metaspencer The medical system is a fraud. The real cures are the natural cures. There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
When I asked my neuro (in 2002) why Benign MS wasn't among the 'types of MS' posted on his wall. He said "Because the drug companies want everyone on drugs" F pharma, they can't have me.
I do not have MS. Just by chance see your documentation. I'm very impressed. You've probably wondered many times why it has even taken you. Because we always need someone who gives us hope. Best wishes to you from Germany.
I have been diagnosed since 95. I'm not in a chair or walker. I was on Copaxeon for 10 years. I have multiple muscle damage and scar tissue in my stomach. I have not taken anything like the MS meds for 10 years at least. I have the same 4 leisions that I've had since day 1. Hang in there.
Claudia Robinson There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Here in Brazil, the Coimbra protocol cure MS in more than 95% of the cases. Even some Americans are using it. See the channel "" MS Hope", here on TH-cam.
MS is a purely personal journey that is different for everyone depending on how many lesions you have and where and how they are progressing. Some people had a CIS 25 years ago and their brain rewired around it. Some people have 25 lesions and a very resourceful brain that has rewired around all of them. Some aren't so lucky...one major spinal lesion and they were taken out. Glad your approach is working for you but I wouldn't presume that it would work for everyone or you would recommend it for everyone without knowing their details. I have been pretty fortunate, considering, but now after 15 years am seeing progression which is pretty typical. I did take actions in the meantime to save more than average, travel and see more than average and set myself up the best I could for the future. I continue to walk forward...with my eyes wide open. I was on Copaxone for 11 years and it is a very low quality drug but what they had back then. There are a lot better options now. Kind of hard to compare them.
I was diagnosed in 98 and didn't take meds till around 2012, but I don't show any signs of a disability. I'm in an MS group on Facebook and I keep seeing newly diagnosed people taking Copaxone, which is one of the abc drugs that have been ruled ineffective and I'm like why are Doctors prescribing a med that's so old and ineffective.
Hi Matt, I don't have MS but I know someone that is symtoms free with meditation, I strongly believe that the state of the mind and emotions has also a big impact in any illness. I know you have worked mainly with the physical side but have you tried to do some research about how meditation and the knowledge of mind and emotions work in our health?.
I have sent this video to every news station in the UK and emailed so many news stations MPS etc newspapers also in the UK. to be ignored. No one cares here in the UK SADLY many more with MS will now sadly die because of that.
I’m BAWLING my eyes out just watching this video. I’ve not seen the entire movie yet. I was just diagnosed with MS last November, 2020. I’m almost 48 yrs old. That’s means PPMS and I have lesions on my spine which means more aggressive MS... and about to start Ocrevus in April... but NOW? NOW? ... I just don’t know. All I know is #fuckms and ##fuckbigpharma
I have MS, dx in 2014 after several years of trying to get answers. No drug I have taken has improved my symptoms at all, infact my mobility has decreased. I'm told I'm stable, as my MRI shows no knew lesions. But my symptoms have gotten worse. The fatigue, the balance issues, the vertigo, the walking..... I'm seriously considering quiting Ocrevus and focusing on diet.
Kelly Fassino * Hi Kelly, I just watched this video for the first time. As I read through the comments, I realize this was from 2 yrs ago, lol. After reading your reply, I'm curious as to what you decided to do about your current MS treatment. Did you stop all MS meds and try a special diet? Maybe you just went cold turkey? I'm really interested to hear what you decided. Or anyone else in this predicament, since I'm at this same crossroads myself. I do not want to take my infusions anymore, but as you are well aware, it's a scary decision. Either way Kelly, I pray Our Father in heaven takes away all your MS pains and symptoms. I pray God heals and restores every single lesion!! Lord Jesus, please take Kelly's vertigo away, enabling her to walk firmly on the ground, in a straight path, with no sense of dizziness!! !! I ask all these things in the name of My Glorious Lord and Savior, Jesus Christ!! 🤗 GODBLESS&❤️ALL Kelly, have you ever tried any treatments just for vertigo?
My son was 21 when he was diagnosed with MS in 2011 and was prescribed Avonex. He told me that his head feels like it's going to explode every time of his injection and this went on for 2 yrs. Then the pill Avonex was approved and he switched so he does not have to deal with the injection. He did not tell me that he made a decision to stop taking medication because he said the side effects are so bad for his quality of life. It's interesting because when his neurologist prescribed Avonex, she told us --- this is a newly approved drug and I'm sorry to say that this is still BUSINESS. If you want to know more about this drug, read about it at the Wall Street Journal because it will have more information than the American Journal of Medicine. I appreciated her honesty --- she also told my son that MS is not a death sentence but it is a life sentence. He was my son's favorite neurologist but has to find a new one due to change in our health insurance. I did a lot of research on HSCT and he will undergo stem cell transplantation in April at Panama City Stem Cell Institute ---- Health Insurance will not pay for this transplantation even though there's a lot of patients (I have followed their blogs) that benefited from this. I know this is not a cure, but if it will alleviate some of his medical issues and will improve his quality of life without the debilitating side effects, then it's all worth it. Health insurance is willing to pay $80,000/yr for medication but not willing to help for stem cell transplantation which is a fraction of the cost.
Can't wait until I can see this whole production. Kudos for standing up for MSers!! This is going to be shown to my neuro and Dr if they want to push big pharma on me next time I see them!
Your neurologist doesn't care. Sorry but it's true. I confronted my MS specialist neurologist and all he did was get angry. How could I DARE question his wisdom?
