Ryan’s Story
We are all told to stay away from “Dr. Google”; however, in the case of our son’s diagnosis of Hypophosphatasia (HPP), we were glad that…
Month: November 2020
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…
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…
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…
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…
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…
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…
Can we identify individuals with an ALPL variant in adults with persistent hypophosphatasaemia?
To read more please click on the link below. Read Article
Biochemical and clinical findings distinguishing between the genetic and the acquired conditions in osteoporotic patients with low serum alkaline phosphatase levels
To read more please click on the link below. Read Article
Alkaline phosphatase: Structure, expression and its function in bone mineralization
To read more please click on the link below. Read Article
