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.

Welcoming a brand-new member of the family

Two weeks ago, I gave birth to another beautiful baby boy named Kylan. Our family is ecstatic about our new addition, and Kylan feels like the last piece to our puzzle. My 6-year-old son, Cayden, and 20-month-old son, Kyree, love to hold him and help do things for their baby…

When plans for my son’s home infusion go haywire

Every month, we receive a package at our house for my 6-year-old son, Cayden, worth almost $14,000. What could cost so much, you might wonder? Life-saving medication. Cayden receives biweekly infusions of Nexviazyme (avalglucosidase alfa), as enzyme-replacement infusions are currently the only treatment option for Pompe disease, which…