Posted by Michael Wonder on 27 Oct 2021
Audrey Ashman’s bone treatment for rare genetic disease known as XLH denied government subsidy
24 October 2021 - Audrey Ashman loves to ballet dance and plays with her brothers — but she needs a special bone treatment that’s been rejected for a government subsidy.
The youngster suffers from a rare genetic disease, called X-linked hypophosphataemia, which left her father’s bones so soft he required rounds and rounds of horrifying surgery.
