My Multiple Sclerosis Story - 2 Years Later

[@JanetLiberto]

Sweetheart! I'm also an MS Warrior. I was diagnosed 16 years ago and I know it can be very hard at times but stay optimistic and keep doing yoga and meditate! xox

[@tabitha1017]

JanetLiberto are you still walking? I was diagnosed 3 months ago

[@JanetLiberto]

Tabitha Glover I am still walking. I use a cane. How I wish I could tell you that I have no issues but that's not the case....

[@tabitha1017]

JanetLiberto how long were you able to walk before a cane was needed? What’s your name? I will pray for you

[@JanetLiberto]

Tabitha Glover I walked without a cane for I guess 12 years. There were a series of stressful events that led to the change in walking. What is your current physical situation? My name is Janet...

[@tabitha1017]

JanetLiberto I just got diagnosed 3 months ago. After my first attack. I’m recovering and about 90 percent bk to my normal self. So I am walking . I am keeping faith that I will walk for a nother 20 years. Please understand hunnie God can do anything. And I will pray that you will no longer need a Cain . You just have to have faith ok.

[@desiderata333]

I am so happy to see you’re doing well. I’ve had MS for 27 years and I have never lost my positive mindset. I could not live any other way. It’s this strength that keeps me going on the bad days along with my faith in God. I may have MS, but MS does not have me! 🙏🏽💃🏻

[@karinmagnusongheddar6476]

Cynthia Dee Thank you. I agree. I refuse to stop feeling optimistic.

[@isaacguerrero6169]

@@karinmagnusongheddar6476 theirs people on my program m.s. is reversing 1st month on program

[@desiderata333]

Karin Magnuson I am sooo glad! Stay strong. 🙏🏽💚💞

[@desiderata333]

Crystalnactor thank you so much. You’re very kind. Be well and stay safe!🙏🏽💞

[@desiderata333]

Owen thanks very much for all this info. I had no idea about sanitation workers never becoming sick. I am going to check that out. It makes so much sense though. God bless you and be well. 🙏🏽💞💙

[@Scrubbini]

I am trying everyday to be like you. Let's stay positive together, MS warrior!

[@richarddavis2107]

Scrubbini why are you not positive? Remember you live with MS that is not who you are you are a person with dreams keep on following those dreams some you will achieve some not, just in life without MS, as Seb said keep optimistic.

[@PoojaKumari-il3oy]

Yeah bring it on

[@Scrubbini]

@@richarddavis2107 did I say I wasn't positive?

[@cherylhorta4131]

Thank you for sharing your story. I was diagnosed 30 years ago. I can completely relate to everything you've said. Well done. Always optimistic and see the joy of the journey. Thank you

[@johnmcnulty1082]

Thank you for your story - it’s truly inspiring. I was diagnosed with RRMS in January 2016. I’m optimistic. I deal with MS one day at a time - there is no other way. I want to go on living as best I can for as long as I can. MS is different for every one who has it. Be optimistic - and let’s hope that the medications for MS continue to get better & better. Be safe - be happy - stay real.

[@TheEDNC]

Thank you Seb, I’m suffering real bad tonight and you put a big bright smile on my sad pain filled face.

[@metaspencer]

Dude, it's nice to hear this follow-up, even if some of the nerve problems have been getting worse. I've also been following up on "my MS story," which seems like a healthy process. As always, you have my support. So hang in there

[@BMax-no9mg]

metaspencer I’m also a KZbinr who has Multiple Sclerosis. My channel is new & I would love if you would subscribe & follow my journey. I use humor as a therapy tool & it’s my hope to touch the lives of other who share the same struggles as me!

[@mdoyle94]

Thanks so much for sharing! I try to tread lightly on the internet out of fear that I'll read something I don't want to hear, but it's so nice to hear positive stories, even if the journey has not been perfect. Thank you again!

[@opheliaslove]

thank you for sharing your story. your honesty, your voice is so comforting. i greatly appreciate your video.

[@robertr.8354]

In the process of being diagnosed. Thank you for your videos.