Here in Brazil, the Coimbra Protocol cures MS, in more than 90% of the cases. Se the TH-cam channel "MS Hope", where an American was cured of MS only using the Coimbra Protocol.
I participated in the Rebif trials at Western university hospital in London and injected it for over 15 years before quitting. I was never evaluated at 10 years or 15 years and when I started to react to the new formula, they would do nothing for me except give me an appointment for an MRI in one year because they did not have anything to compare it to. I said I could get it done sooner locally and they said I would have to wait a year to see them again for an evaluation. I never went back to that clinic after being treated so poorly. I gave them my life for 15 years and they turned their back on me
Diana McCaig Sorry but I has been great to see that your hospital is just like mine, Look for Matt Embry and see what he thinks of the MSsoceity of Canada nothing good as charity the have a D grade. If you would send me ouelepne number I could text youMy phone number is 587-700-9440 and again my phone number is 587-7009440
Julie was drugged up on meds for MS and sadly passed away funeral-notices.co.uk/national/death-notices/notice/Julie+Wingfield/2439939 Julie Wingfield, who died on 24 March, 2010, aged 46, was described as a “one in a million” mother.Julie, who suffered from multiple sclerosis, lived in Syston in Leicestershire with her son Terry.Terry said: “Mum had been diagnosed with MS about four years ago and she was on a lot of medication. She lived here with us and she got drowsy because of the medicine but what happened was completely unexpected. It’s been devastating for us.“She had so many plans. And she was really looking forward to my brother Michael’s wedding in the summer.“I had no idea how to cope. Luckily my neighbours, Sarah and Tony, who live across the street were a great help.“Mum had her eyes closed so we think she just passed away in her sleep.”Before being diagnosed with MS, Mrs Wingfield, whose maiden name was Melbourne, lived in Belgrave, Leicester.She worked at several residential homes across the city, including Pine View in Hinckley Road, Groby Lodge in Groby Road and Silver Birches in Aylestone.She was survived by her father, four siblings, four children and three grandchildren.Terry said: “When we were all kids she made sure we had a holiday every year. She was a great mum.”Daughter Kirsty added: “She was one in a million and we all loved her dearly.“She will be missed and she will never be forgotten. She will always be in our hearts.”
Now that you know the truth, do something about it. Diet is the key. You CAN do it! I am living proof! My family saw the transformation of my health with diet and it's amazing how they protect me, if we go out to a restaurant to eat, they are always the ones to ask about ingredients even when I know what I am eating is safe. I have had my MS in remission for 13 years! At 67 years old, I take no and need no pharma drugs, have no aches and pains and sleep like a baby at night. You can do!
@@Ane127 8 years to be exact . That's what most research points to but 8 years of hard diet and exercising and let's be real, no one in this lazy society will do it.
Sherly Teegs That shouldn’t be the MDs’ decision. We have the right to know what our disease is and how to reverse it if we want to. Plenty of people would choose the option if they knew about it.
Just watching this has made me feel much better about choosing to not take anything. My neurologist keeps trying to push me to take something i did pick something recently but havent felt comfortable about it so i just havent gotten my lab work done.
I just watched. I have MS too. I cried when you cried, you are not alone. I've had this for 10 years. I've been in the chair 1. I hate it. This is not life, it's death by 1000 cuts. I'm from Ontario.
Don't know where you get your info but that is untrue. Here she is at the Cleveland Clinic just a few months ago. th-cam.com/video/Qe6mgabKlp0/w-d-xo.html Diet worked for me too, I was diagnosed 13 years ago and have had the MS in remission for 12 1/2 years. And yes, there is no magic bullet it's lots of hard work and constant diligence.
I AM VERY PROUD of TEAM GB and to so many who supported me with MS thank you.Many sites that supported me from our UK sports sadly the sites I am on for lots I have been hacked.
I'm not saying that this can't be true but as I was patient 4 of a double blind test of a new MS drug over 10 years ago, I know this to be horribly misleading from a personal perspective. I am still on the drug and I am monitored closely to this day. I feel that this is video misleading at best. MS is a horrible ailment and I wouldn't wish it on my worst enemy. That said, I feel very lucky to have been placed on the drug trial when I was and can comfortably say that my dependents and I owe our lifestyle to my treatment. Bad people exist in every walk of life, implying that the entire sector is villainous due to this one side is sad and to a degree irresponsible. I hope people do their own research before making a decision that could impact their friends and family so severely.
I can't wait to watch the whole documentary, I have refused the "conventional" MS drugs, I am taking LOW dose Naltrexone, which has helped me with balance and incontinence with NO side effects other than some vivid dreams. My neurologist who was sceptical of LDN, was truly amazed how well I am doing.
I have worked out every single thing going on around me concerning MS . I had a GP tell me in 2009 that I can die any day in Leicester UK he took 24 years to diagnose me with SPMS the next surgery after my new GP has visited me once only .A total of 39 years of no help properly lots of post traumatic stress caused to me.😢I want a compensation scheme for everyone who's died on MS meds for their families that have all suffered and apologises from drug companies.
when the incidence of relapses decrease, or they are not happening at all for years, how then there is no long term effect? and I am talking about RRMS.
