_I am so happy for my Sister, she got cured of her Multiple Sclerosis just few weeks of using Dr Madida Sam herbal supplements🌿🌿🌱.._

_I am so happy for my Sister, she got cured of her Multiple Sclerosis just few weeks of using Dr Madida Sam herbal supplements🌿🌿🌱._

Thank you!!

One you're fucked the other not as much

Thanks for sharing gives help to others ❤️

MS will lose make the possible look easy! Facilitate Multiple Sclerosis research!! Science confirmed medecal condition causative factors for Neurovascular Diseases Multiple Sclerosis and Covid 19 involve Chronic Cerebrospinal Venous Insufficiency (CCSVI) yet to be fully understood genetics and environmental issues such as infections or food/vitamin nourishment! Science confirmedcausative factors for Neurovascular Diseases Multiple Sclerosis and Covid 19 involve Chronic Cerebrospinal Venous Insufficiency (CCSVI) yet to be fully understood genetics and environmental issues such as infections or food/vitamin nourishment! Science confirmedcausative factors for Neurovascular Diseases Multiple Sclerosis and Covid 19 involve Chronic Cerebrospinal Venous Insufficiency (CCSVI) yet to be fully understood genetics and environmental issues such as infections or food/vitamin nourishment! So happens a protocol of treatment for MS and Neurovascular Disease is CCSVI Venous Angioplasty to fix mechanical Vascular issue and stem cell therapy to repair damage caused by narrow malformed leaky Veins! What is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal flow? Apparently Neurogenisis and Homeostasis side effects of Venous Angioplasty treating Neurovascular Disease CCSVI! ect., Ect., ECT.! As much the unproven autoimmune theory so called MS is being referred to as a slow Stroke! #BloodFlowMatters Keep in mind! Supplying Oxygen and Nutrients to every Cell in a Body, Blood circulation, including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! Nothing else matters! Science!!! FB Group: MultipleStenosisSociety facebook.com/groups/493935520792751/?ref=sharec Apparantly nothing else matters critical Healthcare research facilitate collaboration defining the path forward establishing the understanding and treatment of Neurovascular disease organizing unified clarity in Science knowledge and progress! #CCSVI 'Fluid leaks from small blood vessels and collects in tiny air sacs in your lungs so they can’t fill with enough air' #microbleedings #BloodFlowMatters So happens CCSVI is a MINIMALLY INVASIVE TREATABLE Congenital Science Confirmed Recognized Medical Condition studies show causative factor so called Multiple Sclerosis and role/part 43 other so called Neurological Afflictions Including Migraines, Asperger Autism, Dementia/Alzheimer's, Aphasia, Optic Neuritis, Tinnitus, Transverse Myelitis, Parkinson's Disease, Lyme Disease, Meniers Syndrome, Ehlers-Danlos ect., Ect., ECT.! As much the unproven autoimmune theory so called MS is being referred to as a slow Stroke! #BloodFlowMatters Keep in mind! Supplying Oxygen and Nutrients to every Cell in a Body, Blood circulation, including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! Nothing else matters! Science!!! FB Group: MultipleStenosisSociety facebook.com/groups/493935520792751/?ref=sharec Apparantly nothing else matters critical Healthcare research facilitate collaboration defining the path forward establishing the understanding and treatment of Neurovascular disease organizing unified clarity in Science knowledge and rogress! #CCSVI Establish Venous Cerebrospinal Blood flow treatment, as a primary care option treating Neurovascular Disease, eliminating the cause of disease SymptoMS!!! #CCSVI Multiple Sclerosis is strong and you often need help. Make you be worthy of this help, don't stand in a corner complaining, do your part! 💪 #Symptoms often ease/DISAPPEAR Facilitate Collaboration Neurovascular Disease Research! #CCSVI FB Group: MultipleStenosisSociety t.co/YYPIA4tRuM So happens, to mention apparently, Neurogenesis and Homeostasis, are often side effects of Venous Angioplasty treating CCSVI!! Apparently sooner treatment best possiblity Symptoms easing or disappearing. 1/1 #CriticalHealthcare_Research #CCSVI Cardiovascular/Neurovascular Disease including Heart function & Dopamine related Mental Health Depression Vascular Disease issues! #Vascular t.co/PdmbyVDbcy Time for Learning Science #BloodFlowMatters Apparantly nothing else matters critical Healthcare So happens CCSVI a TREATABLE Congenital Science Confirmed Recognized Med Condition STUDIES show causative factor so called Multiple Sclerosis & role/part 43 other SO called Neurological Afflictions Incl. Migraines, Asperger Autism Dementia/Alzheimer's Aphasia Optic Neurtis Tinnitus Ect! facilitate collhaboration defining the path forward establishing the understanding and treatment of Neurovascular disease organizing unified clarity in Science knowledge and progress! Have you tried learning about best possiblity to eliminate cause of SymptoMS! Can you relate? Connect with others who know about #CCSVI and #neurovasculardisease on FBGroup: MultipleStenosisSociety! facebook.com/groups/493935520792751/?ref=share WORLD CCSVI AWARENESS MAY 3 - 10 So happens CCSVI is a MINIMALLY INVASIVE TREATABLE Congenital Science Confirmed Recognized Medical Condition studies show causative factor SO CALLED Multiple Sclerosis role/part 43 other so called Neurological Afflictions! #CCSVI So happens CCSVI is a MINIMALLY INVASIVE TREATABLE Congenital Science Confirmed Recognized Medical Condition studies show causative factor SO CALLED Multiple Sclerosis role/part 43 other so called Neurological Afflictions! #CCSVI

