From:      bounce-scoliosis
To:        scoliosis-digest@ai.mit.edu
Subject:   scoliosis V1 #579
Reply-To:  
Errors-To: bounce-scoliosis
Precedence: bulk


scoliosis                Sunday, 28 September 1997     Volume 01 : Number 579

Today's subjects for scoliosis and scoliosis-teens:
  Re: DC                  ["Dean A. Hoppenrath, DC" <drdean@interaccess.com>]
  Re: Copes                                    [Peggy <mclay@concentric.net>]
  [Fwd: Re: Scoliosis Docs]                    [Peggy <mclay@concentric.net>]
  Re: SRS             [Linda Racine <lindaracine@denmark-c.it.earthlink.net>]

----------------------------------------------------------------------

From: "Dean A. Hoppenrath, DC" <drdean@interaccess.com>
Date: Sat, 27 Sep 1997 10:55:17 -0500
Subject: Re: DC

the Copes system.  I decided to start this a week or so ago when everyone
started the discussion about it.  I must admit I am not too familiar with
the system but am very interested in any info available.

I thank you for your kind comment at the end of your message and I have
gotten a lot of information from you guys that no one teaches in school.  I
have always thought that doctors can learn more from their patients than
they can teach them and this forum proves it.  When I develop an opinion on
the Copes system you will be the first to know but for now, I don't have
one.

Keep up the good work and if anyone has any questions that I can "try" to
answer feel free.

Dr. Dean

- -----Original Message-----
From: EarthLady3@aol.com <EarthLady3@aol.com>
To: scoliosis@ai.mit.edu <scoliosis@ai.mit.edu>
Date: Friday, September 26, 1997 11:50 AM
Subject: Re: DC



:In a message dated 97-09-26 10:59:20 EDT, you write:
:<< if it is primary idiopathic scoliosis, I would have to say no
: because I would be kidding myself if I thought I would be able to reverse
: the curve. >>
:
:
:Dear *DR.* Hoppenrath, <smile>
:
:Then how do you feel about the Copes system of bracing for adults?  BTW,
:thank you for contributing to this forum, I think it helps to have a "real"
:chiropractor here.
:
:EarthLady3@aol.com
:
:
:For help on using this list (especially unsubscribing), send a message to
:"scoliosis-request@ai.mit.edu" with one line of text: "help".
:
:


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------------------------------

From: Peggy <mclay@concentric.net>
Date: Sat, 27 Sep 1997 17:13:32 -0700
Subject: Re: Copes

> My 4 year old has her appointment with a pediatric SRS in 2 weeks and I
> pray she is in the clear as far as having this, I think of your daughter
> every time I see a posting from you and hope she is doing ok.
> ...
Kathy,
Natalie got her brace and it fits perfect.  Her eyes got wide when it
was first put on.  I think she got a little claustrophobic.  When she
realized he could still breathe, move around etc she relaxed.

I have to buy her lots of pretty t-shirts to wear under it that fit snug
to her body.  Some of the ones she has tend to bunch under it.
She is supposed to wear it an hour longer each day until she builds up
to the 18 hours.  The first day she was only required to wear it one
hour, but we were out shopping and she was in it for 2 1/2 with no
complaint.

The only part that is noticeable under her clothes is the buckle part at
the top of her back. This kind of bulges a little.  I think I will let
her hair grow longer to disquise this a little.
She has fallen asleep in it for an hour on the sofa.  So I know it is
possible for her to sleep in.
She has an apointment in 6 weeks to get the air bladders put in.

She can't put it on or take it off herself, so I'm not sure what we will
do about her gym class at school. I don't know if she can change her
clothes by herself with it on yet.  We haven't tried that yet.
Her teachers have offered that they will help with any special
arrangements she may need.  I hope to keep special treatment to a
minimum.  I don't want her to feel too singled out or different from the
other kids.

Anyway I am delighted that she does not complain about it or seem too
very uncomfortable in it.  I was told it may rub under the arms but so
far so good.

Natalie also had an MRI on Friday to rule out tethered cord and
syringomyelia. Initially childerens was going to do it but they wanted
to  heavily sedate her.  I didn't like the idea of that so we went to
the Allegheny Back Institute and they did not make her take anything. 
She did just fine.  She said it was noisy and a little warm but not
scary at all.  Her dad was able to hold her hand.  She said she didn't
fall asleep because she said it went too fast.  Her Chiropractor will
get the results on Monday.  He does not expect that she has either
condition, but because her curve is to the left and we have no family
history of scoliosis that we should check and rule these causes out.

Good luck with your little ones.  If we have any further updates I will
keep you posted.

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------------------------------

From: Peggy <mclay@concentric.net>
Date: Sat, 27 Sep 1997 17:22:22 -0700
Subject: [Fwd: Re: Scoliosis Docs]

I think Linda could anwer this one for you.  She has been really helpful
to others with these requests.

I am merely excited about a non urgical technique that has been giving
my daughter great results.  Linda eem to be a SRS member and have lots
of info on surgeons.


Linda?

 Peggy - I read your post with great interest.  Do you have knowledge of
>
> 
>



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------------------------------

From: Linda Racine <lindaracine@denmark-c.it.earthlink.net>
Date: Sat, 27 Sep 1997 18:53:50 -0700
Subject: Re: SRS

Hi Kathy..
Thanks for the kind words.  The C after an SRS member's name means
they're a Candidate instead of a Fellow.
Linda

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------------------------------

End of scoliosis V1 #579
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