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

There is a 3rd form of MS called PIRA (progression independent of relapse activity). This is said to be common among RRMS people. It is a new discovery. At the time you first get MS the progressive part is probably so minor that it is easily missed and the neurologist will be focused on the relapses. Also, there have been a number of posts by neurologists saying PPMS and SPMS are the same disease.

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

Another great video. I was told exactly this 35 yrs ago when I was diagnosed. Good optimistic information for the newly diagnosed.

My vision suddenly went blurry one evening which I later found was diplopia, one eye not looking the same direction as the other, and then the MRI showed three oval white spots on my brain. That was all that was needed to diagnose MS.

Thank you.

Why would the neurologist send me to a neuropsychologist?

Walking myself was difficult for me because of my parkinson health situation but am happy that Dr Madida medicine on youtube I was able to get cured. Now I can walk properly🙏🙏

Of course cost effective ness...so we continue to be sick and wait 6-9 months while other organs start failing and then have five Drs and are too sick to keep running for one test at a time for years! This healthcare system is broken! We need to be admitted and all of it done at once! $$$ is always the bottom line! So sick of lazy Drs in this country and hospitals that have to save money!!

My doctor says that my son is suffering from ppms his hands tremors doctor is giving him rituximab injection tap of the spinal cord is normal glands are normal pl advise my son is 26yrs old pl suggest

Alan MacDonald : MS is a parasitosis

I am on Gilenya - 6th year. No dusability yet- but too many plaques in brain, neck, dorsal. No active lesion now. Doc asks me if i should now switch to Ocrevus. I am afaid which is better for me. Follow with Gilenya or NOW switch OCREVUS before too late? On Gilenya, i never had attack- earlier roughly every 6 yrs.

All thanks to DR. OSAKA on KZbin Channel for curing me from multiple sclerosis with his natural herbal diet.

Have been confirmed negative of MS, thank you Dr mason channel on KZbin..indeed your medications works wonders..keep saving lives

It's clear that it's unclear

Listening to these comments is scary! I was diagnosed 5 months ago and moving on to Ocrevus next year. I’m hoping to get onto a plateau and stop deteriorating - please God!

I'm 69 years old and female. I was diagnosed a couple of years ago with (SPMS) and I was beyond scared! My lung function test indicated 49% capacity. After having had flu a year ago, the shortness of breath, coughing and chest pains continued even after being treated with antibiotics. I've been smoking two packs a day for 46 years. Being born without a sternum caused my ribs to be curled in just one inch away from my spine, resulting to underdeveloped lungs. At age 34 I had surgery and it was fixed. Unfortunately my smoking just caused more damage to my already under developed lungs. The problem was having is that I enjoy smoking and don't want to give up! Have tried twice before and nearly went crazy and don't want to go through that again. I saw the fear in my husband and children's eyes when I told them about my condition then they start to find solution on their own to help my condition.I am an 69 now who was diagnose (SPMS) emphysema which I know was from my years of smoking. I started smoking in school when smoking was socially acceptable. I remember when smoking was permitted in hospitals. It was not known then how dangerous cigarettes were for us, and it seemed everybody smoked but i was able to get rid of my (SPMS) lung condition through the help of total cure herbal foundation my husband bought, please email dr for your cure on [[email protected]] has the right herbal formula to help you get rid and repair any lung conditions and cure you totally with their natural organic herbs,it class products at affordable prices. Purchase these medicines and get the generic medicines delivered in USA, UK & Australia,I wish anybody who starts smoking at a young age would realize what will eventually happen to their bodies if they continue that vile habit throughout their life contact him via WhatsApp no +2349056393169 address good luck.

Can the other diseases be found in blood tests?

It’s just diet. You can get to remission using diet. kzbin.info/www/bejne/l2XOgZl3nM53fac There are lots of different diets for multiple sclerosis, but natural cures can’t be patented, so the conventional/allopathic medical system suppresses them. Luckily, the naturopathic doctors are replacing the medical doctors. I’m in the process of permanently curing myself right now using classical homeopathy. There’s also biomagnetic therapy or even MMS/chlorine dioxide, and other options.

What about numbness that lasts for weeks in Late Onset?

Nice

I didn't quite figure the difference between primary and secondary progressive MS? Could someone explain please

Is anyone thinking Isaac Asimov’s doppelgänger?

the best summary

Thanks for this video..I was searching for oral DMD medicines and found here...thanks again.

