Early signs of MS ( Multiple Sclerosis) I Common pre-diagnosis symptoms that are easily missed

[@adanoid]

Thank you for your info. I was so fatigued for a couple of years that every step you take is an extreme effort. The concrete footpath looks like a lovely place to lay down and frequently every about 50 meters I would lay flat on path to rest. One day we took dogs for a walk but I only got about ten paces away from car and could not proceed.

[@memsandi6445]

Fatigue is the worst! People who do not have a chronic condition really don't understand when you say you're fatigued - they just think you need more sleep! Have you had you diagnosis now?

[@trixiekirch434]

I have not been diagnosed yet but I’m having many of these symptoms. I’m awaiting an MRI. Thank you for this video.

[@memsandi6445]

Aw you’re welcome - glad it was helpful! Good luck with your MRI x

[@nabiarahim2524]

Hello

[@memsandi6445]

@@nabiarahim2524 Hello!

[@familylovencarsndogs5495]

What was the results?

[@trixiekirch434]

@@familylovencarsndogs5495 they told me complicated migraines.

[@Huntress_Hannah]

I recently found out I (probably) have MS, not diagnosed yet. Looking back on it I’ve had symptoms for years and just kinda wrote everything off too. From numb limbs to even temporarily losing a bit of color vision in my left eye. Interestingly enough, I too had a double vision and vertigo attack and it was SO severe that I had to go to the hospital, I couldn’t ignore it. They ended up doing an MRI and they found T2 spots on it. I’m waiting to see a neuro but it might be a few months

[@michelelionti9814]

how long did your numb limbs last?

[@sarahlc1978]

I have migraines all the time. Numbness in my face and forehead. Tongue tingles and burns. Muscle spasms. Eyes twitch. Seizures in my eyes. Dizzy spells. Once in awhile I get a rash on my legs. I feel exhausted all the time but cannot sleep. I have panic and anxiety now. I got blood work done a few weeks ago and the ANA was negative but the c-reactive protein was slightly elevated to 13. I'm going in for an MRI on the 22nd. I just want some answers because I am tired of feeling like this every day.

[@kaykayyyyymwaa]

This sounds a lot like my symtoms. I am currently not diagnosed yet either.

[@sophiamia3742]

At this point i'm still very shocked with the negative result I got after suffering from PCOS for so long. 🌿🌿🌿Thanks once again DR RORPOPOR HERBAL on KZbin for your natural supplements

[@sophiamia3742]

Contact DR RORPOPOR HERBAL using this link kzbin.info/door/kZwKW6qES4dXDWzb0YQErA

[@psvillanelle9398]

How did it go?

[@visi7891]

we need more people like you! thank you so much

[@deborahtawadros567]

Before I was diagnosed with PPMS(Primary Progressive Multiple Sclerosis) I was diagnosed with a few other things. First I was diagnosed with tendinitis and bursitis. Then came fibromyalgia and chronic fatigue syndrome. Also arthritis throughout my body. I also was suffered through headaches and migraines including optical migraines. Finally after years of me asking my doctor if there could be just one thing I have instead of all these other diagnoses I went and got a brain MRI. That’s when I got the PPMS. Needless to say I never went back to that doctor especially after she insisted it was all in my head and gave me a prescription to see a therapist. It was her assistant that sent me for a MRI. Since the diagnosis I also developed degenerative spine disease.

[@Skybluewindcool]

Hey how r u now....

[@Rabswood296]

I have ME, tendonitis, lower back pain, joint pain, dizziness, now practically the whole of my back is going numb, i am suffering from a huge amount of stress due to a family issue. Everything i have my doctor says is down to ME or stress so no help.