Death as a side effect? Well let's say thankfully these drugs didn't cause death, because myself and a friend who also has MS are still both here. But we weren't far off! Both of us were on the typical DMD, ones that reduce your immune system, and both of us spent weeks in hospital beds because we caught minor infections (and mine was a weak cough, a cough I wouldn't say was anywhere near as severe as coughs I've had before I was on DMD)! I was on Tecfidera, a drug that personally I'm not sure had any real effect in slowing my MS. But a drug that reduced my lymphocyte count to dangerous levels that a simple cough turned into Sepsis. I could hardly move, and had to be admitted to hospital after falling out of her and not having the strength to get off the floor. But a good job as I had a 103C temperature and atrial fibulation, so my heart rate showed as 250+ bmp! After loads of intravenous antibiotics and drugs to thin my blood, and slow my heart rate, and therapies to reduce my temperature I pulled through. Although what I was told was a psuedo relapse, has resulted in significant physiotherapy to try and get me back to walking with crutches, but months later in significantly more disabled. And of course off this drug that I have doubts really did anything helpful.
This was my neurologist I have the original letter from him from 1999 not recommending drug recommending to monitor. This tells me he was already decided on his stance but couldn't say anything till after he retired 😞
kms386 Diet and supplements. Go to the alternative healers and holistic doctors. There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
It makes you so angry. All these people financially benefiting from the illness and eventual disability of innocent people. The fda and "ms society" should be ashamed of themselves.
I am English and medicine is not forced down us as in America. I am also of an age where there were no medicines so the idea of being pressurised into taking drugs is bizarre. Most of us are desperate to have medicine as some 'new' treatments are not paid for by the local area. If we pay for a medicine privately we become ineligible for further NHS Treatment.
I will always speak out whilst I am still alive after being told that I can die any day via a GP in 2009.Thank you always to Matt Embry for his prayers he has done for me.
Hi Matt, MS Patients in Germany would very much like like to carry Prof. Ebers thoughts and concerns to the wider MS community in Germany. Is there any way to get in touch with Prof. Ebers in order to confirm that he’s ok with that? Thanks!
I'd be a lot more interested in a better quality of life now, considering we _all_ die and lots of people end up with shitty issues as they get older regardless of M.S. Edited to add; and potential side effects are not guaranteed side effects. FFS.
I have secondary progressive MS ans took medications for 2 years. After having horrible side effects I stopped all of this because I was thinking that something doesn't ad up. the medication didn't show any positive but a lot of negative effects and my organs started to take a turn for the worse just as my MS too. The long term effects on the organs is not known or not communicated. That was reason enough for me to stop all this nonsense. MS is developing further anyway, with or without medication. the only difference is that with medication you're distroying your organs too. They say MS is not deadly but it becomes if you take medications.. because the organs fail.
Shawn Moustache There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Thank you for speaking out.... also, please watch your back..... a lot of doctors who spoke out against pharma have accidentally beaten themselves to death............
Here in Brazil, the Coimbra Protocol cures MS, in more than 90% of the cases. Coimbra Protocol means: Take a pill of vitamin D, each day and follow a diet without gluten and lactose.
George Kafantaris there are two videos on TH-cam, both sponsors have MS, the films are independent of each other, and both have advanced MS, each video is about how diet changed the lives of each person, as they were healed from MS. Don’t give up...
Lawrence Hofer here from Dinsmore Hutterite Colony in Saskatchewan Canada I have MS too have gotten Lemtrada a strong drug that has helped me but I'm very interested in Natural resources Our Lord's meds
I have multiple sclerosis was diagnosed at 24 I'm now 27 I am on copaxone injections 3 times a week. I wish and pray for a cure I want my life back.. 😖 And these drugs are scary as hell... I was 1st put on tecfidera it didn't agree with me at the time I was having a relapse aswell I couldn't get off the floor I was 🤮 throwing up sweating losing weight ='(
Here in Brazil, we have the Coimbra Protocol. On averages it cures MS in more than 90% of the cases. Coimbra Protocol means: 1- Take a pill of vitamin D, each day. 2- Follow a diet without lactose and gluten for the rest of his life. ****************** If you want to see a proof of Protocol Coimbra curing an American with MS, on the channel "MS Hope", available here on TH-cam.
I have most of those effects that he listed as side effects right now just from the ms. I am on no meds so I don't know if I would want to take any that would make them worse
Becca M Have you listened to the documentary? Changing the diet is mentioned & vitamin D, and the brain can be affected, which is treatable through surgery, I’m watching the documentary on Amazon prime. But it might be on TH-cam.
Something needs to be done in the United States because pharmaceuticals have so much power above the doctors I’m on disability and I have no help with financial help I’ve lost both my mom and dad and don’t even make $8000.00 a year. I feel like with Medicare they won’t pay for anything besides pharmaceuticals. I started with Betaseron , Tysabri, Tecfidera , and now Ocrevus because I’ve been diagnosed with secondary progressive MS.
Greed by the pharmaceutical companies is a huge problem in the country if not in the world. I would not doubt that there is cures for cancer but I know this is how cruel and evil the industry is for the almighty dollar. Look up Dr. Michael Johnson on TH-cam . This doctor has made amazing progress on MS, please look him up.
The Coimbra Protocol cures MS, in more than 90% of the cases. Coimbra Protocol is: 1- Follow a gluten and lactose free diet. 2- Take a pill of vitamin D each day.