I got diagnosed with sinus tachycardia Cardiologist said its multiple sclerosis related..neurologist said I don't think so Unbelievable.

I've had ms at least 11 years. Diagnosis in 2013. I notice this year... covid, isolation, leaving my lifetime abuser after 19 years, my 4year old having cancer, I have been having a LOT of uncontrollable nerve spasms lately. It is sonfristrating and humiliating when I cant control it in front of others. I worry I'm getting worse or maybe im.just being paranoid and I'm fine and it's just from the stress.

if all cancer are not dealt with with ms it will continue to kill cancer are like dotcom bastard selfish ungrateful and will kill it’s own mother for some money

I keep reading that MS is not fatal. That said, just in August of this year a close friend and coworker died in her sleep. It took until just a few weeks ago for the final coroners report and toxicology tests to come out and the primary cause of death listed was Multiple Sclerosis. She did not fall, did not have pneumonia or any of the other things I have seen listed as possibilities when someone actually dies from MS. She died in her sleep and her husband only realized something was wrong when she would not get up that morning and he turned her over and her lips were blue. The only thing that I do know for certain is that she never ever had treatment or took medication for her MS and I assume she likely had it for years. Just don't understand what actually physically took place within her body that killed her as relates to MS and I have yet to read anywhere that describes anyone dying from it other than from ancillary causes. Something about her MS very definitely caused her death but what(?)

I actually made a video looking at the average Prognosis from MS EPIC UCSF Study: kzbin.info/www/bejne/enikmHZ3h9pnnNE The MS-EPIC study: pubmed.ncbi.nlm.nih.gov/27464... Of those who start with relapsing MS, the proportion who require a cane to walk 100 meters (EDSS 6.0) : 4.7% at 10 years 16.2% at 20 years over 50% at 40 years. Transition to secondary progressive MS is 6.4% at 10 years 24.2% at 20 years over 50% at 40 years.

Appreciate video content! Excuse me for chiming in, I would appreciate your initial thoughts. Have you heard the talk about - Seyrooklyn Salient Supremacy (do a google search)? It is a smashing exclusive guide for overcoming the symptoms of multiple sclerosis minus the normal expense. Ive heard some extraordinary things about it and my old buddy Taylor got amazing success with it.

Cheers for the Video! Forgive me for butting in, I would appreciate your opinion. Have you tried - Seyrooklyn Salient Supremacy (do a search on google)? It is a smashing exclusive guide for overcoming the symptoms of multiple sclerosis minus the normal expense. Ive heard some pretty good things about it and my mate after many years got great results with it.

I’m being tested now for MS. My doc said my physical exam was not horrible but my symptoms were concerning. Sometimes I feel like I’m crazy and it’s all in my head. I just want an answer.

Like when I ate something that I assumed caused by whole spine to swell and lock and put me on the couch for a week, that might not have been a garlic allergy? 🤔

I have maltapal scrousis for 2 and a half years ago

I can’t believe there is a “cure” for leprosy but none for lichen sclerosus?

Comments have been removed because he has nothing of substance worth to say. He assumes any symptoms are related lusus or ms because he has no clue, he has done no case studies and has no studied information other that what others have researched and have reported. He doesn't care enough to put in his own research towards the cause other than for any recognition OTHER that he could possibly salvage on somebody else's behalf. TYPICAL DOCTOR

I'm convinced I have this as well, is it hereditary by any chance?

Some people have lesions but no neurological condition. People have been diagnosed with MS prior to MRI’s. How so ?

I was curious, so I came here. First video I watched, the background music was alittle louder than the voice.👎THEN I came here. No music, very good explaining, and questions. Even though I'm sure my problem isn't MS, I loved the video and Dr. Thank-you very much. 👍

The questions and answers are so clear, so well explained in such short period of time that not only encouraged me to decide to talk to my doctor but kept me calm and attentive to the video..thank you so much.🙏

😳😭😭😭 at least now I have a clue

What about tingling that has lasted over a year? continuously my feet and legs feel like a low watt voltage going through my feet and legs. Muscle spasms all Over and continuous tinnitus that’s getting louder, lasted 2 years so far. My lip and chin when completely numb and that lasted a few hours. My muscle spasms seem to be having a break at the moment but my tingling and tinnitus never goes away. I did have a mri but only to check the tinnitus isn’t something more sinister. (Waiting for results)

