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Khloe

<div>Hola soy Ale o más conocido como Cocuyito playero, soy el más pequeño de los Medici Arceo 
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<div>A mis 11 meses de edad tenía un desarrollo perfecto pero ,
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<div>Como muchos saben el 8 de Diciembre del 2024 el descuido de la persona que me cuidaba terminó en tragedia, me caía a la piscina y estuve en un paro cardiaco por más de 30 minutos ( hace un par de semanas , un doctor le dijo a mi mamá que fueron 40 minutos) .
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<div>La falta de oxígeno por tanto tiempo lastimó mucho mucho mi cerebrito. Perdí todas mis habilidades , ya no puedo caminar, ni comer por boca. Incluso hasta deglutir mi saliva me es difícil. Quedé con discapacidad visual cortical y muchas secuelas más a raíz de toro el accidente.
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<div>Actualmente mis papás me llevan a terapia física 3 veces por semana, terapia visual 2 veces por semana y terapia pulmonar 1 vez por semana
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<div>Cuando salí de Terapia intensiva a mis papás no les dieron mucha esperanza pero yo he luchado mucho mucho .
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<div>Hace 2 años se hizo la primera recaudación con la cual logré mi primera ronda de células madre las cuales me ayudaron mucho a dormir mejor , y empecé a levantar mis brazos estas terapias fueron en Guadalajara , asi como terapias intensivas en Guadalajara y Querétaro .
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<div>Esta recaudación tiene como finalidad reunir el dinero necesario para hacerme otras células madre DESAWA MUSE CELLS , estas pueden ayudarme a regular mi sistema nervioso central , a reducir mi rigidez del cuerpo , a tener mayor atención y sobre todo a crear nuevas conexiones que me ayudan a mi recuperación .
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<div>Estas células tiene un costo de $260 mil pesos , y queremos potenciarlas con terapias intensivas en Querétaro , lo que queremos lograr es que vuelva a comer por boca ya que ahora me alimento por botón gástrico ,estas terapias tienen un coste aprx de $100 000 por tres semanas .
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<div>Ayúdame a llegar a la meta
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<div>A nombre de mis papás Claudio y Monica
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<div>Gracias ,gracias ,gracias
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<div>Este camino es largo , pero mientras haya vida hay Esperanza ,gracias a todo mi ejército que lucha conmigo día a día para seguir avanzando .
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<div>Y les deseo que todo lo bonito que dan regrese multiplicado 7 veces 7
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<div>#todosconcocuyito
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#Todosconcocuyito

<div>Soy Matías de  2 años tengo una malformación renal de nacimiento el cual generó que me complicará con una urosepsis ( una infección grave de las vías urinarias) y requerí  cirugía de urgencia para controlar el foco infeccioso. Ayúdame de favor a pagar mi cirugía que era vital para conservar mi vida  
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Ayuda para solventar mi urosepsis

<div>Update: We raised enough money to cover the cost for Noah's first treatment. In early October we travelled to Duke where Noah received his first round of stem cell therapy. All contributions will now go towards Noah's subsequent stem cell infusions and related therapies. If we surpass our goal, we will be able to afford more treatments.
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<div>Noah is a triplet, born on June 1, 2024, at just 25 weeks gestation. As a micro-preemie, the odds were stacked against him from the start. Noah's first month in the NICU was uneventful, but on July 11th, everything changed. At just over a month old, Noah was rushed to BC Women’s and Children’s Hospital for emergency surgery. What we thought would be a single procedure turned into the first of seven surgeries he would need. Doctors discovered a strangulated inguinal hernia. Thankfully, the surgery saved his intestine—but Noah’s struggles were far from over.
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<div>Shortly after the surgery, his lung collapsed and Noah could not get enough oxygen. While he fought for his life, the doctors asked us to make the impossible choice: to continue care or let him go. We chose to keep fighting. We could not give up on our son.
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<div>Following this, Noah developed a volvulus that required four additional surgeries. In the end, he needed surgical silo and then an ostomy bag, with the hope of reversal surgery once he grew stronger.
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<div>Noah spent a total of 195 days in the NICU. During that time, his lung collapsed again, depriving him of oxygen.
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<div>The lack of oxygen caused brain damage, and an MRI revealed Periventricular Leukomalacia—injury to the white matter of the brain. Doctors told us Noah would never walk or talk, and that he would face severe cognitive challenges. He has since been diagnosed with Cerebral Palsy, with a prognosis described as “severe.”
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<div>Since coming home from the NICU, Noah has been hospitalized twice due to respiratory distress, throwing more hurdles in his way. There is no cure for Noah’s brain injury. The only proven treatments are therapies that help him build strength and skills, little by little.
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<div>However, there is hope. Emerging research on stem cells is showing promising results. Noah has been given the rare opportunity to participate in the expanded access protocol at Duke University, a treatment that may improve his motor function and quality of life.
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<div>But we can’t do this alone. The treatment, travel, and care costs are overwhelming for our family. We are asking for your support to give Noah the chance he deserves—the chance to reach his fullest potential and to experience a brighter future.
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<div>Every donation, no matter the size, brings us one step closer to hope for Noah. Thank you for being part of his journey and for helping us give our little fighter the best chance at life.
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Hope for Noah: Life-Changing Stem Cell Treatment

