2024 Lace Up for Kids Recap

A collage of images with a yellow butterfly in the middle.

Lace Up for Kids: Your Impact on Childhood Cancer Research

At Solving Kids’ Cancer, our mission has always been driven by hope — hope for better treatments, hope for breakthroughs, and most importantly, hope for every child fighting cancer. This year’s Lace Up for Kids campaign was nothing short of inspiring. Together, we’ve raised over $264,000 across the entire campaign, funding innovative childhood cancer research and providing more treatment options for children in need.



From coast to coast, nearly 4,000 participants have stepped up to lace up their gold shoelaces and make a difference. Whether it was through schools, sports teams, or community groups, the show of support has been overwhelming throughout the years. Over 7,823 donations have been made to accelerate new treatments, and the hashtag #CareWearShare has been used 13,864 times, spreading the message far and wide!

A glass jar filled with gold ribbons for childhood cancer awareness

Your Participation Means the World

To every student, teacher, athlete, parent, and friend who participated in this year’s Lace Up for Kids, we want you to know how deeply grateful we are for your help in raising critical children’s cancer research funds. Whether you walked miles, ran races, or simply shared the cause with your network, each act of kindness had a ripple effect.


With 212,500 gold shoelaces distributed, this childhood cancer fundraiser’s message of hope has reached far and wide. Some schools have organized entire days dedicated to childhood cancer awareness, with classrooms buzzing with excitement and determination. Many participants have told us how they felt connected to something larger than themselves, knowing that they were raising funds for children in the fight of their lives.

Stories That Touched Our Hearts

Throughout this campaign, we were fortunate to hear the stories behind the participation. Parents told us about lacing up in honor of their children who are fighting cancer. Teachers shared about students who learned valuable lessons on compassion and empathy by taking part in Lace Up for Kids. These moments remind us of why we continue this important work.



One story that stands out is from Erin Martin, a 14-year-old student from San Antonio, Texas, who has been actively raising awareness for childhood cancer in 2021. Since starting her efforts, Erin and her friends have shared their passion for helping children with their classmates and community, earning a plaque that now proudly hangs in their school lobby.

More Than Just Gold Shoelaces

What makes Lace Up for Kids so special is that it’s about more than just raising money—it’s about raising awareness and standing in solidarity with families facing unimaginable challenges. Every gold lace worn is a symbol of hope. When we go gold for childhood cancer, we remind the world that cancer isn’t something we can ignore; it’s a battle we’re determined to win.

The Smithtown Schools, for example, have consistently gone above and beyond. Over the years, students and staff have organized school-wide cancer awareness days and fundraising challenges, encouraging students to lace up their gold shoelaces and show support for pediatric cancer patients. Their efforts have helped their community foster a deeper understanding of the fight children with cancer face every day.

What Your Support Achieves

Because of you, the funds raised this year will go directly toward advancing life-saving research and treatments for the most aggressive childhood cancers. Your contributions support projects like immunotherapy research1 and clinical trials for less toxic therapies, giving children hope for recovery without the harsh side effects of traditional treatments.


One of our key initiatives is funding the first-ever clinical trials for ETMR (Embryonal Tumor with Multilayered Rosettes), a rare and deadly pediatric brain tumor. Thanks to your support, we’re not only providing access to cutting-edge trials but also driving the development of new treatment protocols that could transform pediatric cancer care.

Support Childhood Cancer Research Year-Round

Even though Lace Up for Kids is over, there are many ways you can go gold for childhood cancer throughout the year. Here are a few simple, practical ways to stay involved:

  • Monthly Giving: Set up a recurring donation to make a consistent impact. Even small monthly contributions add up over time and help sustain critical research projects.
  • Host a Childhood Cancer Fundraiser: Whether it’s a bake sale, garage sale, or online donation drive, you can raise funds in your community to support groundbreaking research for kids with cancer.
  • Spread Awareness: Share stories from Solving Kids’ Cancer and the impact of ongoing research on your social media. Raising awareness is just as powerful as fundraising and helps spread the message.
  • Employer Matching Gifts: Check if your employer offers a matching gift program. This simple step can double or even triple the impact of your donation.
  • Volunteer Your Time: Explore opportunities to get involved locally by volunteering at awareness events or helping to spread the word about childhood cancer research.
  • Stay Informed: Sign up for our newsletter to keep up to date with the latest in childhood cancer research and learn about new ways to support children and families battling cancer.

By staying active and engaged, you’re helping to fuel research that gives children hope for a brighter, healthier future. 


Missed Laces? You Can Still Make an Impact!

