Other than the brief entry I made this past February, I haven't written in over a year... Not one thing. The disease progressed so rapidly and aggressively, I began losing regular cognitive function, thus, making it damn near impossible for me to form a comprehensive thought... However, I'd started a treatment that actually showed promise. My LLMD (Lyme Literate Medical Doctor) decided that I was FINALLY ready to have a PICC line placed and administer IV Rocephin everyday... until recently. <-- (But we'll get to that tid bit later) ... I slowly began to feel different... And eventually: I wasn't in excruciating pain everyday... I mean, still in pain everyday, but not in the fetal position, screaming, in the middle of the floor, pain. Seizure Activity was at an all time minimum My balance and strength was so much better, I didn't have to use my walker anymore My short term memory had improved... ... as well as focus and comprehension... So m
I have been battling a weakened immune system most of my life. And for well over a decade, I've been ill with Late Stage Lyme Disease, but having just been diagnosed, April 2013. Now, USUALLY, I don't like to share my business BUT I'm finding I'm not the only one living a life filled w/ pain. So follow me and better understand my tale of the sheer unnecessary! Whether you can learn/relate OR even get a laugh or two out of this, it's DEF worth the read... ENJOY THE RIDE!!!... somebody has to;)