I’ve been experiencing new symptoms from that which I had in 2014 when I had 2 mri’s that showed lesions but I didn’t have a 3rd scan which showed active lesions so I was told back then they couldn’t officially diagnose ms as they needed all 3 scans to show active lesions. Now 2018 and my b…

ok so I have never been keen on messing with hormones and have always been natural. since diagnosis I have noticed every month 3-4 days pre menstruation my MS feels like I am relapsing and all my symptoms hit me like a train. takes me ages to get over this!! ruins nearly two weeks out the month. so…

Hello friends, what a day I’ve had. My brother-in-law got me and him an appointment with an MP in Westminster today. It was about the decision by NICE to turn down Ocrevus for PPMS folk, like my sister. It was great to have the chance to talk about MS with someone who knew little about it, about …

Right guys, sorry if this is too obvious but in this article i read ….some patients in original group continued to get worse early on after transplant, he added, “but we think that was due to previous disease before the transplant. There can be an early degenerativer phase, but that le…

Hi everyone 👋 I was diagnosed with RRMS in May 2009 and started treatment (Rebismart ) 2 months later which I absolutely hated! #Painful. Was on it until 2014, then I started Gilenya. Another rollercoaster with all the symptoms like fatigue, foot drop, muscle weakness and the list goes on. Those…

Hi all, I have RRMS and my sister has PPMS. My brother-in-law wrote to his MP regarding Ocrevus being denied by NICE. Anyways, he and MS Warrior Vixen have been invited to meet the MP in Westminster next week! There has been so much relevant discussion and debate on Shift which has really informed …