LLMD IN MISSOURI

Discussion in 'Fibromyalgia Main Forum' started by mollies, Aug 19, 2008.

  1. mollies

    mollies New Member

    LLMD IN MISSOURI

    ALSO POSTED ON THE LYME BOARD.

    I HAVE

    BEEN DIAGNOSED WITH CFS FOR 8YRS. I HAVE MY FIRST APPT.

    WITH A LLMD IN MISSOURI. DOES ANYONE HAVE ANY EXPERIENCE

    WITH THIS DR.? JUST WANT TO MAKE SURE I GET TO A

    GOOD DOCTOR. AS I AM SO TIRED OF NOT BEING ABLE TO

    FUNCTION AS HUMAN BEING. WILLING TO TRAVEL FROM INDIANA

    TO WHERE EVER I NEED TO GO FOR HELP!!!


    I WOULD APPRECIATE ANY PRAYERS FOR THIS BIG DECISION. I'M

    LIKE ALOT OF PEOPLE ON THIS BOARD, SO TIRED OF BEING

    EXHAUSTED, AND NOT KNOWING WHAT TO DO FOR HELP.