[@jh1123]

You are incredibly inspiring & positive!

[@BMax-no9mg]

Jill Hansen I’m also a KZbinr who has Multiple Sclerosis. My channel is new & I would love if you would subscribe & follow my journey. I use humor as a therapy tool & it’s my hope to touch the lives of other who share the same struggles as me!

[@jh1123]

Ok. I will be sure to follow you...

[@BMax-no9mg]

Jill Hansen thank you so much!

[@mikeecko]

Great video buddy. Keep on fighting. We're all part of a club that we never wanted to be in. ☹️

[@adobahej8781]

You're doing well and doing the right thing to talk about it. I struggle to talk publicly as I don't want people to see me as weak. Keep strong

[@jenniferpage4211]

Your story gives me hope and comfort. Many, many thanks for sharing......

[@angelusa73]

Ciao, I am the wonan that took Tysabri and the JC an almost took the best of me and was living in the States. I was making videos on You Tube too and I am from Italy originally and now I am back here. I believe in your words and how being positive is very important which was easier for me when I was back in the States. I was making videos in both languages and loved to touch many subjects like you do, now 22 years after the MS diagnose and after surviving the PML I show that we are stronger than we thought and I hoped I was able to share this feeling with others. Thank you for sharing your story and I wish you the very best. Lots if hugs, Angela :)

[@Autumn364U]

Thank you for sharing your update. It is always great to hear positive updates on MS warriors. Keep that optimism and kick MS to the curb. You got this! I now have secondary MS . Take Care of yourself!!

[@1411fly]

Good luck to you seb . Keep being positive

[@Jefff72]

It's great you're doing well. Ya for me, i had a relapse with double vision last summer (2018), in the last month or so, it has improved. My bladder issues are about me trying to let it out. I have never had the problem where I couldn't hold it in, but it's trying to let it go. I need to relax and it's hard if there's tons of noise and stress around me. I often constipated. I try to eat a lot of fruits and vegetables and drink a lot of water to help me pass. Now I have been in the weight room trying to put some mass on my skinny ass for the last year. My strength has improved. Var stark!

[@ajdicarlo8693]

i cried watching this thank you so positive man !

[@carlagarrett3244]

wow a heckler from a longterm MS'er. Optimism, enjoying life till the last breath, is what keeps you doing things, if you have a few or a lot of years. You are a great inspiration, and I suspect he was and is fighting to get his back.

[@riv3rss]

God bless you always sweetheart! 🙏🏻🌸 yes, stay optimistic!! Please keep fighting...your story is very inspiring and touching! 🖤

[@rockymountainrocker5630]

Thanks for sharing (again)! I am also an MS warrior.. will not let this thing win! Keep up the spirit my friend! Bless you.

[@rockymountainrocker5630]

Our minds are so powerful for either good or bad... Optimism is the ONLY way! "It's not what happens to us that defines us.. it's how we deal with it that defines us." Love ya brother!

[@tonyaelrod1869]

Your story touch my heart. I will continue to pray for u and your family every day... God bless u ...thank u for inspiring others.

[@christinev3534]

Thank you so much for your inspiring video I needed to hear your positivity.. I am educating myself as well.. in the process of getting into a neurologist to be tested.. I am losing function of my legs, bladder and bowels and I am now having tingling and numbness in my arms, hands and the right side of my face.. in lieu of those symptoms I do have problems in the L1 to L5 of the spine.. I can only pray for a diagnosis sooner than later bc things are happening fast.. Thank you again for your powerful inspiring message today.

[@BMax-no9mg]

Christine V I’m also a KZbinr who has Multiple Sclerosis. My channel is new & I would love if you would subscribe & follow my journey. I use humor as a therapy tool & it’s my hope to touch the lives of other who share the same struggles as me!

[@sharaeman]

Very beautiful and inspiring video! Was recently diagnosed with MS and had to stop my medication for RA. Now I await treatment for both conditions! So tired of awaiting the start of my new medications, whatever they may be! I needed to see this video tonight!!!!