I don’t know if big Pharma controls all the planet, but it definitely controls much of it! I discovered by accident info about an antipsychotic medication that was banned In all but two countries, & 1 was the US, Despite horrible side effects, including death. This website gave info on how much $$$ each Drug makes for the drug company & it’s in the billions. Very nice for the stockholders but not for trusting consumers.
my neurologist jokingly said if there’s a cure then she would be out of a job!-i walk slower now with an edss of 4.5 still taking this betaseron injectables still walk my kids to their school bus only having to recently fall down and trip due to a right foot drop. i dread the days when it happens and my kids are left alone because i’ve passed out do slamming my head on concrete. we deserve a cure but in this capitalist society like my neurologist stated a cure would leave many thousands without a job, so I guess we gotta take one for the team!-right?
Here in Brazil, the Coimbra Protocol cures MS, in more than 90% of the cases. Coimbra Protocol is: 1- Follow a diet without gluten and lactose. 2- Take a pill of vitamin D, each day. "MS Hope" is the name of a channel on TH-cam, where an American tells what happend to him, when he followed the Coimbra Protocol. He went to a wheelchair to a normal life, in two years.
George Kafantaris There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time. The body heals itself just like when we break a bone or get a paper cut.
I have MS, every week there's a new diet, and someone else making money. But if you all look deeply into this, the people that survive have a change in attitude. Any way enough.
Sounds like you are too gluttonous to stick to a diet. What about exercise? proven beyond a scientific doubt it's neuro protective. Is that a scam too?
Mounia Mouniaa look for the stories on TH-cam, on two women, in separate videos, both were physicians I think, and both healed them selves Completely completely of MS. I believe both used a vegan diet. It’s been a while since I listened to the videos. Both had advanced MS.
I make the same facial expressions when im trying not to cry! I have Ms and i dont want to start any medication. I have always been into natural ways to self heal. The symptoms i experience with MS are real and painful. Even more scarier when i think of having to make a decisiom soon about what to do. I have been diagnose w MS on oct 2017. Apparently my nuero doctor says ive had it since 2014. I understand that now because i tie that into events that were like mid life crisis. I would like to find out how i can make the best with Ms for the rest of my life.
Please watch the video by Dr. Alfred Miller , rheumatologist, as he talks about the Lyme ME connection. Also, Terry Wahl's has a great video on MS called "Minding your mitochondria" .
I too was diagnosed with MS after decades of perplexing symptoms. I have the MS in remission 13 years now exclusively with diet. You can do it too. The diet isn't easy but it's worth it. I say that, "NOTHING tastes as good as feeling healthy feels."
Flora Lopez There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
lea Geronimo There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Merry Christmas 2024 to George Ebers and Matt Embry and to thousands of friends to me I was born on Christmas day 🎄
Thank you brave soul for speaking out! I hope one day we all be happy and completely healthy, living our passions in life!
He said he wouldn't take them himself, he'd rather risk it. That says it all in a nutshell, SMART man!
One of the best parts of the documentary, in my opinion. It's amazing that a leading MS drug trial researcher would have these perspectives
metaspencer The medical system is a fraud. The real cures are the natural cures.
There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Look up Dr. Michael Johnson on TH-cam
When I asked my neuro (in 2002) why Benign MS wasn't among the 'types of MS' posted on his wall. He said "Because the drug companies want everyone on drugs"
F pharma, they can't have me.
I do not have MS.
Just by chance see your documentation.
I'm very impressed.
You've probably wondered many times why it has even taken you.
Because we always need someone who gives us hope.
Best wishes to you from Germany.
I have been diagnosed since 95. I'm not in a chair or walker. I was on Copaxeon for 10 years. I have multiple muscle damage and scar tissue in my stomach. I have not taken anything like the MS meds for 10 years at least. I have the same 4 leisions that I've had since day 1. Hang in there.
Claudia Robinson There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Here in Brazil, the Coimbra protocol cure MS in more than 95% of the cases. Even some Americans are using it. See the channel "" MS Hope", here on TH-cam.
MS is a purely personal journey that is different for everyone depending on how many lesions you have and where and how they are progressing. Some people had a CIS 25 years ago and their brain rewired around it. Some people have 25 lesions and a very resourceful brain that has rewired around all of them. Some aren't so lucky...one major spinal lesion and they were taken out. Glad your approach is working for you but I wouldn't presume that it would work for everyone or you would recommend it for everyone without knowing their details. I have been pretty fortunate, considering, but now after 15 years am seeing progression which is pretty typical. I did take actions in the meantime to save more than average, travel and see more than average and set myself up the best I could for the future. I continue to walk forward...with my eyes wide open.
I was on Copaxone for 11 years and it is a very low quality drug but what they had back then. There are a lot better options now. Kind of hard to compare them.
I have developed 2 after 32 yrs. I was on Copaxone for over 10 yrs.
I was diagnosed in 98 and didn't take meds till around 2012, but I don't show any signs of a disability. I'm in an MS group on Facebook and I keep seeing newly diagnosed people taking Copaxone, which is one of the abc drugs that have been ruled ineffective and I'm like why are Doctors prescribing a med that's so old and ineffective.
Hi Matt, I don't have MS but I know someone that is symtoms free with meditation, I strongly believe that the state of the mind and emotions has also a big impact in any illness. I know you have worked mainly with the physical side but have you tried to do some research about how meditation and the knowledge of mind and emotions work in our health?.
Thank you for making this important documentary.
I have sent this video to every news station in the UK and emailed so many news stations MPS etc newspapers also in the UK. to be ignored. No one cares here in the UK SADLY many more with MS will now sadly die because of that.
