Thank you, it's a great relief to hear I'm not the only one going through the pain of MS alone, inhear your stories and I share the experience of it all, my neurologist stated everyone goes through phases at different rates, it was just a surprise that the Muscletor Degeneration Disease occurred, a further devastation when the doctor indicated a spinal tumour...I am currently a candidate for surgery or radiation but I wanted to know if MDD affected MS patients as part of acquiring MS

My mobility problems came a couple of months after my first flare up (although not diagnosed until five years later.My level of mobility is very changeable,usually associated with my fatigue levels.

I started having problems in my twenties with my left arm going numb then i started falling and horrible pains threw my whole body they found i had bone degenerative disease and started me on steroid injection and nothing helped then finally i had to have neck surgery back in June of 2016 and still wasn't getting any better so i had mri on my brain and cervical spine they found lesions then i had a nerve and muscle test then a lumbar puncture and thats when they diagnosed me with MS in February of 2017 a long with the rest of what i have

I was diagnosed when I was 26 by 31 I couldn't walk at all was diagnosed with secondary progressive

I was diagnosed in 1991 @ 32 yrs Old had kids because I did not want to be alone for the rest of my life! Wish I had listened to the doctors and not had kids they don't want anything to do with me!