[@trixie1556]

Thx for all your videos. I know this is not easy but I’m learning a lot. I truly appreciate you telling us your continuing journey.

[@LifeofSebMS]

Thanks for the kind words!

[@chungseng4155]

Thank you for sharing your story. It’s really comforting to others that have the same conditions.

[@Universalwillful]

Thank you for your calm and warm voice, God Bless You

[@bholahashutosh3300]

This is beautiful! Hats off to your optimism and fight against Multiple Sclerosis :)

[@charlottemclaughlin4706]

really really inspiring .... thank you .... i feel brave enough to go check out my symptoms now

[@steph5260]

Hi was recently diagnosed with MS - was diagnosed with epilepsy a year ago ... than to find out the lesions were causing the Epilepsy all along - waiting for treatments since the holidays- your story is very optimistic which is all I am remaining for now - life is already a struggle at times thanks for the inspirational message!!

[@sugoijade9379]

how are you doing now?

[@venternicky9599]

We all have some kind of health problem, but like you say "never give up " keep on smiling and hoping. You are a beautiful person. Stay strong.

[@Kirarachu]

I was diagnosed 2 years ago as well though my first relapse was mid 2014. I felt compelled to comment because I too have found that the worsened, most prominent symptom for me also is numbness in the fingers of my left hand and the toes of my left foot. I do aerobics for 20 minutes on the weekdays and I notice for the first time in the past months that the feeling becomes quite strong even on days where it isn't hot. I don't notice it as much when I'm walking or doing other things. I haven't had any new symptoms either and I consider myself grateful for this. I read the blogpost you mentioned as well and I find that his view is in general rather dark. Those kind of thoughts remind me that it is better to surround myself with positive thoughts even if I am headed to a similar progression, far better to focus on where I am at this moment. I also read the blogpost you mentioned and I find his opinions in general to be dark and negative. Whether I am where he's at in 10 years or not, I would rather surround myself with positivity in the meantime and to focus on my own journey. xx

[@BMax-no9mg]

Nyssa I’m also a KZbinr who has Multiple Sclerosis. My channel is new & I would love if you would subscribe & follow my journey. I use humor as a therapy tool & it’s my hope to touch the lives of other who share the same struggles as me!

[@bigearsandnoddy1]

I've had MS NOW FOR COMING ON 23 Years and I'm in roughly the same boat as u Seb concerning MS symptoms apart from the walking side of things as my right leg seems to be getting alot worse as in I can't seem to be able to move it where and when I want to I also have dropfoot on my right leg Which constantly makes me trip, I'm also taking gilenya now for the past 6 years and I'm having no problems with taking it I.E. no side effects, how I see it is you just have to get on the correct meds suited for your body so it's totally trial and error but you will get there in the end so stay strong Web and stay safe ✌️ peace ✌️ 🇬🇧🇬🇧🇬🇧

[@LifeofSebMS]

You’re so right! 🙏🏻🧡

[@sheripacori2097]

Yes yes yes. It is true. The mind is powerful. Stay positive. Worry and stress is poison. It will only make things worse. Stay optimistic.

[@jackiefrazier316]

Thank you Seb for sharing your story. You are more courageous than most.

[@kristamunger7915]

God bless you. I was recently diagnosed back in May 2017 and have been taking gilenya as well. I appreciate your optimism; that definitely is keeping me going everyday. Thank you for your story. ❤

[@BMax-no9mg]

krista munger I’m also a KZbinr who has Multiple Sclerosis. My channel is new & I would love if you would subscribe & follow my journey. I use humor as a therapy tool & it’s my hope to touch the lives of other who share the same struggles as me!

[@YANKEEEFEVER]

It does make me feel better that there are people that make this video, I'm 21 right now, and I got it when I was 10 years, at that age, you don't know what it really is, and I still haven't looked up anything becuase I really don't wanna know what can happen, I don't have it bad at all, but it can still do an impact, but thank you for making tbis video

[@jstringer4900]

Thank you for posting this. Hope you have lots of good days. :)

[@27Zangle]

My wife was just diagnosed with PPMS December 2017. We have two young children and she is rapidly declining. Hopefully treatments will slow this down a bit. Thanks for sharing your story!