<div>Dear friends, family, and compassionate strangers, I’m reaching out with a heavy heart to share the devastating story of my best friends, Natasha Ward and Louis McGuire, and their three incredible children—Cruz (5), Willow (4), and Blaze (2)—along with their beloved Labradoodle, Mocha. This family is trapped in a nightmare no parent should face, fighting to save their kids from a life-threatening fungal infection caused by toxic mold. They need our urgent help to save their children’s lives and rebuild their future. Please, read their story and join me in giving them hope.
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<div>A Home That Became a Death Trap
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<div>Natasha and Louis moved to Las Vegas for a fresh start, renting a home they believed was a safe haven for their kids to grow and play. But it hid a deadly secret: toxic black mold (Stachybotrys chartarum and Aspergillus fumigatus) lurking in the walls, carpets, and air vents, poisoning the air their family breathed. They had no idea until their children started falling dangerously ill.
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<div>It began with rashes on Cruz and Willow, and Blaze, misdiagnosed as eczema, that turned into burning, blistering sores. Fevers, vomiting, and crippling fatigue followed, stealing their joy. Little Blaze, only two, suffered the worst—struggling to breathe and enduring terrifying seizures that left Natasha and Louis helpless as his tiny body shook. Even Mocha, their loyal service dog and the kids’ best friend, began coughing, developing rashes, and losing her energy.
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<div>Natasha and Louis raised concerns about mold early, pointing out visible signs and begging for action. Their pleas were dismissed, and they faced resistance when they persisted. Desperate, the family paid for a mold test, revealing a horrifying truth: their home was a toxic trap, with dangerous mold contaminating their furniture, clothes, and air. A judge later declared the house unlivable, but the damage to their children’s health was done.
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<div>A Life-Threatening Crisis: Invasive Pulmonary Aspergillosis
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<div>Cruz, Willow, and Blaze are battling invasive pulmonary aspergillosis, a deadly fungal infection caused by prolonged exposure to toxic mold. This is not a mild allergy—it’s a systemic infection attacking their lungs, blood, and nervous systems. Blood tests show dangerously high Aspergillus levels, causing severe rashes, respiratory distress, and neurological complications. Blaze’s seizures are the most heart-wrenching, risking permanent brain damage or worse. Their lungs show early signs of interstitial lung disease, a scarring condition that could lead to chronic respiratory failure. Even Mocha is suffering from mold-related illness.
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<div>Medical experts warn that invasive aspergillosis in children has a 30-50% mortality rate if treatment is delayed or interrupted. Without immediate, consistent care, the infection could invade vital organs, causing irreversible damage or death. The stakes could not be higher.
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<div>Their Lifeline: Voriconazole
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<div>The only hope for Cruz, Willow, and Blaze is Voriconazole, a potent antifungal drug that fights the Aspergillus infection. It’s their best chance at survival, but it’s brutally expensive: $1,688.42 per child every two weeks, totaling over $5,065.26 every 14 days for all three. They need this medication for at least 26 weeks—a staggering $131,696. 76 that insurance won’t cover. The drug is harsh, causing nausea, headaches, and fatigue, but it’s working to save their lives. Missing even one dose risks the infection rebounding, potentially triggering worse seizures, lung collapse, or fatal outcomes. They cannot stop treatment.
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<div>A Family Forced to Start Over
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<div>When the mold test results came back, Natasha and Louis fled the toxic house, leaving behind everything—furniture, clothes, toys—all contaminated. They drained their savings on hotel stays, air purifiers, and medical tests while fighting in court. When Nevada’s healthcare system failed them, they made the brave choice to return to their hometown, La Crosse, Wisconsin, for doctors who understand mold toxicity. They’ve found a dedicated medical team, but the costs for Voriconazole, lab tests, ER visits, and a safe, mold-free home are crushing. Louis stays home to care for the kids, and Natasha is their full-time caregiver, leaving them with no income to face these overwhelming expenses.
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<div>Why We Must Act Now
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<div>This is a life-or-death emergency. Cruz, Willow, and Blaze are fighting a poison that could steal their futures—lung damage, neurological issues, or worse—if we don’t act. Natasha and Louis have exhausted every resource, but they can’t do this alone. They’re not the type to ask for help, but for their kids and Mocha, they’re putting pride aside. I’m begging you to join me in supporting them with:
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<div>•  Medical Costs: Over $80,000 for Voriconazole, plus ongoing lab tests and specialist visits to monitor recovery.
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<div>•  Mocha’s Care: Vet bills to treat their service dog’s mold-related illness.
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<div>•  Basic Needs: Replacing contaminated belongings and covering living expenses while they focus on their kids.
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<div>Every dollar brings Cruz’s giggles, Willow’s hugs, and Blaze’s brave smiles closer to returning. If you can’t donate, please share this campaign to amplify their story and raise awareness about the dangers of toxic mold. Your shares could help another family avoid this fate.
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<div>A Call from the Heart
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<div>I’ve watched Natasha and Louis hold their kids through endless ER visits, comfort Blaze during seizures, and fight for answers when no one listened. Their love for Cruz, Willow, Blaze, and Mocha is unbreakable, even as they’re pushed to their breaking point. These kids still have so much spirit—Blaze’s tiny smile, Willow’s warmth, Cruz’s energy trying to shine through. With your help, we can give them the care and safety they need to heal and thrive again.
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<div>Please, donate what you can at, share this far and wide, and keep this family in your prayers. This fundraiser is not affiliated with any rental company and reflects the family’s personal experience. Together, we can be the lifeline between survival and tragedy, ensuring no child dies from a poison in their own home.
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<div>With gratitude and urgency,
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<div>Caitlin Slater-Guggisberg, on behalf of Natasha, Louis, Cruz, Willow, Blaze, and Mocha
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Toxic Mold: A Life-or-Death Emergency

