The 3/32 Foundation will mainly work with other childhood cancer organizations to raise awareness about the lack of research funding and the need for less toxic treatments. Any funds raised will be distributed to other childhood cancer organizations.
Locally and nationally Aiden’s Army provides care bags filled of comfort items to children under 2 battling cancer and other life threatening illnesses. We seek to raise awareness for Pediatric Cancer and provide toys, books, and pajamas to hospitals.
Alex’s Lemonade Stand Foundation (ALSF) is changing the lives of children with cancer by funding impactful research, raising awareness, supporting families and empowering everyone to help cure childhood cancer.
To bring dignity and comfort into the harsh world of childhood cancer and other life-threatening diseases.
Fight childhood cancer by: (a) providing support to families of kids with cancer; (b) funding research; © supporting awareness and advocacy; and (d) spreading the B+ message
Our mission is to accelerate the development of better treatments for children with cancer. We do this by supporting international drug re-purposing projects and drug development collaborations between academia and industry.
Fund less toxic therapies for children with cancer; help families emotionally and financially; raise awareness
ASK is dedicated to make life better for children with cancer and their families through emotional, financial, educational and social support.
To eliminate pediatric cancer and to provide hope and support to those who are touched by it. Two major programs:
Bear Hugs: A Bear Hug is a customized experiences designed to brighten the life of a child fighting cancer;
Bear Discoveries: program provides much needed funding for investigators and fellows in their quest to discover new and novel treatments for pediatric cancer.
Beat Childhood Cancer drives childhood cancer research and raises awareness, making a difference in kids’ survival today.
Empower children suffering from chronic illnesses and provide support to their families. The organization helps pediatric cancer patients write and illustrate their very own children’s book, which is then published. Books That Heal hosts signing events to celebrate and empower the children, and donate royalties of books sales to the families of the children and to research centers of their choosing.
Braden’s Hope For Childhood Cancer raises awareness and funds for research precision-based treatments of childhood cancers to shut down the activators of childhood cancers.
To encourage and empower others, especially children, to get involved and make a difference for children with cancer by raising global public awareness of childhood cancer through service project, education and advocacy initiatives; and to raise money primarily for research into earlier detection, newer treatments, and cutting edge, targeted therapies and cures for pediatric cancer that will be gentler and more tolerable through all stages: discovery, diagnosis, treatment, and remission.
We support Advocacy, raise awareness for childhood cancer, and directly fund local families aiding in the financial challenges that come with such a diagnoses.
Cancer Families United provides essential support and services to families of southwest Michigan affected by childhood cancer through financial assistance, family networking, community awareness and advocacy for a cure.
We provide support and services to every new diagnosed patient at Bronson Hospital, Pediatric Oncology Clinic.
The mission of CancerFree KIDS is to eradicate cancer as a life-threatening disease in children by funding promising research that might otherwise go unfunded. CancerFree KIDSCancerFree KIDS’ investments provide seed-funding for innovative, high-risk/high-reward research. This essential, but extremely limited funding is what will propel childhood cancer research forward. CancerFree KIDS has invested in over $5.3 million awarded in life saving childhood cancer research since its inception.
Candlelighters NYC is an organization dedicated to helping families get through the difficult times when a child is diagnosed with and being treated for cancer .We assist through all stages: discovery, diagnosis, treatment and remission- “BECAUSE KIDS CAN’T FIGHT CANCER ALONE”™
The Canines-N-Kids Foundation is committed to finding a cure to the devastating cancers that canines and children face in common. We fund the most promising, humane research and clinical trials to treat canine cancer patients, while answering critical questions that will accelerate a cure for children battling these same cancers.
The Carson Leslie Foundation is dedicated to raising funds for research leading to a cure for pediatric cancer and enriching the lives of teens in the battle. Our mission is achieved through our (3) pillars:
1. Encourage: CARSON’S CORNER | TEENS IN THE BATTLE
2. Research: CHILDHOOD BRAIN CANCER RESEARCH #cureMEdullo
3. Educate: BRAIN CANCER IS THE DEADLIEST DISEASE OF OUR NATION’S CHILDREN
ccThrive’s mission is to build awareness that childhood cancer survivors can thrive by providing visibility to high profile childhood cancer survivors performing at top levels to demonstrate that survivorship is not necessarily defined by diminished physical and cognitive capacities.
