My fiance just released an album dedicated to his mother who has MS. Half of the proceeds will go straight to the MS society. Support good music for a great cause! Please!
i can relate i was diagnosed with ms last Oct. It started when i woke up with a numb arm,i just thought it was where i laid on it,i then lost my balance,started to stubble bump in to things with no control.Then progressed to my whole left side of my body , i couldn't walk, my left leg felt like a ton, i cudnt write and cut my food. its not a easy thing but so many people i
know with it, never lose there smile., and to the guy who made his video i salute you for having the bravery to do it .xx
He has such an inspiring story of his life and how he deals with it, never giving up. This man needs an award (if he hasn't got any) because he gets through to people and proves his point. And fuck you bastards how disliked this video, bunch of arseholes.
Thank you for having the courage to share your story. I'm not sure if I have it or not. I've been in and out of the hospital over the past few months. I've exhibited symptoms of MS and other diseases but the doctors can't quite pinpoint what is wrong. At first they thought a minor stroke and it was later thought to be compressed blood vessel to the brain. How long was it from your first attack until when you were diagnosed? (I'm 26)
I'm a young man who suffered a stroke with left side paralysis when I was 24. I am now 42 & my best friend from high school was just diagnosed with MS & MS is far more challenging than a stroke. I have a lot of respect for anyone diagnosed with this challenging disease
Help Jeff Johnson raise money for research to find a cure for Multiple Sclerosis. Visit his fundraising home page at nationalMSsociety home page and add to the URL /goto/jeffjohnson
@ChronicFatigueSyn MS is on the INSIDE. i dunno about you, but i cant see the central nervous system and brain on the outside of someone. just throwing that out there. lol.
People are not lazy its not their faults they have mercury in their body and THINK they have MS lol.
I can tell you most of the MS people I talk too are dumb as fuck.
Something the mercury does to your brain... eats it up or something?
When I had MS (mercury toxicity) I felt so stupid... my brain was mush!
Soon as I got a metal detox... I felt cured within weeks. Now here I am better than I have ever been. I'm telling you... metal detox is the ONLY way any of you will feel better...
@ChronicFatigueSyn you are some kinda piece of crap. WOW. So really how is someone with MS supposed to look? I look fine but I have it. You need to educate yourself son!
Help Jeff Johnson raise money to find a cure for Multiple Sclerosis. Visit his fund raising home page at nationalMSsociety website and add /goto/jeffjohnson to the URL
that is nationalMSsociety AND dot org AND /goto/jeffjohnson
Herman about how old were you when you started experiencing a lot of these symptoms. I am 31 I have been diagnosed for 7 yrs. I knew I had MS long before the diagnosis though. My mother had it...I knew I had inherited it because I have a chromosome mutation called Klinefelters Syndrome...you should look it up ..quite fascinating. anyways I found your video to open and honest and I am sure others out there as well as myself can appreciate those two traits.
@ChronicFatigueSyn What am I suppose to look like? Then you imply I'm trying to cheat people outta money? Really??? I see you're not the sharpest pencil in the box but I wish you many blessings.
Thanx for the vid man I am 34 and am going on a little over 1 year fighting ms. @ragnarocking. I too have ms and eat a low fat diet. It's the natural progression of ms if you are rrms that the "attacks" come and go. If you are strict with your diet you should see results after a full year.
I'm 50yr old, bricklayer, ride dirt bike, run beagles, I never stop. At least that is what I did until one morning I awoke and could hardly walk. I went to bed, age 47, feeling like 19yr old. I awoke feeling like 70yr old. No balance, bladder prob. People think I'm drunk. I never told people at church. You should see the look on their faces. Sucks that I have had people call police on me thinking I'm drunk. I try to just go best I can. I feel life is over. Lucky that I have no unfinished bus.
poor bastard....i thought i had this 2 years ago....the symptoms came back recently and it turns out it was booze causing it....im cleaning my liver and kidneys and the symptoms are going...
Hi Herman. I was D/X with M.S. in June (i'm male/33yrs old). Can I ask what your diet is like? Since D/X, I've been reading (and practicing) a lot about diet and its affect on AI diseases (and nearly all diseases/sicknesses in general). Since I started a very low-fat diet, then vegan diet - nearly immediately after my d/x - all of my symptoms went away. This could just be the natural course of RRMS and I guess that I'm asking if I'm only wasting my time? Best of luck to you.
@ragnarocking I've noticed the same thing my friend diet diet diet. I'm eating very similar to you. Two books I've been using are 'the ph miracle' and 'healing multiple sclerosis' by ann boroch. They've been very helpful
just watched David Wolfe an Dr. Marcola people who got rid of MS longevity now confrince. something about going all raw even meat, superfoods, herbs mushrooms etc.
Hope you are doing well & Im sorry that you have MS I can relate with you my friend, My doctor's have ran some test on me and I have the same symptoms as you and im scared right now, But that will pass im sure because I have faith, sometime my faith gets a little weak But I still TRY to think positive. Thanks Again, Hope you make more video's soon.
Thank you for being honest. My son is now, 16. He was diagnosed at 11. It's very unusual for a child to be diagnosed. He does not have the progressive type.....thank the dear Lord. But, I do have friends with progressive MS and it is horrific. I take great issue with some of the dumbasses on YouTube who are woefully misinformed. I admire you for being honest. Bless Your Heart. XOXO
One symptom I'm glad to have diminished, id numbness in the fingers. Being an artist it is terrifying to not be able to feel the pen in my hand. Thank God that left me. I still have problems holding on to smooth objects, but hell, I just gaff-tape that shit!
Dude, I hear you. My sympptoms (of course) are totally different, but one thing many MS patients have in common is an ability to joke about it. Before I was diagnosed I saw Richard Pryor's stand-up about MS and I felt uncomfortable laughing at it, but now I think it's hilarious because I can see myself in that situation.
There is now a Reformed Multiple Sclerosis Society that is urging for the medical community to check out Dr Paolo Zamboni's discovery that MS is caused by poor blood drainage from the brain. The answer to restore blood drainage from the brain is angioplasty. Watch the before & afters for this surgery called CCSVI on youtube- simply amazing. In just 24 hours a world of difference
I've had almost the exact same symptoms as you. It was almost eerie hearing you describe them. I've also had a couple bouts of optic neuritis that scared the hell out of me. I was losing my vision and had no idea if it would bounce back after the attack ended. Luckily, it did. I'm tired of having MS. I've tried every treatment they have to offer and the only thing that worked was Mitaxantrone but you can only be on that for about 18 months. It's too dangerous. We need something that works.
i am going to get tested in a few days for MS, i have had symptoms that doctors thought were either Tourette's syndrome or some other neurological condition, since i was about 16. Then as time progressed, i got numbness in my left arm (shoulder area) and atrophy, i had to do 3 months of phys therapy to get it to feel normal again, but in a week or so after therapy it went back to normal, now i am having incontinence so i need to get tested. thanks for sharing I wish you the best.
