My wife's neurologist misdiagnosed my wife's MS as a stroke for eight years. After that he diagnosed MS which she had for 26 years before she passed. She was unable to ambulate for the last 15 years. I was her carer for almost all that time and it had a very significant impact on my own health. I had a heart attack and pneumonia after being her carer for so long.
I'm 18 and was recently diagnosed with RRMS. She ordered me to get an mri, and then a lumbar puncture. She showed me my MRI, and there were small dark areas (it almost looked as if that part of my brain didn't have any light or something). Then I got the results of my lumbar puncture and basically confirmed that the pathogens I had and all the proteins and strips of whatever is in spinal fluid was able for her tell me, "so the results are showing obvious signs of multiple sclerosis" and then she explained to me how it works, why my IGG proteins were so high. She explained each section of the result and was able to answer all my questions.
I was diagnosed within 5 days of my very first attack. Woke up, had tingly feet which quickly spread up to my waist and turned into the most painful pins and needle sensations. I was then admitted to the hospital and given 3 MRIs within 5 days. That was all 20 years ago as of this September!
@@yxvraj_01 The way I define tingling - you know when you sit on your foot and it falls asleep. Those pins and needle sensations. It's like that. I think everyone experiences it in a different way. I've interviewed a few people on my channel about their experiences with MS if you want to check it out- hear how other people experience it.
@@kamarulafiq2485 Yes. My walking is not affected at all in between relapses. I can walk, run and dance most of the time. My last relapse was in 2019 but before that, I went over 10 years with no symptoms.
I spent 5-1/2 years going to the Mellen Center at the Cleveland Clinic, Dr. Rae-Grant. I was sent to at least five other specialists because he didn’t think I had MS. Yet, the other specialists kept sending me back to him saying I most likely did! In all those years, he refused to diagnose me. I’m on disability, my husband is on social security, and our savings account was bled dry. Over 50 trips up there! Multiple tests, pokes, spinal taps (which showed MS properties), MRIs, CAT scans, you name it...I probably had it. Some were so painful! I drew the line when they wanted to do a biopsy of my brain toward the end. My husband and I are very, very disappointed in this group of doctors!
I am in my 60s and have weird symptoms over Twenty years but I have tingling in my hands and feed and trouble seeing more than foot in front of me. My mother was born in Helsinki , Finland and she and my grandmother,who was born in Sweden both had a number of diff ent odd illnesses over their lifetime. I have four daughters and I am fighting this problem for all of us!
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@@herbal_doctor_isiramen I strongly suggest if u can find an herbal 🌿 Dr to help treat ur MS symptoms do it cuz it's so much better for u then the drugs that they r trying to push on u to help suppress ur amune system.
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I was in the hospital for kidney problems from high blood pressure and noticed my left eye vision went blurry. That brought in the neurologist. It was pretty damn scary to find out I have ms. It keeps getting scarier for me. I started a shot 6 months or so ago and my hand constantly hurts. When I sleep both hands hurt so bad they wake me.
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Is your neck injured in anyway. I have a friend whose hands hurt so badly that she had 3 disks replaced in her neck. Doing great now. She had bad disc damage in her neck. Even holding a book to read was painful.
Along with about fifty other symptoms, I get these random, debilitating muscle spasms in my abdomen. It feels like my diaphragm. It can last for seconds or minutes. Recently, I had pain and constriction around my whole torso, from the middle back, ribs, and chest. This went on/off for about a week. Could this be the “MS hug”? I was referred to a neurologist years ago, for an MS assessment. But, these symptoms come and go. So everytime I feel better, I think I’m fine. But, they always return. And I’m really bad about going to the doctor when I should. I keep wondering if this is RRMS.
I have lupus, and recently had scan of brain for lesions for MS because of symptoms im having, walking different color intensity in one eye compared to other, every eye test done i think, they look fine, im a "mystery " as my rheumatologist says, blood work has been good. Haven't had contrast mri, or spinal. Any suggestions
@@paulkeelan7465 thanks for your reply, just this morning I got an added symptom diag that I researched, and it could be caused by MS. Granted it could also be other causes but. My MRI, was not with contrast. So thanks for your reply
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I have been having paresthesia blurry vision and vertigo reacuring every other day for 6 months had ct scans and they all came back fone im 31 currant smoker and i think o have this im getting a mri hope they can help me
@@firefighternumber9277 As the doctor said, Generally MS is the degrading of the myelin sheath over time, and he mentioned the involvement of the immune system, I am definitely not a doctor, but based on that I think we can conclude that it’s an autoimmune disease. So if you think about it, it’s like asking if an accident can cause an autoimmune disease, I don’t think so
@@aaronnorman9755 you are right I've done a lot of research in the last few months and it's exactly what u said... But I think that was the trigger point for me...
I have conversion disorder and essential tremors and have symptoms as if I had a stroke or ms or Parkinson’s and sometime wish I had ms or Parkinson’s cause fnd I’m suffering and it rough and changed my life a lot , so I been documenting my symptoms and made a RU-vid channel on it ..
Conversion disorder is an outdated term used in psychology referring to “it’s all in your head.” The term is defined as converting psychological or mental thoughts or anger toward your parents etc., into physical discomforts. You do not have conversion disorder. This is the mental health fields cruel joke on society.
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Interesting; the way the Aftermath of the Disease can clearly be diagnosed, but The Cause(es) in fact go on Continuously as Undetectable. For example: I take my Car to my Mechanic for my car, that is sputtering and stalling. Mechanic says: Yes, your car - definitely has an Engine Misfire, ...and to Treat the engine's symptoms, I'm going to have to charge you $500-$1,000.00 "each time your car begins having this problem." ( Mechanic knows it's sugar in the gas tank but says nothing...) ..' Well, I say: OK- He's a professional, so I guess it must be done, and I'm out Thousands of dollars each year as the problem comes, goes, and gets worse. But suddenly, something happens: ' Turns out: I just so happened to have a burglar that was spotted at my front door. So my Wife and I watched him, walking up to the front door with tools, wearing gloves and a mask. At the same time, there in the background, was a juvenile from next door, who got into a big fight with my Son, and so We when we looked at the video, We Would see him, the night before We took our car to the shop, and He could be seen, Pouring Cups of Sugar into our Car's Gas tank! Question: !? 🤔 "Are We Merely Treating our Car's Symptoms, or should We have just used a proper camera sooner and went over and had my own Son Kick his Ass..?? Friends, this is Exactly what is happening: All Treatments for Symptoms, but No Research on The Cause of MS. Simple!