Me and Nate on Family Day (Feb 18, 2013)
The purpose of this blog is pretty simple. It’s to keep friends and family up to date with how the treatment is going. It’s to document the challenges and the triumphs of treatment and all those moments in between. This doesn’t mean I don’t want to hear from people via email/text/phone etc, but it does mean that when we do chat, we can focus on other things rather than the treatment update. Plus, I can post pics of little Nate here!
Mitchell and Nate on our Family Day walk.
Before the diagnosis, I had wanted to start a blog just about the everyday things I was up to, but it turns out that all my everyday things keep me very busy! So, the blog fell off my radar. I had settled on a blog title, “Everybody Hearts,” because I liked the idea of blogging about things I like, pop culture, trends, design-y stuff etc. After my diagnosis in December, I thought about blogging again. And I decided to stick with the same blog title because I liked the positive spin on the song “Everybody Hurts,” because yes, everybody hurts, but everybody hearts too.
Everybody Hearts 
You are a beautiful vision of strength! Love this blog.. so nice to see the boys too. xoxoxo
Thanks, love. Hope to see you soon. xo
I couldn’t agree more with Marla ^ ! Your positive outlook through this journey is admirable and will undoubtedly be the most powerful weapon through it all.
HUGE hug. MASSIVE kiss.
Love and miss you tons!!
Thanks, Leah! We have to get together soon. Much love. xo
ahhhhhhhhhhhhh. cutest ever of all time. xoxoxo
You!
Miss you. xo
Thank you Naomi for sharing this with us. Love the pics, you look so beautiful and that little Nate is so yummy. Thinking of you so often sending love and strength HUGE HUGS! XOXO
Thanks, Sarah. Lots of love to the family! xo
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