continues to show improvement in her grueling battle to regain the ability to walk again!
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<div>She was given Botox injections in her left calf a bit over a week ago, which seems to be assisting her movement. It initially relaxed the muscle enough for her to be able to straighten her knee and push her heel down, and then ultimately allows all the muscles in her left leg to strengthen!
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<div>With her strength and determination, she has pushed herself to be able to now walk small distances on a walking frame, and gave crutches a little go in Physio this week. (Just enough to put a few tears in her old dads eyes!) She’s determined to practice and develop her ability, so she can move around home on them with confidence, instead of in her wheelchair at times.
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<div>Talking of home… We were all able to return home last weekend for a night, which was wonderful. It was good to test a few things out regarding access and general mobility around the house.
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<div>There’s been a real lot of boxes to tick before we can safely and confidently bring our girl home. Discharge has just yesterday been confirmed for 2-weeks time - bringing our stay here in Melbourne to 11-weeks!
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<div>Harriet is so (beyond) happy that she can return home to Bendigo and continue her Physio and Rehab! (However, we are all feeling already, that it will be bittersweet leaving her unbelievable Physio and OT ‘family’ here!) We’ll look at adding more schoolwork into her schedule then too.
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<div>Every day throughout Harriet’s stay, her Physio’s, OT and Allied Health staff have really encouraged her love of basketball, having her grab the ball at the end of most sessions, transfer into a sports wheelchair and take herself out to the court, where we all shoot hoops over and over.
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<div>After being convinced by the staff to accept an invitation to join a Para-Sport Wheelchair Basketball session at the High Performance Centre at the Essendon Hangar, Harriet (&amp; Darci) spent yesterday afternoon learning some skills and playing a game.
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<div>We were pleasantly surprised when we were approached by a guy from the Australian Institute of Sport (AIS) who wanted to have a chat with us about her remarkable ability to still consistently shoot hoops from a wheelchair and the skills she’s already developed. Whether it leads to something with development for Harriet one day or not, it was an amazing experience, that’s for sure!
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<div>As we count down the days left of hospital life, we want to loudly echo again, just how much your love, support, prayers and faith in our family have helped us through our time here and Harriet’s fight to walk again!
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<div>By the time we depart, it will be just short of 3-months… yet seriously feels like a lifetime!
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<div>Despite this, we’ve met a lot of other kids and their families here, and have heard what they’ve had to endure over not just months, but years…
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<div>And although we’ve felt that heartbreak too now, we’ll always remember this time fondly and with very thankful hearts.
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<div>Our most genuine huge thanks for being there for us! ❤️ Seeya soon! X
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<div>Hey folks, here’s a quick update, 5-weeks on in our new norm’ at RCH Melbourne.
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<div>Harriet is working hard every day to get her body stronger, and her legs functioning enough to stand and eventually walk again.
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<div>Our days are very busy, going between Physio, OT, strength exercises, hydro, gym and other specialized activities in an attempt to fast track a road to recovery…
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<div>She is doing very well with her core strength and is able to do some pedaling on both a FES bike and a recumbent bike once her legs are strapped in.
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<div>Her right leg is getting stronger every day and she has perfected her transfers in and out of a chair/bed.
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<div>Her left leg that was completely paralyzed, with no reflex at all for the first few weeks, has now gained toe &amp; ankle movements and some leg control.
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<div>The Functional Electrical Stimulation (FES) bike has started to locate a flicker in her hamstring muscle which we can only hope may lead to more signs of muscle movement and regeneration over time.
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<div>With a custom AFO fitted to her left foot/calf, and a specialized support brace to stop her knee from collapsing, she is now able to pull herself up to stand with and take small, slow, supported steps between parallel bars.
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<div>We (Harriet in particular) can’t wait until the day she can improve enough to move back home and continue her rehabilitation back in Bendigo.
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<div>She is strong, brave and resilient, and so very determined to walk again, so digs deep every day in her journey!
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<div>As Harriet’s parents, we are beyond proud of the way she gets on with every day, pushing herself, gritting her teeth, strains, shakes, sweats, breathes, sheds a tear out of pure frustration and then pushes all over again…. Inspirational to say the absolute least!
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<div>The prize at the end of this journey is bigger than any medal or trophy… it’s the chance to be a regular kid again.
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<div>We are blessed to have so many wonderful people in our lives - words don’t do any justice to the support you have given us- our truest heartfelt thanks to every one of you.
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<div>There’s hundreds of people to hug and shake hands with… Lots of love! ❤️
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<div>We are fundraising for Harriet Caldwell and her family.
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<div>Harriet is a happy and active 13-year-old girl who loves playing Basketball and Netball.
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<div>Outside of attending school at Victory Christian College, Bendigo, she enjoys spending time with her friends &amp; family, being with her pets and is always keen to take on creative art projects.
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<div>Three weeks ago on May 4th, Harriet was stretching at home, preparing to go to basketball training, felt a pop in her lower back and immediately felt her legs go numb and couldn’t stand up.
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<div>From Bendigo ER, she was transported to the Royal Children’s Hospital, where after a full week of traumatising and invasive testing on the Neuro ward, it was discovered she had suffered a Spinal Cord Infarct (Stroke).
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<div>Spinal Cord Strokes in children are extremely rare, with only 3 cases seen at the Royal Children’s Hospital over the last 20 years.
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<div>Harriet was informed of the heartbreaking news from the team of Neuro specialists that she may never walk again and had to mentally prepare herself for a lifetime confined to a wheelchair.
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<div>Words cannot describe the heartbreak, tears and utter devastation of the next week as any parent could only imagine.
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<div>Some good news came from the brilliant Physio team who have been able to find some positives from the strengthening of her right leg and her left leg has seen her able to wiggle her toe and on occasions, ankle, which gives us all hope and positivity that little wins may continue over time.
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<div>She has began her rehabilitation journey and remains in the Royal Children’s Hospital for her long road to recovery.
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<div>Due to the busy daily Rehab &amp; OT schedule, Tim and Rhiann are required to be present and very hands-on with Harriet in the Rehab ward and are unable to run their mobile coffee business to the capacity that they normally would.
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<div>Along with everyday living away from home costs, travel, a mortgage, ongoing business expenses and accumulating bills, there will also be a need for additional equipment to support the family in caring for Harriet.
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<div>Tim and Rhi have always shown their generosity to their community in times of need and this is now our opportunity to support them.
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<div>All the messages of love, support and prayers are truly appreciated. X
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The Caldwell family

