How I Improve My Hand Function | Motor Neuron Disease
ฝัง
- เผยแพร่เมื่อ 15 ต.ค. 2024
- This video shows how I use electrical stimulation to improve my hand function.
Links -
MND Information: tinyurl.com/4d...
Stimulator: tinyurl.com/4a...
Electrodes: tinyurl.com/54...
Follow me here -
Instagram: / limping_legend
Disclaimer: The content provided in this video is for entertainment and informational purposes only and is not intended to provide diagnosis, treatment, or medical advice. Please seek professional medical attention if you or someone you know has a medical question or concern.
Thanks for making these vids Emily! I’m a 44 y/o dude just diagnosed and seem to be progressing pretty quick so I’m pretty terrified. Your vids are really encouraging me to get my arse in gear to keep my hands etc as much as possible for as long as possible. Better pull my socks up!
Thanks Emily. I’ve just bought all the kit you showed. This is super helpful for my hands with my MND.
Awesome! So glad to hear the video was helpful.
Thank you very much for doing all your vlogs. So helpful and encouraging.
You are so welcome! I'm glad to hear they are helpful
Thank you Emily. Really helpful video. Just found you, I’m in the UK
Wish you so much good you are awesome 👌👌🌹
Very nice very helpful 👌 good motivation for the patients
Can you show me the exact electro stimulator you bought
44 in Dublin 3 kids diagnosed 2 years ago. Speech gone & mobility weak x
Nice video Limping Legend
Amazing 😯
Very helpful! Thank-you for sharing 🙏
Glad it was helpful!
This is true
How can I purchase it. My father is also suffering with MND.
what is the name of this gadget?
Please tell me The name of the machine that you are using their homes please set it to me
Mam i'm from india (tamilnadu) my father have the same problem MND starting stage so , can u give me a usefull information mam please 🙏
Mam ,Please reply me 🙏 it's an emergency...
Sir Tamilnadu same sir hirayama disease sir pls help me sir
@@kanagarajkumutha3307 entha ooru neenga
@@kanagarajkumutha3307 sir idha pathi therila sir
Wrongly dislike ur post, sorry
where can I find the bottle cap electrode? Thanks
Same question
Good luck your a hero. 🤗
Thank you!
@@limping_legendhow are you doing and why are you not answering recent comments?
Hello I have same disease please recommend me mam
I am motor n d patient please help me
I would be waiting for your request
My brother is very sick and he don’t know any solutions medication on the screen
What type of mnd is it?
I am MND Patient Help Me.From India
My sister is motor neuron disease. From india.pls help her.
❤️❤️
I am motor neuron disease patient pls help me.
Hi How can I help you
Please help me my mother is MND
Hello
How can I help you
Do you ever have difficulty speaking?
OMG Emily hiiiiiiiiii!!
Hi Dr. Jones!!!
@@limping_legend yaaaaayyy. So proud of you. And good to see you :)
Can I just say that I have found very high quality grass fed Whey protein isolate with pure Vitamin C powder very helpful for my Muscles. I have had Symptoms of MND since January 2016 especially in my tounge and face muscles.The Doctors cannot agree on me yet if I have MND or not.
(I have been testing since 2016 up until 2022)I do beilve that freqent feedings of Whey protein(Bulk brand) have helped my muscles and staying fat has really helped me(drinking the whey protein with milk helped this)
I also take Magnesium Taurate and Centrum multi vit a day with high quality Fish oil.
I found that When I dont take Whey protein I feel so much worse,I also never strain my muscles too much.
I just stimulate them enough maybe 10 minutes thats it but slow and easy stretching is the best.
I only ever do walking very short and stretching including lots of spine stretching.
Im currently 19 stone and I beilve keeping myself fat has saved me and helped me live longer,I read somewhere that being fat helps the Neurons to survive longer and better.
Also back in 2018,I started working out hard and after one hard working out session,I devoloped Tounge Fasiculations,but I rested and never worked out hard again and they stopped.
I developed symptoms after a Jiu Jitsu competition where I hurt my Cervical spine.
Hi, what symptoms do you/did you have it you don't mind me asking. Did you have an emg test done?
@@vierrecp3 Hi Deem yes I had a lot of EMGs,s did probably about 12 from 2016 to
2022. Now here's the problem, the EMG is only as good as the person performing it and some specialists said I had MND/ALS but others said I didn't.
They actually told me that EMG is NOT a diagnostic instrument for ALS/MND.
MND/ALS is diagnosed by ruling everything else out and there are some subtypes of MND/ALS where people can live for many years. If symptoms are severe and fast processing it's obvious anyway.
@@lippylennnox do u have mucle atrophy anywhere?