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    Category: HPP Stories

    Soft Bones HPP Advocacy: It’s All About Family

    Hello everyone, my name is Sharon T., and my husband Dave has hypophosphatasia (HPP). He and our family have paid a price in our HPP…

    taralyn_naslonski
    Taralyn Naslonski November 6, 2020
    0 Comments

    Kara’s Journey with her Daughter

    My daughter was only 2 years old when she lost her first tooth. At first my husband and I thought maybe she had an old…

    taralyn_naslonski
    Taralyn Naslonski November 6, 2020
    0 Comments

    A Family’s Fight Against HPP

    On December 21, 2011 our daughter Clara B. was born; at the time we believed she was a beautiful healthy baby girl. Little did we…

    taralyn_naslonski
    Taralyn Naslonski November 6, 2020
    0 Comments

    Living with HPP: Aubrey’s Story

    When I found out I was pregnant, the thought of my innocent little baby having an ultra-rare disease never crossed my mind. I was asking…

    taralyn_naslonski
    Taralyn Naslonski November 6, 2020
    0 Comments

    Living with HPP: Sara M.

    My name is Sara and I have Hypophosphatasia (HPP). I am an individual with a rare disease, a fiancé and mother to two toddlers, a…

    taralyn_naslonski
    Taralyn Naslonski November 6, 2020
    0 Comments

    Living with HPP: Sherri P.

    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…

    taralyn_naslonski
    Taralyn Naslonski November 6, 2020
    0 Comments

    Aubrey

    When I found out I was pregnant, the thought of my innocent little baby having an ultra-rare disease never crossed my mind. I was asking myself questi…
    softbones
    softbones October 14, 2020
    0 Comments
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