Do you have other subtle symptoms associated with your MS?

noise and bright lights totally do me in.

I've had all of these symptoms sadly. I left the workforce at 18 when I was diagnosed. It was aggressive and world shattering for my family who cares for me.

How many times did I blame my dizziness on dehydration? How many times did I blame tripping or stumbling on my shoes? How long did I struggle with depression? Prickly pain? Well, that had to be dehydration right? Fatigue? Oh I must have to take vitamins. I write down my schedule? How can I forget what I have to do each day? Why can’t I recognize where I am even though I’ve been here so many times? The list goes on!!!

When you described the tightness is when I said ok I’m not crazy I haven’t even told anyone about that yet.

I have all the symptoms. The dr at the ER said he thought that was what it was but my family Dr says it's ptsd.😔 I love your videos. They are very informative.

I'm 50 and am mid-diagnosis. My neurologist knows it's MS, just waiting on my cervical and lumbar MRI to know my progression. After reviewing my medical history - ulcerative colitis, endometriosis, adenomyosis, hypertension, a wreck that damaged right knee, a self-diagnosis of ADD, blah blah blah, he suspects that my elevated pain tolerance, my writing off cognitive issues as ADD,and how I have just accepted fatigue as a permanent fixture of my life--- that I've probably had MS for years. I have to wonder how many others do the same, and how much of myself I would still have if MS wasn't such a sneaky B***! THANKS. This felt like an appropriate vent area for this 🥹

I've come to utilize "speech to text" all the time. Or just printing things out on my printer rather than writing. Like grocery lists. Very convenient! But I am always conscious of keeping muscles exercised, knowing that "if I don't use it, I'll lose it!"

I'm so glad I found your channel. Sending you so much love and gratitude 🦋

This is a great video!🧡 These really are pretty sneaky symptoms, and I'm so glad you brought them up so people keep them in mind!

Thanks sooo much for putting this together. I just subscribed !

Thank you. I had some of these symptoms but thought I was wrong.. this really helped me 💞

I have all but one of the early symptoms you listed. have never thought to tie them together before. Thank you for this information.😊

Thank you for making this video. It really helped me.

I’m commenting again for the 2nd time today! Again, thank you for the video. You’re putting to words the feelings I’ve had for SO LONG. The compression in the bottoms of the legs, prickling pain, etc. it’s wild that you can put this to words because I explain my feelings to my husband and he’s like ….thats not a word…… so thank you. This is affirmative.

You have a new follower 🙏❤️. I love the way you described all symptoms related to MS in your videos. I have watched two of your videos and I have all the symptoms you’ve described and others too. This confirms that I am not that crazy 😔. I also have other conditions such as herniated/bulging discs, bone spurs, and pinched nerves in my cervical, Thoracic, and lumbar/sciatic areas, cervical disc disease with myelopathy, lumbar disc disease with radiculopathy, spinal enthesopathy and stenosis in cervical area, Fibromyalgia, and recently diagnosed with TOS, Cervical Dystonia. Have bursitis, tendonitis, tear, bone spur, etc. in different areas in both of my shoulders 😔, multiple join pains, and bilateral numbness, tingling, burning, etc. of arms, hands, legs, and feet. I have some doctors against any surgery to be performed on me because they say I will be in even more pain of what I have right now. I always said I have MS, but my neurologist said I don’t 🤷🏽‍♀️, but I keep researching and looking for solutions. I am afraid I am not taking the right medication I should take to stop or delay the condition. The medications I am taking for Fibromyalgia just put me to sleep, make me drowsy, cause more vision problems, and make my body and mind even more tired. Depression and anxiety is horrible. I have faith in God and still in the Doctors that I will get the proper treatment I deserve to feel better. It will not surprised me if I am diagnosed with MS because I’ve been dialing with all of these symptoms for more than 10 years, problem is that every day it is getting worse and even more after having COVID last year. My problem is that when people look at me (55 years) I may not show my age and/or my conditions. But I will continue to advocate for myself as you said 🙏. Again thank you so much and God bless.

