bluelyme said...
i think she is three months in ?
hoagie - i was hoping to allieviate bullekids anxiety lol not raise yours . i took a very guerilla warfare tactic against these shapeshifters and it seems daunting, shoot supplementation was a ft time job by itself! not to mention the detox and killing games. but one thing my llnp said was "these things dont rest , they never take a break and dont stop replicating unless you take action! " that been my creedo
i picked up my first microscope a old university one for $50 btw and lymenut taught me most . i am back to designing prototypes , reading scematics , playing music but it took the will to win the fight for my brain and heart , these buggers had stolen em!
financially it was a miracle i made it! however ,mine and my families savings are tapped , but i feel like i chose wisely in my treatment options . oral supp in large doses is likely just as effective...only since being sick have i taugh myself kinesiology, pathology, pharmacology, herbalism , acupuncture, methylation, genetic interpretation, microscopy, and most importantly compassion and grace with myself and others . were are the lucky who brave the frontier of unknowns , being pioneers rarely allows for tiptoeing.,...
Thanks bl!
There is a woman on Ellie's FB group that has ALS. She is like you in the sense she does a ton of research and experimentation. From all her research she gathers that many with Als who test positive for lyme, yet do not get better with bvt are dealing with fungal infections of the cns. Apparently, she has slowed down the progression of her als through her modalities, but has not stopped it all together.
Do you still visit the group?