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Thanks for sharing. I have not been formally diagnosed, but I got goosebumps reading about FND. I was convinced for at least a year that I had MS despite doctors saying it can't be. I have been recently experiencing paralyzing muscle contractions that got a whole lot worse when I had to miss my medications for about 3 days. That was the first time that I ever felt like I could not control my ticks at all, and my body was almost entirely stuck in a contraction. I have been thinking about a sort of vlog to a diagnosis, but I'm a bit camera shy, and the thought of having a video of me online starts some anxious feelings. I am glad to see there are other people comfortable sharing.... Perhaps one day I will just jump in instead of imagining what could be

My son is trying Prodrome Glia and a little Prodrome Neuro to fix the brain. Please check it out.

You have nice feet

Good job bro, and greeting from China. Love U❤💪🏻

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Thats nice buddy, keep making videos

Thank you so much for your videos! They've helped so much! I love that you're so down to earth and real about it!

awesome!!

Did it cause fybromyalgia symptoms from it

yupppers

also kia/hyundai have installed both port/direct FI......they used the direct for a long time....toyota is also installing the duel setup.......DIRECT INJECTION is crap to the intake valves.....as recycled crud is deposited on them....with no port injection fuel to clean them

First off...i agree.....they push small engines with TURBO-BOOST......but issues develop...later

Hey. Great video and explanation of FND and your symptoms. You have a really good attitude to dealing with your symptoms. I was diagnosed with FND back in 2019. I had an accident on the ice while lining a hockey game and was knocked out and sustained a TBI. That's when the FND symptoms started. When you mentioned the apnea, I didn't know it could be a symptom....but it makes sense. I did a sleep study and learned I had severe sleep apnea, which I believe was the result of my head injury. Thanks for sharing your story. You did an amazing job explaining things in your video. Cheers!

I wish you'd have shown the bearing removal...for fork and wheel! You seem to have plenty of leg strength to push your butt up into the chair at the end...I wish I could do that but I'm like 210lbs lol

I have fnd thanks for being so open n honest with it I typically get weakness, tremors anxiety poor memory n chronic fatigue n cnt remebrr stuff Hope ur symptoms get better

Thank you for sharing. Great attitude.

Thank you for sharing this, and for explaining your symptoms so clearly in plain language

Great video. You're atitude is very much like mine :-) I hope you continue with these videos. Most people in have spoken to are very scared and stressed by this condition. It makes a difference to keep calm I find. It's refreshing to see you describe what happens with a calm demeanour.

i have some struggles since i was 23-24y old weird things happend, but after 2-3y they found out FND i go to an universitair Hospital, it something i also have to go to accept and also i see thing going little bit back, my legs are sometimes weak, i try as much to walk, but they told me also i have to accept life will be different, i did powerlifting, and ice hockey, now already 2y not doing these sport driving me crazy, idk how this will go futher, like they say nerve damages, Software problem. well now i'm 26 but i am pretty scared cause i still can't accept it that things goe different, i think i still need a long way to accept and just enjoy life, and looking to your videos is like therapy and also i have some epileptic shakings but 2y back to now indeed my body has changed, i need to accept but it is still hard mentally like , i drove back then to Motorcycle etc and now i can drive my car but i am honest with myself that this will be change too in future, am i afraid yes cause idk how, that why i go to special theraphy to accept and learn how life will going in future. - btw your story is also important i learn from it to be positive life is more then the things i used to do,

I was diagnosed with FND last May and I didn’t really want to accept it as here in the uk hardly any medical staff I’ve ever met have known what it is or how to help me? I’ve found it hinders the treatment and way people here help me if I have symptoms of other illnesses that need treatment and I have been told to chase up psychology services by several nhs medical staff members! Including my neurology consultant initially. I am lucky in that I have an FND specialist neuro dept here in Sheffield and so feel I am understood, but it is scary as not much is understood about this still.. so finding someone on here who explains it as simple neuro wiring dysfunction is helpful to show others that this is real and an actual brain disorder. Just because it doesn’t show on standard scans yet- available in the uk as basic mri only- it is real and is not something I made up! ❤

My brain deletes the drivers for my legs regularly... Its taking longer to recover each time...

Thank you. My daughter has fnd. You helped me understand. Light and love to you.

Bro way to open up and talk about this topic

FND is such a wild condition. I hate that other people experience this, but I do feel better that I'm not alone in this. I share several of these symptoms, and I am looking forward to learning more coping skills.

i feel you, even if they are unknown they are still there, and make life so hard

carnivore put alot of my symptoms in remisson*

I was wondering how you were get back into the wheelchair. Glad you can still do your work on cars. New sub. I’m in physio at the moment and I’m picking up tips, thanks 🫶

Thank you for sharing. 🫶

😂 really like you and thanks i have FND too along with me/cfs... always try my hardest to carry on with everything xxx hugs

you're a joy. thanks for sharing your journey with such a positive attitude. wishing the best for you and this strange condition.

good video

its calif certifed......emissions also

toyota is one of few that uses port and direct fuel injection......which helps with intake valves....staying clean

Although you don’t have the strength to move your legs, you still have feeling in your lower limbs, right? Feelings can remind you to move after a long time. Is this much better than who are completely paraplegic?

How about the rear wheel

I'm suffering from dystonia and tremor for three years, so I thought the symptoms would relate to some kind of epilepsy (I went to neurology and took anticonvulsant for about 1.5 years)... but as it turns out, it was just FND. Thank you for explaining many symptoms relating to FND using easy words!

I am so impressed with your attitude about your symptoms. I have been blessed with a supportive team of doctors. My neurologist has encouraged me to learn all I can but have stopped because of all the sad stories. You are an inspiration! I am glad you are improving!

Misses seeing you bud 😮

Missed seeing you!❤

Thank you for this, you have really explained it in such a way that has made me feel at ease with my FND. it's been a long year and getting the hang of it now. My goal is to keep my life as normal as possible with my FND, episodes and all. Also makes me feel not alone that there are people that does understand and get me😊. Thank you

memory foam bean bag helps

it was so awesome to talk to you last night! Your perspective is God glorifying!!

Do you have disability? Thanks

You have a great way of explaining your symptoms, really clear. It’s so helpful as a fellow sufferer to hear how you deal with your symptoms. Wishing you good body, brain and electricity 🙌🏻

Amazing! Respect.

Thank you for sharing these information. I do have question in the blockout do you loss consciousness or you can feel what is going on around you? Thank again for sharing this video and I hope you will get better!

Hello I have a disability I have mild cerebral palsy and I live in Texas I am new to your channel?

Damn bud put a shirt on..... 😂 doing great bud keep up the good work

Love your personality . God Good 🙏❤️‍🩹🙏

I have been a C-4 quadriplegic for almost 18 years. Throughout this time, I've encountered a few pressure sores, and the most crucial lesson I've learned is the importance of promptly addressing any signs of redness before it escalates. Each day, I have my Personal Support Workers (PSWs) take pictures of the areas of my skin prone to breakdown. Living with this condition has brought about a persistent daily anxiety, primarily centered around the fear of developing a pressure sore. Being paralyzed is undeniably challenging, but it is possible to make the best of the situation with the right mindset.