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Hi folks. I was diagnosed with MS 2018. I've recently retired on health grounds and have just been granted PIP which is a great help. I'm very reluctant to visit anywhere where I dont know where the nearest loo is. Nightmare in the current climate !!! (covid19) Mobility is a problem re walking and b...

Hi my name is Dominique. I went into the hospital last week because I had some type of stiffness, weakness on my left side. I instantly thought it was side effects to my medication, but long behold, after a MRI, they found lesions in my brain and spinal cord. Being diagnosed with RRMS and being a ...

Hi, I'm Sofia and I was literally diagnosed last week after suffering very mild symptoms here and there since January 2019 which were overlooked, belittled and misdiagnosed. Unfortunately I ended up going into a massive episode (I still don't know lingo) and i woke up one morning not being able to w...

Has anyone else dealt with hair falling out or hair loss? I've been dealing with MS symptoms for a little over a year and have noticed that my hair falls out much more than it used to. If I run my hand through it I might come away with five or six hairs. I've noticed I tend to lose eyelashes and bro...

Hello Everyone, I am new to this forum. I just wanted to ask for some advice regarding cooling vests/ scarves. My symptoms are much worse during the warmer weather and I was thinking of trying a vest/ scarf. I have looked online and there are many different types available. I just wondered could any...

Hi all, I am 22 and was diagnosed with rrms in July after an attack in May. I’ve just started a dmd. Still have some symptoms - fatigue, feeling faint and I overheat quickly. My managers know, but they just don’t get it. My job is so fast-paced and they still think I can do anything and everything...

My name is Ana. I was diagnosed with MS relapsing remmiting type in 2015. The onset of my MS started in 2011 but I didn't know it. I was diagnosed first with severe Anxiety/Depressive disorder with Panic attacks. I am in constant nerve pain, numbness, spascisity and other symptoms. The evenings are...

Does anyone else experience bruising easy or not remembering where bruises came from. I find bruises all the time and have no idea where they have came from. Could it be ms or my meds, I recently started tecfidera.

When losing your ability to walk is it possible to overcome that symptoms so you'd be able to walk as if nothing even happen or will it sorta be off (never) the same after getting that? Cause I can walk but not even for 30 mins but prior to having MS I used to walk on highways for my exercise now I ...

Hi everyone! I am 31 and currently 6 weeks pregnant with my first baby and I am suffering with the dreaded MS! I was under the impression MS is stable through pregnancy but this has not been the case for me for the last 3 weeks :( I’m just wondering if anyone has had a similar experience at all? ...