Taking a Rare Disease to School

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…
Hello, My name is Morgan Salomon, and I am 16 years old, and I’d like to tell you a little bit about me and my…
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…
When I was born in 1968, my parents assumed everything was fine. They took me home and being her 1st child, my mom thought everything…
If you would like to make a donation to Soft Bones in honor of Cannon, please click the button below! Donate Here Hi! I’m Cannon.…
The US Hypophosphatasia Foundation
141 Hawkins Place, #267
Boonton, NJ 07005, USA.
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