Living with Hemifacial SpasmThis section is a place to share stories about Living with Hemifacial Spasm. 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 Mr 
Its now three weeks since my MVD surgery for left side HFS. My eye still twitches but it is much better. My face and smile are more symmetrical. When my eye does twitch there is no pull on my mouth. I still have diminished hearing on my left side and a fuzzy type of feedback. My balance is improving. I ride my scooter but still have to take it easy.
|
|
Archives:
The submissions from our site visitors do not reflect the opinion of Healthcommunities.com, Inc. (HC). The Content of HC's sites is intended for informational and educational purposes only, and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. HC does not provide medical advice. Never disregard professional medical advice or delay seeking it because of something you've read on an HC website. Always seek the advice of your physician or other qualified health care provider regarding any medical question or condition. (See also: Website Disclaimer) |
email this
