Why Integrated Mental Health Support Matters for Nevada’s Kids

Key Takeaways:

  • Integrated behavioral health combines mental health support directly into medical care, eliminating the need for families to navigate multiple systems during already challenging times.
  • Children with serious medical conditions are 5 times more likely to experience anxiety or depression than their healthy peers according to Frontiers in Pediatrics, making emotional support essential to healing.
  • Cure 4 The Kids Foundation has served over 70,000 patients with embedded psychologists and social workers as part of on-site medical care teams.
  • Nevada ranks 51st nationally in youth mental health according to the MHA’s State of Mental Health in America 2025 report, highlighting the critical need for innovative care models that bring behavioral health directly to where children receive medical treatment.
  • Families report 40% better treatment adherence after receiving psychoeducation and integrated mental health care and experience significantly reduced emergency department visits.

Every day at Cure 4 The Kids Foundation, I meet parents whose children are facing both medical and emotional battles. One common story we hear: a child undergoing chemotherapy has started struggling not just with nausea or fatigue, but with growing panic about needles, tears about missing friends’ birthday parties, and nightmares that started after their diagnosis.

A cancer diagnosis or chronic illness brings fear, isolation, anger, and grief. Parents already juggling treatment schedules and insurance calls suddenly find themselves trying to manage their child’s emotional crises alone. This is precisely why integrated behavioral health—having emotional and mental health support right where your child gets medical care—is absolutely crucial.

A whole-child, whole-family care approach is our philosophy and our promise to every family who walks through our doors. When we address emotional wellness and physical healing together, children engage more fully in their treatment and real transformations can happen. 

That’s why I’m thrilled to introduce Dr. Danielle Bello, our Director of Behavioral Health at Cure 4 The Kids Foundation, as a new contributor to our blog. After a decade of transforming how we care for Nevada’s children, Dr. Bello brings invaluable insights about the intersection of medical and emotional healing.

Dr. Bello, Director of Behavioral Health at Cure 4 The Kids Foundation
Dr. Bello, Director of Behavioral Health at Cure 4 The Kids Foundaiton

The Challenge: When Pediatric Mental Health Care is Siloed

Dr. Bello puts it this way: Traditionally, a child receives cancer treatment at one facility, then parents must find different providers for behavioral health support—and all too often must be put on a waitlist. Travel and coordination is difficult. Insurance authorizations require separate processes. Medical records don’t always transfer seamlessly. With all these barriers, mental health support inevitably drops in priority. In the meantime, kids can grow increasingly anxious and fearful. 

And as Dr. Bello explains, emotional stress not only affects a child’s quality of life but also directly impacts physical recovery. Children who are hospitalized face significantly higher risks of developing new mental health conditions within a year of their stay: 

  • 7% of hospitalized children develop anxiety, depression, or trauma-related conditions (compared to 5% of non-hospitalized children)
  • 8% of children who spend time in the ICU develop a mental health condition
  • Children with non-complex chronic conditions face nearly 3 times the risk—approximately 15% develop new mental health diagnoses
  • Children with complex chronic diseases face the steepest odds at over 5 times the risk, meaning roughly 25% (1 in 4) will develop anxiety, depression, or trauma within a year

Studies also show that children experiencing untreated anxiety during medical treatment can have 28–61% longer hospital stays.

These statistics represent thousands of Nevada children who leave hospitals physically healing but emotionally wounded. Without integrated support from the start, a child’s medical journey can inadvertently create lasting psychological challenges.

“When medical and behavioral health teams work separately, critical information falls through the cracks. A child’s sudden medication non-compliance might stem from depression rather than defiance. Without integrated communication, these connections get missed, and children suffer. Behavioral health integration is essential for providing the comprehensive care every child deserves.”

