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
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
so many years of research and doctors still cant find a cure for autoimmune diseases..makes you lose faith in medicine all in all...of course conventional medicine doesnt have any drugs that are curative..no wonder everyone suffering from autoimmune diseases seeks alternative treatments
I find the claims that anti depressants (im thinking SSRIs and MAOIs) are suitable quite dubious given that there is a rumour of theyre presenting nervous damage. Depression can be treated without anti depressants for fuck sake. There are so many meds out there which are so much safer than the current anti D pharmocopeia
May I add: because of this out-of-conscious-control emotional state, the anger is not taken out "properly", the eyes (yes the eyes) sort of get "blocked". The area around the eyes (basically the whole face) is powerful... Keep in mind that through the eyes energy runs through, in a healthy system. Like a gate. If the eyes "close", the emotion gets blocked within the body. I'm not implying that this is definitely MS, but it's actually something a lot similar. (personal experience)
"certain viruses in temperate climates"!? have i understood right?!! Why do you put it down as a virus!? ....i think it's a heavily emotional issue, because the physiology of the human body is such that it's like a perfect network... and there are specific acupressure points on parts of the body, and the front of the skull is the part of emotion.. i think if emotion is badly handled, with intense anger, then it causes similar problems. The plaques she mentioned, i know that are caused by this.
@gliksmar we met on facebook rResearching CCSVI and the liberation last June we fell in love on skype and were married in Aug 2010 in Toronto she is from Serbia I am from the UK
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
High Saturated Fat diet -> young age (active thymus) -> exposure to herpesviridea or other neurovirus -> high permeability of BBB caused by poor, brittle structure from high saturated fat diet, low levels of vitamin D -> T cells in CNS -> sensitization of T Cells -> later onset of MS -> recovery -> anything that can cause a proper situation for episodes (stress, Epstein Barr, etc.) -> disability
I think this video is the most informative thing I've seen so far.
I have done a lot of research and still feel I learnt a bit more about MS
I still can't quite get my head around how the medical profession and drug companies have measured the success of the treatments. They say "no two cases of MS are the same". So how can (for instance) pumping Glatiramer acetate into your body everyday show any indication to how successful it is in slowing down the progression of MS?
I think this video is the most informative thing I've seen so far.
I have done a lot of research and still feel I learnt a bit more about MS
I still can't quite get my head around how the medical profession and drug companies have measured the success of the treatments. They say "no two cases of MS are the same". So how can (for instance) pumping Glatiramer acetate into your body everyday show any indication to how successful it is in slowing down the progression of MS?
Wow. What an irresponsibly dispiriting first 90 seconds. Turned it off after that. I was diagnosed this week, and whilst I realise there will be challenges, this video starts off with the wrong message to those who don't understand the disease. Instant fear mongering put me off what I hope for others was an ultimately uplifting film.
If you want more information on the benefits of Protandim for people with MS, please just let me know. I'm happy to send you the link to the clinical trial / peer review.
I am Liberated and so is my Wife I have practically no Ms symptoms left after 15 years of it and my wife is much better even thought she has been in a wheel chair for 10 years look up CCSVI Liberation
Low Dose Naltrexone (org) raises endorphin levels affecting the immune system, in this case reducing the hyper-immune response. It is harmless and almost free of side effects. In private practice the results have been incredible for the last 20 years. Many Dr.'s are willing to prescribe LDN. I have used it for 5 years without a return of exacerbations.
Have you heard about the MS research study examining benefits of apoaequorin for those living with MS? You receive apoaequorin, a supplement that may help symptoms of MS, and fill out a monthly survey tracking improvement. It's being done by "HOPE Trials" and you can now volunteer to support MS research and may see real improvement of your MS symptoms!
@gigiontube your an idiot if there was a cure everybody with ms would get it.did you ever think you are in remission because of the nutrition your taking?get all the tests again i bet you still have it asshole
The idiot is you for calling me an idiot when all what I did was to provide you with critical information. if you believe that the doctors are looking for a cure, think again. They don't want you to know anything about nutrition. Is not how they make they money and their comfy living. It's NOT what AMA wants.
I sent a link to a real doctor who recovered from MS.
If you are smart enough, you should go and check it out. If not, die like an idiot; it's what stupid people deserve.
someone with MS could sail a kwikat without much trouble at all...i let a 79 years old man go for a sail yesterday in punta banda. easier than walking, really.
My Mom has M.S. and She's had it since I was 10 , I'm 32 now . She's been progressing ever since, now she's in a wheel chair since the past year. I wish all of you the best. I totally understand what you go through. And I fear one day I will be diagnosed with it as well.