[@leaveittolefty]

"yes, it's all in my head"😜 i see sooo many instances of medical neglect, especially for women

[@leaveittolefty]

in the past 2 yrs i've been diagnosed with myasthenia gravis ( proven wrong), parkinson's ( proven wrong)...peripheral neuropathy ( correct), sensory neuropathy (correct) and Charcot-Marie-Tooth ( genetic test is inconclusive ). in meantime i continue to decline.😞

[@timglasier5593]

@@leaveittolefty congrats

[@EvenSoItIsWell]

Thanks for the video. So glad to see more channels sharing information on diet and lifestyle with MS. Well done!

[@memsandi6445]

Even So It Is Well Thank you! X

[@melissachildress2927]

Your video was very helpful. I'm supposed to find out my MRI results tomorrow. I have migraine headaches bladder issues tremors backache cognitive issues to where I can't think and my my legs get really tight and hurt. Really bad depression. Vertigo. I fall a lot . I fall a lot. I can't keep my balance. I have quite few things wrong. It's been going on for a long time. I'm pretty sure it may be MS.

[@Mah0ganyBr0wn]

This video has been very helpful in giving me a push to go to the doctor & speak up. I tend to brush things off or give symptoms a a reason as an excuse not to see a doctor. TFS!

[@summerdays4092]

I have an MRI in 3 days. I have so many of the symptoms and just want to know what is causing them. My symptoms are so similar to yours, the Vertigo and migraines were the first to arise and since then i've had dizzyness. Numbness down my left side (so badly i thought i was having a stroke at 1 night and its been reacurring ever since) with the numbness came vision loss, constant neck pain that feels like an electric shock, sharp random pains in random parts of my body, Nausia, tremble in my right hand, Feeling drained all the time, my left leg will randomly give out while i'm walking. i could keep going with all the symptoms i'm having, Even if its not MS i hope this mri finds something to explain what is going on with my body. Fingers crossed I will know very soon.

[@memsandi6445]

Yeah to me (obviously not a dr) but that sounds a lot like stuff I’ve experienced with it and I’ve got friends also diagnosed who have had similar too. If it is MS they’ll pick it up quick with an MRI. You might need to have a lumbar puncture too (I did to confirm diagnosis- seems to be a standard thing). How was your MRI though? Were you okay with it? Did they say when you’d have results? X

[@summerdays4092]

Got my results not what i was expecting but so glad to have an answer.I have intercranial hypertension . The symptoms mimic those of a brain tumor . I have to get a lumbar puncture to measure the pressure of the fluid around my brain and then figure out what they want to do to treat it. Its swelling my optic nerves as well. Glad i have an answer to the cause of the symptoms! Its a relief to know. I think treatment ranges from medication to putting a stent in the vessels in the brain that are thinning. Have another appointment in a couple of weeks with neurologist . I was totally expecting MS i think more because my dad passed away from motor neuron disease at 37 .

[@memsandi6445]

@@summerdays4092 so glad you have your answer! Sounds like there’s a lot they can do to treat it which is great. Good luck with the lumbar puncture x

[@kaykayyyyymwaa]

@@summerdays4092 could it be optic neuromyelitis?

[@gabbyfranks78]

Love all ms channels so I can know what to do or expect thank you

[@dylanware2193]

Thank you for the video! It was some good info. My sister has ms and I have been having numbness in a foot and been getting tired easier.

[@melandrodelacruz1584]

Excellent video content! Sorry for chiming in, I would appreciate your opinion. Have you tried - Dinanlinson Taking Peace Approach (just google it)? It is a good one of a kind guide for overcoming your Multiple Sclerosis symptoms minus the normal expense. Ive heard some decent things about it and my m8 after a lifetime of fighting got excellent results with it.

[@meganhenry5795]

I woke up in the middle of the night with insane tingling going through my arms. Now my right arm feels weak and my left foot feels off as well. I have migraines too. Just had one today...seemed to be triggered by heat. Not sure though. Doctors blow me off because I'm "young".

[@memsandi6445]

Sorry I missed this. You have to keep pushing - keep nagging and keep asking to be referred. You know your body and what feels right/wrong. Age has nothing to do with it - yes it’s rarer but there are young ppl diagnosed. I hope you get your answers soon!

