16 Multiple Sclerosis Symptoms Early Warning Signs
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- Опубліковано 8 жов 2024
- Common early signs of multiple sclerosis (MS) include: vision problems. tingling and numbness. pains and spasms. weakness or fatigue. balance problems or dizziness. bladder issues. sexual dysfunction. cognitive problems.
Multiple sclerosis (MS) can cause a wide range of symptoms and affect any part of the body. Each person with the condition is affected differently.
16 Multiple Sclerosis Symptoms Early Warning Signs
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16 Multiple Sclerosis Symptoms Early Warning Signs
By Stay Healthy
Why do most physicians (PCP and Neurologists) think that MS does not cause pain. Pain and fatigue are the biggest two roadblocks. I am tired of getting asked if I am drunk or high.
story of my life!
Many people have MS without physical confirmation, physicians diagnose based on symptoms and ruling out other diseases/disorders. I have also found in my research that 3 out of 4 people diagnosed, are misdiagnosed..studies have found some people die having had MS throughout life with little to no symptoms...the disease is very unpredictable as to how it will affect each individual. I know a mother and daughter whom both have MS the mother leads a rather normal life having flare ups time to time...the daughter by 33 has lost many abilities and function, cannot work, and has terrible memory loss day to day. It varies extremely person to person as to how it impacts their ability to function as they once had....I care for a woman with MS..she can only control her head neck and lift one arm. I am experiencing the same frustration...however no one can explain or believe the pain I am in..mostly because of my age...i have a cyst inside my spinal cord but that isn't the cause to my pain or any neurological symptoms I have "so they say" I am always having medications, tests, and therapy thrown at me instead of someone actually reading my medical history back 15 years and seeing the progress and changes In symptoms
#goodluck #wishyouthebest #staystrongandfight
Tell them next time to take a blood test for alcohol and a 12 panel drug screen...
I used to smoke weed socially when I was younger and I got diagnosed with this so now people actually think I’m high when really I’m suffering in the inside
@@cryptic4446 fuck what people think, no one knows how your feeling but you. Something that I learned in the 8 years of having m.s. I also smoked allot of weed , n still do it kinda helps the pain some what.
my father was diagnosed with MS at 22.. never bothered him majorly until he woke up on his 32nd birthday unable to talk or walk, went into the hospital on his birthday and died 3 months later on his brothers birthday. this disease is terrible, it took my dad away in the blink of an eye. doctors said they never seen MS impact someone so quickly as it did my father (pratically overnight)
I hope research progresses to eventually cure this horrible disease.
RIP Barry A Bower 9/15/1973-12/09/2005
Sean Allen So sorry for your loss. I notice your father was born the same year as me - 1973. He was so terribly young to have died 13 years ago. It really hits home how precious life is. Sending hugs from New Zealand.
So sorry for your loss. My hysband suffered 20 years with that disease before he died. A cure must be found now !
Sean Allen ~ I’m so sorry for your loss.
Accept my condolences. Did any of his siblings or kids was diagnosed with the MS
Sorry for your loss . Thank you for sharing and yes I have a first cousin with ms and I have these symptoms, every single one but I'm starting to give up I've been diagnosed with everything under the sun but never get a solid answer to my problems .
I have had a lot of the symptoms since in my 20's!Saw a handful of doctors, dozens of different tests!Yes there are lesions but 'they are old'!
Here I am in my late 60's suffering tremendously with no help no diagnosis
Still fatigue?
I did not realize that the symptoms were there in my early teen year's. Was diagnosed on Halloween of 2000. Dealing with this disease for 18 year's. It doesn't scare me because I have always been meaner than that. Plus I had to raise 3 young sons'. No was was I ever going to give up. I still won't.
❤❤❤
I have all the symptoms except experiencing seizures or slurred speech. Numbness/tingling sensations used to come and go but now its been a year and consistently lingers making life messerable. I'm only 26!
the scariest symptom of MS is slurred speech. Being unable to speak properly... thinking one thing and it comes out as something else. i cried thinking it was a stroke but my mri said otherwise.
Ornella Sonya Hernandez yeah, i had it,that's how i find out about my ms, it was fucked to not be able to speak normally ,then my speach comes back again like it was before
Look into the coimbra protocol, I am doing it, it works.
Ornella Sonya Hernandez where are you from?
