It has been 6 years since my Mother wrote about my life so far and how we as a family dealt with Pompes. In these last six years a great deal has happened and I’m sorry but recalling every detail would be impossible and would probably bore you half to death, therefore I will try and summarise as best as I can the ups and downs I have encountered living with Pompes and being on Enzyme replacement therapy as a teenager/young adult.
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