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I'm struggling with a coping mechanism at the moment. We are just going into Autumn and already I am freezing; I feel like I am just sitting out in the snow in shorts and t-shirt. I put the heating on or wrap up but then it makes me feel really tired. I know this early on in the year its only going...

Hi everyone! I have RRMS and I found out that I had MS after going completely numb on my left side. Even then the Doctor was still uncertain and chose to call it Tranverse Myelitis. 5 years later, same symptoms. Only this time, I was sensitive to hot and cold. I had an MRI, Spinal tap, and evoked po...

Hi everyone..I need your help / advice please...loooong story so please bare with me. I have been experiencing severe tingling on my left side especially worse in my leg and arm...no facial tingling and no weakness whatsover. Oh yes and a little bit on my right leg for the last year and four months....

Happy Friday! I’m new to this space. I’m currently in the process of ruling out what could be going on with me. This post will be a bit long but figured this is a safe space to get it all out. Late Jan 2021 was when I experienced some of my first symptoms. My left upper lip had some numbness. ...

Hi everyone I know many people go through this, but I am really struggling with being in limbo, with my current symptoms and with fears for the future. I had an MRI in November and saw the neurologist in December - a new area of inflammation was found (he called this transverse myelitis). This is ...

Just wondering if anyone has experienced the MS hug? I've had it a few times in the past but last night I had the worst I've ever had. It lasted about 1 hour or so and I was vomitting and had the shakes. I felt hot and cold, and struggled to find a position to breath comfortably. If you've experien...

Hi all, I’m new to this site but am excited to be here. Im 28 and was diagnosed with RRMS 2 months ago after over a year of numbness, tingling, fatigue and changes in my sense of hot and cold. Doctors suspected I may have Lyme disease so although they found spinal cord lesions in my first mri my dia...

Hi I only got diagnosed 2 weeks ago. I got diagnosed while in hospital and they just told me I had relapse and remission and sent me on my way and told me ill be seen in outpatients the waiting time is up to 10 weeks. I'm really confused and scared I don't understand what's happening what I'm suppos...

Hi, Looking for some advice really. I have had MS for 8 years now and medics believe (after months of decline and no remission) that I have started on the path of secondary progressive. Since last summer, I became a full time wheelchair user due to a severe relapse leaving my left leg paralysed. Si...

Update it has now started to go hot and cold? Like a slight burning sensation but not painful, nurse said it sounds like a new symptom 🤔 but I start my Plegridy for the first time Monday 😊 Good afternoon everyone 😊 I don't know if what I'm experiencing is a ms hug? I woke up and the right s...