Sue Waltermeyer with a patient
Sue Waltermeyer, Child Life Specialist at Cure 4 The Kids Foundation

What Integrated Behavioral Health Care Looks Like at Cure 4 The Kids Foundation

Our behavioral health team—neuropsychologists, social workers, and Child Life Specialists all led by Dr. Bello—doesn’t operate in isolation. They work right on the clinic floor alongside physicians and nurse practitioners, providing brief therapeutic interventions, safety and risk screenings, and assessments of cognitive, psychological, and social needs as part of the medical visit. The medical team knows they can easily call on the behavioral health team when they encounter a concern in a patient.  

In addition to in-clinic support, Dr. Bello provides neuropsychological evaluations through on-site physician referrals, assessing all areas of thinking and mood to make diagnoses and care recommendations. Unlike traditional settings where reports are simply submitted electronically, she communicates directly with physicians and nurse practitioners to discuss case nuances and provide immediate feedback. Child Life Specialists work with patients using techniques from medical play to Virtual Reality to increase a child’s understanding of their medical treatments, assist with pain management, and provide distraction. They ease patients’ fear and provide an environment that encourages play and interaction. 

Additionally, social workers at Cure 4 The Kids Foundation complete intakes of new patients and frequently follow up with established patients to assist with financial and social barriers to care. Social workers complete screenings to identify family stressors and connect them with appropriate services.

Comprehensive Pediatric Care Clinics: Treating the Whole Child, Not Just the Diagnosis

A unique aspect of our integrated behavioral health care model is our comprehensive clinic visits, focused around specific diagnoses like sickle cell disease or cancer survivorship. During these extended appointments, families meet with a full team—physician, nursing, pharmacy, dental, and behavioral health—addressing the whole patient and their quality of life. Dr. Bello often meets patients before their neuropsychological evaluation during these clinics, building rapport and answering questions, then follows up afterward to check status and determine additional needs.

Our team’s coordination is supported through weekly case conferences. When a pediatric oncologist notes increasing fatigue, our neuropsychologist might recognize treatment-related cognitive changes affecting school and mood. Together, they create synchronized care plans addressing the whole child, not just their diagnosis.

The measurable benefits we’ve seen speak volumes, and published studies exploring the value of integrated behavioral health care models corroborate our findings as well: 

That’s why we’re proud to say that at Cure 4 The Kids Foundation, families don’t have to navigate behavioral health screening and assessment alone—our integrated team identifies mental health needs right alongside medical care. We then facilitate referrals for crisis response, hospitalization, or connection to community-based therapy services, ensuring families get the comprehensive care they need.

Pediatric Palliative Care

Overcoming Barriers to Child Mental Health Support in Nevada

Despite proven benefits, systemic challenges persist:

Yet opportunities for transformation exist throughout our state. The Las Vegas Medical District represents a perfect ground for innovative, supportive partnerships. Pilot programs like the TANF Mental Health Pilot demonstrating cost-effectiveness could reshape insurance coverage policies. And Nevada state legislators increasingly recognize that investing in integrated care reduces long-term healthcare costs while improving outcomes, committing nearly $200 million to overhaul our state’s behavioral health care system.

Cure 4 The Kids Foundation stands at the forefront of this advocacy, working with policymakers to expand access statewide and demonstrating how integrated models can transform pediatric care.

Dr. Bello sees systemic change on the horizon: “Healthcare systems nationwide are recognizing what we’ve known for years: treating the mind and body separately is outdated medicine. Nevada has the opportunity to lead by example, showing how integrated behavioral health transforms pediatric care. The barriers are real, but they’re not insurmountable when we work together toward this common goal.”

Expanding Access to Pediatric Therapy Across Las Vegas and Beyond

At Cure 4 The Kids Foundation, our commitment to integrated care grows stronger with each family we serve, ensuring no aspect of a child’s wellbeing gets overlooked. We strongly believe that the comprehensive approach we model at our organization represents healthcare’s future.

We invite you to join this transformation. Whether through financial support, advocacy for policy change, or simply sharing this message with others, you can help ensure every Nevada child receives the integrated care they deserve.

Ready to make a difference? Donate today to support our behavioral health program at Cure 4 The Kids Foundation and help us continue building bridges between medical and emotional healing for Nevada’s children.