This is an excellent video. I too have a hard time explaining or understanding MS symtoms. I so appreciate you sharing this information. Thank you & God Bless.

Great video! I also feel warm in my face when I experience these symptoms: Muscle aches, joint pain, weakness in arms I can't lift them longer than 15 to 20 seconds before they start hurting and getting tired, muscle spasms, balance issues when walking, cog fog, speech difficulties where I stumble over my words and have trouble recalling words, nap straight after work, tremors when I'm feeling cold and not cold, tingling crawly feeling like a bug is crawling on me, cold feet and sometimes hands . I also have ADHD just diagnosed. I had an evaluation done in 2015. I was 21ish and saw a neurologist. He did the needle test on me where he stuck me with needles and tested different parts of my body to check my nerves (I forgot what that test is called). The only thing he found was my left side of my body is weaker than my right but nothing significant. Nothing happend after that. Now this whole week I'm experiencing all same symptoms I mentioned earlier again to the point where I was crying last night from the pain and overwhelming sensations. My mom suggested I'm probably dehydrated and that helped a little drinking water/ electrolytes. Can dehydration really cause all the symptoms I'm experiencing? Is this enough to seek another evaluation from a different neurologist? Should I see a different specialty doctor? I'm lost on what or if I should so something about this. Sorry this is long and thank you for anyone who can guide me 😊

Thank you so much for your videos. I’ve had MS for 23 years and I’m still learning.

I have trouble with exercise since about 6 months before my MS was diagnosed back in November. Does anyone else suffer from extreme fatigue after exercise? I've been trying to take it easy with some slow walking because last time i pushed myself i ended up in bed the next day. 😕

Everything you said I’ve been going thru. Since 2014 when I had my knee replacement surgery I’ve complained about a TIGHTNESS in my calf area. I was blown off. Cog fog- 100%, I can’t focus on anything work related. Omg thanks for this video

Very informative. Loved it! ❤

Very helpful. Thank you so much. I am a patient of Ms since almost 15 years. Finally my symptoms make sense.

I thank you so much for making your videos. They are very informative. I have been putting off seeing my doctor but due to your videos I have scheduled to see my doctor due to these symptoms.

Nausea, eye pain, R. Leg pain. Thanks for your informative videos. Very helpful to describe how and what I'm experiencing. Great job!

Thank you 👋 😊

Sounds alot like myalgic encephalomylitis/ME that was poorly named chronic fatigue syndrome in the mid 1980s. Research found low natural killer cell function, inflammatory cytokines, increased infections, white matter lesions on mri's. Even autopsies found inflammation in the brain and spinal cord of ME pts, yet it is still mostly ignored. Some treatments can help some people such as antivirals and antibiotics but its mostly symptomatic treatments if one can tolerate them.

I'm finally seeing a neurologist after canceling with two in the last few years as both times I moved out of area. Thank you for this video! I realize now I've been having symptoms even longer than I realized! I'm on my 3rd GP that suspects I have MS. There are worse things it could be, so I am prepared for diagnosis ...

I have them all! My double vision hasn't went away for 30 years now. Have it 24/7. Fatigue and depression a big part of my life. I went to the doctors for years and they always took bloods and they were always fine. Finally one doc said it could be ms as the numbness I alway had in my feet moved up to my waist. Finally diagnosed in 2006 after mri. When people ask me what symptons I have, my mind goes blank as there is many of them. Great video. Could have been written for me.

Ironic, I came across this video. I found old date book planners from 2017 until 2022. Not much written, making me wonder? Why the heck did I have this? Since 2022, I have been to every doctor imaginable. My datebook is full. I've had tests, numerous. But insurance dictates medical professionals, and even though I've requested MRI many times...2024, and still no success. I know something is wrong, but gaslighting has caused me to give up. Thank you for giving validation to those of us who have given up.

Thank you!!!

