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>Title: Help LimitlessLindy Reclaim Her Life After Losing over 500 Pounds!
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<div>Story:
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<div>Hi everyone,
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<div>My name is Todd Bockness, host of @TheCarnivoreCure, and I’m reaching out on behalf of my extraordinary friend Lindy Barker who has overcome unimaginable odds. You might know her as LimitlessLindy, a true inspiration to thousands in the weight loss and carnivore communities.
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<div>Lindy’s journey has been nothing short of miraculous. At her heaviest, she weighed 800 pounds. Through sheer determination, relentless drive to be here for her girls, she has lost over 500 pounds—an accomplishment few can even fathom. But as inspiring as her journey has been, it hasn’t come without its challenges.
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<div>The next step in Lindy’s transformation is life-changing skin removal surgery. This procedure will allow her to move more freely, avoid health complications, and live her life with the confidence and comfort she deserves. Unfortunately, due to financial constraints, Lindy is on the verge of postponing this surgery—or worse, not pursuing it at all.
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<div>As her friend and a cohost of 700 Plus and Counting Down, I know she might be upset with me for organizing this fundraiser, but I also know how deeply she deserves this opportunity. Lindy has spent years uplifting and motivating others to pursue their own Carnivore health journeys. Now, it’s time for us to show her that same love and support.
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<div>The cost of this surgery is significant, but together, we can make it happen. Every donation, no matter the size, will bring Lindy one step closer to the freedom she has worked so hard to achieve.
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<div>Please join us in helping LimitlessLindy take this final step in her incredible journey. Let’s show her that she’s not alone and that her community stands with her.
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<div>Thank you so much for your support—whether through a donation, sharing this campaign, or keeping Lindy in your thoughts and prayers.
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<div>With gratitude,
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<div>Todd Bachness
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<div>Founder, The Carnivore Cure
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Limitless Lindys Skin Removal Surgery

<div>Hi there. My name is Anthony and I was diagnosed with stage 4 Gist Cancer (gastrointestinal stromical tumor) in 2022.
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<div>In July of that year I went in to emergency surgery to have the softball size tumor removed from my stomach and intestines. Unfortunately by then the cancer had already metastasized to my liver and I was given 6 months to live after they realized the cancer had been in my body for 6 years undiagnosed.
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<div>I went through 130 days straight of chemotherapy which almost killed me. The chemo turned all of my hair white, caused severe issues with my kidneys and heart causing me to have seizures and mini heart attacks.
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<div>January 31st of 2023 they told me that the chemo had made the cancer worse and spread more. That is when I decided to quit chemotherapy and start changing my lifestyle. I started going to the gym even though my energy levels were down significantly. I’ve done several different 3 month trials with diets including vegan, plant based, carnivore, etc. but I found out I am allergic to a lot of vegetables and every diet I tried fed the cancer except the carnivore diet so that is what I have stuck with. I'm now 26 months carnivore and tumors are stable and some are shrinking.
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<div>Right now I am not able to work and am having a hard time affording the bills to get to all of my appointments. I have several out of town appointments and even out of state appointments that I need to raise money to make happen.
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<div>Furthermore being how chemotherapy almost killed me and the natural approach (the metabolic approach) is extending my life and maken me feel better and cancer is under control, I definitely need help/assistance with continuing the path I'm on!!
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<div>To make myself more venerable I'll be 100% honest. The cancer and surgeries (I've had 5 total since 2022) have disabled me for the time being, and the saddest part is that the disability I receive doesn't cover my normal bills let alone all the cancer related stuff.. I'm currently living in a 5th wheel travel trailer because thats the cheapest option i have besides being homeless at this point in time. I use propane to heat, cook with, and to shower with. The propane is 1 of my biggest expense per month (far is winter time goes). P.s for anyone local to Clallam County Washington you can goto Mount Pleasant IGS (Port Angeles) and they have a sheet for me for prepaid propane/diesel for me from those who want to donate local to help!
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<div>This metabolic approach has cost me everything financially I've had. I've sold everything I've could that's not important to me or that I don't use on a regular bases. Any help financially or even sharing my story/ go fund me is appreciated!!
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<div>Thank you all for your well wishes, positive thoughts, support, shares, prayers, and all the help you all have done for me. I wouldn't be alive still without the support that I've received from every one!!
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<div>P.s. for those interested in my progress and entire storyline, you can find me on social platforms such as Facebook: Anthony Hayduk and YouTube is:
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<div><a href="https://youtube.com/" target="_blank" rel="noreferrer noopener"><a href="https://youtube.com/" target="_blank" class="" rel="nofollow noopener noreferrer">https://youtube.com/</a></a>@anthonysmakencancermybitch?si=Dy0OfwSMbDhGTf6f
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<div>I can't thank everyone enough for the kind words, the encouragement, the prayers, shares and donations! I'm glad to be able to inspire so many people throughout the world do work on their health and mindset.  I'd hope and pray anyone in my position would do the same!!!  
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<div>The biggest issue I've understood (my opinion) about cancer is as a whole, Noone goes after the root issue, they treat symptoms and suppress the immune system which jeopardizes the quality of life and freedom of people, where the metabolic approach helps quality of life and gives back some freedom. I speak of my own experiences on that ❤️
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Support Anthony's Fight Against Gist Cancer (updated)