About the Author: Annette Logan-Parker brings over 30 years of experience in pediatric oncology to her role as Founder and Chief Advocacy & Innovation Officer at Cure 4 The Kids Foundation. She has dedicated her career to improving outcomes for children with cancer and ensuring equitable access to cutting-edge treatments for all families.

About the Author: Dr. Danielle Bello brings over a decade of specialized experience in pediatric neuropsychology to her role as Director of Behavioral Health at Cure 4 The Kids Foundation. A board-certified clinical neuropsychologist, she has dedicated her career to understanding how medical treatments affect children’s cognitive and emotional development, ensuring that every child receives comprehensive support for both their psychological and physical healing.

AI and Childhood Cancer: What Families Need to Know About the New Executive Order

Key Takeaways:

  • A new Executive Order directs federal funding and resources specifically toward using AI technology to improve pediatric cancer diagnosis, treatment, and outcomes.
  • The Childhood Cancer Data Initiative (CCDI) will receive an additional $50 million in annual funding for a total of $100 million per year, helping researchers identify patterns across thousands of cases nationwide.
  • Families should expect to see new pilot programs, research announcements, and technology partnerships at their treatment centers in the coming months.
  • Data privacy protections and equitable access remain top priorities as these technologies develop.
  • AI tools will support (not replace) your child’s oncologist, giving them better resources to personalize treatment.

Over my 30 years in pediatric oncology, I’ve watched families wrestle not only with cancer itself but with the overwhelming flood of medical terms, treatment decisions, unknowns, and policy changes that surround their child’s journey. Now, artificial intelligence in childhood cancer treatment has entered the conversation through a new Executive Order. Like the parents who sit across from our doctors every day, you might be asking: What does this really mean for my child?

As the founder and Chief Advocacy & Innovation Officer for Cure 4 The Kids Foundation, I want to break down this policy in plain language and explain why it matters for the children and families we serve.

What the Executive Order Actually Means for Pediatric Cancer Families

Here is what September 30, 2025’s Executive Order “Unlocking Cures for Pediatric Cancer with Artificial Intelligence” means in practical terms:

Direct Federal Investment: The government is prioritizing AI tools specifically for pediatric cancer. This includes doubling the Childhood Cancer Data Initiative‘s current $50 million annual funding to a total of $100 million.

National Data Coordination: Researchers will combine information from hospitals across the country, helping identify treatment patterns that work best for specific types of childhood cancers. This is especially important since pediatric cancers are rare and no single hospital sees enough cases to understand the full picture.

Accelerated Research Partnerships: Universities, children’s hospitals, and technology companies will work together to develop AI-powered solutions faster than traditional research timelines allow.

Focus on Clinical Trial Access: AI will help match children to appropriate clinical trials more quickly and accurately, potentially opening doors to new treatments sooner.

Why This Executive Order Matters for Your Child’s Cancer Treatment

While this Executive Order opens exciting doors for improving pediatric cancer care through AI technology, we’re also closely monitoring important considerations to ensure these advances truly serve every family.

The Opportunities AI Brings to Pediatric Oncology

Smarter Pattern Recognition Across Cases: When your child’s oncologist reviews their case, they’re drawing on their experience with perhaps dozens or hundreds of similar cases. AI cancer diagnosis tools for children can analyze patterns across thousands of cases nationwide, potentially identifying subtle indicators that predict treatment response or complications before they occur.

Personalized Treatment Matching: Pediatric oncology AI can help doctors analyze your child’s specific tumor characteristics against a vast database of treatment outcomes, suggesting the most promising therapy combinations based on what’s worked for similar cases.

Faster, More Accurate Diagnosis: Pediatric cancer is the leading cause of disease-related death for children between ages 1–19 in the United States. Early detection saves lives, but childhood cancers can be challenging to diagnose. AI technology can help radiologists spot concerning patterns in scans earlier and more consistently, potentially catching cancers when they’re most treatable.

