Edited by concerned sister, 25 August 2008 - 02:07 PM.
Question Re: "sunburn Feeling"
#1
Posted 25 August 2008 - 02:06 PM
#3
Posted 26 August 2008 - 01:04 PM
Squirrel, on Aug 26 2008, 07:13 AM, said:
#5
Posted 26 August 2008 - 01:53 PM
http://www.apparelyz...?showtopic=5063
Neuro pain seems to be fairly common although it is much more severe in some people than others. There are a few different drugs to try, with most drugs you will start off on a low dose and slowly build it up until you get a benefit or until the side effects get too much, so it can seem to take ages before you feel any benefit. Also worth bearing in mind are techniques for dealing with the pain for example cognitive behavioural therapy, literally finding your happy place!
Good luck
Trinity X
Memento Vivere
Memento Mori
#6
Posted 26 August 2008 - 02:02 PM
It take's about four months for the swelling to go down in the spine and that's when all the fun stuff starts - muscle spasms, hypersensitive sensations, etc.
I hate to be the one to tell you this, but your brother has a long way to go, so don't get too hung up on the time frame of his recovery. Some of us are still recovering (physically) after a year. One of my Physical Therapists told me that during her 12 year career she can remember the names of the few who gave up and didn't try to move on. Unless your brother is a quitter, he'll keep working toward his recovery. The best thing you can do is support him where he's at and not push him - it will only cause resentment.
And get him to log in some time, so he can hang with his peeps!
#7
Posted 27 August 2008 - 05:48 PM
#8
Posted 27 August 2008 - 07:38 PM
#9
Posted 31 August 2008 - 08:43 PM
The two pieces of advice that have stuck with me regarding recovery:
Recovery is best treated as a series of small goals to achieve one after another, rather than trying to do it all at once.
Never look at your progress by comparing today and yesterday or even this week and last week. Compare this week with two or three weeks ago to get a sense of how you're doing.
#10
Posted 03 September 2008 - 05:49 AM
#11
Posted 03 September 2008 - 07:44 PM
For your brother's nerve pain:
in addition to standard analgesia, he may want to look into Cymbalta (duloxetine) or Effexor (not sure chem name, but watch out for awful side effects) -- these SNRI's (selective Serotonin Norepinephrine Reuptake Inhibitors) help block pain in the peripheral nerves. Has worked wonders for my Reflex Sympathetic Dystrophy (which is what your brother's sunburn feeling seems to be from). These drugs are often prescribed to diabetics for neuropathy even though originally marketed as antidepressants. While in the pain program at Spaulding Rehab, I was informed that pretty much All the patients with RSD were put on Effexor.
There is a new SNRI being developed; I read about it in a medical journal (doc in the family, so I read up on things often before the public does). The pharmaceutical company developing this SNRI plans to market it exclusively for nerve pain despite its alternate application as an antidepressant; they feel that the antidepressant market is already flooded with options, so they are going for a different target population. Moral of this story -- SNRI's are good for nerve pain. Cymbalta helped me liked nothing else had in 8 years. The effects were truly remarkable. Did not touch a lot of my various kinds of pain, but that stinging burning relentless hard-to-pinpoint pain in not exactly the area of injury is what got managed by the Cymbalta.
Best of luck to your brother.
#12
Posted 04 September 2008 - 01:08 PM
CervInstabilityHMSandRSD, on Sep 3 2008, 08:44 PM, said:
Memento Vivere
Memento Mori
#13
Posted 04 September 2008 - 02:36 PM
trinity, on Sep 4 2008, 09:08 AM, said:
CervInstabilityHMSandRSD, on Sep 3 2008, 08:44 PM, said:
Thanks for the info. Good to know. I personally had no relief from nerve pain while on it. The Cymbalta was a miracle drug for the nerve pain. What I have read about Neurontin is that it is primarily for spasms and has a secondary effect as a mood stabilizer. Having not read about the nerve pain benefits (or felt them!), I was unaware of that. I found the med annoying to take -- every 8 hours. The Cymbalta is a once a day med, much more convenient.
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