Peyton’s Neuroblastoma Fight

Peyton’s Neuroblastoma Fight Peyton’s Neuroblastoma Journey. She’s strong little girl suddenly diagnosed with intermediate NB->high risk-> int NB in 2026.

Helping to bring awareness to this rare and aggressive cancer and advocating for all pediatric cancer!🎗️
•Wichita, KS•

9/19/26 🎗️Childhood cancer awareness month.This is one of the pieces of Peyton’s cancer journey I don’t think I’ll ever ...
09/19/2026

9/19/26 🎗️Childhood cancer awareness month.
This is one of the pieces of Peyton’s cancer journey I don’t think I’ll ever get over. The number of times we had to physically hold Peyton down while she screamed, cried, kicked, and begged us to stop. Blood draws. IVs. Dressing changes. Accessing her lines. Scans. Procedures. Pain. Things we knew had to be done to save her life—but things she was far too little to understand. She didn’t understand that we were helping her. She just knew that something hurt, she was scared, and the two people she trusted most were helping hold her still while it happened.💔 There is a kind of heartbreak that comes with looking into your child’s terrified eyes and saying, “Mommy’s right here,” while also being the one holding their arms down.😭 Every instinct you have as a parent is screaming at you to pick them up, protect them, and make it stop. Instead, you have to hold tighter because you know it can’t stop.

Childhood cancer asks children to endure things they cannot possibly understand and it asks parents to participate in things that break their hearts. 💛🎗️💪

9/17/26One thing we don’t talk about enough with childhood cancer is the other child or children in a family.When Peyton...
09/18/2026

9/17/26
One thing we don’t talk about enough with childhood cancer is the other child or children in a family.When Peyton was diagnosed, our entire world became about keeping her alive—chemo, hospital stays, surgery, scans, traveling, appointments and fear. And in the middle of all of it was Saige.
The one being left with family while we traveled for treatment. The one watching us pack bags to rush off to the hospital for another emergency fever protocol. The one who still needed Mom and Dad but somehow had to learn to “understand” that her sister needed us more. Peyton had cancer, but childhood cancer happened to Saige too. So if you know a family going through this and you don’t know how to help—love on the sibling! I can’t express this enough! Take them for ice cream. Invite them somewhere fun. Show up to their activities. Bring or deliver them a little surprise too, one just for them. Ask about their day. Make them feel important and remembered.Those things may seem small, but to a parent being pulled between two children, they mean more than you’ll ever know.Because sometimes the greatest way you can help us care for our sick child is by helping make sure our other child still gets to be a kid!!! 🫶🏻💛Can’t thank Whip Pediatric Cancer enough for sending Saige her very own “uni-port” dress to match PeyPey. Even a dress to match their dolls🥺🫶🏻🦄🎗️💛💪

9/16/26 🎗️The part of survivorship no one really prepares you for. 💛Today brought an unexpected doctor’s visit after Pey...
09/16/2026

9/16/26 🎗️The part of survivorship no one really prepares you for. 💛
Today brought an unexpected doctor’s visit after Peyton has been complaining that her legs hurt and asking to be carried more than usual. I’ve brushed it off for a couple weeks but decided that I needed to let her health care team know just to be on the safe side. And just like that🫰 they were calling wanting to schedule an appointment to see her.
Before cancer, I probably would’ve immediately thought, growth spurt, long day, not feeling good, literally anything a normal 3 year old could come up with. Now, there’s always that little voice in the back of your mind that wonders, what if it’s not? We are blessed with a diligent healthcare team who wanted to lay eyes on her and did a very thorough assessment, ran her urine for the HVA/ VAN testing that’s done in NB kids( those take a week to result). After measuring here, I was informed she’s actually grown 1inch in just 2 months 😱👏💪💛. That immediately gave me some sense of relief. We’re really hoping this is nothing more than a growing little girl with growing little legs. 🤞🏼 But once you’ve heard the words “your child has cancer,” new aches and pains just hit differently. You learn to pay attention to things you once wouldn’t have thought twice about. The irony of walking into the doctor today and seeing all of these “Fight Like a Kid” signs felt pretty special, though. And of course PeyPey had to show everyone just how strong she is. 💪🏼🎗️. She said look mom they have my ribbon hung up!🫶🏻🥺🤣 So for now, we’re hoping for the most boring explanation possible: a growth spurt. Because after the year she’s had, boring sounds pretty damn good. But again, so VERY thankful for a healthcare team who remains on top of things no matter how big or small💛🎗️💪

