Our good thing is that we are reminded at least every 8 hours (med times!) how precious our little one is to us and just how lucky we are to have him still in our lives.  I’m sure this will come in handy when he becomes a teenager with a stinky attitude, as we all do at some point, ha, ha!

And to Aimee, I just wanted to echo the sentiments of Tina and Elizabeth.  I don’t have a daughter with CAH, but if I ever do, I will have your words in my heart at every doctor appointment.  There have been many times that your words have moved me to the point of tears and I’ve wished that I knew you so that I could tell you in person that you are not alone, and that you are an amazing person.

Please know that you’ve touched many lives and hearts, and that your choice to share your experiences with this community will surely spare many children the pain that you’ve been through.

Blessings,