Hypophosphatasia Pain Management – Paola Genovese, MD

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…
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 Amy. I am a 53 year old newly diagnosed member of the HPP community. I have been living with a mild infantile…
Hi! I’m Denise and I was diagnosed with childhood-onset hypophosphatasia (HPP) at age 50. As a child, I remember that all my permanent teeth…
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…
The US Hypophosphatasia Foundation
141 Hawkins Place, #267
Boonton, NJ 07005, USA.
Organization
Programs
Community
Responses