[@OddlyElly]

Get a second opinion. I've been having issues since I was 22 and finally have a referral to a neurologist (my GP had sent me to rheumatology initially and I have a fibromyalgia diagnosis but I just know, I feel that it is something more).

[@memsandi6445]

@@OddlyElly oh I’m so glad you got some answers though that’s great 👍🏻 Have they given you treatments for fibro?

[@Karen-pk3uv]

@@OddlyElly update?

[@OddlyElly]

@@Karen-pk3uv I've seen the neuro and had an MRI which showed plaque consistent with hemiplegic migraine. I have a followed MRI booked for November to see if anything changes. Going to push for a lumbar puncture test because my vertigo has only gotten worse over the last year. Thankfully my team haven't dismissed my concerns - just that we'd need more testing since there isn't a lot they can see yet.

[@gabbyfranks78]

I had fatigue blurred vision as well as pins and needles in my feet that would come and go. Thank you for the video

[@loisdanes176]

I have all of that. Can't wait for my mri

[@latelyknzi]

I wake up with numbness and tingling in my right arm and hand a lot. I am clumsy, I trip over air. These last 4 months I have been having this weird electric shocks in my left side of my neck. It happens when I move my neck in a certain position. It happens everyday, sometimes more than once today. It’s always brief and scares the living hell out of me. I have loss of sight in my right eye more than my left. But I overall have bad vision. I get muscle cramps in my hands and stiffness in the back of my calf’s. I feel tired all the time, and feel like I have no energy everyday. I haven’t been to a doctor yet, but this electric shock feeling has been the big thing that has been scaring the hell out of me. I get lower back pain from time to time. Opinions? I am 20 years old.

[@memsandi6445]

Honestly that sounds a lot of MS symptoms but it’s a bitch to diagnose without an MRI. I’d pester your dr to refer you so you can get answers. Good luck x

[@traceytansley1659]

Lehermites I think is when you look down, chin to chest and get a shock sensation down your spine, an MS symptom.

[@lindseym3810]

Thanks for sharing this info. It’s such a difficult disease to diagnose.. I meet many of the early signs but I’ve also been diagnosed with connective tissue disorder, high intracranial pressure, chronic inflammation & pots/dysautonomia. My maternal grandmother had MS and some of my health issues increase the risk so I’m always looking for info. Wish you all the best 🤍

[@Loveandkindness33]

Do you have EDS and IIH?

[@lindseym3810]

@@Loveandkindness33 Yes I’ve been told that I have both

[@angelfuentes9132]

I got a brain mri and it came back normal.But my symptoms are Fatigue, blurry , pins and neeldes,face numbing and tingling, toung pins and needles, left leg numbness and tingling, left and right arms and hands numbness and tingling. Heat intolerance. But am at my 3 neurologist and he said its not ms also cause brain mri came back normal and my symptoms don't add up

[@elainer8288]

Thank you so much for this video and this channel! Did you have the MS hug? Do you know to make this simptom better?

[@tinamac5278]

I've been told repeatedly that my vertigo is where I have an injury of a ruptured disc and a pinched nerve high up in my spine connected to my neck and they said it was causing cervical vertigo

[@memsandi6445]

That's great that you have an answer :) Have they given you any options for treatment?

[@larryhofer8853]

Lawrence Hofer here from Dinsmore Colony in Saskatchewan Canada first thing that hit me was double vision but I was lucky enough to find this lady that was helping me with her condition with our LORD'S holly spirit I saw 2 pictures after her treatment I am only seeing 1, 2nd thing was walking went to emergency at hospital and meat my neurologist she gave me a round of Lentrada long story but I can walk again but now I am going totally on or lord's meds God never had drugs in his plans

[@beautifuldisaster8006]

My mom has MS. I been having dizziness, pain, fatigue, and numbness in my left leg/ foot. I am afraid to see a neurologist

[@memsandi6445]

Don’t worry or try not to. You don’t know that’s definitely what it is and it’s always better to have answers. If it is that then at least you can tackle it then - there’s plenty you can do. The worst bit is not knowing!

