Smart Meters, ALS-type symptoms, Lyme and Jaw cavitations...(???)

[Guest guest]

Salut, all. I've had Lyme disese since age 8 and am now 25. No diagnosis until

age 24. Got chemically sensitive at age 21 & now literally feel like I'm dying

from the fx of Smart Meters. It's been 2 weeks of complete removal from exposure

(no power lines or anything else within about 2 miles in every direction) since

my 4-day Smart Meter exposure. I'm still getting a lot of symptoms. Feels like I

had another stroke-like episode & got more nervous system damage. The scary

thing is, I've never had certain symptoms before: ALS-type symptoms, such as

temporary paralysis, weak limbs, choking episodes, trouble holding neck up,

poorer coordination that I ever got from Lyme, 5x mroe microseizures than I ever

experienced from Lyme. Weirdest thing is these developed a few days AFTER

removal from exposure. I've been in the off-grid cabin for about 2 weeks & these

symptoms persist & I even occasionally still get that buzzing, humming feeling

of brain & body being microwaved, which I got the whole time I was around Smart

Meters. Since the towns I'm near will be Smart-Metered by September, I will be a

complete hermit by that point; never going to the grocery store, another doctor,

or to the library again. It doesn't help that my grandfather is dying of ALS as

we speak, as his father did before him, & his best friend. On top of that, I

can't tell if the Lyme is predisposing me to be electrically hypersensitive or

not. And finally, my stroke-like episodes started happening 1 year after I had

my wisdom teeth removed, long enough for bacteria-filled cavitations to develop

in the pockets of bone where the teeth had been removed. I've heard these can

also predispose a person to electrosensitivity (altho I can't afford the surgery

to fix it).

Either way, I just really hope this brief exposure didn't trigger ALS, but if I

go by my intuition & remember how it felt, it may sound crazy, but it was like I

could FEEL genetic damage being done. Some of the fx were even visible to

healthy people, unlike many of the neuro fx of Lyme; after the 4-day, more

intense exposure to Smart Meters, my face & ears turned red & my temp was 102.5;

it rarely goes above 99, even when I've got the flu. I haven't even stayed in a

building with Smart Meter on it; I only stayed in buildings where the NEIGHBORS

had them, & they were 100 ft. away.

Not sure what to do; no money & can't get on disability or even SSI, b/c none of

my conditions are recognized & I don't have enuf work credits. Soon there will

be virtually NO PLACE that I can work. I'm going to try a conductive shielding

hood made from a fabric called Thule, and a Silverell hoodie. The company is

sending the hood to me for free b/c they understand the severity fo my

situation, but then I read the posts on how no shielding seems to work. The

company told me that w/ the shielding fabrics, it's still not clear that

grounding even works. I'm just praying that this damage is reversible, despite

the constant disabling symptoms. Most of all, I pray it's not ALS & it's just

damage from Lyme disease, so that if I eventually get the money to treat the

Lyme, I'll see the worst of the EHS symptoms (temp. paralysis, choking,

increased seizures) diminish. Based on my symptoms, does anyone ahve any ideas

as to why the symptoms have persisted so long after removal from exposure, and

most of all, whether or not this could be more Lyme related or more ALS related?

Thanks so much.

-E. Drew