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They didn’t catch a virus. They caught MS. It started with a tingle. Then came the mysterious fatigue no one took seriously. By 28 days in, society hadn’t collapsed but a concerning number of people were falling over for no reason, losing feeling in random limbs, and quietly Googling “why does my e...

I quit I give up, I don't know what to do anything, I'm sick of exploding when I angry, I'm sick of the tears when I cry, I tired of the fatigue, I just want to be on my own, I just want to disappear, no one cares so why do I bother saying these things, if I have upset you my apologies, I just don'...

Living with Multiple Sclerosis (MS) felt like carrying an invisible weight every single day. The fatigue, the brain fog, the flare ups I had tried countless treatments over the years, but nothing brought lasting relief. I was exhausted, emotionally drained, and losing hope.Then I discovered NaturePa...

I need other opinions only I promise I won’t take your replies as a medical diagnosis…. I had an MRI a few weeks back that showed some lesions and what my DR said was CVS. He told me he suspected MS and ordered a spinal tap which said i had ogliconal bands present and another abnormal result. My ...

Hi all. I'm approaching 60, have RRMS and I've been struggling with worsening fatigue for nine years. I think I'm coming towards the end of my useful life as a technical computer bloke. I'm very lucky to work for the UK government who treat me well, but I need to start looking at the options for Med...

I've come to the realization that I may need to address my fatigue. I have an appointment with my neurologist next month and I'm thinking about asking to be put on medication to combat my debilitating fatigue. As much as I don't want to take another pill 💊, I realize it might be necessary.