From:      bounce-scoliosis
To:        scoliosis-digest@ai.mit.edu
Subject:   scoliosis V1 #922
Reply-To:  
Errors-To: bounce-scoliosis
Precedence: bulk


scoliosis                  Monday, 17 August 1998       Volume 01 : Number 922

Today's subjects for scoliosis, scoliosis-medical, scoliosis-child
and scoliosis-teens:
  Re: DURATION OF PHYSICAL THERAPY      [Margaret  Arth <ma247@columbia.edu>]
  Re: DURATION OF PHYSICAL THERAPY   [Mary_Grossi@edu.yorku.ca (Mary Grossi)]
  Re:  PHYSICAL THERAPY, VERTABRAE & 6 WEEKS POST OP  ["Cyndi King" <cbk.skk]
  Re: Back Pain                                     [R.N.A.@worldnet.att.net]
  Intro                                               [ckeane@mindspring.com]
  Re: DURATION OF PHYSICAL THERAPY          ["Cyndi King" <cbk.skk@snet.net>]
  Anti-inflammatories                       ["Cyndi King" <cbk.skk@snet.net>]
  Re: bad experience of Copes                            [DChare6704@aol.com]
  Re: DURATION OF PHYSICAL THERAPY      [Margaret  Arth <ma247@columbia.edu>]

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

From: Margaret  Arth <ma247@columbia.edu>
Date: Sun, 16 Aug 1998 02:31:19 -0400 (EDT)
Subject: Re: DURATION OF PHYSICAL THERAPY

Hi Lynne,
Well, the reason why I had my last a/p fusion was because of the vertebrae
above and below my previous fusion.  With this kind of surgery, the fused
area acts as if it were one vertebrae...one solid bone in which the stress
is given to the vertebrae above and below the fusion as opposed to the
normal segmented taking it equally.  I think over time those discs become
weakened, although I don't have the medical proof that this happens in
every single fusion case.  But I think this happens as part of the normal
aging process anyway and the fusion just helps accelerate it (again just
an assumption).

As far as PT, I started the week after I got out of the hospital with home
visits 2x/week for about an hour.  Around the 2month mark, I was allowed
to go to the office 3x/week for almost 3hrs.  I am currently 6months
post-op and on the same schedule.  I am still not allowed to twist,
bend, or lift anything of significant weight.  My prescription is up in
Oct, but my surgeon may decide to renew it.  

Here is my normal PT exercise/therapy schedule:
15min stationary bicycle
30min matt work (using physiotherapy ball)
30min treadmill
15min step work
    there is a 5-10min break in between each exercise to ease tension
    pain.
20min heating pad
30-40min massage/ultrasound/SI joint mobilization
10min ice therapy
And of course this all depends on how much pain I'm in at the time.  So if
I have a 9 pain day, then I might skip the bike and reduce time on the
treadmill.  I'm never pushed into anything I don't want to do.  The
schedule is customized for my needs and everything is very flexible.  It
has all worked out nicely.  When I get back to school in Sept I will
reduce my visits to the weekend, but during the week while on campus I
will add swimming 2x/week and light (and careful!) weight training maybe
1-2x/week.  My recuperation is my top priority now (even above school) so
I'm very committed to working hard at it (though balanced as well to
listen to how my body reacts).  And both my drs and my pt are aware of my
'plan'.

Each surgeon is different as to how they want their patients to recover
through physical movement.  As we have seen through recent posts, some
don't want any PT for 6months, some maybe only want slow gradual work, and
others are more aggressive.  Find out your surgeon's plan for recovery.
If there is an aspect that bothers you or you want to do something that's
not mentioned, voice your concern and ideas...maybe there are ways to
accomodate your wishes.  I hope everything works out for you and that you 
feel better.  
- --Megan




______
For help on using this list (especially unsubscribing), send a message
to "scoliosis-medical-request@ai.mit.edu" with one line of text: "help".

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

From: Mary_Grossi@edu.yorku.ca (Mary Grossi)
Date: Sun, 16 Aug 1998 08:40:32 -0400
Subject: Re: DURATION OF PHYSICAL THERAPY

scoliosis-medical@ai.mit.edu writes:
>  I'm wondering what others have experienced 
>post-op.  How long did your PT continue and how far along were you in 
>your recovery when it ended.  Did you continue with other types of 
> ...

