My Multiple Sclerosis Story: Symptoms and Diagnosis | Life of an MS Patient & Explaining Symptoms

Hi there! In this video, I shared my multiple sclerosis story symptoms and diagnosis. Also, I explain all about the life of an ms patient. So if you want to know more details about my multiple sclerosis story: the prelude, the diagnosis, the treatment, the symptoms. Watch the video till the end. This is my story of how ms became a part of my life and how the multiple symptoms had been around before I was diagnosed. Hear me talk about how I made it to the current day and what ms treatment I am on today.

⌛ Timestamp
0:00 ➔ My MS (Multiple Sclerosis) Story, Prelude
1:20 ➔ the Diagnosis
4:20 ➔ the Treatment
6:13 ➔ My Symptoms Today

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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📺 Watch My Other Videos:
★ 5 reasons why you should join an MS community
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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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[cardinalrobbins]

Thank you for sharing your journey. You (and Selma Blair) have given me the courage to share mine as well. The more I learn, the more I realize MS has been a major part of my life for an extremely long time. But we are warriors! We will adapt and continue to live life to the best of our ability. <3

[shrutijoshi]

As a psychologist, I understand all of your pain.., the depth of disease. I pray to God to give courage & strength to all of them who are suffering. You are strong enough dear people.

[KatiiieCakes]

Wow 20 lesions, you poor guy! I'm recently diagnosed but only had 3. My attack/relapse was very different from yours. Tingling from the neck down then paralyzed on the right side for just over a week. I see a lot of people arguing in the comments. This disease is individual for every single person. It is not a competition. If anything we need to ban together. Thank you for sharing, it helps hearing peoples stories.

[melymichu]

I didn't know the exact symptoms of MS till I saw Selma Blair talking about them. I am a huge fan of hers and seeing her go through such a debilitating disease and fighting it, just impacted me hugely. My heart goes to everyone suffering from this disease. I admire also all the people coming out and posting these videos and sharing their stories to create awareness and more understanding on this. I hope one day there will be a cure. Blessings to all <3

[reynasanchez]

My mom was diagnosed when I was in the 6th grade.. I’m 32 yrs old now and still blessed to have my mom in our lives. I do not wish this on my worst enemy, hate this disease

[mandypdx]

My mom had MS!! The most beautiful human in the world...she has past but will forever be my hero 💜💜💜

[S-jw]

Hello everyone best of luck fighting against ms I got diagnosed when I was 19 I had complete paralyzes on the left side of my body I couldn't speak either and I had optic neurits all in one attack I'm 22 now starting treatment soon relapses have been on and off affecting walking speech and vision . However I'M currently studying two degrees and working part time, we are all in this together and I believe that by sharing our stories we are encouraging each other to keep going . Healthy diets everyone without saturated fats and excerise . Keep positive 😉

[mellydodge]

I too have MS. After years of various symptoms I was finally diagnosed in 1998. I don't have any medication but have a vit b12 injection every 3 months. I have a positive attitude, even when I am having a bad time. It's holistic and I will not let it rule me....well, not my mind anyway. Good luck to you my

[MeikeBC]

I got diagnosed with a ridiculous amound of lesions yesterday because of the exact same reason; double vision and loss of speech and walking. it is very nice to listen to other people right now to get through the initial shock. In the hospital now. I very much hope you are doing good and well. thank you for uploading this video.

[Iambrittanyisis]

Wow, your bravery gives me chills. I’m still learning to accept MS and the way it will affect my life, and yet, I persist on living my best life! I hope you will too!

[missymogfossy]

Hope you're doing well now. I've had MS for over 25 years, no disease modifying drugs in the past ten years. Stay strong and keep a positive mental attitude. x

[metaspencer]

hey, I just wanted to let you know that, after watching your "my MS story video, " I finally got off my a#% and posted my own. so thanks for the inspiration! :)

[MsMOLLYKINS]

Hey sweetheart, I am 46 and have lived with lupus all my life . I now have ms because lupus attacked my Milan sheath . It's hard some days and I struggle walking these days and my eye sight is very poor . Never give up hope and faith because that is what gets us through the hard days. Stay strong and keep blogging I am listening xoxoxo molly from Sydney Australia

[mcw]

I'm here watching this video after falling in love with someone living with MS.... Thanks for sharing 😘

[treasurecompanion]

Gorgeous man I'm so sorry to hear of your health struggles and just want to wish you love n happiness.

[adishmaryahu]

Wow! I can so relate to your story and symptoms. I hope you are managing well with this disease. Don't lose hope. I was diagnosed with relapsing-remitting 27 years ago and I am currently very active.

[黃祐宇]

I’m 16 and I have MS too
Let’s fight it together

[hebneh]

This is the 2nd spinal tap scare story I've encountered in these videos. I had one when I was 6, and it was nothing. That was 60 years ago. Now, I can be grateful.

[wmccullough]

Thank You...I'm starting my journey, I noticed symptoms about a years ago. The constant pain, especially my back, legs, arms and neck, headaches, vision changes, my balance, and this uncontrollable sleepiness and walking slowly with a cane now...It's shameful 2 doctors thought I was faking! Going to see specialist in major city next week.

[Naveen.Jayananjachar]

My Daughter got diagnosed with MS today, She had double vision. Continuous hiccups, pain in legs. We r treating her. Thnx for sharing your story. Stay Strong. Miracles happen you will be fine in one day.