Coping With BrachymetatarsiaThis section is a place to share stories about Coping With Brachymetatarsia 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 Me and My toe I am 17 years old and only have this disorder on my right foot. The left looks like any humans-beings toe. When I was small I loved it. I would show it to everyone who cared to look and when people asked me whats was up I was happy. But when I was 12, boys started teasing me about it, calling me “deformed-foot” and “piranna foot” since I got fed up with this one boy who kept asking “what wrong with your foot” and sick of giving the anwer “I was born that way!” so I told him a piranna bit it off. They weren’t very nice and it made me unblieveably self-confice of it. To a point where I refused to wear flip-flops or any shoes that showed my feet and if i had to go bare-foot I would put a bandage on. I am slowly getting over it. My friends ask me why i don’t get surgery but I am torn in two. I want it to feel confident but then I think I was born like this, no one I know has this. Why should I take something away that was given to me. I am slowly starting to realise that my toe is a part of me, no one else (I know of) can say “Look at my toe!” and it makes me an indivival. Comments
January 2009
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