Living with NeuropathyThis section is a place to share stories about Living with Neuropathy Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation. You may also Help others by sharing your story. To quickly access health information from your website's browser, download Without hope? 1 yr. ago Neuropathy attacked me with a vengence. It started with hands,feet,arms,my butt. My left hand curled and my right foot dragged when walking. Before I knew it, it “crawled” up my legs, lower half of my face and scalp. My neurologist put me on 3000mgs. of neuronton a day. Right away I shook, jerked when walking and jaw jerked when talking and could barely a get a word out. I cut it back to 2000mgs. a day. It has uncurled hand and don’t drag foot. But barely took the “edge off.” I take 100mgs. of Elavil 2 hrs. before bed. Only way to get some sleep. I take vicodin and Soma when need it which is every day. All this occured after husband lost his job and insurance gone. We’ve had to pay for tests Dr. visits and labs. All this came out of what little retirement $ we had. I need an mri but no $. In this past yr. I had 2 days of no pain and was so grateful! I buy vitamines/minerals from Canada. They are made for neurapathy. I don’t expect to be pain free. I just want it managable. This has effected every area of my life. I’m 52yrs. old. I can’t work. It takes my whole being to just function. Clothes hurt me I hardly talk to folks about it. There is no way they can understand without being in my shoes. So why burden them? It’s a hidden disease. Over 20 million are suffering and I thought it was only me in this world,suffering. I would not want ANYONE to suffer so. In a heartbeat I would let the medical world study and test me. The pain is that severe and debilitating. Comments
June 2007
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