Mrs.D and en bloc,

Thank you for your discussions on the Plaquenil. It was informative.

Mrs.D, thank you for researching and posting the link on Plaquenil. This is a great help for those current and future posters who are currently on Plaquenil.

I will never know if it was indeed the Plaquenil which caused my neurological symptoms. Technically, I am neither here nor there, the neurologist does not categorized me of having a PN because of my normal NCV and EMG and my skin biopsy is normal....but the pain the continues.

It will be a real concern if, assuming I have AI, and I need to be on Plaquenil (being the first line of treatment). I agree with en bloc that other medicines for AI have more serious side effects. Thinking about it makes me scared.