Living with Essential TremorThis section is a place to share stories about Living with Essential Tremor 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 Hiding My Hands All Those Years I am 54 and have been living alone with essential tremor until right now. When I was in 7th grade I remember walking to the front of the class to read my report. My hands shook so badly I couldn’t turn the pages of my report. My voice also locked up that time, and I was mortified. I stumbled through a few more words then went back to my seat, head down. I think the teacher and class realized something was wrong and nothing was ever said. From that point on I would become anxious about public speaking and the condition accelerated rapidly. By the time I reached college I was hiding my hands at every opportunity and avoiding public speaking. I avoided most speech in groups. Sometimes I wouldn’t eat rather than tremble trying to eat or serve myself. I had already made the decision to be a writer–something that I see now was a choice made because of my ET Luckily, I am a good enough writer to make a living at it, but I wonder how much more I would have done if the ET was treated and controlled back then. My fear of public shaking kept me from engaging in debate, aggressive negotiations and even conversation if I was in the company of someone who caused me the least bit of stress; ie., teachers, bosses and really good looking, succesful guys! I spent part of my 30s and all of my 40s in counseling for Social Anxiety disorder. During the course of that I was given many different drugs. With the internet I began researching the drugs and about four years ago ran across the term Essential Tremor associated with an anti-depressant called Effexor EX. I looked up ET and found only a couple websites but when I read the descriptions I was amazed. There was a name for what I had. After more than a decade of going to shrinks and taking antidepressants and lorazepam and Xanax, I finally found an elderly doctor who didn’t ask much but always wrote the prescriptions as long as things were in moderation. I told her I wanted to take Effexor (earlier I had tried Propananol, but it just made me forget things.) I started the Effexor, but didn’t see any real change. I was having some trouble sleeping and a girlfriend gave me a couple of Trazadones to take at night. She was a flight attendant, and I thought she gave me a non-narcotic sleep aid. The next morning when I was making coffee I did not spill the grains. I repeated the motion and marveled at my steadiness. I took the pills two more nights and spent a totally tremor-free day. I called my friend to find out the name of the pills and beg her for more. I looked up Trazadone and immediately found where it said it had been used for ET. I went to my shrink and got a prescription. I had told her about the ET but I don’t think she was very informed about it. I’ve been using the Effexor and Trazadone ever since. I’ve discovered I’m a wonderful group teacher and lecturer. I’m involved in the best relationship of my life and am more active and productive in life than ever, and I no longer take any sedatives. Last month I tried to suggest to my shrink that I get off the Effexor. She basically said why mess with something that’s working? I agreed. Today I googled ET and found dozens of great sites, including this one. Things have really changed! I also found several doctors within 50 miles that I can visit and be prescribed specifically for my ET, not the social anxiety disorder that I never had, by a physician who is more a pill peddler than a doctor. Wow. What a relief. I’m not some freak. I’m just a person with ET who was really, really good at hiding it for a really, really long time. Thanks. Comments
June 2007
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