My daughter's surgery was on July 13, and our next visit to her specialist
is on Aug. 25...
NO PT in the interim.... the physio-therapist that saw her in hospital
basically said that all they
wanted her to do was to let her body heal, not overdue any kind of
physical activity, and to 
get back into doing as many of the regular activities around the house as
she could WITHOUT 
lifting any heavy weights, too much twisting etc....
Possibly the difference is because of her age... she's 14, or maybe the
difference is just
philosophical?  Not sure!
Mary  =;->




______
For help on using this list (especially unsubscribing), send a message
to "scoliosis-medical-request@ai.mit.edu" with one line of text: "help".

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

From: "Cyndi King" <cbk.skk@snet.net>
Date: Sun, 16 Aug 1998 09:43:39 -0400
Subject: Re:  PHYSICAL THERAPY, VERTABRAE & 6 WEEKS POST OP

I am 6 weeks post op and began PT 4 weeks ago.  I began with 10 minutes at
a very slow pace on the treadmill, leg and foot extensions (all out in
front) and the therapist stretched my calves and legs while I laid on the
PT table.  As of last Monday I have added upper body exercises.  One where
I sit on a chair and use a rope pully above my head to stretch my arms (no
weights).  Then I use 2 pound weights in each hand doing bicep curls from
my sides to my shoulders.  Also use the weights with elbow on table, hand
hanging over from wrist and do wrist curls, palm down and palm up.  The
last exercise is the digi-flex, a hand squeezing device that improves
strength in your hands.  After that then I have a soft tissue massage of my
back and very light massage around the incisions.  This helps with the
itchy sensations of the healing.  It is all very easily paced and I am
carefully monitored so that nothing is too difficult for me.  To answer
Cathy Lutz, I'm not sure how long they will allow me to have PT.  I have
gone a lot this year.  I would like to believe it is up to the surgeon, but
with what I'm reading here lately, I don't know.  I would speak to your MD
and your insurance company.  There is nothing stopping you from joining the
YMCA or a gym and just continuing with your PT routine there.

Lynne, it is my understanding the newer rods take this into consideration
in that they are 3 dimensional as compared to the older 2 dimensional rods.
 In other words the rods are placed in the spine after the surgeon uses the
French bending tool to bend the rods to fit your spine side to side AND
front to back.  The scoliotic, lordotic and kyphotic curves are all
considered.  In my case, the condition of the vertabrae and discs were
considered as well.  The disc below L2 was very healthy so my fusion ends
there.  There was no reason for him to begin above T4 as all was strong
there as well.  My surgeon, Dr. Brown, wanted to keeep the fusion as short
as possible so that I would have the lumbar mobility.

As an aside, Bonnie Stone brought me lunch on Friday and she looks great! 
She was fused in the lumbar spine in December and last we met she could not
sit in a dining room chair.  Not only did she sit in a chair, but when I
dropped a napkin, she squatted down to pick it up!!  WOW!!

I am now home alone with my 8 year old daughter, Sarah.  My mom left a week
ago and my dad left yesterday.  I am taking it slow.  Allowed to drive
short distances and am attempting light housework.  Sleep comes easy at or
before 11PM.  Usual waking time is 8:30AM.  Often an afternoon nap around
4.  PT three days a week.  Sarah is good about helping.  My friends and
neighbors have been great!

Regards - CBK



______
For help on using this list (especially unsubscribing), send a message
to "scoliosis-medical-request@ai.mit.edu" with one line of text: "help".

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

From: R.N.A.@worldnet.att.net
Date: Sun, 16 Aug 1998 10:39:06 +0100
Subject: Re: Back Pain

Sindy--

The pain or rather discomfort is more in the center of the back and 
radiates from there. At times the discomfort worsens just a bit when I 
breathe which is why I think it might be the muscles. 
I'm not taking any over the counter anti-inflammatories but I assume 
Linda was talking about Advil, etc.
I don't have a post op brace and won't wear any kind of corset until I 
check with the doctor which is next week.

Lynne



______
For help on using this list (especially unsubscribing), send a message
to "scoliosis-medical-request@ai.mit.edu" with one line of text: "help".