[@laurathompson8500]

Hi , I have had strange episodes where my left arm feels disembodied for a few seconds and almost feel like a rush of blood to my head . I noticed my left eye the vision can go funny when this happens . I have had cramp in left too but do lots of running . I have an autoimmune condition hashimotos so not sure if linked to that.

[@vividesu9943]

what ways did you change your diet and life style to help you? i know it can vary in how much it helps and what can help, but i'm curious! i'm looking for life style changes to help with my symptoms!

[@Memeaux2]

Thanks for the video. I don’t have an ms diagnosis but am having another mri in the next week or two. I’m having many of these symptoms. Blurred and sometimes double vision, migraines, muscle spasms, confusion, numbness, occasional myoclonic spasms, and the most crushing fatigue. It’s hard to explain to people how extreme the fatigue is. About three years ago I had an episode where the left half of my body went numb and my vision got super bad on one side. I had an mri then to check for MS but it came back clear. At this point, I just want to know what’s causing all of this

[@johnnyguitar7921]

hello there, i feel you 100% ,,, im at a point where sometime i even fantazise about euthanasia becuase my quality of life is so bad becuase of all the symptoms and specially the fatigue and back/neck muscle rigidity lack of movement problems,,, and Drs are like "oh its nothing",,, being that im a Ratioal being i try to live with this "its nothing approach" and i have to say my quasi scientific observations denote something liek a switches bieng pulled at random and its not in my control,,,

[@melissachildress2927]

I also have blurred vision really bad. I will let you know how my MRI goes.

[@tinamac5278]

No it's when you sit down and you haven't you haven't slept or eaten or or gotten any rest at all and you sit down in your eyes are rolling in your head and you're yawning and you're trying to stay awake and you just got up an hour and a half before and you can't figure out why you're so tired you go make the bed sleep for two or three hours and you get up in the same thing it's outrageous it's like when you're pregnant just total exhaustion fatigue strain to lift the muscle strain to lift anything there's it's human becomes so I'm having trouble breathing because I'm just so weak I'm tired and I'm breathing so shallow they say you got to take a deeper breath but they don't understand how tired I am and then when I started losing words I sound like an idiot and it's with every conversation that I have God I need help

[@rachelwainfur]

I have had most of these symptoms now since Feb 2019, but all of my mri's and lumbar puncture was clear, so the neuro has discharged me. I have since developed more problems of vertigo and trigeminal neuralgia but am just on painkillers now via my gp. At a dead end :(

[@memsandi6445]

I’d say if your MRI is clear it prob isn’t MS - those lesions are pretty clear. I hope you get your answers soon

[@rachelwainfur]

@@memsandi6445 Thank you. My gp has ordered another brain MRI as he wants to see what is causing my bladder problems and my TN and vertigo as they are new issues.

[@user-ux7yg2ch6i]

​@@rachelwainfur I hope you managed to get some answers and are doing OK. My aunt suffered years of trigeminal neuralgia aka 'the suicide disease' and vertigo. Nothing was apparent on her mri until many years later. She now has advanced dementia.

[@morryswigs2005]

​@@rachelwainfurhope you got an answer. I had bad vertigo and really bad tmj pain at the same time.

[@spicyreyes]

I had an MRI today looking for MS so I'm watching this while I wait for the results 🤣

[@tinamac5278]

I've got double vision I've got blurriness out of nowhere I've got headaches outrageous headaches numbness and tingling all over my face my eyes and my lips twit all the time of disturbances in my bowel can't control them explosive frequent unusually frequently and hard to control urinary tract problems my feet going dead my arms going dead my hands going dead it'll be fine and all the sudden my arm will go weak and unfortunately I've been told I got so much pain right now so please forgive me I spent 4 hours in the doctor's office yesterday after 15 years of these symptoms getting worse and worse and they're still putting me off I don't know how to go about getting a diagnosis so I can get into treatment any suggestions

[@Deltro61]

Like a lot of other people here, I have experienced many of the symptoms, and waiting to do an MRI. You mentioned some treatments that have all but eliminated relapses, and I'm really curious about diet and treatment. Could you elaborate?