<div>Sadly Kurt passed away today 5/24/24.
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<div>Katie and her family are grieving the loss of such a wonderful soulmate, father, grandfather, son and friend to many, many people in our community.
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<div>Kurt N. Smolek, 50, of Westfield, WI (formerly of Francesville, IN and Medaryville, IN) passed away peacefully following a brief illness on Friday, May 24, 2024 at St. Mary’s Hospital in Madison, WI. He was born on September 7, 1973 in Denver, CO to Theodore and Phyllis [Ewing] Smolek. Kurt was a 1992 graduate of West Central High School in Francesville and a 1995 graduate of Purdue University. He continued his education at Madison Area Technical College and University of Wisconsin. Kurt married the love of his life, Katie, on September 14, 2002. He was a proud father to their three children and an even prouder papa to his grandson. Kurt lived in Northwest Indiana until 2008, and in 2009, the family joined him in Wisconsin. He was an inventor, author, and business owner. Kurt loved fishing and couldn’t wait for the yearly family fishing vacation. He also loved football, sports cards, and just being by the water somewhere. Kurt enjoyed meeting and talking to everyone, especially in the shop he and Katie created two years ago - Sasquatch’s Variety Shop in Princeton, WI.
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<div>He is survived by:
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<div>Katie Smolek, Wife
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<div>Trevor (Emily) Hammond, Son
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<div>Hannah Smolek, Daughter
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<div>Bret Smolek, Son
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<div>Jack Hammond, Grandson
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<div>Arden and Phyllis [Ewing] Bathke, Parents
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<div>Many beloved relatives and friends
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<div>He was preceded in death by:
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<div>Theodore Smolek, Father
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<div>Lisa Bathke, Infant Sister
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<div>Robert and Alma Ewing, Grandparents
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<div>James and Opal Smolek, Grandparents
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<div>Otto and Hilda Bathke, Grandparents
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<div>Many beloved relatives and friends
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<div>A Celebration of Kurt’s life will be held on Sunday, June 2, 2024 from 2:00 to 6:00 PM (CDT) at Steinhaus-Holly Funeral Home in Westfield, WI.
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<div>A Celebration of Kurt’s life will also be held on Monday, June 10, 2024 from 2:00 to 6:00 PM (EDT) at Frain Mortuary Querry-Ulbricht Chapel in Medaryville, IN.
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<div>In lieu of flowers, memorial contributions may be made to the family c/o Katie Smolek.
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<div>WISCONSIN SERVICE;
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<div>A Memorial service will be held on June 2, 2024 from 2:00-6:00 pm at Steinhaus-Holly Funeral Home and Cremation, Westfield, WI
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<div>INDIANA SERVICE;
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<div>A second Memorial service will be held in Indiana on Monday June 10th 2pm to 6pm est
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<div>Frain Mortuary Querry-Ulbricht Chapel
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<div>Medaryville, Indiana
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<div>We ask that you keep the Smolek family in your thoughts and prayers. Please continue to share this go fund me page even more now in hope to receive further donations to help with not only the medical bills but the funeral expenses.
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<div>Please hug your family a little bit more and appreciate what you have, because tomorrow isn’t promised.
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<div>God Bless!
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<div>Our family is raising money for Kurt &amp; Katie Smolek. Kurt had been admitted in the hospital with severe medical conditions that came on suddenly. He has been in the hospital for almost a two weeks and in that time, Katie has been unable to work due to Kurt’s ever changing medical conditions. In that time he coded was in dire need of medical intervention. His family is suffering financially and the medical bills have been piling up along with no income for the family.
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<div>We are personal friends of this wonderful family are asking that you please pray for the entire Smolek family while they are dealing with the devastating loss of Kurt. If you could please help by donating to our cause by helping this selfless family who gives and gives back to our community, it would be so much appreciated. God Bless!
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Support Katie with Medical Bills & Funeral Expenses

