Has anyone experienced neuropathy with polycythemia vera (PV)?

Has anyone been experiencing Nueropathy with PV? The tops of my hands and feet/ shins are burning. I’m having tingling in my face also. I am in menopause also and am finding it hard to differentiate what is causing what? For now I just want to know what to take to help… The internet is not much help, I’m taking hydroxyurea and a baby aspirin currently along with phlebotomies about every eight weeks. Last one was about three weeks ago.