Neuromyelitis optica spectrum disorder | Mechanism of disease

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Neuromyelitis optica spectrum disorder (NMOSD) is a rare, lifelong and debilitating autoimmune disease of the central nervous system that damages the optic nerve and spinal cord. Watch this video to learn about the science behind NMOSD, including the role of interleukin-6 in the body’s immune response and what causes the symptoms of this condition.
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[@ernestoleonardoocadizchave4097]

I was diagnosed a little less than two years ago, I have recovered almost 100% from transverse myelitis, I feel optimistic and trust in the treatment of this disease, greetings from Mexico

[@Jokent16dec63]

I am so glad to have found this. This wonderful disease came into my life in January 2019. I am happy to say, I can walk and I have a wonderful doctor. God bless who have this and maybe can't do all the things they did before.

[@roche]

Thanks for sharing your experience. We are working on Doing now what patients need next.

[@greenery5102]

My brother's 2.5 yrs child suffering this desease last 10 days how can we do?

[@dylanzuniga2284]

Well explained video. Unfortunately an old friend of mine has this disease and I came here for better understanding... I hope science can manage to discover the solution.

[@vijin.p.chandran]

What is the condition of your friend Now..? Any progress? Actually my relative has diagnosed the same last week please reply.

[@sontung5661]

thank you very much, very well explained video and beautiful animation

[@bradatfema]

Diagnosed 2019. NMOSD ended my career, and left me with 50% of my prior strength, and debilitating fatigue. I was 52 when diagnosed and not ready to stop doing everything I loved. Miserable disease!

[@abdullahal-noman5201]

@Roche would you please upload the management update on NMOSD?

[@nooralhoda8529]

thank you very much😍

[@bridgetllewellyn7682]

have had this since March 2010

[@MrAnurag1411]

How are you now?

[@WalterSylvia-f4v]

Jean Lodge

[@sh.shaini]

Can someone write me who has this sickness please?!

[@Albanian_traveller]

I don't have it but my husband got diagnosed with it only yesterday.

[@vijin.p.chandran]

@@Albanian_traveller Mrs Leila. What the doctors said about this. Actually my relative has diagnosed the same day before. Please reply.

[@Jokent16dec63]

@@Albanian_traveller how is he doing? I have this and that is why I am asking. I don't know how it effects men, it killed my sex drive. I can no longer go swimming like before. Meaning, an indoor pool, I wear a wet suit. From waist down, my body just do feel the same. It's hard for me to get into a swimming pool if it isn't as warm as bath water.
I take lots of meds now, lots of vitamins , watch the foods I eat due to the inflammation they can and do cause. I now receive 2 infusions a year. Find you a great / neurologist and also a support group/ system. I don't know what all he is dealing with, but I find myself really depressed and I think mostly frustrated with it at times. I also deal with Fibromyalgia , DDD ( spinal issues ) and that makes it hard for them to make me pain free , I'm not. I live with chronic pain. I hope he has good doctors.

[@briancatt3648]

My wife passed away with it in 2018

[@ИгорьАндреев-и6е]

you need to clarify the content

[@Jokent16dec63]

what's missing?.

[@joannboyd8855]

Smh

[@ReynoldsBenedict-q5p]

Crooks Light