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Good morning MS community 🤗. I was diagnosed in July with relapsing ms and have had it for four years before diagnosis. I am due to start my injections once the nurse has visited to show me correctly how to do the injection. I had worries about medication (family all have died of liver cancer or p...

Hi, just recently diagnosed so still figuring it all out! I have a chest infection and a gross cold that I can’t shift, doctors have given me antibiotics but Im so scared It will cause another episode? Any advice?!xx

Hello! I'm 17 and new to this site, I've joined because I might have MS... So my first two symptoms of MS were trigeminal neuralgia and leg pain on walking, no matter the distance. I have been to my local GP a number of times, sometimes referred to my nearest hospital. Fast forward to now and I hav...

So I’ve been back to work for about 2 weeks. It’s been almost 3 years since I was diagnosed. I’m never really sure if my fatigue and pain is caused by stress, an unrelated symptoms, caused by temperature change, or just me imagining things. It’s frustrating. I don’t want to complain, but this week h...

In addition to medication, I use a stick for short distances. I have a stint because my left foot drops a lot and can cause me to trip. For longer distances, I use a walker to keep my balance. Of course, though if anybody offers me an arm to hold I will always take it because it is the best.

In March I was diagnosed with MS at 25. Yesterday I was diagnosed with Lichen Planopilaris, an autoimmune type of hair that is also incurable and causes permanent scarring. I’m trying to keep my head up but I’ve been knocked down so many times this year. Everything has been taken away from me. I’m w...

I was diagnosed with MS about 5 years ago. Since then, I have suffered many, many symptoms and been put on numerous medications. It's been very difficult physically but try to keep a positive outlook. Yesterday I had an appointment with a new neurologist. She looked over my history and told me tha...

Hi All, I'm new to this forum and glad I've found it as there are many others out there with very little activity. Anyway as the title suggests... I have Primary Progressive MS that was diagnosed in late 2022. However, I also have CML which is Chronic Myeloid Leukaemia which was diagnosed in 2017, ...

How many of you lovelies have had a clear brain MRI? I'm feeling really small and dramatic until I have another serious spell of a migraine or numbness. I just spoke up n asked if there are any other tests the neurologist could do. I know that them finding a grade 5 pfo which is the tiniest grade an...

How do you know when the MS symptoms/pain are being caused/triggered by a secondary condition? I feel like my guts are being torn up from the inside; it's making it hard to eat/shit. Without questions or testing, the hospital says, 'That's just the MS.' Is anyone else experiencing this too? Is it ju...