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How To Find Motivation To Recover From Dystonia. A patient's experience

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Dr. Farias' Dystonia Recovery Program

Dr. Farias' Dystonia Recovery Program

Күн бұрын

Excerpt from the boxing class for Dystonia created by Schultz Abrahms Kavunenko.
Dr. Farias' Dystonia Recovery Program.
Manage your symptoms naturally with neuroplasticity, meditation, dance therapy, balance exercises, boxing, martial arts, nutrition, Yoga, and many other tools specially created for dystonia patients.
Join the biggest community worldwide using a holistic approach to treat their dystonias at:
www.dystoniare...
#Physicaltherapyfordystonia
#focaldystoniatreatment
#dystonia
#Handdystonia
#focaldystonia
#musiciansfocaldystonia
#Blepharospasm
#Spasmodicdysphonia
#Cervicaldystonia
#Spasmodictorticollis
#Runnersdystonia
#Legdystonia
#Dystoniarecoveryprogram
#oromandibulardystonia
#Dystoniaexercises
#Boxingfordystonia

Пікірлер: 6
@apersonagainsthatred
@apersonagainsthatred 2 ай бұрын
What an absolutely beautiful viewpoint!
@user-qq5ez2jr4t
@user-qq5ez2jr4t 14 күн бұрын
Good man yourself
@macintoshimann9892
@macintoshimann9892 3 ай бұрын
This is such great advice. I was still very symptomatic when I started crushing weights in the gym which really helped me to KNOW I could recover.
@AdamBlumer
@AdamBlumer 7 ай бұрын
Yay! It's Schultz. Thank you so much for highlighting him. He's an inspiration.
@ldpiazza
@ldpiazza 7 ай бұрын
Great idea, no matter what your challenges.
@elainemcgran8828
@elainemcgran8828 7 ай бұрын
Think you have it same place I have. My shoulder comes up and head turns into the shoulder. My Doctor gives my Botox injections every 3 months I'm due my second round in a week, the first injections didn't work great but I was told it could have been because I had a hip replacement 12 days after I got the injections and hopefully the 2nd round will do better. I find the mire walking and moving I do the worst it gets. Now I was on a waiting list for 8 & half years before I got to see a neurological doctor and it of course got worse over those 8 & half years, my own doctor couldn't give me anything until I was diagnosed. I love gardening and I do it but I find the next day I'm worst. It's terrible in work people look at me as if I'm an ailen it so embarrassing I have my breaks on my own I've stopped socialing just go to work and go for walks again that makes it worse just go out when I have to. Even to text and write is a nightmare because of my head and shoulder
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