I’m BAWLING my eyes out just watching this video. I’ve not seen the entire movie yet. I was just diagnosed with MS last November, 2020. I’m almost 48 yrs old. That’s means PPMS and I have lesions on my spine which means more aggressive MS... and about to start Ocrevus in April... but NOW? NOW? ... I just don’t know. All I know is #fuckms and ##fuckbigpharma
I have MS, dx in 2014 after several years of trying to get answers. No drug I have taken has improved my symptoms at all, infact my mobility has decreased. I'm told I'm stable, as my MRI shows no knew lesions. But my symptoms have gotten worse. The fatigue, the balance issues, the vertigo, the walking..... I'm seriously considering quiting Ocrevus and focusing on diet.
Here in Brazil, the Coimbra Protocol cures MS, in more than 90% of the cases. See a proof on the channel "MS Hope", here on TH-cam.
Kelly Fassino * Hi Kelly, I just watched this video for the first time. As I read through the comments, I realize this was from 2 yrs ago, lol. After reading your reply, I'm curious as to what you decided to do about your current MS treatment. Did you stop all MS meds and try a special diet? Maybe you just went cold turkey? I'm really interested to hear what you decided. Or anyone else in this predicament, since I'm at this same crossroads myself. I do not want to take my infusions anymore, but as you are well aware, it's a scary decision. Either way Kelly, I pray Our Father in heaven takes away all your MS pains and symptoms. I pray God heals and restores every single lesion!! Lord Jesus, please take Kelly's vertigo away, enabling her to walk firmly on the ground, in a straight path, with no sense of dizziness!! !! I ask all these things in the name of My Glorious Lord and Savior, Jesus Christ!! 🤗
GODBLESS&❤️ALL
Kelly, have you ever tried any treatments just for vertigo?
@@daltonagronomo1652 * Thank you for this information. I'm going to look into this . Hopefully it's still on YT, lol. God bless you ❤️
You’re stable with no new lesions BECAUSE OF THE OCREVUS! But go ahead and stop taking and watch how fast your life falls apart around you.
MS since 20119.....thank you for educating me. Your great
My son was 21 when he was diagnosed with MS in 2011 and was prescribed Avonex. He told me that his head feels like it's going to explode every time of his injection and this went on for 2 yrs. Then the pill Avonex was approved and he switched so he does not have to deal with the injection. He did not tell me that he made a decision to stop taking medication because he said the side effects are so bad for his quality of life. It's interesting because when his neurologist prescribed Avonex, she told us --- this is a newly approved drug and I'm sorry to say that this is still BUSINESS. If you want to know more about this drug, read about it at the Wall Street Journal because it will have more information than the American Journal of Medicine. I appreciated her honesty --- she also told my son that MS is not a death sentence but it is a life sentence. He was my son's favorite neurologist but has to find a new one due to change in our health insurance. I did a lot of research on HSCT and he will undergo stem cell transplantation in April at Panama City Stem Cell Institute ---- Health Insurance will not pay for this transplantation even though there's a lot of patients (I have followed their blogs) that benefited from this. I know this is not a cure, but if it will alleviate some of his medical issues and will improve his quality of life without the debilitating side effects, then it's all worth it. Health insurance is willing to pay $80,000/yr for medication but not willing to help for stem cell transplantation which is a fraction of the cost.
why no new videos 😣 are you ok matt?
All MS drugs have failed me. I am no longer on any. 15 years of dead end drugs.
Thanks for standing up. I am behind you..and agree.
Thank you for being a voice
THANK YOU! For the big faith and endurance for this research. The pharmaceutical industry is so unfair
Daniel Spreitzhofer Pharmaceutical companies are indeed unfair, unethical, corrupt, greedy, and more.
Can't wait until I can see this whole production. Kudos for standing up for MSers!! This is going to be shown to my neuro and Dr if they want to push big pharma on me next time I see them!
Your neurologist doesn't care. Sorry but it's true. I confronted my MS specialist neurologist and all he did was get angry. How could I DARE question his wisdom?
There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Here in Brazil, the Coimbra Protocol cures MS, in more than 90% of the cases.
Se the TH-cam channel "MS Hope", where an American was cured of MS only using the Coimbra Protocol.
Watching from Ireland! Thank you.
A #publicinquiry is needed into all #MS deaths and what medications they all took.
Your an angel
Thank you for sharing all these information with ppl who really in need
Thaaaaaank you soooooo much
I participated in the Rebif trials at Western university hospital in London and injected it for over 15 years before quitting. I was never evaluated at 10 years or 15 years and when I started to react to the new formula, they would do nothing for me except give me an appointment for an MRI in one year because they did not have anything to compare it to. I said I could get it done sooner locally and they said I would have to wait a year to see them again for an evaluation. I never went back to that clinic after being treated so poorly. I gave them my life for 15 years and they turned their back on me
Diana McCaig
Sorry but I has been great to see that your hospital is just like mine,
Look for Matt Embry and see what he thinks of the MSsoceity of Canada nothing good as charity the have a D grade.
