Melody pretty much said it all, and please check out the Peripheral Neuropathy forum here....she gave you the link. You'll get so much great feedback, as there are so many others similar to what you are describing....

She also brings up a good point on the 'stressful/trauma' issue......
I truly believe that can be a part of the mix.
Amongst several medical issues, at the time I was suffering major grief after losing my brother. We were very close and it was such a blow to me, I thought a part of me had died also.

Please hook up with the PN folks - there is SO much important info in that forum

Best Wishes
Rae

Hello Hermes.... I am still on vacation, but I would suggest you come to our PN forum and start reading.

Especially look at the SubForum here on the subject.

Some drugs and toxins can damage nerves. There is a thread about that there. Also tight clothing and belts can compress nerves that exit out the L4 area and provide sensory coverage of the front of the thighs. This is called Meralgia paresthetica.
We have a forum for this type of neuropathy too.

Also some vitamin/nutrient deficiencies may cause this. My MP in my right leg came after a C-section. Some surgeries may cause it too.

I have a thread on magnets, and these may help you too:
http://neurotalk.psychcentral.com/sh...hlight=magnets
I would think using them on the back lumbar area near L4 may help. Lidoderm patches also are useful for MP.
The links on that thread to the 3D graphs showing nerves help with placement.

I'll be back in a week or so...so I hope you can post questions on the PN forum for me there, when I can go into more detail.
(I don't have internet access on this vacation, other than free wifi at our laundromat).

I managed my years long MP with Lidoderms, and it went into a remission (after much pain). I don't think oral drugs you have been offered will do much for you... but that is just my opinion.

Hello and welcome to NeuroTalk. Happy to see you have come to be with us. Just let us know if we can be of any help.

There are great number of fellow members here to assist as possible. My thoughts and prayers are with you.

Again welcome, looking forward to seeing you around.

Darlene

im christine im still going from nero pain for 4months and still trying drugs and still not helping and getting lots of pain i was on nertoin my feet and legs were swelling samething from lyraca