Eight months later, I examined optimistic for Lyme illness, however my physician advised me it was doubtless a false optimistic. On the time, there wasn’t quite a lot of info and information about Lyme—particularly the place I lived in Southern California.
For the subsequent 4 years, I continued to go to medical doctors, in search of solutions, as a result of my weird signs didn’t finish there. I started experiencing Bell’s Palsy (a situation that causes muscle weak point on one facet of the face), nerve ache, persistent cough and sore throat, mind fog, and reminiscence loss. Wanting again, I used to be experiencing so many traditional signs of Lyme, however I didn’t understand it on the time.
I additionally began having cardiac points, particularly a bundle department block, which messes with the guts’s electrical indicators and makes it troublesome to beat correctly. What’s extra, I had retina harm in my eyes. I used to be experiencing all of this whereas additionally elevating a new child child.
Medical doctors by no means dismissed my signs, however I used to be subjected to a variety of assessments—MRIs, CAT scans, and lots of extra optimistic Lyme assessments. Inside that point, I used to be advised I doubtless had lupus, points with my adrenal glands, and even that I wanted again surgical procedure. However I knew in my intestine that none of these conclusions pinpointed what I used to be going by. I stored hopping round to completely different medical doctors, and doing my very own analysis.
Again then, you actually couldn’t discover a Lyme physician in California. Finally, I reached out to a specialist in Boston, and I faxed him all my medical information. He advised me I wanted to hunt care instantly, particularly because the illness was impacting my coronary heart, so he linked me with a health care provider in Los Angeles who may assist. This physician definitively identified me with Lyme illness.