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I’m loosing hope I’m crying non stop everyday I can’t take it anymore. I can’t. I can’t. I can’t. I don’t have Ms because I can’t. My neurologist had to lying, I know he did when he said I have Ms. I want to be normal, I am normal I don’t have Ms.. I’m going on ocrevus soon but I genuinely can’t. Be...

What do you do to keep your mind positive? Hobbies or things to pass the time? I work as a veterinary nurse. And as a disabled person, it rips my heart out to euthanize pets who have a disability that can thrive when given a chance. So, I take surrendered newborns from the clinic that would have b...

I now have three doctors (including my MS neurologist’s opinion) that I may have MS. My brain and cervical spine MRI appear normal but my symptoms and physical assessments show MS symptoms and all doctors say CNS difficulties. Experienced some mild symptoms for years but in July my right arm went se...

I was diagnosed with MS June 2011 and I was married for 28 years … six months after I was diagnosed my wife asked me for a divorce. She looked into the possibilities that I could be in in the future and it wasn’t the life for her or the children so this is why she wanted a divorce because it frighte...

In the last few years I get around with or on wheels due to MS disability, so I need to know about accessibility. And I don’t know if it’s just us dog loving Brits but I started to notice a strange phenomenon sometime last year when checking out accessibility of venues. Here’s my rant about it from ...

I rather focus on the positive or the dope shit I have left, fuck all that somber shit, no negativity for me, I AM TOO MUCH OF A FORCE for that bullshit, ayy someone tell m.s to go suck a di.. KCM👑

Hi, I was diagnose over 15 years ago (I’m 43) and obviously in that time my MS has developed from being almost totally ignorable to something I have to think about every second of the day however….i try to live as I always have (within reason), continue to do the things I enjoy with adaptions or v...

Hi everyone, This is mostly aimed at those of us capable of carrying children. My partner and I have been talking about children and what we want to do going forward. Relevant info: I've been diagnosed since 2022, RRMS, no recent relapses and minor, intermittent symptoms (fatigue, migraine, brain f...

Im being admitted in the hospital again for the 2nd time in 5 weeks. Im having a really bad flare that my body is having a really hard time recovering from ive had m.s fot 10 years but have never had a flare quite this bad. My symptoms are as bad as they've ever been and i dont seem to be bouncing ...

Yes I am just sitting here and trying to think if my legs and arms are vibrating more as I can’t walk anymore so if out I am in one of my wheelchairs but I am due another transfusion on the 26th so I’ll say to them as yet again I don’t feel my latest drug is helping or doing its job yeh I am single ...