Karla's Journey: Beating Cervical Dystonia And Myoclonus With Functional Neurology

Published 2022-10-30
Karla's journey with chronic neck pain, cervical dystonia, and myoclonus was marked by misdiagnosis and ineffective treatments. After years of struggling with involuntary movements and severe discomfort, she found hope at Northwest Functional Neurology. Please visit our website to get more information: northwestfunctionalneurology.com/

Dr. Zielinski and his team used innovative diagnostic methods and personalized treatment plans to help Karla regain her life. This video shares her inspiring recovery story and highlights functional neurology's effectiveness. If you're dealing with similar conditions, watch Karla's journey to discover practical solutions and hope for your recovery.

This video is about Karla's Journey: Beating Cervical Dystonia And Myoclonus With Functional Neurology. But It also covers the following topics:

Recovering From Cervical Dystonia
Dystonia Healing Process
Chronic Neck Pain Rehabilitation

Video Title: Karla's Journey: Beating Cervical Dystonia And Myoclonus With Functional Neurology

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Welcome to Northwest Functional Neurology! We specialize in treating challenging conditions like concussions, traumatic brain injuries, dystonia, and dysautonomia. Our intensive therapy model delivers outstanding results for patients worldwide. Watch our testimonial videos to see real-life success stories. Subscribe to learn more about our innovative treatments and stay updated with our latest content. Join our community and witness the future of functional neurology!

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#cervicaldystonia #dystoniarecovery #chronicpain #neurology #healthrecovery #functionalmedicine

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All Comments (21)
  • @renahurst4743
    I have had Dystonia for 7 years. This month I walked without help for the first time in those years. Cervical Dystonia is amazingly silent. Tremors gone. I saw a huge change by changing my diet to a carnivore diet. I would encourage others to pursue keto or Carnivore removing all sugar and carbohydrates.
  • She didn't give much info on what the treatment entailed, but I did find it interesting when she mentioned "staring at dots on a wall." I have a severe pull on my left, and the right side constantly fights it, making me shake uncontrollably and giving me intense pain. But one night, I saw a video about looking as far left as you can for 30 seconds and then the same on the right, and it did give me temporary relief. The video was about resetting certain nerves. I really wish she had gone into more detail on the treatment.
  • @retrorenagade
    Australia is in desperate need of this kind of treatment, if anyone knows somewhere that does it Iā€™d be so grateful, Iā€™m really desperate.
  • So interesting the procedures they used that actually helped. For me staring at a tv screen for about an hour was the best thing I ever did for my recovery from dystonia šŸ˜…. Im so glad people like you that have made these miraculous recoveries that share your story with the world. You helped me believe I could get better, now Iā€™m one of the strongest dudes at the gym. Together we are all going to rewrite the textbooks and create a far better world for those that will get this diagnosis in the future. I really do believe if I could learn to heal myself here on YouTube, in time doctors will know exactly how to get people back to 100%!
  • @user-qi8vp5sy3z
    M going thru the same.. I can totally get what you are saying... Feel for you Sister.. šŸ™
  • I've had Dystonia since I was 21. I turned round to my wife and said is my head shaking? No why? Please look at it I can feel it moving. So I went to see my doctor, who kept saying everybody's head moves. Yes, I know that but my head is moving all the time. I'll give you this medication and that should help. It never did. Then after two years, I started to get these ticks and spam's all over my head and started moving where ever it wanted to. And we had our daughter and she was only three weeks old. And I knotted her right in her face. The thing is I could have killed her not knowing when they were going to come on. That's when I thought I can't go on with this no more. So we had to take her to the hospital I had to explain to the doctors that it was me who knotted her in the face. We had social services the police and everyone else questioning me about what I did. If it was;t for this surgeon who looked at me and saw my head shaking knotting from left to right. They would have taken my daughter off us and I would have been arrested for cruelty to a child, And he said to me how long have you been like this with not only your head but your full body. So I told him. And sent me to have these x-rays of my brain and he said you have a condition called Dystonia. I thought thank God someone has noticed it. Not knowing what it was. But I still was worried about my daughter. Because she was also having X-rays on her face and head. Luckily enough she was okay. Then I started having Botox in the back of my neck to steady the ticks. They never worked after having them for three years. In the end, I had deep brain stimulation. And even now at 58 I'm still suffering where all my toes are more like a claw and turned in. And get cramps in every part of my body. Now I'm in a wheelchair walking about with a Zimmer frame and walking sticks. The only thing they can do with my toes is break every one of them. Plus have another brain operation. I get fed up with me falling and being black and blue with bruises all over my body not even knowing I've even fallen. I've broken my leg twice and broken bough my eye sockets. I wouldn't wish it on my worst enemy
  • @MrStanwillis
    Thank you for sharing, Karla Long Happy Life.šŸ˜Š
  • Hey Karla Iā€™m going through the same situation at the moment thanks for the advice
  • @showorker
    Thanks for sharing your story. I was diagnosed with FND (motor) a few years ago. My story is sooo similar to yours! It started as a neck muscle issue. I had emgs that should it was in a spasm. I had PT, chiropractor visits for years. Craniosacral treatment, acupuncture, etc etc. Nothing helped. Then the movements started. My neck would just whip to the side. Then it spread to my arm and trunk (all on left side). I've made funny videos to cope with the uncertainty. Doctors just passed me around, agreed it was FND. I'm in constant pain. It's been over a decade. I'm a young mom too. Wish I could get the help you were able to find.
  • itā€™s 6am & iā€™m crying because iWant to get my neck straight so bad & start talking like normal
  • With me it started when I was 13 years old. I'm 74 years old. I get botox injections. That's all. It ruined my whole life. I'm from the Netherlands and I guess the doctors here are not as advanced as they are in the States. I wish her neurologist would place some exercise video's on YouTube.
  • Hi Karla, did you get lasting relief from this therapy? Is CD coming back ever since you took this therapy?
  • Moj si ima 36 god pati od cerikvalne dostojnije vratni misica vec 5 godina odao je kod mnogi doktora i razne masaze uključujući i elektro stimulans nsta .dabi mu tek prije 2 mj neurolog dao konacnu dijagnozu tortikolis ili cerikvalna distonija..prije 15 dana je dobio tri botuks inekcije vjer tip A ali i dalje i ma pomjeranje i trzanje vratnih misica tj kontrakcije .šŸ˜¢
  • Ayurveda, an ancient system of medicine from India, views health and disease through the lens of balancing the body's three doshas: Vata, Pitta, and Kapha. While Ayurveda offers a unique perspective on health and well-being, it is essential to approach cervical dystonia with caution and consult with qualified healthcare professionals like Planet Ayurveda's Expert team for appropriate diagnosis and treatment.
  • Thank you for sharing your story. I am considering going to get this therapy. I have lived with cervical dystonia for over 40 years and have tried many different types of therapies to treat the cervical dystonia. I'm wondering if this therapy can help me like it has helped you. Thank you
  • @camillecali22
    I didnt hear the cervical dystonia diagnosis. I got a CD diagnosis within 2 secs of being in the neuro office. Seems like this was deeper then CD