I was put on levorphanol for pain and wonder if anyone else has had as much relief as I have? I have been on it about 6 months now and I am pleased with the relief I have found with it! I have severe pain from nerve damage. I cant stand anything touching my foot, its awful. My right side was completely damaged from a stroke. This medicine was used in the 1950s. And the company closed, Many years later someone else bought the rights to it. All I know is it has helped! I still find days hard but⦠read more
Ive got one implanted had it for about 7 years batteries wont charge anymore helped alittle but i loved it
Not sure what you mean that Seattle has some program
There are resources I suppose but the problems I have are beyond comprehension
Barry in Seattle
I have PTNS for years but now i use it ones a week this 2 mounths i got a lot of effort painwise . I am curious if others has this experience.
@Willemein
Thank you my sweet friend. I am praying hard that it does work. My doctor is very confident that it will work.
Hugs&Blessings &Love
Susie
Do not let anyone burn your nerves causes more damage
How do I relieve severe burning stabbing nerve pain in my legs feet and toes which is worse at night. The pain is excruciating
Thanku Peter for such an informative reply.
I've just been reading about neuromodulation also known as Spinal cord Stimulation as a treatment for chronic pain and wondered if anyone has had opportunity to try this? Its not a widely available treatment. I live in the U.K. where there are 1 or 2 specialist places you can go for the treatment. The Walton Centre is one of them. They implant an electrode or drug delivery system near the spinal cord.
I assume it is helping you is that Correct ? I too am interested in one
Because my nerves are damaged I have constant chronic pain. My stimulator acts like a TENs machine but internal and attached to the spine. It trys to block the synapses from firing to help block the⦠read more
I get for two years Percurtaneous Tibial Nerve Stimulation for my overactive bladder ( not funcional urge ,loss, bladderpain ) ones in two weeks in a hospital . It is a little electro needle in my leg who stays 30 minutes in contact with my bladder nerve. Today they cold that i can do a pilot and treat myself at home after a course with injecting the needle. Does anybody treat her or him self with PTNS and how are your expiriences.
Bedbound is nasty but thats also not nice always your catheter with you and never go out for a walk again. I have pudendus nerve damage luckley i can walk 1 or sometimes 2 miles but the pain was / is⦠read more
At one point I was on 12 T3βs a day for the lower back pain from the collapsing discs; especially S1-L5. The next step was to go on Opiods (hope I spelled it right) anyway. I decided to go for a breast reduction and pain management instead. Anyone else?
I did all that
I have lower back pain for years. Now I have Sciatica along with everything else. I have gone to Neurologists, Ortho guys, my Primary, a Chiro and a few others, and mostly the only thing offered to me is Drugs. I can have "anything I want" from Asprin to Percoset. I dont want any of it. I want to find a treatment or cure that I can actually live with. PT doesnt work for me bevause it only brings on more pain. I'm 71, I'd like to enjoy the years I have left.
Yes Yvonnelewis. Does tiger balm help your joints.thanks Lorraine xx π