[tri-med] Re: Ups and Downs
- From: "Michelle Wilson" <mewildflower@xxxxxxxxxxx>
- To: tri-med@xxxxxxxxxxxxx
- Date: Sun, 30 Sep 2001 11:22:49 -0500
Hi Laurie, I am sorry that I have no answer for you, but I am sending you
some peace of mind and will be thinking about Brianna.
Michelle Wilson, mother to Faren and wife to Rick
>From: TRIER9@xxxxxxx
>Reply-To: tri-med@xxxxxxxxxxxxx
>To: tri-med@xxxxxxxxxxxxx
>Subject: [tri-med] Ups and Downs
>Date: Fri, 28 Sep 2001 21:25:44 EDT
>
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>Content-Transfer-Encoding: 7bit
>
>Hello everyone,
>I'm not sure is this email is even going to go through, but I need to write
>to you all....at least for therapeutic reasons..
>My little girl had a dexa scan this week and her results are back. Her
>pediatrician called today and says he does not know what to do next.
>He read the results to me over the phone, but I did not absorb much. I did
>get that she is at significant risk for bone fractures. I'm just sick, to
>say
>the least.
>He says IF she has osteoporosis in her hip and spine (this is where they
>tested), then she most probably has it throughout her body. :(
>I''ve cried so hard today, my head is throbbing and I'm slightly
>hysterical,
>but can anyone give me any information on this? I know our kids are at risk
>for bone problems and that some of our children have lost their ability to
>walk in their teen years. Please, anyone...please chime in her and let me
>know what I should do next.
>Thanks so much-Always!
>
>P.S. for those of you following Brianna's inability to sweat effectively
>issue, we now have a diagnosis. It is called Ectodermal
>Dysplasia(spelling?)...I'll write more later on this one if anyone would
>like
>to know more....
>Laurie
>Mom to Brianna age 12 with Trisomy 9p/21
>
>
>
>
>
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>To: 9Tips@xxxxxxxxxxxxxxxx
>From: TRIER9@xxxxxxx
>Date: Fri, 28 Sep 2001 18:31:31 EDT
>Subject: 9TIPS:Ups and Downs
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>Hello everyone,
>I'm not sure is this email is even going to go through, but I need to write
>to you all....at least for therapeutic reasons..
>My little girl had a dexa scan this week and her results are back. Her
>pediatrician called today and says he does not know what to do next.
>He read the results to me over the phone, but I did not absorb much. I did
>get that she is at significant risk for bone fractures. I'm just sick, to
>say
>
>the least.
>He says IF she has osteoporosis in her hip and spine (this is where they
>tested), then she most probably has it throughout her body. :(
>I''ve cried so hard today, my head is throbbing and I'm slightly
>hysterical,
>but can anyone give me any information on this? I know our kids are at risk
>for bone problems and that some of our children have lost their ability to
>walk in their teen years. Please, anyone...please chime in her and let me
>know what I should do next.
>Thanks so much-Always!
>
>P.S. for those of you following Brianna's inability to sweat effectively
>issue, we now have a diagnosis. It is called Ectodermal
>Dysplasia(spelling?)...I'll write more later on this one if anyone would
>like
>
>to know more....
>Laurie
>Mom to Brianna age 12 with Trisomy 9p/21
>
>
>
>--part1_132.24701c5.28e65443_boundary
>Content-Type: text/html; charset="us-ascii"
>Content-Transfer-Encoding: 7bit
>
><HTML><FONT FACE=arial,helvetica><FONT SIZE=2>Hello everyone,
><BR>I'm not sure is this email is even going to go through, but I need to
>write to you all....at least for therapeutic reasons..
><BR>My little girl had a dexa scan this week and her results are back. Her
>pediatrician called today and says he does not know what to do next.
><BR>He read the results to me over the phone, but I did not absorb much. I
>did get that she is at significant risk for bone fractures. I'm just sick,
>to say the least.
><BR>He says IF she has osteoporosis in her hip and spine (this is where
>they tested), then she most probably has it throughout her body. :(
><BR>I''ve cried so hard today, my head is throbbing and I'm slightly
>hysterical, but can anyone give me any information on this? I know our kids
>are at risk for bone problems and that some of our children have lost their
>ability to walk in their teen years. Please, anyone...please chime in her
>and let me know what I should do next.
><BR>Thanks so much-Always!
><BR>
><BR>P.S. for those of you following Brianna's inability to sweat
>effectively issue, we now have a diagnosis. It is called Ectodermal
>Dysplasia(spelling?)...I'll write more later on this one if anyone would
>like to know more....
><BR>Laurie
><BR>Mom to Brianna age 12 with Trisomy 9p/21
><BR>
><BR></FONT></HTML>
>
>--part1_132.24701c5.28e65443_boundary--
>
>
> Building ___ooOOoo__ Rainbows
> www.trisomyonline.org
> Families Helping Families On-line
>
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