Hypophosphatasia Externally-Led Patient Focused Drug Development 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…
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…
Howdy! My name is Connor, I’m eighteen years old and I live in San Antonio, Texas! I have been officially diagnosed with HPP for almost…
The US Hypophosphatasia Foundation
141 Hawkins Place, #267
Boonton, NJ 07005, USA.
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