Coping With Bell's PalsyThis section is a place to share stories about Coping With Bell's Palsy 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 Bells Palsy In 1992, i was a sophomore in high school, i developed bells palsy Back then no one new anything about it so i had facial electro therapy and many many shots of vitamin b.(for about 2 years) it is now 2009, and i am still struggling with this. I do not have my smile anymore and although i am able to close my eye, i feel very insecure about what has happened to me. Half of my tongue doesn’t have a sense of taste but i have pretty much gotten used to that. I really would like for some doctor to help me with my facial paralysis. And its is so ironic how it has affected my face, and as my profession, i work with make-up.(make-up artist) if god would grant me just one wish, it would be to have my face back with my gummy smile. I miss it. -alejandra d. Comments
September 2009
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