[@KayDon11]

27Zangle - Would you mind if I connected with you and/or your wife? (Instagram or Facebook, maybe?) If not, I completely understand. I have RRMS but it shows no signs of slowing, no matter what medicine I'm on. Hoping maybe we could share ideas that might benefit each other.

[@27Zangle]

Yes. My wife said she is willing to correspond via email or maybe Facebook message. Obviously no personal information should be shared publicly.

[@KayDon11]

Just sent you a private message, (and potentially a duplicate), through KZbin with my email address.

[@27Zangle]

Nothing has come through.

[@KayDon11]

27Zangle I jumped ship from the KZbin messages. I messaged you via Google Hangouts

[@steffanyhenderson7964]

Stay positive! You’ve got this!!😊

[@vk1990]

God bless you brave heart

[@trondgran]

Got ms early in mai this year, thank u for the video

[@LifeofSebMS]

Stay strong! 💪🏻

[@GrayStoneAngel]

i lost the only man that i called, “father”, ( my stepdad ) due to MS 😢. i just wish i had more time with him to let him know how i felt about him. I Your Strength 💪🏻 Gives Me Strength … keep going sweetie. You Are Loved. ♥️

[@LifeofSebMS]

Thank you 💪🏻😘

[@extofer]

I think it's great to be optimistic! I am optimistic every day despite the MS!

[@elifraser2783]

We’re still here, alive and kicking!

[@BMax-no9mg]

Hey Eli Fraser! I’m also a KZbinr who has Multiple Sclerosis. My channel is new & I would love if you would subscribe & follow my journey. I use humor as a therapy tool & it’s my hope to touch the lives of other who share the same struggles as me!

[@elifraser2783]

Bullsh*t with Britt Thanks! I subscribed 😊

[@BMax-no9mg]

Eli Fraser thank you so much!!

[@Kaiwaza]

Keep up the good work! We all have to approach life on our own terms.

[@andythrash.]

I am starting Gilenya in the following days since the Tecfidera I am taking isn't doing a very good job for me. I am a little scared of the Gilenya tbh but this has to be done and I'm optimistic! I am meeting my neuro tomorrow to book my first pill observation, the box is sitting right here beside me as I'm typing this lol. Thank you for your videos Seb 😊

[@dianedurham8817]

Ur voice is very calming. I like listening to you.

[@LifeofSebMS]

Thank you! 🧡🙏🏻

[@shaneworsham8624]

Thank you so much for sharing your story and for encouraging others. I recently came across the Wahls protocol. I haven't started it yet, but it was created by a doctor who was diagnosed herself with ms. She has a video on KZbin that's quite interesting. Her MS symptoms have greatly improved. Just thought I'd share. I wish all the best and much happiness despite the many challenges you face

[@johnhornby7806]

inspirational, handsome and thankyou for sharing your life story up to now

[@MatidaJane]

Because I have had MS undiagnosed for more than 50 years even though I knew I had it by my symptoms I have just lived my life and got on with it. Putting MS to the back of who I am. Had four children when all the advice was don’t. They are all range from 57 to 65 in age and have had no problems with MS. Vanity prevented me from taking medicines so I just put up with what MS throws my way. I know you are probably thinking OK for you but Seb M S is just a part of the whole lovely you. We make adjustments we have to but that’s OK too. So love your videos and wish you a,long life. ❤️

[@LifeofSebMS]

Thank you for sharing your thoughts and journey, dear Jane 🙏🏻🧡

[@potsak]

Be brave sir and think positive. God bless

[@jenniferbeer1290]

Thanks for your video, helps me feel positive about my future with MS

[@almudallalrana]

We all supporting each other spritely I guess ... I am an MS , I recently was told I Am with ms , I suffered since 2011 and didn't know what's going with me , today in 2018 finally I knew why I went through all that pain when I didn't know nothing about , till the doctor said its serious U have MS. It's a shock yet I am still digesting it perhaps I was told to try ozone therapy

[@chrisnickens4619]

Hey Seb. Great video! You are a natural instructor and you speak with knowledge and passion. I'm a year post HSCT (@Northwestern in Chicago) and improving every day. All traces of MS are gone. (I can relate to the the hand numbness/pain) Yoga has been an amazing part of my recovery. If you ever want to chat about HSCT lmk.