I've have problems speech for months as described now I'm scarred , even I told told. Someone's got laughed at called me stupid, and have had 2 hiking sticks to walk
I can't stand it when I stumble for words. I'm not ashamed though. It's a product of the MS & I will not apologize for something the disease is causing me to do.
I was diagnosed with MS a few months ago when I turned 18... Idk why I'm looking up Ms videos because it is truly stressing me out😭 I hope that all of you live long and healthy lives
Wow so sorry to hear that I’m only 19 years old and was diagnosed a month ago💔💔
@@o_o3323 I haven't really gotten the opportunity to talk to another person with ms before. I hope it isn't too hard on you
Lily xox I have my days but same too u 💯 be strong u will get threw this 🙏
@@o_o3323 Thank you 🙌🏽 Wishing you for all the best
Lily xox same to u god bless🙏💙
I wasn't a afraid of haveing Multiple scrousus until I watched all these videos....😎😢😢😢😢😢
It might give you anxiety.
Not to worry i know persons who are in their late 70s and have had ms in their twenties.
@@shawnmcanthony5724 in wheelchairs? Or still standing?
You ever get checked?
I was diagnosis with MS in 2002 I woke up I was numb from the neck down. I went to the hospital. One of my father's good friend. My father was a family physician Dr call my dad told him I needed a neurology it was horrible I said to myself now I know how faster felt laying on a bed of nails. I haven't had a system or any sign of MS.
I had a live in love he smoked pot. I started smoking it. Within two weeks I could feel my toes then I felt better. It helped me. I have relapse remitting kind of MS.
Michele Dunsworth my mom had MS and I was diagnosed in 2007. Is their any indication that could tell if you were going to have an relapse? My biggest thing I deal with is fitgue
I have been smoking weed when I started having symptoms and the numbness and tingling has gone away for the most part.
K Javonne where do you get the tingling ?
I have almost all these symptoms except paralysis but I have SCD also a progressive lifelong condition
Before I was diagnosed I woke up one morning and could not sit up in bed for two weeks. The room was spinning so severely that I could barely walk. And it lasted and different levels of severity for 3 months. I also suffered from vision loss that would come and go, figured it was just an ocular migraine. One day my vertigo got so bad that I went to the hospital and they did an MRI and found lesions on my brain. It completely freaked me out when the doctor came in the room and started talking about MS.
wike1138 is it vital to gave a spinal tap test or can I refuse and still be diagnosed with MS?
I woke up like you with vertigo and maybe MS
So said MRI
Double vision
Just about every symptom on here.
Scary maybe overdue for check.
Cheerful voice for finding out you're doomed.
16 signs Blurred Visions.TIngling and numbness.Pain and Spasms.Fatigue and weakness.Promblem with your gait.Bladder and bowel Problem Cognitive Problem Emotional disorder.Seizures.Hearing loss....
I was diagnosed with MS many years ago. Just this past month i was diagnosed with ALS Lou Gehrig disease.. Now which one is it? One or the other. Or can you have both.
You can have both
It's no coincidence that these symptoms are also related to insulin resistance (a.k.a. hyperinsulinemia) . The more you know.
I have MS and it does cause a lot of pain
Other symptoms mentioned here can also be a signs of other diseases such as Peripheral Neuropathy, Atherosclerosis (on peripheral artery), Stroke, Diabetic neuropathy, Potassium deficiency, Vitamin B12 deficiency (Pernicious Anemia), Dry beri beri (Vitamin B1 Thiamine deficiency), Fibromyalgia, Myasthenia Gravis, ALS. Guillain-Barré syndrome. etc.. and worst case, brain tumor
Add folate deficiency to the vit B deficiencies. Often go together if baby malnourished in utero.
ALS ...noooo.. why mention that..
I've been sick since June of 2000, the 1st doctor I went to told me nothing was wrong 1 told me it was in my head at this point I'm in a wheelchair and everything was a big blur & double vision so this 1 dr.said i think i know what it is but i don't believe in this disease and treated me like trash, I've went all over the place different states to every kind of doctor there is and I had ALL these symptoms and more but no-one wanted to help me, finally in 2009 I went to a Indian neurologist where I live(that other doctors told me not to go to) examines me and looks thru all my medical records & all the tests they did on me and asked me why haven't the other doctors helped me its right here what's wrong with you, you have MS all I could at that time was😢😭if it wasn't for him I'd still be lost. after looking at some post now I know more about my MS & how to deal with it
cassandra richardson so sorry for the treatment pot
To go to some many so called ‘Health Professionals’ and receive such poor service is deplorable, to say the least.
cassandra richardson I am so sorry for what you have had to deal with .. it’s awful that not 1 of those doctors was able to make a diagnosis way back then .. Again just shows how we have to be our own advocate and fight for treatment and testing and human right !!! I hope and pray that you are getting good treatment and care now and that it’s manageable.. take care my dear I will pray for you
Thank goodness u found someone to help u!!
cassandra richardson could you share a doctor's name because I have had the same problem. To many doctors and no answers and this has been going on since 1994. Thank you for any help!