[@clairejevron6146]

I now have fatigue every afternoon, pared with itchy tingling sensation in the evening goes from my face to my scalp to my shoulders, to my fingertips. Poor concentration and weakness. I m praying it’s not MS.

[@memsandi6445]

I hope you get your answers soon. Just remember MS isn’t the end of your life if you’re diagnosed with it x

[@priscillajay-thepjs6561]

How are you now Claire? Those could also be vitamin deficiencies. Low vitamin d, magnesium and folate. Try getting those checked if you haven’t already.

[@Gallopinjohn]

Thanks for the video. I like you had pins and needles in my toe about 7 years ago now that just wouldn't go, went to the doctors and was told it was anxiety. I've had really bad migraines and vision problems, was told I needed glasses. similar episodes over the years have either been ignored by me or I've been told it's anxiety. only recently I've had a really bad episode that my doctor has said he thinks it might be MS. just waiting for my neurology. I've had most of the symptoms for years now. I really just want to know what's causing it so I can get on with my life.

[@memsandi6445]

The not knowing is the worse bit! Honestly once you find out you can just move on and get on with it! If you’re having lots of symptoms try changing your diet like I did and see if that helps!

[@kassandrachmarzynski1572]

Thank and thats how mine started ❤

[@rebeccaperez7711]

Hello!! I’m 24 years old and suffer from really bad anxiety… however 8 days ago I noticed that I was getting a head ache so I went to sleep early that night and have felt pressure in my head ever since… the head ache comes back when I start to panic but goes away…. And only thing left is pressure in my head. I have never experienced this before and it’s really scaring me I show no other symptoms other than I’m dizzy because my head feels heavy. Other than that no vision issues or anything….. was just wondering if your head aches were constant…..? Or if they would come and go because mine have had me in my bed for 2 days

[@sophiamia3742]

At this point i'm still very shocked with the negative result I got after suffering from PCOS for so long. 🌿🌿🌿Thanks once again DR RORPOPOR HERBAL on KZbin for your natural supplements

[@sanjaykumar6599]

How are u now

[@henp99]

Share your video because I have a lot of family members and I worry about my sister

[@mollycoughtrie5854]

I’m 17 and I’m waiting to have an MRI scan for this as I developed double vision around a year ago my Gran on my dads side had MS so they just want to make sure, as of today I have had a very strange feeling in my legs like they are cold? Not numb but cold and I’m absolutely terrified as my only experience with MS was my severely disabled grandmother and well obviously I don’t want to be disabled, if anyone could tell me what it’s like to actually live with MS and ensure me that it’s not as terrible as it sounds that would be great

[@memsandi6445]

Try not to worry! I was 27 when I was diagnosed and I literally thought my life was over but if anything I’m now healthier and fitter than I was then cos you have to step up and take care of your body more- pay attention to what you eat and exercise. Yes, there are days when you have a symptom and you get fed up or even scared but you know that you are stronger than it and you get through it. There is loads you can do to manage it and meds have come a long way since the days when your gran had it. I’m very happy to answer as many questions as you need. Stay strong x

[@mollycoughtrie5854]

Me, MS and I do you mind me asking what age you are now? And if you have deteriorated at all? And what the treatments do? My Gran passed when I was around 8 so I’d imagine there are a lot more you can do to treat it now than what you could when she had it but that being my only connection with the illness really terrified me, and showing symptoms at such a young age makes me think that I’ll be in the same shape as she was.

