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I had my son in February and I was told during my pregnancy that I was high risk of relapsing in the first 3 months Post partum. Ofcourse my body decided to have that relapse in the April. I was on steroids and finished the, then had to have an MRI. Unfortunately my MS was still active after the ste...

Anyone ever try? Benefits? MS fatigue is SO different than the fatigue/tiredness I remember pre Dx. Boundaries are my go to currently but my MS fatigue doesn’t necessarily need physical activity to trigger. #PPMS https://multiplesclerosisnewstoday.com/news-posts/2024/09/27/acupuncture-shows-benefit...

Hello all, I know that talking about long term prognosis with ms is like asking how long a piece of string is, but I'm going to try and pick your collective brains anyway! I was diagnosed at 16 years old (rrns) and my ms probably started when I was 14 or so. I am 39 next month and although my ms i...

Hello my fellow MSers I have RRMS and one of the permanent issues I have are bladder and bowel control. I've returned to work after a relapse (triggered by work-related stress) and have asked if I could have the ability to reserve a desk near the bathroom (we book desks) as part of my OH workplace...

My MS nurse said this medication can manifest genital herpes, cold sore etc as it can be triggered from the chicken pox I had as a teen… wondering how likely this is and if anybody has had any side effects like this 😭

*LONG WINDED POST IM AFRAID * It's been 7 years since i was diagnosed with Fibromyalgia. I spent the first few months after that diagnosis on such strong painkillers, I was almost constantly nauseous and I struggled to get out of bed most days. I became depressed, because i felt like i couldnt do a...

I’m getting ready for a slew of tests. I know I have ddd in my lower back. I have so many symptoms that I now know are possible Ms. But, they could be also ddd. However, if I collectively think about all of the things I have happening currently and all the things I’ve had in the past… it’s hard to c...

Hi All. Hope your well. I am new to this and just wanted to share my journey. After almost a year, I’ve finally been diagnosed in March with MS. My main symptoms were pins and needles in both legs/feet and numbness in my upper torso region. I am not currently on any treatments as I’m still awaitin...

Hi all, does anyone else have illness after illness? I’m not a poorly person and never have been but this last month or so I’ve had an infection, then Covid and now I’m ill again. Not used to this at all! I already take the recommended dose of vitamin D and multi vitamins. When I’m feeling poorly it...

So I was diagnosed with RRMS in 2014, after an initial episode in 2006 which was diagnosed as stress related swelling on the brain. The episodes I have experienced previously have been triggered by stress. I sat in the GP’s surgery and sobbed this morning and told him I had tingling in my left leg, ...