Where did September go? Or even more accurate … Where did that YEAR go?! My baby boy is ONE year old tomorrow! When did that happen? I swear I was just telling people we were expecting yesterday!
What a year it has been. If you told me a year ago that we would have done the things we have done, I would not have believed you. Ryan has made our lives even better than we could have imagined. It’s hard to put into words having a son who at first is your worst fear embodied: a genetic disorder! When we found out that Ryan has achondroplasia, at first I could only think about medical hurdles, social difficulties, and physical limitations. All things that were completely on the opposite end of the spectrum from what I had envisioned for 9 months! It didn't take long to fall for Ryan. And as Scott and I learned about achondropliasia and about Ryan’s specific case, we found ourselves pleasantly surprised that little people have perfectly normal, happy, healthy lives! Of course we have had a few extra doctor’s appointments and/or minor issues … but they are just that. Minor. And to top it off, Ryan has risen above everything that has come his way. It’s hard to explain, but I am overwhelmed with pride when I think of Ryan’s past, present and future. He’s more than just “normal” – he’s my Ryan: perfect in every way.
Here are a few pictures looking back over this first year …
Here I am at one of my showers … I’m 33 weeks here!
Happy family:
Homecoming!!
First time meeting his feline brother Tobey:
Helping mom and dad find the perfect Christmas tree for his first Christmas!
Yay for Holidays!
One of our “less fun” adventures …
Say cheese …
My little bunny and his first Easter Basket …
First time at the race track!
First birthday party!
Go Giants!
First time at the family cabin …
First swim class!
Fight On!
First vacation … what a vacation it was!
First Snorkel ...?
It’s fitting that Ryan’s birthday is at the end of September … right in time for October - which is National Dwarfisim Awareness Month! Ryan has opened my eyes, my heart and my mind. I can’t wait to learn more about dwarfism and to help make a difference. I feel lucky that today, people are more accepting of differences, but we still have a long way to go! Thankfully, Ryan has a massive support group in our friends and family.
Here’s to Ryan! … the most amazing, perfect, lovely boy – I couldn't ask for anything more.
... On to the next adventure!