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Are headaches common with brain leisons in MS?

HOLA PALS :D Hope you're all well. I had an MRI scan a couple of week ago and the neurologist always sends a letter to my GP with results and I also get a copy of the letter. It took myself and my mum a good while to work out what the letter actually said but basically suggests although they have f...

Does anyone here suffer with depression as well as ms I've suffered with ms since 2012 11 years I've been on gilenya since 2013 I've 50 leisons on my brain which I've a brain like a sieve 🤣

Just had my first mri results back since starting Ocrevus, I have no new leisons and the lesions that developed during my first attack in July last year are decreasing in size but the report says this recovery is most compatible with a demylenatating process such as adem, any thoughts or experienc...

Hi even though I have multiple leisons on brain and spine the neurologist still will not diagnose, but she has suggested the GP prescribing Gabapentin for chronic pain. Was just wondering whether anyone else takes this and if so how effective is it?

Hello everyone! I hope you are all well? I have a question that the internet cannot provide answers to so I have turned to you lot the true experts! I am having a relapse and now will fit criteria for HSCT as long as my MRI shows new lesions, I have an MRI booked through the NHS at the end of the ...

I have just recently being diagnosed with quite a few leisons on my brain and spinal cord and have suffered symptoms of ms for years (although never knew that that's what they were) but my neurologist will not diagnose ms, has anyone else had this problem? At first the neurologist wasn't going to se...

Hi all, I was recently advised to start treatment as I have developed new leisons in my spinal cord! I had the choice of 3, which all seem much the same, with similar results and side effects. I chose Plegridy due to it being allowed to be out of a fridge longer (I like to travel) and only 1 injecti...

Had an appoitment today with my neurologist he just went over the MRI i had in June and has told me i have a new leisons and will be finally starting Ocrevus shortly! Can anyone explain if you will feel abit funny after the first infusion? Thank you!

I was diagnosed with Ms in 2011 after about with optic neuritis and MRI showing lesions on my brain. I was always hesitant to believe this diagnosis. Maybe I was just in denial, I'm not sure. I have been off medicine since March of 2018, and feeling pretty good. I thought I was having a relapse a fe...