Hi there. I had a morton's neuroma 3 years ago on my right foot and had it surgically removed. I now have one on my left foot and just got back from the hosipital after having an MRI. ( I live and work in Germany.....so it's hospital care). However....even though I KNOW I have the MN.....they saw nothing on the MRI. Is it possible that it wouldn't show up? Should I go ahead and ask for the surgery....I've had it for over a year? When they did my right foot they also saw nothing but I was in so much pain I asked them to operate...and sure enough that is what they found. I've been researching this for years....and I work and play on my feet every day. What is your advice?? Ask for the surgery and have it done where my insurance will cover EVERYTHING.....or go to the states and get it done....on my own dime? I'm confused. Was the MRI my last resort?
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