Enjoy another sneak peek from Samantha Moss’ memoir titled My Medical Musings: A Story of Love, Laughter, Faith and Hope; Living with a Rare Disease! Purchase this book here! * * * “Loves And Losses” A friend recently posted a question in a Facebook Group, asking how we can gain freedom in a chronic illness life, so we can …
Today’s author blog post brings you a special treat! Enjoy a sneak peek from Samantha Moss’ memoir titled My Medical Musings: A Story of Love, Laughter, Faith and Hope; Living with a Rare Disease. Purchase this book here! * * * “The Day My Femur Broke” My left femur broke spontaneously on October 6th 2014. It just snapped …
My name is Kale Sudhoff. and I am 17 years old. I am a Junior at Celina High School in Celina Ohio. I am on the Track and Golf teams at school and I like to fish and draw in my spare time. I have always liked to draw and writing stories is a …
I hear others within the chronic illness or disability community urging others not to let one’s illness or disability define themselves. When I was younger, I followed this sentiment but as the years have gone by, I no longer relate to this sentiment. Nor do I want to. I inherited a genetic mutation from my …
How I Stopped Hiding in the Shadows of Rare Disease (by Jenny Jones) Read More »
In Memory of Oliver Collins 9/16/1993 – 04/21/21 When we set out on a quest to create our Chronically Empowered book, we never imagined one of our own would pass away before the book was released. The news of Oliver’s passing has come as a great surprise and is so very saddening. As we thought …
Sneak Peek of Chronically Empowered (by Oliver Collins) Read More »
