Living with Sleep DisordersThis section is a place to share stories about Living with Sleep Disorders. 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 Myoclonus (Lance-Adams syndrome) I had an accident last 6Sep2003 which left me deaf and disabled. I think a brain trauma resulted in having to suffer what the doctor in the Philippines termed as Myoclonus where I could not control my right body particularly my right hand. While I could control my left hand, not so much the tips of my fingers that’s why I eat like a pig with my left hand. I’ve undergone Occupational Therapy in 2 hospitals but I feel it’s not helping me for the Therapist just tells me to relax. I asked myself, is this how you conduct Occupational Therapy to your patients where you just tell them to relax to achieve control? I feel using Psychology to cure something Physiological is inappropriate. What is happening to me is purely Physiological. That’s why my Father and I researched the Internet often. There’s one drug that my dad researched and the doctor heeded, it’s called Piracetam (generic name Nootropil) It helped a great deal to reduce the shaking, but after a while, its effects weren’t as dramatic. I think my body has developed immunity which I also read holds true. I thought the drug researched by my dad called Sodium Valproate whose side-effect was that it makes you feel drowsy, was what I need for I’m not getting enough sleep. There are times when I couldn’t sleep at all. I’ve read that lack of sleep is not age-related but symptom-related, so most likely it has something to do with my accident. I’ve been taking Clonazepam (which I read was the first drug of choice for Myoclonus) for quite a while but it doesn’t seem to work. I had a CT scan done in the hospital where I was confined only a few months after the accident and an EEG requested by my current neurologist. Before when I would attempt to button my blouse my nail bled and my right fingers would hurt. But I think thru constant practice and the right medicine this doesn’t occur anymore. My succeeding visits to my neurologist seems to go nowhere for he keeps on prescribing anti-depressant drugs when depression is not my main problem. I was prescribed again an Antidepressant with generic name Mitrazepan and brand name Remeron. But it didn’t work, then he prescribed Keppra (generic name Levetiracetam which I suggested based on what I found in magazines). He was cautious because this drug is relatively new (but the reason why I suggested this anti-epileptic drug which I also read is applicable to Myoclonus, is because its side-effect once more is sleepiness). I received a confirmation from a TBI website that I may indeed be suffering from myoclonus although I failed to mention that I was diagnosed with Lance-Adam’s syndrome, but when I read about it, the symptoms do not appear to coincide with what I’m suffering. Comments
July 2007
|
|
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) |

