Eight months later, I examined optimistic for Lyme illness, however my physician instructed me it was probably a false optimistic. At the time, there wasn’t loads of info and information about Lyme—particularly the place I lived in Southern California.
For the subsequent 4 years, I continued to go to docs, searching for 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, power cough and sore throat, mind fog, and reminiscence loss. Looking again, I used to be experiencing so many traditional signs of Lyme, however I didn’t notice it on the time.
I additionally began having cardiac points, particularly a bundle department block, which messes with the center’s electrical alerts and makes it tough to beat correctly. What’s extra, I had retina injury in my eyes. I used to be experiencing all of this whereas additionally elevating a new child child.
Doctors by no means dismissed my signs, however I used to be subjected to a variety of checks—MRIs, CAT scans, and lots of extra optimistic Lyme checks. Within that point, I used to be instructed I probably had lupus, points with my adrenal glands, and even that I wanted again surgical procedure. But I knew in my intestine that none of these conclusions pinpointed what I used to be going by means of. I saved hopping round to completely different docs, and doing my very own analysis.
Back then, you actually couldn’t discover a Lyme physician in California. Eventually, I reached out to a specialist in Boston, and I faxed him all my medical data. He instructed 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 might assist. This physician definitively identified me with Lyme illness.