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>Sot na nevojitet ndihma juaj me shume se kurre . Bebet kane nevoje urgjentish te dergohen jashte shtetit per operim . Dy bebe rrezikojne te humbasin shikimin   dhe dy bebe  nese nuk marrin ndihmen e shpejt rrezikohen edhe ata po me te njejta  pasoja . Ata kane hemoragji ne syte , pasi arteriet e syve cahen . Doktoret ju komunikuan sot qe bebet urgjentish duhen te nisen brenda javes per te kryer keto nderhyrje  pasi ne Shqiperi nuk i marrin aty kujdes qe ju nevojitet dhe eshte  rrisk shume i larte . Ju lutem bejeni share sa me shume te mundeni , le te bashkohemi te gjithe qe ketyre 4 mrekullive ti shpetojme dhe te gezojne dhe shikojne jeten si te gjithe femijet . Cdo kontribut mund te shpetoje jeten e tyre 
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<div>My brother-in-law Geraldo and his wife Rozeta were blessed with quadruplets and wanted to blass them and see if we can help them with raising this beautifull kids named Roal Alroa Roar and Auro.
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<div>If you can and would like to help would be most appreciate it by them and all of family members.
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Help Geraldo and Rozeta's Quadruplets

<div>Hello, my name is Nykirah. My sister Crystal unfortunately passed away on November 4th, 2025, at the age of 27. On December 31st, 2020, Crystal was attacked and nearly fatally wounded before she was left for dead by the attacker. On New Year’s Day, we received the call that she survived the attack. After years of hard work trying to recover from said attack, Crystal suffered a stroke and was admitted to a nursing facility for better care that our family was uneducated to provide from home, until she passed in recent days. On November 5th just one day after crystals passing out mother Klena joined Crystal in heaven after finally getting rest from her battle with heart failure. 
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<div>My family is asking kindly if you could spare a moment to share this so we can raise funds to get my sister and mother cremated and brought home. All additional funds will be used to help aid my transition into living without my mother and moving out.
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Honor Crystal's Memory: Cremation Fund

<div>My name is Deontae, and for as long as I can remember, I have been a fighter. Living with Spastic Cerebral Palsy means every single day is a marathon the simple things others take for granted require my full strength and focus.
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<div>But right now, I am facing a wall I cannot climb alone.
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<div>Due to a sudden decision by my uncle to sell his house while we’re in it, my family and I are being forced to completely start from scratch.This transition is an incredible weight on us right now, especially because my mother has been diagnosed with Congestive Heart Failure. We have been left with no choice but to rebuild our lives from the ground up on a very tight deadline. For someone in my physical condition and for my mother’s recovery, a stable environment isn't just a luxury—it is a necessity for our survival and dignity.
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<div>My mission is to buy a house for my family so that our security can never be taken away again. However, due to how quickly this move is happening, we need to secure a rental immediately as a bridge while we work toward that 100% goal.
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<div>This fundraiser is designed to provide my family with a complete fresh start. While our primary goal is permanent housing, these funds will be used to cover all essential costs and unforeseen expenses that arise during this transition. This includes housing, moving logistics, household necessities, transportation, and general living expenses as we work to rebuild our lives. Your support provides the flexibility we need to navigate this difficult move and ensures we have the resources to handle any challenge that comes our way.
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Help Deontae Before It’s Too Late

