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. 🙏
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.
Left a comment on another of your videos. Like you I’m also the first one to figure this out haha 😃 Just want people to know psychedelics do work for dystonia! I used DMT mostly as opposed to psilocybin. For me, it was the beginning of understanding I could indeed still use the muscles I hadn’t been able to in years. The “how” took some time and effort through meditation but it really was the psychedelics that exploded my brain out of the dystonia. Please please please do not put this off for years like I did, thinking God would be impressed with my morality for some reason. I really think I would have had a very easy recovery had I taken them early on. I feel really compelled to share my experience here on TH-cam soon, just a little nervous but the world needs to know about these therapies. They do work!
Thank you for sharing! I really think you should share the story anonymously with us - people in the medical community need to hear this and the best way to reach them is through journals. Again, I am working with a researcher in the field collecting case reports for publication - reach out through the website and submit your story! It’ll help many others 😊 www.hopefordystonia.com
Good evening dear, how are you? Regarding psilocybin mushrooms, how much do you use per day? What type is it? Pills or lotions? How long did you use the treatment? When did you start feeling better?
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 😢😢😢
I have cervical dystonia on it's a nightmare I also found a really bad overbite since I was little. Is that going to need to be corrected in order for this to work
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
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 .
Ready to start on the holistic path to dystonia recovery? Check out www.hopefordystonia.com/welcome and watch the video on the Eight Steps of the Hope for Dystonia Recovery Roadmap! Read what others have to say: www.hopefordystonia.com/testimonials The Self-Healers Club is now complete, stay tuned for future dates!
You are misunderstanding how this works - the mushrooms help promote neuroplasticity. It is up to you to direct the learning process and rewire your nervous system to re-integrate your hypotonic pathways. You need guidance to map out your cranial nerves and develop the right exercises before you consider mushrooms.
Hope for dystonia is right it’s not as simple as the mushrooms just fixing you. However, once I was on my healing path I found that on the days I Microdosed I had so much better movement and less pain that I’d just do a lot more life everyday and being out, having new experiences in new environments did wonders for my brain. I have also experienced litle to no benefit from psychedelics before I learned how to reprogram my nervous system.
@@hopefordystoniahi fede, are you talking about the same exercises as per recommended by dr Farias out of Toronto? Starting microdosing at the moment together with rehab exercises for the past 4 months: how long does it take to see the first results?
@@benoitleleu7840no, I’m talking about a specific protocol that I developed to target the specific cranial nerves that are impacted. With that targeted protocol you can be a lot more effective.
Thank you! I do not have dystopia but I do have chronic pain issues that are similar and this type of approach and conversation about these types of issues is essencial. It gives me hope for what we can achieve and how many routes to better health we truely have available.
Hoping youre feeling better already but you’re on the right track for sure. My chronic dystonia pain was the easiest thing to fix actually. Would highly recommend a daily meditation practice as well, I find it more powerful than psychedelics personally. You will be away from the suffering soon enough friend! Keep your attention on healing and it will happen!
We are all different but we all have common principles that govern our experience. Maladaptive neuroplasticity is a shared feature of most cases of dystonia.
@@hopefordystonia Doctor Lee was a waste of time and money lol healed myself similar to you did with some small tricks and learning proper mechanics of movement...how to activate the left eye...toes...heel...pelvis movement ect
![[TH] FS vs BME - VCT Ascension Pacific - Lower Bracket Final](http://i.ytimg.com/vi/wnygqsR2Fig/mqdefault.jpg)
I function WAY better now after microdosing, the results seem lasting so far. I'm not cured but I'm more functional more often.
Would you consider submitting an anonymous report so we can publish and help more people? 🙏
I am so looking forward meeting you on October 6th 🙏🙏🙏
The feeling is mutual 🥰
Hi Fede ! thanks for the info! What are your thoughts on DBS ? and mushrooms for generalized dystonia, not just focal/cervical ?
Thanks for your comment. I never considered DBS because I wanted to address the root causes. And everything I say applies to generalized dystonia.
I had generalized and psychedelics did work for me
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. 🙏
Thank you for sharing!
Volume is so low
Yeah I made a mistake with the microphone :-/
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.
Sounds great Adam, let’s make it happen! I look forward to chatting
Left a comment on another of your videos. Like you I’m also the first one to figure this out haha 😃 Just want people to know psychedelics do work for dystonia! I used DMT mostly as opposed to psilocybin. For me, it was the beginning of understanding I could indeed still use the muscles I hadn’t been able to in years. The “how” took some time and effort through meditation but it really was the psychedelics that exploded my brain out of the dystonia. Please please please do not put this off for years like I did, thinking God would be impressed with my morality for some reason. I really think I would have had a very easy recovery had I taken them early on. I feel really compelled to share my experience here on TH-cam soon, just a little nervous but the world needs to know about these therapies. They do work!