If you would send me ouelepne number I could text youMy phone number is 587-700-9440 and again my phone number is 587-7009440
Diana McCaig
Phone number 547 no is 587
77Zero 7 9440
Seven (hindred) 8440
I was just warhatchinh the guy who worked for the feet rebid stilugy
Julie was drugged up on meds for MS and sadly passed away funeral-notices.co.uk/national/death-notices/notice/Julie+Wingfield/2439939 Julie Wingfield, who died on 24 March, 2010, aged 46, was described as a “one in a million” mother.Julie, who suffered from multiple sclerosis, lived in Syston in Leicestershire with her son Terry.Terry said: “Mum had been diagnosed with MS about four years ago and she was on a lot of medication. She lived here with us and she got drowsy because of the medicine but what happened was completely unexpected. It’s been devastating for us.“She had so many plans. And she was really looking forward to my brother Michael’s wedding in the summer.“I had no idea how to cope. Luckily my neighbours, Sarah and Tony, who live across the street were a great help.“Mum had her eyes closed so we think she just passed away in her sleep.”Before being diagnosed with MS, Mrs Wingfield, whose maiden name was Melbourne, lived in Belgrave, Leicester.She worked at several residential homes across the city, including Pine View in Hinckley Road, Groby Lodge in Groby Road and Silver Birches in Aylestone.She was survived by her father, four siblings, four children and three grandchildren.Terry said: “When we were all kids she made sure we had a holiday every year. She was a great mum.”Daughter Kirsty added: “She was one in a million and we all loved her dearly.“She will be missed and she will never be forgotten. She will always be in our hearts.”
Well just wow. I am always the seeker of Truth. This is just as disturbing as the MonSter itself.
This is me. 18 years worth of 6 failed drugs. I feel so dooped , angry, and lied too!
Now that you know the truth, do something about it. Diet is the key. You CAN do it! I am living proof! My family saw the transformation of my health with diet and it's amazing how they protect me, if we go out to a restaurant to eat, they are always the ones to ask about ingredients even when I know what I am eating is safe. I have had my MS in remission for 13 years! At 67 years old, I take no and need no pharma drugs, have no aches and pains and sleep like a baby at night. You can do!
There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
@@jerseygrl5 What diet are you on? You keep on yapping but never give details.
@@Ane127 8 years to be exact . That's what most research points to but 8 years of hard diet and exercising and let's be real, no one in this lazy society will do it.
Sherly Teegs That shouldn’t be the MDs’ decision. We have the right to know what our disease is and how to reverse it if we want to. Plenty of people would choose the option if they knew about it.
Just watching this has made me feel much better about choosing to not take anything. My neurologist keeps trying to push me to take something i did pick something recently but havent felt comfortable about it so i just havent gotten my lab work done.
Don’t take anything for it. They don’t work. I’m speaking as one who knows.
I just watched. I have MS too. I cried when you cried, you are not alone. I've had this for 10 years. I've been in the chair 1. I hate it. This is not life, it's death by 1000 cuts. I'm from Ontario.
Please watch this video. th-cam.com/video/KLjgBLwH3Wc/w-d-xo.html
You know she's not doing very well now. There is no magic bullet.
Don't know where you get your info but that is untrue. Here she is at the Cleveland Clinic just a few months ago. th-cam.com/video/Qe6mgabKlp0/w-d-xo.html Diet worked for me too, I was diagnosed 13 years ago and have had the MS in remission for 12 1/2 years. And yes, there is no magic bullet it's lots of hard work and constant diligence.
She's very sick. Watch even thia entire video. She's been sick for a while. Go find new videos of her.
I watched the entire video and she looks healthy and sharp mentally. Clearly you are looking for something negative that isn't there.
I AM VERY PROUD of TEAM GB and to so many who supported me with MS thank you.Many sites that supported me from our UK sports sadly the sites I am on for lots I have been hacked.
I'm not saying that this can't be true but as I was patient 4 of a double blind test of a new MS drug over 10 years ago, I know this to be horribly misleading from a personal perspective. I am still on the drug and I am monitored closely to this day. I feel that this is video misleading at best. MS is a horrible ailment and I wouldn't wish it on my worst enemy. That said, I feel very lucky to have been placed on the drug trial when I was and can comfortably say that my dependents and I owe our lifestyle to my treatment. Bad people exist in every walk of life, implying that the entire sector is villainous due to this one side is sad and to a degree irresponsible. I hope people do their own research before making a decision that could impact their friends and family so severely.
I can't wait to watch the whole documentary, I have refused the "conventional" MS drugs, I am taking LOW dose Naltrexone, which has helped me with balance and incontinence with NO side effects other than some vivid dreams. My neurologist who was sceptical of LDN, was truly amazed how well I am doing.
Look up Dr. Michael Johnson on TH-cam
Here in Brazil, the Coimbra Protocol cures the MS, in more than 90% of the cases.
Where can i see the full doc? Thanks
luis fernando I've only just come by this documentary myself, www.seelivingproof.com might show you where to find the full thing.
Amazon prime 😊
I have worked out every single thing going on around me concerning MS . I had a GP tell me in 2009 that I can die any day in Leicester UK he took 24 years to diagnose me with SPMS the next surgery after my new GP has visited me once only .A total of 39 years of no help properly lots of post traumatic stress caused to me.😢I want a compensation scheme for everyone who's died on MS meds for their families that have all suffered and apologises from drug companies.
when the incidence of relapses decrease, or they are not happening at all for years, how then there is no long term effect? and I am talking about RRMS.
