The Truth About Accepting Multiple Sclerosis | What They Did Not Tell you
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- Опубликовано: 29 июн 2024
- Accepting a life with Multiple Sclerosis by your side is tough to accept and you may be longing for the day when you will accept it. The truth is not that simple, unfortunately…
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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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#LifeofSeb #multiplesclerosis #ms #livingwithms #mssymptoms #msdiagnosis #msawareness #msfighter #multiplesclerosisawareness #invisibleillness #autoimmunedisease #thisisms #multiplesclerosiswarrior #mswarriors #mscommunity
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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" RUclips 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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Awe Seb your always such a beautiful person inside and out. I have always loved how you speak from the heart. I love this community you have created for all of us to hear from such kind, caring, kind soul. ❤ Seb you are truly loved by all of us. Have a beautiful night xox❤️🤗😘🥰❤️
Thank you so much Rose. It really warms my heart to know that I am bringing comfort to the community. Hope you had a beautiful night too 🥰🧡
@@LifeofSebMSI always look foward to your videos seb your a very genuine and decent man.
🥰🧡
Yes, it seems like every day we need to check in and say "so what can I do today"? and accept that today may not be a good day for a long walk but know that doesn't mean that tomorrow won't be! Never making demands but always asking the question. We have to be more in touch with ourselves than others which, in a way, is somewhat of a blessing...to live with that vulnerability. We can make not demands but always hope.
And in turn we are encouraged to be our own best friends 🤗🧡
Love you Seb. My way of accepting the dreaded MS is to 1. Put my hope in Heaven (2 Cor 5:1-2) 2. Do my best with what I have each day 3. Not be ashamed when people ask why I am limping when outwardly I look fine. MS sucks. But life is worth living and we WILL keep going and not give up. God bless. Xxx
Beautiful, thank you for that 🙏🏻🧡
I’m so thankful to have found your channel. I’m just starting this MS journey and it’s all new to me. Your videos have helped me so much already. I’m sure this community will continue to be an encouragement for years to come. ❤
Thank you so much for your recognition! I sure hope that this channel will continue to provide you with some guidance and moral support 🤗🧡
Hi Seb, I’ve seen this acceptance deal over and over each time it gets harder to do. Knowing you see it as I do makes the difference. Please keep making your videos they make so much sense. Love and hugs from the UK X
So good to know that there’s more people who understand😓🧡
The goal is and will always be to have "the serenity to accept the things we cannot change, the courage to change the things we can and the wisdom to know the difference".
Already accepting the fact of our finitude with which we are all born is quite a challenge. That's why every second counts and tomorrow is now, at this very moment. Go ahead, lovely human being.
You speak words of truth! Thank you so much for sharing this shard of wisdom 🤗🧡
@@LifeofSebMS
I am the grateful one Seb. Until next time.
I do not have MS. But I have limitations, as so many do. What I try to do is ask myself each day, "What can I do fairly comfortably today? Can I go to the store, can I do some yard work, can I do some housework, can I wash the car or do some laundry? Physical fatigue and weakness can undercut the best of intentions. But doing things slowly and one small piece at a time will get things done, and if there are things left over you cannot do today, there is always tomorrow. On days when it seems everything is beyond what you can or want to do, do nothing except rest, eat healthy and delicious food, read a great book, listen to some favorite music, and maybe take a nice, soothing shower or bath. That is plenty for one day.
Beautiful 🤗🧡
MS definitely keeps,us on our toes (or off of them 😉) with the potential changes day to day. You are so right that we need to adapt.
