Sweet Olivia Poppy…

I wasn’t there for your two minutes here on earth but your few breaths were so special to your family. You were so tiny and so perfect. Three pounds of a perfect angel. It’s always sad to meet people like your parents in these circumstances but I am thankful to have met them and I love them dearly. They are no doubt, friends for life. Keep an eye on your big brother and send signs to your mommy and daddy that you are around, they will love it!

Baby Olivia was born with Trisomy 18. A condition that causes severe developmental delays due to an extra chromosome 18.

Little Heroes was called in at 1am to capture “Livy” and her parents. I honestly can’t imagine this service not being offered. NILMDTS is a program that does most of these in the hospital but sometimes they aren’t available so Little Heroes gets the call. If you love what we offer and either on a personal level or have a business that would like to donate before year end, we are a 501c3 that can give you a receipt for your donation. Little Heroes runs off of donations and no donation is too small.

What these families receive:
Session
Digital files
Keepsake Slideshow
5×7 prints of all images
Wall portrait(s)

Our annual fundraiser is coming up in November. It is our 11th year!! Beautiful portraits, Santa, snacks, craft, and giving hearts!! It’s a magical time of year!! Message me if you would like a link to book and/or more information.

How to donate:
I get a lot of questions on how to donate…
Please use one of the following ways to donate:
1. Venmo @kam-neth
2. PayPal: kamslittleheroes@gmail.com
3. Check: Little Heroes, 2825 N. 26th St. 83702