TED's
#1
Posted 27 June 2006 - 07:51 PM
Thanks
Dex
#2
Posted 27 June 2006 - 07:57 PM
My injury is low, so that may have something to do with it, I don't know.
I hated them too, blckchns.
Edited by Joed, 27 June 2006 - 07:58 PM.
Female. Incomplete para following a cord stroke in '03. Spina-bifida, severe scoliosis. 18 surgeries total...five spine-related: Three fusions w/hardware, two tethered cord releases.
#5
Posted 28 June 2006 - 11:30 AM
#6
Posted 29 June 2006 - 08:28 AM
I walk all the time, however, now and again my ankles & feet swell pretty bad, so I put em on for a week or so.
All the best.
C-5 Incomplete, Diving Accident in Mexico. Walking with crutches, In controlled pain !
Big respect to all SCI people !
#7
Posted 07 July 2006 - 05:22 PM
I found that wearing TEDs every day has helped this very old issue of mine in amazing ways. I wear the long thigh-length ones. My feet are no longer ice-blocks when I go to bed at night. The most helpful thing is the lack of dizziness I now have while I'm in my chair during the day. The incremental compression of the TEDs helps for circulation and subsequently allows more blood-pressure regulation, which for Para's like myself, is crucial for quality of life issues.
Yes, it's a pain to put them on in the morning. Yes, my girlfriend makes fun of them by calling them my "Manty Hose". And Yes, it's not the most stylish thing to wear - but the benefits far outweight any of that stuff for me. I wish I had found out about these years ago.
When your brain is receiving the correct amount of blood/oxygen because of better circulation, your whole life can feel better.
-Seth
#8
Posted 08 July 2006 - 01:56 AM
dose any one other then me have this?
and dose any one have any opinions on what to do to stop it?
..........One Day I’ll Be Free, Free To Be Anything I Want To Be, Until That Day You’ll See What They Want Me To Be ..........
..........It's Better To Be Hated For Who You Are Than Loved For Who Your Not..........
#9
Posted 09 July 2006 - 12:01 AM
russ1, on Jun 28 2006, 07:30 AM, said:
I tried not wearing them. My feet just turned really red, but when I elevated them, they got their color back. My legs, ankles, and feet didn't swell though. I already don't wear them when I sleep.
#10
Posted 09 July 2006 - 12:04 AM
bubbleandsqueak, on Jul 7 2006, 09:56 PM, said:
dose any one other then me have this?
and dose any one have any opinions on what to do to stop it?
I just pull up on them every once in while. It helps a little.
#11
Posted 09 July 2006 - 04:34 AM
#13
Posted 09 July 2006 - 05:28 AM
tsutiff, on Jul 9 2006, 12:34 AM, said:
Intersting....I stopped wearing the binder a long time ago. Wonder if I could wear the binder and not the TEDS. Only one way to find out
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