Steve McCulloch

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Vault on success card payment method

Platform is iOS v11.0.0 and above

Desktop users

Person ids

United States (US) users

allow yuno fundraisers for test

Mexico country code

Posters INTL

NPO Profile Opted-In

iOS at or above 12.4.0

non-US recurring donors

Canada Campaign Owner Group

Fundraiser Without Meta Link

Scheduler payment tester gorup

charityCommunityId

Charities allow to be claimed unclaimed (PRD)

Canada (CA) users

currencyCode

UC Tipping v20250115 International

pymk_production_xplr_fe_team

Android at or above 12.2.0

Profile photo entry point audience

smart goals (fundraiser/manage) on test01

Activity Tracking v1 Beta Testing

writePath

Stream Notification

start gfm intl allowed locales

Platform is iOS v11.2.0 and above

unclaimed charities

prod_ach_audience

AI Chatbot Audience

amp13 only new funds (prod) (anyword auto)

UC Flow Enabled (Prod)

Payment Identity Beneficiary Verification - Production

shared notification bell audience

Custom users

ach frontend audience

Android v11.0.0 and above

Users Receiving Payments Paused Notifications

smart goals test01

Manage Coach - US English Organizers Only + new funds only

Team EGG - IP Address list

Fundraiser Without Instagram Deep Link

Native 11.4.0 and above

UC Tipping v20250107

Users Receiving Braze KYC Validation Failed

Native 11.3.0 and above

Influencer - Prod

US fundraisers and US users

ai_title_page

anyword

openai

control

manual_entry

userEmail

template_id

userId

fundUrl

isCharityCo

email

appVersion

shouldBucketIntoExperiment

partnerId

donationCadence

isActiveFundraiser

isPartner

isMobile

npoProfileOptIn

fundIsLinkedWithMeta

hasSessionDonation

isCampaignOwner

fundHasInstagramDeepLink

Native 11.4.0 and higher

New funds eligible - Video Sharing (PROD)

GB Donation Upsell audience 

Auto Thanks V3 Rollout Audience

Thank you V3 testing whitelist

isRecurringFriendly

Is Recurring Friendly

Excluded funds - Video Sharing

Logged In Users

CH Donation Upsell audience

Android v10.6.0 and above

userCurrencyCode

Localized Currency

v11.5.0 and above

testAudience

pathname

Survicate

appVersion is at or above 12.8.0

Non-charity fund

isChallengeFundraiser

challenge-fundraisers

Payment Identity Launch Verification - Production

New funds eligible - Posters v2

CAD Donation Upsell Audience

Steve McCulloch

Steve McCulloch

Featured causes

Help a brother out

Supporting Mel, Kaili, Montana and Thomas.

Supporting Renee: Strength for a Mother of Four

Help Simon Get Back On The Road

Koben’s liver transplant and ongoing care

About me