I "climbed" the WHO pain ladder as recommended by my neurologist for my chemo induced peripheral neuropathy and found that only Percocet worked for me...45mg/day. Not pain free but at least I can sleep better. We pain patients are being persecuted due to a hysteria created by PROP and one Dr. Kolodny...go ahead...look it up for yourself. It's unconscionable!

At first my neurologist said that what I had. That she said it was all in my head. Because I had major depression. Years later I was diagnosed with fibromyalgia. Now I have Lupus and migraines and neuropathy and peripheral neuropathy. So I probably could force myself to do more.But I don’t lately I have serious pain in my feet. What really hurt is I have no family support.In May I will have skin cancer surgery for 8 times. I am a 73 female. I just keep going when I can.

What do you mean

Thank you

Hello Marie, Please ask your doctor to test you for SLE, aka Lupus Disease. Lupus is a wolf in disguise. Please keep in contact with me. I would like to leave you with some good advice--No one will understand because they are not walking in your shoes.
Please know, many people are suffering like you are but, they have LUPUS>
Many Blessings
Michele aka Mickey
(Email address can only be seen by the question and answer creators)