Stumbled on to this video. I'll definitely look for the others. You're right - we're all different and I learned about symptoms I haven't been confronted with. Love listening to you speak!
Wow I am grateful for your voice I was diagnosed this december I thought i WAS going completely nuts..now on avonex for the last 5 months great...tried the copaxzone (ms).no intended misspellings ...but that got old and depressing i mean every day my god! I was terrified by needles and wow my client who is 78 yrs old told me she was on avonex once a week im 30yrs but it is impowering me to know that I am doing something pl
Can you still drive? I have to do work that concerns driving but I lose focus sometimes like my mind daydreams out of the blue. I probably will have to look into at home work on the computer. thanks for sharing your story.
@PsalmsNmyrrh Yes I can still drive. When I first got diagnosed in 2005 my legs would shake when I'd drive. But things are better now. My driving is back to normal. If you're looking to work from home. I have a postcard program I've been using that you may be interested in. Go to PeopleLoveCash * com
Ms is the biggest bollocks to happen to me. Because I dont show any symptoms people forget I have it, even those closest to me. And while, thank god it doesnt affect me badly, it has an effect on everything I consider myself doing. But I thank god every day for what I have and know I am lucky. God bless. X
i have pretty much all the symptoms you have. except the bathroom thing haha. but i never thought he writing thing was from MS... im 16 now and when i write my name in school it looks like im writing my name in kindergarten. my handwriting never really got better.
I have a new found understanding of MS. I recently found out that one of my closest girlfriends has been in the hospital for the past two weeks because she suddenly couldn't walk. She is now in rehab to learn to walk again and there is a strong possibility that she has MS. Thank you for sharing/
I relate with this video. I've had ms for 9 years the numbness the tremors(both hand and feet) now I use a crutch tnow. I don't write again, I just use the computer. have blurred vision, my right eye don't see beyond 3m. The bathroom stuff he talked about is exactly like mine, done it on myself a couple of times, learnt to only take fluids when a toilet is close
However, I learnt that the intensity of the symptoms depend on my emotions-Anger agitation flares symptoms up
If you're interested in natural supplements which may improve your MS symptoms, you should research the study being conducted by hopetrials! You can receive a supplement which is currently being studied for it's effectiveness for MS symptoms.
I'm a hypochondriac, and my latest scare is MS. I've thought that since my mind is so foggy, i have trouple with linear thought, my whole body shakes when I yawn or stretch, my extremities fall asleep easily that I had MS. I've been a pot head for 2 years now. I'm going to clear my mind up and see if it helps with all this anxiety I have. I also get the chills very easily when I'm nervous. Sometimes, wearing black, in the 80degree heat, I shiver. You're a good person, and I wish you luck with MS
So far I am only having the problems you describe with my legs. I was always able to walk around all day without even thinking about it ....and I am sure finding it hard to accept the idea that this is only going to get worse, I would sooner have a fixed disability like having lost a leg or something.
hey man your video cleared up alot of stuff for me, im trying to put my mind at ease and the symptoms your having are alot harsher than the ones im having, im just having discomfort in my muscles from what i believe to be depression.
This might sound a little crazy but I just started using food grade hydrogen peroxide 35% it adds more oxygen to my blood stream it might help you as well
I have congestive heart failure my symtoms are the same as yours I take 2 drops into a bottle of water it does help with numbness and can breath better when i go to move around.I've been on this now for a month going shopping was a big problem I would have to stop and caught my breath every 3 minutes not anymore fred_bynum@yahoo.com
This might sound a little crazy but I just started using food grade hydrogen peroxide 35% it adds more oxygen to my blood stream it might help you as well
I have congestive heart failure my symtoms are some what the same as yours I take 2 drops into a bottle of water it does help with numbness and can breath better when i go to move around.I've been on this now for a month going shopping was a big problem I would have to stop and caught my breath every 3 minutes not anymore fred_bynum@yahoo.com
This might sound a little crazy but I just started using food grade hydrogen peroxide 35% it adds more oxygen to my blood stream it might help you as well
I have congestive heart failure my symtoms are some what the same as yours I take 2 drops into a bottle of water it does help with numbness and can breath better when i go to move around.I've been on this now for a month.going shopping was a big problem I would have to stop and caught my breath every 3 minutes not anymore fred_bynum@yahoo.com
Thanks for this nice video i have the same symptoms you have ... but am a girl and what hurt me the most i can't wear high heels shoes which i was like too much .. i really wish to be your friend coz u know here in middle east ppl don't even know what ms and that hurts no one can understand your pain .. anyway thanks that was nice to accept MS with a big smile :D
My symptoms are very similar as well! I was formally dignosed 02-07-2011. One day I'll have to get a camera and make a video, too! Thank you for yours!
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I can relate... I've had most of the symptoms you are talking about. My first serious attack scared the hell out of me. I had double vision and I couldn't walk without stumbling around. This was before I was diagnosed with MS so I didn't know what was going on. I have also had the numbness on both sides of my body from head to toe twice. Been on avonex 7 months now, and so far I haven't had any attacks so I hope this continues to work for me.
If you’re diagnosed with Multiple Sclerosis, cheer up because the cure for MS is already discovered, and it’s called “CCSVI,” or “The Liberation Treatment!” This cure was discovered by “Dr. Zamboni!” You can search this here on You Tube. Just search: “CCSVI,” and/or “The Liberation Treatment,” and/or “Doctor Zamboni!” You can also log on Facebook and check”CCSVI in Multiple Sclerosis!” Feel better!
If you’re diagnosed with Multiple Sclerosis, cheer up because the cure for MS is already discovered, and it’s called “CCSVI,” or “The Liberation Treatment!” This cure was discovered by “Dr. Zamboni!” You can search this here on You Tube. Just search: “CCSVI,” and/or “The Liberation Treatment,” and/or “Doctor Zamboni!” You can also log on Facebook and check”CCSVI in Multiple Sclerosis!” Feel better!
Thank you for sharing. I especially like you saying "MS career", I'll use that. What helps me a lot is taking high doses of Omega 3 supplements and Magnesium for my restless muscles. I've had embarrasments too, not a pretty sight but, as long as I offload in the mornings, the day is OK. Peace and love.
I love your videos! You are an excellent public speaker and I enjoy hearing about MS symptoms from you. Having MS sucks for us all. Stay strong and beautiful!
I agree you are a lovely looking man. I was diagnosed in 87 and know what you are going through. Keep strong and show the world that MS has made the wonderful person that you are.
Look up neurovax. It stopped the progression of MS entered phase II clinical trials and then the company that was going to produce it went bankrupt. This drug needs to be approved.
@hmack2005 You're welcome. You seem like a very kind person and I enjoy your videos. I hope that vaccine gets picked up by another company and gets approved or the company gets the funding it needs. People as kind as you need to be cured now. Let those who choose to follow בעל זבוב have this suffering . I'm a great believer in יְהֹוָה and I believe if his servants ask and truly serve then he will heal them and not allow בעל זבוב to harm his servants.
