Oh lady do I feel your pain....
For two years I went through every test
known to man...
No one could pinpoint what it was. I was
finally told it was
in my head. I had to get a second
opinion... I felt like someone
was telling me I was crazy. The next
doctor slapped the label
cfs because I didn't have a rash.... In
the beginning I did
not pull a positive ana... I was
fatigued, had severe joint pain,
ulcers in my mouth, uv sensitivity.
A few months later.... My doctor got a
new "partner" a younger
doctor who got "stuck" with me. Thank
god she did... She
saw a pattern and started monitoring
things very carefully.
She finally found my demon with a urine
protein test. 6months
later the anas started coming back
positive....
The moral to this story.... Lupus is hard
to diagnose. If a doctor
double checks a previous diagnosis its not
a bad thing. There are
so many indicators for lupus that could be
another auto-immune
disorder. There are also so many things
that can be mistaken for
lupus.
Definitely obtain your medical records.
Review them with the new
doctor. Ask questions.... Don't let it
shake you... Again remember
the more you know and understand the more
active you can become
in your own recovery and wellness.
Remember this is his/her job
but your life!!!!

heather