<div>Meet Shane and Amy, a loving couple united not just by love but by an extraordinary journey of overcoming adversity. Both are blind; Shane has been so since birth, and Amy lost her vision due to diabetes. Together, they face life's challenges with grace, strength, and determination.
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<div>On June 15, 2023, they began a new chapter in their lives by embracing the Carnivore Diet, a decision that has led them to better health and well-being. Their story is one of triumph, resilience, and inspiration, as they have found joy and vitality in a lifestyle that nourishes their bodies and souls.
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<div>But life has thrown a new curveball at Shane and Amy. Shane's work hours have been significantly reduced, making it increasingly difficult for them to afford the quality meat essential to their Carnivore Diet. This setback, however, has not dampened their spirit or commitment to their health.
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<div>In return for your support, Shane and Amy plan to share more and more YouTube videos of their inspirational journey. They'll document their experience navigating the Carnivore Diet sightless, offering a unique and heartening perspective on resilience, health, and life.
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<div>What Your Donation Will Do:
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<div>Provide Nutritious Food: Your contribution will enable Shane and Amy to purchase the quality meat necessary for their Carnivore Diet, supporting their ongoing health and wellness journey.
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<div>Empower Their Independence: By helping with their dietary needs, you are empowering Shane and Amy to lead an independent, fulfilling life despite their unique challenges.
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<div>Spread Inspiration: Shane and Amy's story is one of inspiration and determination. By supporting them, you are joining a community that believes in overcoming adversity and celebrating human spirit.
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<div>Whether you can contribute financially or simply share their story, your support means the world to Shane and Amy. Together, we can make a difference in their lives and encourage others to embrace resilience, hope, and transformation.
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<div>Thank you for your kindness and generosity. Please continue to follow Shane and Amy's journey here and on their YouTube channel.
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Help Shane and Amy On Their Carnivore Journey

<div>Hello, I'm Kerry. I've personally experienced a profound transformation through the Proper Human Diet, and now, I want to share this life-altering journey with the world. I'm setting out to create a comprehensive documentary that uncovers the incredible potential of the Carnivore Diet, showcasing real-world examples from real people. I need your help.
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<div>"Healing Humanity The Power of a Proper Human Diet" aims to explore the impact of the Diet through real, heartfelt stories of individuals battling various health issues. Over the course of a year, we will document their progress, showcasing the tangible effects of this diet on their physical and mental well-being. Additionally, we'll incorporate expert insights from doctors who champion the the Proper Human Diet to provide scientific context and understanding.
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<div>But creating a documentary of this magnitude requires significant resources. From equipment, post-production, and professional consultation, to ensuring our participants' health and safety throughout this journey - the costs add up.
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<div>That's why we're asking for your help. Your donation will not only help fund the production of this eye-opening documentary but also enable us to bring these transformative stories to light. No contribution is too small, and every bit of support brings us a step closer to our goal.
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<div>For those who can't contribute financially but still wish to help, please consider sharing our project within your networks. The more people know about our cause, the more likely we are to reach our funding goal.
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<div>Join us on this extraordinary journey of transformation and discovery. Your support will not only help us create this documentary but also could potentially change countless lives.
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<div>Thank you for your time and consideration.
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<div>Best,
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<div>Kerry
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Healing Humanity: Proper Human Diet Documentary