The AI Challenges We’re Watching Carefully

Protecting Your Child’s Privacy: Your family’s medical information deserves the highest level of protection. While the Executive Order emphasizes privacy safeguards, we’re advocating for transparent consent processes that clearly explain how your child’s data will be used, who can access it, and how it’s protected from misuse.

Ensuring Every Child Benefits: Advanced AI tools shouldn’t be limited to major research hospitals. Cure 4 The Kids Foundation is advocating to ensure children treated at community hospitals and rural centers have equal access to pediatric AI innovations. Geography or insurance status should never determine whether a child benefits from top-quality care.

Maintaining Human Expertise: AI excels at processing data as FDA-regulated medical device software, but even the most advanced machine learning cannot replace the clinical judgment, experience, and compassion of your child’s oncology team. These tools must enhance, not diminish, the doctor-patient relationship that’s so crucial during cancer treatment.

What Changes Families Should Watch For

As this Executive Order takes effect, here’s what you might start seeing at your treatment center:

  • New consent forms asking permission to include your child’s de-identified data in national research databases
  • Pilot programs where AI assists with treatment planning or side effect prediction
  • Research announcements about AI-driven studies specifically focused on your child’s type of cancer
  • Technology partnerships between your hospital and universities or tech companies developing pediatric cancer solutions
  • Enhanced molecular testing through programs like the Molecular Characterization Initiative, providing free genetic analysis of tumors

If you notice these changes, don’t hesitate to ask your oncology team how they might benefit your child’s specific situation.

What is the Childhood Cancer Data Initiative (CCDI)? 

The CCDI is a National Cancer Institute program that collects and shares comprehensive data on childhood, adolescent, and young adult cancers across the United States.

Why the CCDI matters for rare cancers: Childhood cancers affect around just 15,000 children in the United States annually. This means no single hospital sees enough cases to understand optimal treatments, making nationwide data sharing essential.

How the CCDI helps families:

  • Accelerates research discoveries by combining data from thousands of cases
  • Enables more precise treatments based on real-world outcomes
  • Expands focus on ultra-rare pediatric cancers that previously lacked research attention
  • Provides insights into long-term effects and survivorship

Key feature: The Molecular Characterization Initiative (MCI) offers free comprehensive molecular testing for many pediatric cancers, sharing de-identified results to benefit future patients while providing immediate insights for current treatment.

How Cure 4 The Kids Foundation is Advocating for Your Family

At Cure 4 The Kids Foundation, our focus remains simple and unchanged: We will continue to bring every possible tool to the fight against childhood cancer while making sure families feel informed and supported along the way. Every year, we care for over 7,000 children with cancer and complex medical conditions, ensuring through our Charity Care Plan that every family receives the same research-driven, high-quality care and treatment regardless of their financial situation.

This new Executive Order is promising, and that’s why we’re committed to:

  • Monitoring Implementation: We’re tracking how quickly and effectively these policies reach actual treatment centers, not just research institutions.
  • Advocating for Equity: We’re working with policymakers to ensure AI advances reach every child, regardless of their family’s income, location, or insurance coverage.
  • Protecting Privacy and Ethics: We’re pushing for the strongest possible data protection standards and clear, understandable consent processes for families.
  • Translating Complex Policies: We’ll continue breaking down technical developments into practical information families can use in treatment decisions.

A Message of Hope: What This Means for the Future

Policy changes don’t happen overnight. However, this Executive Order represents a powerful, national commitment to using some of the world’s most advanced technologies in the fight against childhood cancer.

Change takes time, but every step forward matters. The children we serve today will benefit from better diagnostic tools, more personalized treatments, and improved outcomes. The children diagnosed tomorrow will enter a system that’s learning and improving every day.

To stay updated on AI advances and how this Executive Order impacts your child’s care options, sign up for our newsletter and follow us on social media using the links below.

About the Author: Annette Logan-Parker brings over 30 years of experience in pediatric oncology to her role as Founder and Chief Advocacy & Innovation Officer at Cure 4 The Kids Foundation. She has dedicated her career to improving outcomes for children with cancer and ensuring equitable access to cutting-edge treatments for all families.