Thanks! Shouldnt have watched this video. I have almost all these symptoms. Thats what i get trying to self diagnose. ✌
Have you found out your official diagnosis?
Hope all is well.
You ever get checked?
Sighhhh..damn computer voice 😠😠😠
I feel the same as you!
Dude it’s so annoying
it's often pull who are hearing impaired so they type it out to computer
I'm pretty sure I have this and I am so sad. It all came on so suddenly.
Do you have to have blurred vision? Could someone have all of these symptoms and not the vision
You don't have to have the blurred vision. It didn't affect my vision in the beginning. Years later but not in 2010 when I was diagnosed.
How do thay find if MRI scans are fine
Crazy my Dr diagnosed me with Parkinson's...yet more of my systems are MS related. No real test have been done due to no health insurance. So now on maximum dose for Parkinson's. Ugh.
That’s awful.
What symptoms did you have
Who to diagnose what are the test please guide.
i had pretty much all of these sympotms a year ago and then they dissapeared. Now, they are back. idk what to do. doctors dont take it seriously...
You need to see a neurologist who will schedule an MRI. This is the most telling and reliable way to see.
Agree with the MRI thing. Spinal tap only if needed but not at the top of the list. I had a neurologist order one and damn if I had just done the MRI. Horrible thing. I'll never have another spinal tap in my life.
@@raptureready3015 im getting a mri soon. Were u diagnosed with ms thru the spinal tap?
Oh hell no. I was diagnosed through MRI but he had me do a spinal tap as well and that was so crazy and I was already so scared. They found 2 small lesions on my left frontal lobe and the absolute best advice I can give to you babe is to be proactive and ask for the very best treatment immediately. I know you're scared. You gotta be. Listen. I waited 2 years. I went from 2 small lesions to my entire brain being covered in them. I went on Tysabri. It's an infusion drug. Every 28 days. Last year I switched to Ocrevus. Ask about those drugs. There are so many different drugs now that can help you stabilize this nasty disease. Watch your diet and don't forget that we are called warriors. Love to you. ❤️
@@raptureready3015 Thank you so much for your kinds words. ❤️ If The mri shows that i have ms ill take your advice! Could be Something else too, i dont know... Sending love back to you 🥰
Is it possible to have all these symptoms with a clear brain MRI, and still have MS? I’ve heard that’s what happened to Montel Williams, that his brain scans kept coming back fine and was misdiagnosed for 16 years! I truly believe I’m being misdiagnosed but can’t get my neurologist to listen to me, I feel like just giving up😞
Tina Lancaster From what I have researched, yes you can have a clear brain scan and still have MS. My doctor wasn't sure with my brain scan so he ordered a spinal tap, he said it would take 6 weeks to find out but 1 week later he called me back in his office to tell me there was no doubt I had MS.
I was mis diagnosed for 10 yrs I was numb and tingling and my vision went out in one eye for 2 weeks..all this at the same time in 99 so yes you need to look for another neurologist Dear ❤ I was finally diagnosed in 2009. Best Wishes Love
Tina Lancaster ... yes, this is what happened to me
yes and it feels horrible even when your dr doesn't want to do a spinal tap test. I've been so fed up with my dr not wanting to test further and giving up on me until I go blind again or cant walk or talk or move my arms... so she wants to wait for the worse to diagnose me all cause my mri came back clear but the issue was that i had to wait over a month for my mri cause there were no sooner spots open and during the time i was waiting i was blind in my right eye and slurring my speech and having seizures non stop. by the time i got my mri everything was already pretty much gotten better, almost completely gone but just cause my mri was not soon enough they basically just missed it... I'm suffering at home and tbh here in cali theres way too many ppl here that also go to the drs so that will slow down the chances of getting help and being rightly diagnosed on time. In the past they miss diagnosed me with lupus and fibromyalgia up until i went blind so now they have taken off lupus and fibro from my chart... treatments for the both never worked for me either and they still kept wanting to say it was lupus and fibro.... some drs will play you for money for as long as they can even with clear sign that treatments are not working and will make you feel like you're crazy up until you go blind or cant speak well and so on. Ive changed many many many drs cause of that and thank god my mom was there for one of my appointments to witness how a past dr tried to play me. So my point is dont stop trying to find a dr that will help you, find one who is interested in your well being who is willing to work with your opinions and ideas like a team, a dr who wont have a stick up their ass acting like they know what you feel who then wont agree to keep doing routine blood work or mri imaging just cause they dont think its necessary. they are NOT in your body and don't know the suffering you could be going through. The only dr that refused to do my spinal tap was my neurologist which i haven't changed cause I needed to see her a couple times to be able to change neurologists. If moving to another state will help then so be it. My family and I are moving out of cali cause of how expensive and packed with people its getting here but also to hope to find the better care for me.