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

From: ckeane@mindspring.com
Date: Sun, 16 Aug 1998 12:55:01
Subject: Intro

Hi, 
I have just joined this list and was so glad to find it. It's hard to find
people who understand through experience. I was diagnosed with scoliosis at
age 11. While I can't recall the exact degree of my double curve, I believe
they were 25 and 60. I was treated at age 12 for idiopathic sclerosis,
spondylolisthesis and thoracolumbar scoliosis. Treatment included 2
Harrington rods and spinal fusion from T5 to sacrum. I am now 30 and the
last 18 years have been pretty much trouble free, until recently. I have
pain occassionally in my lower back, like today, that scares me a whole
lot. I'm hoping to find people on here who have similar symptoms and just
learn more in general about how I get through the next 18 years. If it
isn't obvious, today is a worry day :) Thanks for listening and for being
here.

Colleen




______
For help on using this list (especially unsubscribing), send a message
to "scoliosis-request@ai.mit.edu" with one line of text: "help".

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

From: "Cyndi King" <cbk.skk@snet.net>
Date: Sun, 16 Aug 1998 13:39:58 -0400
Subject: Re: DURATION OF PHYSICAL THERAPY

Megan - Where does the PT apply the ultrasound?  I was advised not to have
it as the rods impair it's effect and it could heat the rods and cause
burns. Regards - CBK

- ----------
From: Margaret  Arth <ma247@columbia.edu>
To: scoliosis-medical@ai.mit.edu
Subject: Re: DURATION OF PHYSICAL THERAPY
Date: Sunday, August 16, 1998 2:31 AM

30-40min massage/ultrasound/SI joint mobilization



______
For help on using this list (especially unsubscribing), send a message
to "scoliosis-medical-request@ai.mit.edu" with one line of text: "help".

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

From: "Cyndi King" <cbk.skk@snet.net>
Date: Sun, 16 Aug 1998 13:52:17 -0400
Subject: Anti-inflammatories

I have been advised by my surgeon to not take any anti-inflammatory drug
for the next 18 months as it will interfere with the fusion process. 
Before taking anything like Advil, etc. check with your surgeon.  It takes
up to 2 years for the fusion to solidify.  95% of the fusion is complete in
18 months.  Remember, as Dr. Brown reminds me, you are a Faberge egg! 
Don't allow any cracking!  Regards - CBK

______
For help on using this list (especially unsubscribing), send a message
to "scoliosis-medical-request@ai.mit.edu" with one line of text: "help".

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

From: DChare6704@aol.com
Date: Sun, 16 Aug 1998 16:27:33 EDT
Subject: Re: bad experience of Copes

My son has a neuromuscular condtion and we are considering a Copes brace.
Would you mind telling me what the cause is for Christian's scoliosis/

______
For help on using this list (especially unsubscribing), send a message
to "scoliosis-request@ai.mit.edu" with one line of text: "help".

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

From: Margaret  Arth <ma247@columbia.edu>
Date: Sun, 16 Aug 1998 20:27:50 -0400 (EDT)
Subject: Re: DURATION OF PHYSICAL THERAPY

> 
> Megan - Where does the PT apply the ultrasound?  I was advised not to have
> it as the rods impair it's effect and it could heat the rods and cause
> ...

Wow Cyndi, I never knew that.  What a scary thought.  My PT uses the
ultrasound on my SI joints in which there is no hardware.  I'll have to
ask him about that though.
- --Megan




______
For help on using this list (especially unsubscribing), send a message
to "scoliosis-medical-request@ai.mit.edu" with one line of text: "help".

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

End of scoliosis V1 #922
************************

You're reading a composite here: the scoliosis-digest is a daily
encapsulation of messages sent to four different mailing lists:
scoliosis, scoliosis-medical, scoliosis-child and scoliosis-teens.  If
you're responding, you can determine which list message above was
posted to by looking at the message footer.  To post your own email to
scoliosis, send it to "scoliosis@ai.mit.edu".  To post your own email
to scoliosis-medical list, send it to "scoliosis-medical@ai.mit.edu".
To post to scoliosis-child, send your message to "scoliosis-child@ai.mit.edu."
To post your message to scoliosis-teens, send it to
"scoliosis-teens@ai.mit.edu".  Be sure to see the scoliosis web page
at "http://www.ai.mit.edu/extra/scoliosis/scoliosis.html".  For help
on using the scoliosis-digest, (especially unsubscribing) send an
electronic mail message to "scoliosis-digest-request@ai.mit.edu" with
one line of text: "help".  Spammers and promotional posts not allowed.