Thanks for sharing. I am studying to be a doctor and your descriptions have greatly helped my understanding. I'll be better able to provide advice in the future as a consequence. All the best. J
wana say,for the past 5 years ive had numbness in my face and tingling in my arms,neck,hands and my doctor put it down to panic attacks.ive had a MRI 3years ago which was clear,now I have painfull joints,now I have confusion and weakness in my body also tremor in my left thumb and hand,what im trying to say im sick of prople saying that its all in my mind. I know my body,and somthings wrong,I wish someone could help me. What do I do? Please help me find an answer!
@tonyurmate Sounds like benign fasciculation syndrome, but with the painful joints it sounds more like fibromyalgia. Neither of which would show on an MRI, though benign fasciculation syndrome could show up on an EKG. You should see if they'll do a nerve conduction test. If it comes back that you don't have anything and your Rheumatoid Factor is low, yet you still have these symptoms, you could have a strong case for fibromyalgia. On the other hand a diagnosis of fibromyalgia is hard to get.
@guitarobsessed85 Thank you for your comment,I still get tingling in hands,arms legs and back and joint pain,it can last up to two weeks to a month,it always goes away for mabey a month or so but comes back.
my doctor puts it down to stress and i have suffered with panic attacks also since I was 7years old,I also suffered with very bad growing pains in my teens,with hip back and knee pain.
Ive just been diagnosed with arthritis in both hips,im now 38.
@tonyurmate Your joint pain could be caused by migratory arthralgias due to your prior infection. Panic attacks can cause parasthesias like tingling and numbness, but so can benign fasciculation syndrome. I you have extreme fatigue and stabbing sensations you probably have fibromyalgia.
@tonyurmate You have my sympathy. I know how horrible it is to be told this crap by doctors and so called experts. All the unessesary vaccines, food additives and fluoride in drinking water etc over many decades has a lot to do with why so many people are going down with MS, ME, Lupus and many other mystery diseases.
I have MS, the 5th in my family and sometimes it does not show up. There is never enough helpful information. Don't let them fob you off, of course you know your own body!
after 4 years of tingly feet, i just had my first mri which showed 5 3mm lesions on my brain. family dr gave me the news on friday and i'm going to call my neuro tomorrow. any advice? thanks for the video . . . :) (other symptoms: i'm a marathoner (did 5 this year, including a personal best!) and when i run with some slower friends, i've tripped.)
My mother has all of the symptoms of MS but she hasn't been diagnosed with it because her MRI scans always come up negative (she doesn't have the damaged myeline sheath or nerve cells) But I was curious to ask a question if you don't mind. How often does your face go numb and what side of the face?
My mother has Symptoms of MS but she hasn't been diagnosed because her MRI scans always come back negative (she doesn't have the damaged myelin sheeth)
However, i'm very curious if you don't mind me asking about the numbness in your face, How often does it happen and what side of your face the right or the left?
@realityword I think CCSVI is great. I think all MSers should get checked for it. I found out that my left jugular is 90% blocked and my right is 50% blocked. So I'm getting the procedure done down in San Diego next week :)
@wisdaniel No meds my friend. I did rebif for 2 years. And for the last 2 years I've been med free. I've been doing everything all natural. The meds didn't help me.
ye had all them syptoms except the bladder problems the writting one really sucks but also had the pain that you didn't. hope your not having too much of a problem at the moment
@johnnyd101 I've made really great improvements since I made this video. I'm not 100% but better than I was...thank GOD. Lookin into CCSVI. I found out that my left jugular is 90% blocked and my right is 50% blocked. I'll keep everyone posted :)
Partial Facial numbness that lasted a few days and back numbness that lasted a few mins. Shooting warm feelings in legs. I always had vibrations in my legs and thought it was normal. Never really had any vision issues except photosenstivity (can this be optic neuritis? Or does it always impair color vision?) This is over the course of two weeks. Numbness is gone in my face but I'm still getting hot sensations in my legs. Are these symptoms of MS or are they too mild?
@guitarobsessed85 I have two relatives with ms. I went running the other day and my whole shoulder went numb along with my face. The shoulder numbness only lasted a few minutes but the facial numbness lasted 3 days. My legs twitch a lot. I experience no weakness or ataxia. Do symptoms tend to be more mild in the beginning of MS or does it usually hit strong? And are there always vision issues? I'm freaking out right now. I have no health insurance.
@guitarobsessed85 unfortunately my friend evryones symptoms vary so much I don't know if I could lable it MS. My suggestion would be to go to your doctor or free clinic and let them know what's going on. Try not to panic. You can beat whatever is going on. Stay strong my friend.
@hmack2005 Thank you. I will be going to the doctor as soon as I have health insurance which is in two weeks. I hope they find a cure for this disease. I'm a biologist of all things haha. I will hopefully not have the disease and be able to get into research for a cure. I hope that you go into permanent remission.
Thanks for posting this, it's important to let people know some of the things we go through. It's also good just to talk about it. I have only had "accidents" in or near my house, thank goodness. But I still map the bathrooms when I'm out.
@hmack2005 well i had found an interesting approach and some ppl report success with MS, it is called watercure (hydration therapy) , address is watercure2 D()t org, check out their testimonials. Caffeine and ethanol are diuretics.
@hmack2005 No problem. If U dont drink caffeine and alcohol, there is only one thing left to ask. What do U drink generally and what is Your water and salt consumption daily ?
I just found out I have MS a few weeks ago.... just now getting brave enough to look at stuff online, I was worried that I would see people all fukrd up and one day I'm gonna look like them........... it hasn't really been like that tho, thank God.
Thanks for sharing yourself, if you get a chance, I'd love to chat with you more.
You can message me here but yahoo is better, they block youtube at work...lol
leigh_massengill@Yahoo.com you can look me up on myspace or facebook too
have you checked out the paleo diet to relieve your symptoms? i have an auto immune condition called ulcerative colitis and thats greatly helped me. the science of it all makes so much sense.
Im really sorry man, I dident even know what ms was untill and hour ago maby. I honestly hope there might be a cure in our lifetime. Just dont let it beat you man please. I cant say i feel for you cause i dont know what its like man but after watching this i care for ya like a brother man I hope you get through it all you will be in my prayers
@tidusgang123 Hey brah thank you for the kind words. Please dont be sorry cuz everything happens for a reason. What doesn't kill me will only make me stronger and I my strong mf. Many blessings and much success :0)
I don't have MS but I know what it is like to loose the ability to walk. My legs felt like they were on fire for two days and then all of a sudden they stopped working, but I can still feel. I am sorry you have it. It is horrible. To this day the doctor's don't know what I have.