We encourage children with cancer to be as active as possible, both physically and cognitively and once off treatment, to be proactive and persistent in their full rehabilitation and entry into competitive pursuits.
Children’s Cancer Cause ensures that the needs and perspectives of children with cancer, their families and survivors are integrated into national deliberations on health care, research, and cancer policy. We give survivors and families the resources and tools they need to be effective advocates in Washington and in their communities.
Children’s Cancer Research Fund is a charitable organization that acts courageously on donors’ behalf to improve childhood cancer outcomes.
• By funding critical research needs, nimbly and responsively. This includes providing seed grants for innovative research projects that hold great promise but don’t yet qualify for federal or larger funding;
• By collaborating with leading researchers who stay keenly attuned to the ever-changing landscape of cancer research
• By educating our nation about childhood cancer and its long-term effects,
• By supporting children and families affected by cancer, funding innovative services and fostering relationships that enhance quality of life.
• By fearlessly asking for the donor support needed, because every dollar matters in the search for a cure.
The Christina Renna Foundation is dedicated to supporting childhood cancer research and furthering awareness and education through the support of cancer groups and outreach program for the direct support of those in need. “A prayer, a wish and a dream of a cancer free world.TM”
To advance cures and means of prevention for pediatric catastrophic diseases through research and treatment, while providing access to quality medical care for the uninsured, underinsured, and medically indigent children of Nevada with complex medical issues; through a charity care plan, education, research, and advocacy – consistent with the vision of our founders, that no child be deprived of care based on a family’s inability to pay for services.
CURE Childhood Cancer is dedicated to conquering childhood cancer through funding targeted research while supporting patients and their families.
The Cure4Cam Childhood Cancer Foundation seeks to raise community awareness about childhood cancer and supports the development of new and more humane therapies for children with these diseases.
CureSearch has a laser focus on finding new and better therapies for children with cancer. We contribute specifically to pediatric drug development by only investing in projects that have commercial potential. We address outdated systems to create connection and community between stakeholders by providing platforms for engagement to allow critical conversations to occur.
The Daniela Conte Foundation is dedicated to raising awareness and research funds for Rhabdomyosarcoma with a particular interest in Embryonal Rhabdomyosarcoma (ERMS). We also provide financial support to families of kids with cancer.
To provide emotional, educational, financial and practical support to families battling childhood cancer.
Dragon Master Foundation’s mission is to find and accelerate cures for cancers and other diseases by fostering and rewarding a community of collaboration and innovation. We seek to expedite research, development, and treatments as well as to improve the quality of life for patients and their families.
Educate others about childhood cancers and raise money to fund research to cure childhood cancers with an interest in alveolar rhabdomyosarcoma.
Our mission is to Activate the Cure(TM) for childhood cancer by raising awareness and funding for innovative childhood cancer treatments that are less toxic and more targeted, such as immunotherapy, and supporting families facing childhood cancer.
Provide financial support for research and clinical trials that will cure neuroblastoma, with an emphasis on non-toxic treatments.
The mission of the organization is to fund the most promising basic, translational and clinical research on neuroblastoma, and support patient wellness programs for pediatric cancer patients currently in treatment.
The mission of Fabulous Faith’s Foundation is to end the suffering caused by childhood cancer by supporting cancer research, affected families, providers, and facilities while promoting awareness and hope that a cure will be found.
The For a Day Foundation is committed to creating emotionally therapeutic experiences for children with cancer – and providing them and their families with a joyful and much needed diversion from the strain of chronic treatment.
Specifically, we host themed parties in hospital playrooms, like Queen & Hero for a Day, and arrange family experiences outside of a hospital setting. Since founding in 2000, we’ve served over 8,000 kids and we currently operate in 16 local chapters.
Supporting children and families affected by childhood cancer.
