Lyme Disease & ER4YT?
Hello!
I was just wondering if anyone here who has been on the diet for a
while and has Lyme Disease has any info on how they progressed with
ER4YT and their regime? I have had Lyme for about 4 years
now, ..Doctors have been no help! :0( I don’t take any antibiotics as
I am COMPLETELY against them now. ( I don’t feel they are neccessary)
I live in Northern CA and have gotten bitten by ticks several times
when I used to live in the country basically. The last one was
different and I felt sick, but this was nearly 4 years ago!
But my troubles REALLY began I’d say (since I don’t even remember
WHEN I got bitten exactly) about 3 months later when I started to
take erythromycine for acne when I was 14.(which I know is a poison
for O’s!) Then I got mono shortly after, from my dad we suspect since
he was sick for 3 months, but never got tested. I took
the “poisonous” antibiotic throughout that(STUPIDLY) so as a result I
have never recovered. It’s like the mono never left, so first we
thought it was CFS… but it seems to kind of be a mix of both since
EBV seems like a VERY likely culprit as well. I do have an autoimmune
disorder since my..I forget the name of the test I took..:0/, but my
body is attacking itself that is for SURE!
A couple weeks ago before starting ER4YT I was a vegetarian for 13
years, and wanted more info. I have NO problems with the meat really,
and actually was surprised! :0) FINALLY no bloating after eating! ;0)
It was a little hard to make myself do it, but I REALLY want to feel
better!!
My chiropractic doctor put me onto the diet a year ago..but I didn’t
FULLY understand the concept and realize until a few weeks ago that
maybe vegetarianism isn’t what is BEST for “me”. So he has been the
ONLY helpful doctor really. He was the one who was able to get me the
Lyme test last August..it was kind of over the scale ;0/.
Anyway, I am taking colloidal silver, but maybe not enough? I am on a
CS list though and make it myself. I take about a cup a day of 10ppm
or so. I am now VERY curious about the effects of olive leaf and
Lyme!! My question is that I am able to get some olive leaf “powder”
in bulk at a resonable price, and can make my own caps..but I have
heard (since I already checked the archives) that people found great
results from olive leaf “extract”?? I assume this is more expensive
than the powder and was wondering if they work the same??
My BIGGEST complaint is the brainfog:0(. Last summer I had some knee
troubles though. I still do if I try to exercise too much and they
are very stiff, but I am REALLY not looking forward to the HEAT,
which seems to make me feel VERY sick. So I look forward to having my
memory back and having things seem REAL again, at least depression
isn’t much of a problem since I have the CS! :0) (it was never in my
nature but I have struggled with it since I became ill) I have been
seriously ill for over 3 years now..seems more though.. But this is
just the “BRIEF” version of my story of deteriorated health..;0)
I am very appreciative of all information and advice offered in
advance!
Thank you!
Nicole :O)
PS. I also have adrenal exhaustion and am looking for any information
on things for that besides locorice?