If you couldn’t join us for Lace Up for Kids, there’s still a way to be part of the mission. Your donation supports groundbreaking childhood cancer research and gives hope to children and their families. Every contribution, big or small, moves us closer to a future without childhood cancer — because every kid deserves to grow up.

A pink button with the words `` give today '' written on it.
Source:
1 Immunotherapy of Neuroblastoma: Facts and Hopes – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9344822/
A man and a little girl are sitting in front of a wooden wall.
By duda November 20, 2024
Ahana’s Story of Strength with High-Risk Neuroblastoma Every day, over 1,000 children worldwide are diagnosed with cancer,1 and for many families, that diagnosis means facing an uncertain future. At just 20 months old, Ahana was diagnosed with a rare and aggressive cancer that had already spread through her small body. Her family’s search for life-saving childhood cancer treatments led them from South Africa to Spain and possibly toward a clinical trial in New York. Ahana’s journey shows the importance of supporting organizations like Solving Kids’ Cancer, which works to find, fund, and advocate for advanced treatments that give hope to families fighting against tough-to-treat rare pediatric cancers.
A poster for 2024 year in review for solving kids ' cancer
November 11, 2024
Advancing Childhood Cancer Research: SKC’s 2024 Milestones
A girl is standing in front of a car in a parking lot.
September 2, 2024
Gold Laces for Childhood Cancer Awareness Month: Erin’s Story 
A group of children are standing in a circle with their shoes on the floor.
August 8, 2024
Smithtown Goes Gold for Childhood Cancer Awareness Month!
A poster for lace up for kids with a butterfly on it
August 6, 2024
Childhood Cancer Awareness Month: Lace Up for Kids 2024
A man standing on top of a mountain with the words osteosarcoma survivor to surgeon dr. kurt weiss ' story
August 1, 2024
Osteosarcoma Survivor to Surgeon: Dr. Kurt Weiss’ Story
Jacob 's journey : a childhood cancer survivor 's story
May 10, 2024
Jacob’s Journey: A Childhood Cancer Survivor’s Story Every battle has its heroes, and among the bravest are young children like Jacob Mozer, who faced stage 4 high-risk neuroblastoma when he was barely old enough to walk. Diagnosed at only 16 months old, Jacob’s early years were filled with constant medical appointments and intense treatments. Despite these challenges, today, Jacob is a shining example of the remarkable progress in pediatric oncology. He’s not merely surviving; he’s thriving as a pharmacy resident, driven to give back to the medical community that gave him a second chance at life. During National Cancer Survivors Month this June, we honor and celebrate fighters like Jacob who have battled cancer and emerged stronger. This month also serves to amplify the conversation about pediatric cancer survivorship and push for vital research that continues to save lives. Solving Kids’ Cancer (SKC) plays an essential role in this effort, supporting children like Jacob by funding crucial clinical trials that enhance survival rates and improve the quality of life for those fighting fatal childhood cancers.
A close up of a person holding a test tube in a laboratory.
May 2, 2024
Trailblazing Treatments for Pediatric Brain Tumors Picture a fortress built to guard precious treasure but accidentally also keeps out the very allies it needs in a time of crisis. This is the challenge faced by medical researchers when dealing with the brain’s natural defense — the blood-brain barrier — especially in children with brain tumors. At Columbia University Medical Center, Dr. Luca Szalontay is leading the charge to breach this fortress with groundbreaking approaches. Recently, Dr. Timothy Cripe from Solving Kids’ Cancer’s podcast, This Week in Pediatric Oncology (TWIPO) , interviewed Dr. Szalontay to delve deeper into these innovative treatments. This Brain Tumor Awareness Month, we’re shining a light on these important advances in treating children’s cancer. Understanding the Challenge Treating pediatric brain tumors like diffuse midline glioma (DMG) is especially tough because of the brain’s own protective shield, known as the blood-brain barrier. This barrier keeps out most chemotherapy drugs as well as large molecules, like antibodies, making it hard to treat the tumors effectively. Dr. Szalontay describes the dilemma: “Our field hasn’t been able to advance as quickly as it has with leukemias or other solid tumors because the drugs don’t penetrate the brain efficiently.” She adds on the nature of this blood-brain barrier, “It’s evolutionary, very important to protect us from different toxins and harmful agents, but this is a shield which protects the tumor as well.” Even when drugs work well in lab tests, they struggle to get to the tumor in strong enough doses without harming the body. Dr. Szalontay also points out that DMG tumors are found in very sensitive areas of the brain, making traditional surgery or radiation risky because they could damage vital brain functions. This makes finding safe and effective treatments for these tumors even more challenging. So, what’s being done to tackle these obstacles and help kids fight these tumors?
A group of stick figures are holding hands around a globe.
April 4, 2024