Our MISSION is to help families, fund research, and raise awareness for DIPG and pediatric brain cancer. Gabriella’s Smile Foundation provides families with the necessary resources during the most critical times. No family should fight cancer alone.
To raise awareness and inspire action for childhood cancer initiatives for every child, everywhere.
Gold Rush Cure Foundation supports childhood cancer patients and families through their Pot of Gold Program for children’s hospitals around the country giving a gift of compassion to children during their difficult journey. We also support advocacy and awareness through federal legislation that benefits children fighting cancer and promotes increases in research funding, drug development and compassionate use.
Our mission is simple: to provide students battling cancer a stress-relieving, individualized learning experience to not only stabilize their academics, but also to rekindle their interests in STEAM. Through free, one-on-one digital classes, students will experience an effective form of learning that can allow them to both maintain the academic standards found in the school environment, and also to dive deeper into the custom fields of interest tailored to each student’s asking.
We strive to provide continued motivation for cancer patients to pursue their academic dreams. By working with students in all stages of treatment (including post-treatment), we can make the seamless transition from treatment to normal school life a reality.
Hope4ATRT is a research entity of Out of Zion Inc., dedicated to directing resources and research to families in the fight. Hope4ATRT provides a single dynamic site where parents can go to find all the information they need to navigate their child’s diagnosis, to know exactly what to do, where to go for treatment, and what resources are available to them. The organization has experts in the field that make sure parents have the relevant information they need, presented in a way they can easily understand. Hope4ATRT provides resources to parents, as well as supports ATRT research.
Raise awareness and funding to provide the research necessary to help cure childhood cancer; help children suffering with cancer in any way possible.
I Care I Cure Childhood Cancer Foundation raises awareness and funds for cutting edge research for targeted and less toxic cures and treatments for childhood cancer.
Jack’s Angels mission is awareness and research for DIPG and pediatric brain tumors, and advocacy for children with cancer.
The mission of The Jeff Gordon Foundation is to support children battling cancer by funding programs that improve patients’ quality of life, treatment programs that increase survivorship and pediatric medical research dedicated to finding a cure.
In addition, the Foundation provides support to the Jeff Gordon’s Children’s Hospital in Concord, NC, which serves children in the community by providing a high level of primary and specialty care, regardless of their ability to pay.
Create moments of joy for families based on our founding philosophy of paying it forward and the belief that a little caring can go along way in creating hope. Provide Holiday Gifts to families in Northeast Ohio who have children in treatment, award PAYA college scholarships to survivors and siblings, host an annual event for siblings, and work with local (Northeast Ohio) hospitals to provide mini-wishes where and when appropriate.
Our mission is to encourage every kid fighting cancer to Never Ever Give Up by CONNECTING with their family, bringing AWARENESS to their story, providing them helpful RESOURCES and sending them continuous doses of ENCOURAGEMENT throughout their journey.
Raises funds and awareness of rare pediatric cancers, specifically sarcomas, blastomas, and brain tumors and for research and clinical trials at Levine Children’s Hospital. Joedance, held annually, is committed to screen films of Charlotte film producers, writers, and directors.
Joey’s Journey Foundation was created to enrich the lives of children walking the rocky path of cancer and other life-threatening illnesses. Our mission is simple. With donations, Joey’s Journey will grant wishes, raise awareness and fund research to help families fighting pediatric cancer.
Our mission is to fund research that focuses on kidney cancers affecting children and young adults, raise awareness and provide support to families affected by childhood cancer. Our foundation is supported by an active Board of Directors operating solely on a volunteer basis. 100% of all donations made is used towards research and treatment options, patients care and advocacy for developing less toxic therapies to treat kidney cancer among children and young adults.
Dedicated to: funding immunotherapy research at Seattle Children’s; increasing advocacy and awareness about need the need to make funding childhood cancer research a national priority; enhancing the lives of children battling cancer through our iPAD program.
Julia’s Grace Foundation® brings moments of happiness and support to children with cancer and their families.
From giving special moments for a family to share, to providing items to make the long days in the clinic feel shorter, Julia’s Grace® helps children with cancer and their families smile with our special “hugs”.
