Gait and MS Part 1 - National MS Society
ฝัง
- เผยแพร่เมื่อ 2 มี.ค. 2010
- MS Learn Online is the National MS Society's online educational webcast series. This video features part one of a discussion with Francois Bethoux, MD, who talks about the common issues associated with gait and multiple sclerosis. www.nationalmssociety.org/Symp...
This hits home for my MS I can barely walk the past week I'm so over it :( 11 years of crap.
My legs feel like they carry bowling balls sometimes 😎
Thanks everyone involved! Great source of information, very professional and straight forward!
My right leg takes on a mind of its own!! Especially after sitting for a while right when I stand up it just goes nuts to the point where I can't walk for a while!! Just started doing that 20 years ago!!! Symptom onset was 38 1/2 years ago!!! I'm a rare case, unmedicated, came up with own treatment regimen and have steadily been improving in The last 5 years I'm a across country cyclist, Bikepacker!! I am coming out of retirement and finishing my goal of ridding the miles around the planet, to raise money for MS starting in the middle of June this June!! I am the ((Natural Born bike packer)) riding for MS!! To make a difference!!!!🚴👊 No one should have to live the way I did!!!!!
What did you do to recover?
@@youknowtherules8888 I changed the pH of my body from acidic to alkaline and went on the Terry walls Ms protocol diet!!
I walk like I’m drunk, but at least I’m walking.
Let Them Talk haha I am the same after a 100 m I start listing and bumbling
I walk like I’m drunk and I’m so scared I have PPMS
Me too!
Same
Yea 🙌 I am always like people think I am drunk!
Have you seen the Bioness L300 Foot Drop System? It uses Functional Electrical Stimulation and a gait sensor to help you walk more naturally and correct foot drop from MS, Stroke, CP, TBI and SCI.
This is a great series of videos. I was diagnosed with rrms in July of '05. Thank you NMSS!
Just got it and I’m struggling
im realy sick of my ms.
Same
He looks like the young Davey Jones from The Monkees lol
I have all these symptoms. Working hard to improve! 🤗
Thanks for this great Video about Gaitproblems in MS. 🌻🐞🦋
Can we please figure out the root cause. There are only so many factors. can we run them through a computer algorithm. It’s 2020
I totally agree with you.
Mast cell activation and co infections, such as SARS, Epstein Barr virus and Mold Toxicity. Calm the mast cells and treat any co infections that should slow down or even stop the MS process. For any damage already done, it maybe too late to repair tho.
Very infromative..thank you
I walk spastic and legs hurt and tire in 1 Bock it's impossible to walk farther.
I have very bad shoulder pain going down my arm into my hand. And in my neck.
Calf muscle very sore.
Long sight goes bit blurry at times.
I feel my balance is disturbed when I standing still.
Do I have early signs of ms.
I been diagnosed with mds
But now hospital not sure.
Got to go to bigger hospital for different tests
My doctor is in a state of denial. Medicare is my only medical coverage. I am 73 years old and have MS. Getting help is out of the question. Would like any advice someone could offer.
Barbara Stephens try state Medicaid as well! Department of Rehabilitation Services.
Try it all!
Hello, I'm awaiting test results. I also have DDD & Spinal Stenosis. Does anyone else have all 3?
You need to show the patients not only the doctors
Well geez a visual example would have been quite helpful to the viewers.
Anyone on Ampyria?
Im a hot MS lol. I wear an AFO for my drop foot
i walk with a gait i have LESSION ON THE BRAIN.
Many times others asked what I been drinking. Lol One person was calling but my speach was slurred. But hey life goes on and we cannot change to the better.
Another success story for and MS patient using Feldenkrais Method ,
Lifestyle and Dietary change:
th-cam.com/video/yzBwXKNlEDA/w-d-xo.html
Fatigue, makes me wonder how many are hypothyroid.
I can only speak of myself, but I imagine it applies to most patients diagnosed with MS, but I was thoroughly tested for other conditions before I was diagnosed with MS. (Including hypothyroidism and other conditions that are closely similar to MS).
I don't know, my thyroid and one neurologist said MRIs are fine, it's all in your head! I felt such anger well up in me... I had taken neuroleptics in the past but not anymore. Sice the MRIs look fine, they want to take me to neuroleptics. I am never psychotic, never out of control, not fighting anyone. Do not see things or talk to someone not there, do not hear voices, and never have. But these drugs can cause demyelination also.
useless... you should be talking about researches and cures. You just "chat" about issues... that are all well known.