Diagnosed exactly a year ago today, Previously in 2014 diagnosed with CIS.I had an episode of facial numbness and walking like I was drunk especially when walking over black and white floor tiles. Had settled down then my neurologist retired plus COVID changed the world and I was forgotten about. Fast forward to 2022 assaulted at work knocked out ,then over the next 16 months it was one thing after another subtle yes... Then one day climbing the stairs the pain I experienced was like getting shot in the hamstring area. I couldn't walk further than a couple of meters. Eventually I had a new neurologist and after he examined me he said in my opinion you've MS wow. Full head and spine MRI the next day. Results a fortnight later. Haven't worked since going through the process of I'll health retirement. Honestly everything you said in the video every single subtle symptom I had but put it down to work stress getting old or just tired. Male 55

I live with many of the symptoms you described in your video to varying degrees but the one symptom that is difficult for me to control is the unusual sensation of feeling wet, cold and damp legs, when they are DRY! The other sensation is waking up in the morning with an iced cold right hand. When I run cold water 💦 on the hand, the water feels warm. The truth is I don’t know what to expect from day to day but fortunately there’s one medication which helps me more than others.

I concur with your sentiment 100%♡ Australia

Thanks a lot

You're AMAZING!! 🥰😘

100% what I'm going thru...everything you said I'm feeling one thing that is driving me crazy is the burning sensation on my body started in my feet now everywhere Shoulder blades burn like coals on my shoulder blades ...touching my skin hurts to I have noticed my right side of my body is the worst ...I have no energy...sleep helps alot

i’m currently in a phase of noting and recording many little weird signs i’ve been having - which when i’ve researched, have pointed to ms (or some type of nervous condition). the main one recently being a persistent thumb twitch that lasted a month and tremors when bending the same wrist. i strongly feel that my cognitive abilities have been decreasing over time - my short term memory is terrible, i really struggle to relay or note down new information or just speak from memory in general - i can’t talk a straight sentence basically. i had one scary instance of intense pain going down one side of my head down to my teeth (lasted about 10 seconds) - that was very alarming as it had never happened before but also hasn’t happened since. the list goes on but for years, specifically since a severe vertigo episode that lasted a day, i have not felt the same - always feeling tired, on the weak side, just off in general. but taking note and recording twitches etc should help in the future. i just feel a little silly calling the doctors about it as i’m quite young and i don’t feel that my symptoms are persistent enough, i know it would be a case of waiting and seeing how it goes. very informative video though, thank you!

Undiagnosed, the top of my right foot developed numbness about a week ago after some excruciating occipital neuralgia pain. Its so subtle, I can still feel but its different when compared to my left foot.

A have had weird symptoms for years but just recently have been taking the falling over thing more seriously. Well losing your job because you can’t stop falling over will do it. I thought it was all low blood sugar all this time but was recently told by a Doctor I don’t have hypoglycemia. When googling the causes for falling over MS came up and when I looked up the symptoms it was shocking. I have dealt with problems for years it would be a relief to finally know whats wrong.

Funny you mentioned looking for blisters, I was convinced I had a blister on my heel as it was so sore but definitely no blister there. I’ve checked several times but no blister has snuck up on me. When the weather is warm I frequently feel like it is raining, phantom rain syndrome I call it 😂

I can relate to the many years of doctors of many specialties. I am finally getting my first MRI to "rule out" MS. I'm not so sure it will be ruled out. I have pretty much every symptom you just listed and many more. I have been going to doctors for over 10 years with many of the same complaints and seen ortho, GI, rheumatology, hematology (had a PE and nearly died), physical therapy, gynecology, urogynecology.....and probably more.

Thanks for sharing! I am managing MS for 9 yrs now..

I was diagnosed with Fibromyalgia some years ago, but things have gradually got worse. With some of the symptoms you have described. My fatigue is the worst. I'm drained all of the time. No matter what I do. How can I ask my dr to look at my diagnosis again? Don't get me wrong, fibromyalgia is awful, but a lot of symptoms can overlook others. I live like a hermit with the fatigue. I hate it

I have had the honor of dealing with trigeminal neuralgia, and there is nothing subtle about that. I have a neurologist that I do like but after I had gone through two rounds of gamma, knife surgery, they only had relief for four months each and then the pain came back, and my neurologist said he was not a pain doctor and could not help me At that point, I went to a acupuncturist rather than The brain surgery that Could provide Relief bye placing a Teflon sheet over the trigeminal nerve. However, I did not follow through with that surgery and resorted to acupuncture which I wholeheartedly recommend After five visits the pain what about 90% gone and I could stop caring Orajel in my pocket all day !!!

