Hey, everyone I just joined MS connection although I've had MS for about 6-7 years. I am now 29 there were a lot of bumps in the road when I first go diagnosed. I hate seeing people having difficulties getting diagnosed because ironically the doctor diagnosed me but said that my symptoms were worsening because of stress, anxiety and depression. Basically I felt like everyone thought I was crazy when I knew I wasn't but as a nurse I know how hard it is for a patient to advocate for themselves. I had this problem I honestly thought I was crazy for a long time. I have now found an inner peace and have been really try to get back on the train tracks of life and continue going.
Anyway just wanted to say Hi, and thank everyone who is on here for giving support to everyone on here. Thanks hope everyone has a great holiday!
Hi Gabrielle! Welcome :) I hope you had a nice Thanksgiving.
MS Navigator Carla
I was diagnosed with Multiple sclerosis in late July of this year after a brain MRI came back showing lots of MS lesions and a spinal tap came back positive for high amounts of elevated protein 'o' bands. I read your profile, I feel for you and what you've been through. It is difficult, I don't have many people in my life who support my MS and no one else in my family has even been diagnosed with it. I agree you have to advocate for yourself and if others judge you cause they can't see your MS (the often invisible illness) then they don't deserve to be in your life and you're better off without them I say.
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