Optimism and Teamwork Keep Toddler’s Rare Cancer at Bay
Wednesday, June 2, 2010
Toddlers don’t usually come out of the operating room (OR) with an idea for a Halloween costume, but Hailey Coniber is no typical toddler. Over the past year, the 3-year-old has been through half a dozen surgeries and many more hospital visits, and yet her optimism and curiosity have prevailed over what might have otherwise seemed like a dire situation.
Jospe found that Hailey had an overactive adrenal gland, which was causing precocious puberty, and a CT scan later revealed that Hailey had an apple-sized tumor on her left adrenal gland. Jospe referred the Conibers to Walter Pegoli, M.D.
, chief of Pediatric Surgery
at Golisano Children’s Hospital. Two days later, the family met with Pegoli to talk with him about removing Hailey’s tumor.
“It was very overwhelming. We kept trying to reassure ourselves,” said Hailey’s mom.
The surgery, which took place April 8, was expected to last four hours but took only 45 minutes. Pegoli met with the family afterwards and told them he had excised, or taken out, the entire tumor and the affected adrenal gland. Though the likelihood of the tumor being cancerous was less than 1 percent, Pegoli wanted to run it through pathology to be sure.
Unfortunately, the test was positive for cancer.
“It’s extremely rare that an adrenal gland has a cortical tumor, which is cancerous, as opposed to a neurogenic tumor, which tends to be benign,” said Pegoli. “I’ve only seen two of these cases in my 20-year career.”
Hailey went home the day before Easter but ended up back that same day to be treated for ileus – an intestinal blockage that can occur after abdominal surgery. Hailey’s CT scan picked up two spots on her right lung. Since it was difficult to tell at that point whether the spots were cancerous, Melissa and Jason were advised to monitor Hailey and to come back three weeks later to see if the spots had grown.
When the family returned for the next CT scan, it appeared that Hailey’s spots might be cancerous lesions. Hailey had her second surgery on May 29 and Pegoli performed a thoracotomy – an incision into the pleural part of the chest to get access to the lungs. He resected, or removed, three lesions from Hailey’s right lung. Later, results from pathology showed that the cancer had spread to her lungs.
One month later, on June 5, Hailey returned to the operating room yet again, this time to place a central venous line so Hailey could begin her vigorous cancer treatment. A central line is a catheter tube passed through a vein to the chest portion of the large vein that returns blood to the heart.
The Conibers tried to maintain a sense of normalcy for Hailey. They kept two Curious George stuffed animals on hand to take turns being with Hailey during her procedures. On June 5, the Conibers began meeting with Lauren Bruckner, M.D., Ph.D.
, assistant professor of Pediatrics and Oncology
at Golisano Children’s Hospital, for Hailey’s chemotherapy treatment. It was important to both the family and pediatric oncologist that they develop a strong working relationship.
“We talk about how the care of a child with cancer is truly a partnership between the family and the child’s health care providers,” said Bruckner. “There isn’t a better example of this than the way in which Melissa and Jason have advocated for their daughter.”
Bruckner was struck by how thoroughly the Conibers prepared for appointments with questions and a list of Hailey’s medications and reactions to treatment. “Dr. Bruckner was very good about listening to us and looking through our notes with us,” said Melissa. “We felt almost bad bombarding her with questions.”
Melissa and Jason took notes daily, and even hourly. Note-taking, as it turns out, was instrumental to Hailey’s treatment. Hailey was taking 24 medications to fight cancer and replace hormones that her body was no longer able to produce since her left adrenal gland had been removed. Hailey’s medications came with just as many side effects, all of which were carefully observed by her parents. Melissa and Jason got to the point where they could predict the timing of the drugs’ side effects within the hour.
Despite their diligence, Hailey began to run the other way when she saw her parents coming because she knew another dose of medication was coming with them. Her nausea, a side effect of the chemotherapy, also made it difficult for Melissa and Jason to persuade Hailey to eat.
The Conibers asked Bruckner and Pegoli about inserting a gastrostomy feeding tube that could supply Hailey with the medications and nourishment she needed. The tube, which looked like a button on the belly and would be surgically placed through the stomach into the abdominal wall, meant another surgery for little Hailey, but Bruckner and Pegoli agreed that it would make it easier to manage her treatment in the long run.
On Aug. 11, Pegoli worked with the Division of Pediatric Gastoenterology to insert a feeding tube. The decision proved to be beneficial for everyone involved. Hailey was getting everything she needed more easily and she no longer saw her parents as “the bad guys.” Hailey has since come to love her “tubey” which looks like one of the Mickey Mouse buttons, as if it were always part of her.
During her many visits to the hospital, Hailey also came to adore her surgeon, “Dr. Goli.” When Halloween came around, she decided to dress up like her “boyfriend” and proudly sported a surgeon’s outfit when she went out trick-or-treating. The nurses on 4-3600 came to know and love the bright-eyed little girl who liked to sit with them at the nurses’ station.
“Hailey was pretty good about being her own advocate,” said Melissa. She described how Hailey learned how to unhook herself from IV tubes properly and always asked, “What’s this?” when nurses or doctors gave her a dose of medication.
Hailey’s positive outlook on her hospital experience reflected the kind, appreciative and receptive demeanor of her parents.
“You see the best in people and you see the worst in people when their children are sick,” said Pegoli. “Some parents exercise such grace and dignity not only to rise to the occasion, but to rise above and think about others.”
Pegoli recalled that despite the difficult position Melissa and Jason found themselves in, they often brought candy and cookies in for the residents and nursing staff. The Conibers recognized that providers were doing their best to help their little girl and were grateful for it.
The Conibers worked with Pegoli and Bruckner to determine the best options for Hailey. A CT scan Oct. 28 showed that Hailey had another spot on her right lung. Pegoli suggested waiting to do the surgery, since Hailey was neutropenic, which meant she had an abnormally low number of neutrophils, an important white blood cell that fights off infections, and her platelet counts were also very low.
Pegoli explained that Hailey would have a better chance at recovering if they waited until Hailey’s immune system had strengthened on its own. The Conibers agreed.
“Dr. Pegoli was always honest and had very strong standards,” said Melissa, as she recounted the story, “I really admired that.”
After a few weeks, Hailey’s blood count levels were high enough for the surgery, which the family scheduled for Nov. 12. Pegoli removed a lesion, located in a hidden area of Hailey’s lung that was difficult to access, along with two other suspicious-looking spots.
After completing the six cycles of chemotherapy prescribed by Bruckner and the most recent surgery with Pegoli, there are no cancerous cells to be found in Hailey.
“I think we’re at the best possible place we could be right now,” said Bruckner. “We have no evidence of any disease.”
“It was a positive experience, thank goodness,” said Melissa, ever the optimist, “We’re still close with everyone. We still visit the nurses and see the doctors. Things happen and it stinks but so far, we’ve had a good outcome.”
Tune in to Children's Miracle Network's News 10NBC Telethon
to meet the Conibers, along with four other Miracle Kid families and Golisano Children's Hospital supporters and providers. The Telethon will take place during Miracle Weekend, 7 to 11 p.m. Friday, June 4, and 3:30 to 8 p.m. Saturday, June 5, on News10NBC. To make a gift, dial (585) 241-KIDS to donate during the Telethon, donate online
or give $10 by texting "Strong" to 85944.
The Stroll for Strong Kids
fundraising walk will also take place during Miracle Weekend from 8 a.m. to 1 p.m. Saturday, June 5, at the University or Rochester’s Fauver Stadium. To sign up or learn more, visit www.bit.ly/Stroll4Kids