My 20+ Year Journey With Lyme Disease & What I Wish People Knew

Eight months later, I examined optimistic for Lyme illness, however my physician advised me it was possible a false optimistic. At the time, there wasn’t numerous data and data 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 spot on one facet of the face), nerve ache, persistent cough and sore throat, mind fog, and reminiscence loss. Looking again, I was 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 indicators and makes it tough to beat correctly. What’s extra, I had retina harm in my eyes. I was experiencing all of this whereas additionally elevating a new child child. 

Doctors by no means dismissed my signs, however I was subjected to a variety of assessments—MRIs, CAT scans, and plenty of extra optimistic Lyme assessments. Within that point, I was advised I possible 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 was going by means of. I stored hopping round to totally 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 information. He advised me I wanted to hunt care instantly, particularly for the reason that illness was impacting my coronary heart, so he linked me with a physician in Los Angeles who may assist. This physician definitively identified me with Lyme illness.

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