Author: Kerri Theriault

Makayla’s story: Living with Leri-Weill Dyschondrosteosis

Makayla hip dysplasia lead image

Our daughter Makayla was born perfectly healthy on April 5th, 2014, passing all of the usual newborn screenings without issue. From day one, her personality shone through. She was strong-willed and had a smile that would light up her eyes before her mouth even showed a hint of joy. But over the next 3 months, Makayla wasn’t eating well and wasn’t gaining enough weight.  Our pediatrician referred us to Dr. Elizabeth Hait, a gastroenterologist at Boston Children’s Hospital. Dr. Hait would change Makayla’s formula multiple times and put her on medication for her acid reflux. Her pediatrician also tested her for a milk allergy, since her brother had one as an infant, but it was negative. It was recommended Makayla have an upper GI to make sure everything was anatomically correct.

The technician suggested everything looked good, so we left feeling that Makayla was perfectly normal. But a call from her doctor that afternoon turned our world upside down.

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