<img src="https://d2g8igdw686xgo.cloudfront.net/52377150_1604620160567324_r.jpeg" alt="52377150_1604620160567324_r.jpeg" width="100%" media_type="3" />Logan waking up after his first cast. <br /><br /><br />Logan was born March of 2013 - and we thought we had every new parent's dream - a happy, healthy baby. For a few months he grew, he ate, he met and blew past his milestones, and then it came time to sit upright.. and he had a lean. We thought it was a balance issue, but it never self-corrected. At 8 months old, we took Logan to the doctor and found he had a very large spinal curve - and was diagnosed with Infantile Progressive Scoliosis - We don't know why this happened, we don't know what caused it.  His spine just started to curve, and wants to keep going. We suspect, but have not yet been able to confirm yet, that he has Ehler's Danlos Syndrome, (Mom has it too). Many kids with EDS have scoliosis early on. <br /><br />At a year, we had an MRI done under anesthesia - it showed us the detailed curve (at 60 degrees) but no definite reason why. He started treatment at a local Richmond, Va. hospital, which included them putting him on a table (that looks a lot like a medieval torture stretching rack), under anesthesia, forcibly straightening his spine, then wrapping him up in a body cast from armpit to hip bone. We got some correction, but nothing that truly held fast, a few days out of his cast, and he was back to our curvy little guy. <br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/52377150_1604623040748998_r.jpeg" alt="52377150_1604623040748998_r.jpeg" width="100%" media_type="3" />His most recent x-ray. 10/28/20<br /><br />For the next 4 years, we went through THIRTEEN more casts. We transferred hospitals, to a hospital in Philadelphia, 5 hours away. Each time we'd get a little correction, but the doctor warned us that we were 'kicking the can down the road' for surgery. We accepted it, and trudged along, missing time from work, putting our little guy under anesthesia repeatedly, missing time from school. <br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/52377150_1604622538573345_r.jpeg" alt="52377150_1604622538573345_r.jpeg" width="100%" media_type="3" />Silly man showing us his "Happy Face" despite being encased in fiberglass webbing. <br /><br /><br /><br /><br />At 5 we could no longer reliably get any good corrections from casts, so we were forced to stop, with his curve at 49 degrees. We've tried bracing, but his curve has been slowly progressing. At our last visit, he was at 65 degrees. We are getting to the point where we can no longer 'kick the can' any longer.  70 degrees is the cut off for our doctor to want to operate. The farther it goes, the more vertebrae have to be involved.<br /><br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/52377150_1604622756904668_r.jpeg" alt="52377150_1604622756904668_r.jpeg" width="100%" media_type="3" />Logan and one of his buddies. <br /><br />We have two choices now. We can put Logan through growth-rod surgery. This involving opening him up directly beside his spine, implanting growth rods (called MAGEC rods) alongside it, anchoring it in place, to force his spine straight. Every 4 months we'll have to take him back up to Philadelphia so they can lengthen the rods (with magnets, done externally) to go along with his growth. <br /><br />Insurance will cover this. It is a reliable method of correcting scoliosis. The issues come when you factor in the probable Ehler's Danlos (EDS), which causes serious problems with healing, and his age. Growth rods have a 2-3 three year life span, and then need to be replaced. Logan, because he's so young, is looking at 2-3, possibly 4 sets of these, each requiring their own surgery, risks, and recovery. At the end, Logan will end up with a partially fused spine. Some of it fused by growing around the growth rods, and a large chunk fused by the doctors to hold his spine straight after removing the rods. <br /><br />Our second choice is why we need help. There is another surgery available. It is called Vertebral Body Tethering (VBT/ASC). The hospital Logan is currently treated at offers it, but they have very strict criteria and Logan is 'too young' by their standards. If he qualified, we would not be in this financial situation. There is another surgeon, the one who pioneered VBT/ASC surgery and got it FDA approved, and he has performed this surgery on kids even younger than Logan, and with far larger curves, with fantastic results.  <br /><br />Instead of facing the likelihood of 5-6 major spinal  surgeries, (MAGEC rods have issues, they break, they cause skin problems, etc.), Logan would be facing JUST two. The original VBT, and the likely possibility of a revision much later in his childhood, after the majority of his growing is done. Even better, instead of a 12"+ incision, it is just a 4" incision in his side. Then there's the BEST part - NO spinal fusion at the end. He won't start out his adult life with his mobility and flexibility already limited. <br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/52377150_1604624604113496_r.jpeg" alt="52377150_1604624604113496_r.jpeg" width="100%" media_type="3" /><br /><br />The problem is insurance. Our insurance will cover the hospitalization, and everything up to the surgeon's fee. He's out of network, and they will pay only a tiny amount. <br /><br />We're still waiting to hear what the bottom line will be. From what we've been told, the worst case scenario: We'll owe $50,000 for just this surgery, then face another later, 6-8 years down the road. The amount is staggering to us, but if we have even the chance to turn 5-6 surgeries, each with a week stay in the hospital, and the pain of recovery, into just 2, maybe even one.. We have to try. <br /><br />We're going to do everything in our power to raise this money by taking equity from our home, savings, etc. but Mom is disabled, and the financial burden of the family is already carried solely by Logan's Dad.  <br /><br />We need help to cover the costs of the surgeon's fee.  We need help to cover the costs to treks up and down to New Jersey, and the costs of the stay when the time comes for the surgery. He'll be in the hospital at least a week. Anything that is donated will be used for that purpose. If we cannot raise it all, and are forced to go with the MAGEC rod surgery, the money will go to the same medical costs, just in a different direction. (Costs of staying in the hospital and future care.) <br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/52377150_1604623102526304_r.jpeg" alt="52377150_1604623102526304_r.jpeg" width="100%" media_type="3" />Logan and his best buddy, his kitten, "Nintendo" <br /><br />Throughout all of this - Logan has shown us what true strength is. From the first time he woke up with this.. THING on him.. he had to learn to balance again with a new center of gravity and a cast that added 20% to his body weight at first. He'd stumble, and fall, but even at 14 months old, he'd get up, dust himself off, and try again. He had to learn how to do things again, as a toddler, without being able to bend at the waist. It has NEVER stopped him for a second, and he has remained our happy, loving, guy. If anything we think it has made him more determined. <br />He rarely wanted any help, preferring to figure things out for himself, but he knew when it was time to ask.. and taking a page out of his book, we realize that we need help to help him. <br /><br /><br /><img src="https://d2g8igdw686xgo.cloudfront.net/52377150_1604624482564470_r.jpeg" alt="52377150_1604624482564470_r.jpeg" width="100%" media_type="3" />Chillaxin' waiting for the Doc. <br /><br />We would greatly appreciate any help that you can give us towards helping our son get the best chance at living a life with as few problems related to scoliosis as we can possibly give him. This economy isn't fabulous, and we understand that. If you cannot help financially, sharing on social media would mean a great deal to us.

