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Hi all New to the site. Been given 3 options for treatment and I am siding with Rebif as we are thinking of starting a family soon. What’s people’s thoughts on it? So much information to take it. I’m feeling very confused and overwhelmed. Got diagnosed about 3 weeks ago. Thanks in advance Lucy

At this point I have to just laugh. I was in hospital last week, was diagnosed with MS. Discharged last Friday, put on steroids while in hospital, symptoms cleared up by Tuesday and I woke up this morning with a very, heavy arm with horrible cramps and pins and needles. Tried to contact enable but n...

Hi folks. I was diagnosed with MS 2018. I've recently retired on health grounds and have just been granted PIP which is a great help. I'm very reluctant to visit anywhere where I dont know where the nearest loo is. Nightmare in the current climate !!! (covid19) Mobility is a problem re walking and b...

Hi my name is Dominique. I went into the hospital last week because I had some type of stiffness, weakness on my left side. I instantly thought it was side effects to my medication, but long behold, after a MRI, they found lesions in my brain and spinal cord. Being diagnosed with RRMS and being a ...

Help!! I'm a size 6. I've been trying to get some FEMALE incontinence knickers in size XS. Couldn't believe that apparently, no one had ever inquired about an extra small size @Always discreet. Tena sent an xs unisex sample pant. Incontinence clinic suggested childrens Pull-ups.... Say no more!!

Hello! I think I need advice from someone a bit more experienced than me. Does any of you have both glaucoma and MS? How do you get it diagnosed? After my recent optic neuritis (in march) my optician suggested a week ago that I might have glaucoma, but that she is not certain, as it damages nerves i...

I have primary progressive MS, and have been trying for a long time to get access to ocreveus, they tell me you have to have recent activity in your brain or you will not get it, i feel my condition has worsened and surely this treatment is worth trying whether you have any brain activity or not, i ...

Hi there! First time posting here. I was diagnosed with RRMS 8 years ago and am recently experiencing major fecal urgency. It’s scaring me. Does anyone have any insight or advice? I’m terrified that I’ll be out and the urge will hit me and there won’t be a bathroom nearby.

and what to do about lockdown isolation. - https://www.newscientist.com/article/mg24732951-700-the-surprising-ways-little-social-interactions-affect-your-health/

In the future, when our kids are the parents... 🤔 ‘Oh my god, these kids are doing my head in. Six weeks is so long.......’ Six weeks? SIX WEEKS?? Try six chuffing months! You parents today haven’t got a clue what we went through in 2020. Six months of entertaining you little shits, and we could...