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Hello I hope everyone is doing well ! I was just wondering if anyone else has experienced hard lumps under the skin !? I spoke to my GP and he told me it could be a cyst or my lymph nodes and I think it is my lymph nodes. Does anyone know how this correlates with Ms ?

Hi there im just wanting some advice and help really. In a nut shell I am 25 years old and had this illness since just shy of my 16th birthday (great gift that was) anyway last year after my birthday i suffered a miscarried (first time pregnant as well) and that sent me down a dark dark hole anyway ...

Hi friends. It's been a while since I posted so I'll give you a quick run down. I went off all ms meds in sept of last year due to having a 1 in 100 chance of contracting PML. Then in december I had a flair up that had me in bed until march. It was horrific to say the least. So in march I started my...

Hi to my old friend! That is SHIFT MS! - Not you, well it could be? I guess a stranger is a friend you just haven't met just yet! I was speaking to my OT via video call at hospital during this crazy and unusual time. She suggested going on SHIFT MS and it is a website I joined several years ago and...

I felt really good today, i didn't do much just played some video games but by 6pm i was exhausted. i lay down for a nap but i woke up exhausted, dizzy and it felt like my heart beat was in my head i could hear and feel it. it this common and caused by MS?

Hi! I’m Jenny-May,I’m 21 and I’ve recently been diagnosed with relapsing remitting MS. I’ve been advised to join because I’m quite ‘lonely’ as my therapist says 🤦🏼

I don't qualify for Ocrevus either. What I believe is helping me is Low Level Light Therapy. I found a chiropractor who uses it on primarily MS patients. It take about fifteen minutes a treatment: the doctor uses a wand on my spinal cord on my back. I've been using it weekly until the Stay at Home o...

Hi everyone, I'm wondering whether anyone on here has had any virtual consultations with their Neurologists or MS Nurses? Either over the phone or even more excitingly over a video call of some sort? I've not had one myself, but I wanted to know what experiences people may have had, positive and or...

Hi everyone, even though I’ve had MS for over ten years I’m pretty new to the forum scene. I haven’t really spoke or sort advise on anything like this? I’m thinking of purchasing an electric wheelchair as my mobility over the last couple of years as become worse. Can anyone make any recommendations,...

Hi I’m looking for some advice if poss.... I have been on copaxone for 10 years and the sight reactions are much worse which has made me seek alternative DMTs. I’ve chosen Tecfidera and got the green light so just waiting on starting. My issue is I work in public facing role for civil service and h...