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| Mishari
Al Mohamed By Wendy Al Mohamed |
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Mishari was born in the
UK by emergency C-Section on 7th August 1995 (5 weeks early) due to a very
flat trace on the monitor. He weighed just 3lb 10ozs and spent 7 weeks in
the special care unit. He was diagnosed at 2 weeks with diabetes insipidus
and at 3 months with SOD, panhypopituitaryism and Moebius syndrome (facial
paralysis being the most obvious sign). He is currently on DDAVP, Thyroxine,
and just recently Hydrocortisone. He is scheduled to have growth hormone
testing this month. We have not yet got an accurate idea about his vision
but we know it is fairly useful.
Mishari has the gentlest nature and is content and very happy (so long as you don't try to cut his nails or hair!!) and the silliest things make him laugh. He is extremely sensitive to light and must wear a hat and sun glasses outside (this is partly due to the moebius syndrome as he cannot squint or close his eyes), he looks so trendy. He loves to get under things an since he's got more mobile we never know where we'll find him, and his favourite position is upside down. He is trying to crawl (he does commando style crawling but still loves to get around on his back, much to my disgust as he's got a huge bald patch on the back of his head!). He's happy to walk a little with support but will still not sit unsupported. Mishari has two brothers, Faraaj 3 1/2 and Talal 1 year, and we all live in Bahrain which is just across the water from Saudi Arabia.
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This website has been
designed to help empower parents of children with ONH/SOD. All the information
herein is subject to opinion. If you suspect your child may have ONH/SOD
it is recommended that you seek professional advice from a certified pediatric
ophthalmologist. No one individual or company connected with this website
assumes any liability or responsibility |
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