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Hi there, is anyone aware if Tecfidera is an immunosuppresant? As far as I'm aware it's on the lower scale compared to other drugs? If anyone has any information, I'd appreciate it. Thanks, Katie

Hi all, first post. I'm 22 and slogging through the long and troublesome diagnostic process to figure out what's going on. My strong suspicion is MS, but my objective clinical indicators are either barely there or nonexistent ⁠— I have small demyelinated lesions and speckled ANA blood titer, but tha...

Hi there, I just finished my 1st cycle of Mavenclad treatment...free now for 4 weeks before the next lot No real side affects...just a little exhausted...more than the usual kind I could feel burning sensation while swallowing the medication..make sure anyone taking this medication has plenty of w...

Hi all, I started on copaxone 4 weeks ago. The first two weeks went really well & I had no side effects. Since then every time I have injected I’ve come out in a hot red swollen rash, which has then turned into a hard lump, like a marble (sometimes bigger) in the injection site. Has anyone e...

I’ve had bladder issues for the past 5 years and had just started to get things under control with Intermittent catheterisation, medication for overactive bladder and accupuncture. Over the last couple of months things seem to be getting worse again. The anxiety I feel over this is so overwhelming a...

I am a scientist based in the UK. I'm doing some research in the area for SMART technologies ie technology that improves the patients experience when they need to take medications. Specifically, I am interested in two technologies that have been introduced for MS patients. The first is for patie...

I apologize in advance for the long post. I know MS is different from Person to person, My ms consists of numbness in my right hand and neurological pain in my abdomen and fatigue and I experience these symptoms on the daily. When I 1st knew something was wrong was my 1st clinical event that happe...

Hi everyone, I'm currently planning on moving to Dublin, Ireland within the next 6 months and I'm starting to think about changing neurologists. I will obviously have to get a referral from my GP to see a neuro. I've been told that it can take up to 6 months to get an appointment!! Does anyone ha...

good afternoon everyone it's been a while since I last posted anything! My neurologist didn't give me anything new to help my ms she still prescribed me copaxone and she said to stop taking it for a few months and then start taking it again! Since I stopped taking it I have been feeling great having...

Hi everyone, I am new to this, I am just wondering if anyone suffers with leg cramps through the night and what medication they are on to help these, I have tried lots of things but nothing seems to be helping. 😀