“Three-Year-Old Girl’s Uncontrollable Craving for Plaster, Foam, and Wool Due to Rare Diagnosis”

Three-Year-Old Diagnosed With Rare Condition, Develops Unusual Eating Habits

In a heart-wrenching plea for help, Stacey A’Hearne from Blackwood, Wales, shared the challenges she faces with her three-year-old daughter Wynter, who has been diagnosed with a rare condition and an unusual feeding disorder.

Wynter’s journey began when she was just 13 months old, as her mother noticed her becoming non-verbal and developing peculiar eating habits. These habits escalated rapidly, leading Wynter to consume items like plaster off walls, sofa foam, and even attempting to eat glass and photo frames.

Stacey A’Hearne, aged 25, described her daughter’s condition as “literally eating the whole house,” expressing the difficulties of constantly monitoring Wynter to prevent her from ingesting harmful substances. Despite being fussy with normal food, Wynter exhibits a strong urge to consume objects that are not safe to eat, a characteristic of the rare feeding disorder known as pica.

Pica, often associated with autism, generates cravings for non-nutritive substances and is more common in children with sensory processing issues. Stacey noted that Wynter has severe autism, which contributes to her limited speech and behavioral challenges.

Reflecting on her daughter’s journey, Stacey shared her initial concerns when Wynter began putting things in her mouth as a baby, but she didn’t perceive it as a serious issue until Wynter’s behavior changed drastically at 13 months old.

After seeking medical guidance, Wynter was diagnosed with pica and autism in January 2024 through a series of tests. Stacey emphasized the importance of closely monitoring Wynter’s actions to ensure her safety and expressed hope that Wynter will eventually outgrow this challenging phase.

The story of Wynter’s rare condition and Stacey’s perseverance serves as a poignant reminder of the complexities faced by families dealing with unique medical challenges, shedding light on the need for continued research and support for individuals with rare conditions and their caregivers.

Sources By Agencies

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