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Dystonia - can anyone help?

by WAIN, Aug 01, 2007 07:54AM
Does anyone suffer from Dystonia ?  I would like to share symptons
also , we are awaiting and EEG and an ENG test to confirm diagnosis, does anyone know what an ENG test is and how this would confirm DYSTONIA?
Member Comments

by 22685, May 16, 2008 10:26AM
To: Wain
I have been a sufferer of Dystonia ( Torticollis ) for the past 26 years , It took 11years to be Diagosed... I had no EEG OR ENG test to confirm i was suffering with Dystonia .
My head kept turning on it`s own to the right, luckly enough i got the right neurologist who new what he was looking for .There are different types of Dystonia ..
Blepharospasm - Affects the muscles of the eye.
Cervical Dystonia - Affects the neck muscles.
Laryngeal Dystonia - Affects the vocal cords
Myoclonus Dystonia - Jerking movements
Hand/Arm Dystonia - Tremors that cause difficulty writing.
Paroxysmal Dystonia - A group of rare conditions where Dystonia affects the whole part of the body.
Oromandibular Dystonia - Affecting the muscles that move the mouth , tongue and jaw.
I hope this helps.

by BhumikaMD, May 16, 2008 10:53AM
Hi,

In dystonia, muscles contract involuntarily — causing an uncontrollable twisting of the affected body part. Symptoms can be mild or severe, and often interfere with the performance of many day-to-day tasks.

You could read more about the condition at the following links -

en.wikipedia.org/wiki/Dystonia

and

http://www.mayoclinic.com/health/dystonia/DS00684

Electrical sensors (EMG) inserted into affected muscle groups, while painful, can provide a definitive diagnosis by showing pulsating nerve signals being transmitted to the muscles even when they are at rest.

Let us know if you need any further information.

Regards.

by Twisted959, Jun 03, 2008 07:28PM
To: WAIN
I was diagnosed with Cervical Dystonia on April 29/08 by a neurologist.  No tests have been done todate.  I am awaiting an MRI and have been informed that my options are, and I quote:  "Live with it or try Botox"  Today I have been informed that I have an 18 -24 month wait before a Dr who does medical botox will see me.  I have been in alot of pain and this Dystonia has very negatively affected my life, I am unable to cook, clean, exercise, cut the lawn, garden, - any of the everyday activities that most people can do.  The medical community has not been very helpful and it has taken over 18 months to get this diagnosis.  I have been searching for answers on my own, and at my own expense, since most of the treatments are not covered by any medical plans.  I have tried chiropractic, accupunctture, physiotherapy, I.M.S., deep tissue massage, freezing at the base of my skull, chinese herbal products, homeopathic remedies, topical creams, prescription drugs, anti-inflamatories, magnets, heat therapy, ice therapy, and sacral cranial therapy; all to no avail.   It has been suggested that I seek medical assistance in the U.S.or another country.  If anyone has any information about treatments in other countries I would be interested in hearing from you.
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