I have cell phone viberations in my legs and stomach did anyone ever have this symptom?

Thank you hon for this. My maternal grandmother had MS and my sister has it. I am pretty sure I do too; I have all the symptoms. I am an Exercise/Yoga Therapist, and I really think that is what keeps me in control with this disease. Thank you and Blessings. Deedee

getting tired/zoning out during conversations

My trigeminal neuralgia was always on the left side of my mouth The pain was so bad that I always refer to it as the best diet you never want to have My pain was triggered by cold air, hitting my mouth, and luckily Fate worked in my favor that face mask had to be worn, so Nobody thought I was crazy for wearing the mask

great video :D feared i had MS but my doctor thinks its stress :D but thankfully this video gave me peace, i don't think i have MS no more, but will keep looking out for symptoms , you are amazing and a strong woman! :D

Hopefully patients are on high orders of b12…. B12 I think is a huge part of correcting these symptoms..

I've been so interested in your videos. I am going to get an app....I just have so many symptoms and besides having the rare Klippel-Feil Syndrome I have on my medical chart a hoard of "I think you have...diagnosis: lupus, myasthenia gravis, liver and kidney enzymes suddenly going way way up or kidney disease (liver enzymes went away and back to normal after 8 months???). I do have a brain tumor (meningioma only) in the right cavernous sinus that is quite large. I've been dealing with terrible migraines labeled cluster headaches and trigeminal neuralgia. I can't possibly have allll of these things!!!! I really believe that I have MS and that the severity of the cervical spine condition was constantly hindering the diagnosis.

Dee Dee was my favorite doll I had as a child. Anyway, my Dad had progressive MS. Within 10 years he was totally paralyzed. It was got wrenching to watch his pain. Has feet crossed and he begged me too pull them apart. I wasn't strong enough. Anyway, I am now dealing with some of what he did. I have been diagnosed with Dementia, but wonder if it's MS. Thanks for your valuable video and God Bless You.

This has been very helpful. I’ve had many of these and some like dizziness and balance issues with increasing regularity. I am awaiting my first MRI. I don’t know if anyone else has felt this but when my symptoms were bad, I was 100 percent convinced that I have MS and to be honest, I was relieved because it explained so much BUT…as my various issues improve I start to feel like a fraud. Like maybe I am just being a hypochondriac. My wife assures me that every symptom I have is valid and it’s becoming more problematic and more apparent but now I am actually worried that my MRI is going to be normal and I will be left with all of those questions again. I am not worried about the disease. I conquered Leukemia (CML) and have been receiving the all clear since 2000 and I have always been one of those “make the best of it” kind of guys and I am 57 so it’s not like I am planning my future. Did any of you feel this sort of “imposter syndrome” leading up to your diagnosis? Once you had convinced yourself that it all made sense?

Same 8:13 I have gotten diagnosed with adhd and migraines and lower back issues, now I have excessive neck pain

They need you to do a Ted talk!!🙏

I'm not yet diagnosed with MS but some of my doctors are starting to suspect it. There is just too much that hasn't been explained by any of the other specialists yet. One of the most obvious to me, and to my PCP, is that I've been having periods of difficulty walking. Sometimes I can walk almost fine. But sometimes I feel as if I've forgotten how to walk. Like I have to concentrate so hard on every little movement to get my legs to keep stepping ahead. Like I'm both a puppeteer and a marionette. Like my brain and my body just don't quite connect. They're definitely not working in unison as one. And I've noticed that standing from a sitting position has become almost impossible. I've passed muscle testing from 4 different specialist. And yet my legs seem convinced that they can't get me up. Or more accurately, that my legs are not hearing the signal from my brain saying, "Get up!". Once I use my hands to push up on whatever is nearby my legs seem to hear the signal to engage. But until then they just stare back at my brain saying, "What?" As if they're wondering why my brain is so annoyed. And those are just some of the more recent things that none of the specialists have said could be from anyhing in their department. I do have a lot of other neurological stuff, too. Like my feet feeling wet so often that I've almost quit checking my socks. My spine specialist said it's not from my lumbar spine. But my rheumatologist said that weird neurological stuff like that could be from Fibromyalgia, which he diagnosed me with. Even he said that some of my weird symptoms are not from his department, though. Anyway, I could go on and on. And my PCP and I are going to send me to a neurologist soon. But I wanted to say that yes, I do relate to a lot of what you said. Most of it, actually. Especially the part about these weirenesses having the ability to come and go. I didn't realize they could do that. Mine definitely do. So I'm glad to hear I'm not just going insane. Thank you for making this video. I appreciate you.

