• kim,l's Avatar
    04-20-2014, 07:45 PM
    thanks nonna I agree but I worry she will go to any length even try to go to usa to get help she is already emailing and calling. I worry she will...
    3 replies | 53 view(s)
  • kim,l's Avatar
    04-19-2014, 11:01 PM
    I have joined local online support group and I a worried about one girl she seems to have been told that the usa at the mayo clinic is doing research...
    3 replies | 53 view(s)
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3 Visitor Messages

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    hello tabatha just checking in to how you are doing and to wish you a merry christmas hugs
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    hello tabatha i have sent friends request if you need to talk message me anytime i check the boards 5 times a day.
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    Hello tabathabroaden,

    Welcome to WeHaveLupus.com!

    Please read the rules and enjoy your stay!
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About tabathabroaden

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About tabathabroaden
Biography:
My name is Tabatha. I am 41 years old, mother of son, 20 (until 12-15) and a daughter, 4. Happily married to my fantanstic husband since 2004. I was diagnosed with Lupus Erythematosus in 2002, Fibro in 2007, and a small anuerism in 2008. Origninally from California, I have lived in Michigan since 1990.
Location:
Detroit, Michigan
Interests:
Baking, Movies, My children

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by tabathabroaden on 10-30-2011 at 06:56 PM
Hi My name is Tabatha. I have recently turned 41. I was diagnosed in 2002. Since that time, I have gone thru a series of doctors. My concern is I have been diagnosed as having Lupus by positive ANA and other tests. I have some symptoms, such a chronic fatigue, swelling of joints, legs, hands and feet. Chronic pain and deep depression. I have no signs of organ failure, including heart and kidneys, I only get a very light rash on my cheeks from time to time. But, I do have the headaches, dizziness,

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Throwing the towell in.....

by tabathabroaden on 08-27-2010 at 03:11 AM
Hi, I have been diagnosed with Lupus since 2002. I have experienced many challenges during this time. First off, my doctor who originally diagnosed the disease unfortunattely had a stroke and that started the long frustrating road of the doctor trail. Each doctor I see just seems to listen selectively or really quick to put me on additional meds. when I question, the answer is always, " well, we just dont know. My issues have escalated to the point where I have now lost my job. My current rheumys

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