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Moyamoya Related Topics >> Moyamoya Related Information and Support >> Downs and moyamoya http://www.moyamoya.com/cgi-bin/yabb2/YaBB.pl?num=1141533792 Message started by emmas mom on Mar 4th, 2006 at 11:43pm |
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Title: Downs and moyamoya Post by emmas mom on Mar 4th, 2006 at 11:43pm
My daughter has the surgery at Stanford in 2000 (when she was 5) and has downs.... she is now complaining of dizzy spells and tingling in arms and legs. Anyone else out there with downs... how about the symptoms. This website is amazing! When we searched after her stroke in 1999 it was so hard to find any info on the internet!!!! [smiley=worried.gif]
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Title: Re: Downs and moyamoya Post by Dane on Mar 6th, 2006 at 6:08am
Hi Emmas Mum
Our son Dane aged 12 has just undergone his surgery. He has had both right and left STAMCA plus an additional 4 burrs holds placed in his top centre section. He had his Right side done in August, left in Sept and the burr holes in Dec 2005. Pior to his operations he had pain in his left arm and leg quiet regularly. Dane Right side provided a very good artery and it was able to provide a dual bipass whereas his left side artery was quiet small and provided a smaller bipass lower on his brain. The concern from this was that his upper central sector may not get the required blood flow and therefore the burr hole operation. This operation was less intrusive and he was only in hosp for 5 days. The burr holes are expected to allow veins, arteries to grow down to his brain from the skull tissue over the next 6-8 mths. I am not aware of Emmas situation but if she has not had Danes level of surgery it may be good to investigate if some additional surgery may provide further blood supply. It was expected that Dane would require all his operations over the next years but as he had a TIA not long following his first proceedure it was decided to do what we believed would provide the prevention as early as possible. Regards Dane's dad |
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Title: Re: Downs and moyamoya Post by mg12061 on Mar 6th, 2006 at 10:23am
My daughter had her surgery at Boston exactly 4 yrs ago she too was 5. Kathleen ahd some pretty severe strokes before her suregeries so she has a lot of things going on that I don't know are realted to the strokes or the MM.she ash good days and not so good days.She really doens't ahve the language to tell me if she's dizzy or has tingling.Waht I can tell you is she gets VERY tired very easily, she seems to ned 12 hours of sleep.She has days that she seems "out of it" and her concentration is poor.She may even have trouble with school owrk that she previously knew how to do.She has times something will "set ehr off" and she'll cry like something hurts but when I ask her she won't even respond.I have no clue what she's feeling through any of these days so I just work with it and hope that someday she'll be able to tell me. If I can answer any more specific questions let me know. Our girls arent too far apart in age.Kathleen, previouse to the strokes did just about everything right on time,she walked at 18 months,and was talking pretty good, but she lost it all when she had her strokes.She's making her way back slowly.She's reading writting and doing math in school she's in a reg classroom with and aid and special ed teacher.She get PT OT and speech.I owuld love to hear more about your daughter and how she's doing...
Mary Grace mgrace5@nycap.rr.com PS does your daughter get follow up MRI's still,if not how long has it been since ehr last? |
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