To all my fellow lupies

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Hi Everyone im new to this site but is finding it very helpful and cool so far. I never knew there were so many persons living with this horrible disease. Anyhow Ive been diagnosed with lupus since 2003 and since then my health has been a roller coaster ride. Even my immediate family members seem to be burdened by me and my constant cries for pain not to mention my hospital visits, numerous blood tests and monthly medication and specialist bills etc Trust me this is no walk through the park, and at times you may feel overwhelmed, frustrated and even hopeless but DONT GIVE UP! We are in this together and should lean on each other for support. After all this is a part of what this site is here for. So good luck to each and everyone of you and inspite of everything, stay positive and remember God loves you and will never give you more than you can bare, and what doesn't kill you, only makes you stronger! LOVE YOU ALL, MWAH! By the way is there anyone who is currently being treated with bromocriptine due to having a high prolactin level?? What side effects are you experiencing and does lupus affect sex drive??

Updated 04-08-2010 at 10:14 AM by Ms_Determined

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  1. stillkicking's Avatar
    WOW.. exactly how I feel.

    sorry.. don't even know what that drug is thank God! Thanks for your encouraging words though.