What can I say? I have a MS I’ve had it since I can kind of remember. I was in college and I want numb from the waist down. I was in my in the first MRI machines at New York University medical center in New York City and all they found was what they called you UBO’s (Unidentified bright objects 😂 In my brain and was attributed to drug use and I went on with my life knowing there was something wrong but not concentrating on you know It was the 80s.
I felt fine I had other things happening In my life. I didn’t know for sure I had MS until my 30s and I fell off my horse and I had been competing at high levels for years – it really put a kibosh on everything for me including my relationship which is now over after 20 years because of my MS and I’m alone at 55 1/2 That was a bitter pill to swallow. More better than my diagnosis my feral treatments my whatever I’ve been through God we’ve all been through it at whatever level MS we have whatever level we suffer at were all there.
I think I know that there are different degrees but there are different degrees of pain it’s a family you may have severe MS in a husband who loves you. I have RR MS and a husband who left me. And I am a watercolor artist. I love my dogs. I bought myself a place where I can try and be happy again and I’m living and I hope to hell I don’t have bad exacerbation...
I really listen to my body. I exercise like a fiend – I don’t take care of myself as well as I should, I don’t eat right, I don’t take MS meds and I am terrible but on the other hand I’m living and that’s more important to me so I hope you guys understand where I’m coming from and please go to the creative center where I put my art and that’s what I’m all about this is I think that you’ll enjoy that. Or at least I hope you’re well and if you have any questions feel free to ask because I have taken lots of medication then it’s made me sicker than I feel right now. This is a treasure for me feeling this way which is alive !
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