Thank you for your reply. But as you will note in my post, I have already researched Reiter's online. I am looking for people that might be willing to share their personal experiences with the disease. So if anyone, any additional information above and beyond that on line, I am very interested. Thank you again.
sure r many tests for ReA : C reactive proteine, CPR, ASO, HBLA27 that prove inflammation in the body
all my tests came negative, no swelling no inflammation just migratory pain from joint to joints my left side is the worst.i have time when i had elbows pain , than knees , hips, shoulder now i have in my feet sole. MRI didnt show anything is like a mistery this pain.
still believe is ReA but incomon tha this usual ReA with swelling and redness in the joints
for how many years do u suffer. i have right now 2 years, started 2 years ago in Nov.
Post Edited (UncleBill48) : 4/3/2012 10:28:17 PM (GMT-6)