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Smells like quackery.. Another charlatan looking to take advantage of desperate people.. Stay away

I entirely agree with you regarding the fact that we are all accountable for our own actions and we should not be looking for saviours…. I have been microdosing since 1,5 months, do daily physical training ( Farias Technique) but yet I can’t just still see the bottom out of it… my pharyngeal dystonia keeps deteriorating again and again and I still can’t figure it out how to properly enhance the right motions of my tongue, my jaw, my tonsil, my lips despite being able to to do it naturally a few months before…

Interesting heads up! Have you come across a similar initiative/ approach/ location about a clinic accessible in Europe or closer than SK ?

Your dystonia is completely different from what others have and not everything helps everyone the way it helped you.👈God bless you.

Hello… I registered my mail id and name. Couldn’t get through and so far no response. How to see it?

I'm amazed and inspired by your journey Fede. I've a strong sense that you can help me and I've booked my 30 minutes for Monday. Feeling hopeful about my issues in a way that I haven't for years. Thank you.

كل الشكر والتقدير اليك ايها البطل ! استمر ❤

Questions!: 1) My 8yo has CP from HIE at birth. Breech baby who aspirated, didn't breathe for 18 minutes. Cooling bed for first 3 days worked wonders. Walking talking, just fine motor and speech is hard. His hands are dystonic while his legs are more spastic. Do you think you're more methods could help his dystonia? Also we just found QNRT therapy. I am wondering if we resolve some of the first trauma if some of his nervous system protection will lessen. It's worth every effort.

I am SO grateful to have found you and you’re channel. I feel more understood and seen then ever. Since I was 14 I began to show symptoms of Cervical Dystonia. It was on and off for several years after that and I had no idea what was happening to me. It was devastating and I shamed myself so much (this is something I still am yet to overcome) but after it started getting terrible after a traumatic emotional event I finally opened up to the Drs..... they all had no idea what was wrong with with me and over a year ago I discovered Cervical Dystonia and cried because I KNEW that’s what I experience. Since then I told my Dr but she never looked into it. I don’t think she’s heard of it so she blew me off and labelled it as Fibromyalgia.. in this time I have discovered that yes I need to find ways to detox, address my trauma and implement neuroplaticity. I started to lose more function after a toxic relationship and heavy breakup. During this relationship I had a drug induced psychosis on 🍄 (however during that trip there was a correlation between having braces during my childhood and experiencing severe pain). I learned that neurotoxicity can contribute to this disorder and so I have been hesitant to touch the plant medicine again even though I have considered microdosing. I know my nervous system is extremely sensitive. The last several months to a year I have been at my lowest and the idea of doing all this work to heal is hard to covercome. Atm I cannot work and I don’t leave my house or couch much. I say no to all social events and feel so isolated and truly worthless. I know my emotional wounds that create this sickness revolve around feelings of unworthiness, ugliness, a fear or being seen and that I cannot be confident and also my abandonment wounds. I also had an experience when I connected deeply to my body and I asked it where it held the trauma and it said “my teeth and from getting braces” atm the correlations don’t make sense but I’ve come so far and learnt so much. I known this isn’t the end even though I’ve felt like my life was meant to end many times. Thank you for sharing you’re wisdom, journey and knowledge. I may be a bit behind you in mine but it gives me hope to heal because I AM WORTH IT

Thanks you 😊

You dont do more videos?

Heres the thing why do people who suffer with such a dibilitating problem and how much we suffer and you want to charge sufferes for there suffering people like you are low lifes

Thank you for sharing your story. There is much to digest here. Federico Bittis Ted talk is also worth watching. I have lived with Dystonia for over a decade now but most days you wouldn't even know I still had it. I too was incapacitated for over a year, but a holistic approach to my wellbeing including lifestyle changes in my diet and social habits(keto and abstinence) has seen the symptoms reduce to manageable levels. While I fought it, I lived in misery. Accepting dystonia as part of my life was the first step. I take a small dose of baclofen but my main therapy is physical and spiritual. (Meditation) There appear to be a number of routes out of this pain this horrible condition causes. They need to be shared.

