Brayden will be meeting with Dr. Singh today for his 4 month check up. We have a list of questions to ask the dr about his up coming surgery in May when he turns 6 months. If everything looks ok with Brayden, we will have his 1st surgery in May.
Tomorrow Brayden will be having a MRI done. The 1st time he had one, they only did a MRI on his lumbar spine. So this time around they want to do a whole body one and make sure he doesn't have the nevus on his brain. His apt tomorrow is at 10 am and he can't eat after 5 am. Poor baby! I don't know how we will do that, when he gets hungry, he's hungry and he wants to eat right now....just like his mom! ha! Since mommy will be working tomorrow, daddy & Grandma Vauble will be taking him to his MRI. They have to put a gas mask on him to put him under and the whole MRI will take an hour.
Just thought I would give everyone a quick update with Brayden and what he will be going through this week.
Please keep him in your prayers
Thank you for following Brayden's Journey. He is truly such an amazing little boy, always so happy and full of smiles. Brayden was born on 11/01/2010 with Giant Congenital Melanocytic Nevus. 1 out of 500,000 babies are born with this, so a lot of you may have never heard of this before. Continue to follow Brayden's Journey and you will learn all about nevus. We really appreciate all of your support.
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