<div><a href="https://www.gofundme.com/f/2026-flood-relief-fund" target="_blank" rel="noreferrer noopener"><strong>2026 Fund Here</strong></a>
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<div>Flooding is one of the most devastating natural disasters in the US, causing billions of dollars in damage each year and displacing thousands of families. Too often we see people create fundraisers on the GoFundMe platform asking for help in the wake of destructive floods.
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<div>GoFundMe.org has launched this fund to provide direct and immediate support to those impacted by floods this year. Tax deductible donations will go to individuals and families impacted, and to the nonprofit organizations who are responding on the ground. Every dollar will go directly to the communities in need. Your support will help flood survivors begin to rebuild—stronger and together.
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<div><strong>Current Need</strong>
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<div>On December 9, 2025, an atmospheric river began sweeping through Washington state and the greater Pacific Northwest, resulting in widespread flooding and damage. We will be issuing grants to verified folks impacted as donations are raised.
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<div>On October 12, 2025, Typhoon Halong swept through Alaska’s Yukon-Kuskokwim Delta, resulting in widespread flooding and damage, and over 2,000 people being displaced. New donations raised will be granted to support this community.
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<div>We are currently raising money to support victims of the deadly flooding in Gila County, Arizona.
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<div>Torrential rain on this August caused historic flash flooding across southeastern Wisconsin, damaging over 1,800 homes and 20+ public schools. Streets, schools, and neighborhoods in Milwaukee County were overwhelmed as rivers reached record levels. Thousands of families are now displaced, schools are facing costly repairs, and FEMA is still assessing the full extent of the damage.
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<div>Over the July 4th weekend, catastrophic floods swept across Central and South Texas, devastating homes, displacing families, and leaving entire communities underwater. With little warning, rising waters destroyed businesses, washed away roads, and forced emergency evacuations. Thousands of Texans are now navigating the aftermath—mourning lives lost, cleaning up what’s left, salvaging what they can, and facing an uncertain road to recovery.
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<div>In mid‑June, San Antonio was slammed by a flash flood when over 6 inches of rain fell in just a few hours, sweeping away vehicles and killing 13 people. This marked the city’s worst flooding in over a decade, causing extensive infrastructure and road damage.
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<div><strong>Who we help</strong>
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<div>We deliver cash grants directly to those impacted by domestic floods. We grant to verified individuals who qualify and are fundraising for themselves or on behalf of someone else. We may also provide grants to fundraisers benefiting small businesses and community relief efforts, and to vetted nonprofits coordinating long-term recovery.
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<div><strong>Why donate to this fund?</strong>
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<div>We provide swift support (within a few days) to individuals and communities who are directly impacted by a flood, supporting as many people as we can. Donations to this fund are tax-deductible to the extent allowed by U.S. law. We’ll send you a receipt upon donation completion.
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<div><strong>Stay informed of our impact</strong>
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<div>We’re deeply committed to operating with transparency and strive for maximum impact. We post regular updates to this fund about how donations have helped which are emailed directly to donors.
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<div><strong>Thank you</strong>
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<div>Thank you for supporting this critical relief fund. Every single donation is meaningful, no matter how small. Together, we can show up for people in times of crisis and let them know they are not alone.
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<div>For more information, <a href="https://www.gofundme.org/wp-content/uploads/2025/07/GoFundMe.org-Flood-Relief-Fund-Overview.pdf" target="_blank" rel="noreferrer noopener">click here to review a one-pager about this fund</a>.
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<div>To donate via DAF, please select the DAF Pay option as the payment method once you click 'donate now' on this page. If you would like to donate to this Fund via stock, ACH/wire, crypto, check, or by Private Foundation please visit our <a href="https://www.gofundme.org/off-platform-donations/" target="_blank" rel="noreferrer noopener">offline donation page</a>. and we will add your donation to this fund as an offline donation so that your contribution is recognized on this Fund page.
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<div><em>GoFundMe.org is a registered 501(c)(3) nonprofit organization (EIN 81-2279757) that works to swiftly mobilize donations raised to support individuals and communities impacted by crises, natural disasters, and social inequalities. We accept tax-deductible donations from donors into funds created for a specific philanthropic purpose. From these funds, we issue grants to charitable classes of individuals, nonprofit organizations, and charitable projects.</em>
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<div><em>Donations to this fund are tax-deductible to the extent permissible by U.S. law. Money will be given to verified charitable needs at the discretion of GoFundMe.org.</em>
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2025 Flood Relief Fund