I have a question for anyone that can answer... I dont really think I have MS but was wondering if this means anything... My hands dont always want to work. i have a hard time doing tedious tasks for longer than just a few seconds. they tire quickly and i drop things just out of the blue, for no reason. Its irritating to me and i want to know why... if anyone could help
@MyBaby91307 hi, I don't think the internet is the best place for an answer on this but here's my opinion, what you describe COULD be normal, depending on how often it happens and what the activity is.OR it could be an indicator of somethingg else, I don't want to worry you but I think you should get this checked out by your doctor/a neurologist as it is not normal for hands to drop things and not work, especially if it is after a few seconds. Get it checked out, if only to put your mind at ease
KEVIN GARNETT
RossTheBalla05 1 week ago
This has been flagged as spam show
My fiance just released an album dedicated to his mother who has MS. Half of the proceeds will go straight to the MS society. Support good music for a great cause! Please!
itunes.apple.com/us/album/jnewryep/id476015357
Blessings
JessicaSunshineMusic 1 week ago
I FEAR GOD, bless you
wehbe505 2 weeks ago
i can relate i was diagnosed with ms last Oct. It started when i woke up with a numb arm,i just thought it was where i laid on it,i then lost my balance,started to stubble bump in to things with no control.Then progressed to my whole left side of my body , i couldn't walk, my left leg felt like a ton, i cudnt write and cut my food. its not a easy thing but so many people i
know with it, never lose there smile., and to the guy who made his video i salute you for having the bravery to do it .xx
beckybananasx1 2 weeks ago
He has such an inspiring story of his life and how he deals with it, never giving up. This man needs an award (if he hasn't got any) because he gets through to people and proves his point. And fuck you bastards how disliked this video, bunch of arseholes.
DavidQuinn101 3 weeks ago
Take care my friend. I wish you health and longevity.
harmagician1 3 weeks ago
MS is very common in Scotland due to the miserable, freezing weather.
karezza6 1 month ago
Thank you for having the courage to share your story. I'm not sure if I have it or not. I've been in and out of the hospital over the past few months. I've exhibited symptoms of MS and other diseases but the doctors can't quite pinpoint what is wrong. At first they thought a minor stroke and it was later thought to be compressed blood vessel to the brain. How long was it from your first attack until when you were diagnosed? (I'm 26)
hippykiller1 1 month ago
@hippykiller1 I found out about a month after I starting seeing signs
hmack2005 1 month ago
God bless you and your courage bro. I'm not half the man you are.
jedimind28 1 month ago
@jedimind28 thanks for those kind words :)
hmack2005 1 month ago
I'm a young man who suffered a stroke with left side paralysis when I was 24. I am now 42 & my best friend from high school was just diagnosed with MS & MS is far more challenging than a stroke. I have a lot of respect for anyone diagnosed with this challenging disease
MrDarkmarius 1 month ago
This has been flagged as spam show
Help Jeff Johnson raise money for research to find a cure for Multiple Sclerosis. Visit his fundraising home page at nationalMSsociety home page and add to the URL /goto/jeffjohnson
Ekorn999 2 months ago
@ChronicFatigueSyn MS is on the INSIDE. i dunno about you, but i cant see the central nervous system and brain on the outside of someone. just throwing that out there. lol.
staceyfenster 2 months ago
Slowly people with MS will realize I'm right... then MS will be over!
DOCTORS CAN'T TEST FOR MERCURY, BUT THEY SURE THINK THEY CAN.
YOU MUST FIND A WELLNESS CENTRE!
vancouverislandbass 2 months ago
People are not lazy its not their faults they have mercury in their body and THINK they have MS lol.
I can tell you most of the MS people I talk too are dumb as fuck.
Something the mercury does to your brain... eats it up or something?
When I had MS (mercury toxicity) I felt so stupid... my brain was mush!
Soon as I got a metal detox... I felt cured within weeks. Now here I am better than I have ever been. I'm telling you... metal detox is the ONLY way any of you will feel better...
vancouverislandbass 2 months ago
@ChronicFatigueSyn you are some kinda piece of crap. WOW. So really how is someone with MS supposed to look? I look fine but I have it. You need to educate yourself son!
missrizzo1 2 months ago
This has been flagged as spam show
But mercury is not in the blood or urine. It is in the tissues. It has to be
provocated out of the tissues by a chelating agent in order to be measured.
Hair analysis may sometimes show levels of mercury in the body but it is often inaccurate.
vancouverislandbass 2 months ago
This has been flagged as spam show
MS is very difficult to diagnose. Yet, believe it or not,
mercury poisoning is almost never considered during the
MS diagnosis procedure. Even though MS symptoms are identical
to mercury poisoning. According to OSHA chronic mercury
toxicity cannot be distinguished from MS. Mercury levels
cannot be assessed by either blood or urine levels. Blood
and urine tests are the only tests that the medical system uses for mercury.
vancouverislandbass 2 months ago
This has been flagged as spam show
Help Jeff Johnson raise money to find a cure for Multiple Sclerosis. Visit his fund raising home page at nationalMSsociety website and add /goto/jeffjohnson to the URL
that is nationalMSsociety AND dot org AND /goto/jeffjohnson
Ekorn999 2 months ago
@ChronicFatigueSyn we are just laze? You are an ignorant POS
rewind2grace 3 months ago
Herman about how old were you when you started experiencing a lot of these symptoms. I am 31 I have been diagnosed for 7 yrs. I knew I had MS long before the diagnosis though. My mother had it...I knew I had inherited it because I have a chromosome mutation called Klinefelters Syndrome...you should look it up ..quite fascinating. anyways I found your video to open and honest and I am sure others out there as well as myself can appreciate those two traits.
rewind2grace 3 months ago
@ChronicFatigueSyn No, there not. Montel Williams has multiple sclerosis, and he is very active and positive.
shelbielynnVEVO 3 months ago
HOW DO YA HAV 3 DISLIKE. PEOPLE CAN BE SOLELESS
thallious9876 3 months ago
@ChronicFatigueSyn
Shut the eff up! You know nothing! people are born with this you jack ass.
SavahRoss 3 months ago
@ChronicFatigueSyn What am I suppose to look like? Then you imply I'm trying to cheat people outta money? Really??? I see you're not the sharpest pencil in the box but I wish you many blessings.
hmack2005 3 months ago
I feel your pain brother
vertigotronix 4 months ago
Thanx for the vid man I am 34 and am going on a little over 1 year fighting ms. @ragnarocking. I too have ms and eat a low fat diet. It's the natural progression of ms if you are rrms that the "attacks" come and go. If you are strict with your diet you should see results after a full year.
furiousbrysko 4 months ago
:(
LaSexyNativa 4 months ago
I'm 50yr old, bricklayer, ride dirt bike, run beagles, I never stop. At least that is what I did until one morning I awoke and could hardly walk. I went to bed, age 47, feeling like 19yr old. I awoke feeling like 70yr old. No balance, bladder prob. People think I'm drunk. I never told people at church. You should see the look on their faces. Sucks that I have had people call police on me thinking I'm drunk. I try to just go best I can. I feel life is over. Lucky that I have no unfinished bus.