Death as a side effect? Well let's say thankfully these drugs didn't cause death, because myself and a friend who also has MS are still both here. But we weren't far off! Both of us were on the typical DMD, ones that reduce your immune system, and both of us spent weeks in hospital beds because we caught minor infections (and mine was a weak cough, a cough I wouldn't say was anywhere near as severe as coughs I've had before I was on DMD)! I was on Tecfidera, a drug that personally I'm not sure had any real effect in slowing my MS. But a drug that reduced my lymphocyte count to dangerous levels that a simple cough turned into Sepsis. I could hardly move, and had to be admitted to hospital after falling out of her and not having the strength to get off the floor. But a good job as I had a 103C temperature and atrial fibulation, so my heart rate showed as 250+ bmp! After loads of intravenous antibiotics and drugs to thin my blood, and slow my heart rate, and therapies to reduce my temperature I pulled through. Although what I was told was a psuedo relapse, has resulted in significant physiotherapy to try and get me back to walking with crutches, but months later in significantly more disabled. And of course off this drug that I have doubts really did anything helpful.
This was my neurologist I have the original letter from him from 1999 not recommending drug recommending to monitor. This tells me he was already decided on his stance but couldn't say anything till after he retired 😞
What should we take for autoimmune disease then?
kms386 Diet and supplements. Go to the alternative healers and holistic doctors. There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Look up Dr. Michael Johnson on TH-cam
. This doctor has made amazing progress, please look him up. This doctor also deals with autoimmune diseases.
Also avoid gluten, sugar, dairy, and grains. Fasting helps too.
The Coimbra Protocol is a cure for MS, in more than 90% of the cases.
It makes you so angry. All these people financially benefiting from the illness and eventual disability of innocent people. The fda and "ms society" should be ashamed of themselves.
Then how come some patients 20 years later after beta 1 b still don't have significant disability and stable MRI.
Exactly why I've never been on any DMD.
@8:50 all I needed to hear.
I am English and medicine is not forced down us as in America. I am also of an age where there were no medicines so the idea of being pressurised into taking drugs is bizarre. Most of us are desperate to have medicine as some 'new' treatments are not paid for by the local area. If we pay for a medicine privately we become ineligible for further NHS Treatment.
I will always speak out whilst I am still alive after being told that I can die any day via a GP in 2009.Thank you always to Matt Embry for his prayers he has done for me.
No remorse and no ms recognition from bad people Im afraid
Hi Matt, MS Patients in Germany would very much like like to carry Prof. Ebers thoughts and concerns to the wider MS community in Germany. Is there any way to get in touch with Prof. Ebers in order to confirm that he’s ok with that? Thanks!
I'd be a lot more interested in a better quality of life now, considering we _all_ die and lots of people end up with shitty issues as they get older regardless of M.S.
Edited to add; and potential side effects are not guaranteed side effects. FFS.
I have secondary progressive MS ans took medications for 2 years. After having horrible side effects I stopped all of this because I was thinking that something doesn't ad up. the medication didn't show any positive but a lot of negative effects and my organs started to take a turn for the worse just as my MS too. The long term effects on the organs is not known or not communicated. That was reason enough for me to stop all this nonsense. MS is developing further anyway, with or without medication. the only difference is that with medication you're distroying your organs too. They say MS is not deadly but it becomes if you take medications.. because the organs fail.
Shawn Moustache There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Look up Dr. Michael Johnson on TH-cam
. This doctor has made amazing progress, please look him up.
The Coimbra Protocol cure MS in more than 90% of the cases. In fact, here in Brazil, this is the standard treatment for MS.
Thank you for speaking out.... also, please watch your back..... a lot of doctors who spoke out against pharma have accidentally beaten themselves to death............
Very true and important , god protect him
IM GEORGE 56 FROM AUSTRALIA,,,MS RUINED MY TEENAGE YEARS AND BEYOND...
Here in Brazil, the Coimbra Protocol cures MS, in more than 90% of the cases.
Coimbra Protocol means: Take a pill of vitamin D, each day and follow a diet without gluten and lactose.
George Kafantaris there are two videos on TH-cam, both sponsors have MS, the films are independent of each other, and both have advanced MS, each video is about how diet changed the lives of each person, as they were healed from MS. Don’t give up...
Thank You for this.
As there has never ever been a public enquiry into #MS deaths on the meds then many more will die on them SO SAD :(
Lawrence Hofer here from Dinsmore Hutterite Colony in Saskatchewan Canada I have MS too have gotten Lemtrada a strong drug that has helped me but I'm very interested in Natural resources Our Lord's meds
I have multiple sclerosis was diagnosed at 24 I'm now 27 I am on copaxone injections 3 times a week. I wish and pray for a cure I want my life back.. 😖 And these drugs are scary as hell... I was 1st put on tecfidera it didn't agree with me at the time I was having a relapse aswell I couldn't get off the floor I was 🤮 throwing up sweating losing weight ='(
Here in Brazil, we have the Coimbra Protocol. On averages it cures MS in more than 90% of the cases. Coimbra Protocol means:
1- Take a pill of vitamin D, each day.
2- Follow a diet without lactose and gluten for the rest of his life.
******************
If you want to see a proof of Protocol Coimbra curing an American with MS, on the channel "MS Hope", available here on TH-cam.
I have most of those effects that he listed as side effects right now just from the ms. I am on no meds so I don't know if I would want to take any that would make them worse
Becca M Have you listened to the documentary? Changing the diet is mentioned & vitamin D, and the brain can be affected, which is treatable through surgery, I’m watching the documentary on Amazon prime. But it might be on TH-cam.
The whole infrastructure is wrong concerning #MS
This is so disturbing
Money money 💰 money 💵
KM: And GREED, greed, greed!