I have all of these symptoms you speak of for years and my GP always put it down to fibromyalgia which I was diagnosed with 10 years ago, I finally got referred for an MRI and was found to have a lesion on the right hemisphere of my brain but nothing else evident on the scan so now I'm having a scan every 6 months and a review of results with a neurologist every 6 months, he says he cannot diagnose me with MS right now but looks like I may progress enough in the future to be heading toward a diagnosis........can only manage myself symptomatically

Beautiful hair!

I am not diagnosed (and having a horrible time getting in to see a neuro) but I'm starting to suspect MS, and thinking back it may have started in 1990 when I was 18. Since then I've had every blood test for autoimmune disease (mostly negative, a mildly positive ANA), been diagnosed with fibromyalgia, and seen countless specialists for various symptoms that might last for a few months and then vanish, occasionally resurfacing months or years later. My cog fog was dx as ADHD; whether that's right or not, the meds have been helpful. It's been frustrating and I am sure my medical chart has notes about my hypochondria, but now that I recognize what it might be, I have hope that eventually I'll be able to be tested.

Omg. I have everyone you mention except the prickling. My feet, ankles. shins, thighs and now fingers and toes "freeze up" in pain. It's awful and will wake me up from a deep sleep. I used to have beautiful handwriting and now it's barely legible. My fingers are always one off the correct keys when I type. I have a different chronic health condition I have always attributed the symptoms to be from, but never with confidence. I know something else is going on.

I get this weird sensation where it feels like cold water is being poured down one side of my head. I feel every bit of it. It doesn’t hurt but always makes me wonder why I get them

Thank you for this. I have so many of these symtoms. I recently was diagnosed with intracranial hypertension but i just feel like something aint right. I tick so many of these boxes. Im due to see my neurologist soon so hopefully he can clear it up for me. Currently my left foot keep getting pins snf needles and same leg feels so weird and like numb inside. I cant explan it.

I have a diagnosis of fibromyalgia but I'm unsure I can relate to this so badly

There is ALWAYS a reason Mitochodrial, micotoxins, parasites, circadian rhythm disruption, dehydration, emotional trauma etc Blaming MS, age, menopause etc are just excuses and don’t give strategies towards correcting the problem We are our best advocates with bodies that can heal Due diligence, commitment, and consistency to self care is a daily job to positive well being🧘‍♀️☀️❤️

The weirdest symptoms I had was change of smell. Everything smelled and tasted the same for 4 months. EVERYTHING. Peanut butter smelled like a bowel movement. Sweat smelled like yogurt. I struggled to eat anything except strongly flavored foods for months before diagnosis. This corrected itself after my first round of steroids.

18 years for me before I was properly diagnosed

I don't know if I have ms or not. I saw you on utube discussing MS Hug. I started reading your comments. For almost two years I wake up with 5my ribs feeling they are in a crushing squeeze. Sometimes hard to breathe. I said i need a new mattress. They are expensive so i havent done it. . After about 10 minutes of walking around , 80% goes away but lately, my bra feels too tight all the time. I have a reason for that possibly. . I have carpal tunnel syndrome that's now in my arm. Numbness. I can't hardly hold a pen to write. So many other symptoms but I can explain each one away, , but put them all together, it worries me. With that info on the ms hug, that did it. I'm going to see a neurologist. I'm 79, so it's probably not likely, but reading you can have mild symptoms for years, then it raises its ugly head; I'm so glad I saw your video.

