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Hello, I am new here, so just call me Drak

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    Hello, I am new here, so just call me Drak

    my name is Kheri, sounds like Carrie but not bodily injury obtained from speaking to me. I am new to this MS site. My Ms story...

    ... It started in 2003, June 15 of 2003 to be exact. I woke up one morning to get ready for work and my right hand was asleep. So, I went to work as normal. But my day just got worse from there. I could not write, when I spoke my words stated to slur, I couldn't even tie my shoes!! One woman I worked with had been a nurse ( thank God she was there) and she said " if I didn't know better I would say you are having a stroke".

    Well I went to the ER and to my surprise that ER doctor had no idea what was wrong with me. He said " if it were not for the fact that you know where you are, what year it is, just plain coherent, I'm stumped. So we are sending you to JMCGH to see a specialist.

    After a spinal tap and CT, and MRI this doctor came in. You have multiple sclerosis. I just stared at him, half grinning because I could only move half of my body. My mom just asked "What is that"? She literally went home after hearing what it was and looked it up online. Now keep in mind this was 2003. Not a lot of home computers then. Internet was still new. Shoot I had to get online with a second phone line and "Earthlink". Raise your hand if you remember that!!!

    I went on for three years before I had my first relapse. I thought three years was a big deal. Everyone I knew that has MS said it was good.
    That was in 2006, July 2006. I got pregnant with my daughter in August 2006. I have not had a relapse or flair-up since July 2006. Now it is 2019 and in that span of 13 years I have had two children, got divorced, got remarried and graduated college.

    So when someone asks me how my MS is doing, I show them my children and husband. Because without them my MS would control my life not me controlling my life.

    Vent, scream, sing, dance, cry, but above all these laugh. Laugh hard, laugh often but never laugh alone.

    Drak

    ** Moderator's note - Post broken into paragraphs for easier reading. Many people with MS have visual difficulties that prevent them from reading large blocks of print. **
    ​Kheri "Drak" Battles

    #2
    Hi Drak and welcome to MSWorld! We're glad you found us and thanks for sharing your story. It's wonderful to hear that MS has not affected you as much as it has others. Have you been on a DMT during those "flare free" 13 years?

    It's always nice to hear from someone with an upbeat attitude, but if you ever need to cry, scream, vent, etc. we're also here for you. Hope the future keeps you free of flares!

    and yes, I remember Earthlink - it's still in existence!

    Take care and come back often
    1st sx '89 Dx '99 w/RRMS - SP since 2010
    Administrator Message Boards/Moderator

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      #3
      Hi Drak

      Welcome!

      Thank you for sharing your story.

      Hope you continue to post and let us know what's going on, and how you're doing.

      Wishing you and your family all the best!

      Take Care
      PPMS for 26 years (dx 1998)
      ~ Worrying will not take away tomorrow's troubles ~ But it will take away today's peace. ~

      Comment


        #4
        Hello Drak,

        Thanks for sharing your story. Welcome to MSWorld please hang out a while and join th e conversation. There are a lot of great people here with tons of knowledge.
        The future depends on what you do today.- Gandhi

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