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11 ways that make MS an invisible illness
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31,500 Views ā€¢ Sep 11, 2021 ā€¢ Click to toggle off description
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 šŸ”” so that you never miss any updates. Thanks for watching :)

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šŸ“ŗ Watch My Other Videos:
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Ā Ā Ā ā€¢Ā 5Ā reasonsĀ whyĀ youĀ shouldĀ joinĀ anĀ MSĀ c...Ā Ā 
ā˜… MS Yoga: Twists and stretches for spinal fluidity
Ā Ā Ā ā€¢Ā MSĀ Yoga:Ā TwistsĀ andĀ stretchesĀ forĀ spi...Ā Ā 
ā˜… MS and I: Am I following the Coimbra protocol?
Ā Ā Ā ā€¢Ā MSĀ andĀ I:Ā AmĀ IĀ followingĀ theĀ CoimbraĀ ...Ā Ā 
ā˜… Workout threshold with MS
Ā Ā Ā ā€¢Ā WorkoutĀ thresholdĀ withĀ MSĀ Ā 
ā˜… MS Yoga: Ease your MS symptoms - Pamper Your Neck
Ā Ā Ā ā€¢Ā MSĀ Yoga:Ā EaseĀ yourĀ MSĀ symptomsĀ -Ā Pamp...Ā Ā 
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What is Multiple Sclerosis ā“
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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āš ļø 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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Views : 31,500
Genre: Entertainment
Uploaded At Sep 11, 2021 ^^


warning: returnyoutubedislikes may not be accurate, this is just an estiment ehe :3
Rating : 4.953 (19/1,591 LTDR)

98.82% of the users lieked the video!!
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User score: 98.23- Masterpiece Video

RYD date created : 2024-05-15T20:12:00.707652Z
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YouTube Comments - 233 Comments

Top Comments of this video!! :3

@Slyma

2 years ago

May God help you and all MS patients šŸ’•

73 |

@Ken1Isis

1 year ago

Insomnia please add this as Iā€™m tired of people thinking it is a choice to not be able to sleep

33 |

@jaynebuck5163

2 years ago

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

59 |

@kaladixon2024

10 months ago

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.

10 |

@visionvixxen

10 months ago

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

7 |

@roberture5903

1 year ago

ThalnkyĆ²u .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.

8 |

@seinawhite4400

1 year ago

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

11 |

@186Sexylady

2 years ago

Thanks for highlighting all these symptoms. My son who is now 34 has MS and have all those except pains. His depression and anxiety is so bad that he don't want to get out of bed. Happy to see you looking so great, keep on fighting.

18 |

@arielatomhc

2 years ago

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.

17 |

@Grimace_SYLB

1 year ago

My brother just got diagnosed with MS today. It was hard for me to understand what heā€™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!

5 |

@karenmurphy7066

5 months ago

šŸ˜® 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

1 |

@wernervdz2710

1 year ago

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

11 |

@vandanajain6993

1 year ago

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 šŸ™

2 |

@jlongino51823

11 months ago

I was diagnosed yesterday. Finally. I have a reason why I feel like I do. ā¤

2 |

@stevewildeagle965

8 months ago

May the Great Spirit Bless you, your keeping Awareness about MS alive, Afternoon Fatigue & nightly leg spasms šŸ˜©. 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. ā¤ļøšŸŒˆšŸ™

2 |

@kimpiha7489

1 week ago

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

|

@janedoe381

7 months ago

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

2 |

@richellevanchiere7604

1 year ago

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

3 |

@Chumpess_X

9 months ago

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

2 |

@ecoonce23

2 years ago

Loved your vdo and nailed it right to the cross for me because unfortunately Iā€™ve been diagnosed with Tumefactive MS. Thank you for posting how I /we all go through and more.

4 |

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