Senator Rosen to bring Nevada teen reliant on Medicaid to Trump’s Congress address

U.S. Senator Jacky Rosen announced she will bring a Las Vegas teenager, Dominic Rampa, and his mother, Rebecca Ennis, to President Trump’s Joint Address to Congress Tuesday. Dominic, who has relied on Medicaid since childhood, requires the program to cover treatments for nine genetic disorders, including two immunodeficiencies and juvenile rheumatoid arthritis. Without Medicaid, his healthcare costs would exceed $200,000 annually.

“Since he was a young child, Dominic has relied on Medicaid to get the health care he needs to stay alive. This critical program is a lifeline for Dominic and his family, and I’m grateful to be joined by him and his mom at the Joint Address to Congress,” said Senator Rosen.

Rebecca Ennis, Dominic’s mother, emphasized the importance of Medicaid, saying, “Having a child with multiple rare diseases is very difficult. The cost is more than most people could afford, so losing Medicaid would cause my son to lose the treatments that keep him alive.”

Senator Rosen has been a vocal critic of Republican budget plans that propose cuts to Medicaid to fund tax breaks for the wealthy. She opposed a recent budget resolution that would reduce funding for programs like Medicaid and SNAP, which are vital for many Nevadans. Rosen urged President Trump to reject these legislative plans, which she argues would increase the cost of living for Americans.

Governor Joe Lombardo has expressed strong opposition to potential Medicaid cuts, warning of the severe impact on nearly 800,000 Nevadans who depend on the program. In a letter to Nevada lawmakers, Lombardo emphasized the critical role of Medicaid in supporting low-income individuals, children, seniors, and people with disabilities.

It comes after Congressional Republicans have eyed $880 billion in cuts to the committee that handles health care spending, including Medicaid. President Donald Trump and House Speaker Mike Johnson insist they won’t cut entitlement benefits, but experts say those targeted spending cuts won’t be possible without rollbacks to entitlement programs like Medicaid, which covers hundreds of thousands of people in the Silver State.

In a press conference outside the statehouse last week, state Senate Majority Leader Nicole Cannizzaro called on local congressional leaders to halt the proposed cuts. She noted that Nevada would be the third hardest-hit state in the country, with 50% of all births in the state covered by Medicaid. Cannizzaro warned that rural hospitals would be severely affected, and neonatal intensive care units (NICUs) in the state could face elimination.

Blood Drive and Bone Marrow Registry Event Exceeds Goal

The Cure 4 The Kids Foundation Blood Drive and Bone Marrow Registry event on Valentine’s Day was a huge success, impacting the lives of 177 people who will benefit from the life-saving blood donations and many more who may find a bone marrow match.

A total of 59 units was collected by the Vitalant team, which translated into a 211 percent increase above the event’s goal.

Read more at NonprofitNews.Vegas

 

Critical Care Comics Fundraiser Will Help Cure 4 The Kids Foundation Patients

Superheroes, comic books, and joy! That’s what the team from Critical Care Comics brings to our patients during their regular visits. Usually twice a month, you’ll find Spiderman, Batman, Black Panther and a long list of other superheroes stopping by our clinic with a healthy supply of comic books.

  • 8 News Now recently featured the nonprofit organization and what they do for our patients during their Acts of Kindness segment. Thanks, Critical Care Comics!

Gwen Stefani and Cure 4 The Kids Foundation – A Donation That Keeps On Giving!

Gwen Stefani continues to thrill audiences during her Las Vegas residency performances at the Zappos Theater inside Planet Hollywood Resort & Casino. We’re extremely honored and grateful that Gwen Stefani chose to support Cure 4 The Kids Foundation when she came to Las Vegas. In fact, a portion of every ticket sale is donated to our organization! This is a gracious and lasting gift to Cure 4 The Kids Foundation that will benefit our patients.

We’re also happy to see that her incredible show remains one of the “8 Hottest Las Vegas Residencies!”  Tickets are available for concerts through November of 2019.

Read more in Haute Living