In Re The Dependency Of V.w.

Court of Appeals of Washington·Decided December 18, 2023·No. 84395-8·Unpublished

Opinion

IN THE COURT OF APPEALS OF THE STATE OF WASHINGTON

In the Matter of the Dependency of:

No. 84395-8-I

V.W., DIVISION ONE

Minor Child.

UNPUBLISHED OPINION

CHUNG, J. — Infant V.W. struggled to gain weight in the care of his mother, M.W., who has cognitive disabilities. After several hospital stays, V.W. had a nasogastric (NG) tube inserted to ensure adequate nutrition. M.W. was unable to learn how to properly use the NG tube. Based on concerns about V.W.’s failure to thrive in M.W.’s care, the Department of Children, Youth, and Families (the Department) petitioned for dependency for V.W., resulting in an order of dependency and out-of-home placement.

M.W. appeals the finding of dependency based on abuse or neglect and the trial court’s determination that the Department made reasonable efforts to prevent the need for V.W.’s removal from the home. M.W. also challenges the court’s disposition ordering her to refrain from cannabis use. We affirm.

FACTS

M.W. first became involved with the Department in 2012, when B.W., her 10-month-old child, struggled to gain weight. The Department filed a petition for

dependency, to which both parents agreed. Social workers observed that M.W. and the father were not feeding B.W. adequately, did not appear to understand his development needs, and did not follow directions for feeding. A psychological assessment focused on parenting capacity or fitness to parent diagnosed M.W. with cognitive difficulties, including borderline intelligence and Cognitive Disorder NOS. 1 Psychological testing showed that M.W.’s ability to recall verbal and visual information after a 20- to 30-minute delay was in the “Extremely Low” range. Her delayed memory performance was consistent with Cognitive Disorder. The report identified weaknesses such as “limited intelligence, poor memory functioning, and extremely poor academic skills. She lacks basic skills to structure, organize or plan.” Additionally, M.W. “does not appear to understand what led to her child being placed in foster care, and does not consider what she provided to be abusive or neglectful.” The assessment noted that “[t]o be helpful for her services need to accommodate her learning disabilities, limited intelligence, and memory problems. She should not be expected to read and comprehend what she reads.” M.W. subsequently relinquished her rights to B.W.

The child who is the subject of this dependency action, V.W., was born in February 2021 to M.W. and an unknown father. 2 The Department received a “risk-only intake” shortly after M.W. gave birth to V.W. due to its previous

1 “NOS” means not otherwise specified.

2 While V.W.’s birth certificate names M.W.’s husband as the father, M.W. acknowledges

that her husband is not the biological father, and a paternity test confirms this. M.W. does not know the name or whereabouts of her husband or V.W.’s biological father. At the time of the trial, M.W.’s husband was seeking to disestablish paternity and dissolve the marriage.

involvement with B.W., as well as possible instability in M.W.’s housing situation in a “tiny house village.” 3 In May 2021, the Department received an intake reporting that 3-month-

old V.W. was admitted to Swedish Hospital for inadequate weight gain and failure to thrive, with concerns that he was not being fed enough. Dr. Mark Johnson, primary care physician for M.W. and V.W., made the referral because V.W. was not gaining weight as needed for proper development. Dr. Johnson testified that “despite all the medical interventions I recommended and knew of [V.W.] was still not gaining weight appropriately. When [V.W.] was in the hospital with all the support and all the nursing care, [V.W.] was able to gain weight. But when [V.W] wasn’t in the hospital, he wasn’t gaining weight.”

During V.W.’s stay at Swedish Hospital, social worker Alizia Shook worked with M.W. She testified that M.W. was frustrated and did not have a lot of patience with V.W. during feeding. Shook explained that M.W. was required to be present in the room for 24 hours while V.W. was gaining weight before discharge. However, V.W. lost weight during the time he was in M.W.’s care at the hospital. In order to discharge successfully, Shook and the Department worked to create a plan for additional community health supports and resources to assist M.W.

3 A tiny house village is comprised of small units, each with power and a shared kitchen

and bathroom. The record is unclear as to whether each unit has running water. M.W. testified that she had running water. However, social workers testified the units did not have running water.

Shook believed the Department needed to stay involved due to concerns V.W. would lose weight upon returning home to fulltime care by M.W.4 Swedish Hospital discharged V.W. to his mother’s care. Eight days after V.W. left the hospital, Dr. Johnson, noted that his weight had decreased, he had an elevated pulse, and he showed evidence of dehydration. M.W. took V.W. to Seattle Children’s Hospital (SCH). After several days in the hospital, medical testing revealed no medical diagnosis to explain V.W.’s weight loss. SCH physician Dr. Jessica Meikle believed his faltering growth was due to inadequate formula intake because of feeding difficulty. V.W. was a “tricky feeder” and was not meeting feeding goals, even when fed by experienced staff. Additionally, Dr. Meikle was “concerned that perhaps he wasn’t offered enough opportunities to feed based on his mother’s recall of the feeding regimen and what the nurses observed in the hospital of her ability to stick to a feeding schedule.” A nurse observed M.W.’s frustration and overheard her tell a fussing V.W., “Why don’t you just shut up already. You have kept me up since two a.m.”

As a result of V.W.’s inadequate formula intake by mouth, SCH placed an NG tube and established a strict schedule of seven feeds a day with formula

4 The Department’s petition alleged additional facts relating to V.W.’s earlier hospital

stays. For example, it alleges that when M.W. provided care, the time between feeds was too long and the feeds themselves were too short. It also alleged that despite the nursing team providing M.W. with extensive education, reminders, and prompts for feedings, M.W. was “inconsistent” in her ability to provide care including properly mixing formula and adding extra formula “for the calories” and that the incorrect formula to water ratio can lead to dehydration. But at trial, the evidence relating to feeding deficiencies focused primarily on the later hospital stay at Seattle Children’s, through testimony from Dr. Meikle, nurses, and social workers from Seattle Children’s. We do not consider the unsupported allegations from the petition.

offered by mouth and the residual fed through the NG tube. An NG tube goes into the nostril and down to sit in the stomach. Caring for an NG tube requires training in feeding and basic maintenance, as well as additional training in how to place the tube in the nose and stomach. The first step for an NG tube feed involves mixing the formula to the dietician’s recommendation. For pump-fed NG tubes, the caregiver must insert a cartridge into the pump and press a button in order to prime the tubing to get the air out of the line. Then, the caregiver programs the pump with the rate and dose of the feed. 5 Prior to attaching the pump to the NG tube, the caregiver must verify the placement of the NG tube in the stomach by injecting a small amount of air with a syringe and listening to the stomach with a stethoscope. Once placement is confirmed, the caregiver connects the tube from the pump to the NG tube and starts the pump. If programmed correctly, the pump will provide the feed and stop automatically. When the feeding is completed, the NG tube must be flushed with water. NG tube care also requires changing the tape that secures the tube to the face.

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