I have had MP for over 30 years. It is diagnosed by history and exam. It does not show up on nerve conduction tests or EMG's since it involves a sensory nerve. Prolonged standing and walking will usually exacerbate the symptoms. For years mine was just an intermittent annoyance with brief pain but would immediately subside upon sitting. It has progressed to severe levels with constant pain at various fluctuating levels. It forced me out of the workforce. Some people have it go away on its own but rarely if you have had it for over a year or more. I would suggest that you take action before it gets worse especially if you are in a work situation that involves prolonged standing.

Feel free to contact me at any time as there are not many still around and active with MP. There are a few and very helpful but it is a small number in comparison to the other conditions on Neuro.

I did physical therapy (aqua), oral medications, lidoderm patches, Tens unit, nerve blocks, etc.

I would seek help from a neurologist and/or a pain management specialist. I would not spend too much time with general practitioners as they are not usually familiar with the condition. They may want to do x-rays, or an MRI to rule out radiculopathy or other possible conditions, which is a very good idea.

I would not just ignore it and hope it goes away as the longer you are untreated, the more damage to the nerve and the more the LFCN nerve will affect your life. Sometimes the cause may be something you can modify, or it may be of unknown origin. Mrs. D has lots of advice on supplements that may be of help. Glenn is a great wealth of info. He has been a tremendous help to me.