9/15/26🎗️💛🎗️
09/16/2026

9/15/26🎗️💛🎗️

9/14/26🎗️childhood cancer awareness month🎗️
09/15/2026

9/14/26🎗️childhood cancer awareness month🎗️

9/13/26🎗️This post might hit hard, it might be triggering, and it might hurt feelings. But good. I want the reality of c...
09/14/2026

9/13/26🎗️This post might hit hard, it might be triggering, and it might hurt feelings. But good. I want the reality of childhood cancer to make others sick like it makes us. We created a platform and we plan to use it to the fullest because the general public is SO unaware that we need a change. People say,“It’s just hair. It’ll grow back.” And yes, it does. But watching your child’s hair fall out is often the moment cancer becomes visible to the rest of the world. Nothing about Peyton’s cancer journey has stuck with me quite like the day we had to shave her hair. It felt like we lost a piece of our daughter that day. Like we were taking the PeyPey we knew and loved and watching cancer create a whole new version of her — a version she never asked to become. But the hair is only what people can see. What they don’t see is the nausea. The pain. The exhaustion. The infections. The transfusions. The surgeries. The LONG hospital stays. The fear. And even when treatment ends, the damage doesn’t necessarily end with it. Cancer treatment can leave children facing lifelong consequences. Damage to their heart, hearing, fertility problems, developmental effects, organ damage, and even an increased risk of developing another cancer later in life. And these are CHILDREN‼️‼️
This may be controversial, but I think it’s a conversation worth having: I wonder what cancer treatment would look like if adults were expected to endure the same intensity of treatment and the same risk of lifelong consequences that we have somehow learned to accept for children? I’m not saying adult cancer is easy. It absolutely isn’t. Cancer is devastating at any age. But watching pediatric cancer treatment firsthand has made me question why adults can go through the same treatment and live their life as “normal” while our small children are struggling to survive each and every day. If adults were facing treatments that threatened decades of their future health just for the chance to survive, would we accept the same pace of progress? Would research have to fight this hard for attention and funding? Would we be louder about demanding treatments that don’t require doing so much damage to a person in order to save their life? I’ve seen far too many adults this year alone who you could look at from the outside and never even know they were battling cancer, while at moments Peyton was struggling for her life. I had a patient tell me they had over 36 rounds of chemo under their belt- all while looking like they never went through a day of chemo in their life. And all I could respond with was “my daughter absolutely would not survive going through that many rounds”. This is when we have to demand a change! Because our children deserve more than treatments that simply give them a chance to survive.
They deserve more research.
More funding.
Better treatments.
Less toxic treatments.
Children should not have to pay for survival with the rest of their lives.
And they sure as hell deserve more than 4 f*cking percent of federal cancer research funding. 💛🎗️💪

9/12/26 🎗️Childhood Cancer Awareness Month🎗️ consider this your ~friendly~ fall guilt trip to Skip ONE pumpkin spice lat...
09/12/2026

9/12/26 🎗️Childhood Cancer Awareness Month🎗️ consider this your ~friendly~ fall guilt trip to
Skip ONE pumpkin spice latte. Skip ONE b**r at the football game. Skip ONE drive-thru lunch. That $5–$10 probably won’t change your week… but when hundreds of people do it, it can change the lives of families facing childhood cancer. Peyton has done enough fighting. The least we can do is sacrifice a little caffeine or b**r money. 😉 🎗️💪💛

Local⤵️
⏩️ Wichita's Littlest Heroes
⏩️ Carter Tough Foundation
⏩️ BabyJay's Legacy of Hope
⏩️ Love, Chloe Foundation

NYC/MSK⤵️
⏩️ Whip Pediatric Cancer
⏩️ Candlelighters NYC
⏩️ Memorial Sloan Kettering Cancer Center

9/11/26 🎗️Childhood Cancer Awareness Month🎗️I can’t help but wonder… what if we were looking for childhood cancer sooner...
09/12/2026

