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    Hi Im new here my . This is my story it started back in 1995 my eyes would just go black would only last a few minutes. I couldn't even see shadows. This happen few times a week for approx. 6 weeks. I did see a Dr. at that time she never even looked at MS. She said it was anxiaty.

    Then in 1997 while pregant my right leg would give out. I thought it was the way my baby was position and I was extremly exhausted. It to passed. Had a few other thing happen over the next 12 years. Then I started in the fall of 2010 noticing that my feet would catch on the foot. Then over the next several months fatigue hit and hit hard.

    Then by Feb. of 2011 one night after working I went to the store and it took all I could do to walk through the store to pick up supper for my family.(I can tell what I bought that night .) I still didnt see or think something was wrong until numbness started on my lower right back and in a few weeks it came around to my stomach. I now knew something was wrong went to the Dr.and she started to run testsand in one week my right leg went numb and was using a cane to walk.I saw the Dr. and she saw a big change she refered me to neuro and was tested two days later. The neuro saw me in two day after that and gave me my dx.

    I took it very well it wasn't cancer on ALS latter .I feel blessed because it wasn't either of them.I reallized life is and always is changing. I'm ok I have great support from my husband and family. My mom struggles with grasping that I can't go like I once did. I use the slowing down to stop and smell the roses that still come my way.

    #2
    Hi
    Sorry to welcome you here. It's a good place though to listen to others and find out that you are not alone in this struggle. Sometimes you might want to check in and say something.

    I don t have children but your story sounds familiar. Im sure you are going to learn a lot. Be strong, positive as you can. It helps
    [I]Tellnhelen
    Progressive Relapsing MS

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      #3
      Glad you found this place. Sorry that you have to be here. I have dealt with my diagnosis much better than my mother has. I dont really understand it but have to understand that we all deal with this in our own way.
      I hope you look around and see that there are many more like you and that someone is always here to lend a shoulder

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        #4
        Welcome to MSWorld, OliveDeb!!

        I also went for years with various weird symptoms until the last flare had me diagnosed within 24 hours! It's usually a strange emotion we go thru dealing with a dx. Glad that one's not going crazy or having a more serious dx, but shocked and saddened that it's MS.

        Sounds like you have a great attitude and support system in place - that is crucial! Please come back often and share stories, questions and comments! Take care
        1st sx '89 Dx '99 w/RRMS - SP since 2010
        Administrator Message Boards/Moderator

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