Story Time - My niece said what?!

I loved telling this story. It will be one I remember forever! I liked getting Emma's reaction, and I got to educate yall too. I hope you enjoy it!

My name is Kathryn and I have SMA (Spinal Muscular Atrophy) type 2. I may have a disability, but I’m really just your average country girl. I have written a book! You can buy it exclusively on amazon! I love drawing on my laptop! I have taught myself how to draw digital artwork, and I’m not trying to brag, but I’m pretty good lol. I have the best family anyone could ask for, and we do a lot of stuff together. We especially love camping! I love playing video games with my awesome boyfriend! Music is a big favorite! I listen to a little bit of everything. And I like watching movies. So see I’m really not that different from anybody. Thanks for stopping by my channel! ❤️

Follow me!
Facebook -   / camochick202  
Instagram-   / camochick202  
TikTok - https://www.tiktok.com/@kathrynhicks2...

Buy My Book
eBook- https://www.amazon.com/dp/B09D3WSK96
Paperback - https://www.amazon.com/dp/1736906917


Address
Kathryn Hicks
PO Box 538
Six Mile, SC 29682

I’m making these videos to show that people with a disability live normal lives just like anyone else!

SMA is a genetic disorder that causes muscle to weaken and stop working. SMA is caused by a mutation in the survival motor neuron gene 1 (SMN1). In a healthy person, this gene produces a protein that is critical to the function of the nerves that control our muscles. Without it, those nerve cells cannot properly function and eventually die, leading to debilitating and often fatal muscle weakness.
SMA affects approximately 1 in 10,000 babies, and about 1 in every 50 Americans is a genetic carrier. SMA used to be the number one genetic cause of death for infants. Now theres three FDA approved treatments for SMA that are helping people live a much longer life! 😊