There is so much going on now with Oliver’s sloth petition everyday. It’s overwhelming. We are trying to keep up with everything going on and share stuff with you guys here on Oli’s page but we are tiptoeing on that line between celebrating all the amazing things happening and being completely obnoxious with too many posts.

We have met and talked to so many amazing people in the last few weeks because of this. People who have also lost children. Parents with VACTERL kids, kids with limb differences, kids with other rare conditions. Their stories uplift and inspire us. They are setting the example Alyssa and I need to help guide our journey as we try to do the same for other in Oliver’s name.

We’ve said it many many times before, but thank you to everyone reading this from the bottom of our hearts. We will keep posting updates because this journey is far from over. � ❤️ ��