[@MsMustang58]

thanks for this, stay positive ! you are an inspiration

[@brendallscott6879]

Thank you for sharing your story. I am scheduled for the spinal tap and 2nd MRI in 5 days. The symptoms that you described are very similar to my own. I have been trying to find out what's wrong for about a year now. Hopefully I will have some answers soon. I am up late surfing the web for information and I am really glad I got to watch your videos. I have hope.

[@jazzlall3971]

How did you get on?

[@MarianFit]

Ni imaginas lo mucho que me relaja escucharte y todo lo que me transmites☺Gracias por compartirlo con nosotros. Me alegro de verte tan bien Seb😊😘

[@cidh9531]

Thank you, I cried and laughed. Optimism, humor, and love is so imprtant. When your friends only allow you to use plastic wine "glasses" is just funny. Well Wishes.

[@alrightwithms845]

Thanks for the update - Fantastic yoga move!

[@alaaadel8900]

*اللهم صل على سيدنا محمد وعلى اله وصحبه وسلم تسليما كثيرا عدد خلقك و رضا نفسك وزنة عرشك ومداد كلماتك و عدد ما كان وعدد ما سيكون وعدد الحركات والسكون.*

[@bizzye]

What’s good homie, don’t give up on this journey, we got this, wish you the best

[@kekecatty]

I was dx with Sciatica a few weeks ago and all my symptoms now are scaring me I have a limp on my right side, both legs and feet have that tingling sensation, including hands and my back. I woke up yesterday and my eyes were so blurry. I wear glasses! I wake up every hour, or sooner, but I'm a side sleeper and both hips can't stand the pressure......I have severe charlie horse cramps that start from my feet all the way up to my thighs. Auto immune disorders runs in my family, my son has plaque psoriasis. I made an appointment with my primary Doctor........ I was dx with Breast Cancer two years ago.......I'm 56 years old and scared......

[@BMax-no9mg]

keke catty I’m also a KZbinr who has Multiple Sclerosis. My channel is new & I would love if you would subscribe & follow my journey. I use humor as a therapy tool & it’s my hope to touch the lives of other who share the same struggles as me!

[@willcortez5]

Sorry to hear, but it sounds like you've been through a lot in the past. And I think a great attitude and optimistic outlook steered u through that. U are strong and you can get through this. God bless u and ur family

[@XTCBiscuit]

wow you give me optimism because I realized that I worried much about trivial things and that I wasn't taking the time to appreciate the good fortune of having friends/family and myself in relatively good health As for the liver and alcohol, i'd like to relate my story of how less than a glass of wine is enough to give me a headache and nausea (like a hangover i assume), but within about an hour. This is due acetaldehyde dehydrogenase deficiency, a functional lack of the enzyme needed to detoxify one of alcohol's toxic by-products: acetaldehyde. So there are some things that your liver will still be better at doing, and defending against alcohol is one of them, well relatively speaking compared to me anyway All the best

[@MrBass-nt5fw]

Thanks for your courage. it can keep you strong .

[@brianpan6453]

You are a very charming and handsome man, Seb. I wish you continued and steadily improving good health. Remember, you are not your body. The body is a place holder for your spirit for a set amount of time. I hope you are, also, surrounded by good friends who will watch over you. Peace and good wishes, brother.

