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Just focus on the good things I have in my life, as small as it might be! It helps me by miles and definitely hope 👌🏼

Hi am new to this site and don't know what I am really doing :( I have not yet received a diagnosis , I have my first brain MRI this Saturday. I had a spinal MRI nearly a year ago after some leg symptoms that lasted around 6 weeks and nasuea and off balance that was diagnosed as vertigo by my GP. By...

So it has come to my attention a fair few of you have mentioned you are unable to deal with the fact you have the phantom illness well in my experience over the past few years i have had a struggle and half and im not expecting my first child SO MY Positive thinking to keep me goign and help me de...

I’m in mourning for my brain this week as I’ve had to make the decision to go for medical retirement after 11 years of continuing to work with MS chewing away at my cognitive function. Recently been retested at neuropsychological service and the decline was shockingly apparent. Even having the OT co...

Distance walk everyday more 10 km good food like fish 🐠 meat 🥩 vegetables 🥗 no smoke 💨 no alcohol and positive thinking stay with positive people with people how u feel happy and not will hear in your body sclerose multiple be strong 💪🏻 be strong warrior

Is it just me that celebrates small achievements such as testing my balance by walking from the car into a shop without an aid. Knowing that I may not be able to do that the next day doesn’t matter to me, the fact that I could do it today means a lot to me #positivethinking

I was diagnosed with MS 2 years ago when I was 56 in 2016. I saw a neurologist once! Apparently he can't see me as he is only seeing "The newbies" We only have one neurologist in Plymouth! My MS nurse is really not much help as she hasn't helped me much at all! I went on Steroids for my first relaps...

I have a very special friend, who is a fantastic counsellor/art therapist, but yesterday, she was telling me about a friend of hers who is a hypnotherapist and how she believes in power of the mind and that every day if we just believe in our ability to believe we have new cells every day, or words ...

Signed paperwork today to start tysabri in 2 weeks and just thought to ask others if they have any tips for me, like I had with avonex (keeping hydrated etc) I am JCV positive if that makes any difference to advice. Before today I was a bit worried about the risk of PML but my nurse assured me today...

Be happy, what ever type or how bad you are try & be happy. Positive thinking keeps things @ bay, otherwise you'll feel C*** & make things worse. Stay Happy & keep well, all of Us out there with MS :-D