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

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...

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, 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...

Hi Guys been told by docs regarding my MS that my speech is slurred i dont see it at all nor my mum. I’m fine !! i believe anyway anyone else speech due to MS affected? Mine is not at all but 2 Neurologists have said it in their notes!

Hi, Thanks for adding me to this group. I was recently diagnosed with MS. I had slurred speech which was treated with steroids. I've been having trouble passing urine, sometimes I go normally, other times I have to sit and wiggle before passing a pathetic amount of urine. Had a bladder scan but not ...

Hi everyone im new to this site, my MS nurse advised a take a look. My symptoms since getting diagnosed 3 and a half years ago are: Complete numbness from kneck down on both sides. Sleep insomnia ( Sleep walking) Neurological bladder Poor memory Slurred speech when tired Anxiety Moody Li...

Hi Everyone. I haven't been diagnosed yet but I have had 2 relapses that were absolutely awful. Comparable to a round of Chemo since I had 4 rounds of that too. I need to make major changes in my eating and soaking up everything I can get my ears on since I've been bed ridden for day 25 now and m...

Hello! This is the very first online community I've join since my diagnosis and I figured a good place to start was with an introduction and my own story. So hello everyone (or anyone who may stumble upon this!) (: ! My name is Melissa, I am 28 years old, and I was officially diagnosed with Relaps...