Re the patches--perhaps more important than pain--do the patches assist with hair growth? That is what I want to hear!

Wasn't this aspirin (from willow bark)?
I also have no financial connections with them, or indeed with any of their competitors. I found fentanyl a disaster, all the side effects, none of the benefits! One man's meat....

heheheh
 

yes, there is

1) willow bark --source of salicylates, aspirin

2) there is pine bark-- OPCs which are antioxidants

3) there is cinchona bark---source of quinine

4) there is cinnamon-- for controlling blood sugar

5) slippery elm bark-- for coughs etc

6) yohimbe-- for male erectile dysfunction

That is all I can think of right now... yohimbe sort of stopped my mind for a while! LOL:p

i wonder how many guys are looking up the yohimbe tree right now.

Recently diagnosed
 

I was recently diagnosed with Idiopathic PN at the Mayo Clinic. My neurologist did the nerve conduction study and ran several blood tests to check my levels of vitamin B and E and for diabetes. However they all came back normal.

She said the next step was to put me on an "anti-depressant" used to treat PN. I told her that I didn't want to start with an anti-depressant. That I really wanted more testing to see if we could figure out "why" I have this in the first place before committing to a drug that has side effects.

I just turned 50, have never drank, didn't do drugs, was physically fit so none of this made sense. When I asked her for additional blood tests to check for Lyme or a Gluten sensitivity she said that my regular doctor could do those if I wanted to. When I asked about maybe a MRI or CTSCAN she said that I could see an Ortho for those tests.

I was so frustrated, both with her and myself. I wish that I had pushed harder. What was the point of traveling to a "World Class Facility" only to be told to see my regular doctor. It was as if she was saying "I told you it's Idiopathic PN, now take this pain med and go away". With so many people experiencing this you would think that doctor's would be more open to figuring out what specifically is each person's cause.

I really appreciate finding this site and reading all of the great information that others have posted. It gives me hope that I will find a doctor willing to do more than just pat me on the head and write out a prescription.

Thank you all for your posts.

Welcome to NeuroTalk:

First off, you need a copy of your test results for the B12 and E.

Lab ranges in the US go down below 400pg/ml which is the new lowest normal. So to be sure your B12 is okay, you need the numbers. And yes even Mayo can be wrong.

April, I sure hope you find a better doctor soon.

Me too! I go see another doctor next week.

:) thanks!