Julia’s Grace Foundation® also grants monetary assistance, or “graces”, to families experiencing financial hardship due to the direct result of a child’s cancer treatment and care.
Julia’s Grace® brings “happiness, hope, & hugs” to families affected by childhood cancer.
Kellen’s Krusade raises funding for clinical trials in neuroblastoma. We collaborate with researchers who are prompting less toxicity in the future of cancer therapy.
We help children and young adults (to 29 y.o.) with cancer and their families; we help to underwrite pediatric cancer research and treatment; and we educate the public about pediatric cancer.
As a nonprofit, Ladybug House will offer intermittent stays to families who are caring for their children with life challenging illnesses so they can have time for rest and quality time together.
Ladybug House will have two options for stay: one for the entire family and the other for the child to stay solo. Ladybug House will be an option beyond the hospital or home environment for end-of-life care offering an extra layer of support.
Ladybug House will consist of an interdisciplinary team of healthcare professionals, specially trained pediatric staff, and volunteers who provide 24/7 loving care and support.
This care will be provided with no out of pocket cost to the family.
We strengthen families living through childhood cancer by providing restorative retreats and helpful resources.
Support research and raise awareness to improve the quality of life of patients and their families, in the hope of finding a cure for pediatric brain and childhood cancers. LEF financially assists children and their families in treatment for pediatric cancers.
Our goal is to Live Like Lukas did, every day. Lukas faced every last challenge head on. Our vision is to honor him and keep his memory alive by supporting families fighting childhood cancer, childhood cancer research, and local non-profit organizations that Lukas loved. All proceeds or donations will be allocated based on three areas of focus: Family Assistance, Nonprofit Foundation Support, and Childhood Cancer Research.
Lolo’s Angels, Inc.’s mission is to fund life-saving research for pediatric cancer research, sponsor blood and bone marrow drives, raise awareness for pediatric cancer, and serve kids and families through their cancer journey.
The Make Some Noise: Cure Kids Cancer Foundation was established by a child with cancer with one purpose in mind: to fund pediatric cancer research. To that end, the foundation serves as a vehicle to secure private funding to distribute to research facilities and promote awareness through its fund raising activities. The designation of funds to various research facilities is cancer specific and based on the foundation’s annual evaluation of the latest research.
Mattie Miracle Cancer Foundation is dedicated to increasing childhood cancer awareness, education, advocacy, research and psychosocial support services to children, their families, and medical personnel. Children and their families will be supported throughout the cancer treatment journey, to ensure access to quality psychosocial and mental health care, and to enable children to cope with cancer so they can lead happy and productive lives.
The mission of The Max Cure Foundation, Inc., is to fund research for the development of pediatric cancer drugs, including funding to discover less toxic treatments for children with cancer, and as its research mission, to fund an Immune Cell Therapy Lab at Memorial Sloan-Kettering Cancer Center, to financially assist low income and military families battling cancer in their children, and through advocacy, to pursue legislative and regulatory changes that seek to benefit children with cancer and at the same time, raise awareness to the needs of those fighting pediatric cancer.
MIB Agents is a leading pediatric osteosarcoma nonprofit dedicated to Making It Better for our community of patients, caregivers, doctors, and researchers with the goal of less toxic, more effective treatments and a cure for this aggressive bone cancer.
Momcology is a national community-based organization directly serving caregivers of children with cancer through facilitated peer support programs, information distribution, partnerships with treatment centers, and engagement in projects and programs that address the ongoing needs of families affected by pediatric cancer from diagnosis, through treatment and into survivorship or bereavement care.
Our main objective is to raise awareness of Childhood Cancer and desperately needed funds for research to bring less toxic, more effective treatments for these children. We also strive to enhance the lives of children battling Childhood Cancer through inpatient hospital parties and the granting ‘Wishes’ whenever possible. Our ultimate goal is to find a cure for all the children afflicted with this very painful and aggressive disease.
The Neuroblastoma Children’s Cancer Society is a group made up of volunteers, many of whom have children or relatives who are victims or survivors of this disease. Our organization is an advocate for the children who suffer from neuroblastoma and is dedicated to serving as a support center for their families. The primary focus of the organization is to raise money to assist local research in neuroblastoma cancer, and to raise national awareness to focus additional research and funding until a cure can be found.