[@memsandi6445]

@@mollycoughtrie5854 that’s completely understandable! I did work experience in a care home when I was at school and there was a lady in a wheel chair who had MS and that was my only experience too when I was diagnosed. Just know that theyre now more often than not the rarer cases. I’m 36 now. I take a drug called Avonex which is injected weekly. My dose isn’t very high. One of my good friends (who also has MS) that didn’t get on with Avonex goes to the hospital every 6 weeks for an infusion called Tysabri which is stronger stuff but she calls it her gogo juice. There are loads of meds u can take now depending on severity and what suits you. There’s also loads more understanding of how diet affects you as well. X

[@Skybluewindcool]

@@mollycoughtrie5854 hey how r u now

[@warlordqueekheadtaker7960]

Did you get pain in your left arm and left foot

[@Nini-gq6qi]

How do you get rid of your dizziness

[@memsandi6445]

Well I don’t have it anymore through changes in diet etc. When I did have it I just had to sit down and wait for it to pass - it was never constant x

[@sheilawhitmire2218]

I had a Dr say I had MS but I was never sent to a Neurologist in 2014 well here it is 2021 and I'm now getting sent.ro.a.neurologist finally Had shocking in legs falling alot bladder issues and lots of gait issues so I'm.praying this is figured out very soon

[@sophiamia3742]

At this point i'm still very shocked with the negative result I got after suffering from PCOS for so long. 🌿🌿🌿Thanks once again DR RORPOPOR HERBAL on KZbin for your natural supplements

[@sophiamia3742]

Contact DR RORPOPOR HERBAL using this link 👇 kzbin.info/door/kZwKW6qES4dXDWzb0YQErA

[@tinamac5278]

I guess I'm in real trouble cuz I've got all of those and the ones that you said that you don't have or other symptoms that other people have had I've got those also so I'm in trouble dear God I don't know how to get to doctors to listen to me and I'm on good old Obamacare and nobody wants to take it from what I understand there's no actual test for this they just kind of throw all these symptoms together and they go oh aha I mean I'm nauseous I can make something to eat and be so exhausted by the time I finish fixing it I don't need it I get so nauseous when I go to the bathroom I literally feel like I'm going to puke when I'm having a bowel movement just and I'm talking I've got the trash can up to my chest and I'm doing everything except puking while I'm having a bowel movement something is wrong that is not normal muscle spasms outrageous muscle spasms I can't touch my feet I can't put socks on without causing spasms in my hands and my feet and my calves and my butt just trying to put on my socks can't raise my legs up to where I can do that so what I'm afraid of and after watching a series of these films is I'm much further along in Ms than you are and what's making it worse is I'm 60 years old I was told by a nurse that nobody's really going to take you serious because you're an old person and you don't have real insurance and because of that they're not going to put much effort in so that scares me on top of this other mess so it's a good thing that I believe in God

[@mzmarvel29]

Thank you. Just had MRI.

[@dr.froghopper6711]

Thinking back, my earliest symptoms that went undiagnosed were occasional spasms in my thoracic back and sexual dysfunction. I was in a Special Forces command trying to keep up with Navy SEALs (wasn’t one myself) and going to sick call was frowned on. What 23 year old man is gonna go to sick call with problems getting an erection? That was in 1975. Macho was everything and I was young enough and dumb enough to believe it.

[@memsandi6445]

It’s amazing when you really think back to the early symptoms - so many are easily missed or put down as something else!

[@brigittescott2438]

I’ve got double vision in both eyes

[@SylviaGroves]

I believe I have MS my walking is worse my vision is bad and my hands are really bad.

[@lesleysprake1045]

I’ve had all that for years and put it down as other things? I was diagnosed with Sjögrens and fibromyalgia in 2018. But been having more intense all round those symptoms but lasting longer 4/5 last bout. And my new GP referred me back to neurologist with misdiagnosed MS he said just off history and these symptoms he could make the diagnosis but wants me to have mri scan. But it’s getting worse I’ve had terrible fatigue today and odd headaches ?

