kalise
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my son lives with moyamoya.
Posts: 36
westernaustralia, Australia, australia, 21, 203, WA, Western_Australia
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hi everyone, my name's kalise, and i have just joined this amazing group. My son Mitchell, who is nearly 4 was diagnosed with moyamoya at 15months of age, after having two strokes, he had two lots of brain surgery before he turned two, and is going quite well, though he still experiences T.I.A's, and seizures, maybe a couple of times a month. He takes 27ml of Tegretol daily, i'm too scared to put him on the asprin. He has brain damage to the left and right frontal lobes, he is an amazing little boy, and will always be my little hero. His next mri is on the 27th nov, the day after his fourth birthday. i hope to get to know many of you. take care...kalise
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