In re G.M.

CourtCourt of Appeals of Kansas
DecidedMay 15, 2020
Docket121254
StatusUnpublished

This text of In re G.M. (In re G.M.) is published on Counsel Stack Legal Research, covering Court of Appeals of Kansas primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re G.M., (kanctapp 2020).

Opinion

NOT DESIGNATED FOR PUBLICATION

No. 121,254

IN THE COURT OF APPEALS OF THE STATE OF KANSAS

In the Interest of G.M., A Minor Child.

MEMORANDUM OPINION

Appeal from Sedgwick District Court; RICHARD A. MACIAS, judge. Opinion filed May 15, 2020. Affirmed.

N. Trip Shawver, of Wichita, for appellant natural mother.

Julie A. Koon, assistant district attorney, and Marc Bennett, district attorney, for appellee.

Before GARDNER, P.J., WARNER, J., and ROBERT J. WONNELL, District Judge, assigned.

PER CURIAM: Since he was a baby, G.M. has been treated for a host of medical conditions. These involved several invasive surgeries and required G.M. to take multiple prescription medications with serious side effects. By the time he was 11 years old, G.M. had not attended school for over a year and appeared to be losing his mobility. These various treatments, procedures, and medications were provided based on reports of symptoms by—and often at the insistence of—G.M.'s mother, sometimes contrary to the advice of G.M.'s doctors. In February 2018, medical professionals reported concerns that G.M. was the victim of caregiver-fabricated illness—that is, that the treatment, procedures, and medication G.M. received were unnecessary because the symptoms his mother reported could not be objectively verified. The providers were also concerned the multiple overlapping treatments he underwent were exacerbating his conditions.

1 After hearing several days of evidence, the district court adjudicated G.M. a child in need of care. G.M.'s mother now appeals that adjudication. Because there is sufficient evidence in the record to support the court's findings, we affirm.

FACTUAL AND PROCEDURAL BACKGROUND

Though he is young, G.M. has an extensive and complicated medical history. Beginning when he was less than two years old, G.M.'s mother (Mother) reported symptoms to his medical providers that led to diagnoses of—and treatment for—multiple serious conditions, including global developmental delay (later classified as autism with intellectual impairment), seizures, migraines, somnolence (excessive tiredness and sleeping), sleep apnea, cyclic vomiting, eosinophilic gastroenteritis, difficulty urinating, and failure to thrive. In February 2018, the State filed a Child in Need of Care (CINC) petition on behalf of G.M., who was then 11 years old, alleging he was the victim of medical child abuse and caretaker-fabricated illness in a child—that is, claiming Mother exaggerated or fabricated his symptoms to procure unnecessary and harmful medical care.

G.M.'s father and Mother waived their rights to temporary custody hearings, and G.M. was placed in temporary custody with a foster family. G.M.'s father did not contest the CINC petition. Mother, however, challenged the adjudication.

The district court held an evidentiary hearing over the course of several days in the fall of 2018. During that hearing, the court heard testimony from multiple witnesses, including the reporting physician, several of G.M.'s treating physicians and health care providers, G.M.'s structured learning teacher from his home-schooling, and G.M.'s foster mother. Mother also testified, along with several of her friends and family members. The evidence presented during the hearing revealed the following history.

2 G.M. was born in 2006. Beginning in 2008, Mother took him to see a neurologist in Wichita, reporting a variety of symptoms. Over the course of several years, these reported symptoms included headaches (including migraine headaches), dragging his right leg, aversion to noise, seizures and epilepsy, sleep deprivation, and autism.

G.M. has been prescribed multiple medications for seizures since 2010, sometimes four or five medications at one time. Mother continued to report G.M.'s seizures despite this medication, and in 2014 doctors implanted a vagal nerve stimulator (VNS)—a device connected to the vagus nerve that releases electrical impulses to disrupt and decrease the number of seizures. In September 2017, G.M. underwent a second surgery to replace the battery in the VNS. In February 2018, G.M. had the VNS and was also taking four prescription medications to treat his seizures. At the hearing, a number of friends and family of Mother testified they had witnessed G.M.'s seizures. But G.M. has undergone at least nine EEGs, including two lasting several days, and none showed brain activity indicating seizures.

One of the side effects of G.M.'s anti-seizure medications was somnolence. G.M. began experiencing excessive sleepiness in 2014. Mother reported that this condition was particularly severe in the second half of 2016; during that time, G.M. would sleep all the time and would wet and soil the bed. Mother reported that she had to use a wheelchair to take G.M. to medical appointments because he would be asleep when they needed to go somewhere and was too big to carry. She also indicated G.M. was not able to attend school because of this sleepiness, compounded by his other medical conditions.

Excessive sleeping can lead to low blood-oxygen saturation. In March 2014, Mother reported that G.M.'s lips, hands, and feet turned blue while he slept. She thus obtained a pulse oximeter to measure G.M.'s oxygen saturation while sleeping; his saturation level was 84%. After doctors performed a sleep study in April 2014, G.M. was diagnosed with sleep apnea and placed on a continuous positive airway pressure (CPAP)

3 machine while sleeping. Because his saturation levels continued to dip below 90% even with the CPAP, G.M.'s doctor placed him on supplemental oxygen when asleep.

Another side effect of an anti-seizure medication prescribed to G.M. in October 2016 was elevated liver enzyme levels. To monitor G.M.'s enzyme levels, doctors had to draw blood every six weeks; G.M. was often uncooperative, and doctors feared they would have to sedate him during the draws. To avoid the possibility of sedating him for every draw, G.M.'s primary care physician referred him to a surgeon in August 2017 to implant a Mediport—a port which provides direct venous access for injections and draws.

Seemingly unrelated to the seizures, Mother took G.M. to see a pediatric gastroenterologist—Dr. Mayssa Zayat—in January 2013, reporting that G.M. was vomiting once per week. Dr. Zayat performed an endoscopy, which showed eosinophilic gastroenteritis in his throat. G.M. was placed on several dietary restrictions and prescribed medication to control the vomiting. In follow-up visits, Dr. Zayat found nothing wrong with G.M.'s throat, and G.M. showed no signs of continued vomiting. Nevertheless, over the course of the next year, Mother continued to bring him to Dr. Zayat, reporting that G.M. was now choking and gagging when eating, was a picky eater, and experienced routine pain and nausea. The gastroenterologist referred G.M. to an allergist in case he was experiencing an allergic reaction and performed two additional endoscopies—both of which came back as normal. G.M. was also within the normal weight range for children his age.

In July 2014, Mother consulted Dr. Zayat about the possibility of surgically inserting a feeding tube to make sure G.M. was receiving proper nutrition. The doctor explained she did not believe the feeding tube was necessary, as G.M. was within the proper weight range—he was actually gaining weight—and implanting a feeding tube is an invasive procedure. Nevertheless, at the urging of Mother, Dr. Zayat provided the phone number of a surgeon in case G.M. wanted to consult someone else about it.

4 When G.M. next met with Dr. Zayat in September 2014, the feeding tube (or G- tube) had been implanted.

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