My husband is suffering from Multiple Sclerosis and back sugeries. We are in need of donations to cover medical debt. Please if you can find it in your hearts to donate or simply spread our website around it would mean the world to us and our family. We are accepting donations at medicalbillsdebtdonationsms.weebly.com Thank You and God Bless we need a miracle!
My husband is suffering from Multiple Sclerosis and back sugeries. We are in need of donations to cover medical debt. Please if you can find it in your hearts to donate or simply spread our website around it would mean the world to us and our family. We are accepting donations at medicalbillsdebtdonationsms.weebly.com Thank You and God Bless we need a miracle!
My husband is suffering from Multiple Sclerosis and back sugeries. We are in need of donations to cover medical debt. Please if you can find it in your hearts to donate or simply spread our website around it would mean the world to us and our family. We are accepting donations at medicalbillsdebtdonationsms.weebly.com Thank You and God Bless we need a miracle!
Thanks for uploading this excellent video. very well done. I have had MS for six years. On some days it kicks my bum, but on a lot of days, I kick IT's bum.
Had a neighbor with MS who went through SCC International (407) 610-4248 who coordinated a medical evaluation by an Asian doctor. They had to travel to an overseas treatment center, but their condition totally REVERSED. it was incredible.
I was diagnosed with MS in '04 and in 4 years I took all the different medications to try to stop the progression with no success. In '08 I had stem cell treatment that worked amazingly well in my case. iLoveMyNewStemCells
Hi all, I haven't post any comment since a long time. But reading my previous posts by people, taking the same natural ingredient I have took to fight MS (Black Seed Oil) and thanking me a lot for the mysterious results they have found, encourages me to repost about my try.
As a sum, I was infected by MS and by chance I've tried to take the Black Seed Oil and it has done fantastic results with me. I CANT ADMIT my try to be a cure of MS, but I think that;1-getting rid of all the remains of MS 2-providing me with power to continue my life 3-MRI tests proving the stop of demyelation 4-living free of MS attack since I took the black seed oil from 7 years! 5-benefits of many people that have read my posts and took the Black Seed Oil SHOULD BE TAKEN INTO CONSIDERATION.
If u thing that 1-my intention is to market for BSO (coasting 6 usd / month) 2-my intend is to be famous even by stating my name with such a diseaseDon't respond to my post
If you would like to have a chance for my try respond to me with a message a even add me on MSN to help you thoroughly; saad_fakhoury@hotmail
Exercise and take vitamin D3 10'000iu per day vitamin B12 1000 iu per day (for balance) Magnisium citrate 1-200 mg a day , I've had MS for 15 years Ive walked 10 miles in the last 4 days no fatigue no brain fog and no systems after I started doing the above. I dont want anything off you just try it! and God bless :) look at my vids over the last year for proof
I'm waiting to see a neurologist next week. Apparently my MRI results showed some type of disease process. I've had quite a few weird symptoms which seem to fit MS. I'm a bit worried. How do I find out for sure if it is or isn't MS?
An MRI will show periventricular lesions. They will take some CSF from you via a lumbar puncture. The pathologist will be looking for oligonal bands and mononuclear cells.
Also you would get a lot of symptoms that are not explained by the presence of one lesion in the brain. This because MS can attack any sensory or motor pathway in the CNS while leaving the others unaffected. It can even damage the cerebellar which reproduces many of the symptoms of being drunk, the only difference is they don't go away in the morning when you start to sober up.
neurological diseases are the worst. out of all of them, Huntington's has to be the absolute worst. Parkinson's, Lou gehrigs, multiple sclerosis, Alzheimer's. i think we have so much potential to cure these horrible things as people its ridiculous. im sad that these things still exist. =[
I dunno if i have ms or not but I was told in 03 i had a stroke. in the brain stream but for 2 years before this the same time of year i had numbniss weakniss on the left side i was healthy until 2 months ago but now its on my right side but just numb not tingly. I always have some troubles with eye sight seeing headlights street lamps seeing streaks and also after images, Medical insurance is pending so hard for me to get tests any info?
Stroke is usually pretty easy to pick up on an MRI scan. The radiological presentation is very distinctive and an MRI is accurate enough to hone in on the smallest of lesions. You might have had another stroke afterwards. Not all strokes are apparent with obvious motor and sensory signs. Your sight problems could be explained by a stroke in the brain stem. Have they done a lumbar puncture yet for oligonal cells and mononuclear cells in the CSF?
for all MS patients, Id like to mention an important fact; I was infected with MS from around 8 years and got rid from all my permanent disabilities and stopped the demeylation by taking the BLACK SEED OIL.
