Well i've had some time to rest, and think about my appointment and the look on my face is still....
I've been staring at the place on my arm where the doctor touched as if its contaminated. All these ah-ha moments come flashing to me....
1. why i almost passed out when i had to have an IV in that part of my arm, and i STILL TO THIS DAY CAN FEEL WHERE THEY PUT THAT DAMN NEEDLE and that was 2.5 years ago....
2. Why carrying things is sometimes more difficult.... flash back to TOYS R US days when i had to carry boxes... when i worked at the nursing home and had to lift patients by my arms, why i would get an instant headache....
3. carrying my kids not only hurts my hips but after a prolonged time i get headaches, and pain...
where that bottom arrow is .... that's about the spot my doctor pressed. I almost want to buy arm guards now haha!
The type of lupus he diagnoses me with is cutaneous Lupus... I do not yet have Systemic Lupus... which i feel is the worst diagnosis to get...
Systemic lupus erythematosus (SLE) is an autoimmune disease, which means the body's immune system mistakenly attacks healthy tissue. This leads to long-term (chronic) inflammation.
In order for me to be diagnoses with SLE i have to have a POSTIVE ANA blood test. Wich i have not had one. However, i do show signs of inflammation in other tests... 10% of cutaneous Lupus patients will develop SLE so i will have to go in every couple of months to test the inflammation in my blood.
For now my Kidney's are in the care of Dr. Polkit Patel. We are still trying to determine why i get kidney infections so easily... Since seeing him.... I've yet to have one... wierd..... However Dr. Schue did order a urinalis to test for protien and blood in my urine... because i do not want to develop Lupus Nephritis... which is where the kidneys are attacked by lupus...
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