[@memsandi6445]

Mmm sounds about right - it’s unfortunately really hard to diagnose without an MRI so hopefully having one will give you some answers. Fatigue is a bitch- try changing your diet - cut out gluten and dairy and see if that helps you at all x

[@lesleysprake1045]

@@memsandi6445 I have osteoporosis but use soya/oat/almond milk mostly. Drastically cut down on bread etc but got underactive thyroid doesn’t help

[@memsandi6445]

@@lesleysprake1045 that’s a great start. Gluten is in LOADS! Not just bread so have a go trying to check ingredients more and avoid it. Also try eating anti-inflammatory foods like turmeric, ginger, salmon, sweet potatoes... The other thing you could try is supplements - I take flax seed oil, high dose vit d, vit b complex, MSM, calcium and a prebiotic everyday (I have done since soon after diagnosis and they’ve helped me). X

[@kp7032]

I’m coeliac with lactose intolerance so haven’t had gluten or dairy in years, but still get severe fatigue. Someone suggested coconut oil helps them, and coincidentally I add it to fruit smoothies, but to be honest any dietary changes for the good that I’ve made over the years haven’t made a difference to the symptoms themselves. Vitamin D and using a SAD light can sometimes help with fatigue; light exercise, building up from a couple of minutes to 30 minutes+ can also help with improving energy levels. With trial and error I’ve found out that for me, keeping as stress free as possible and listening to what my body’s telling me has been the most useful way of managing my symptoms, even if it means on some occasions I end up sleeping a weekend away with the occasional waking up periods for comfort breaks and food! Having a hobby to keep your brain active also helps. I’m unable to work, but I can still knit, so I try to do that between frequent power naps! 🥱😴😁 I think it’s a case of trying different things and seeing what works for you,

[@nabiarahim2524]

She Arab ples??

[@lucasluc7341]

I'm 16 i have problem urinating and straining to poop and a mild tingling in my feet for 2-3 months now is this can be also sign of ms? or is this something else?

[@ml3598]

Maybe you have spina bifida occulta or tethered cord

[@litlangl09]

How often were you having episodes before you got better?

[@memsandi6445]

Jessica Vasquez I was having 1-2 big episodes a year before so ones that were lasting a few months with a few months in between. I just have a few random symptoms now and again now. Haven’t had a relapse in over a year 😊

[@fannyissac7398]

Please contact Dr. Eric Berg

[@michaeldixon1982]

Can I ask when you get very stiff muscle do you wake up with them all do’s it come on gradually few out the day please

[@memsandi6445]

Michael Dixon I don’t get any stiffness with my MS, just numbness but generally symptoms come on gradually, keep getting worse then plateau before getting better.

[@michaeldixon1982]

Me, MS and I ok cool just have this bad feeling I have ms don’t know what it is I just have a feeling had this Achy pain in the buttocks and groin and one of my eye twitches now and again

[@butaorrak4484]

How u recover from it with diet plese share your diet plan with us......

[@memsandi6445]

Hi Buta - I can’t say I’m recovered from MS, I still have it but I don’t suffer symptoms (or have them very rarely). In essence I don’t eat gluten, dairy, caffeine, refined sugar or alcohol. I try to eat a lot of vege and fruit and not too much red meat. I have to stress that everyone is different - some ppl have more sensitivity to different things like tomatoes or legumes. You have to experiment with what affects you more. I did do a vid on clean eating so check out that one for a bit more detail x

[@butaorrak4484]

@@memsandi6445 thanks gorgeous lady for replying me back I also on Dip diet I don’t know that I m suffering from M S but I have some symptoms like fatigue in my right side of body and also sometimes double vision in my right eye.. mam could u please tell me the right tests for M S diagnosis

[@memsandi6445]

@@butaorrak4484 you would need to see you dr first and request an MRI. if that shows lesions on your brain then you’ll be referred to a neurologist and usually have a lumbar puncture to confirm the diagnosis. Hope that helps!

