Powering Through Pompe – a Column by Keara Engle

Keara is located in south-central Pennsylvania and has lived there her whole life. Keara is a single mother to a little boy with Pompe disease who was born in 2018. She hopes that her column, “Powering Through Pompe,” will bring comfort to those that are also dealing with Pompe disease. She remembers how scary it was when her son was first diagnosed and wants to help guide others through their journey. Keara is excited for this opportunity and is proud to be working with this site’s publisher, BioNews.

When a temporary nurse steps in to help my son at school

I’ve become so used to my routines that when an abrupt change happens, it throws me off. Recently, a substitute nurse filled in for the one who usually attends school with my 5-year-old son, Cayden, who has infantile-onset Pompe disease. Cayden is accustomed to having a nurse with him…

Adding nutrients to my son’s diet led to unexpected issues

My 5-year-old son, Cayden, has seen a nutritionist his entire life. In his younger years, this was important because Cayden was underweight. Recently, he has gained weight, but the visits are still necessary because he’s tube-fed. Thankfully, Cayden is able to see his nutritionist at the same time as…