9/11/26 🎗️Childhood Cancer Awareness Month🎗️
I can’t help but wonder… what if we were looking for childhood cancer sooner?What if we routinely checked HVA and VMA in kids’ urine at certain well-child visits? What if we started checking blood pressure consistently at younger ages, rather than waiting until they’re older? What if we were “swabbing” our kids as frequently as doctors want to always test for Covid/ flu? I say “swabbing” because we all know anytime we take our kid in with a concern they want to swab for flu/Covid right off the bat 🥴🙄. I believe now from living this personal version of hell, that a lot gets overlooked for our kids. But then, from a nurse and mother standpoint, I understand that not all kids are potty trained as early as Peyton was. Her older sister Saige definitely wasn’t, in which straight catheterizing her for a urine sample would have been an absolute no for me. But what about blood pressure checks? Upon diagnosis Peyton’s blood pressure was absolutely sky high, yet her blood pressure had never been taken because she was under the age of 3.
Neuroblastoma can grow silently. Its symptoms can be vague or easily mistaken for normal childhood illnesses—and some children may have very few warning signs. Yet many neuroblastomas produce catecholamine metabolites that can show up in urine, and some can also cause high blood pressure.
I’ll always wonder: if Peyton’s urine had been tested earlier, or if something as simple as her blood pressure had raised a red flag, could we have found her cancer sooner?
Before her tumor became massive.
Before it wrapped around major blood vessels.
Before it had the opportunity to spread.
I understand that routine neuroblastoma screening isn’t currently recommended for every healthy child, and neither urine testing nor blood pressure would catch every case. But after watching my child battle this disease, I think we’re allowed to ask: Are there simple, non-invasive ways we could be catching some of these kids earlier? I mean adults have the “luxury” of screening for different cancers so why can’t our kids?!? Maybe it’s a urine sample. Maybe it’s a blood pressure reading. Maybe it’s paying closer attention to subtle changes that don’t quite add up. Childhood cancer may be rare, but earlier detection deserves a much bigger conversation. 💛🎗️💪

9/10/26🎗️Childhood Cancer Awareness Month🎗️This one is for the dads out there. The dads who carry a weight most people w...
09/11/2026

9/10/26🎗️Childhood Cancer Awareness Month🎗️This one is for the dads out there. The dads who carry a weight most people will never see. The dads who hold it together in front of everyone else and later fall apart when no one is looking. Behind so many little warriors is a dad quietly fighting right alongside them. 🎗️💛💪

9/9/26🎗️Another ugly side of childhood cancer that nobody prepares you for: you don’t just fight cancer. You fight insur...
09/09/2026

9/9/26🎗️Another ugly side of childhood cancer that nobody prepares you for: you don’t just fight cancer. You fight insurance, too.
In less than four months, Peyton had 174 insurance claims totaling $1,837,024.58 billed to insurance. Let that sink in for a second. Nearly $1.84 MILLION DOLLARS with 174 individualize claims!!! Obviously, I am incredibly thankful we have insurance. But having insurance does not mean you can just hand over your card and focus on keeping your child alive. I wish it were that simple. Instead, somewhere between chemotherapy, surgeries, scans, labs, hospital stays, medications, traveling for care, working, and trying to keep some sense of normalcy for our family, I basically had to take on another unpaid job: learning how to navigate our health insurance system. My biggest advice to any family going through something medically complex: ‼️‼️CALL YOUR INSURANCE COMPANY AND REQUEST A CASE MANAGER ASAP‼️‼️
Our case eventually became complicated enough that we had two incredible women helping me navigate it. They worked endlessly behind the scenes, and I genuinely don’t know what I would have done without them. But even with their help, the amount of work that still fell on me was ridiculous. Hours on the phone, tracking claims, reading EOBs, checking authorizations, making sure providers were in network, comparing bills to insurance claims, documenting phone calls, disputing charges. Following up again…and again…and again. I work hard for our family to have good insurance coverage and what insurance put us through this year is a disgrace. All while taking care of our child with cancer.🤬
Within 24 hours of Peyton’s diagnosis, I knew we had already hit her deductible and out-of-pocket maximum. Yet bills continued pouring into our mailbox like wildfire. And then came the fun part: trying to figure out which ones we actually owed. Was insurance still processing it? Was it applied correctly? Did it count toward our out-of-pocket maximum? Was the provider billing us prematurely? Was it something we were actually responsible for? And when I didn’t immediately pay bills I believed were still being worked through insurance? Collection letters started showing up just as fast. So then, on top of everything else, I was sending dispute letters almost weekly.
Recently, I finally asked our case managers to make me an Excel sheet showing exactly which claims out of the 174 we were actually responsible for paying because I couldn’t keep up with everything. And bless their hearts that they did. 🙌🫶🏻
Because I refuse to blindly pay every medical bill that lands in my mailbox simply because someone printed an amount next to “Amount Due.” I will pay every dollar we legitimately owe. But I will not pay one dollar more. Parents should be spending those hours holding their children—not fighting a healthcare system on the phone. But until that changes, LEARN your policy and ADVOCATE like hell. Because nobody will protect your family, your child’s care, or your bank account quite like you will. 🎗️💛💪

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327 E 64th St
New York, NY
10065

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