Lyme and Lupus
I have been told for the past year that I have chronic Lyme disease. I have been treated with antibiotics and natural remedies, to the tune of thousands of dollars, only to find out that form further tests, that I most likely have Lupus and not Lymes. I'm beyond frustrated that 6 doctors couldn't figure out to test for all things first before asking me to pay so much money for treatment, that insurance did not cover. Now, they are acting like Lupus is no big deal and I can just take a pill. I refuse to take any drugs for this and will deal with it naturally.
Anyone else have a similar experience?