All. Every single one.

Yes, sometimes when I work out or do anything cardiovascular activity hiking , treadmill,spinning bike My feet feel numb and prickly Also experience wet sensation on my skin or burning prickly pain on my skin mostly thighs

6:00 literally still always taking off my shoe to look for pebbles that aren’t there, even after diagnosis.

I enjoyed this informative clip but please don’t forget about us with PPMS. Our symptoms don’t ’come And go’, unfortunately

I have recently had the term MS used by my neurologist. She also mentioned "White Matter" that was evident in a recent MRI. She has recommended a lumbar punch as a confirmation of MS. I do have some symptoms but would like your opinion on my next steps.

My symptoms started last year. I had tingling and numbness in one of my hands., And then I had it in the other hand. I started to get stroke-like symptoms, and they took an EEG scan and didn't find anything at the time they took an MRI of my brain and there was a white spot on my brain ( or at least that's how they described it). Dr. pegg said that white spots come up all the time, it could be nothing. Then he retired. 🙄 I have muscle jerks, brain fog, one side of my face goes numb, I smell things that are not there, and I'm in constant pain at the same time. And yes it comes and goes with stress. I was diagnosed with fibromyalgia.

I had an mri on brain but not my spine which I feel should have been done as well and it showed nothing on it however I have all of the symptoms you described when I have what I guess is a flare up!? The only time I had relief was when I was on a cortisone pack for a tooth infection that was treated with a root canal. Once I was off the meds for a week the symptoms came back again. My doctors keep dismissing me so I give up. It all started when I couldn’t see out of my eye one day for a few seconds. Then I started getting spasm through out my body which all went away except for one eye that still does it but no as bad. I still get tingling on left side of my face and nose and lips. I have a prickly sensation on foot that comes and goes. The cold wet sensation occasionally. Forgetfulness. Fatigue. My throat spasms sometimes too on occasion. Dizziness at times or vertigo. Arm will feel strange at times like it’s heavy. It’s all definitely neurological. I’ve been to two dentist. Two eye docs. Two doctors and they all think that as well. There are times when I see blurry or double in one eye. I’m like can y’all just help me here. Sigh. 😔 so frustrating. My primary doc said he’s going to set me up with a neurologist. So just going to have to wait and see. Thank you for the informative video.

I have high anxiety and depression, my balance has effected me sometimes swallowing problems and high muscle twitching and had days of being off I looked oops and mispronounced words.

I need my doctor to run more tests. I have so many symptoms and I'm frightened.

Thanks for asking. It's a mixed bag, isn't it??? It's my cheeky jelly legs for me. I keep on walking and building up my strength, stability, and endurance. I try to practice functional exercises as promoted by Dr. Gretchen here: kzfaq.info/get/bejne/nNeghs5eyb2co6M.html

Yes to 98% of these

Now add Adhesive Arachnoiditis symptoms on top of MS… then you’ll have a very interesting presentation

I have AS but I'm getting so much nerve pain in my face and ulcers roof of mouth. I'm so exhausted

Wow, I have the same sensation in my left calf as you! I especially feel it while walking for exercise. I have all these symptoms. MS was ruled out because I do not have brain lesions. I have not had an MRI of my cervical spine. Did you?

i feel like i walking on sponges, pain in between sho ulder blades, feelings like cold water running down my face, chest bothers me. i still waiting on mri. i been having symtoms since April, neorologist is slow

This is a good video. I have never been diagnosed with MS but I have dealt with symptoms for about 15 years. I did go and get a blood test and went to the eye doctor early on and they didn't find anything there. I wasn't even thinking MS at that time though. The last time I went to a doctor was about a year ago and he wanted to refer me to another doctor to get an MRI. He said he saw white blood cells in my eyes and thought I might have a more serious situation and he did not name it. I have had a gait problem years ago and it never came back. One arm felt tired and was shaky as hell for a time but it never came back. My eyes though have been coming and going the whole 15 years. One pupil is bigger than another at times. I get double vision frequently and sometimes double vision with just one eye and the other closed. Should I remain happily ignorant or at least hold onto the possibility I don't really have it or is it better to know?