grady1610 4 months ago
Comment removed
MsCSimmonds 4 months ago
oh by the way...DON CROFT PARASITE ZAPPER will help with the symptoms loads
hallwoodsgadgets 4 months ago
he seems like a decent bloke too...illnesses only happen to good people while all the cunts and rapists are 100% healthy
hallwoodsgadgets 4 months ago
poor bastard....i thought i had this 2 years ago....the symptoms came back recently and it turns out it was booze causing it....im cleaning my liver and kidneys and the symptoms are going...
hallwoodsgadgets 4 months ago
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i am a 11 year old boy and my mom has ms
hackz77 4 months ago
Hi Herman. I was D/X with M.S. in June (i'm male/33yrs old). Can I ask what your diet is like? Since D/X, I've been reading (and practicing) a lot about diet and its affect on AI diseases (and nearly all diseases/sicknesses in general). Since I started a very low-fat diet, then vegan diet - nearly immediately after my d/x - all of my symptoms went away. This could just be the natural course of RRMS and I guess that I'm asking if I'm only wasting my time? Best of luck to you.
ragnarocking 4 months ago
@ragnarocking I've noticed the same thing my friend diet diet diet. I'm eating very similar to you. Two books I've been using are 'the ph miracle' and 'healing multiple sclerosis' by ann boroch. They've been very helpful
hmack2005 4 months ago
just watched David Wolfe an Dr. Marcola people who got rid of MS longevity now confrince. something about going all raw even meat, superfoods, herbs mushrooms etc.
thallious9876 4 months ago
@thallious9876 thanks i will check this out :)
hmack2005 4 months ago
@thallious9876 , raw meat harbors many parasites, one that's particularly dangerous is the Tapeworm
PantheraAtrox 4 months ago
I have MS and I can relate to you totally. I'm going to send you a friend invitation to my channel. Hope you will accept.
dragonflywhisperer1 4 months ago
Hope you are doing well & Im sorry that you have MS I can relate with you my friend, My doctor's have ran some test on me and I have the same symptoms as you and im scared right now, But that will pass im sure because I have faith, sometime my faith gets a little weak But I still TRY to think positive. Thanks Again, Hope you make more video's soon.
BlistardPussy 5 months ago
@BlistardPussy Continue to think positive. Things will get better. :)
hmack2005 4 months ago
Thank you for being honest. My son is now, 16. He was diagnosed at 11. It's very unusual for a child to be diagnosed. He does not have the progressive type.....thank the dear Lord. But, I do have friends with progressive MS and it is horrific. I take great issue with some of the dumbasses on YouTube who are woefully misinformed. I admire you for being honest. Bless Your Heart. XOXO
fyates8485 5 months ago
One symptom I'm glad to have diminished, id numbness in the fingers. Being an artist it is terrifying to not be able to feel the pen in my hand. Thank God that left me. I still have problems holding on to smooth objects, but hell, I just gaff-tape that shit!
alfrank2000 5 months ago
Dude, I hear you. My sympptoms (of course) are totally different, but one thing many MS patients have in common is an ability to joke about it. Before I was diagnosed I saw Richard Pryor's stand-up about MS and I felt uncomfortable laughing at it, but now I think it's hilarious because I can see myself in that situation.
alfrank2000 5 months ago
There is now a Reformed Multiple Sclerosis Society that is urging for the medical community to check out Dr Paolo Zamboni's discovery that MS is caused by poor blood drainage from the brain. The answer to restore blood drainage from the brain is angioplasty. Watch the before & afters for this surgery called CCSVI on youtube- simply amazing. In just 24 hours a world of difference
2ndSamuel710 5 months ago
I've had almost the exact same symptoms as you. It was almost eerie hearing you describe them. I've also had a couple bouts of optic neuritis that scared the hell out of me. I was losing my vision and had no idea if it would bounce back after the attack ended. Luckily, it did. I'm tired of having MS. I've tried every treatment they have to offer and the only thing that worked was Mitaxantrone but you can only be on that for about 18 months. It's too dangerous. We need something that works.
MrFuckinSunshine 5 months ago
yes it does and we hope for the best.
TheGlamWay 6 months ago
I'm sorry for all of you that have MS. I wouldn't wish it, on anyone! God Bless You.
heatherlikey 6 months ago
I just want to say thank you for letting us know what it is to have MS.
RealmOfTruth110 6 months ago 12
@RealmOfTruth110 No problem :)
hmack2005 6 months ago
i am going to get tested in a few days for MS, i have had symptoms that doctors thought were either Tourette's syndrome or some other neurological condition, since i was about 16. Then as time progressed, i got numbness in my left arm (shoulder area) and atrophy, i had to do 3 months of phys therapy to get it to feel normal again, but in a week or so after therapy it went back to normal, now i am having incontinence so i need to get tested. thanks for sharing I wish you the best.
ilovepinatas3179 7 months ago
Stumbled on to this video. I'll definitely look for the others. You're right - we're all different and I learned about symptoms I haven't been confronted with. Love listening to you speak!
vsjcat 7 months ago
@ForeverAchiever Thanks I will check out these videos. I really appreciate the suggestion
hmack2005 7 months ago
Exactly what I went through.
TheKatieb1991 7 months ago
Wow I am grateful for your voice I was diagnosed this december I thought i WAS going completely nuts..now on avonex for the last 5 months great...tried the copaxzone (ms).no intended misspellings ...but that got old and depressing i mean every day my god! I was terrified by needles and wow my client who is 78 yrs old told me she was on avonex once a week im 30yrs but it is impowering me to know that I am doing something pl
us 3,000ui of vitamin D ..... say life is choices
Ken1Isis 8 months ago
Can you still drive? I have to do work that concerns driving but I lose focus sometimes like my mind daydreams out of the blue. I probably will have to look into at home work on the computer. thanks for sharing your story.
PsalmsNmyrrh 8 months ago
@PsalmsNmyrrh Yes I can still drive. When I first got diagnosed in 2005 my legs would shake when I'd drive. But things are better now. My driving is back to normal. If you're looking to work from home. I have a postcard program I've been using that you may be interested in. Go to PeopleLoveCash * com
hmack2005 8 months ago
@hmack2005 good you are feeling better and thank you for site, I will check it out.
PsalmsNmyrrh 8 months ago
This sounds like me? Best wishes from England. richie979X.
