Spasmodic Torticollis (Cervical Dystonia) Remedies

Spasmodic Torticollis:

For years I had muscle spasms in my lower back and tried Lugol's Solution, but it made me very nauseous so instead I switched to Potassium Iodate by Vitamin Research (you can find it on Amazon). It comes in capsules of 50mg, but since it's in a Potassium Iodate solution, only about 24mg of the iodine is available for absorption. Best of all, it acts like a buffer slowly absorbing into your system. At first I took it at night, but after a week or so it started keeping me up at night, so I switched to taking it in the morning with my Breakfast.

I don't even need coffee anymore and the pain and spasms in my back are completely gone!

Hi Iboro

How to apply casteroil, cut cloth 10 by 8 inch.get frying pan-low heat with some casteroil to warm up.then fold cloth to the size you need and get it soaked in frying pan.now put soaked cloth on neck.cover with plastic wrap and put a electric blanket over the plastic-wrap. 2 hours then take a break and use same cloth over and over adding alittle casteroil when its getting dry.You can re-use for a month and then make a new one. Store in fridge when you dont use it.

When you are not putting casteroil pack you should apply 2-3 drops of D.M.S.O. Oil and rub gentley the area, it will fix nerves in the neck.

God Bless

Gary

I have on and off torticollis from neck trauma from 14 years ago. It comes and goes every few months. Not sure what brings on the spasms but when they start it's hard to get rid of...makes daily functioning difficult...and takes many weeks to get range of motion back and pain to diminish. I've tried chiropractic adjustments, massage, moist heat, Tylenol for inflammation, elect. stimulation, ultrasound. All help to a degree but nothing earth shattering. But I've recently been reading about castor oil packs and when the symptoms returned this month, I tried it...with great success!!

After the 1st night with the pack, 80% improvement. 2nd night...95% improvement. I never made it to the 3rd treatment (3 are advised) but over the next 2 days, everything left seemed to resolve on its own and I was back to normal again. I was completely and utterly amazed.

I used the standard method for applying a castor oil pack...but left it on my neck overnight as I slept, instead of an hour during the day. I didn't sleep that well...as I'd wake up often to reset the heat. And it got a little messy (extra towels and old clothes are necessary) since I shifted a little during sleep.

The 2nd night I added extra packs to other areas besides my upper neck, that were feeling pain or tenderness...like my scapula/spine area.

During the day...if there was any pain or spasm coming about... I'd dig my fingers into that area, press down very hard and massage it for a minute or two. It sort of disarmed the spasm, forcing the muscle to relax again.

I'm so so thankful for castor oil packs. I'm now using it on my hernia (after 1st night it's gone down by half).

Where do buy the Castor oil packs? I had spasmodic tortiscolis back in 1985 & it was so bad that I had surgery. I have no problem with it for 30yrs and it has come back on me. I have taken my first Botox injections which have helped but don't like the way it makes me feel. I would like to try this castor oil to see if it helps. I'm always searching for any treatments that would really work.

I was diagnosed, finally, with Spasmodic Torticollis.

I suggested to my neurologists and chiropractor that my 20+ year dental work may be affecting me. They said that was a crazy idea until I consulted the US Olympic team's chief council, Dr, Arnold Takemoto of Scottsdale, AZ who agreed with me there was mercury poisoning from 20+ mercury amalgam fillings in my mouth. Mercury is the 2nd most toxic element and a silver filling consists of 50% mercury, 35% silver... The mercury inside your mouth vaporizes 24/7/365 and attaches to your central nervous system, but notably your jaw-the hardest bone in your body that gets less blood flow. Your mouth has 10x more nerves than anywhere in your body, thus your taste buds. Bureaucratic Medical Associations will not agree with this, but they are the ones who put mercury in our mouths when they knew it was deadly. Of course it is a conspiracy.

He shared a story of a woman he treated who was paralyzed from the waste down, took his detox protocol and had the fillings removed. Within a month she received mobility and years later her muscles have become normal with regular use.

I am documenting my severe dystonia and my path to recovery. I believe it will be an extreme relief for the dystonia community. If you have not yet considered mercury fillings and any dental work or inorganic surgeries then it is time to reconsider.

Bennymang, Fountain Hills Arizona

people try ayurvedic medicine it realy work afte 1.5 month of shirodara I feel no pain at all I hope be healthull

We first sought a neurologist who said my husband wasn't in bad enough shape for any treatment at all. Then we found a Chiropractor who has additional training as a Natural Doctor. Understand the state of Fl doesn't offer a Natural Doctor's license anymore, so look for acupuncturists, chiropractors, etc. Anyway. My husband undergoes weekly neck adjustments and electro stimulation as well as takes supplements 3x per day of Ligaplex, Relax All and adreneloin. This is not a cure, however it has lessened the frequency, severity and pain associated with the shakes

Hi, Go to stclinic.com. This is a website that brought me hope. Hope it helps you.

I will second Ginger's claim about stclinic.com. THey offer a totally natural plan that has brought me great relief as I travel the rocky road toward recovery from ST

I would not be so quick to discount botox... I've suffered with severe torticollis for about 8 years, and without my regular botox treatments, I would be permanently disfigured by now (I've seen the poor folks who spent years of their lives untreated, and it isn't pleasant). Botox isn't perfect, but it is the best remedy that medical doctors have come up with so far, and I highly recommend you try the injections for your daughter before her disease causes irreversible harm.

