I was asked to put my experiences with Pompe and Myozyme on paper. And while I realised this...
Author: Robert van Putten
October 20, 2011
Haley, a child with Pompe Disease
Author: Haley Hayes
Video Testimonials
October 5, 2011
I was diagnosed in 2002 at the age of 51, Pompe is not a new visitor to our...
Author: Raymond
September 27, 2011
I was born on July 19, 1986 with a very normal delivery, after a pregnancy without any problem....
Author: Pamela Pieralli
September 14, 2011
My name Nisa means ‘brave woman’ but my parents call me their little sunshine or mouse. I was...
Author: Nisa Karatekin (written by her mother Aylin)
August 25, 2011
At the beginning of the year 2006 I received the news that I was allowed to participate in a...
Author: Theo van der Voort
August 14, 2011
I thought I would let you know how John (aged 68) is doing after he started enzym replacement...
Author: John and Val Shaw
August 4, 2011
Since childhood I had onconventional, but otherwise accepted weaknesses. They were regarded as a child’s expected particularities. The...
Author: Ismael Portilho
July 11, 2011
Nidhi Shirol- 12 year old girl having a ultra rare genetic disorder called "Pompe".
Author: Nidhi Shirol
Video Testimonials
June 28, 2011
Lucas was born on 3rd February 2002. Apparently everything was normal with him and he seemed to have...
Author: Javier (Lucas' Father)
April 6, 2011
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