IFFFFF ud like you know more about my state, write to me.
my mom has had MS and bipolar disorder my entire life. I hate my life. she has no correct judgement. my childhood has been taken away from me because of this god forsaken disiese. If my dad were alive everything would be better
i have to agree with AletheReneW . MS has you . she's right everyday is different. what is LDN . i use Copaxone and steroids once every two months. i'm not the same person w/ the steroids. i'm not the same person i used to be lol . someone out there please reply. i feel so alone. surrounded by family yet so alone.
i am waiting to find out if I have ms. This is Thurs. and my appointment is on Tues.
I'm very nervous. I have had a MRI, MRA, a Spinal Tap, blood work, and a bunch of other stuff. This video is has been very helpful. I hope that I don't have ms, but with research and videos like this I belive I am ready.
F150FORDMAN01...Im also going to get MRI's tomorrow 12/01. I have lost my family. My husband has left me for another woman(he says they are just "friends"), and my daughter is looking to her as a mother and loves to send word back through her friends that she goes to movies and just whatever with this woman. They love to go on topix and make fun of me, they make fun of the way I dress, etc. Im about as sad as sad can get. They hate me for something I cant help or change.
Maybe it has something to do with malfunction of the glial cells. glial cells nourishes the neurons. Maybe the virus kills off the glial cell so that affects the neuron's myelin shelth.
MY dad has ms and i am only 14 my mom works 3/4 of the day and he cant do anything, he has ms for over 3 years. If u have any idea how hard it is plz pray for everyone with MS u guys.
I have twitcing all over my body since nov 08, as well as tingling in my soles, as wellas fingertips, have been to my GP who did a physical nuero exam and said i dont have MS, unconvinced I asked for nuros opinion who did a nuro exam in April this year and again said you are fine, these sypmtoms have been constant I mean the twitching, burning sensation and tingling. its pretty sad i dont get a diagnoses and ben in limbo land.
Instead of searching for a diagnosis to "label" yourself, look at ways to improve these feelings you are getting. People get too caught up in diagnosis's but everyone is different so you should just focus on the symptoms and try to treat them.
dx'd 2000. good luck to everyone! MS is no joyride... keep pushing and be productive! work out the ultimate muscle: the brain! and live with dignity...
Hello everyone. I'm a 20 year old male and im unsure of whether i have this disease. I remember the Doctor in the video talked about how location of your first 15 years of life can have an affect on whether you have the disease or not. I was born in Vancouver, BC and moved to Calgary AB when i was 12. My possible symptoms for now seem to be urinary irrgularity some days, math seems to be a real challenge, a bit of long/short term memory issues. No one in my family has MS.Please share some advice
LYME disease is known as the " GREAT IMITATOR." Within the Lyme community, patients have been diagnosed with MS, ALS, ADHD, CFS, and the list goes on and on. Lyme disease for the most part is a treatable disease. Would be happy to email anyone a Lyme disease brochure.... Elaine in VA
This was well done and pretty informative for those who don't have MS. I was diagnosed 3 years ago and do daily shots of Copaxone along with other meds for symptom management. The only thing that annoys me and many of my fellow MS'ers is the statement " I have MS, MS doesn't have me". This is bull, MS has you whether you admit it or not. When every decision you make on a daily basis is determined on how your MS is affecting you today, it has you. Just a pet peeve for a lot of us.
Until there is a cure there is LDN. Please everyone should look into LDN for MS. It has been a miracle for my husband. He has been on it for 4 years now. I can send anyone his full story if you send me an e-mail. Or you cna look up LDN and MS on the internet. This drug is cheap, has minimal side effects and most people report no progression in their MS. Please look into it!
hi. i'm studyin this illness at university, and i'm interested in this ldn-low dose naltrexone-. could you please tell me more about it or caould you tell me some website where to find info? my books don't say almost anything about ms therapies...thx a lot.
I was diagnosed 2 weeks ago. I live in San Diego, too. This was very informative and I even forwarded this to my loved ones to share the information and perspectives with them. Thank you so much for this video.
@CaliCousin it is all out of date she knows nothing I have had MS for 15 years and live a normal life! Because of what I learnt and because I am Liberated
This video was extremely well-made in many aspects.I wanted to know what my client/friend goes through on a daily basis.I wish there were videos this good for all types of illnesses.400000 is like 1 in every 750 people in US which is a big number.
Old MSers KNOW ALL THAT1 because we LIVE that every second of our lives. Perhapsit might help other understand but if you have over 30 year of MS u sort of know every manifestation andalso KNOS THERE IS NO CURE!
Hi Luis, My husband Paul grew up near you in Palisades Park. His parents now live in Saddle Brook. Paul and one of his sisters have MS. She still lives back there. Paul and I live in Calif. You are right there is no cure, but Paul has reversed all of his symptoms with LDN, diet, exercise and suppliments. I know LDN has heled thousands of others. It does not promis to reverse symptoms, but 85% of people report lack of progression in their MS. That is huge. If you want info just let me know.Aletha
Thank you for uploading! I got diagnosed with MS a year ago but cant really believe that its true. Unfortunately it is.
