Team Joella

Our sweet baby girl was born with a rare skin disease called Epidermolysis Bullosa. On the day she was born our lives changed forever. Through her life God has shown us his power, comfort and healing hand. We are blessed to be Ella's parents and can't wait to see what God has in store for her life.

Saturday, August 1, 2020

AJ's Bike and Yes Day

›
Hello everyone! In the last week, we have completed two Summer Bucket List items! Last weekend, AJ took off the training wheels on his bike....
3 comments:
Saturday, July 18, 2020

Our Tennessee Trip

›
 Hello everyone! Last week my family and I came back from Pigeon Forge, Tennessee! The trip was so fun. Along the way, our friends the Gr...
Thursday, July 2, 2020

Sorry

›
Sorry everyone. I could not upload the video. It says it is too large. I don't know what that means, but it is not letting me upload i...
1 comment:

Maggie Jo turned 3!

›
My little sister Maggie Jo is now 3 years old! She turned 3 on June 30th. Not a lot happened on her birthday. First, she woke up to he...
Monday, June 22, 2020

I am a teenager!

›
Yes, you did read the title right. I turned 13 yesterday! I think yesterday was the best birthday ever! First, my mom made DELICIOUS b...
Saturday, June 20, 2020

Ella Day

›
Today was another bucket list item! Today was Ella Day. A few weeks ago we had AJ Day on June 9th. You might ask "Ella, why are you n...
3 comments:
Friday, June 19, 2020

Hello!

›
Hi everyone! It is me, Ella! I know is has been a few years since the last post, but now I am going to run the blog! I will update on wh...
7 comments:
›
Home
View web version
Powered by Blogger.