Dave, I would very much like to communicate with you about focal dystonia. I was a French horn player. About 20 years ago, I was preparing for a recital, as well as getting ready to transfer to the New England Conservatory, when I began to experience muscle spasms in my lips. In a short period of time the spasms grew worse. Ultimately, they ended my career as a musician, as I was no longer able to play. To this day, if I try to play the horn, I experience the spasms. Please contact me to discuss
My Name is Thomas Wade. I was diagnosed with Oromandibular Dystonia in 2006. I was a singer/ recording artist and suffered a decline in ability that is very much like some of the experiences in this video, with the added challenge that after my voice quality , strength and range were gone, it became difficult to form words. I am now on the mend largely due to hypnotherapy, and a great deal of learning about neuro-plasticity. Read "the brain that changes itself" and " Evolve your brain" amazing!
I am a cellist and it seems that I have focal distonia; after a year going to many doctors and doing physical therapy I've finally got a diagnosis; my problem is having my right thumb in place (bow arm)
it's from playing with too much tension. It is treatable by retraining your hand to function with no tension. it takes a long time to undo, but that's the answer. I tried botox, accupuncture, etc. nothing works except physical therapy, ie. for a guitarist like myself, you can use a guitar with thread instead of strings and do finger exercises and undo the tension. it does come back but it's reversible
Don't be fooled by the medical cartel, I recovered. There is a way out of dystonia. Soon I will be putting up videos to show dystonia sufferes how to help themselves. Deep brain stumulation is a farce and so is botox, figures they would go find something expensive to inject us with so they can make money.
Thanks for posting the extended interviews with Joachim and his students. I am a faculty member at the Berklee College of Music and have suffered with focal dystonia for two years. I have been working with Joachim for about 6 months. I thought I was making some progress but in the last month I feel alot worse. It was very helpful to listen to the two trombonists talk about their experience , I think it's enabling me to refocus on the way I'm approaching this condition.
Hi Dave. Thanks for your helpful videos as there many FD sufferers like myself who have been seeking answers and treatment. I would not mind sharing my story with you.
Hi Dave. Is there anybody in the UK I could talk to about this problem? My playing began to deteriorate in 2003. I gave up on it after four years. I recognise most of the symptoms as those I have experienced. Thanks for your time and the videos!
Dave, I would very much like to communicate with you about focal dystonia. I was a French horn player. About 20 years ago, I was preparing for a recital, as well as getting ready to transfer to the New England Conservatory, when I began to experience muscle spasms in my lips. In a short period of time the spasms grew worse. Ultimately, they ended my career as a musician, as I was no longer able to play. To this day, if I try to play the horn, I experience the spasms. Please contact me to discuss
animalliberator 6 months ago
My Name is Thomas Wade. I was diagnosed with Oromandibular Dystonia in 2006. I was a singer/ recording artist and suffered a decline in ability that is very much like some of the experiences in this video, with the added challenge that after my voice quality , strength and range were gone, it became difficult to form words. I am now on the mend largely due to hypnotherapy, and a great deal of learning about neuro-plasticity. Read "the brain that changes itself" and " Evolve your brain" amazing!
rockitboy2004 1 year ago
I am a cellist and it seems that I have focal distonia; after a year going to many doctors and doing physical therapy I've finally got a diagnosis; my problem is having my right thumb in place (bow arm)
clodoaldoljr 2 years ago
This has been flagged as spam show
Por favor un video en español!! es muy importante para latinos que no dominamos el ingles gracias..
321men654 2 years ago
it's from playing with too much tension. It is treatable by retraining your hand to function with no tension. it takes a long time to undo, but that's the answer. I tried botox, accupuncture, etc. nothing works except physical therapy, ie. for a guitarist like myself, you can use a guitar with thread instead of strings and do finger exercises and undo the tension. it does come back but it's reversible
sireel 2 years ago
Don't be fooled by the medical cartel, I recovered. There is a way out of dystonia. Soon I will be putting up videos to show dystonia sufferes how to help themselves. Deep brain stumulation is a farce and so is botox, figures they would go find something expensive to inject us with so they can make money.
nonsulen 2 years ago
? ?
Loonatiks3 2 years ago
HI everyone,
the last posting came from my son's youtube sight, so if anyone wants to reach me I'm at sherstudios, not coolmamiacs360!
sherstudios 3 years ago
Dave,
Thanks for posting the extended interviews with Joachim and his students. I am a faculty member at the Berklee College of Music and have suffered with focal dystonia for two years. I have been working with Joachim for about 6 months. I thought I was making some progress but in the last month I feel alot worse. It was very helpful to listen to the two trombonists talk about their experience , I think it's enabling me to refocus on the way I'm approaching this condition.
coolmaniacs360 3 years ago
Hi and thanks for your comments. I would be very interested in hearing your story. Please email me when you've got a spare minute..
Dave
davescragg 3 years ago
Hi Dave. Thanks for your helpful videos as there many FD sufferers like myself who have been seeking answers and treatment. I would not mind sharing my story with you.
All the Best
guitarsoul77 3 years ago
Please note!!
If you try to email me through the golobalbones site, they may not get to me at the moment!!!
Best to contact me through youtube!!
D
davescragg 3 years ago
Hi Dave. Is there anybody in the UK I could talk to about this problem? My playing began to deteriorate in 2003. I gave up on it after four years. I recognise most of the symptoms as those I have experienced. Thanks for your time and the videos!
slowmovingclot 3 years ago
Hi, can you email some contact details and I'll get in touch ..
Dave
davescragg 3 years ago
Super intresting!!
celticberrybhoy 3 years ago