Don't let them make you feel stupid or crazy. You have the right to question and ask and let them know they you are educated in health and medical, research it! Cause you'd be surprised that your dr could have been avoiding a blood test just to keep you coming back wasting your time and money on so many unnecessary medications and visits.
My tip for you if you believe its ms is that you change your diet to be at least vegetarian, if you cant handle that then at least cut out all dairy and red meats and go for chicken snd turkey meat. If you also dont get enough sun, have your drs do a vitamin d test cause ms can be frequent more in ppl with low vitamin d. if your vitamin d levels are low then you'll want to start taking vitamin d3. Also have your cholesterol checked, eating healthier will make it so your body doesnt have too much inflammation going on so it wont be in constant stress which will make your immune system out of wack, remember ms is an autoimmune issue and you want to keep as much stress away from it as much as possible.
Yes my eye dr wrote a prescription for a MRI and MRA she added if negative for MS do a lumbar puncture
I am doing the coimbra protocol for my MS. I am doing a lot better. No new symptoms.
Here goes,
Posting this here because I know some of you do research and think I may have stumbled upon a very important insight concerning the etiologies of various neurodegenerative disorders and maybe degenerative disorders in general.
I’ll cut to the chase and ask the question and then explain how I got to the hypothesis. It is: Is it possible that distinct neurodegenerative and musculoskeletal degenerative disorders are in fact be specific symptom complexes that correspond to dysfunction of specific substructures of the cervical ganglia which subsequently alter certain functionalities of the choroid plexus and have downstream effects on the basal ganglia and spine?
A recent medical situation in my life prompted me to conduct some personal research to better understand my condition. As a result, I became familiarized with the dynamics of a specific system of structures in the body that, if better understood and regarded as a unified whole, could potentially shed a brighter light in the etiologies of degenerative disorders.
Essentially, my research led to make connections between three structures in the neck and head: the cervical ganglia, the choroid plexus, and the basal ganglia.
A few observations became key in developing this idea about cervical ganglia involvement in degenerative disease. The first had to do with the basal ganglia. Basal ganglia dysfunction can cause a dearth of dopamine in the brain and subsequent cluster headaches and Parkinsonism/movement disorder symptomatology. This structure controls voluntary movement in the body and so in the case of movement disorders, it is usually the culprit. The question then becomes what is the fundamental cause of this dysfunction?
jamanetwork.com/journals/jamaneurology/fullarticle/784785
Thinking about a specific syndrome called Eagle’s Syndrome which often presents with symptomatology similar if not identical to that of neurodegenerative/movement disorder. Eagle’s Syndrome is an abnormal ossification and elongation of the styloid process at the base of the skull that interferes with the cervical ganglia and carotid arteries in the neck and creates symptoms.
actascientific.com/ASDS/pdf/ASDS-02-0202.pdf
I wondered if superior cervical ganglia dysfunction could have downstream effects on the basal ganglia and cause disorder. So I began to attempt to understand the dynamic relationship between the cervical and basal ganglia.
