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    Category: HPP Stories

    Patient of the Month- Sharon M.

    My Journey with my Soft Bones: The only hint my parents had that something was wrong with me was my teeth. My baby teeth had…

    emma_richter January 3, 2023
    0 Comments

    Patient of the Month- Rachel S. and Christine S.

    Hi Everyone,  Instead of Rachel and I (Christine) writing two separate stories, we thought that since our lives are so intertwined, it is best to…

    emma_richter November 30, 2022
    0 Comments

    Patient of the Month- Morgan S.

    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…

    emma_richter October 31, 2022
    0 Comments

    Patient of the Month- Nicole S.

    I was born premature, broke bones easily throughout childhood, and had a few setbacks with development. My parents didn’t think much of it thinking that…

    Denise Goodbar October 5, 2022
    0 Comments

    Patient of the Month- Denise K.

      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…

    Emma September 1, 2022
    0 Comments

    Patient of the Month- Nellie S.

    Hi, I am Nellie and this is my HPP story:  I absolutely love spending time with my family. My husband and I have two sons,…

    wpengine August 4, 2022
    0 Comments

    Patient of the Month- Chris D.

    I became aware of HPP when I was about 38 years old, but in retrospect, I’ve been on this journey for a long time –…

    wpengine June 30, 2022
    0 Comments

    Patients of the Month- Amy and Suzanne

    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…

    wpengine June 8, 2022
    0 Comments

    Living with HPP- Sierra

    Hello..my name is Shelly and I am Sierra’s mother..I had gotten pregnant with Sierra and thought everything was fine..the ultrasounds of her came back perfect…

    Taralyn Naslonski June 24, 2021
    0 Comments

    Living with HPP- Courtney

    In the spring of 2020, I was officially diagnosed with Hypophosphatasia through genetic testing. In retrospect, the signs and symptoms have been evident since my…

    Taralyn Naslonski March 1, 2021
    0 Comments
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    Mail Address (P.O Box)
    The US Hypophosphatasia Foundation
    141 Hawkins Place, #267
    Boonton, NJ 07005, USA.

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