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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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June 2008
- Years of Not Knowing - by Jan - (Fri, Jun 27 2008)
This is a “Whew”!! I have always been a walker. Approximately 8 to 10 years ago, I noticed my left foot was “just not right”.
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- Ms - by LINDA - (Wed, Jun 25 2008)
Today after many years of back and forth to the surgery I have finally been diagnosed as having a Mortons Neuroma ( I had suspected this for so long and it took an MRI scan to confirm as it did not convince the surgeon on examination) I have been advised to have surgery.
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- Morton’s Neuroma - by Paula - (Mon, Jun 16 2008)
This is miserable. My left foot has a bunion but then the 2nd toe has become a hammer toe and then there is a wide separation between the 2nd and 3rd toe, which is caused by the MN, when I stand.
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- Cortisone shots - by Joseph - (Tue, Jun 10 2008)
I have this condition on the left foot and walked in pain for almost 3 months before I went to the podiatrist back in March 2008.
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- Still walking - by jbh - (Mon, Jun 09 2008)
I just wanted to update since my last comments back in March 2008. I have continued on with my Ultra Sonic Sound Therapy on my MN and I am pleased to say I am doing SO well.
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- multipal surgeries for mortons neuroma - by Donna - (Mon, Jun 02 2008)
I have had morton’s neuroma in both of my feet for about thirteen years. I just went through my fourth surgery a week ago.
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