Richie979 8 months ago
Ms is the biggest bollocks to happen to me. Because I dont show any symptoms people forget I have it, even those closest to me. And while, thank god it doesnt affect me badly, it has an effect on everything I consider myself doing. But I thank god every day for what I have and know I am lucky. God bless. X
123jsbach 8 months ago
i have pretty much all the symptoms you have. except the bathroom thing haha. but i never thought he writing thing was from MS... im 16 now and when i write my name in school it looks like im writing my name in kindergarten. my handwriting never really got better.
zachboggs360 8 months ago
I have a new found understanding of MS. I recently found out that one of my closest girlfriends has been in the hospital for the past two weeks because she suddenly couldn't walk. She is now in rehab to learn to walk again and there is a strong possibility that she has MS. Thank you for sharing/
curvygirl63 8 months ago
I relate with this video. I've had ms for 9 years the numbness the tremors(both hand and feet) now I use a crutch tnow. I don't write again, I just use the computer. have blurred vision, my right eye don't see beyond 3m. The bathroom stuff he talked about is exactly like mine, done it on myself a couple of times, learnt to only take fluids when a toilet is close
However, I learnt that the intensity of the symptoms depend on my emotions-Anger agitation flares symptoms up
sky1927 8 months ago
If you're interested in natural supplements which may improve your MS symptoms, you should research the study being conducted by hopetrials! You can receive a supplement which is currently being studied for it's effectiveness for MS symptoms.
MSHopeTrials 9 months ago
I'm a hypochondriac, and my latest scare is MS. I've thought that since my mind is so foggy, i have trouple with linear thought, my whole body shakes when I yawn or stretch, my extremities fall asleep easily that I had MS. I've been a pot head for 2 years now. I'm going to clear my mind up and see if it helps with all this anxiety I have. I also get the chills very easily when I'm nervous. Sometimes, wearing black, in the 80degree heat, I shiver. You're a good person, and I wish you luck with MS
leciasslave 9 months ago
So far I am only having the problems you describe with my legs. I was always able to walk around all day without even thinking about it ....and I am sure finding it hard to accept the idea that this is only going to get worse, I would sooner have a fixed disability like having lost a leg or something.
peterjol 9 months ago
hey man your video cleared up alot of stuff for me, im trying to put my mind at ease and the symptoms your having are alot harsher than the ones im having, im just having discomfort in my muscles from what i believe to be depression.
God bless
-WSP
WoodlandSurvivalPro 9 months ago
@WoodlandSurvivalPro God bless you too my friend :)
hmack2005 9 months ago
This might sound a little crazy but I just started using food grade hydrogen peroxide 35% it adds more oxygen to my blood stream it might help you as well
I have congestive heart failure my symtoms are the same as yours I take 2 drops into a bottle of water it does help with numbness and can breath better when i go to move around.I've been on this now for a month going shopping was a big problem I would have to stop and caught my breath every 3 minutes not anymore fred_bynum@yahoo.com
22y32g9 9 months ago
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This might sound a little crazy but I just started using food grade hydrogen peroxide 35% it adds more oxygen to my blood stream it might help you as well
I have congestive heart failure my symtoms are some what the same as yours I take 2 drops into a bottle of water it does help with numbness and can breath better when i go to move around.I've been on this now for a month going shopping was a big problem I would have to stop and caught my breath every 3 minutes not anymore fred_bynum@yahoo.com
22y32g9 9 months ago
This might sound a little crazy but I just started using food grade hydrogen peroxide 35% it adds more oxygen to my blood stream it might help you as well
I have congestive heart failure my symtoms are some what the same as yours I take 2 drops into a bottle of water it does help with numbness and can breath better when i go to move around.I've been on this now for a month.going shopping was a big problem I would have to stop and caught my breath every 3 minutes not anymore fred_bynum@yahoo.com
22y32g9 9 months ago
Thanks for this nice video i have the same symptoms you have ... but am a girl and what hurt me the most i can't wear high heels shoes which i was like too much .. i really wish to be your friend coz u know here in middle east ppl don't even know what ms and that hurts no one can understand your pain .. anyway thanks that was nice to accept MS with a big smile :D
aromauae 9 months ago
excellent vid. true soldier! im in limbo right now, its been a rough month
TheVillain365 10 months ago
Dude this sounds horrible. Your very strong! <3
TheLipstickhippie 10 months ago
sorry to hear that.... i am going to pray for you.... god bless
ladycateyes 10 months ago
My symptoms are very similar as well! I was formally dignosed 02-07-2011. One day I'll have to get a camera and make a video, too! Thank you for yours!
mark13728 10 months ago
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CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Gregmills007 10 months ago
This is one of the most saddest videos on youtube. I pray for you. Greetings from Denmark
Learncountriescom 10 months ago
I can relate... I've had most of the symptoms you are talking about. My first serious attack scared the hell out of me. I had double vision and I couldn't walk without stumbling around. This was before I was diagnosed with MS so I didn't know what was going on. I have also had the numbness on both sides of my body from head to toe twice. Been on avonex 7 months now, and so far I haven't had any attacks so I hope this continues to work for me.
gbugss 10 months ago
@gbugss That's good to hear my friend. I'm happy avonex is working for you
hmack2005 10 months ago
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If you’re diagnosed with Multiple Sclerosis, cheer up because the cure for MS is already discovered, and it’s called “CCSVI,” or “The Liberation Treatment!” This cure was discovered by “Dr. Zamboni!” You can search this here on You Tube. Just search: “CCSVI,” and/or “The Liberation Treatment,” and/or “Doctor Zamboni!” You can also log on Facebook and check”CCSVI in Multiple Sclerosis!” Feel better!
MSpinalcord 10 months ago
This has been flagged as spam show
If you’re diagnosed with Multiple Sclerosis, cheer up because the cure for MS is already discovered, and it’s called “CCSVI,” or “The Liberation Treatment!” This cure was discovered by “Dr. Zamboni!” You can search this here on You Tube. Just search: “CCSVI,” and/or “The Liberation Treatment,” and/or “Doctor Zamboni!” You can also log on Facebook and check”CCSVI in Multiple Sclerosis!” Feel better!
MSpinalcord 10 months ago
HEY YOU SHOULD DEFINITELY CHECK OUT DR SEBI, P.S. LISTEN
peacenlove2810 11 months ago
@peacenlove2810 I will thanks :)
hmack2005 10 months ago
Thank you for sharing. I especially like you saying "MS career", I'll use that. What helps me a lot is taking high doses of Omega 3 supplements and Magnesium for my restless muscles. I've had embarrasments too, not a pretty sight but, as long as I offload in the mornings, the day is OK. Peace and love.
RaeleneMcDual 11 months ago
@RaeleneMcDual No problem. I will try upin' my dosages on the Mag and Omega 3 Thanks
hmack2005 10 months ago
Great video. It's helpful to hear someone with similar symptoms. God bless you dear. You are still handsome though! :)
SkyBlue1031 11 months ago
Invaluable information. I don't have this but I don't take anything for granted. I never have. Thanks to my mother.
