Impact of Pediatric Hypophosphatasia on Behavioral Health and Quality of Life – (2021 Soft Bones Virtual Meeting)

WRITTEN BY JULIA C. If you sat in a class with me, there are a few things you might notice right away. I talk a…
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Hi, we are twin sisters Amy and Suzanne, we have been dealing with symptoms of HPP for a lifetime. Our diagnosis seemed as though it…
My name is Sherri Palackdharry, I have Hypophosphatasia along with two of my daughters, Maya, 16 and Syreeta, 21. Our journey began when Maya was…
I was 22 years old when you were born and had a kindergartner, your brother, as well. I knew something was going on with you,…
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