I began to look more closely at the cervical ganglia, in particular the superior cervical ganglia. This structure innervates the eye, parts of the face, the throat and sinuses, stimulates mucous production, has a part in regulating heartbeat (an aside: the disruption of the cervical ganglia when an Eagle’s Syndrome sufferer turns their head can result in panic symptoms: palpitations, dry mouth, gagging, so this could be a tool when thinking about mental heath physiopathologies as well), and also found that it is the only peripheral structure that sympathetically innervates areas of the head and brain. In particular, it innervates a structure in the brain called the choroid plexus. This was the next bridge on my way to the basal ganglia.
en.wikipedia.org/wiki/Superior_cervical_ganglion
The choroid plexus and found that it has a few very important functions: 1. To release transferrin that promotes iron homeostasis in the brain 2. Send agents to bind with antibodies to be flushed out of the system when infections are resolved and 3. Stimulate production of cerebrospinal fluid. That all struck me as fairly promising.
en.wikipedia.org/wiki/Choroid_plexus
I started with antibodies and found articles about post-infection movement disorders (specifically PANDAS, about which there is now literature about non-pediatric cases) where it is shown that sufferers have anti basal ganglia antibodies.
www.ncbi.nlm.nih.gov/books/NBK333433/
It struck me that if a substructure of the cervical ganglia that innervates parts of the choroid plexus that promote production of antibody binding agents is dysfunctional, an infection could very well trigger an indefinite autoimmune response, attacking the basal ganglia and other systems. Some neurodegenerative and degenerative disorders like MS are thought to be autoimmune, and disruption of the cervical ganglia and subsequent introduction of infection could precipitate an indefinite autoimmune response. Symptom progression might depend on the nature of the ganglia dysfunction (if it is ongoing, say, due to injury and resulting occlusion, or intermittent, say, due to Eagle’s Syndrome, in which turning the head causes ganglia disruption), theoretically accounting for the different subtypes of MS.
www.nationalmssociety.org/What-is-MS/Definition-of-MS/Immune-mediated-disease
I also had the thought that if iron deregulation in the brain could be caused by dysfunction of a specific substructure of the cervical ganglia and subsequently the choroid plexus, maybe iron irregularities in the basal ganglia would be observed in sufferers of movement disorders, and sure enough, it’s observed in most, if not all of them. At this point I felt like I was really onto something.
www.ncbi.nlm.nih.gov/m/pubmed/22266337/
And then a thought occurred to me: what if the first domino to fall in the etiologic chain of ALL of these degenerative disorders begins in the cervical ganglia? This could be why there are peripheral nervous system symptoms that manifest early in diseases like MS (the cervical ganglia innervates the eye and throat and heart, so vision dysfunction, dysphasia, heart rhythm problems etc would be some of the first symptoms you’d expect to see in this etiologic formulation). I’d seen papers talk about a corticothalamic basal ganglia circuit, but not much of anything about the cervical ganglia or choroid plexus, and I thought, “maybe the cervical ganglia is part of that circuit, affecting it indirectly but very profoundly.”
Not everyone who suffers from degenerative diseases would have Eagle’s Syndrome of course, but maybe there would be occlusion/tortuosity of the ECA or cervical ganglia, or maybe a trauma shifted their positions leaving the cervical ganglia susceptible to injury, or maybe genetic degenerative disorders’ gene expressions simply omit instructions for certain substructures of the cervical ganglia to form and subsequently instruct the choroid plexus.
So the idea is, if there are three main tasks of the choroid plexus, then there are seven combinations of those tasks (1; 2; 3; 1+2; 2+3; 1+3; and 1+2+3), and there are two ways for each of those tasks to dysfunction (over-firing or under-firing, although I’m not exactly sure about this detail), then each combination of simultaneous or sole dysfunction of cervical ganglia substructures which correspond to areas of the choroid plexus that are involved with completion of one of these three tasks would represent a distinct symptomatology-i.e., a distinct degenerative disorder.
Important to note is that for antibody binding dysfunction due to lack of transferrin to become part of a neurodegenerative symptom complex, it may require an initial infection of a certain type to kick-start an autoimmune response strong enough to manifest in this way. In my reading about PANDAS I came across mention of “molecular mimicry,” and I thought maybe it was possible in the case of infections that feature such molecules, and in patients that have cervical ganglia dysfunction, that since the infection that the immune system (now totally unchecked by transferrin-aided antibody binding) is targeting resembles healthy structures in the body that all of these factors compounded could lead to ongoing destruction of healthy body tissue.
It may be the case that I’m off base, or there are ways to easily prove false all that I’ve said, but I don’t know that. That’s why I’m posting, because in the unlikely event that this is not totally crazy, and might actually be plausible, it will be in the hands of people who can do something with it. A theory is judged by its explanatory power, and to me, this one seems to explain a lot. Could it be the skeleton key that unlocks understanding of these diseases and leads to new treatments and potentially cures? Is it simply that the cervical ganglia needs to be attended to more intensively when these disorders manifest?
