Wednesday, February 27, 2019

CHD Awareness Chloe & Isabel Jewelry Party

I'm hosting a CHD Awareness Jewelry Party and it ends tonight at 8pm. 

My friend Becky is the consultant running the sale and she is donating her proceeds.

❤️100% of my commission from Kinsley’s party will be donated to CHD Awareness via Run For Little Hearts❤️

When placing your order make sure it says 
1)"you are shopping in Rebecca Crotts' Boutique" 
2) you say “yes this is part of a pop-up” 
3) select “Kinsley’s CHD Awareness Jewelry Party” from the drop down box.

Here is the special party link to order from:
http://www.chloeandisabel.com/boutique/beckycrotts/kinsleys-chd-awareness-jewelry-party

Please let me (Rebecca Crotts) or Kinsley know if you have any questions.

#chdaware #runforlittlehearts #love4lydia




Friday, February 22, 2019

Henry is why we have to keep fighting.


This is why we fight. This is why I write the blog.  This is why I flood your Facebook feed with CHD awareness. This is why I ask you to Run for LITTLE Hearts. Henry is why. Lydia is why. Every other baby born with an incurable CHD is why.

Paige is a friend from Washburn University. We didn't keep touch after graduation but remained connected on Facebook. I still remember the exact moment I found their blog about Henry's CHD. It was just days after we found out Lydia would be born with a congenital heart defect. Henry, Paige, and Jason have been a source of information and inspiration for us. I admire their courage and bravery.

I think of you everyday Henry. 

Here is more on the story of sweet Henry:



The year I didn't post because it was overwhelming, and I'm not sharing that part yet.

I've been meaning to post Lydia's medical update since her comprehensive clinic visit on July 3, 2024.  The notes have been written ...