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 »
This blog kicks off the month of May because May is Melanoma Awareness month. Today’s blog is a special surprise for everyone! We’ve been learning about how the company started as well as all of the heart and soul that has been built throughout the company since we started a few years ago. Today we would …
