01/22/2026
Char here….bare with me I’m going to put myself out there, I’m not a super social, put myself on camera kind of gal, but I’m holding myself accountable on here to start posting about our daily life dealing with diagnosis of ALS and caregiving. Sterlings a fighter I’m a fighter, we are constantly researching, studying, trying everything and anything to fight this beast. We are very determined to figure this out, not only for us but for all the ALS families in general that we have come to love so much and so far we have been successful with keeping most the symptoms at bay, keeping positive (we are working on this every minute of every day and night) this doesn’t mean Sterlings life is easy and what he goes through hour by hour is not hard, I live with him, I’m his arms, legs etc! I truly don’t even understand it myself. But with all that being said it’s hard to put it on camera, being a caregiver is not easy it has all the feels, but mostly feels intimate. So here I am holding myself accountable! We are going to start sharing our day to day life. Right now we had to sale our dream home to build a safe one level home for us to live in and this has been difficult with all the other stuff we do on a daily basis, we are starting to see the light at the end of the tunnel to get into our own home where I believe Sterling is going to see some huge wins being able to move around more and go outdoors to get fresh air on his face!
Thanks for the listen get ready to see awkward NOT professional videos and pictures 🙈
Again I have to always say thank you for the support and love you all show us, the prayers, fundraisers all of it! We couldn’t do this fight alone