When your child has cancer, you need a team of compassionate experts. Neovita’s pediatric oncology program offers world-class treatment, cutting-edge research, and whole-family support for children, teens, and young adults.
Hearing the word “cancer” in relation to your child is every parent’s greatest fear. In this moment, you need more than just medical experts; you need a partner who understands that treating a child is fundamentally different from treating an adult. At Neovita Oncology, our dedicated Pediatric and Adolescent Oncology Program is built around this core belief. We combine the most advanced, evidence-based medical treatments with a profound commitment to protecting your child’s emotional well-being, development, and future. From the moment you walk through our doors, our mission is to surround your entire family with hope, expertise, and unwavering support.
We have a child-centered, family-focused approach to care where a multidisciplinary team of specialists regularly meets to discuss every part of your child’s journey. This ensures that treatment is not only effective against the cancer but also managed in a way that puts your child’s quality of life, growth, and long-term health first. Your child’s dedicated care team includes pediatric oncologists/hematologists, pediatric oncology nurse navigators, pediatric surgeons, radiation oncologists, child life specialists, pediatric psychologists, social workers, pediatric nutritionists, and pain management specialists. They are all focused on keeping your child strong, nourished, and comfortable.
We have a comprehensive approach to treating childhood cancers and blood disorders, focusing on the most complex cases. Our treatments are specifically designed for the unique biology of pediatric cancers and the delicate bodies of developing children. We use precision medicine and genetic sequencing to analyze a child’s tumor, allowing us to identify specific mutations and choose targeted therapies that reduce long-term side effects. As a leading institution, we also provide access to cutting-edge therapies through pediatric clinical trials from the Children’s Oncology Group (COG) and other consortiums, ensuring our patients are among the first to benefit from new, groundbreaking treatments. Furthermore, we leverage the latest in immunotherapy, including CAR T-cell therapy, to harness the child’s own immune system to fight cancer cells. This approach has proven revolutionary for certain types of leukemia and lymphoma. We also have specialized Leukemia & Brain Tumor Programs with ultra-specialized teams that follow protocols representing the global standard of care, guaranteeing your child receives the best possible treatment.
Healing is about more than just fighting cancer; it’s about nurturing the spirit and supporting the whole family so a child can still be a child. Our comprehensive support services are integrated directly into your child’s care plan. The Child Life Program, led by certified specialists, uses therapeutic play and medical preparation with dolls and models to help reduce a child’s fear and give them a sense of control. For older children, we offer School Reintegration & Education Support through a dedicated education coordinator who works with your child’s school to keep them connected and facilitate a smooth return to the classroom. We also provide Age-Specific Psychosocial Support tailored to each stage of development—from play and art therapy for young children to private counseling and support groups for teens dealing with unique challenges like body image and isolation. Finally, our Creative Arts & Music Therapy provides a powerful outlet for expression, helping to reduce stress and bring joy to the hospital environment.
When a child is sick, the entire family is affected. We provide a strong network of support to help you navigate this journey together. Our resources for parents, siblings, and families include parent support groups and counseling, led by licensed therapists who can help you manage stress and anxiety. We also have a Sibling Support program, called Sibshops, which gives brothers and sisters a fun, supportive space to express their feelings and connect with others. To help with the financial side, our financial advocates can assist with insurance, co-pays, and applications for financial aid. Lastly, our Parent Resource Library offers a curated collection of books and online resources to help you understand your child’s diagnosis and how to best support them at home.
The AYA (Adolescent & Young Adult) Oncology Program addresses the unique medical and psychosocial challenges faced by teens and young adults between the ages of 15 and 39, a group often underserved in both pediatric and adult care settings. Our dedicated program offers specialized medical expertise because cancers in this age group can have different biologies. A standard part of our care is a discussion on fertility preservation at the start of treatment, where we provide urgent referrals for options like sperm banking and egg/embryo freezing to protect future family-building potential. To combat isolation, we also facilitate peer connections through dedicated support groups, social events, and online communities, ensuring that young patients have a space to connect with others who understand their experiences.
You don’t have to navigate this journey alone, as we offer extensive resources to support both you and your loved ones. We provide specific resources and support groups For Caregivers, recognizing their vital role. You can also access our comprehensive online Patient & Caregiver Education Library, which is filled with helpful articles, videos, and guides. Finally, our Support Groups allow you to connect with others who truly understand what you’re experiencing.
External Resources:
National Cancer Institute (NCI):
American Cancer Society (ACS):
American Society of Clinical Oncology (ASCO):
A: A Child Life Specialist is a certified professional with a master’s degree in child development or a related field. They are a vital part of the medical team. They use therapeutic play, medical education (using real medical equipment on dolls), and preparation to demystify procedures, reduce fear, and teach coping skills. They are your child’s advocate for normalcy and play.
A: We have a dedicated Pediatric Pain Service made up of anesthesiologists and nurses who specialize in acute and chronic pain management in children. We use a multi-modal approach that can include child-friendly medications, numbing creams, distraction techniques, nerve blocks, and complementary therapies to ensure your child is as comfortable as possible.
A: This is a common and incredibly challenging situation. Our pediatric psychologists and AYA team are specially trained to help. They work with the teen to understand their fears and anxieties, address issues of control and autonomy, and help them re-engage in their care plan in a way that respects their growing independence while ensuring they receive life-saving treatment.
A: Yes. Beyond support groups, we host numerous events throughout the year, both in-hospital and in the community, such as summer camps, family picnics, and holiday parties. These events, run by our psychosocial team, allow patients and siblings to form deep, supportive friendships with others who truly understand their journey.
From the first lab test to the final follow-up appointment, our entire team is dedicated to achieving the best possible outcome for your child—in body, mind, and spirit. We are here to answer your questions, ease your fears, and fight alongside your family with every resource at our disposal.
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