[@dishabydeepanagesh]

hi I am Deepa Nagesh from India I live In India I really love your videos and I am following your videos and you are such a positive person I like that keep it up your positive energy and being A Hindu I like your tattoo that's full of positive energy and ahimsa means no violence so it symbolise that you are so so so energetic and positive thinking person so keep it up keep smiling have a great health and happiness

[@jenniferbeer1290]

Have you read Bruce Lee's - Wisdom for daily living - think you would enjoy it - one of my favourite quotes are: 'Greatness is in the act of trying - in great attempts it is glorious even to fail' To be discouraged is to be defeated' 'Optimism is the faith that leads to success' 'Faith and belief is wasted if not acted on' Thanks again for your positive video going in for Lemtrada treatment next week and your positive attitude is a breath of fresh air

[@adobahej8781]

Hey Seb, thanks for this. Very inspiring!

[@sofoniaszemichael8596]

Hello SEB! MRI showed 2 lesions in my brain and I will most likely be diagnosed with MS in january. About that double vision. U could get prism glasses, which I got. Extremely helpful

[@panthersprung5161]

how did it go if i may ask?

[@hectorraulruizgongora5329]

you are so strong and a truly Human inspiration and warrior , you have a beautiful body and soul, I'm sending all my positive vibes.PD: you are very handsome too.

[@TalhaKhan-ml2gj]

I wanto contact you

[@rmetal2792]

You can listen to him all day. How i wish there will be a definite treatment for MS.

[@laurenvillegas6103]

Me more. Sometimes I rather have it be fibromyalgia or even epilepsy like my husband.

[@Evenfall-s3g]

I'm too a Ms Warrior..I am happy to see that beautiful hindi Tattoo on your arms..your story is encouraging...All The Best😊

[@isabilas]

Just found your story...very similar to mine!!! Hope to hear more from you!

[@isabilas]

And I became a yoga teacher!

[@michycruz1145]

You are sooooo strong and bold !!! ❤️❤️❤️

[@geraldkeene6172]

You are so handsome and your personal strength shines through

[@carnunicoleta]

Hi Seb! I think you should try looking into the Vit C liposomale because it is non acid and much better assimilated by the body. I think Solgar has it and I believe it’s called Esther C or Solaray etc etc... and you can have it at 2 to 3 grams a day. Vit C it’s the only one you can not over dose ever!!! if you attained the dosage your body needs you just eliminate the rest just gets excreted through your kidneys without affecting them. And the first thing that it will do to you would be helping your liver and with time it will also start helping your immune system. Just look into it. I wish you all the best !!!

[@hanimasyi94]

seb, 9 April 2020 was my 2nd years live in MS. new symptoms i am experienced it now...at age of 26years old. 1. i having problem speaking.. 2. Balance worst 3. Sharp pain on my right chest keep on n getting bad 4. Numbness on my left legs worst.. before just my right leg..now its both... 5. my hand shaking while writing or holding something like pen/stick... my doctor said the only steroids can slow down the symptoms..BUt i am in bad emotion..sad..stress out.. i dont want to eat dont i have to control my diet calories and everything yoga n so on..but end up i feel like better i die. nobody able to help... when look so skin n sick people talk about it when i gain weight because of steroids people talk about it.. what should i do then...i also stuck n dont know. y dont people just shut up n together pray. its much valuable. love n hug from Malaysia.

[@valansley]

Looking GR8 = Yoga clean food meditation and fresh air help me to cope = Keep teaching

[@MenetO7]

thank you seb :) your video did cheer me up and gave me more hope

[@LifeofSebMS]

Stay strong 🧡💪🏻

[@lastanetaarion]

I'm taking Avonex injections every week. After 2 years of taking it liver markers in the blood tests were just above the norm (around 42 and 60). Someone recommended me taking this thingy: en.wikipedia.org/wiki/Silybum_marianum - 2 tea spoons freshly ground in a coffee grinder (about one tea spoon before grinding) every day. Being me I was a little worried about the tests (quite unusual, because I used to not get along so well with my "corpse" - now the relation is a little bit better :P) so I started taking it (but 2 tea spoons every 2-3 days) and for one year now my results for the liver are oscillating in the middle. I don't encourage you to take it due to mixed results you can read about it but it seems it works for me so I will keep taking it ;). P.S. Sorry if something wasn't clear - English is not my first language.