<div><strong>A parent's worse nightmare is losing their child. Our daughter Lydia is 3 years old. </strong>She is so full of life. She loves playing right along side with her big sister. <strong>But her little body is dying. </strong>Before her disease takes over her body and brain damage starts to occur, we have one chance to change her fate &amp; it has to happen soon. What if money was the one thing that stands in the way of your child's chance to live? <strong>We need your help to save our sweet Lydia. </strong>**donations are tax deductible**
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/80764751_1718400734232974_r." width="100%" />
<div><strong>Our Story</strong>
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<div>When Lydia was born, we were so excited. Her big sister was so happy to have a forever best friend. Our hearts were so full. She had a perfect birth. The doctor said <strong>“she’s perfect”</strong>. We were so in love with her. We were so happy to have our new girl to take home with us. 18 months of our lives were just full of happiness. Until April 4, 2024, <strong>the day our lives changed forever</strong>.
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<div>Our sweet Lydia was diagnosed with a rare genetic disorder called <strong>Sanfilippo Syndrome </strong>type B, which is <strong>terminal</strong>. Life Expectancy not passed teenage years. Our hearts were shattered and it was a dark place I cannot even explain. How was our child slowly dying and we did not even know it?
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<div>In March, my mother sent me a TikTok of a little girl named Olivia with the TikTok account "Saving Liv". This little girl could have been my Lydia's twin. It was a gut punch when I saw the diagnosis of Olivia being a terminal illness. Of a disease I did not even know existed. So I started researching more of the disease, with symptoms that went along with it. I found frequent ear infections, sleep disturbances, distended belly, GI issues, and prominent thick eyebrows, which were all the symptoms Lydia had. The thick eyebrows were something I thought she inherited from my husband. Everyone always said "They look just alike". I knew then when I saw the symptoms, this was what my daughter had. My gut told me so but my heart told me there was absolutely no way (it is 1 in 70,000) that my baby who has met all milestones in her life and to me, was a healthy baby as I thought.
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<div>I took my concerns to our pediatrician in our hometown of Natchitoches, Louisiana. I showed him side by side pictures &amp; the TikTok I had seen. He told me "I have never been asked this before, nor have I ever seen a child with it". He told me he would have to go do research himself and come back into the room. He came back into the room and tells me <strong>"I cannot come back in here &amp; tell you she does not have it, </strong>so I will order you the genetic testing for it, but you will have to do it at another hospital because our town does not have that type of ability to test for it. I want you to assure you that this is very rare, and children come in all the time with issues not sleeping, constipation, and frequent ear infections still after tubes". I was so grateful that he listened to me, ordered us the testing, and did not make me feel crazy. We went to another hospital to have the testing done the very next day. It was a blood test and a urine test.
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<div>A week of anxiously waiting to "rule it out".... the following Thursday I pull up my patient portal to see <strong>POSITIVE MPS III </strong>(Sanfilippo Syndrome). That exact moment was the worst feeling of any day I have ever had on this earth. My heart sunk, I felt like I could not breathe. <strong>The instant feeling of "my baby is going to die". </strong>
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<div>This dark place my husband and I were in last for about 2 weeks. It was then, I was ready to <strong>fight</strong> for her. I contacted the <strong>Cure Sanfilippo Foundation</strong> to figure out what I could do as a mother to fight for her and the treatments available for her. There are no current treatments or cure approved by the FDA, only clinical trials. <strong>But there is HOPE.</strong> The clinical trials have a gene therapy treatment and an enzyme replacement therapy. In Sanfilippo Syndrome, Lydia's body is missing an enzyme that is used to breakdown sugar molecules. Without this enzyme, <strong>toxic waste build up in her body. </strong>This would explain her distended belly from an enlarged liver. That I thought was just from constipation. As the years go by and more toxic waste build up, it will start affecting her brain, causing damage, leading to her to <strong>lose or forget all of her abilities such as walking, talking, and feeding herself, </strong>everything she has already learned. This is why it is called Childhood Dementia. She will also eventually endure pain and suffering, and then die. <strong>This is 100% fatal.</strong>
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<div>Luckily, we were able to get diagnosed early because of TikTok and our pediatrician. The <strong>regression usually starts around age 3 and 4.</strong> But every child with this disease is different. This would mean we have about a year or less before brain damage begins &amp; takes over. Fast forward 18 months after we got the diagnoses, THERE NOW IS A TREATMENT OPTION. We need 6 million to fund a treatment that could be available for her as early as this summer 2026. 3.8 million by December 1, 2025 &amp; the rest by spring 2026. This is how you can help us <strong>Save Our Lydia.</strong> So one day, when my 6 year old daughter, Heidi, is able to understand, I will not have to explain to her that her little sister is going to die. The words I never want to hear is <strong>"I don't want my sister to die"</strong>. After the diagnosis, that is the moment I am dreading. She is the best big sister to her. Her sister deserves a chance at life.