Khultan 11 months ago
Thank you so much for sharing your experience. Your kindness and love helped me so much when I was being diagnosed!
emconner1 11 months ago
@emconner1 I'm happy that I was able to help ya a bit :)
hmack2005 10 months ago
check out dr nemeh he is a healer he is a man of god. love april
AWDESIGNS8 11 months ago
@AWDESIGNS8 thank you so much i will check him out.
hmack2005 11 months ago
Look at it another way, MS will be sad it caught a dose with you ;-)
TheSpankymonkey 1 year ago 6
@TheSpankymonkey true true :)
hmack2005 1 year ago
I love your videos! You are an excellent public speaker and I enjoy hearing about MS symptoms from you. Having MS sucks for us all. Stay strong and beautiful!
dswenson1411 1 year ago 5
@dswenson1411 thank you. I'm smiling right now :)
hmack2005 1 year ago
I've had ms for 10 years, great new product MS cooling shirt.
fros-t cooling.com
justbran12 1 year ago
I agree you are a lovely looking man. I was diagnosed in 87 and know what you are going through. Keep strong and show the world that MS has made the wonderful person that you are.
parrotchops 1 year ago
@parrotchops Thank you for your kind words
hmack2005 1 year ago
This is a great video, and says alot about the symptoms I have. I hate it!
dedeyemaxx 1 year ago
Look up neurovax. It stopped the progression of MS entered phase II clinical trials and then the company that was going to produce it went bankrupt. This drug needs to be approved.
guitarobsessed85 1 year ago
@guitarobsessed85 thank you for sharing this info
hmack2005 1 year ago
@hmack2005 You're welcome. You seem like a very kind person and I enjoy your videos. I hope that vaccine gets picked up by another company and gets approved or the company gets the funding it needs. People as kind as you need to be cured now. Let those who choose to follow בעל זבוב have this suffering . I'm a great believer in יְהֹוָה and I believe if his servants ask and truly serve then he will heal them and not allow בעל זבוב to harm his servants.
guitarobsessed85 1 year ago
Thanks for sharing. I am studying to be a doctor and your descriptions have greatly helped my understanding. I'll be better able to provide advice in the future as a consequence. All the best. J
jdoc1350 1 year ago
wana say,for the past 5 years ive had numbness in my face and tingling in my arms,neck,hands and my doctor put it down to panic attacks.ive had a MRI 3years ago which was clear,now I have painfull joints,now I have confusion and weakness in my body also tremor in my left thumb and hand,what im trying to say im sick of prople saying that its all in my mind. I know my body,and somthings wrong,I wish someone could help me. What do I do? Please help me find an answer!
tonyurmate 1 year ago
@tonyurmate Hey my friend please check out Noel Batten and CCSVI videos on youtube. Please shoot me an email if you have any questions.
hmack2005 1 year ago
@tonyurmate Sounds like benign fasciculation syndrome, but with the painful joints it sounds more like fibromyalgia. Neither of which would show on an MRI, though benign fasciculation syndrome could show up on an EKG. You should see if they'll do a nerve conduction test. If it comes back that you don't have anything and your Rheumatoid Factor is low, yet you still have these symptoms, you could have a strong case for fibromyalgia. On the other hand a diagnosis of fibromyalgia is hard to get.
guitarobsessed85 1 year ago
@guitarobsessed85 Thank you for your comment,I still get tingling in hands,arms legs and back and joint pain,it can last up to two weeks to a month,it always goes away for mabey a month or so but comes back.
my doctor puts it down to stress and i have suffered with panic attacks also since I was 7years old,I also suffered with very bad growing pains in my teens,with hip back and knee pain.
Ive just been diagnosed with arthritis in both hips,im now 38.
i have had rumatic fever when I was 26.
tonyurmate 1 year ago
@tonyurmate Your joint pain could be caused by migratory arthralgias due to your prior infection. Panic attacks can cause parasthesias like tingling and numbness, but so can benign fasciculation syndrome. I you have extreme fatigue and stabbing sensations you probably have fibromyalgia.
guitarobsessed85 1 year ago
@tonyurmate You have my sympathy. I know how horrible it is to be told this crap by doctors and so called experts. All the unessesary vaccines, food additives and fluoride in drinking water etc over many decades has a lot to do with why so many people are going down with MS, ME, Lupus and many other mystery diseases.
I have MS, the 5th in my family and sometimes it does not show up. There is never enough helpful information. Don't let them fob you off, of course you know your own body!
parrotchops 1 year ago
after 4 years of tingly feet, i just had my first mri which showed 5 3mm lesions on my brain. family dr gave me the news on friday and i'm going to call my neuro tomorrow. any advice? thanks for the video . . . :) (other symptoms: i'm a marathoner (did 5 this year, including a personal best!) and when i run with some slower friends, i've tripped.)
wendymyers 1 year ago
@wendymyers See what your neuro says and see if you suffer from CCSVI
hmack2005 1 year ago
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Asian beauties are waiting for you "busizz4me.info"
kzkleyoile 1 year ago
My mother has all of the symptoms of MS but she hasn't been diagnosed with it because her MRI scans always come up negative (she doesn't have the damaged myeline sheath or nerve cells) But I was curious to ask a question if you don't mind. How often does your face go numb and what side of the face?
counting100sheep 1 year ago
My mother has Symptoms of MS but she hasn't been diagnosed because her MRI scans always come back negative (she doesn't have the damaged myelin sheeth)
However, i'm very curious if you don't mind me asking about the numbness in your face, How often does it happen and what side of your face the right or the left?
counting100sheep 1 year ago
@counting100sheep I've had no numbness on my face my friend
hmack2005 1 year ago
@hmack2005 , thank you for what you are doing, you gorgeous my brother, I see the ring, are u hooked up? otherwise I would say hook a sister up!
miobing 1 year ago
@miobing married but thank you for the compliment ;)
hmack2005 1 year ago
@realityword I think CCSVI is great. I think all MSers should get checked for it. I found out that my left jugular is 90% blocked and my right is 50% blocked. So I'm getting the procedure done down in San Diego next week :)
hmack2005 1 year ago
Hmack, are you on meds. Has it helped??
wisdaniel 1 year ago
@wisdaniel No meds my friend. I did rebif for 2 years. And for the last 2 years I've been med free. I've been doing everything all natural. The meds didn't help me.
hmack2005 1 year ago
ye had all them syptoms except the bladder problems the writting one really sucks but also had the pain that you didn't. hope your not having too much of a problem at the moment
johnnyd101 1 year ago
@johnnyd101 I've made really great improvements since I made this video. I'm not 100% but better than I was...thank GOD. Lookin into CCSVI. I found out that my left jugular is 90% blocked and my right is 50% blocked. I'll keep everyone posted :)
hmack2005 1 year ago
Feel you dude! MS sucks tail pipe. So true on the restroom comments. Big ups bro, Thanks!
nyc0053 1 year ago
Partial Facial numbness that lasted a few days and back numbness that lasted a few mins. Shooting warm feelings in legs. I always had vibrations in my legs and thought it was normal. Never really had any vision issues except photosenstivity (can this be optic neuritis? Or does it always impair color vision?) This is over the course of two weeks. Numbness is gone in my face but I'm still getting hot sensations in my legs. Are these symptoms of MS or are they too mild?
guitarobsessed85 1 year ago
@guitarobsessed85 I have two relatives with ms. I went running the other day and my whole shoulder went numb along with my face. The shoulder numbness only lasted a few minutes but the facial numbness lasted 3 days. My legs twitch a lot. I experience no weakness or ataxia. Do symptoms tend to be more mild in the beginning of MS or does it usually hit strong? And are there always vision issues? I'm freaking out right now. I have no health insurance.
guitarobsessed85 1 year ago
@guitarobsessed85 unfortunately my friend evryones symptoms vary so much I don't know if I could lable it MS. My suggestion would be to go to your doctor or free clinic and let them know what's going on. Try not to panic. You can beat whatever is going on. Stay strong my friend.
hmack2005 1 year ago
@hmack2005 Thank you. I will be going to the doctor as soon as I have health insurance which is in two weeks. I hope they find a cure for this disease. I'm a biologist of all things haha. I will hopefully not have the disease and be able to get into research for a cure. I hope that you go into permanent remission.
guitarobsessed85 1 year ago
@hmack2005 I definitely understand the bathroom issues. The staggering and numbness on my tongue. Eating sucks. I liked your video thanks.