[@lkog5r-0]

I recommend you to start diet based treatment (avoid protein especially cows and eat a lot of vegetables) fasting also helps. There are a lot of videos about this on KZbin

[@ritalahlou1620]

Could plz recommend any that match with the fasting diet

[@jh1123]

What a complete shame that this other MS patient tries to deflate your optimism...he must be extremely angry & bitter. It has been proven that a positive mindset is very therapeutic along with healthy eating, exercise, etc. I don’t have MS (at least I have not been diagnosed), but I know a lot about the power of positivity, prayer, living as healthy as you can as I do suffer from other life changing issues. Please stay the way you are...awesome!

[@LukeHughesfromBournemouth]

Stay positive mate! It's proven scientifically the power of positive thought

[@meganhenry5795]

When I get tired, I see a flash of light in my left eye that coincides with my heartbeat. Dr said I'm "insane" to think I have M.S. I get pins and needles, numbness in my hands during the night. Constantly feel like I'm on a g-damn boat. That's the worst symptom as it makes me nauseated and feel like I'm on the verge of a violent vertigo attack.

[@LifeofSebMS]

So sorry about that, that sounds horrible :(

[@sumeenahmed5099]

How r u now did u get ms

[@TorkomMovsesiyan]

Never change!

[@JUSTME190-p1x]

Oh I wish I was doing that good today my downs seem to last 4 ever . I dont even care if I get Corona today I feel so bad I try to stay positive it's just it's so hard to when it hurts to walk 10 steps ..

[@notion14]

Hi.. How are you doing these days..

[@JUSTME190-p1x]

@@notion14 good days and bad days around and around hope all is well with u..

[@jsmith317]

Awesome! Thanks for the attitude you have. Keep that optimism. It's wonderful! You make excellent points.

[@summersinclair8211]

Seb, I think you’re a beautiful person inside and out .How old are you?Where are you from. I also have MS.I just started taking Tecfidera..I been getting flushing from it.Sometimes I feel down but your video made me feel better that I’m not alone.

[@heng-s-intuition1688]

Thank you for sharing again.

[@sabrinareddington8751]

Keep pushing yourself

[@SoulTarot90]

I am going to take the tests i am 90% sure i have the same... i am 28 years old... i feel i die... horrible symptoms and 3 years roaming from doctors to doctors with no help... 3 brain mri, analyses...everything i cld think of... last night i thought i will die... i don t know how i ll cope with the thought of having this...

[@susanaviegas3350]

Thank you Seb! It´s nice to hear your calm tone of voice and tranquility! God bless you! Did you heard about Coimbra Protocol, with high doses of vit d? It works very well for MS and other autoimmune deseases. please serach for this. in fb there are few groups about the protocol that can help you know more, and lot´s of youtube videos too with Dr Cícero Coimbra, a neurologist that created this amazing protocol. All the best! Susana

[@nuttersnut2000]

Hi there, I am sure that you have gotten this question before but I have to ask.....have you changed medications since your first videos to help with MS lesions? Or have you found that the medication you have used works? I've been told that my medication isn't working well enough and I need to try something harder. Thanks for your videos, they make it seem a little less intense.

[@Lugmillord]

Yes, let's stay optimistic :) I'm at 1.5 years now.

[@BMax-no9mg]

Lugmillord I’m also a KZbinr who has Multiple Sclerosis. My channel is new & I would love if you would subscribe & follow my journey. I use humor as a therapy tool & it’s my hope to touch the lives of other who share the same struggles as me!

[@ghizlaneabdouni6403]

Hi am a new fan from morocco , i want to asck you about diet do you think diet can help us to improuv our quality of life, and how about hsct i hear it can help a lot

[@LifeofSebMS]

Diet can definitely help you with your energy levels, as for hsct it is supposed to be very effective but I’m too scared of it…

[@florindalucero3236]

Were you not tested for PML, before beginning the Gilenya? I can't take it, because I came up positive for JCV.

[@gabbyfranks78]

Love ur videos.

[@mehdimellak6240]

Search for HSCT Bro they are practicing it in uk , chicago ,moscow , Singapour, italy