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Thread: New member

  1. #1
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    Default New member

    hello everyone
    I was diagnosed with lupus SLE with an over lap of Scleroderma in 2004 I also have Raynauds Phenomenon. I am lucky to have never been in the hospital for more than a couple of hours. I am so happy to have found a website with actual people on it.

  2. #2
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    welcome to the forum....
    The worse the bad times are the more we appreciate the good things in life..

  3. #3
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    Welcome to the site Davita28

    Glad you found us. Nothing more frustrating then finding a site and no one really interacts on it.

    This is a warm friendly group of people. Looking foreward to more posts from you.

    I'm 49 yr old female, I've not been diagnosed as yet. Lupus runs in my family. I have many of the symptems but my blood work is all over the place.
    Oh look ... a cookie

  4. #4
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    Default hi

    Just to say hello and welcome and glad you found us.

    Love
    Angel.xx

  5. #5
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    Hi Davita...

    Welcome aboard!

    Glad you found us and decided to share.

    You'll find many understanding, compassionate people here that are willing to listen and share their experiences.

    Fondly,

    Lori :P

  6. #6
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    Welcome Davita :!:

  7. #7
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    Welcome!!!! I am so happy you are here! You have found a place where you can come and be yourself. You can share anything and everything you want to and we will help you get through it all. You are going to love it here. You jut became a member of an amazing forum family
    As I grow to understand life less and less,
    I learn to love it more and more.

    Age 29, Lupus for last 7 years

    Medications: Methotrexate, Lyrica, Celebrex, Flexeril, Theophylline, Bactrim, Xopenex, Lisinopril, Ultram

  8. #8
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    welcome Davita,

    this is a great group of people and I hope you find calmness in sharing experiences with everyone. thank goodness your hospital experiences have been for a couple of hours. I usually get admitted, then I have to struggle to get out a couple of days later. They all want to be the one to find out what the problem is, and then they all write it off as "oh well it must be the lupus".

    share a smile today,

  9. #9
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    Hi davita,
    Welcome to our little home on the web.

    Kasey

  10. #10
    Saysusie's Avatar
    Saysusie is offline Super Moderator Super ModeratorEmperor of the Universe
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    Hi Davita;

    Welcome to our family :lol: My name is Saysusie and I am the moderator/administrator here. I am glad that you've joined our family and, as you can see, the people here are very caring, supportive, informative and understanding. Yes, we are real people who live with this disease and its many over-lapping illnesses and we want to help you as much as we can. Again...Welcome :lol:

    Peace and Blessings
    Saysusie
    Look For The Good and Praise It!

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