It's been a while

Wow. I feel like I have really neglected Cameron's blog!

Cameron is doing phenomenal. He is moving about everywhere and crawling so well! Cameron also began pulling up in his playpen last week which is obviously another HUGE step for my sweet boy. Sometimes I can hardly believe all that he is learning and doing. We were told he would never do any of this and yet I know that much more is to come.

Things happening in the Jordan household:

Cam is a little stingy with his kisses but that makes them even more special!

He is really enjoying feeding himself.

Cameron is pulling up! He gets onto his knees and then he pulls himself into standing!

Cameron is finally able to pester Caden as every little brother does and it is hilarious.

These goofy boys are having constant laughing fits while playing together every day and I absolutely love it!

Cameron is enjoying rolling the ball back and forth to big brother. He loves this game. These things may seem small to you, but they are huge for my little man's brain!

We are missing Cameron's Occupational Therapist, Lynea (she moved-good luck Lynea!)

As I was typing this email this is what Cameron was doing.

At least its only paper in there! He was very proud.

Big News!

We have known since the moment we met Cameron that he is an amazing little guy and he continues showing us that every day.

This past week we were very blessed to take a family trip to Disney World. We had an incredible time and will never forget it! 

Not only did we have bundles of fun seeing the sights, but Cameron had some surprises in store for us. If you keep up with us on Facebook than I'm sure this is old news to you. While we were there for our week long stay Cameron began crawling! That my friends is HUGE! He also will lean in and give us kisses. It is the sweetest thing. It's so wonderful to see his eyes light up with excitement over his accomplishments. 

Caden and I have always loved to do patty cake with Cameron and last week Cameron started doing it with us! He can even make a fist with his hands and attempts to 'roll 'em'.

Yesterday I took Cameron to see the family doc because little man wasn't feeling too good. I was so excited to go and brag on my guy. For such a grim outlook to have been painted for Cameron it is a great feeling to be able to tell his doctors that because of Jesus Cameron is defying all odds! We were told to expect him to begin declining rapidly and there was no hope, but we have been praying faithfully and I know that so many of you have been as well and I thank you for that! The doctors are literally speechless.Our neurologists is going to be doing some different testing based on Cameron's progress. He now thinks that Cameron may still have a white matter disease, or a leukodystrophy, but maybe it is a type that stops progressing at random and the brain learns to adapt around the damage.

Cameron still has a lot of learning to do, but he has come miles and miles! He is a happy healthy angel and we are so blessed to have him in our lives. 

I will be posting videos of Cameron crawling etc as well as Disney photos soon.

Thank you everyone for continuing to pray for Cameron and our family!