[tri-med] Re: Partial Trisomy 1, Partial Monosomy 6

hello i'm gina son taylor triosmy 8 mosaic and he is 8 years  old  have you 
tryed the chrosome 8 web site thru yahoo i know there are some 8q on that list 
gina
-----Original Message-----
>From: Tiffany Sprishewsky <tiffanysprishewsky@xxxxxxxxx>
>Sent: Jan 27, 2009 4:32 PM
>To: tri-med@xxxxxxxxxxxxx
>Cc: tiffanysprishewsky@xxxxxxxxx
>Subject: [tri-med] Re: Partial Trisomy 1, Partial Monosomy 6
>
>  Hello, this will be my first post on the site too. So forgive me if I mess 
>up. I have two boys Paul 13 and Danny 10. They are both severely mentally 
>disabled. Along with that other health problems have come and now were dealing 
>with seizures, which they have always had but now the meds don't seem to be 
>controlling them.  Anyway, Three years ago we finally found out their 
>diagnosis. They have a partial monosomy of 6q and a partial trisomy of 8q. 
>They inherited it from me which means I'm a balanced translocation carrierer 
>and they are unbalanced. I was wondering if Sue and the childrens father were 
>tested for the chromosome disorder? And yes I also would like to see if there 
>are anybody else with this same rare translocation?   Thank you. 
> 
>Tiffany Sprishewsky
>--- On Tue, 1/27/09, jwaite <jwaite@xxxxxxxxxxxxx> wrote:
>
>From: jwaite <jwaite@xxxxxxxxxxxxx>
>Subject: [tri-med] Re: Partial Trisomy 1, Partial Monosomy 6
>To: tri-med@xxxxxxxxxxxxx
>Date: Tuesday, January 27, 2009, 10:54 AM
>
>----- Original Message ----- 
>From: "Sue Stockton" <tgsrrs@xxxxxxxxx>
>> This is my first post to this site, and I'm curious if anyone else has
>a 
>> child or children with this particular diagnosis. I have had three 
>> children with this condition. Two have died. My son, Timmy, died at the 
>> age of 2. My daughter, Sheila, died at 11 1/2 months. Her twin sister, 
>> Becky, is 12 now, and has many physical diagnoses, and mental retardation.
>
>Hi and welcome Sue! Glad you've found us but sorry you had a reason to do 
>so.
>
>First off, I can't even come up with adequate words to say with the loss of
>
>your 2 children..........hugs to you at the very least.
>
>Secondly, those of us without a tri-18 or tri-13 diagnosis are considered 
>'rare, rares'. Tend to be few of us around.
>Don't think anyone here has the EXACT same diagnosis (same is true for
>quite 
>a few folks around here) as you dealing with.
>
>While our kids may not have the same dx often they share many common issues 
>be they medical, physical, emotional, social, etc.
>If you have any issues or questions there is often someone here who has had 
>some experience, knows a direction to send someone for help or at least a 
>word of encouragement.
>
>You just never know where a question or comment will lead that benefits so 
>many in some way! (a 'behold the power of the list' moment).
>
>I look foreword to hearing more about Becky.
>
>Michelle mom to Alex (21, partial trisomy 14 mosaic) and Molly (18)
>MichiganUSA
>
>
>                  Building ___ooOOoo__ Rainbows
>                       www.trisomyonline.org
>                  Families Helping Families On-line
>
>
>
>
>      
>                  Building ___ooOOoo__ Rainbows
>                       www.trisomyonline.org
>                  Families Helping Families On-line
>

                  Building ___ooOOoo__ Rainbows
                       www.trisomyonline.org
                  Families Helping Families On-line

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