Something needs to be done in the United States because pharmaceuticals have so much power above the doctors I’m on disability and I have no help with financial help I’ve lost both my mom and dad and don’t even make $8000.00 a year. I feel like with Medicare they won’t pay for anything besides pharmaceuticals. I started with Betaseron , Tysabri, Tecfidera , and now Ocrevus because I’ve been diagnosed with secondary progressive MS.
Greed by the pharmaceutical companies is a huge problem in the country if not in the world. I would not doubt that there is cures for cancer but I know this is how cruel and evil the industry is for the almighty dollar. Look up Dr. Michael Johnson on TH-cam
. This doctor has made amazing progress on MS, please look him up.
Jasmine Johnson thank you I will look for the doctor here on TH-cam.
The Coimbra Protocol cures MS, in more than 90% of the cases. Coimbra Protocol is: 1- Follow a gluten and lactose free diet. 2- Take a pill of vitamin D each day.
Big pharma industrial complex. As it interfaces with big Agra & environmental/weather control.
Here in Brazil, the Coimbra Protocol cures MS in more than 90% of the cases.
I don’t know if big Pharma controls all the planet, but it definitely controls much of it! I discovered by accident info about an antipsychotic medication that was banned In all but two countries, & 1 was the US, Despite horrible side effects, including death. This website gave info on how much $$$ each Drug makes for the drug company & it’s in the billions. Very nice for the stockholders but not for trusting consumers.
my neurologist jokingly said if there’s a cure then she would be out of a job!-i walk slower now with an edss of 4.5 still taking this betaseron injectables still walk my kids to their school bus only having to recently fall down and trip due to a right foot drop. i dread the days when it happens and my kids are left alone because i’ve passed out do slamming my head on concrete. we deserve a cure but in this capitalist society like my neurologist stated a cure would leave many thousands without a job, so I guess we gotta take one for the team!-right?
Low Dose Naltrexone, and Vitamin D3 Therapy
Swank, Jelinek, Wahls, vegan, Mediterranean, etc. Choose a diet and stick with it.
How would they be out of a job since they treat numerous diseases. Don't be dense.
Look up Dr. Michael Johnson on TH-cam
. This doctor has made amazing progress, please look him up.
Here in Brazil, the Coimbra Protocol cures MS, in more than 90% of the cases. Coimbra Protocol is: 1- Follow a diet without gluten and lactose. 2- Take a pill of vitamin D, each day.
"MS Hope" is the name of a channel on TH-cam, where an American tells what happend to him, when he followed the Coimbra Protocol. He went to a wheelchair to a normal life, in two years.
I just quit copaxone. I do not feel supported by doctors.
LESSIONS IN HEAD DONT GO AWAY.......ONLY HEAD TRANSPLANT CAN WORK,,,,,
George Kafantaris There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time. The body heals itself just like when we break a bone or get a paper cut.
Actually their have been MANY reported disappearances of Brain Lesions after following long term diet protocols.
I have MS, every week there's a new diet, and someone else making money. But if you all look deeply into this, the people that survive have a change in attitude. Any way enough.
Sounds like you are too gluttonous to stick to a diet. What about exercise? proven beyond a scientific doubt it's neuro protective. Is that a scam too?
Here in Brazil, the Coimbra Protocol cures MS in more than 90% of the cases.
hi, where can I find the whole documentary ?thank you ^^
Watch "Living Proof" for FREE on Amazon Prime at www.amazon.com/gp/video/detail/B07D7PF9HR/ or get DVD and digital copies from www.seelivingproof.com/
Who healed from Ms
Mounia Mouniaa look for the stories on TH-cam, on two women, in separate videos, both were physicians I think, and both healed them selves Completely completely of MS. I believe both used a vegan diet. It’s been a while since I listened to the videos. Both had advanced MS.
@@janetpattison8474 i think you talk about tery Welles
There is no “healing” from MS as MS has NO CURE
The host looks like his neck is off, the C1/C2/C3 are misaligned. Maybe that's whats causing his "MS"?
I make the same facial expressions when im trying not to cry! I have Ms and i dont want to start any medication. I have always been into natural ways to self heal. The symptoms i experience with MS are real and painful. Even more scarier when i think of having to make a decisiom soon about what to do. I have been diagnose w MS on oct 2017. Apparently my nuero doctor says ive had it since 2014. I understand that now because i tie that into events that were like mid life crisis. I would like to find out how i can make the best with Ms for the rest of my life.
Please watch the video by Dr. Alfred Miller , rheumatologist, as he talks about the Lyme ME connection. Also, Terry Wahl's has a great video on MS called "Minding your mitochondria" .
I too was diagnosed with MS after decades of perplexing symptoms. I have the MS in remission 13 years now exclusively with diet. You can do it too. The diet isn't easy but it's worth it. I say that, "NOTHING tastes as good as feeling healthy feels."
The same diet Matt Embrey promotes.
Flora Lopez There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Look up Dr. Michael Johnson on TH-cam
. This doctor has made amazing progress, please look him up.
Yeah taking those pills gave me more discomfort and depression..the drugs literally drugged you, horrible experience!
lea Geronimo There are many MS diets. Dr. Swank, Dr. Jelinek, Dr. Wahls, Mediterranean, vegan. Choose one and stick with it. We do remyelinate, but it takes time.
Look up Dr. Michael Johnson on TH-cam
. This doctor has made amazing progress, please look him up.
See the channel "MS", where an American tells how the Coimbra Protocol cured his MS.
Protocol, Build a Protocol, I'm still Building, Good Health to you all.
Get a homeopath.
Where can I see the full doc?
james flana : I’m watching it on Amazon prime.