Carnivore Diet can cure MS... period. Refer to Dr Shawn Baker, Dr Ken Berry amongst others.

The Carnivore diet is the best and most natural way to treat and cure MS.

Thank you Dr. Shin your very compassionate

I've been diagnosed with MS and LEMS (Lambert-Eaton syndrome), they both have almost the same symptoms. I was supposed to start Ocrevus treatment for MS. But I just called (just before I posted this) and told them, "Let's hold off on that", until I can get a 2nd opinion. Half a dozen reasons: Having 2 diseases with the exact same symptoms? Possible, but not as likely: If I do have both, MS treatment alone is probably not going to do anything (Ocrevus does not treat LEMS); If I do take MS treatment and treatment for LEMS, could there be a reaction of the 2 drugs? I have heard a lot about MS being misdiagnosed (My neurologist is not a specialist in MS). Everyone I have watched on KZfaq says they were given a choice of treatment. Not me! We are putting you on Ocrevus. End of story. Throwing the dice for all the side effects I've heard about Ocrevus when I'M thinking it may not work anyway because of LEMS (if I even have that?). Yeah....NO!

Why... Is their so little info on this!?

Wow, this video is full of practical insights, delivered with professionalism from a true expert in MS. You can feel Laurie's compassion - Wonderful!

What is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal Blood flow?? #CCSVI #BloodFlowMatters TY DR CCSVI is definitely one of the causes of MS. The novelty for some years is that we are certain that, after studying at the La Sapienza University of Rome, there are 3 types of CCSVI: * a 1 type with patients suffering from an obstacle to the endovacular venous discharge, i.e. due to congenital or acquired anomalies that restrict and block the drainage of the investigated veins (jugular, vertebral, azygos) * a 2nd type with patients suffering from an extra-vascular venous obstruction, i.e. due to external compression of the vessel * a 3 type with patients suffering from endo-vacular and extra-vascular venous obstruction So to simplify we can say that there is a CCSVI of the "hydraulic" type (1 type), a CCSVI of the "mechanical" type (2 type) and a "mixed" CCSVI of the two previous types (3 type), the 2 and the 3 type represent about 85% of cases. A patient with type 1 CCSVI will have a greater indication for angioplasty treatment, a patient with type 2 CCSVI will have a specific indication for specific physiotherapy decompressive treatment (RIMA Method), a patient with type 3 CCSVI it will have an indication for both an endo-vascular dilatation treatment and an extra-vascular decompression treatment. The RIMA Method devised by Dr. Domenico Ricci of Bari is able to release compressed veins throughout their course, as shown by a publication of June 2015 after a one-year study (Internal jugular Venous Compressione Syndrome: hemodynamic outcomes after cervical vertebral decompression manipulations-Pubmed). For information: Dr. Domenico Ricci cell.3393828399 MRI IN MS VASCULAR PATHOLOGY www.dropbox.com/s/m0yvgmufgfcys1v/MRI%20IN%20MS%20-%20VASCULAR%20PATHOLOGY%20.pdf?dl=0 