Possible MS
Im wondering if anyone has some advice or info about this whole disease as ive just been told they are 99% certain that i have it and are waiting for my MRI date anyone got any info or help etc.
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Every single person here can help you in some way. As you wait for your MRI, know that even if you have MS, your life is still your own. There are so many variations of types of symptoms, frequency of symptoms ——we are all like snowflakes! A little bit similar, but no two are totally alike. And quite a lot of people, looking back, suspect they may have had MS for years prior to their diagnosis. Best thing is not to have it. Second best is to be diagnosed so that you can quickly start meds to make it hard for MS to be active. Write out your top questions for the doctor’s appointment and DO take someone with you who can help listen and perhaps ask questions, as time permits. Hopefully you have a doctor who will take a good chunk of time to consult and educate you on the MRI reading. Always check here for input from us “regular people”. 😁
Thankyou for your reply that puts me at ease abit i have only had 2 symtoms of this over a year ago but just getting my firs MRI result looks at over a year later which i think is crazy concidering my GP told be everything was fine with it but i was just getting referred incase of future occurrence. Apart from that ive never once had any of the symptoms but from the scan they are relatively certain i have it