KARI422 1 year ago
For all, here is my story with MS and my CURE of it taking the black seed oil.
it is true, and many of people that had followed me find good results, read it please;
seedoil.net/vb/showthread.php?p=2135#post2135
saadfakhoury 1 year ago
@saadfakhoury i take black seed in a pill its for imflamation and that is what ms is .
AWDESIGNS8 1 year ago
Please look into CCSVI..
omexmc80 1 year ago
@omexmc80 Thank you very much. I will do that asap
hmack2005 1 year ago
Thanks for posting this, it's important to let people know some of the things we go through. It's also good just to talk about it. I have only had "accidents" in or near my house, thank goodness. But I still map the bathrooms when I'm out.
kodybryson 1 year ago
Mi Bro has dat he knows how you feel he is only 15 i don't know how it feel but I know where your coming from.
ekechii 1 year ago
@ekechii Thanks my friend. Let your little bro know he can reach ou to me if he has any questions about this stuff.
hmack2005 1 year ago
Mi Bro has dat he knows how you feel he is only soo i don't know how it feel but I know where you coming from
ekechii 1 year ago
Do U drink coffee ? If yes, how much ??
maciejwrotek 1 year ago
@maciejwrotek no coffee my friend
hmack2005 1 year ago
@hmack2005 What about other caffeinated beverages like tea. And what about alcohol ?
maciejwrotek 1 year ago
@maciejwrotek I don't drink any of that stuff why do you ask?
hmack2005 1 year ago
@hmack2005 well i had found an interesting approach and some ppl report success with MS, it is called watercure (hydration therapy) , address is watercure2 D()t org, check out their testimonials. Caffeine and ethanol are diuretics.
maciejwrotek 1 year ago
@hmack2005 heard about it?
maciejwrotek 1 year ago
@maciejwrotek I knew nothin about it. But I thank you sooooooo much for sharin' this info.
hmack2005 1 year ago
@hmack2005 No problem. If U dont drink caffeine and alcohol, there is only one thing left to ask. What do U drink generally and what is Your water and salt consumption daily ?
maciejwrotek 1 year ago
@hmack2005 So, what do u drink on daily basis ?
maciejwrotek 1 year ago
I just found out I have MS a few weeks ago.... just now getting brave enough to look at stuff online, I was worried that I would see people all fukrd up and one day I'm gonna look like them........... it hasn't really been like that tho, thank God.
Thanks for sharing yourself, if you get a chance, I'd love to chat with you more.
You can message me here but yahoo is better, they block youtube at work...lol
leigh_massengill@Yahoo.com you can look me up on myspace or facebook too
take care!
leighsknees 1 year ago
@leighsknees Hey... I just sent you a message :0)
hmack2005 1 year ago
u r so honest....I too have MS.Mine has been alot like urs plus a little more.Noone understands what we are going thru because we look healthy.
Thanks for sharing.I AM NOT CRAZEE!it all happened to me from the legs to the bathroom issues.
mro1010 1 year ago
@mro1010 no problem just here to help :0)
hmack2005 1 year ago
have you checked out the paleo diet to relieve your symptoms? i have an auto immune condition called ulcerative colitis and thats greatly helped me. the science of it all makes so much sense.
wordey123 1 year ago
@wordey123 No but I will check it out ASAP Thanks
hmack2005 1 year ago
@hmack2005 Send me a message if you actually try the diet and post a couple vids about starting it and the effects a few months later.
wordey123 1 year ago
i love the video i have ms for 10 years i am a comedian for 10 years an tour around the world with ms thanks for the video.
illwillcomedy 1 year ago
Its no prob bro, Just stay strong and never lose faith
tidusgang123 1 year ago
Im really sorry man, I dident even know what ms was untill and hour ago maby. I honestly hope there might be a cure in our lifetime. Just dont let it beat you man please. I cant say i feel for you cause i dont know what its like man but after watching this i care for ya like a brother man I hope you get through it all you will be in my prayers
tidusgang123 1 year ago
@tidusgang123 Hey brah thank you for the kind words. Please dont be sorry cuz everything happens for a reason. What doesn't kill me will only make me stronger and I my strong mf. Many blessings and much success :0)
hmack2005 1 year ago
wow , thanx bro helped me allot!
Americajuana 1 year ago
@Americajuana No problem my friend. Thats why Im here
hmack2005 1 year ago
I don't have MS but I know what it is like to loose the ability to walk. My legs felt like they were on fire for two days and then all of a sudden they stopped working, but I can still feel. I am sorry you have it. It is horrible. To this day the doctor's don't know what I have.
lovemybones88 1 year ago
@lovemybones88 thank you for sharin'
hmack2005 1 year ago
thanks for sharing
kizu00 1 year ago
@kizu00 No problem. I just wanna let others know that they're not alone
hmack2005 1 year ago
Man I hear you brotha
amarcelous 1 year ago
@amarcelous Thanks for checkin out my video :0)
hmack2005 1 year ago
@amarcelous LOL LOL
hmack2005 1 year ago
I have a question for anyone that can answer... I dont really think I have MS but was wondering if this means anything... My hands dont always want to work. i have a hard time doing tedious tasks for longer than just a few seconds. they tire quickly and i drop things just out of the blue, for no reason. Its irritating to me and i want to know why... if anyone could help
MyBaby91307 1 year ago
@MyBaby91307 hi, I don't think the internet is the best place for an answer on this but here's my opinion, what you describe COULD be normal, depending on how often it happens and what the activity is.OR it could be an indicator of somethingg else, I don't want to worry you but I think you should get this checked out by your doctor/a neurologist as it is not normal for hands to drop things and not work, especially if it is after a few seconds. Get it checked out, if only to put your mind at ease
alexaria 1 year ago
"what's wrong with that cat" thank you for sharing this info., you're pretty funny too
wowoak 1 year ago
HAHAHA
danecolless 1 year ago
so many symptoms, so much shit. life is good though. gotta love life.
onojmai 1 year ago
thanks for sharing!
Zebatshi 1 year ago
thanks for sharing
sdibaja 1 year ago