And I am the typical 'victim' of it: woman, 30 years, blinded on my rigtht eye, and from Europe.
Life's a bitch...
anjajune 3 months 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 3 months ago
19:38 You were working 20 hours a day? What?
tackcatta 3 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
Ekorn999 4 months ago
Very good informations! (^_^)
dennychoi 4 months ago
spinal cord IS part of the central nervous system, Dr. 3:30
ramiarabas 6 months ago
I believe I have MS, but I have yet to get it diagnosed! I have like every symptoms though!
atvchick09 7 months ago
This has been flagged as spam show
so many years of research and doctors still cant find a cure for autoimmune diseases..makes you lose faith in medicine all in all...of course conventional medicine doesnt have any drugs that are curative..no wonder everyone suffering from autoimmune diseases seeks alternative treatments
wreyoG 7 months ago
I find the claims that anti depressants (im thinking SSRIs and MAOIs) are suitable quite dubious given that there is a rumour of theyre presenting nervous damage. Depression can be treated without anti depressants for fuck sake. There are so many meds out there which are so much safer than the current anti D pharmocopeia
ElectraOnAzaleaPath 7 months ago
@ElectraOnAzaleaPath so true
wreyoG 7 months ago
Comment removed
ElectraOnAzaleaPath 7 months ago
May I add: because of this out-of-conscious-control emotional state, the anger is not taken out "properly", the eyes (yes the eyes) sort of get "blocked". The area around the eyes (basically the whole face) is powerful... Keep in mind that through the eyes energy runs through, in a healthy system. Like a gate. If the eyes "close", the emotion gets blocked within the body. I'm not implying that this is definitely MS, but it's actually something a lot similar. (personal experience)
pansagittarius 8 months ago
"certain viruses in temperate climates"!? have i understood right?!! Why do you put it down as a virus!? ....i think it's a heavily emotional issue, because the physiology of the human body is such that it's like a perfect network... and there are specific acupressure points on parts of the body, and the front of the skull is the part of emotion.. i think if emotion is badly handled, with intense anger, then it causes similar problems. The plaques she mentioned, i know that are caused by this.
pansagittarius 8 months ago
She has a lovely mullet and wide set eyes. She may be related to Billy Ray. But she is recommending drugs that she doesn't understand. Beware.
WoundedEgo 9 months ago
@gliksmar we met on facebook rResearching CCSVI and the liberation last June we fell in love on skype and were married in Aug 2010 in Toronto she is from Serbia I am from the UK
gekiryudojo 10 months ago
This has been flagged as spam show
Avoid any Mercury intake, eliminate Mercury from your body and get well.
perryhtc 10 months ago
Avoid any Mercury intake, eliminate Mercury from your body and get well.
perryhtc 10 months ago
This has been flagged as spam show
Why people suffering Multiple Sclerosis?
The answer is " Chronic Mercury Poisoning".
Mercury is a neural-toxic heavy metal ! and it is the second most toxic thing in the world.
Dental Amalgam have 50% Mercury. Too many vaccine using Thimerosal (A Mercury compound) as a preservative.
perryhtc 10 months ago
this neurologist clearly has problems with CNS!Al that she said about MS and that is apsolutly nothing is allredy well known.CCSVI bitch:)
buysomeremzbitch 11 months ago
very imformitive
AcostaFernandoA 11 months ago
This has been flagged as spam show
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 11 months ago
High Saturated Fat diet -> young age (active thymus) -> exposure to herpesviridea or other neurovirus -> high permeability of BBB caused by poor, brittle structure from high saturated fat diet, low levels of vitamin D -> T cells in CNS -> sensitization of T Cells -> later onset of MS -> recovery -> anything that can cause a proper situation for episodes (stress, Epstein Barr, etc.) -> disability
seekirk 1 year ago
I think this video is the most informative thing I've seen so far.
I have done a lot of research and still feel I learnt a bit more about MS
I still can't quite get my head around how the medical profession and drug companies have measured the success of the treatments. They say "no two cases of MS are the same". So how can (for instance) pumping Glatiramer acetate into your body everyday show any indication to how successful it is in slowing down the progression of MS?
It's all a bit vague.
mrbsred 1 year ago
This has been flagged as spam show
I think this video is the most informative thing I've seen so far.
I have done a lot of research and still feel I learnt a bit more about MS
I still can't quite get my head around how the medical profession and drug companies have measured the success of the treatments. They say "no two cases of MS are the same". So how can (for instance) pumping Glatiramer acetate into your body everyday show any indication to how successful it is in slowing down the progression of MS?
It all a bit vague.