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<div>As a mother, feeling helpless and knowing this disease is out of my control.. the only thing I know to do is fight for her. Fighting for her in this case is making awareness of this disease, sharing her story, fundraising, and in hopes her story will reach the world. <strong>Hoping the world will help save her.</strong> We pray everyday for this. We will never stop fighting for her. Every dollar counts. <strong>We need a miracle and this world of a community could be our miracle</strong>. Along with all the other children and families suffering with this disease and heartbreak.
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<div><strong>Our goal is to raise $6 million dollars to help fund treatments </strong>and give our Lydia a chance at growing up, a chance at life. We can't just sit back and accept that she is going to die with knowing there are treatments out there. Previous clinical trials done for Sanfilippo Syndrome have shown real promise. The treatments WORK. <strong>Our Lydia needs treatment!! </strong>This campaign for her LIFE is as urgent as it gets. <strong>It's now or never for Lydia. This is our last chance to save her life before brain damage begins. 3.8 million by December 1st. </strong>
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<div><strong>This is truly our only hope.</strong> Her story has already reached millions. People Magazine, VT, Daily News, &amp; News stations. Help us keep sharing her story. In hopes it will reach a celebrity or millionaire that will be these children's spokesperson and help fund for them. They deserve a chance at this life. A parent's love is like no other. If you are a parent, you understand.
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<div><strong>There are three things we are asking you to do.</strong> A campaign like this can grow quickly if supported and if shared with great mass. We can reach this goal if it goes viral.
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<div><strong>1. Please donate what you are able. </strong>All donations go to the 501c3 <strong>nonprofit Cure Sanfilippo Foundation</strong> (Tax ID: 46-4322131) to fund a clinical trial and are tax deductible.
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<div><strong>2. </strong>Please take a few minutes and share our GoFundMe everywhere you can. It’s really easy to do. Just click the “Share” button and send it everywhere you can. Please help this reach the right people. I know if they see it, this can happen.
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<div><strong>3.</strong> Please leverage any avenue you have to make this go viral.
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<div><strong>Thank you for making it this far in our story. I hope you are able to help save our girl.</strong>
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<div><strong><em>-Morgan &amp; Kirk</em></strong>
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<div>Other ways to donate:
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<div>-- By check: Cure Sanfilippo Foundation, PO Box 6901, Columbia, SC 29260. Include “Save Lydia” in the memo.
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<div>-- Donate via Venmo, ACH, digital wallet or digital wallet, go to <a href="https://give.curesanfilippofoundation.org/save_lydia" target="_blank" rel="noreferrer noopener"><a href="https://give.curesanfilippofoundation.org/save_lydia" target="_blank" class="" rel="nofollow noopener noreferrer">https://give.curesanfilippofoundation.org/save_lydia</a></a>
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<div>-- Make a recurring donation, go to <a href="https://give.curesanfilippofoundation.org/give/630751/#!/donation/checkout?recurring=1" target="_blank" rel="noreferrer noopener"><a href="https://give.curesanfilippofoundation.org/give/630751/#!/donation/checkout?recurring=1" target="_blank" class="" rel="nofollow noopener noreferrer">https://give.curesanfilippofoundation.org/give/630751/#!/donation/checkout?recurring=1</a></a>
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<div>-- By stock gift, email <a href="https://CureSanfilippoFoundation.org" target="_blank" rel="noreferrer noopener">[email redacted]</a> for details.
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<div>Follow us
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<div>-- TikTok: <a href="https://www.tiktok.com/" target="_blank" rel="noreferrer noopener"><a href="https://www.tiktok.com/" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.tiktok.com/</a></a>@hopeforlydia
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<div>-- Instagram: <a href="https://www.instagram.com/hopeforlydia/" target="_blank" rel="noreferrer noopener"><a href="https://www.instagram.com/hopeforlydia/" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.instagram.com/hopeforlydia/</a></a>
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<div>-- Facebook: <a href="https://www.facebook.com/profile.php?id=61561244030850" target="_blank" rel="noreferrer noopener"><a href="https://www.facebook.com/profile.php?id=61561244030850" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.facebook.com/profile.php?id=61561244030850</a></a>
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<div>For media
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<div>For additional information and photography for the media, please go to <a href="https://CureSanfilippoFoundation.org/Save_Lydia" target="_blank" rel="noreferrer noopener"><a href="http://CureSanfilippoFoundation.org/Save_Lydia" target="_blank" class="" rel="nofollow noopener noreferrer">http://CureSanfilippoFoundation.org/Save_Lydia</a></a>
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<div>Credits
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<div>Special thanks to Joe Lane of Anointed Media LLC (<a href="https://www.anointed.media" target="_blank" rel="noreferrer noopener"><a href="https://www.anointed.media" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.anointed.media</a></a>) for lending his tremendous videography, video edit, music and audio editing skills, and passion to this project.
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Save Lydia