According to the literature, somewhere between 80-95% of Eagle’s Syndrome patients who undergo styloidectomies have complete cessation of symptoms. If I am right about the cervical ganglia’s role in degenerative disorders, and some of these patients’ styloid process was in contact with their ECAs and cervical ganglia, the neurological symptomatologies that presented may well have progressed into full-blown neurodegenerative disorder if left unaddressed. It could very well be the case that these successful surgeries represent instances of the curing of previously thought to be incurable neurodegenerative conditions. But again, Eagle’s syndrome merely represents one mechanism of action that could cause cervical ganglia dysfunction.
I’d appreciate any response, even if it’s to tell me why I’m off base. I hope you’ve read with an open mind, and were willing to ask yourself “what if?” So, the question is: is it possible that superior ganglia dysfunction is the primary etiological feature of a host of neurodegenerative disorders? That this could be a unifying theory?
Hey , I've tried read the whole literally paper u wrote , but I have some questions hopefully u can answer???
oh god. im having tests done tomorrow. hope i don't have ms. i have these symptoms.
How did it go?
Been having ms for 10 years now. Sucks!!! I'm 36 now, it does cause me to be tired. I drink energy drinks daily...
Many MS sufferers have found relief using high dose vitamin D3, vitamin B12, magnesium , omega 3 oil, CBD oil please do some research into alternatives , the earlier you treat the symptoms the better the recovery. Good luck
Look up dr. Alan MacDonald. You'll learn what causes MS and how to properly treat and maybe heal it (among other autoimmune and emotional problems).
I have 12 symptoms and it's freaking me the hell out! 😔
Why do you constantly show flashes of white which hurts our eyes. Very inconsiderate.
I'm showing several of these I'm 54
I just got diagnosed with ms today anybody have any tips ? I’m 27 years old btw
I am sorry that you have to face this scary disease. It seems unfair and my heart goes out to you. As horrifying as it may seem and perhaps even as hopeless you may feel. Please know that there have been huge advances in understanding and treatment of the disease in just the last couple of years. Get preventative treatment as early in the disease as possible. My wife was diagnosed in 2013 with RRMS (although we know she had a flare up the year before). I still remember when we found out how scared I felt for my wife and how helpless she felt and how helpless I felt to assuage her fears. I was scared what was in her, mine, our future.
Just keep up on the science and emerging news as much as possible there is extreme optimism to be had in the arena of stem cell therapy (which is likely a cure if the immune system is killed with chemo and then rebooted with stem cells). There has also been huge strides in immunosuppressant therapies which drastically reduce or eliminate activity all together. These are still so new that their effectiveness can only be assumed tentative because there hasn't been enough time to tell (5 year data still shows NEDA or no evidence of disease activity in many of the patients). Change your lifestyle, if you don't eat healthy or aren't active...change that. Workout, eat as healthy and clean as possible. Cut out all processed foods and preservatives. Start taking vitamin D3 and establish a healthy gut biome. I know it sounds weird but they think there may be a link with leaky gut, which is caused by eating foods that poke holes in your stomach/intestines, or and by killing off good gut bacteria through things like antibiotics.
There was a few years of trying several different drugs with relatively good outcome Gileyna and Tecfidera. We had no health insurance when she was first diagnosed and so she got the Gilenya through a dosage drug study at the MS center in Seattle, WA. However, she got plenty of free MRIs with contrast that helped establish the course of her disease activity. She was still getting silent lesions on her brain MRI scans (meaning the disease was still progressing) but they were presumably mounting at a much slower rate that without drug intervention. Just because you feel fine and show no outward symptoms doesn't mean that the disease isn't reaking havoc on your brain. Your brain has an incredible ability for elasticity meaning it can be under attack and receiving damage and alternate nuero pathways will be used so that you feel no symptoms even though your in an attack. My wifes silent lesions were such that her neuro said it was a fairly aggressive disease. She was persuaded to take a more aggressive approach by taking Tecfidera. She got Tecfidera for free somehow through the MS center and because we were not married at the time and so the state paid for everything. Tecfidera did even better than Gileyna but the drug is considered very dangerous as it can reduce a certain type of immune cell to the point where you are susceptible to brain infection and death. As I said, there was still 'silent' lesions on her brain MRI though which means technically the disease is still progressing but at a markedly slower rate which is not comforting because you are still progressing towards some sort of unknown disability.
