Well it is now 8 months later & after 1 C.A.T. scan, 4 M.R.I tests, 3 M.R.A tests, several blood tests, 12 E.R. visits, a trip to Nevada to see a specialist, 3 stays in the Hospital, countless Doctors, losing the ability to move her right arm, ending up in a wheel chair twice, having a constant migraine type headache 24 hours a day, vision changes, having a bad reaction to every medication she has been given, developing red marks/rash on her legs that never seem to go away and for a teenager is a big deal, stomach issues, her ankle turning in sideways and locking for hours at a time, missing 6 months of school & we still don’t have any answers.
Some people don't think I have stressed enough about what has happended to my daughter. I really could fill up a book at this point. But I have a hard time telling everyone about the sleepless nights and scary as heck days of wondering am I gong to lose my little girl. I have faith that God will heel my daughter and that we have gone thru all of this for a reason. But I have to say that this is truly the hardest thing I have gone thru. Even harder than losing My precious daughter Jaidyn.
I have had countless days where I am scared I am losing my daughter because nobody can figure out what’s wrong with her. I have finally contacted the Mayo Clinic in Minnesota and she is scheduled to see several different Doctors starting September 22nd to help diagnose her. She is also on the canelation list if anything else comes up earlier. Please help us get her to Minnesota and figure out how to help her.
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