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Hello everybody. I just found out about this forum and looking forward to connect and share our experience 🙂 I've been diagnosed a year ago and still learning on how to " collaborate" better with my new friend MS. I am based in Romania, Bucharest. I hope all of you are safe during this hard period!

I'm newly diagnosed with RRMS. I'm rather young and frightened... can anyone give me advice and support? Thanks

Hi, I was wondering if anyone has had trigeminal neuralgia present as teeth pain! I have had sinuses the made my teeth hurt before but not this pulsating, shocking kind of pain along the upper row of teeth on left side. I thought tn was more like head/face pain? At first I thought it was sensitiv...

Hi Has anyone had any news regarding DMT treatments in the UK now? My MS nurse is waiting to hear when they might be able to re-start, and I am on the list for the initial Ocrevus infusion - hoping this will be soon, of course.. Wishing you all well.

How would you describe your emotion in this moment? Calm? 🙂 Sad? 😢 Angry? 😡 Anxious? 😨 Happy? 😄 - In episode 6 of 'PPE for the Mind' episode, Jo asks us to observe our bodies, noticing any areas of discomfort or emotions 💆‍♀️ To get the most out of the episodes, grab a cuppa ☕️, take a ...

Well I'm back to see if anyone knows anything. I've had problems with movement disorder since 2018. - while it's being worse the past few days alongside my spasticity. The thing that confused me is it's like I've got this new tic disorder or maybe it's just worse i dont know. Basically in the pas...

https://www.youtube.com/watch?v=ySih1Ef64lU&list=PLVUOB-ZqvZOHIdZD3nrpGPgoSqrOyxoat&index=1 In our new series ‘MS, my Baby and Me’, our MS Reporters are on a mission - to start a conversation about the postpartum period & MS Woman feeding babyBaby In Ep 1, Carla, Rosie & Grace talk surprises, chall...

Hi all, I'm new to Shift MS, nice to meet you all. I got diagnosed over a year ago, but haven't talked to anyone else with MS before, so just looking to say hi and catch up with someone who might be having a similar experience. How do people deal with day to day stuff? My most annoying thing is work...

I am switching from Tecfidera to Ocrevus. I'd been waiting since the beginning of the year and then the coronavirus came into play. So now I am still waiting. It seems that I had new lesions on my last MRI scan even though I'd been on Tecfidera for the last five years. I just hope this thing starts ...

New here and not sure how to find friends. Is this like FB for MS?