Now we are married and on a better health insurance plan and my wife takes Ocrevus which is only a few years old. You go on, get an infusion and the drug works in you for 6 months. The drug has a good safety profile as it has been in use for other auto immune diseases for like 20-30 years (it is reformulated with human protein instead of mice protein). She gets 1-2 MRIs a year and there has been ZERO activity on her scans. That is also what is being reported for most if not all who take it. This is the first therapy for primary progressive MS as well. Long story short, this drug in conjunction with lifestyle change is a God send. My wife has had MS now for approx. 7-8 years and has no disability, except for slight numbness in her pinky toe that is from her initial flare up in 2013. She goes to the gym, we go on hikes, she plays with our son. She is in better shape now and can do more physically then when we first met 14 years ago. Also pharmaceutical companies will work with you. Our insurance pays for about 35K of the Ocrevus and then the pharmaceutical company pays the rest for us. If you don't have insurance apply for drug studies, trials, and work with bio tech companies, they will help people who can't afford the drugs.
Attack MS from as many angles as possible (i.e. get on a treatment EARLY, workout, eat right, live healthy, supplement your body with inflammation fighting foods, take probiotics, become an expert, etc). They are starting to believe that with early intervention and the available drugs out there, that MS progression may be preventable. Basically as long as you get MRIs with not activity, you are not being attacked by MS and therefore, you don't really have MS. I hope this helps.
Take b612,it's great for ms.
i have most of this symptoms but when i go for check up, everything was normal including my mri. I also have double vision, but at the time the doctors check my vision, everything was okay, i dont see double vision but the shaking images. The next day, i start to see double vision again. This is so frustrating. I cant go to the hospital again because of the charge.
MRI for FLAIR if negative get a lumbar puncture
DD/ GCA
I got a flu shot 3 months ago and have had leg pain and little muscle twitches in my calfs ever since. Normal blood tests and negative ANA test. I'm still terrified I have some horrible disease.
I have a similar problem, hope you have discovered the problem.
@@umbusongcobo8039 I haven't
@@blixasice are the symptoms still there?
@@umbusongcobo8039 yes
My twitches move all over with numbness of hands when sleeping and burning feets everyday like peripheral neuropathy. All the test came normal, from MRI head contrast, nervous conduct and EMG
The voice split and kept talking about two topics. This is very unusual!
Scariest symptom by far is choking.I hate it.Also losing my voice.
All these symptoms are common with Lyme disease.
I have lyme disease and just got informed I also have MS last week. After doing a loaddddd of research, there's a ton of people who believe that MS is actually neurolyme or untreated/undiagnosed lyme disease. Which actually makes some sense considering there is no actual cause known for MS....I'm not sure if I believe that or not but you're right the symptoms are extremely common.
There are several components to reducing multiple sclerosis quickly . One place I found which successfully combines these is the Denelle Multi Care (google it if you're interested) it's the most useful plan that I have ever seen. Check out all the awesome information .
Kathleen Gustafson YES THAT'S WHAT IM GOING THROUGH
I don’t think all of these symptoms are the same with Lyme, but most, and that’s why they try to rule out Lyme. You can diagnose this with MRI and Spinal tap, and can’t with Lyme, that I know. I was bit by a deer tick 3 times in just a few months while living near Wisconsin. I had the large bullseye mark and was given antibiotics, but the doctor never told me what it was, I was in the Navy, and it was boot camp, and I’m not sure I trust those doctors. Over the years I’ve had signs of Lyme or lupus, but never considered MS. I was even diagnosised with anxiety and depression, then bipolar, but even now I question it all and come back to Lyme, and recently saw all this! I have all over these symptoms, I also have the poor heat tolerance and overheat so fast, especially at night, my vertigo and numb limbs now has been going on for almost two years. Yet this deer tick bit me almost 16 years ago. I could have been just having MS symptoms coming and going for years and worsening, some symptoms they chalk up to my bipolar, if it even is bipolar, and others, JUST aren’t bipolar symptoms! Anyhow I at least have an ENT appt this week to rule out BPPV and then I move on to nuero! Wish me luck, my primary has mentioned I should get a MRI as is since my last manic episode was just more like a severe MS attack.
My ENT was delayed! Waiting longer :(
I got TMS at age 14 now I'm 22
All these symptoms are similar to spine subluxation, how weird.
