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Lyme Disease Discussion on Lyme Disease, Also known as ticks disease/lyme arthritis


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  #1 (permalink)  
Old August 21st, 2009, 03:09 PM
Kritters is a fungus magnet
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Andalusian Dogs Presents: Under The Eightball

Can't remember if anyone posted this before....

Kritts
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Old August 21st, 2009, 03:25 PM
Kritters is a fungus magnet
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I don't know about anyone else but I think the music totally drowns it out. I'm going to email them about it.
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Old August 22nd, 2009, 10:17 AM
faithinacure is obsessed in unravelling this hideous puzzle
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Kritts: Thanks for posting that. The children and parents were so innocent; they had no idea what they were getting themselves into.
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Old August 22nd, 2009, 10:49 AM
Kritters is a fungus magnet
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Faith,

Yabutt, I would never sign my child up for any experiment unless it's life saving and they had no other alternative, you know?

Did the music drown it out for you, or is it me?

xoKritts
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Old August 22nd, 2009, 11:53 AM
Sadsack is Praying for a Miracle
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Kritters -

I agree - but even when the music wasn't playing, it was hard to understand what they were saying.

I am having a bit of trouble understanding the connection between this experimental site (Ft. Detrick) and the point of the film which is evidently about Lyme. I am sure they must be saying that is where it was developed. Was Lori one of the kids who was subjected to the experiment? They didn't say.

About Under The Eightball
In 1951 at Fort Detrick, Maryland, construction crews built a hollow metal sphere four stories high. Inside germ weapons were to be exploded, creating mists of infectious aerosols for testing on animals....and people. Employees called it the eight ball.
In the summer of 2006 my sister Lori was afflicted with an illness that, ten months later, has yet to be definitively diagnosed. Less than one year ago she had full function of her body, regularly riding bicycles, swimming and gardening with her son Jackson. One day, while helping Jackson onto his bicycle her leg gave way beneath her and she collapsed. Although it felt no different it just wouldn’t respond.
She quickly sought treatment for what she thought was simply a pinched nerve. However, after seeing a specialist she was told that due to the quickly lost muscle function Guilian Barre Syndrome, a rare autoimmune disease, could be the culprit. She was started on a rigorous and extremely expensive course of intravenous immunoglobulin, or IVIG, which boosts antibodies to help the good guys fight the bad guys. But why after a month of treatments, when improvements should be seen in a few weeks, was Lori not getting better but getting worse?
Countless hours and myriad visits to Munson Medical Center in Traverse City, University of Michigan in Ann Arbor and other traditional and homeopathic specialists only fueled confusion and frustration. Lori soon lost function in her other leg and motion in her hands deteriorated. Finally, after months of testing, poking, scraping, and analyzing, the diagnoses began arriving. They seemed forced and without tangible evidence, some symptoms conflicting with others: Guilian Barre Syndrome, Multiple Sclerosis, Lupus, Lyme disease, Lou Gehrig’s disease, then Lyme disease again, Lou Gehrig’s disease again. Once being told by her neurologist that “Everyone dies”.
During one visit to the doctor’s we crossed paths with a friend who had recently been diagnosed with Multiple Sclerosis. What were the odds that two people who knew each other would contract similar disease in such a short time? we began to dig a little deeper. Lori realized that she knew of five people in her neighborhood that had been diagnosed with MS, ALS, fibromyalgia or a similar degenerative disease. This could not be a coincidence.
Two diagnoses took rein: Lou Gehrig's disease or ALS, incurable and fatal, and Lyme disease, an easily treatable and often durable ailment.
At the time my knowledge of Lyme was the same as others --What’s Lyme? A disease -- How do you get it? Ticks – What does it do? Makes you sick. Right? – Well, Lyme disease can be hard to diagnose with its vague flu-like symptoms. However, when Lori described a bite she had that was surrounded with Lyme’s trademark round red rash, commonly called a “bulls-eye”, why didn’t doctors start her on a routine regimen of antibiotics? If untreated Lyme’s can cause debilitating arthritis and joint swelling, meningitis, blindness, fatigue, droopy eyes and other serious conditions. Why wouldn’t doctors prescribe the harmless antibiotics?
We were all very scared at what was happening to Lori and we had discovered, but even more frightening was the possibility that this was something that could have been prevented.... or worse that it was intentional in the name science and National Security... I had questions... many questions. And I'd be damned if they went unanswered.



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Old August 22nd, 2009, 01:06 PM
kmar is a believer that with effort wishes can come true!
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This is a heartbreaking video.

Under The Eightball

" All neuromuscular genetic testing has been negative.

Dr's we have spoke with believe this stemmed from 1 of 3 things: genetic, a toxin, or a virus. Since Alex has an identical twin and all genetic testing has come back normal we believe it is one of the other 2.

She did test positive for HHV-6 (virus) and pro-inflammatory markers were all normal. There are so many confusing things about Alex's illness which makes it so difficult to proceed with proper treatment.

Everyone we write chose to ignore Alex. We have struggled to find the help Alex deserves to help save her life.

A Dr in Colorado who was misdiagnosed with ALS and was positive with lyme flew to Alex and clinically diagnosed her with lyme as well. "


READ THE COMMENTS to this video on You Tube.

YouTube - A Family's Fight for Hope, Faith and Courage
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Old August 22nd, 2009, 01:09 PM
kmar is a believer that with effort wishes can come true!
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Thanks Kritters for posting this very important link.


Kmar
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Old August 22nd, 2009, 01:20 PM
Kritters is a fungus magnet
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Kmar~ you're welcome and thank YOU for the above! Alex was the one I posted a thread on a few months ago asking for everyone's help. I got that request from the newsletter. I had emailed Alex's mother (sheer boldness on my part since I'm really not all that informed) because I really wanted to help any way I could. After my 3rd email to her with questions, (she had been replying all along with 'yes's) she told me I was making her hair stand on end and thanked me profusely for the info I sent. I haven't heard from her since and I have been thinking of her. I hope no news is good news, but I'm worried that it isn't. the poor little girl was a paraplegic, had lyme, and had multiple vaccinations just prior to this happening.

Kmar...one other thing... "She did test positive for HHV-6 (virus) and pro-inflammatory markers were all normal. There are so many confusing things about Alex's illness which makes it so difficult to proceed with proper treatment. "......

HHV-6 HERPES VIRUS!!!!positive!!!! that so supports Herpes being involved in Lyme and probably Morgellons, as far as I'm concerned. You know of course, being a nurse and researcher, that a virus needs the dna of something to multiply and proliferate. Is it the Borrellia bacteria? Is it the fungus (maybe Candida or Aspergillis?) How are all these things connected?

thanks again,
Kritts
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Old August 23rd, 2009, 02:26 AM
jonsi is live and let live. Let's get through this!
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right on kritts,

This video hits the nail on the head. It is a "must see" for anyone posting under this link. I didn't have any problems understanding what they were saying.

Andalusian Dogs Presents: Under The Eightball

Itwl,
~jonsi
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There is a reason I have "Morgellons". Helping and teaching others how to survive in our toxic world may be the reason. Hang in there everyone who has this.
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