World Health Day: Pediatric Cancer’s Global Divide Imagine this: Two children, born at the same moment, oceans apart. In a country brimming with medical resources, one child quickly gets top-notch treatment for cancer. Meanwhile, across the globe, the other child faces a drastically different reality, with limited access to basic care. This isn’t just a thought experiment — it’s the harsh truth of pediatric cancer treatment worldwide. Observed every year on April 7, World Health Day shines a light on the mission to make healthcare accessible for all. This day is particularly significant in the context of pediatric cancer, where vast disparities in treatment availability highlight the global challenge of ensuring every child has the opportunity for health and healing. The Stark Contrast in Survival Rates: A Look at Pediatric Cancer Statistics Every day, more than 1,000 children are diagnosed with cancer, and the chances of survival vary greatly depending on where they live.1 Pediatric cancer survival rates serve as a clear indicator of the disparities between high-income countries (HICs) and low- and middle-income countries (LMICs). In wealthier nations such as the United States and Western Europe, the 5-year survival rate for children with cancer is over 80%, thanks to advanced healthcare systems and access to the latest treatments.2 But, here’s a troubling childhood cancer statistic: in LMICs where 80% of children with cancer live, fewer than 20% survive.1 This gap is due to several factors, including late diagnoses or, tragically, no diagnosis at all. Many children succumb to the disease without access to pain medication, and the burdens of travel and the high costs force most families to abandon care. These challenges are compounded by limited access to necessary treatments,3 as well as a lack of specialized equipment and trained healthcare professionals needed for effective pediatric cancer treatment. Addressing this divide requires a concerted global effort to improve early detection, make treatments more affordable, and enhance healthcare infrastructures, giving every child a fair chance to beat cancer. Navigating the Access Maze Access to cancer care shouldn’t be a treasure hunt. Yet, for many in LMICs, it feels like that — a relentless search for something seemingly out of reach. Here’s the reality revealed in childhood cancer statistics worldwide: many areas lack enough doctors who specialize in children’s cancer4 and the prices of cancer drugs can be sky-high.2 Even getting to a hospital can be an ordeal, with some families traveling hundreds of miles. And the financial strain? Devastating. The cost of care can quickly add up to more than a year’s income, forcing households into deep financial distress. In many LMICs, the lack of comprehensive insurance coverage means families are often left to pay for pediatric cancer treatment entirely out-of-pocket.5 Families often face the impossible choice between their child’s health and their financial survival. Solving Kids’ Cancer: Bridging the Gap Solving Kids’ Cancer (SKC) isn’t standing by; we’re on the front lines, actively working to make a difference in the global pediatric cancer landscape. Beyond funding research, advocating for policy changes, and fostering global partnerships, SKC is committed to educating and empowering the community to take action. We understand that while we might not have a global foothold to address every aspect of the pediatric cancer divide directly, there’s power in collective action. Through our efforts, we aim to catalyze advancements in pediatric cancer treatments and care that could dramatically change outcomes for children worldwide. • Research: We direct funds into cutting-edge studies, searching for breakthrough treatments that promise a brighter future for all kids, regardless of where they live. • Advocacy: We advocate for children’s needs by steering research funding towards unmet challenges and collaborating with experts to prioritize all children, including expanding trials to international sites to maximize access.2 • Global Partnerships: We don’t do it alone. By teaming up with researchers, hospitals, and other organizations across the globe, we’ve helped fund clinical trials that have extended to over 250 institutions across 15 countries worldwide . Uniting for a Cause Solving Kids’ Cancer extends its mission beyond research by fostering community and collaboration. Our signature event, Lace Up for Kids , held annually during September Childhood Cancer Awareness Month, is a powerful testament to this mission, drawing communities together to stand in solidarity against childhood cancer. Additionally, supporters can create their own fundraiser and have a platform to engage their local communities, sparking crucial conversations and garnering support for the cause. These initiatives highlight an important fact: While the challenge of pediatric cancer is significant, each of us has a part to play. By working together and supporting each other, we can fund the research needed to possibly change the direction of pediatric cancer treatment and care worldwide. World Health Day: A Chance for Every Child The fight against pediatric cancer is a stark reminder of the work ahead of us.6 It’s a battle that Solving Kids’ Cancer is dedicated to, but we need more than just our efforts — we need a global movement. This World Health Day, let’s rally for every child’s right to fight cancer on an even playing field. Donate today to help fund more innovative research and one day find a cure for childhood cancer — because every child, no matter where they are born, deserves a chance — a chance to fight, a chance to survive, and a chance to thrive.