I’ve been recently diagnosed with it. Fatigue, lack of coordination, breathing issues and the shakes are bad. It kind of came out of nowhere. It’s scary as fuck.
How about the
Lymphatic System!??
Chengfu Saechao well the hypothalamus is very important
My doctor has given me this diagnosis. My health insurance has decided to not give me an MRI. United Health Care deems me too old at 59 to mess with. Private insurance has gone the way of Socialist medicine
Start complaining about severe shooting headaches, they may want to rule out an anurism. You've got to work around the insurance companies.
So sorry. I don't have money or insurance and can't get anything done.
If you go in having passed out and having a severe shooting pain in your head all the way through and tingling and numbness in your arms or legs , they will do an MRI at the emergency room if you go to a decent hospital. They have to. Then you can just send 5 or 10 dollars a month with each bill they send you. Also look online for an MS support group who may be able to give you ideas and help. Do what you have to do to get help.
The most challenging symptom is muscle spasms.
Ornella Sonya Hernandez yes! I was just diagnosed with MS. My major problem right is leg spasms every morning along with weakness. I'm only 47 but walk like I'm 80. Terrible.
No, its the vestibular disorder...
@@philcartier994 that was my first symptom to..
I have drop foot left side and paralysis left arm and hand 55 years old use to be a truck driver trainer and auto body /mechanic 😞
Montel Williams says marijuana has helped him with his
MMAFighter38 Montel Williams has Lupus, not M.S.. but I have heard that it does help both and so does raw veganism with B12 injections.
He has MS, but marijuana has helped him on pain and burning sensations on legs and to sleep. Marijuana doesn't cure anything.
Jaska Mäkynen burning sensation in legs is part of the disease?
It takes pain away, sleep is way better and CBD oil with thc is the best thing I ever used.
@@jameswilliam9160 It can be everybody has different symptoms
What kind of person talks like that. That was unpleasant for me, someone with MS, to listen to. Get real people to do the voiceover.
i got mri on the 1st i got most these
Howd it go?
I think I have. This , but can't afford a dr, if. I. Did
How are you now?
shit...
Dang! I've experienced every one of those symptoms.....except the sexual thing.....I've been celibate for a long time. How long? So long I can't remember the last time I was sexually active.
How many people with MS who have commented up here are still alive? Like this comment for a show of hands! 2019 anyone?
Why are the symptoms for MS almost identical to diabetes?
Because diabetes also causes damage to the nerves
Pork can cause MS.
Hello hypercohndriacs...
*wriggles eyebrows*
😓😩😭
Hi! 👋
Hello 2 years later 🖐️
So when I'm at an AA meeting and I start to twitch at random, it's not because someone just said "higher power" again. ITS MS! What a relief, now I can say, " I thought it was the drugs but turns out I'm dying, I have MS."
At the end of the meeting I'll be passing around my own basket to practice the 7th tradition.
i hate all of the symptoms
Some of these symptoms could be something else. ._. These just makes me paranoid. lol I looked this up because I just found a numb patch of skin 2x3 inches on my left ankle.
The computer voice hides the foreign language that presents this Channel
Does anyone else experience facial twitching after a hot shower...?
There is some good info in here I suppose, but whay can't you get an actual person to narrate? These virtual voices are just terrible to listen to.
This video sounds like a robot is delivering it.
Just... stop using the computer voice. Seriously, not that much work to say it yourself/hire someone to do it.
it's often hearing impaired ppl doing videos by typing
444 people just "got MS" lol
jessica Caldwell yes me too! lol
I've developed severe pain in the brain....after trying to listen to this WORST ROBO VOICE EVER. (I have many of the symptoms, but there are better and far less "spastic" sites to check out regarding this topic. So, why did I put myself through this one? I MUST be sick! )
I hate computerised voiceovers
WHY DO PEOPLE USE DISGUTING AND OBNOXSIOUS ROBOT VOICES..... I could use this information but I CAN"T WATCH/LISTEN TO THIS VOICE
often times hearing impaired ppl do these videos by typing
@@jdssurf I understand that however if that's the case just let people read it.
@@sharongagnist6428 bleh i hate reading lol. plus if i'm cooking or something i like to listen. I know, the voices sound shit though.
computer voice and i click to the next vid in 1 second
often times it's a hearing impaired person typing to the computer for voicing.
nnn
Mog is ms?