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Some people don't understand what us MS patients go through but it's a challenge emotionally mentally and physically only we do and it's very frustrating at times

I've had the worst week so far. But determined to enjoy myself and get on with life.

Hi, I am confused whether or not my symptoms are of MS or Parkinsons Disease. My Neurologiest is not being helpful. He sent me to every medical profession the ends in a "ist" for months. Im getting tired of his avoidance, I would like to compare similarities with one that had/has the same. If you s...

F*#$ MS

When I got diagnosed it was a shock couldn’t believe it but now I just keep trying everyday

Who has found difficulty in adjusting what you eat or drink? I still find it difficult 😞 anytime I eat something my bowels start moving and wants to go toilet immediately.

To me it seems truly effortless and pointless to continue knowing I'm going to be a crippled or gimp. No more drive to accomplish things in life,don't see a need to excel through life and career anymore, it's all stupid AF to me. What is the point?? I watched someone with Ms develop bed sores the ...

I've been diagnosed since 6th June 2023. Found out because of an accident that happened when me and my then 2 year old was playing a game. He headbutted me directly on my nose/between my eyes. I then started getting tingles in my face, my head and all down my right side. Led to several MRIs and the...

Not sure about my numbness. Think that I might have ms. Any information is appreciated. Started in my feet and now up to my scalp.

Hi All. Hope your well. I am new to this and just wanted to share my journey. After almost a year, I’ve finally been diagnosed in March with MS. My main symptoms were pins and needles in both legs/feet and numbness in my upper torso region. I am not currently on any treatments as I’m still awaitin...