.
mrbsred 1 year ago
Comment removed
mrbsred 1 year ago
Wow. What an irresponsibly dispiriting first 90 seconds. Turned it off after that. I was diagnosed this week, and whilst I realise there will be challenges, this video starts off with the wrong message to those who don't understand the disease. Instant fear mongering put me off what I hope for others was an ultimately uplifting film.
shamelesshussy 1 year ago
If you want more information on the benefits of Protandim for people with MS, please just let me know. I'm happy to send you the link to the clinical trial / peer review.
ProtandimDistributor 1 year ago
what's all this talk I keep hearing about multiple scrotums? why is that such a bad thing?
personally, I wouldnt mind having and extra 2 scrotums, you know, in case I ripped my ballbag open while I was masturbating with sandpaper.
i like fast cars.
vampurile 1 year ago
@gliksmar your right I have been on it for 7 months and so has my wife
gekiryudojo 1 year ago
I am Liberated and so is my Wife I have practically no Ms symptoms left after 15 years of it and my wife is much better even thought she has been in a wheel chair for 10 years look up CCSVI Liberation
gekiryudojo 1 year ago
This has been flagged as spam show
Low Dose Naltrexone (org) raises endorphin levels affecting the immune system, in this case reducing the hyper-immune response. It is harmless and almost free of side effects. In private practice the results have been incredible for the last 20 years. Many Dr.'s are willing to prescribe LDN. I have used it for 5 years without a return of exacerbations.
savingbeauty 1 year ago
Comment removed
savingbeauty 1 year ago
XMRV XMRV XMRV XMRV
omv08 1 year ago
I can't believe some assholes DARE posting spam to "cures"
knuckleisgodlike 1 year ago
This has been flagged as spam show
Have you heard about the MS research study examining benefits of apoaequorin for those living with MS? You receive apoaequorin, a supplement that may help symptoms of MS, and fill out a monthly survey tracking improvement. It's being done by "HOPE Trials" and you can now volunteer to support MS research and may see real improvement of your MS symptoms!
MSHopeTrials 1 year ago
Multiple Sclerosis is CURABLE.
Please go and see this doctor who is recovering herself from MS through nutrition and electrical stimulation.
YES.... it is SO SIMPLE! NUTRITION PEOPLE, NUTRITION !
[take the spaces out from the link below of course]
h t t p : / / w w w . t e r r y w a h l s . o r g /
Good luck and good health to all.
gigiontube 1 year ago
@gigiontube your an idiot if there was a cure everybody with ms would get it.did you ever think you are in remission because of the nutrition your taking?get all the tests again i bet you still have it asshole
jessie472 1 year ago
@jessie472
The idiot is you for calling me an idiot when all what I did was to provide you with critical information. if you believe that the doctors are looking for a cure, think again. They don't want you to know anything about nutrition. Is not how they make they money and their comfy living. It's NOT what AMA wants.
I sent a link to a real doctor who recovered from MS.
If you are smart enough, you should go and check it out. If not, die like an idiot; it's what stupid people deserve.
gigiontube 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
someone with MS could sail a kwikat without much trouble at all...i let a 79 years old man go for a sail yesterday in punta banda. easier than walking, really.
bvrcrap56 1 year ago
My Mom has M.S. and She's had it since I was 10 , I'm 32 now . She's been progressing ever since, now she's in a wheel chair since the past year. I wish all of you the best. I totally understand what you go through. And I fear one day I will be diagnosed with it as well.
MeanMissC 1 year ago
This has been flagged as spam show
MedicalBillsDebtDonationsMS.weebly.com
My husband is suffering from Multiple Sclerosis and back sugeries. We are in need of donations to cover medical debt. Please if you can find it in your hearts to donate or simply spread our website around it would mean the world to us and our family. We are accepting donations at medicalbillsdebtdonationsms.weebly.com Thank You and God Bless we need a miracle!
DonatePleaseMS 1 year ago
This has been flagged as spam show
MedicalBillsDebtDonationsMS.weebly.com
My husband is suffering from Multiple Sclerosis and back sugeries. We are in need of donations to cover medical debt. Please if you can find it in your hearts to donate or simply spread our website around it would mean the world to us and our family. We are accepting donations at medicalbillsdebtdonationsms.weebly.com Thank You and God Bless we need a miracle!
DonatePleaseMS 1 year ago
This has been flagged as spam show
MedicalBillsDebtDonationsMS.weebly.com
My husband is suffering from Multiple Sclerosis and back sugeries. We are in need of donations to cover medical debt. Please if you can find it in your hearts to donate or simply spread our website around it would mean the world to us and our family. We are accepting donations at medicalbillsdebtdonationsms.weebly.com Thank You and God Bless we need a miracle!
