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373 Views • Apr 3, 2023 • Click to toggle off description
This is one of the many unfortunate comments you may get from random people about Multiple Sclerosis. Try to not get furious! 😂
To learn more about Multiple Sclerosis. Stay connected with "Life of Seb" Do LIKE, COMMENT, and SHARE. Don't forget to hit the SUBSCRIBE button and the BELL 🔔 so that you never miss any updates. Thanks for watching :)
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What is Multiple Sclerosis ❓
Multiple sclerosis (MS) is a potentially disabling disease of the brain and spinal cord (central nervous system). In MS, the immune system attacks the protective sheath (myelin) that covers nerve fibers and causes communication problems between your brain and the rest of your body. Eventually, the disease can cause permanent damage or deterioration of the nerves. Signs and symptoms of MS vary widely and depend on the amount of nerve damage and which nerves are affected. Some people with severe MS may lose the ability to walk independently or at all, while others may experience long periods of remission without any new symptoms. There's no cure for multiple sclerosis. However, treatments can help speed recovery from attacks, modify the course of the disease, and manage symptoms.
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Views : 373
Genre: People & Blogs
Uploaded At Apr 3, 2023 ^^
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RYD date created : 2023-04-04T06:22:11.028085Z
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YouTube Comments - 42 Comments
Top Comments of this video!! :3
My twin brother and sister thinks they have MS as well... lord
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This is something I hear from people close to me, even, and I am just speechless when it’s said.
I usually say nothing, but it 1) it feels like a minimizing of my symptoms and hurts my feelings and 2) burns me up because they have no clue what it is like to have a combination of symptoms all at once and to have gone years now through a frustrating diagnosis process.
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I’m so happy you’ve been able to get out hiking it feels so good for the soul we manage our steps. That’s fabulous! Disregard the lady though it’s frustrating to hear comments like that. The “oh I’m tired too” If only going to bed earlier one night would help. All the best in gratitude and appreciation for what we can do ❤
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oh my goodness. I can't stand people like that!
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People I see in the shops think I have had a knee replacement. When I explain I have transverse myelitis in the setting of MS, they usually tell me of people they know in our area with MS. Usually when people find out, they tell me I look really good. Then I never know what to say so I just thank them.
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I began following your journey years ago as I was being tested for MS. For me, my diagnosis ended up being FND vs MS, but I continue to follow your story as your strength and openness - I admire and draw my own strength and courage from. Thank you for helping so many come to terms with the unique-ities in our own lives!
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Initially that would have made my eye twitch too!
I believe a lot of people have body pain issues. These can include illnesses such as, chronic fatigue, certain movement disorders and fibromyalgia.
I hope her encounter with you, helps her seek some answers surrounding her health.
In saying all of that, I know exactly where you're coming from. I was watching a TV programme with my friend and her mother many years ago. An old lady who had passed away, was found to have a fossilised baby in her womb.. my friend's mother piped up and said, that's probably what's wrong with me because I have pains in my stomach😂
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It depends on how they ask what I say. I always tell them to get tested for one reason MS does mimic other illnesses and 2. I guess because I was misdiagnosed for 30 plus years I didn't find out I had it til I moved to Ireland to be with my husband. Started having symptoms double vision and walking very weird. Went to hospital emergency room, and after being poked in the back ,mri finally got my diagnosis. was 45 then 59 now and it has been a lonely few years.
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I don’t tell people that I have MS. I do feel off balance sometimes but nothing crazy. At least just yet. My main problem is brain fog and fatigue. When I have it very bad at work I try not to talk to people at all.
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Try not to hurt those ignorant fools!
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Being recently diagnosed its haed for me to not be sarcastic back at them because some people don't either really understand or just are plain dumb. I get kinda defensive because it is such a hard blow. Just like 2 weeks ago the eye dr i went to took ut as a joke that i have ms. Im going for a second opinion because i am dealing with black floaties and blurred vision
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Unfortunately, so many symptoms can be a multitude of things but it never hurts to get tested. Sometimes even if they aren’t causing pain. As a child, I hated rollercoasters because the rush of blood to the head from any upside down loops would be way too much for me and would often tingle at the back of my neck. Turns out that’s a common symptom, but I never said anything because it didn’t hurt. So moral is: just because it doesn’t hurt, doesn’t mean nothing is going on. If something feels unusual, even if not painful, tell your doctor.
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Commenting as one who has not been diagnosed with MS but having similar symptoms and questioning, I think it’s relatively easy to just assume one has ms when they have ms like symptoms when you don’t understand how those symptoms are so similar to other things like migraines for example. Migraines sometimes present with some ms symptoms. With concerning symptoms people generally assume what is, in their mind, the worst possible diagnosis.
Then on the flip side, it’s human nature to when you see others struggling in similar ways and are a little more in tune with that struggle, whatever struggle that is. In this case it would be folks with ms recognizing ms in others.
As for me, I’ll probably have to end up in a wheelchair in order to get diagnosed. I’ve been a medical mystery for 3 years now.
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yeah i had medical staff at my old neorologist i said its hard for me to get up and i get off balanced and shes like i do that too and she wouldnt write it down as a symptom its like um i hate drs and i wouldnt be here if i didnt think it was nothing
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I just encourage them to get tested. no skin off my nose.
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it's really strange that wen you are experiencing something, with MS
someone might say, ooooooooo i must have MS too.😮
as tho it's something cute
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Hey seb how are you doing..is all well
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@Eddies186
1 year ago
Lol 😅 get tested . Years ago way before i got MS i had a lady ask have i ever had a scan for MS she had MS i wasnt feeling any of the symptoms was really energetic and active so many times years later i wondered so many why she asked like was i showing symptoms than or was it a MS 6 senses Now i see people that R showing the very earliest signs i just wanna ask have u ever been scanned but i do to this day wonder what she saw .the earliest sìgns R symptoms of so many thing
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