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Hello people I am a little new at this posting questions. But I thought I’d give it a go. Who better to ask than the ma community. I was diagnosed with ms after having optic neuritis About 8-9 years ago. Since then I have very few symptoms. I do suffer what I Describe as a ice cold feeling/ pain ...

My name is karen. I was born in England. I will be 43, this year. I had three older siblings. All of them were born three years apart... Five years later I was born. Back in 2002-03, my second oldest sister started having symptoms. It took along time for her diagnosis. By 2020, and my sister can do...

The next meeting (wobble) for those interested is next Saturday at 11am UKtime online via Zoom. The meeting ID is 301-350-0141 and the passŵord is Wobble1 Everyone welcome regardless of where in the world you are. No fixed discussion points just shooting the💩 with others who you don’t have to ex...

Hi all, The last couple of days I have been experiencing some weakness in my left leg, going from the area around the base of my spine all the way down to my foot. Sometimes it extends upwards into my left arm and shoulder. This is a totally new symptom for me and otherwise I feel well but this co...

Hi, I was wondering if anyone has had trigeminal neuralgia present as teeth pain! I have had sinuses the made my teeth hurt before but not this pulsating, shocking kind of pain along the upper row of teeth on left side. I thought tn was more like head/face pain? At first I thought it was sensitiv...

I am wondering if anyone has seen either a geneticist or immunologist in the context of your MS. My brother is encouraging me to go, and he is also encouraging me to eat a keto diet. He doesn't quite articulate what he thinks these other doctors can do for me. My brother reads a lot of books about h...

Well I'm back to see if anyone knows anything. I've had problems with movement disorder since 2018. - while it's being worse the past few days alongside my spasticity. The thing that confused me is it's like I've got this new tic disorder or maybe it's just worse i dont know. Basically in the pas...

Happy Tuesday everyone! So I was really chuffed yesterday, I went out on the board for the first time in a year. The family and I love going to Sandbanks and we had a good day in the harbour. I was nervous, because last year, my brother and I (Identical twin) went for a swim and I realised very qu...

Hi everyone. Apologies that my question is not MS related but as Psoriasis is also an autoimmune condition I'm hoping someone will have some advice. For the least 5 years, my friend has been struggling to get treatment or even get an appointment at the local NHS Trust because her "condition is not ...

Hi! I am hoping to get some feedback. I am dx RRMS. Doing pretty well, on Glatopa (copaxone) about three years. Anyway, I am having serious joint pain in both hands and mainly thumbs. Maybe carpal tunnel but I have much joint pain in other areas like knees and feet. But the hands are the worst. An...