I have most of these symptoms, but did not get a diagnosis. The doctors did not say anything why I am suffering.

I’m in Jacksonville Florida I am declining and I CAN’T GET ANY DR TO HELP ME

I have been referred to neurology query ms. I have endometriosis, painful bladder syndrome, raynauds. I have been experiencing restless legs syndrome, hands tremors, pins and needles in my feet and now spreading up my legs and numbness in the legs. Chronic bowel issues, back pain, blurred vision and balance problems. my symptoms are getting worse rapidly. Could you give me advice on what I should bring/ write down for my first appointment, thanks. I and only 28 and I am worried what is going on.

How about numbness in the palm s of hands..and front of legs...feet etc.

I get pain in my legs like it’s swelling but no swelling especially in the summer. It’s fustrating

I have many ms symptoms but here's two I wonder about... Excruciating cramp like pain in limbs (varies, could be both legs, one arm, etc)... its so bad I'll lay in bed stretching writhing tossing and crying until it passes. I believe this is one of the first symptoms I experienced many years ago. Strange tightening in my abdominal /pelvic area. Both tingly and tight. Swelling of legs and feet. Especially in heat. To the point none of my shoes fit. Besides these.. I was diagnosed with carpal tunnel in both wrists at 25... then went to dr for electric shock type pain down my neck into my shoulder. I had a newborn at the time and the pain was so sudden and intense I was afraid I'd drop him. Dr sent me for xray to check for arthritis which was negative so he gave pain meds. Maybe a year later went to ER with drop foot. On call neuro wanted to operate on my spine then and there but I said no and got a referral for second opinion three months out. It went away on its own so I canceled. I've been diagnosed also with interstitial cystitis due to constant urge to urinate but can't. But also sometimes will pee myself while coughing or laughing. Currently my right outer thigh is numb but also at times prickly hot and painful to touch. I get horrible migraines that start and eminate from the back of my neck /base of skull.. I know I'm leaving stuff out but after having many drs dismiss me or throw pain meds at me I've given up. Feel sure it's ms but now I'm just waiting til it's bad enough to diagnose

How about hand/eye coordination issues?

Is Sedrate and or CRP elevated with MS? My husbands sed is 116 and crp is 11.1 .. just started autoimmune disorders

I am experiencing almost all of these symptoms I m desperate

i am 67, woman. seeing a doctor is a waste of time here. they say " stress" " anxiety" even though i have neither. i say, ok i can see why you might draw that conclusion but let's look at my labs and imaging. also, i've not been clinically diagnosed with anxiety by a qualified professional. thanks anyway. goodbye. and then i go home frustrated and in the same condition as i was before seeing a doctor.

For the last few I can not stand to be touched lightly, I feel like I am going to crawl out of my skin. Could this be related

What tests does your doctor order to confirm MS or rule it out?

Does anyone have white spots under their skin on their feet? Mine come and go. When I exercise I feel ill after, sometimes flu like aching all over or fatigued.

I have numbness on one leg and have 2 other autoimmune disease, my doctor is now suspecting I have MS, I am scheduled for an MRI on 4 days ! I am scared ! wish me good luck 😔

I had started getting a weird change of colors, in my left eye. (Things are a grayish, washed-out color). My right eye seems to be ok though. I have a lot of other issues but, nothing that points to MS quite yet. I've had dizziness / balance issues for a while as well. Sometimes I get the weird numbness in random areas. Speech problems bad head fogginess. Depression / anxiety...yep. (Who doesn't have it) I can't drink alcohol because of it. (Probably a good thing). I take up to 10 motion sickness pills a day, depending on what I'm doing. The doctors I've been to have no idea what's going on. No tests really show anything besides my minor health issues. Idk what to think about it! I just have to wait and see if it gets worse, I suppose to go see a Dr again. Maybe it isn't MS but, who knows.

Didn't see the symptom tracking apps. Is it possible to get the names?