I can see I am very fortunate to not have the extreme variety of Spasmodic Torticollis. But my head used to pull to the left, and down, and it was coupled with a tremor that I still have. I think honestly, by my Spasmodic Torticolus exercises, which many a mom has done on their babies with ST, has changed the degree of ST for me. I also walk about 6 miles a week which helps with all sorts of pain in my back and neck. Since I came to EC, I now use Magnesium and have been helped with both the ST, and the tremor. I take 400 Magnesium per day (right now have Mag. Malate, but prefer Glycinate) and also 200 mg per day of Mag. Citrate. I wish I could take all Citrate but it causes me to have diarhea.

My foods are full of anti-inflammatory properties, like Ginger, Turmeric, and Cinnamon.

I drink a home-made tea every day, sometimes 2 of the 1 and 1/2 Cup per day. The doctors also started me out on Botox, 2 in one side, 3 in the other, every 3 months, for about a year. I stopped those, because of lack of money to continue them, but continued on Clonazapam that the Neurologist prescribed.

I am still trying to get off my .5 miligram, but the calming effect when I get anxiety, or irritablility is hard to give up. But I take just a half of the .5 now, every other day.

Hi Juan,

I just read your post of 2016 and checked with Amazon for the Potassium Iodate. Unfortunately, it isn't available from Amazon any longer.

I am wondering how your Spasmodic Torticollis is today. Thank you. MJ

Dear sir, my brother (34yrs old) has been suffering from spasmodic torticollis since 8 months very severely, he had botox a month ago, but after botox the pain shifted to another muscle, now he is not at all able to bear pain and he has to wait for another botox for 3 months more, he left his job since last 8months, not able to eat, sit and sleep. He is the only person in the family who earns, but now he left his job, he is married and had a kid too. Please tell me how to control the pain.

Please how is the castor pack made for management neck pains and twisting from Torticolis?

Please how is the castor oil pack and how is the heat applied to the pack? Please help me, I am in pains for a long time from the condition. Thank you.

I had my mercury fillings removed several years ago. My dystonia at the time was barely noticeable. It has gotten much worse since then. I do agree mercury is bad and possibly even a root cause but so could a lot of things if we are just guessing. I would recommend removing the mercury fillings but don't expect a miracle.... I didn't get one.

My only child is suffering from cervical dystonia.he has taken botox thrice but always it worked for 3/4 months and it is very painful injection as doctors say that they have to inject in the deep muscle. Recently he started taking ayurvedic treatment & sirodhara is one of them. Could you please let me know how long it takes to get cured?

Hi, does anyone know of natural treatments for torticollis or dystonia? Medical doctors point us to botox but we do not want to do that. My daughter has had the condition very badly for seven years. Thanks to anyone who can help us.

I was just diagnosed with cervical dystonia which I have had since I can remember. I am now on Soma medication because I am not comfortable with the idea of Botox injections. My Soma medication is a muscle relaxer that makes me feel tired all the time but I have never slept better in all my life. However, I feel that it is too strong for me. If anyone has any suggestions I would really appreciate it.

Hi, I can also confirm that the method of stclinic.com works. After 5 months following the method, my neck has started to straighten out quite well. However, my ST is not gone. Therefore I will travel to South Korea to a clinic that treats ST patients by balancing the temporomandibular joints. According to Dr. Lee, the method yields permanent results.

I had the botox last year and it did not help relax the area but did make it extremely hard to raise my chin up. I was very hopeful for botox but it has not been a compatible working option for me. I had surgery when I was 6 years old but my mother and I do not speak often and she can not recall what the details are... she also never took me to rehab for full and extended recovery.. I believe that is why for 30 something years I have had pain with ST, my right ear pulls down and my chin points up and to the left. Over the years I noticed through pictures that my face grew slightly less symmetrical which is likely due to the ST always pulling.. I have shoulder and hip trouble too.. I have been on pain and muscle relaxers but they are temporary fixes and like many other the muscle relaxers helped some but mostly just made me tired & I am a mother of 4 children so I have to be fully functioning... I find warm heat and stretching helpful and when I can afford regular chiropractic visits they are also very, very helpful..there are days when I can't drive because the pulling or stiffness is so strong... Has anyone out there heard about brain stimulation for ST? I am going to visit the stclinic. Also, has anyone heard if inversion tables help?

Happy to find a place to chat with others like me!!

myIndy husband has suffered from ST for 4 years now. He has tried everything the so called Drs have suggested. Nothing worked, including Botox. He sought the help of a fantastic Chiropractor named Dr Stephen Cooper in Phenix City, AL. He performs a 3 day outpatient procedure called Manipulation Under Anesthesia (MUA). It isn't a permanent cure, but he goes from being practically bedridden from pain and the need to walk with a cane due to constant falls to functioning normal with very little to no pain. The first time he had the procedure he was good for 9 months and then the 2nd for 1 1/2 years. Hope that helPs. He is going to the magnesium oil and see if that helps.