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Does anyone else feel they have to bite their tongue more often than normal people? I recently was informed by my neuroptomoligist that my MS has decided to steal my eye sight along with everything else it has already taken. Yet I feel as though my "support" team here at home believes I'm not allowe...

So what a few worldwind months I have had! Waited 6 months for my treatment and when I had my first full dosage afterwards instantly became 🤰 . I am nervous about what the relapse will/if do to me after the 👶🏻is born in November. I am excited but so so nervous & anxious because never for the life...

My brother went to a new Neurologist. She said are u willing to try this? Supposably theres a ned iut, depleting both antibidies and your body resets itself. Ahe stated people are being cured. I will oost more ince I get more info.in Michigan

Hello All, I have been tested positive in JCV antibody(Index value 3.37), the blood sample was taken before my 1st tysabri infusion and results came 3 weeks after my infusion. Now my neuro is advising me to stop tysabri since the count is too high(PML risk) and switch to either ocrevus or kesimpta....

I'm currently in the u.k and on ocrevus, if I were to move to Australia could I continue with this treatment, would it be covered by insurance or public healthcare and what is the criteria for getting this medicine in Australia..thank you in advance for any info

Hi all, I’m just asking this as I don’t know of anyone else who this happened too. But I lost my vision in BOTH eyes in April 2023. I know many people only have it effect 1 eye, I had major double vision and then just blury. I may aswell have been blind. Just curious. It lasted about 9 weeks before...

Hi. I have had an epuside of transverse myelitis 2 years ago. Mri showed just a 16.5mm lesion in my spine. I have a diagnosis of cis. I have random symptoms of leg weakness. Mild but annoying and i am clumsy and had a fall last week. But not too bad generally sometimes I think I am ima...

I just got diagnosed about a month ago. I feel like I should have found out sooner. I've been walking with a Walker for 3 years now. I'm trying to stay positive I don't know what's to come. I haven't seen the neurologist yet, any advice?

Has anyone used ice baths or cold water plunges to help with their symptoms? If so how have they found them and have they helped? I have spasms and joint pain and wondering if it will help with this. I did a cold plunge back in November and like the day after started to have the worst relapse I have...