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I’m crying listening to this as I have had stroke like symptoms my body seizes up and I go stiff I can’t breathe. My abdomen seizes up and I can’t open my diaphragm to take breathe I want to heal and need answers I’m part of a pot’s clinic and get no help. I want to know I can get better ❤️‍🩹

But what is the treatment? Just a 20 minute video of a woman crying.

Were mycotoxins part of the testing and B1?

Thank you for coming out with this. Losing and forgetting a sentences and words for me feels like impossible. Very hard to live that way.

Going on 3 years and third neurologist. Why? It’s sad and really there’s no excuse for anyone to have to go through that.

Come back to spend thousands of dollars each time?

I want to be friends with this woman. I feel seen, just listening to her story.

£££££££$

ya what's up with Dr's gaslighting people when they cant come up with a solution to something

hello if i got med-induced dystonia can the treatment also help? thank you @northwestfunctionalneurolo5250

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.

Did you get tremors when you moved

Identical to me

Thank you.

Thank you for sharing! So happy you could be helped!

Can u lie flat on bed without pillow. I still can't lie flat on floor or on bed. I feel so dizzy. But yes can manage. Exercises and meditation helped me a lot in improving balance and headaches

I had this driving home from work. It was like a light switch and the world was spinning. Luckley pulled over and felt like i was going to pass out someone helped me get ambulance. Tried getting out my van collasped throwing up everywhere couldnt stand up. Blue lighted to hospital they thought id had stroke has i have high blood pressure. In from thursday till saturday end up on stroke ward after all tests then came back as this took me 5 weeks to get my balance back. It was horrible especially the thought of when will this end will i ever be normal again.

Are you still severely symptomatic?

Thank you!

I sustained TBI from a bashing to the head in 2205. I have struggled with seizures ever since & stopped meds in 2012 bcause of s/effects & some drugs were making the seizures worse. I am tying the keto diet.

27 year TBI survivor here from a bad car wreck from 3/31/97... I was in the hospital 26 days and in Physical Therapy 18 months... I struggle with repeating myself,poor multitasking skills,poor short term memory etc... I attempted and failed at several careers-(Special Education Teacher,Car Salesmam,911 Radio Dispatcher)...The combination of TBI issues,PTSD issues and Career Failures led to increased Depression,anxiety and Suicidal Thoughts... I FINALLY have a somewhat decent quality of life now... I FINALLY received SSDI-(Social Security Disability Income) after 15 years,4 appeals and 3 attorneys... I drive for a Car Dealership part time and build model cars part time as a hobby... These activities bring meaning to my life,help me deal with my TBI and PTSD issues,and improve my self esteem...

I am so happy for my Sister, she got cured of her Multiple Sclerosis just few weeks of using Dr Madida Sam herbal supplements.

I have found my hobby of Model Car Building very beneficial to deal with my TBI issues-( And it has given me a substantial boost in my self esteem as well!!)..

I am very limited when it comes to employment... I attempted and failed to become a Special Education Teacher,Car Salesman and a 911 Emergency Dispatcher.... After several years( and tears) of crashing and burning,I now recieve SSDI,Food Stamps,Medicaid,Medicare,and Section 8 Housing and can only work part time driving for a local car dealership...

TBI is one if the most misdiagnosed conditions... TBI is not a "One size fits all" condition... Since 1997,I struggle with repeating myself,anger,frustration,anxiety,depression,and memory.... TBI: Yoy only know it if you live it!!

When this girl can recover ,then i can too.😊

I supposedly have dystonia. My shoulder has been stuck elevated for 5-10 years. I don’t have tremors or head tilt. I have c0-3 fusion. I’m in so much pain on the right side of my neck into scapula.

I have had cervical dystonia four about 5 years and it is horrific!

Thanks for your sharing.

Thank you for sharing your story. It made me not feel so alone. I went through the same thing and almost four years later I am still not back to normal. I hope you are feeling better! You give hope to others. That concussion centre sounds amazing! They need to have them everywhere.

I love the testimony’s but I would love more details of the condition so people can somewhat relate and get there anxiety down to know one is not crazy lol

Loving all the testimonials lately!

Thank you for this encouraging example ❤

About the Doctors making you feel like your crazy

I can understand what your saying.😢

Similar outcome

That’s great your almost fully recovered crossings my fingers for a

I have CCI and dystonia now as well. The team has helped me too but my CCI is severe so they are one important aspect as I continue other healing treatments for my neck 🫶🏻happy to hear you found so much relief for the dystonia. It’s so hard

I know your pain 🧘🙏

Wow i need this treatment

My POTS and digestive issues responded well to Mestinon (Pyridostigmine). This medication stimulates the vagus nerve and parasympathetic nervous system. Pyridostigmine was developed 75 years ago, making it inexpensive since it's off patent. It also has a long track record for safety. Guanfacine/Clonidine further treated my POTS, since I have the hyperadrenergic type of POTS.

Good for you Kim. I have had Long Covid Dysautonomia for 3 years and am getting some online treatment. My hospital does not have a clinic. So many doctors miss this diagnosis because there is not yet a lab test for it. I had over 50 lab tests that were negative. I hope I can find a doctor who can treat this.

I am most grateful I came across dr Liam ogbebor herbal centre CZcams channel ,his treatment has helped me and a lot of other people, all my symptoms of Ménière’s disease including the constant ringing sounds in my ears(tinnitus ) are all gone, all thanks to his treatment 😊😊😊

Just got diagnosed with POTS/MCAS been battling for 2 years. Good luck in everyone’s journey. We got this.

I'm doing the beef only diet, taking 80mg propanolol a day and 50mg sertraline for 3 weeks and attacks have practically stopped completely. I have had ibs for 19 years now and can't eat fruit or much vegetables but I also don't want to stay on the carnivore diet for long as it's incredibly boring and anti social and I don't know what foods I can live on and not trigger migraines but I do want to figure it out soon because I own a busy bar and have a good social life.

I suffered a TBI concussion 1 1/2 years ago. I continue to suffer from horrible migraines, dizziness, nausea, light and sound sensitivity, cognitive problems and so much more. I am happy for your success, Angela. I hope one day I will feel better, too, and have relief from these disabling symptoms. The dream of putting on heels once again would be oh-so nice.

How do you get here and do you take insurance? I need help. This has devastated my entire life. Please doctor

Hi , Im'ma from (MIT) university freshmen. I've encountered a recent incident that has left me in need some advice . I wanted to share that I recently experienced a concussion two days ago, and unfortunately, it has occurred again in the same right side. I'm wondering, would a sudden sideways motorbike collision with a cycle at a speed of 30 km/hr., causing a forceful movement of my torso to lurch and my head in relative (lateral flexion) in the same area of the first concussion ,can it potentially cause some DAI and possibly axotomy to the previously concussed neurons ? very worried since i am difficulty speaking like finding right words and articulating fluently and even slight difficulty understanding words and its been 1 month no recovery? i initially have no symptoms after the incidence like nausea or dizziness , does it cause any permanent deficits or it is just temporary ? and Does this injury lead to the diminution of a handful of neurons?

Thank you for sharing your story. I pray for the day to be able to tell mine. I've been through the exact same thing, working on 9+ yrs of getting little to no help. Its exhausting, ive lost so much of me while others have just belittled my health. Meeting with a specialist Feb 9th. 🤞

What is the treatment for mold?