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...
Hello, I’m Delia.👋🏻
Before my diagnosis in 2025, I was a Zumba instructor and a mobility instructor for older adults and people with disabilities, with two years of experience.
This diagnosis was a huge shock, but I’m trying to find something positive in it. I’ve realized that when I help othe...
Hello, I’m Delia.👋🏻
Before my diagnosis in 2025, I was a Zumba instructor and a mobility instructor for older adults and people with disabilities, with two years of experience.
This diagnosis was a huge shock, but I’m trying to find something positive in it. I’ve realized that when I help othe...
Hi ms fam,
I was dxd in august of last year and started Ocrevus in January. Had my first 6month mri with no new activity!!! Yay! Also my doctor said they do not anticipate any future relapses. This could be due to Ocrevus or because my there were only a few lesions when we caught it (I’m on the spec...
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...