Thank you for sharing! I really think you should share the story anonymously with us - people in the medical community need to hear this and the best way to reach them is through journals. Again, I am working with a researcher in the field collecting case reports for publication - reach out through the website and submit your story! It’ll help many others 😊 www.hopefordystonia.com
great
This is very interesting, I will contact you and I think we might have some research mutual interests. Warm regards from Colombia.
Please do! Warm regards back 😊
Where can you buy Psilocybin mushrooms?
Don’t just do this at random!
Good evening dear, how are you? Regarding psilocybin mushrooms, how much do you use per day? What type is it? Pills or lotions? How long did you use the treatment? When did you start feeling better?
Mushrooms cannot be taken like you take aspirin. They won’t help. They require guidance, precise intention and specific practices.
How do we get in touch with someone who can help with taking them?
@@amyb774have you booked your initial consultation on www.hopefordystonia.com?
@@hopefordystonia I haven’t. I’ll check it out. Thank you. 😊
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 😢😢😢
Hi Nida, start by watching the video at www.hopefordystonia.com/welcome then book a consultation on the website!
I have cervical dystonia on it's a nightmare I also found a really bad overbite since I was little. Is that going to need to be corrected in order for this to work
You can begin to get better regardless
@@hopefordystoniathe tremors and spasms are ruining my life :(
Schedule a free consultation then and see how you can get your life back!
Combien ça coûte ?
How do we get them!?
Check your local laws as a first step
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 Erick, please book a time to speak on hopefordystonia.com to discuss this
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 .
Hi Susilah, thank you for your comment. Please book an initial consultation on www.hopefordystonia.com
Ready to start on the holistic path to dystonia recovery? Check out www.hopefordystonia.com/welcome and watch the video on the Eight Steps of the Hope for Dystonia Recovery Roadmap!
Read what others have to say: www.hopefordystonia.com/testimonials
The Self-Healers Club is now complete, stay tuned for future dates!
Do micro doses cure or do you have to take them regularly? Thanks 🙏
You are misunderstanding how this works - the mushrooms help promote neuroplasticity. It is up to you to direct the learning process and rewire your nervous system to re-integrate your hypotonic pathways. You need guidance to map out your cranial nerves and develop the right exercises before you consider mushrooms.
Hope for dystonia is right it’s not as simple as the mushrooms just fixing you. However, once I was on my healing path I found that on the days I Microdosed I had so much better movement and less pain that I’d just do a lot more life everyday and being out, having new experiences in new environments did wonders for my brain. I have also experienced litle to no benefit from psychedelics before I learned how to reprogram my nervous system.
@@macintoshimann9892it's overwhelming. I have cervical dystonia
@@hopefordystoniahi fede, are you talking about the same exercises as per recommended by dr Farias out of Toronto? Starting microdosing at the moment together with rehab exercises for the past 4 months: how long does it take to see the first results?
@@benoitleleu7840no, I’m talking about a specific protocol that I developed to target the specific cranial nerves that are impacted. With that targeted protocol you can be a lot more effective.
I dont understand your language or it is speedy. Kindly translate it in Indian english as it is more helpful because I am also have dystonia.
maybe the video at www.hopefordystonia.com/welcome will provide more clarity
thank you so much for give me a hope
So glad it resonated ❤
hows that? the micro dosing sir?
Life-changing in my experience if done right, working to integrate hypotonic pathways!
what exaxt dosage sir for the psilocybin mushroom?
It’s not about the dosage, it’s about the nervous system work around it. It requires guidance
👀 👀👉 psychedtripx for 🍄🍁 n more 🛳🌐.
On tele-gram...
Thank you! I do not have dystopia but I do have chronic pain issues that are similar and this type of approach and conversation about these types of issues is essencial. It gives me hope for what we can achieve and how many routes to better health we truely have available.
Indeed! The body wants to heal!
🆙☝️You can always order from him, he's legit & reliable,he's got magic shrooms,LSD,DMT and many more, he's the best 💯 Natural.
Hoping youre feeling better already but you’re on the right track for sure. My chronic dystonia pain was the easiest thing to fix actually. Would highly recommend a daily meditation practice as well, I find it more powerful than psychedelics personally. You will be away from the suffering soon enough friend! Keep your attention on healing and it will happen!
DYSTONIA not dystopia
Thanks you 😊
🥰
Your dystonia is completely different from what others have and not everything helps everyone the way it helped you.👈God bless you.
We are all different but we all have common principles that govern our experience. Maladaptive neuroplasticity is a shared feature of most cases of dystonia.
@@hopefordystonia Including spasmodic dysphonia?
@@remembermeordieof course. That’s just your tenth cranial nerve being confused
@@hopefordystonia has your program helped individuals with SD?
@@remembermeordieyes
Great video my friend, we talked years ago on Facebook
So happy it resonated! I can’t recognize you from your profile but whoever you are I hope you’re doing great 😊
@@hopefordystonia
Doctor Lee was a waste of time and money lol healed myself similar to you did with some small tricks and learning proper mechanics of movement...how to activate the left eye...toes...heel...pelvis movement ect