DonatePleaseMS 1 year ago
Thanks for uploading this excellent video. very well done. I have had MS for six years. On some days it kicks my bum, but on a lot of days, I kick IT's bum.
teslagirlM 1 year ago
go and check "ccsvi" dr Zamboni there is a cure. its for real!
IsaacG1965 1 year ago 4
This has been flagged as spam show
@IsaacG1965 yes man u r great :)
530BigBen 4 months ago
@IsaacG1965 it's not a cure. it's a treatment for some symptoms in some people with MS that have problems with vein blockages. It's not an MS cure.
LadyLahdeedah 1 month ago
Had a neighbor with MS who went through SCC International (407) 610-4248 who coordinated a medical evaluation by an Asian doctor. They had to travel to an overseas treatment center, but their condition totally REVERSED. it was incredible.
search4acure 2 years ago
I was diagnosed with MS in '04 and in 4 years I took all the different medications to try to stop the progression with no success. In '08 I had stem cell treatment that worked amazingly well in my case. iLoveMyNewStemCells
hollyhuber 2 years ago
Hi all, I haven't post any comment since a long time. But reading my previous posts by people, taking the same natural ingredient I have took to fight MS (Black Seed Oil) and thanking me a lot for the mysterious results they have found, encourages me to repost about my try.
saadfakhoury 2 years ago
As a sum, I was infected by MS and by chance I've tried to take the Black Seed Oil and it has done fantastic results with me. I CANT ADMIT my try to be a cure of MS, but I think that;1-getting rid of all the remains of MS 2-providing me with power to continue my life 3-MRI tests proving the stop of demyelation 4-living free of MS attack since I took the black seed oil from 7 years! 5-benefits of many people that have read my posts and took the Black Seed Oil SHOULD BE TAKEN INTO CONSIDERATION.
saadfakhoury 2 years ago
If u thing that 1-my intention is to market for BSO (coasting 6 usd / month) 2-my intend is to be famous even by stating my name with such a diseaseDon't respond to my post
If you would like to have a chance for my try respond to me with a message a even add me on MSN to help you thoroughly; saad_fakhoury@hotmail
saadfakhoury 2 years ago
@saadfakhoury Why would you want to help infidels?
ancbcc 1 year ago
@ancbcc
you are right!
you are completly right. i could go away or even dont post my comment even
but i Like to help other and I'M SURE ill be profited from Almighty GOD when doing that
saadfakhoury 1 year ago
This has been flagged as spam show
excellent worker!
1888junkteam 2 years ago
excellent worker!
1888junkteam 2 years ago
I'm worried about the cost of diagnosis and treatment because I dont have a health insurance
DeliciousRipon 2 years ago
Exercise and take vitamin D3 10'000iu per day vitamin B12 1000 iu per day (for balance) Magnisium citrate 1-200 mg a day , I've had MS for 15 years Ive walked 10 miles in the last 4 days no fatigue no brain fog and no systems after I started doing the above. I dont want anything off you just try it! and God bless :) look at my vids over the last year for proof
gekiryudojo 2 years ago
this is what I am doing until the Day we all can get the liberation treatment check out CCSVI
gekiryudojo 2 years ago
Check out the Liberation Treatment on YouTube.
OvisArie 2 years ago
I'm waiting to see a neurologist next week. Apparently my MRI results showed some type of disease process. I've had quite a few weird symptoms which seem to fit MS. I'm a bit worried. How do I find out for sure if it is or isn't MS?
SisterSunnshine 2 years ago
An MRI will show periventricular lesions. They will take some CSF from you via a lumbar puncture. The pathologist will be looking for oligonal bands and mononuclear cells.
piddleton 2 years ago
Also you would get a lot of symptoms that are not explained by the presence of one lesion in the brain. This because MS can attack any sensory or motor pathway in the CNS while leaving the others unaffected. It can even damage the cerebellar which reproduces many of the symptoms of being drunk, the only difference is they don't go away in the morning when you start to sober up.
piddleton 2 years ago
i think i have it
Jethawk72 2 years ago
neurological diseases are the worst. out of all of them, Huntington's has to be the absolute worst. Parkinson's, Lou gehrigs, multiple sclerosis, Alzheimer's. i think we have so much potential to cure these horrible things as people its ridiculous. im sad that these things still exist. =[
chadinterrupted 2 years ago
thanks for this video
pochlomin 2 years ago
This has been flagged as spam show
New miracle treatment for multiple sclerosis!
