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 Hemifacial Spasm 
I was just diagnosed with this and am still learning about it. I, too wish there were more options for treatment. I am just starting on the medication for treatment to see if I can tolerate it. The thought of continually getting botox injections really scares me, as I have a lot of allergies and asthma I am worried I will have a reaction to the injections. If anyone else can enlighten me further, I would appreciate any knowledge I can gain.
February 2009
|
|
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
