Two things to share:
One is the link to Simon's blog. You can see Dr. Polley's amazing work just hours after surgery. Haven is SO lucky to have the best pediatric surgeon in the country to take care of her.
The other is something really special to me. When we first found out about Haven's cleft, we had a few days of confusion, anxiety, and worry about what the future would hold. I turned to the internet to start researching everything I could about cleft lip and palate. I came across a blog that changed my whole perception of this journey--I still cry every time I watch the video on her blog but from the first time I saw it--I knew that everything was going to be ok. We are all on a path in life and this was ours--it wasn't bad or different it was just the road that our family was meant to travel. I've said before that I feel like this experience has changed our family and opened our eyes to what REALLY matters in life so I want to share this link with you.
No comments:
Post a Comment