I was originally diagnosed Essential Tremor and researched into the effects of psilocybin on the condition. I had emailed the hospital university in London (and their trials at the time on depression and further PD). I asked 'off the record' if there was a possible positive response to taking mushrooms and the lessening on tremors. I was told yes. But the trials had ended and the brief window into this research was halted. I assume its still ongoing elsewhere due to the legalities here in the UK. There are studies into PD using psilocybin to help with the dystonic tremors ongoing apparently. 🙏

Im only 3mins into this. I suffer bruxism and have lost back teeth as a result. Cervical dystonia and a vocal tremor onset at a very stressful time in my life. How is it that a lot of people took the trip to SK when I can't afford a B&B at the seaside?? 😂❤

thank you so much for give me a hope

Is lions mane usefull.? I am having this but i cannot afford the preciblin mushrooms and its not legal here. Can u plz suggst if i can take this

I was prescribed long term benzo and antidepressants for 13 years by these evil doctors. I left them cold turkey and since then i vr dystonia and left side body is tight pulls n my spine is deformed . 2.5 years am bedridden lost my life my career. Now no oone here in india understands. I ve a six year old son. Now i have no support no money. Starving as i cant work nor does govt help.i would love to have the mushrooms n help but i dont knoe if i can afford. Am giving up😢

I live in US ! if I want to connect you , do I have to go to CA ? I see a video consultation is that sufficient to follow your guidance?

What an incredible story! Thanks for sharing. I don't have dystonia but I have acquired really bad spasms of my neck after a laser surgery of my cervical spine back in August 2023. I travelled from Australia to the Deukspine Institute in Florida to have my C5-C6, C6-C7 discs decompressed to freeup my C6,C7 nerves on the left side. The surgery was a total failure becuase I woke up with a dropped head syndrome, severe tighhtness of of my neck with very limited motion. Since I have come back last year my neck has been getting very tight, cramped. Not only this but also feel lots of tightness of my traps, shoulders, back muscles. I am also getting numbness of my legs, feet accompanied by painful pins and needles. In the last 4 months now my right side has become symptomatic and get a lot of pain there too. Sleep is impossible nearly every night. I used to be a very fit person riding push bikes and going to the gym from 2002 to 2022. Unfortunately I have been run over by cars while riding in the bike lane in the last 11 years. My body is in constant pain, I am depressed due to this tightness of the neck. I have seen lots of physios, doctors, specialist but no one can help me except for prescribing oppioids, neuropathic medicines and antimflammatories which are not healthy for the body in the long term. Recently I had to reduce my walking activities and even gentle stretches cause me pain. I am hoping that I may learn something from your experience. Alfred

Da li ste vi imali distoniju? Ja trebam vas video na nemackom jeziku...❤bila bi vam zahvalna Imam problem da mi s eglava okrece na levu stranu, to ke normalan polozaj glave ... "Schifhals"nemam bolove....i mofu glavu i ka desno da okrenem bez problema ALI pravo nikako ne mogu ..pravo da gledam -glava pravo da bude Strasno😢

How do you use the mushroom 34:00

I am suffering from cervical dystonia now it is been 1 year but no recovery my head is towards left side muscular spasm How could you help me out to get rid of it. Do you advise me to go korea for my treatment? Waiting for your response

Re-ayurveda: 1 cup of herbal tea made of holy basil 3 times a day has made a difference for me. Also, 365 breathing.

What were your symptoms? My neck twists and jerks to the right.

I am Focal hand dystonia patient. It is very Painful Problem 😢

I was seriously considering going to YJ Clinic a month ago, only deterred by the cost and time I had to spend there. This video is very helpful.