[@Nini-gq6qi]

I have a lot of unbalance don’t know what to do , my doctor might think is MS

[@memsandi6445]

Could be so many things - best thing to do it get tests done x

[@vanitharadhakrishnan1769]

Can you give tips on how you are controlling it.what are the lifestyle changes you have made?

[@memsandi6445]

Hi Vanitha. The biggest changes I made were to my diet - I completely quite gluten and dairy. I have very limited refined sugar (if any), I don't drink and I have very little caffeine. I also exercise daily which really helps and I practice yoga daily (excellent for strengthening your core and helping balance). I drink 2 ltrs of water a day and ensure that I get enough greens and different coloured foods in everyday. Finally I take a high dose of vitamin d, a vitamin b complex, flax seed oil probiotics, msm and calcium daily. It's a lot but if you do a bit at a a time and work up. Quitting dairy and gluten are key though. x

[@lordzmusic8461]

VERY HELPFUL VIDEO ...... I'M HAVING ALL THE SYMPTOMS OF MS ..... BUT I DIDN'T GO TO NEUROLOGIST TILL NOW ..... AND DID A CT SCAN REPORT CAME NORMAL ...... I THINK I HAVE TO DO MRI 😭😭😭😭 ......

[@memsandi6445]

Yeah CTs don’t show anything just MRIs. Good luck

[@lordzmusic8461]

Can i close my eyes during a MRI

[@pinap1602]

@@lordzmusic8461 yes you can 🙂

[@Skybluewindcool]

@@lordzmusic8461 Hey what yours mri report came

[@lordzmusic8461]

@@Skybluewindcool I didn't go for any MRI . It's been 1 year I'm commenting . At that time , doctor suspected maybe I'm having chronic anxiety and that's what happened . He told me that if you don't wanna do MRI . Then wait for a few month if you get your symptoms worse then you should go for a MRI . He also added not to search the symptoms in SEARCH ENGINES (GOOGLE or anything ) . It's happening dur to it the more I'm searching that more I'm getting anxious . I did all the thing what he said . And i noticed all the symptoms were vanished within a month . So that's it

[@modmodeliani8774]

🙏🏻🎩🌹

[@lovetorres5985]

I have ms I am very scared?

[@memsandi6445]

Try not to be - I know that’s not easy but there’s loads that you can now do for it and carry on leading a very normal life. Don’t let it become you, it’s just something you have to deal with and you will deal with it - you’re stronger than you think x

[@SylviaGroves]

Waiting for my insurance to kick in

[@tinamac5278]

Donald move on just move on give a list of your first symptom second symptoms third symptoms the track that you took to get doctors to listen to you what was the method that they came together and said okay this and this and this and this tells us you have MS that's what I need what kind of doctors do I go to they've got me going to pain management and and they keep taking x-rays the same damn x-rays over and over and they keep telling me all I've got is arthritis well from what I understand with Ms you have arthritis I was diagnosed with arthritis at the age of 11 they've been trying to put me in a wheelchair since then never was I it ever mentioned to me that the numbness the tingling the burning sensation the the dropping things losing control of my hands to where I can't even hold on to the steering wheel the confusion is the thing that just started happening I happen to be highly intelligent but I'm dropping words I know what the word is or what it means but I can't remember what the word is I need help and these doctors are driving me crazy because they're telling me I'm crazy I'm in pain right now severe pain and having muscle spasm like crazy and they won't give me anything for it I need help I've gone to doctors and gone to doctors I finally had an emergency room doctor says well that goes along with your Ms and I said what do you mean my MS I've never been diagnosed with MS well maybe you need to check into that well I'm just trying to and she flat shot me down I mean did not discuss what Ms looks like did not ask me a line of symptoms they tried to blame smoking on this and that's b*******

[@tinamac5278]

Oh my God you just mentioned another one I can't even watch the TV show all the way through I just feel like how stupid you're wasting my time get to the point even while ago I said to you get to the point and I have to throw all that cute thing and you know just just say what you got to say