Providing HOPE and HELP to Northwest Indiana families affected by childhood cancer and supporting promising research so that all children with cancer can be HEALed.
To inform people of the need, and raise funds, for pediatric cancer research in all areas where funding is lacking.
Working to eliminate the challenges of childhood brain tumors.
Find a cure for childhood cancer. This is accomplished through the support of research, state of the art equipment/ instruments and patient/parent care for world-renowned doctors at the hospitals.
Our mission is to raise awareness of Childhood Cancer and to unite the childhood cancer world to speak as “One Voice United Against Childhood Cancer”.
Precious Jules Childhood Cancer Foundation’s mission is to create, operate and support fundraising initiatives & events to raise & provide funds for the discovery, advancement and treatment of pediatric oncology research; promote public awareness and advocacy through such events; and to provide support for children & adolescents with cancer & their families.
Our mission consists to ensure that all children who suffer at the hands of cancer have the opportunity for a better prognosis and quality of life.
A hospital experience can be terrifying and traumatic for both a child and their family. While others strive to find a cure, Ryan’s Case for Smiles helps with the stress and emotional impact of illness in the here and now. Our whimsical pillowcases give children an emotional boost, while resources and tools help families better understand and cope with the experience. CopingSpace.org offers tools and resources in a web-based format for caregivers, siblings, schools, and the community of a sick or injured child. Resources for the child’s caregiver provide evidence-based information that will help them cope with diagnosis, treatment and recovery while building resilience along the way. These resources alert them to the risk of Post Medical Traumatic Stress and provide age appropriate explanations and scripting for caregivers to reference as well as tips on how to build resilience in themselves and their child.
Sam Day Foundation strives to fund research for rare pediatric cancer and life-giving experiences so kids with cancer can survive and live well.
Sammy’s Superheroes Foundation’s is a 501(c)3 non-profit that raises money for life-saving childhood cancer research for all types of childhood cancer that will lead to modern treatments of this horrible disease. We seek out doctors and researchers who are doing ground-breaking, innovative work and help fund their projects to ensure that advances are being made towards a cure for childhood cancer.
We will honor the life of Sebastian Ortiz by increasing awareness of childhood cancer and by raising money to fund research for less toxic, more targeted childhood cancer cures.
The work of Smashing Walnuts is to change these statistics by funding much needed research and clinical trials to find “cures.” By focusing our efforts specifically on childhood brain cancer research, the second-most-common cancer and the most deadly, we act as a catalyst, changing the situation. Sources of funding for childhood brain cancer research are scarce, but through our financial support, lobbying and directed resources, we have already moved the needle.
Solving Kids’ Cancer finds, funds, and advocates for breakthrough treatment options to cure children with the most fatal pediatric cancers (neuroblastoma, sarcomas, and CNS tumors).
Provide financial support to children undergoing cancer treatments and to their families. Sophia’s Fund also works to help increase childhood cancer awareness, funding, and research.
The relentless pursuit of the a complete and permanent cure for Ewing’s Sarcoma.
Fight childhood cancer by providing support to pediatric cancer initiatives focused on complementary and alternative treatments to chemotherapy. To continue to further the push for awareness of childhood cancer, and to provide assistance to families with children battling the disease.
The Steven G AYA Cancer Research Fund is committed to supporting Adolescent and Young Adult (AYA) Research, teaching survivorship to patients and their families, and awareness building on the issues related to this dreaded disease.
The Swifty Foundation was founded to celebrate the life of Michael Gustafson, who died at age 15 from medullablastoma. Michael started the foundation before his death so “No other child would have to go through what he did.” Michael wanted to be a scientist, and donated his tissue to researchers to help find a cure. Swifty’s mission is to promote tissue donation, fund pediatric cancer research, and raise awareness through social media campaigns and events. 100% of all donations go straight to research, and no expenses are paid with Swifty Foundation funds. Michael’s parents pay all foundation expenses.
The Taylor Matthews Foundation is dedicated to raising awareness and funding pediatric cancer research.
