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My name is SCHULZ ALICE and i am 46 years old . I was born on 19/01/1974 in Carinthia (Klagenfurt)Austria . I grew up there till the age of 20 when i started having Vision problems,Fatigue and weakness,Bladder and bowel dysfunction,Sexual dysfunction,Cognitive problems. Since i was still young i nev...

Hi, I have rrms, diagnosed in 2010, symptoms since 2007. I started copaxone in 2018, had MRI new lesions. So started tecfidera in February this year. I just wondered as i have not been on dmds for 8 years after being diagnosed. Whether the dmds would be less effective going forward, I know t...

hey just went to the cafe and work to a get a coffee, and upon trying to pick it up with my right arm i was hit with almost unbearable muscle pain. this isn't one of my usual muscular gripes that we all face day to day, but rather feels like i've torn a bicep or something. super painful and now am ...

Does anyone else get this.... I am seeing double but only in my right eye pain under and to the back of my eye. Been of phone with the ms nurse she said it doesn’t sound optic neuritis or classic symptoms of. Please I Just want to know if I’m going mad or not

Hi All; I am new to the forum and i will be honest in that i have a problem speaking to my GPs due to neglect in the past which lost me my first born.. I have strong symptoms of MS and dared to mention it to 2 diferent GPs but was fobbed of,especially when i mentioned the heat intollerance; all i go...

Sorry long post!! Finally got a diagnosis in March this year. Been a long haul from 2013. In the last 4 days I've had excruciating pain in my face and a banging headache. Back in 2013 it was optic neuritis I was diagnosed with but I ended up with more symptoms and everything got worse over the years...

Hello everyone, hope you are all well.......... It looks like I am/ have been starting to relapse. For a few weeks now my legs are heavy and numb and I am waking up in the morning needing almost 30 minutes to get my legs moving before I can get out of bed. My vision is going hazy throughout the day...

Hello everyone, as the title suggests I'm new here. Although, I've been lurking for some time. I got diagnosed with MS last week after a lot of barking up the wrong tree. I'm a Police Officer and in 2016 I decided to apply to transfer to firearms. The fitness test is a bit harder for this but didn't...

Sorry in advance ... I just need to vent a little and I thought this would be the right place. It's nice to have a group of people that know what you're going through. I'm seriously on the struggle bus. I've been deemed "high risk" for covid so I've been exiled from my home and banished to my nanna'...

I'd like to hear first or at most second hand an account of what it's like for a PwMS to go through COVID. I'm surprised and a bit concerned that I've not seen one here yet. Either we're very good at shielding, or we tend to die of COVID, or both. Or it's just a quirk of stats, and the rate of inf...