That sounds frighteningly familiar in many ways... I had tingling on right side of face& hand, thought it was stroke went to a& e they sent me home went off next day, this happened a few times, put down to anxiety & prior medication. 3 neurologists countless MRI scans( non specific white matter they say....& small vessel disease, like its a minor thing, but they say it doesn't corolate with my physical symptoms.. 🤔🤯😱) one radiologist suspected Cadasil, saw a professor who in consultation said "you DEFINITELY don't have it" "phew" thinks me👌👌👌🍻, only to recieve official written report afterwards, saying thinks like "unlikely he has it" " Don't THINK.. your symptoms are typical" ....NOT so reassuring now,💥🙈 so genetic test begged for from another Neurologist he agreed & did test , that should take 8 weeks , waited 8 MONTHS for results, constantly having to chase EVERY THING , and I still don't have a conclusive result. Mri list since 2015 _4 brain inc 2 cervical spine, A full spine ( current neurologist wouldn't even look at it actual film, just vague report..because my gp ordered it) refused to do lumbar puncture ( despite a professor recommending I had one , to rule out inflammatory diseases)because he said " you DON'T have m.s!!! " ( ok... I'm not saying or insisting I do... but, I have many similar symptoms) I cant walk properly, feels like the weight of a 10 stone person pushing down on my legs , heavy pressure on the back of my neck& head, sort of giddy etc,I get scratchy pricking all over my body that comes & goes, cold wet sensation since December in right side of my head,weakness on my right arm and leg, reduced dexterity in my right hand, tight band around my groin, repeat negative afterimages of everything I look at 4 referrals in last year to see a neuro ophthalmologist, only to see regular ophthalmologist EVERYTIME! , MY sight gets worse, eyesight has greatly deteriorated over last year and a half, eye ache on n off strange sensations I can't explain, visual aura migraines ( without much pain ) fir a year now. ALL... I would like is to be looked at properly and by someone who will actually listen too and look at investigate my symptoms as everyone else I've encountered so far , has had done, instead of bits of tests here & there & them to actually know what they are on about & not treat me like a hypochondriac, this all started since 2015, & after a previous gp incorrectly prescribed some hefty mental health medications, after a very low dose medication change for panic attacks( I wanted to come off them but he recommended I try a different drug, it made me feel suicidal, which I'd NEVER felt before, & my legs went funny, but did he take me off them??? Nah.... he upped them one week, downed another, added another & sleeping tablet & laxatives cus I could not poo because of the meds. one bad one after another, that sent me off my head, I'm now drug free 3 + years but the stigma remains ! It's all GOT to be in his head!!! Also get muscle tremors & twitches in my eyelids, twitchy legs occasionally, mild cramps in both forearms come & go. The legs sometimes feel almost normal when I first stand after a nights sleep, but the longer I stand , after a couple minutes standing, the heavy pressure pushing my legs down worsens, if I stand still the longer I stand the stiffer & clumsier my legs get. Beyond the End of my tether😭😢 #LookingForAMiracle

Good bless oll

Can someone help me find out if I have this or hell me how to find out?

They can expect horrible horrible things and losing everything a long the way including but not limited to family home ENERGY strength and TIME!!! It steals your time!!! The pain is the worst. I have PPMS and it has taken everything from me my muscles my limbs my teeth the list is never ending. Driving going out making plans that goes away to. Cooking showering coordination speech and I just am not using comas. Find a doctor that actually listens to YOU. Not their other patients that aren't you! It should be individual care not factory care. Amd because we don't look sick my response is You don't look stupid my mistake. Lol when it progresses you can expect to be bed ridden. They hardly know because we all suffer differently yet the same in so many ways. The day they get big pharma out of their back pockets is the day MS suffer's will see REAL progress. #Freetheweed #wewantchoices #Wewantacure not bandaids

I see so many negative comments. After MS diagnosis, this is the life we have now. Other people have it worse. Whatever fate we have, quit bitchin and make the best of your life NOW!! While you have a fucking chance. We’re staring down the barrel of a shotgun. The fuck is wrong with you. Even if you’re in a wheelchair you can still live an awesome life. Freddie’s wife can’t unfortunately God Bless her. But if you can type your bullshit poor me complaints, then you can do something productive too other than whining and crying. I suffer symptoms everyday and you wouldn’t know because I have a life to live while I still can.

Can I have both lupus and ms?