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Well, so much dor not relapsing. Now people think I’m having a stroke 🤦🏻‍♂️

Hi all. 7 years ago my first ms symptom was my speech slurring. 7 years on I feel like my speech has never been the same as before I got diagnosed. However everyone around me says nothings wrong with my speech but I feel like they don’t understand. Has anyone else been through the same? And did you...

Hi everyone. This is my first post. Thank you for all the support so far. I am feeling a little lost. I'm four weeks in to taking tecfidera. Hot flushes are daily but the most upsetting symptom is feeling not with it. This has got worse since the heat wa c e. Finding words. Brain fog. Having the e...

What the reason for slurred speech in MS? I slur my words everyday. Surely there must be a fix for it #speech #slurred

Hello, I am the World's Strongest MS Warrior. Story: When I was 11yrs old I was mis diagnosed and had 3 foot operations to "fix" numbness tingling and pain in my legs. It wasn't until 2019 that I was diagnosed with MS. By this time I had almost completely lost my ability to walk. I was experiencin...

I have days where I’m fine. Days where I have accepted this disease and then there just stays like today where I look at myself in the mirror I think it’s just really want my life is like now like my speech is slurred. I used to be the girl who was fun in would always have a comeback on the quick a...

Hi all, I have noticed recently that I'm suffering bouts of slurred speech. I know in the past when I've been tired I've struggled with the odd word, but more recently when I'm talking I hear the words coming out and have to go back and correct them. I'm currently training placement students so I'm ...

I'm currently hospitalized in a town away from home. About 4–5 years ago, I had multiple lesions on my cervical and thoracic spine, plus hyperintensities throughout my brain (especially frontal lobe). The neurologist charged $400/visit with no insurance coverage. Has anyone here experienced total pa...

Hi everyone, i’m newly diagnosed. I have yet to even see neurology outpatient. I went into the ER thinking I was having a stroke and my MRI results showed a different story. They did a spinal tap so I’m waiting for those results to come back. I’m here because I’m not really Sure what to expect with...