Help Fund 7 yo Logan's Spinal Surgery

Kerry Mann

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<div><strong>Help Transform Diabetes Care: Support the American Diabetes Society</strong>
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<div>Visit our website to donate!
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<div><a href="https://www.americandiabetessociety.org/" target="_blank" rel="noreferrer noopener">American Diabetes Society website</a>
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<div>If you would like to volunteer send your resume to support @ drberry . com
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<div><br />
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<div><strong>What Sets ADS Apart?</strong>
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<div>It has become clear that the American Diabetes Association has failed people with diabetes on multiple levels.
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<div>The ADS is different...
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<div><strong>Unwavering Transparency</strong>: We commit to full transparency in our operations. Every donation, financial statement, and fund allocation will be openly available on our website, ensuring you know where our donations came from, and exactly how your contributions are being used.
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<div><strong>Independence from Big Industry</strong>: The ADS will never accept donations from big-food or big-pharma companies. Donations exceeding $10,000 will require board approval, maintaining our unbiased commitment to your health. Our advice to people with diabetes will never be swayed by million dollar donations.
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<div><strong>Practical Support</strong>: Our website will offer low-carb recipes and lifestyle tips that genuinely help lower blood sugar levels, and keep your blood sugar normal.
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<div><strong>Research for the Future</strong>: We are dedicated to funding critical research aimed at finding a cure for type 1 diabetes and proven methods to help those with type 2 diabetes reverse their condition with minimal or no medication.
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<div><strong>Education and Advocacy</strong>: We will educate healthcare professionals on the most effective diabetes management techniques and advocate for dietary changes in hospitals, long-term care facilities, and schools to prevent and improve diabetes more effectively.
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<div><strong>Public Policy Influence</strong>: ADS is set to challenge and change the public perception and policy regarding diabetes, advocating that type 2 diabetes is preventable and reversible, and that type 1 diabetes can be managed with significantly less insulin, and fewer hypoglycemic episodes.
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<div><strong>Your Impact</strong>
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<div>By donating to the American Diabetes Society, you are not just giving money; you are supporting a movement to transform diabetes care and prevention. Your contribution will help us:
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<div>Educate and train healthcare providers to improve patient outcomes.
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<div>Develop resources for effective diabetes treatment, reversal and prevention.
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<div>Advocate for healthier food choices in public institutions, including schools and hospitals.
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<div>Encourage and support research that will lead to breakthroughs in diabetes care.
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<div><strong>Join Us in Making a Difference</strong>
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<div>Every donation brings us closer to a world where diabetes can be effectively improved, reversed or even eradicated. Your support is vital in helping us provide these life-changing services. Together, we can ensure that every person with diabetes—or at risk of developing it—receives the best possible education, care and support.
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<div>Donate today and be a part of a healthier tomorrow. Your contribution will change lives, improve lives and save lives.
</div>
<div><br />
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<div><strong>People with Diabetes Deserve the Truth - Donate Now!</strong>
</div>