This quantification of the disease pathology will help! #CCSVI Venous Hypertension >microbleedings >iron >inflammation >free radicals >neurodegeneration #multiplesclerosis M.S. - Mystery Solved Mysterious Autoimmunity = CCSVI Neurodegeneration M.S. - Mystery Solved Mysterious Autoimmunity = CCSVI Neurodegeneration Keep in mind! Also venous hypertension ➡️ impaired CSF absorption ➡️ reduced G Lymphatic drainage ➡️ interstitial peptides accumulation ➡️ NEURO INFLAMMATION #CCSVI Eliminating cause of the Symptoms of so called Multiple Sclerosis will End MS. Apparently it is unquantifiable the length of time Symptom$ can be treated! If you hadn't noticed Who Knew?? #BloodFlowMatters What is the role of proper/improved Blood flow? #CCSVI Apparently #BloodFlowMatters Stroke common occurrence in Individuals diagnosed with Diabetes, unproven autoimmune THEORY so called MS Supplying Oxygen and Nutrients to Cell in a Body. Blood Circulation through and including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! #CCSVI #Healthcare game changer when the cause The doctor of the future will give no medicine, but will interest his patient in the care of the human frame, in diet and in the cause and prevention of disease. -THOMAS EDISON Best possiblity easing/eliminating cause of SymptoMS! You can relate! If your veins are blocked they should be opened if you have SymptoMS or not! MRI IN MS VASCULAR PATHOLOGY www.dropbox.com/s/m0yvgmufgfcys1v/MRI%20IN%20MS%20-%20VASCULAR%20PATHOLOGY%20.pdf?dl=0 Who Knew?? #BloodFlowMatters What is the role of proper/improved Blood flow? #CCSVI Apparently #BloodFlowMatters Stroke is a common occurrence in Individuals diagnosed with Diabetes Neurovascular Disease Multiple Sclerosis is beingreferred 'slow Stroke'. What is the role of proper/improved Blood flow in both conditions as much CCSVI has been Scientifically confirmed a causative factor in Symptoms of so called MS! Supplying Oxygen and Nutrients to every Cell in a Body. Blood Circulation through and including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! #CCSVI #Healthcare game changer when the cause of the Symptoms of Medical conditions are eliminated! The doctor of the future will give no medicine, but will interest his patient in the care of the human frame, in diet and in the cause and prevention of disease. -THOMAS EDISON Best possiblity easing/eliminating cause of SymptoMS! You can relate! If your veins are blocked they should be opened if you have SymptoMS or not! A Vascular problem led to the crippling nightmare of Multiple Sclerosis The real Multiple Sclerosis nightmare started at the point of NeuroDx The disaster of diagnosis being made by general physical observation over time,. Especially when Time is something you can’t afford #CCSVI Multiple Sclerosis is strong and you often need help. Make you be worthy of this help, don't stand in a corner complaining, do your part! 💪 #Symptoms often ease/DISAPPEAR Facilitate Collaboration Neurovascular Disease Research! #CCSVI FB Group: MSS facebook.com/groups/4939355…!

I understand, just wanting to know what's wrong.