A woman is hugging another woman in front of a doctor.
March 18, 2024
Childhood Cancer Resource: 7 Things to Do After Diagnosis Nothing can ever prepare a parent for the moment they learn their child has cancer. As reality sets in, so does the question: “What comes next?” To help navigate this challenging time, Scott Kennedy, SKC Executive Director, and Donna Ludwinski, SKC Director of Research Advocacy offer some insights. Both have personal experience with the emotional and practical aspects of this journey, having faced their own children’s cancer battles. They’ve dedicated themselves to improving treatment options for the most difficult-to-treat cancers, drawing from their personal experiences and professional expertise. Scott, motivated by his son Hazen’s fight, co-founded Solving Kids’ Cancer, while Donna, driven by her son Erik’s journey, has contributed to pediatric cancer research on a global scale. Their insights can serve as a valuable childhood cancer resource for families facing a diagnosis. Here are 7 essential steps they recommend parents and caregivers consider: 1. Educate Yourself About the Disease Facing a new and scary diagnosis can feel overwhelming, but gaining knowledge about your child’s cancer can be one of the most powerful tools in your arsenal. “Understanding your child’s cancer is the first step towards empowerment,” Scott advised, “Start by learning as much as you can about your child’s specific type of cancer. Utilize reputable online resources and pediatric cancer resources to gather information. This knowledge will help you to make informed decisions and ask the right questions when discussing treatment options with your child’s medical team.” To give you a head start, here’s a list of questions you can ask your child’s oncologist about their specific cancer type. 2. Create a Community of Support Drawing from her extensive experience advocating for parents and families, Donna emphasized the value of building a support network and strengthening family bonds: “It takes a village to navigate the challenges of childhood cancer. Seek out childhood cancer support groups for guidance and shared understanding; Reach out to friends and family who can offer a helping hand with daily tasks, such as meal preparation, household chores, and caring for other siblings, to conserve your energy for where it’s needed most.” Creating a community of support is not just about logistical help; it’s a source of emotional strength . Donna also highlighted, “Make sure to keep open communication within the family to help acknowledge everyone’s feelings and fears.” Sharing this journey can bring a family closer in unexpected ways. 3. Keep a Record of Everything Keeping track of medical information might seem daunting, but it’s a crucial step in managing your child’s care. Scott suggested, “Start a binder or digital folder to store all the important documents and notes you take. This habit will not only keep you organized but also make you feel more prepared for appointments and discussions with your child’s healthcare team.” 4. Advocate for Your Child “Never underestimate the power of a parent’s intuition,” Donna shared. “You know your child best, and in the medical world, your voice is critical.” She reminded that parents and guardians should fully understand the medical information presented and not shy away from asking questions or expressing concerns to their child’s doctors. Here is a glossary to help you understand medical terms related to oncology. Adding to her advice, Donna highlighted, “Seeking second opinions is also part of advocating for your child . It’s about exploring all options and being confident in the treatment plan.” To help drive changes in treatments and care, she also encouraged parents and caregivers to get involved in pediatric cancer advocacy. 5. Prioritize Self-Care Scott, whose son Hazen bravely battled cancer, knows firsthand how mentally and emotionally taxing this journey can be for a parent. He stresses the benefits of self-care: “In the midst of caring for your child, don’t forget to take care of yourself too. It’s essential to carve out moments for self-care , even if brief.” Whether enjoying a quiet cup of coffee in the morning or taking a short walk in the evening, finding small ways to recharge can significantly enhance your ability to stay strong and supportive of your child. 6. Where to Go for Treatment If the diagnosis is made by a pediatrician or general practitioner, a child is typically referred to the nearest Children’s Oncology Group (COG) hospital. The child’s oncologist will make a treatment recommendation based on a standard protocol, or recommend enrollment on a current frontline clinical trial. In most cases, the closest COG hospital will treat your child the same as any other hospital. Some very rare childhood cancers do not have standard protocols and are treated based on tumor board recommendations, and different approaches may be available at other large centers.  7. When to Request Additional Testing While some pediatric cancers, like leukemia and lymphomas, have seen profound increases in survival rates with advanced treatments, there remain some tumor types that are difficult to treat. If you are facing a less favorable prognosis, talk to your oncologist about additional testing that may reveal targets that can be treated with new drugs or immunotherapies. Many rare tumor types are now being treated based on genetic mutations or antigen expression.
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