Search Youtube for HOW WEED WON THE WEST
watch?v=MzT1a1NKoKM
SacredCowProductions 2 years ago
Could a stroke be confused with some on has ms? the mri back then didnt show any plaq but was told it could take years to see.
aheroawakend 2 years ago
I dunno if i have ms or not but I was told in 03 i had a stroke. in the brain stream but for 2 years before this the same time of year i had numbniss weakniss on the left side i was healthy until 2 months ago but now its on my right side but just numb not tingly. I always have some troubles with eye sight seeing headlights street lamps seeing streaks and also after images, Medical insurance is pending so hard for me to get tests any info?
aheroawakend 2 years ago
Stroke is usually pretty easy to pick up on an MRI scan. The radiological presentation is very distinctive and an MRI is accurate enough to hone in on the smallest of lesions. You might have had another stroke afterwards. Not all strokes are apparent with obvious motor and sensory signs. Your sight problems could be explained by a stroke in the brain stem. Have they done a lumbar puncture yet for oligonal cells and mononuclear cells in the CSF?
piddleton 2 years ago
This has been flagged as spam show
for all MS patients, Id like to mention an important fact; I was infected with MS from around 8 years and got rid from all my permanent disabilities and stopped the demeylation by taking the BLACK SEED OIL.
IFFFFF ud like you know more about my state, write to me.
saadfakhoury 2 years ago
my mom has had MS and bipolar disorder my entire life. I hate my life. she has no correct judgement. my childhood has been taken away from me because of this god forsaken disiese. If my dad were alive everything would be better
coolchris303 2 years ago
This has been flagged as spam show
There is an amazing new medical technology known as MEDSONIX... Look it up here on youtube... ABC News Reports on Medsonix... There is hope!!
erwinmeyer 2 years ago
my friend's father was just diagnosed with ms...
louiesthe1 2 years ago
This comment has received too many negative votes show
what the hell is up with that ladies mullet or is that a crew cut?
agent1up 2 years ago
i have to agree with AletheReneW . MS has you . she's right everyday is different. what is LDN . i use Copaxone and steroids once every two months. i'm not the same person w/ the steroids. i'm not the same person i used to be lol . someone out there please reply. i feel so alone. surrounded by family yet so alone.
pyretta66 2 years ago
I hope you are doing good! You are not alone! :)
I have MS too... But we have to stay positive. :)
roxy782 2 years ago
This is noting new for a person with the disease
trojantjl 2 years ago
I feel sorry for people who have ms and cancer.love always cutiekyla2002
cutiekyla2002 2 years ago
that was a sweet comment buetiful
jermeal385 2 years ago
This has been flagged as spam show
Nice try. Keep it up check out esteembpo + com for social media marketing. rgfdg
QuentinTilley 2 years ago
This has been flagged as spam show
Nice try. Keep it up check out esteembpo + com for social media marketing. rhtk
isabngeryer 2 years ago
i am waiting to find out if I have ms. This is Thurs. and my appointment is on Tues.
I'm very nervous. I have had a MRI, MRA, a Spinal Tap, blood work, and a bunch of other stuff. This video is has been very helpful. I hope that I don't have ms, but with research and videos like this I belive I am ready.
F150FORDMAN01 2 years ago
I hope things go good today let us know...praying for you. MS does suck but, it becomes your life and, you start to deal with it...hang in there.
Jones0da 2 years ago
F150FORDMAN01...Im also going to get MRI's tomorrow 12/01. I have lost my family. My husband has left me for another woman(he says they are just "friends"), and my daughter is looking to her as a mother and loves to send word back through her friends that she goes to movies and just whatever with this woman. They love to go on topix and make fun of me, they make fun of the way I dress, etc. Im about as sad as sad can get. They hate me for something I cant help or change.
mitzydawn 2 years ago
Maybe it has something to do with malfunction of the glial cells. glial cells nourishes the neurons. Maybe the virus kills off the glial cell so that affects the neuron's myelin shelth.
xEternalx 2 years ago
MY dad has ms and i am only 14 my mom works 3/4 of the day and he cant do anything, he has ms for over 3 years. If u have any idea how hard it is plz pray for everyone with MS u guys.
yomommazzz 2 years ago
I have twitcing all over my body since nov 08, as well as tingling in my soles, as wellas fingertips, have been to my GP who did a physical nuero exam and said i dont have MS, unconvinced I asked for nuros opinion who did a nuro exam in April this year and again said you are fine, these sypmtoms have been constant I mean the twitching, burning sensation and tingling. its pretty sad i dont get a diagnoses and ben in limbo land.
rezza01 2 years ago
You even had an MRI and a spinal tap?
NamekianPikkoro7 2 years ago
Instead of searching for a diagnosis to "label" yourself, look at ways to improve these feelings you are getting. People get too caught up in diagnosis's but everyone is different so you should just focus on the symptoms and try to treat them.