<div>Diego es un niño que aparentemente nacio con atresia de vias biliares y a los 75 dias de vida le realizaron una cirugia llamada kasai y estuvo al rededor de 8 meses inrenado y logro salir del hospital y estuvo estable un tiempo sin embargo se le formo una fistula entero biliar en donde era el drenaje de su cirugia y con el tiempo se cerro sin embargo en esa zona se le formaron varices y estas provocaron hemorragias por ersa zona. En mayo de 23 lo embolizaron en el IMSS sin embargo como secuela le resurgio la fistula biliar y por esa area ha estado sangrando desde entonces pero ahora de manera interna. Esos sangrados ya tienen mas de un año y solo lo internan y lo transfunden pero no hay un tratamiento que las mitigue y nos indican que el transplante de higado es la unica opcion sin embargo nos indican que el exito en mexico es de un 20 a 40% porque no hay recursos para los tratamientos post ransplantes y en otros paises son de 90 a 95% pero hay quie pagar por ellos y nosotros queremos luchar porque Diego reciba la mejor atencion y que las posibiliadades sean mas altas ya que tiene 9años de vida y cada vez su condicion se complica mas y no hay opciones en mexico que nos den un mejor panorama. Asi que les suplicamos nos apoyen para encontrar una mejor opcion de atencion y calidad de vida para Diego. 
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Dona para ayudar a Diego

<div>Hola me llamo Eva Tolentino y estoy recaudando fondos para mi hijo Fernando Isaac quien por segunda vez está luchando contra el cáncer, la primera vez lucho contra la leucemia y ahora tiene cáncer en un testiculo, es por eso que pido de su apoyo para poder solventar sus gastos médicos, mi hijo es un niño muy valiente que todos los días lucha por volver a vencer el cáncer, tiene sueños que quiere cumplir, por favor les pido su ayuda para que mi hijo siga viviendo. Mi hijo quiere vivir. Mi niño necesita 15 radiaciones para tener una calidad de vida buena, cada radiacion tiene un costo de $2990 pesos y son 15 radiaciones , $44,850 pesos. Pido de su apoyo para poder juntar el dinero y pagarlas y empiezan a radiar a mi hijo. Se los agradezco mucho cada uno de ustedes por su apoyo, un pesito o lo que ustedes nos puedan apoyar.
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POR SEGUNDA VEZ LUCHA CONTRA EL CANCER.MI HIJO QUIERE VIVIR

Laura Staub-Garcia

Laura Staub-Garcia

Laura Staub-Garcia

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