Yeah the road of symptoms and dealing with Drs is very frustrating. It doesn’t help matters. Stress is around every corner and God forbid going through any serious live stressors like divorce and losing loved ones.

Hi! I'm 72 and have had MS since age 29 when there were no MRIs or DMT's - first symptoms were TM treated w/ steroids and recovered 97%. I did have other relapses after but didn't know what they were and I recovered w/out steroids. When the last relapse didn't remit 15 years agp but worsened I was on Copaxone for years and am now on Kesimpta for 2 years. My symptoms have traveled up my body so it is now toe to head. It advertises as for SP (my last relapse never remitted but continues to worsen) and my ms neuro said that this addresses SP. Is the advertising bogus? Was my llast ms neuro mistaken? t I saw a new ms neuro recently who said that K does not treat any progressive MS and that there are no meds for PP or SP and she would have me return to Copaxone - that K is too dangerous for me at my age because of infections - I have had 1 - thrush in my throat that has created problems w/ spasms in my throat. I have looked at the studies of aging folks w/ ms and seems the study is somewhat inconclusive and I do not want "new problems./lesions/brain damage" You mentioned that there was something for PP but didn't say wnat it was. And you didn't mention any DMT for SP. Are there any? As you mentioned every neuro has their own "opinion" about things, esp w/ it comes to these phenotypes and interpretation of studies. Confused. I'm interested in your thoughts! Thank you!

I said this years ago now i have a cane😢 Good friend has ALS i'm glad i have you ms

Wow i was diagnosed 4 yrs ago but have had symptoms years ago

Good comments so I figure I'll add for posterity .... I am a male diagnosed w/ MS at 55. From NY living in SoCaL for past 12 yrs. I had tingly hands and feet for a year and thought diabetes... Had a bad attack after a flight, when I got home and saw the Dr I got an MRI for ultimate MS diagnosis. After one year... Dr unsure if RR or PP. Time will tell. Taking full med right out of the gate (Rituximab and daily Gabapentin), I get flares but never get back to "baseline". Just gotta fight the fight.~ Meds, Diet, exercise, no stress. I don't have a lot of strength or ability to work hard, cog fog, with a little bit of trbl walking. I watch a lot of Dr Aaron Bolster on YT to learn. My neurologist (younger male) doesn't have a very good bed side manner. I think I have Primary MS but at a yr in it is hard to tell.

The carnivore diet has changed my life!

Everytime I watch your videos, first thing I do is give them a thumbs up and like the video but then I walk around my house questioning why I put up with my stupid neurologist. All 3 of mine have never addressed those 5 mentioned areas!! THANKYOU FOR EDUCATING ALL OF US IN AUSTRALIA. I’m sending this link to them now! 🇦🇺 😍🙏😉💗

I been waking up with numb hands and fingers almost every day for the past month and a half. I was asked how long do your hands stay numb for , I said 3 minutes or so. And I was told the numb feeling had to last 24 hours . So is that 24 hours of numb feeling non stop?

Neurology is as subjective as MS itself. Don't rush to believe, or not to, a diagnosis, just based on a few generic tests. I've had rrms, spms and now ppms. Every Dr, of the 8 I've had, has their own opinions and they've almost never agreed. I've also used almost all the mainstream ms meds including Lemtrada and Rituxamab. B-cell depletion therapy is the ultimate for ms, especially with stem cell transplant, but there's no guarantee. Your ms will change and evolve from within you. Do your own research but not off the internet gossip columns but from John's Hopkins, Mayo Clinic and specialist Like them.

There is a microbiome connection. Could it be that our body is fighting a disseminated invasive microbe? And there is a collateral damage?

A great video for us MSers. Thank you for sharing! 🙌🧡

What if you have attacks early on that remits but have a slow deterioration?

"Missed" opportunity...? My ass. There isn't any money in it.

I was so lucky to get rid of my Multiple Sclerosis (MS) after using DR ALAHO OLU on KZfaq herbal supplements for three weeks. He has medicine for HPV, HSV, ALS and MND……….

