Brady now turned 1, and what a year it's been! It wasn't always easy, and it wasn't all good, but the great memories and milestones really outweigh everything. Brady has a mouth of chompers and is a spunky little boy. He isn't walking quite yet but he sure gets around, and into everything. He babbles all day and is full of slobbery smiles and kisses.
Brady is still on his beta-blocker treatment and he'll be on that until Jan 1 (that day can't come fast enough). His hemangioma is looking great. There are areas that are back to normal skin color and the rest is well on it's way. On Wednesday this week Brady will be having a laser surgery on his hemangioma. Dr. Drolet thinks the treatment will be very effective in getting rid of some of the color still left. It was a big decision for us whether or not to do this, but for Brady's sake we're going for it. Cross our fingers and say lots of prayers that it all goes well.
It's crazy to think that sooner than later our little boy won't see doctors, won't be on meds, and won't have the red little face that we love so much.
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i wanted to say hello my daughter izabell was born with phace syndrome. your sone is very cute!! my daugter is almost 4 now and i can remember back to ther first year or the blur it was. the tought of missing her pink face and its warmth. she still has some pink left on her face and it gives her a nice blush to her pale skin.
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Our daughter is two months old and she just recieved her second dose of Vincristine and Children's. It is nice to see what dramatic results it had for your little boy. How long did you stay on Propranolol?
ReplyDeleteBrooke
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