My channel is about inspiring others to do what they love to do. Despite having a setback or two. It's important to live life to what is given to us, and it's meant for others to share. I do everything of living life differently and how I see the world. I have experience with working with my hands and many other things, and it's time to give back to the world. Enjoy and follow me as we live on this incredible journey called life!
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
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
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! ❤
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 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 🫶
Yah, they have Federal and California for the Cat. But of course getting to involved in the video about that would take away the attention for the audience on other matters and topics. But yes thanks for commenting
@@livingdifferently470 i agree.....explaning CARB requirements on your video🤣🤣......just wish there would be one standard for all 50 states...using the calif standard
You. I hate direct injection because of that reason. I've seen the intake valve myself when changing out an injector on a Travers engine 3.6 And man. When I had my legs, I'm not even kidding you. I had both legs on the motor and pulling.... it finally budged with me ejecting backward. I absolutely hate direct.
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?
My brain stopped sending signals down to my legs. And I have spasticity also. It is very controversial in that topic with Healthcare and me and others. The fact is, is that I'd rather not go to doctors because they're looking from outside my body and only see a body. But they don't know what I feel and deal with daily. And I would want to live a happy life versus go into a doctor's room and ask what's going on with me when I already did that, and got bad results. To hell with knowing what can be or could be. To hell with looking at doctors and think they're people who have the answers and solutions. Because they're the worst patients. No one knows what is and isn't. What can or will be. The best way Ii see it and has worked for me. Accept and move on. You'll be better off.
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!
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
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 🙌🏻
Yes. My neurological symptoms are very real, very obvious, and they're not very common in the medical field. But we do live on with better lives despite our symptoms. I hope you subscribed because i like making videos for people.
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!
I don't lose consciousness. I can hear everything around me. I can even tell you what you did around me. And if you touched and where you touched me. I just can't respond to you. I have gotten much better since my video. I've started to drive again. .y symptoms are very minimal and rare now. Except the paralysis and tics. The stuttering and blackouts only occur under extreme cases and I've started to take medication that help a lot
That happens to me too! I actually started what I call passing out (I've never done it while drinking, I know cause I don't drink lol, so don't know if it's like that) just before and during the eclipse 😮😅
I'm so glad you're doing better. That's so great that you can drive again!! I'm so new at this and have so many questions, and it's seems too me that you must be the best embassador out there😀💕
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.
Yes I always think of different kinds. The reason why Im using my foam is because my friend Harold told me how many air cushions he's popped due to both his and mine's line of work. So My air would be more for other times. I do plan to purchase more robust cushions in the future though. The softer the better
@@chantelle1654 oh it is. And spacious enough to record properly without all the small stuff on the counter tips. Excellent soft light etc. So I will starting here pretty soon thanks for your support
@@livingdifferently470 I've no doubt it will grow in popularity, especially talking about FND which is so poorly understood around the world and so little money being put into research and treatment, we're kinda left alone. I'm sharing you're vlogging here in the U.K FND community.
@@chantelle1654 I am considering about making a video of how FND is known and understood to be real, but how the medical field lacks knowledge that people need to further understand. How paralysis can occur without a spinal or brain injury.
@@livingdifferently470 that would be so helpful to so many sufferers and their Support People👍🏻💝 But I think that the Videos you've made are so awesome and just need exposure and shared more! I'll share them especially on 🇨🇦 sites for sure! I think you'd be great in Interviews!
