"newbie" To The Forum
#1
Posted 30 September 2009 - 09:13 PM
Since my spinal injury was properly diagnosed in 1986, although it actually occurred in 1964, I've realised that I'm "in between" most groups as I'm neither paralysed nor fully able.
To explain, my injury originated from a fracture in a transverse facet and following a "Buck's Fusion", removal of discs at L5/S1 and a subsequent decompression of the nerves running down both legs, I've been left with phantom pain in the lower legs, feet and thighs. Through my own research, I eventually discovered the spinal cord neurostimulator. The first was fitted in 2002. Because of a non-rechargeable power supply, the second was fitted in March 2006 - still functioning as I write! The amelioration provided has been excellent increasing my mobility from some 30% to about 50% - my estimations.
I've never been able to find, for example, pain management courses that deal with nerve damage as opposed to muscular or skeletal damage. Nor, even though the hospital I attend is very helpful, have I been able to find physiotherapy of the right type.
I would also like to ask advice about the connection (if any) been tinnitus and spinal injury and whether or not prostate function can be compromised.
Any ideas, please.
#2
Posted 30 September 2009 - 10:16 PM
I hope this helps.
#3
Posted 01 October 2009 - 12:17 AM
jacques, on Sep 30 2009, 10:13 PM, said:
Since my spinal injury was properly diagnosed in 1986, although it actually occurred in 1964, I've realised that I'm "in between" most groups as I'm neither paralysed nor fully able.
To explain, my injury originated from a fracture in a transverse facet and following a "Buck's Fusion", removal of discs at L5/S1 and a subsequent decompression of the nerves running down both legs, I've been left with phantom pain in the lower legs, feet and thighs. Through my own research, I eventually discovered the spinal cord neurostimulator. The first was fitted in 2002. Because of a non-rechargeable power supply, the second was fitted in March 2006 - still functioning as I write! The amelioration provided has been excellent increasing my mobility from some 30% to about 50% - my estimations.
I've never been able to find, for example, pain management courses that deal with nerve damage as opposed to muscular or skeletal damage. Nor, even though the hospital I attend is very helpful, have I been able to find physiotherapy of the right type.
I would also like to ask advice about the connection (if any) been tinnitus and spinal injury and whether or not prostate function can be compromised.
Any ideas, please.
Hi Jacques
Your symptoms sound like mine were till july this year. I'm L4 L5 too. Could walk 20 - 25ft with stick, chronic pain,pins and needles in legs/feet. tought it was just me with tinitus !!! drives me mad at times. I've now lost all from waist down. Hope you find your answers, there are some very friedly and knowledgable guys and gals here.
All the best
Al
#4
Posted 01 October 2009 - 05:29 PM
Shooting With Still Fingers - http://shootingwiths...s.blogspot.com/
#5
Posted 01 October 2009 - 05:44 PM
#6
Posted 01 October 2009 - 05:51 PM
As for the pain mgmt stuff, I'm new on that sort of thing - so far, I'm just trying to sort it out with meds and self-imposed physio, but it's not going very well, IMO. I'd be interested in saying hi in chat and hearing your experiences firsthand, maybe comparing notes?
Glad you're here!
-S
#7
Posted 01 October 2009 - 09:26 PM
#8
Posted 01 October 2009 - 09:35 PM
#9
Posted 02 October 2009 - 08:53 AM
Welcome to the forums though, I have found more help here on how to describe my condition to medical people and about what is "normal" for SCI injured and how to deal with some of the complications. I am sure you will find the site helpful and will gain a lot from being here.

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