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Hi ?? I've got my home assessment coming up for pip soon and I am absolutely terrified. I've heard so many horror stories about it and I can't cope. I have RRMS recently diagnosed but it has taken over 1 year since first bout of mylitis back in August of last year (when I was 12 weeks pregnant) T...

I live alone in Cleveland Ohio with my dog, Never married and no kids, I was diagnosed in 2018 and it’s been really sad being alone with no one to comfort me or share my pain with, I often wonder if it’s best I’m alone so no one experiences how fatigued I get or how much pain I’m in when the pain co...

Hi All! Is anybody really struggling with Avonex? Side effects and actually doing the injection? For the last few months I have sat in tears every injection night and having a panic attack trying to do it. Last night it was so bad I just couldn't do it. I've tried getting someone else to do it and a...

Hi everyone, I’m not sure if anyone has experienced this but I have a friend who has been experiencing some pretty intense neurological symptoms for the last couple of years and is currently dealing with what I would describe as a relapse. (He’s been told that he either has a brain tumour, MS or bra...

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...

I'm currently waiting to find out if in having a relapse or a flare up. I'm slowly weaning my 1 year old (he's mainly doing it himself as he's sleeping a lot more). Has anyone experienced a relapse when their hormones start to come back. I've not had a period so not fully back but I was warned by th...

Is anyone else having a really hard time with trying to do better health wise. After my diagnosis of RRMS I got so depressed. It seems like I cannot find even an ounce of motivation to get me to eat better or exercise. I just don’t even understand. With everything else I have to deal with, kids, inj...

People often mention how important their support networks are. My partner is supportive but doesn't have anyone to add to the support. I have friends but only a couple of them live nearby, and they all have their own lives to deal with but they do help when they can. I have multiple conditions on to...

I’m a lil upset as I just wrote a funny, meaningful post but there was an error :( I personally think it was the language I used. Anywho take 2 So I’m 37 female whose V has died. My OT says it’s my battery level and fatigue that’s causing me to feel this way. I want my sexy time back, life is grey...

Hello. I have a partner with MS and we are both in our 20s planning a future together . He’s got RRMS for 9 years now and he’s got rare relapses with fatigue and balance being the main issues, only brain lesions. I was using Google to understand how our future would look with his MS journey. I was ...