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This section is a place to share stories about Coping With Morton's Neuroma
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.
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January 2009
- my horrible feet - by amanda - (Fri, Jan 30 2009)
Ive had problems with my feet for about 6 years..had insoles, funny things for behind my toes etc u name it ive tried it..I was diagnosed with claw toe
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- MN - by Liz - (Tue, Jan 27 2009)
I have had 4 MN’s removed in the past 10 mos..2 on each foot.
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- Me too - by Lisa in MD - (Mon, Jan 26 2009)
I finally went to a foot doctor about the pain and “clicking” in my left foot. He diagnosed me with MN immediately and gave me a cortisone shot.
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- Surgery IS possible for Morton’s Neuroma? - by louiese - (Mon, Jan 19 2009)
I have been so surprised to read stories from people who suffer from Morton’s Neuroma and have had surgery. I have suffered with M.N. for approx 6 years and have been told that they cannot operate. I have visited many specialists and they only offer orthotics pain medications, and cortisone injects.
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- Morton’s Neuroma Post-Surgery Alcohol Sclerosing - by SS - (Tue, Jan 06 2009)
I had dorsal surgery to remove a .5mm Morton’s neuroma in late February 2008.
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- MRI’s do not tell all - by AC - (Tue, Jan 06 2009)
I have dealt with Morton Neuroma pain for 3 years. I had 2 MRI’s during that time both saying I was negative for Mortons Neuromas.
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