I can empathize with everyone on the pain issue.

After many years...and trying so many different approaches to pain treatment, over and over again, I find myself staying with the opiates.
Morphine 3xday and dilaudid for breakthrough pain.

These do not totally relieve pain for me; yet, they help.
So many meds had so many side-effects and some of them gave me worse pain immediately.
Some of the meds used for neuropathic pain spark an autoimmune condition for me right away, too.

I am always looking at new options.

I sincerely hope everyone can find adequate pain relief. :grouphug:

DejaVu

Hi Rae
I am going into hospital tomorrow to get the infusion, woohoo - I cant wait until Wednesday, I might wake up pain free:D - my pain manager said he is expecting it to work for 6-8weeks, fingers crossed and I will keep you posted
Arlene x

I am very keen to know how this will affect you. Good I hope. I have read a bit about this procedure - still pretty new here.

My best of hopes with you, Mere

Thanks so much Mere - so far so good, I have started another thread on this and intend to add to this every day and hopefully my progress will be positive for other folks.
Arlene

what i am missing in all the comments is electricity on the needle is also called PENS or percutane electrostimulation.This technic is used for people with severe neuropatic pain and helpes regeneted the nerves.I am using in combination with actyl-l-carnitine and alpha lipon acid but the needles help me more the the supplents