I was so lucky to get rid of my Multiple Sclerosis (MS) after using DR ALAHO OLU on KZfaq herbal supplements for three weeks. He has medicine for HPV, HSV, ALS and MND……

The best video ! I have MS from 98 !!! Thanks,yes the sexuality is part of your life!!!❤

my uncle had it and he died ms he was 22 years old

I was refused DMT due to not taking the covid vaccine

What is " high cholesterol "?

You can’t fight your purpose. It was meant to be! 🧡

What an amazing video. Hero! 🧡

Dr, I'm not slamming you, but if you've had MS, like i do, for +40 years and can function so well, go to college for ?yrs and get a neurology degree and now go to an office to see patients, you Do Not know our World. You may have a few symptoms but so do millions of people. Many people have lesions in the brain and are incorrectly diagnosed with MS.

I was diagnosed with MS 11 years ago, but because my MS was very mild, I was in denial that I had it. For years, I thought I was misdiagnosed. I took my medications sporadically and, during Covid stopped taking them for about 18 months. Recently, I started feeling numbness in both feet and two fingers on my dominant hand. I rushed to start taking treatment again, but I am nervous that I stayed in denial and relaxed with taking my meds for too long. I am taking prednisone for the numbness, but it isn't working at all. I am hoping the numbness will remit soon, but I will be certain to stay on my meds this time. No more bs denial; I have the disease.

I was diagnosed with Multiple Sclerosis 4 days ago, I’ve never thought I’d catch something like this and my symptoms really sucked. The worst part of MS is when people ask me “how are you doing” or “how are you feeling” deep down inside we know we’re not okay but in the outside we look okay.

I was diagnosed this past may so very recent. Been feeling scared beyond belief. Felt like life was over. But watching this gave me so much hope.🎉❤

It takes a village

I'm just recently diagnosed with m.s. can anyone suggest anything to help with pain and fatigue?

Every relapse is permanent damage done though. Your only getting older, the damage is harder and harder to recover from. It's already hard to get insurance putting you on the highest efficacy treatment available off the bat so why would you delay the possibility of upgrading the treatment when a relapse occurs?

Nothing for PPMS...SPMS....

No one could possibly understand this disease unless you have ms like myself. It’s indescribable. Everyday is different and really tough. God bless us all. I understand what this gentleman is talking about and understand how he feels

Hi, thanks for your story and insights. I have been having symptoms for 1-2 years. Off and on. Recently I had a brain, c spine, thoracic, lumbar and sacral MRI spine. Scanned with 1.5 Tesla without contrast. All came back normal with no evidence of lesions of demyelination. My dad has MS. I wonder if the scan was strong enough or if something was missed or if this is all in my head now, what do you think Steve or should I rule out MS? Thanks

This woman is so giving the wrong impression about rrms . I had it for 20+ yrs before I became spms . Not once did I return to baseline after a relapse . Most people ( especially over time and repeated relapses) don’t go back to baseline . They are left with some disability or problem which never goes back to normal . This is why over time your disability worsens and problems increase . Like bladder weakness , worsening mobility , lack of finger dexterity and cognition problems . This woman over and over repeats how you go back to being a normal person between relapses which for nearly all ms’ers just isn’t true and gives an untrue picture to people newly diagnosed .

The Dr. found several lesions in my periventrical region. The radiologist said possible MS differential diagnosis. I have many ms symptoms. I dont know what to do. My Neurologist doesnt do anything at all. Not even explaining the MRI's ect. What do i do now?😢😢😢😢

Business bs

Who is this dr?

I have had MS for 29 years. It is not a nice thing to have. Stress can be horrible if you have MS. The main thing with is don't let it get you. Also don't fight it. Accept that you have MS and learn to live with it. Most people do not understand MS.. Just please, please do not let it beat you and you can still have a happy life. My heartfelt felt best wishes to all MS'ers.