KTSKING 2 years ago
my mother has this desease i just found out two weeks ago i am 20 years old i love my mother
787puertorico 3 years ago
So informative! A must for anyone with MS (me) or anyone who knows someone with it.
cathie62 3 years ago 4
dx'd 2000. good luck to everyone! MS is no joyride... keep pushing and be productive! work out the ultimate muscle: the brain! and live with dignity...
omons 3 years ago
i've been on LDN since lat July..the stuff is great, look into it guys.
estaesloca 3 years ago
Hello everyone. I'm a 20 year old male and im unsure of whether i have this disease. I remember the Doctor in the video talked about how location of your first 15 years of life can have an affect on whether you have the disease or not. I was born in Vancouver, BC and moved to Calgary AB when i was 12. My possible symptoms for now seem to be urinary irrgularity some days, math seems to be a real challenge, a bit of long/short term memory issues. No one in my family has MS.Please share some advice
Apollexis77 3 years ago
Just wanted to share some info......
LYME disease is known as the " GREAT IMITATOR." Within the Lyme community, patients have been diagnosed with MS, ALS, ADHD, CFS, and the list goes on and on. Lyme disease for the most part is a treatable disease. Would be happy to email anyone a Lyme disease brochure.... Elaine in VA
ecftube 3 years ago
How is that, though? They only have like a few minimum similarities. Why is it a great imitator?
NamekianPikkoro7 2 years ago
This was well done and pretty informative for those who don't have MS. I was diagnosed 3 years ago and do daily shots of Copaxone along with other meds for symptom management. The only thing that annoys me and many of my fellow MS'ers is the statement " I have MS, MS doesn't have me". This is bull, MS has you whether you admit it or not. When every decision you make on a daily basis is determined on how your MS is affecting you today, it has you. Just a pet peeve for a lot of us.
Renoandi 3 years ago
So do you have to have eye sight lose first inorder to be diagnoised?
LastKitten06 3 years ago
Until there is a cure there is LDN. Please everyone should look into LDN for MS. It has been a miracle for my husband. He has been on it for 4 years now. I can send anyone his full story if you send me an e-mail. Or you cna look up LDN and MS on the internet. This drug is cheap, has minimal side effects and most people report no progression in their MS. Please look into it!
AlethaReneW 3 years ago
hi. i'm studyin this illness at university, and i'm interested in this ldn-low dose naltrexone-. could you please tell me more about it or caould you tell me some website where to find info? my books don't say almost anything about ms therapies...thx a lot.
gkublok87 3 years ago
omg its almost a hour long
zezsn1p3r 3 years ago
I haven't been diagnosed yet, but MS is the #1 suspect. It's been four months since my initial attack. It is crazy how long it takes to diagnose.
murfdog19 3 years ago
I was diagnosed 2 weeks ago. I live in San Diego, too. This was very informative and I even forwarded this to my loved ones to share the information and perspectives with them. Thank you so much for this video.
CaliCousin 3 years ago 9
i woke up today and had unusually sore muscles and a little tingling in my leg.....should i be worried?
johnowensjr1234 1 year ago
This has been flagged as spam show
i woke up today and had unusually sore muscles and a little tingling in my leg.....should i be worried?
johnowensjr1234 1 year ago
@CaliCousin it is all out of date she knows nothing I have had MS for 15 years and live a normal life! Because of what I learnt and because I am Liberated
gekiryudojo 10 months ago
This comment has received too many negative votes show
virus?
don't think so.
The signals are electrical.
MS exists as long as the electrosmog.
We are surrounded by electricity.
It's quite likely that it's the reason.
JOscHAou 3 years ago
This video was extremely well-made in many aspects.I wanted to know what my client/friend goes through on a daily basis.I wish there were videos this good for all types of illnesses.400000 is like 1 in every 750 people in US which is a big number.
kaos60 4 years ago 5
Old MSers KNOW ALL THAT1 because we LIVE that every second of our lives. Perhapsit might help other understand but if you have over 30 year of MS u sort of know every manifestation andalso KNOS THERE IS NO CURE!
Best regards,
LuisM
Hoboken NJ
Sefardisafran 4 years ago
Hi Luis, My husband Paul grew up near you in Palisades Park. His parents now live in Saddle Brook. Paul and one of his sisters have MS. She still lives back there. Paul and I live in Calif. You are right there is no cure, but Paul has reversed all of his symptoms with LDN, diet, exercise and suppliments. I know LDN has heled thousands of others. It does not promis to reverse symptoms, but 85% of people report lack of progression in their MS. That is huge. If you want info just let me know.Aletha
AlethaReneW 3 years ago
As someone who was diagnosed 2 days ago, I found this to be very informative, thank you uctv.
msquarednet1 4 years ago 3
Very informative, Explains what to expect if you have or know someone with MS. Lets find a cure now.
ACMELIGHTING 4 years ago 4