Understanding multiple sclerosis and what it does to the body
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- Опубликовано: 26 сен 2015
- Multiple sclerosis (MS) is a disease of the central nervous system estimated to affect 2.3 million people worldwide. It is a chronic disease in which the immune system abnormally attacks the insulation and support around the nerve cells (myelin sheath) in the brain, spinal cord and optic nerves, causing inflammation and consequent damage. MS is a leading cause of non-traumatic disability in young people, usually striking between 20 and 40 years of age. There is no cure for MS, but research continues to better understand and treat the disease.
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As someone who’s only in my 30s, being diagnosed feels like a death sentence.
Also, Thanks Kursgesagt For animating this video!
Thank you 🧡 Information I was seeking delivered by one of my favorite educational tubers! 😁
It’s still unbelievable to me that I was diagnosed with MS in grade 5 (11yrs old). Have a crazy story that I will probably make a book on one day.
Mine was at 6 or 7 years old and they sent me home immediately saying oh that car accident that dented your skull and destroyed your brain didn’t do anything pssh, go home!
Not even 30 now and bedridden, cannot walk, on an 8 on the disability scale, suffering PPMS. Now everybody is starting to know stuff about ms, feels too late for me personally, but hopefully not for others who got it super young like us.
@@MotherRuss1ajust read your comment 💝 wishing you well.💫
You also 🌻💫
Who ever is diagnosed with this disease, i just want you to know if i ever had chance to meet you guys I'll have hugged you with all my heart and had a great conversation, I wish you guys well
I was confirmed to have MS less than a week ago. I showed this video to my loved ones to help them understand what is happening to me and I find it to be really comprehensive and helpful, thank you for this! I am Wishing everyone all the best 🙏🏾💛🙏🏾
Thanks for sharing your experience with us. Stay strong. Have a nice day ahead.
❤️
My mother has it and it is really hard to live without worrying for her
Really helped my understanding of the condition. Thankyou!
Wow you explained it soo right! Full of details!😲
Thanku so much for this video and I have been diagnosed since 2019 and I'm still going strong thankyou Father God Jesus 🙏
A very good teaching tool!!
that was amazing and verey emational
Excellent video content! Forgive me for butting in, I would appreciate your thoughts. Have you researched - Liyaraah Sclerosis Redemption (probably on Google)? It is an awesome one off guide for overcoming the symptoms of multiple sclerosis minus the hard work. Ive heard some amazing things about it and my good mate called Gray after a lifetime of fighting got amazing results with it.
Thank you for this information
Excellent gives the information about this condition
Amazing video thank you
Sometimes i wish if it was recorded in different languages :"( Thank you for your help and support.
Same. Bc i am a greek and also i have MS and..well i forgot many words about English language 🙁
Thank you so much this videos
such great animation!
This should be redone at kurzgesagt.
I am doing a research paper and presentation about MS. Your video is awesome! Great presentation! Very fun and easy to understand! Love love it! Thank you for sharing!!! ^_^
My mum has it it’s been tough growing up like this
Thanks ever so much
Now you know! I take meds for it !
I have Ms and I am 18 years old. Had it since 15 years old and had 2 attacks, yeah it's scary.
Super video nice to see youcg
❤quando me m'hanno detto è stato tremendo..ora ci convivo ma non ho accettato..ero sano..giocavo pallone...lavoravo...ora tutto questo..non più..come faccio..è una vita diversa..anche se dicono..di no...bisogna esserci...😢😢😢😢😢
I got diagnosed at 15 💀 well I am 15 but I’m 16 tomorrow
How are you now? I just got diagnosis yesterday. Believe me, it's stressful like heck.
How you doing now?
I have MS too. This has inspired me to start my owm RUclips journey. Please check out and support.
Take it one day at time
Laiba Khan i was diagnosed 1 month ago but found at today at age 15... almost 16 and i was reading my doctors note and it says it can “aggressively worsen overtime most likely” how are you taking it?
U let me 4get the disese and enjoing ur demonistration😅I thank u a bunch🥰🥰🥰
I don’t know the protocol...how do I go about featuring this video on my channel. I would love to educate my followers using this information.
Hello! I am an IB student and I am working on a project that is due on the 8th of this month. I was wondering if I could use your video on a web page that I'm working on? If not, that's alright as well :)
Don’t think they care buddy
Basically your body is shutting itself down
You’re welcome
The immune system part reminds me of the clones executing Order 66
What happened to the Arabic version of this video?
What's the next episode?
People who don't understand the seriousness of this disease
Why did I felt like I was watching a movie?
i felt the same way. lol
Bc of the music? Maybe
Christy CoOl his voice as well
My sister's has and I have systoms
Roche company.
Please make another video without music
I have everything every symptom. Doc said fibromyalgia. Took years alone in pain. An cuz I look fine I get ignored. Help. I was not like this in my younger days strong. Now weak that is hard to deal with. Every day I try but it's getting worse over the years
Hello!
Thank you for getting in touch with us.
If you have questions regarding a treatment or medication, please consult your healthcare provider first or get in touch with one of our offices in your country. You can find a detailed list of Roche offices: www.roche.com/about/business/roche_worldwide.htm. It’s not that we don’t want to help, but social media is not the right place to discuss private health information.
Wishing you all the very best.
Ana on behalf of the Roche Social Media team
I have MS too and made a video about my story. We will get through this.
Christina Applgate brought me here.
Ms freaking sucks. Diagnosed in 2012 and my quality of life has went down the 💩 er ever since. From my eyes to my bladder it’s taking everything from me. I look healthy on the outside but I have sooo many issues on the inside. Plus Crohn’s disease wanted to take up residence in my body around 2020 and here we are today. Sigh.
Ga bisa bahasa enggres