Join The ADS in Revolutionizing Diabetes Care

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Fundraiser Saved Payment Method Rate Limit Bypass (Production)

leaderboard-partner-id-audience-givepanel

New funds eligible - Video Sharing (PROD) (amp17)

Version 9.2.1 and above

AUD Donation Upsell audience

fundraiserCountryCode is US/EN

Austria (AT) users

DAF Internal

Netherlands (NL) users

Platform is iOS v11.0.0 and above

Desktop users

Person ids

United States (US) users

allow yuno fundraisers for test

Posters INTL

iOS at or above 12.4.0

non-US recurring donors

Fundraiser Without Meta Link

email

Scheduler payment tester gorup

Ireland (IE) users

charityCommunityId

Charities allow to be claimed unclaimed (PRD)

Canada (CA) users

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

start gfm intl allowed locales

United Kingdom (GB) users

Platform is iOS v11.2.0 and above

NPO upsell education category

unclaimed charities

prod_ach_audience

AI Chatbot Audience

amp13 only new funds (prod) (anyword auto)

Payment Identity Beneficiary Verification - Production

shared notification bell audience

 Custom users

Sweden (SE) users

userEmail

public_profiles_redesign_prod_test_audience

ach frontend audience

Norway (NO) users

Android v11.0.0 and above

Users Receiving Payments Paused Notifications

Excluded funds - Video Sharing (amp15)

smart goals test01

Manage Coach - US English Organizers Only + new funds only

Team EGG - IP Address list

Fundraiser Without Instagram Deep Link

ai_title_page

anyword

openai

control

manual_entry

template_id

userId

fundUrl

isCharityCo

appVersion

shouldBucketIntoExperiment

partnerId

isMobile

fundIsLinkedWithMeta

hasSessionDonation

categoryGroup

isCampaignOwner

fundHasInstagramDeepLink

Native 11.4.0 and above

checkout headers audience

Native 11.3.0 and above

Native 11.4.0 and higher

New funds eligible - Video Sharing (PROD)

NPO email opt-in candidates

GB Donation Upsell audience 

Auto Thanks V3 Rollout Audience

Thank you V3 testing whitelist

Excluded funds - Video Sharing

Fundraiser Without Instagram Deep Link (amp15)

NPO upsell animals category

NPO upsell disaster relief category

Logged In Users

CH Donation Upsell audience

Android v10.6.0 and above

NPO upsell essential needs category

NPO upsell medical category

userCurrencyCode

Localized Currency

NPO upsell cancer category

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

iOS App Version

Kerry Mann

Kerry Mann

What Kerry cares about

Kerry’s featured causes

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Limitless Lindys Skin Removal Surgery

Support Anthony's Fight Against Gist Cancer (updated)

Support Katie with Medical Bills & Funeral Expenses

Help Shane and Amy On Their Carnivore Journey