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mitchell's story (Read 2881 times)
kalise
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my son lives with moyamoya.

Posts: 36
westernaustralia, Australia, australia, 21, 203, WA, Western_Australia
Gender: female
mitchell's story
Nov 13th, 2003 at 7:47pm
 
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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DJ
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Been there, done that...

Posts: 721
Wichita, KS
Gender: male
Re: mitchell's story
Reply #1 - Nov 13th, 2003 at 10:12pm
 
Hi Kalise,  Smiley

Welcome to our group!  Sorry you had to find us, but definately glad we could be here for you!

Thank you for your story about Mitchell.  It's always good to hear sucess stories about Moyamoya.  I hope Mitchell continues to improve and grow into an active 'little man'.

Stay in touch!

DJ
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Adversity does not build character... it reveals it...  I help my neighbor and my neighbor helps someone else. Life is a wonderful circle!
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