The TeamConnor Childhood Cancer Foundation mission is to serve families, build awareness, and raise funds for research to help cure childhood cancer.
Achieve the goal and objectives in the childhood chapter of the TN Cancer Control Plan. The Childhood Committee developed 5 regional action teams comprised of representatives of over 30 childhood cancer organizations. Action teams set regional priorities and work The TN Cancer Coalition is a “Comprehensive Cancer Control Program” sponsored by the CDCtogether on statewide initiatives. We unite to: (a) raise awareness; (b) advocate; (c) provide resources; and (d) make our voices heard
Our mission is to fund neuroblastoma research.
The Grayson Saves Foundation is a 501(c)3 non-profit organization that aids children and families afflicted with pediatric brain tumors. The Foundation’s goal is to provide monetary assistance to help promote awareness of pediatric brain tumors and support the research efforts to treat pediatric brain tumors.
The Lilabean Foundation for Pediatric Brain Cancer Research (LBF) seeks to (1) fund critical childhood brain cancer research and (2) to help raise awareness of the severity of this fatal disease.
The Morgan Adams Foundation funds kids’ cancer research. We raise awareness of, and educate our communities about, the need for pediatric and young adult specific cancer treatments.
Working with leading researchers and physicians, we fund new and innovative ideas that will improve cancer treatment effectiveness, overall outcomes, survival rates, and quality of life while minimizing the devastating side effects current treatments have on our children.
The mission of The Oliver Foundation is to drive research into the environmental toxicants that have caused pediatric cancer to soar 50% in the USA since 1975 – in order that we as a society take the necessary steps to reduce our exposure to the pollutants triggering cancer in ever greater numbers of our children. Our key project is a pioneering online global epidemiological study, TheReasonsWhy.Us (www.thereasonswhy.us) in partnership with Baylor College of Medicine
To end pediatric brain cancer, funding innovative research that will lead to successful, non-toxic treatments for children battling brain tumors.
This Star Won’t Go Out is making a difference in the lives of children with cancer, one family at a time. By providing funds to help pay for travel, a mortgage or rent check, and other cost of living expenses, TSWGO frees up families to focus on their child who is in treatment. A gift of money is really a gift towards quality time as a family—and that’s a gift that is beyond value.
Fight for the voiceless youth in the pursuit of elevating childhood cancer awareness and generating bold action through online story-sharing, events, and media with hopes to change the percentage of dollars invested in childhood cancer research and make a real difference for a cure.
The Ty Louis Campbell Foundation is a nonprofit organization (EIN: 45-1858390) that funds innovative research and clinical trials specifically geared toward the treatment of the most aggressive childhood cancers. Our mission is to help fund the intelligence and technology that will improve long-term survival rates and minimize side-effects for children diagnosed with the deadliest cancers, while helping to care for families when their child is in treatment by providing financial assistance and uplifting experiences.
The mission of The Tyler Robinson Foundation is to strengthen families financially and emotionally as they cope with the tragedy of a pediatric cancer diagnosis by offsetting out-of-pocket life expenses.
WithLove is on a mission to spread love across the country and pride ourselves on giving back to the community with toy drives and tailored programs benefiting children with cancer and their families. We are called to inspire and give children with cancer the opportunity to be simply what they are… kids!
With Purpose is a youth and community-led movement dedicated to making sure kids with cancer have access to safe and effective treatment options. We advocate for families affected by childhood cancer, empower youth and community leaders to take action and invest in ground-breaking initatives that remove the barriers to advancing treatment for childhood cancer. With Purpose attacks three distinct pain points in the complex problem of advancing treatment for kids with cancer and which, in turn, gives families hope for a better future: lack of funding for research, lack of “proof of concept” research, and lack of incentives for drug development.
Support research ; provide financial support to families in need; support kids during their treatments; advocate and raise awareness about childhood cancer and the problems related to treatment
The mission of the Zoefia Alexandria Foundation is to honor Zoefia’s life and her courageous battle against Brain Cancer. Through contributions we help to enrich the life and development of Cancer Children and their families by supporting Education and Housing.