<div>While driving through Nashville with my parents, we came across Clark—a disabled veteran who recently lost his apartment and financial stability. I truly believe it was no coincidence that our paths crossed. We sat and talked, shared a meal together, and were able to get him a hotel room for a bit. Clark has served our Country. Today, on Veterans Day, we take time to honor those who have sacrificed for our freedom. He did not ask for any handouts, yet it’s clear he could really use the support right now. If you feel the calling on your heart to support Clark, I know he would be deeply grateful. Clark, thank you for your service! Let's continue to be the light of the world! ❤️

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Support Clark: A Veteran in Need

<div>My name is Michael Wolff. I’m the author of four books about Donald Trump and his political rise: <em>Fire and Fury </em>(2018); <em>Siege </em>(2019); <em>Landslide</em> (2021); <em>All or Nothing </em>(2025). I also co-host with the <em>Daily Beast’s</em> Joanna Coles, the podcast "Inside Trump’s Head"; and post short videos on a nearly daily basis on Instagram about what I’ve learned is taking place in the White House—including many details about the involvement of Donald and Melania Trump in the Jeffrey Epstein scandal. This has put me in considerable conflict with the White House—a stream of frequent invective directed towards me as well as past efforts to interfere with publication of my books. Trump seems to have been particularly alarmed about by my reporting about Epstein, who I interviewed extensively before his death.
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<div>Trump family lawyers have now announced their intention to sue me for $1 billion, just as they have similarly sued and threatened others, for statements I have made about the relationship of the President and First Lady to Epstein. This is clearly an effort at intimidation, designed to close down discussion of the Epstein story. Others who the Trumps have sued, understandably afraid of the President's power, have acquiesced and apologized and retracted their comments.
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<div>I am not going to do this. In fact, with your help, I intend to fight the Trumps and to make every effort to force husband and wife, under oath, to testify about their relationship with Epstein, or to hold them to account for why they won’t. And, as well, with the subpoena power of a lawsuit, to call other witnesses who can help explain the nature of Donald and Melania Trump's long involvement with Epstein.
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<div>This GoFundMe page is not only meant to help pay these legal costs but to fund the opportunity for all of us to see behind the dark curtain of the Epstein affair. I hope you’ll help support this effort. Thank you.
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<div>All funds will be transferred to my representing firm's escrow account.
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Help Michael Wolff in His Legal Fight Against Melania Trump

Aaron Richmond

<div>They really need your help ppl help Bella and Lexi 
</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/96502939_1763047475481095_r.jpeg" width="100%" />
<div>Hi there our names are Bella Lexi
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<div>we are trying to raise some money so we can see our love ones we are 1 years old and we need a operation because we are going blind so we are hoping there are some nice people out there who can help us get better
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Help Bella and Lexi have a successful operation

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Aaron Richmond

Aaron Richmond

What Aaron cares about

Aaron’s featured causes

Help Bella and Lexi have a successful operation

Help Geraldo and Rozeta's Quadruplets

Honor Crystal's Memory: Cremation Fund

Help Deontae Before It’s Too Late

Save Lydia