Thank you so much for this video!. I'm 59 years old and I remember since my late twenties having this twisting and muscle spasm on my right side, the TMJ dysfunction also that started in high school and is stronger on the right side. I do infrared sauna, stretching massage therapy, acupuncture red light therapy.. I really just want a Botox shot in that one muscle spasm just to get relief. It's just chronic. I go to sleep with it. I wake up with it. I can stop it from twisting but it doesn't stop the pain. Anyway, Just found you on this video. And will now have more options. Oh and let's not forget. I had scoliosis surgery when I was 12 so I have a rod in my back from t1 to about l4 which I imagine contributed somehow to this too

Omg. That doctor who was supposed to be a fancy pain specialist on Park avenue should be reported for his unprofessional and cruel behavior.

Hi Fede, I have had cervical dystonia (at least symptomatic) for just over a year. I also live in Michigan, where mushrooms are decriminalized. I am beginning a 12-week medical leave from my employer and would love to work with you to provide a start-to-finish case study for my recovery. Please let me know how we can make this happen. Headed to the website now.

Hello, where can I find out which mushrooms you are talking, please? Thanks.

Hi one of my family members suffers from severe dystonia. I am willing to explore more helpful intervention. How can i be in touch

So this is curable ??? RIGHT?IF it's so I got a new hope

Hi l along with many others would like to see videos of you whilst in your previous phase of Dystonia as l am sure you would have many documented. This would definitely convince everyone to join you on your journey of ongoing wellness.I look forward to seeing many videos soon. The medical professionals would take your method of recovery very seriously once seeing your vids.

Is there any way to receive professional help also in Germany? I suffer from dystonia since I am 22, so more than 25 years.

I don’t think I have dystonia I have suspected FND - I have quick reflex movements, jerks, tics, awkward stiffness, I recently saw a movement specialist she is keeping me under close Monitoring until march but as of yet no diagnosis - anyhow with that being said can these mushrooms 🍄 be of help to me and relief / cure me of my current symptoms described

Hi i m nida from pakistan my mother is facing oromendibular dystonia including her eyes tongue and lower jaw she in pain suggest me what can i do for her 😢😢😢

Helo. My name is Susilah from Malaysia. I hv dystopia. Left side , facial spasms n chronically affecting my eyes,eyelid shutting down. Pls respond for me to get in touch personally .

Great video my friend, we talked years ago on Facebook

I saw doctor lee and had over a 100 treatments and never noticed any improvement...if anything it made me more anxious. He puts people into EXTENSION which is HORRIBLE if your nervous system is already in extension

Hey bro, how's it going? I went to south korea too (was working there at the time) and visited dr. Lee

You are the Savior 💖🙏💖

I have periods of whole body dystonia. It's very painful and stressful. I do suffer from severe spinal deformities which pull and push on my nerves as well as stretching and constricting muscles tendons and ligaments. Lately I have been having sleepless nights because my body is stiff. I'm not sure what to do.

i have meige syndrome and blephorspasm i take alpha lipoic acid and magnesium it helps me alot i also take velerian root these pills have made my condition 90 percent better i got my meige syndrome and blephorspasm from psych meds i had to quit the dangerous pscyh meds my torso was moving back and forth violently for about5 min once i quit taking the psych meds my symptoms got 50 percent better then 2 years later my symptoms were getting mildy worse were i had problems seeing and walking becaues of the blephorspasm then i started taking ala and magnesium and velerian root now my symptoms are alot better they only bother me 15 percent the symptoms are very mild im able to walk out side adn see alot better thanks to the pills i take i also stopped takign caffeine i went to a so called dystonia proffesional the lady told me there is nothing she can do for me no pills or treatment can help me thank god i figured out how to help my self

This was so helpful to me. Thank you.

I'm going to the website I've dealt with cervical dystonia for 18 years

I have this I need help 😩

👍👍👍👍

Your words help.

Amazing! You’re speaking my language!