I was diagnosed with RRMS this month, although my neurologist suspects I could have had it for around 10 years. I’m feeling so much grief and anger at the minute. Anger at the GPs who dismissed my symptoms as anxiety over 10 years, anger that lesions on an MRI of my spine last year weren’t flagged,...

So all my ms people i has be bladder stem implanted in my back n its not working any longer... they got me on fully cath for 3 weeks n either i have to have surgery get implant removed or surgery try n fix it...but now theyre talking about a permenant cathater and I'm not sure how i feel about it......

So I find that my vision blurred instead of double vision. Does anyone else seem to have that problem?

I have been seriously Donald Ducked by a recent relapse. As a result of a new lesion, I have pretty much lost the use of my right hand. I can't write, can't draw, can't paint, can't even do my ruddy shoe laces up anymore. So given a choice between giving up and learning to use my left hand, I am ...

I've been at the hospital all morning and had lots if info thrown at me and I've seen my brain and spine scans, I've had blood taken, urine test and chest xray. I'm going to start Ocrevus as soon as possible and I've got some pregabalin. Advised to up my vitamin D intake to 4 times my current dose...

Good morning, I had my first dose of Kesimpta yesterday. The nurse came to my house and showed me how to do it, she was lovely and it was easier than expected. Last night was awful, headaches like I’ve never had before, chills, nausea, weakness, just feeling generally unwell, and I’m pretty sure I s...

Hey y’all if you didn’t see the post, follow my instagram dedicated to my health journey living with MS. @myhealthyig_ Motivational posts, clean eating post, just me taking steps to become a better me and beat MS in the process. See you there!