It took 5 years to diagnose me and in that time I have been diagnosed with fibromyalgia, migraines, ibs, arthritis, degenerative disk disease, bi-polar, lupus, my vision is fading fast, lots of dental issues, etc. etc. etc.
At this time in my life, I had the same nurse practitioner the whole time. She saw the bullseye on my arm and was still reluctant to name it as lyme. I had two different dipstick tests through Labcorp that stated no lyme. I went to Dr. Erias in New Jersey. She drew blood and found the lyme parasite in my blood. There is no denying that.
I have had morgellons for a few years now. I am getting familiar with the cycles of it.
I recognize it in others. Many, many people have it. At first I tried to tell people, but because it is not recognized, they do not accept the information.
I have to leave for the day. I will check in this evening! Have a great day.
Hope you are having a great day also. It both hurts and helps to hear the stories of others journeys through the confusion. I shared in a contest tonight an older post about my journey and i thought you may enjoy the spectacle. https://steemit.com/contest/@svosse/43rd-daily-steemit-upvote-lottery#@jazzresin/re-svosse-43rd-daily-steemit-upvote-lottery-20180302t030452131z
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