11 ways that make MS an invisible illness

MS is often ignored because of how it is invisible to other people. But here are 11 reasons why these symptoms most often escape the untrained eye.

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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⚠️ DISCLAIMER:
My channel is in no way supposed to provide medical advice or guidance and I do not claim any medical knowledge of Multiple Sclerosis. I merely discuss MS-related topics from a patient's point of view. If you have a serious medical condition, please consult your medical practitioner immediately. By using this channel you do so at your own risk. "Life of Seb" YouTube channel accepts no liability in part or in full for any damages or injury caused by the use of any content provided.
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[Slyma]

May God help you and all MS patients 💕

[kaladixon]

Have had MS for 7 years now and this year alone is the first for me to be having major issues. It is amazing and helps alot to know that i am not alone in this crazy journey. Thank you so much.

[KenIsis]

Insomnia please add this as I’m tired of people thinking it is a choice to not be able to sleep

[jaynebuck]

That is because we are masters at hiding all of those awful symptoms!

[roberture]

Thalnkyòu .Seb, I've experienced all those symptoms that you pointed out. Unfortunately a lot of people that don't have MS have no clue what we go through to get through the day. As always thank you Seb.

[seinawhite]

Thank you for putting this out for all to see about MS because it's terrible to us.

[Grimace_SYLB]

My brother just got diagnosed with MS today. It was hard for me to understand what he’s been going though (symptom wise). I appreciate you putting this out her on social media to help me get a better understanding. Much love!

[visionvixxen]

You never know what your body is going to do or not do and always looking for a public bathroom everywhere you go

[arielatomhc]

Your all Warriors. I had Optic Neuritis but not MS so I can relate that much as I'm left with poor vision in one eye. I see you all as Warriors getting on with your lives.

[vandanajain]

Good to see that you are doing well. Take very good care of yourself. I have MS and was diagnosed 11 years back. My symptoms are mainly, Depression/Anxiety and Numbness/tingling. Sometimes double/blur vision. I even had relapses almost every year, but by god's grace doctors could pull me out of those phases and could walk normally now. I pray for everyone who is an MS patient. Give them courage and strength to fight with it strongly 🙏

[karenmurphy]

😮 Thank you for sharing! I subscribed to your channel because I have a good friend that has MS. I wish and pray for healing for all.

[gh-wtip]

Fatigue for me is the worse, I have other issues but the fatigue is just taking over my life

[wernervdz]

Hope that a cure
comes for us within reasonable time. We have no normal future like this.
Everything stands stil in life.😫

[jlongino]

I was diagnosed yesterday. Finally. I have a reason why I feel like I do. ❤

[kimpiha]

Appreciate the post, have been treated for health Paranoia and ptsd for a year and a half after two years of extensive testing with no results as "tramua does incredibly weird things to the body", now all of a sudden I have MS and Rheumatoid arthritis and none of its phycio-somatic. Grateful i have a MH team so i can get over the trauma of not believing my body. PS visual effects made me feel like the room is spinning and was falling through the floor lol

[stevewildeagle]

May the Great Spirit Bless you, your keeping Awareness about MS alive, Afternoon Fatigue & nightly leg spasms 😩. ATM I've a purple right foot from where my legs just turned off for a split second, but enough to go down like a rock onto it. Some people expect you to park your car then fall out and crawl to prove an illness they can't see.
Keep doing what your doing, your Soul shines through your works.
❤️🌈🙏🏼🌀🦅

[Chumpess_X]

I have RRMS and work part time in retail. I’ve been in customer service in some capacity for over 20 years now. Customers (especially the difficult ones - they’ll smirk because they think they have me rattled when it’s not the case at all) often think I’m new at the job because I can’t remember where things are sometimes, or my hands will shake, or a stutter or can’t find the words I’m looking for. Part of me wants to say, “I have MS, I’m not new”…but it’s none of their business. The only ones I tell are the colleagues I’m closest to, or the ones I train…because I will forget their name and they notice my difficulties and are concerned they’re being trained by someone who doesn’t know what they’re doing. It’s frustrating. It’s tiring. Some days I’m just over it and want a body transplant.

[janedoe]

Thank u for this ive gotten yelled at for using my cane in public because i quote "dont need it" by a stranger, I've been struggling so this meant so much

[richellevanchiere]

My mom also has relapsing - remitting MS diagnosed in March of 2011 and like you said it's invisible until it isn't

[badGrl]

As recently diagnosed with MS. It’s an emotional roller coaster. I am waiting for the balance ❤