Exactly! 🙏🏻🧡
Once again? AMAZED WITH YOUR PRESENTATION. Just also accept that as life changes for us then we don't get bored. But a more challenging time
Thank you brother! You are so right! 🙏🏻🧡
In my head I'm still 25 years old and the world is open. there are no obstacles. but then Mr. MS knocks. now and then. And it's tough to accept again and again. But over the years I have learned to be better at accepting my MS. But I don't see myself as an offer. And I rejoice in the fact that I believe I can do just about everything. I have dreams and my MS can't reach them. 😊
That’s beautiful 🤗🧡
Your videos and the wisdom you share are always a gift 🙏🏻
Thank you so so much 🥲🧡
Today Your Channel came across my RUclips feed. You talked about accepting and living with MS. Man, your statements really hit home with me. My diagnoses was in 2010, after some years of oddball symptoms and events. And still today, I struggle with accepting MS on some level(s).
Many people with MS will say terms like, "my MS."
AND I don't want to claim it. So I don't say "my MS."
But will say, "I have MS." There may be no difference whatsoever between those two phrases. ???
Your smile and gentle spirit are like a breath of fresh air.
I hope you are doing well. God bless you.
I think “my MS” can be appropriate in the sense that everyone has a different version of the condition, but there definitely is that undertone of becoming your illness with that wording! 🤗🧡
first off awesome backdrop.... looks like you may be in paradise!! regarding your message, I appreciate you bringing it up as I am still struggling with accepting the fact that I have MS, especially being diagnosed within this year at 52 years old. very much appreciated my good man
Be strong!! 💪🏻🧡
Much prefer your approach to MS…calm, honest discussion and acceptance rather than the “MS Warrior” anger mindset. Thanks for inspiring so many of us. 🌞
Thank you, Mary ☺️ I used to be all about the warrior type, but time has taught to take a more peaceful approach 🙏🏻🧡
Well said. This is great advice. I think you are right on the money. Thank you.
Thanks brother 🙏🏻🧡
It's not good news, but it is true and must be realized to be accepted.👍👍
Hi Seb.✌
Hi brother!! 🤗🧡
Hi Seb thanks for checking in ❤
🙏🏻🧡
I still deny it. After 15 years I don't waste time with neurologist or neuro opthamigist, they can't stop atropy of optic nerve so why bother. The 4 attacks the confirmed and the 4th did permanent damage. Nut they did nothing with the first 3. Just confirmed I see cardioligist, GI doctor, physical therapy and my faith. Neurologist offered me nothing else. My heart attack at 47 due to microvasular disease (not bad living or high cholesteral or type II or uncontrollednlood pressure) was scarier. But EVERYBODY has good and nad days. I just yhink people with MS look better. Cause rveryone tells me I look great. We a good looking bunch.❤😊
Hahaha we do indeed look amazing!! 😅🧡
Have you ever considered the possibility of you not having multiple sclerosis and it being something else? Like a deficiency in some vitamin, perhaps?
Haha no… I’m pretty sure it’s multiple sclerosis unfortunately 😉🧡
That thumpnail got the Muscles going on 😊
Hahaha I actually find kneeling very comfortable… must be the yoga! 🤷🏼🧡
@@LifeofSebMS its a complement your very toned kneeling for any length of time almost kills me but its not the kneeling its the toned arms you look good ! Idk about you but if someone gives me a complement now idk how to take it with my MS some times i don't feel human not speaking for anyone but myself i think they said it just to make me feel good cause i have MS .Would never do to anyone you actually look fit and good hope all is well with you 🧡
Hows the Wahls protocol going?
Still doing on it but currently on a rough patch due to being outside my comfort zone… 🙏🏻🧡
wahl's protocol still being followed?? acceptance? i'm more of a Supertramp's Fools Overture kind of person.. give it a listen if you want some inspiration....
Yup, still being followed 😉🧡
tough trying to gauge progress when looking at yourself,,, but i have to tell you, it only took about 6 hours to recover from shopping yesterday, as opposed to usual 2 full days of doing nothing!! i see that as significant improvement! and i'm not as stiff first when i wake.. think my toe drop has improved too. could it be that Wahl's magic is kicking in?? you seeing any small changes since you began??@@LifeofSebMS
❤❤❤🙏🙏🙏
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