Published on Jul 25, 2012: In the 1970s, a mysterious and deadly illness began infecting children in a small town in Connecticut. Today it’s a global epidemic. A real-life thriller, this shocking festival hit exposes the controversy surrounding chronic Lyme disease. Following the stories of individuals fighting for their lives, director Andy Abrahams Wilson reveals with beauty and horror a natural world out of balance and a human nature all too willing to put profits before patients.
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this is why it is very important to clean the skin when you go out in the
mountains …
See Dr Robert Cassar skin cleaning protocol … recipe for alcohol is on
earthshiftproducts.com : look under skin cleaning recipes
This disease has taken my freedom…hopefully temporarily. Don’t let it
take yours!!!
Write to your Senators, tell your Doctors, tell your friends and tell your
family…just do something!!!
This is an epidemic and not nearly enough is being done!!!
read lab 257 ..amazon
read lab 257 ..amazon
Culling the herd……population control……a dirty little secret
Lyme
Thank you for shedding light on this!!!! : ) I have been affected and will
be going on a mission to bring about awareness!!! We need to collaborate!
This disease has taken my freedom…hopefully temporarily. Don’t let it
take yours!!!
Write to your Senators, tell your Doctors, tell your friends and tell your
family…just do something!!!
This is an epidemic and not nearly enough is being done!!!
The guy at the end that can’t remember his research and discovery.. my
heart.
Thank you for making this. I’ve been fighting a myriad of symptoms for
about 3 years now, and I’m so tired of doctors telling me I’m crazy and
it’s all in my head. There aren’t enough words to express my gratitude.
I was recently diagnosed. Apparently have had this for decades. Symptoms
came to a head a couple years ago. Doctor after doctor and no diagnosis. If
you are feeling awful physically, psychologically, or both, and docs won’t
give you a satisfactory answer, go get tested! (Igenix is the ONLY
reliable test provider). The symptoms, for me, are in the dozens and
change daily and sometimes on the hour. It’s a baffling, horrific illness.
The answer is simple, we all need access to any treatment we want or to practice curing people without a license. Consumer report type organizations can monitor the successes of these practitioners. Insurance companies then should pay out to those who are the most successful and cheapest. True competition will find all cures. This can be done with a new amendment to the constitution that allows anybody to use any treatment and for anybody to provide it and no drug prohibitions whats so ever. Other drug additions should be treated medically not jail. To those are infected now could do… Read more »
http://www.prweb.com/releases/2013/2/prweb10402216.htm?PID=6154686
Colorado Rockies!
Doctors are only human and quite fallible yet tend to be far more arrogant
than your average human due to the social status they have, do keep that in
mind.
Talk about a witch hunt! It’s disgusting to see how the system tries to
ruin doctors who are merely trying to help their patients… isn’t that
what doctors are supposed to do???
MMS
Yes and it presents long term antibiotic treatment as if it was the answer.
I did antibiotics for over 4 years with little improvement. In fact, I was
worse. Now I only do alternative treatments such as iv peroxide which was
really helpful and put me in the longest remission I have ever had
Imagine a world where peoples’ lives are more important than corporate
greed, money and politics! Be hopeful and prayerful!
I got tested for Lyme disease some years ago, and it came back positive. I
got the normal 10 day antibiotica cure and thats it. I also got the Chronic
Fatigue Syndrome diagnosis last year. But what is it realy.. Is it Chronic
Fatigue Syndrome that gives me all the sypmtoms or could it still be Lyme
in my body..? I dont know, and the doctor dont take me serious and do not
listen. The only solution he got, is to send me to a facility that “trains”
ppl back to normal.. I dont know what to do… :'(
I bought a zapper two years ago and used it regularly. I did not notice a
difference. Several things have helped me immensely tho. IV peroxide, LDA
shots, and high dose vitamin C.
This is really good film
Scheiß Werbung.
Three years into Lyme. I supposedly no longer have the disease, but I have
twitches, and aches, and fatigue, and that mind fog, and, and, and,…. I
go to an herbalist who has been more helpful than the doctors.
For shame on the slime that are turning their backs on the Hypocratic oath
and patients. With greed rampant why is it patients don’t group together
and file class action lawsuits against the medical boards that are
persecuting the true effective doctors??! LIp service only goes so far
but doesn’t help change the landscape profiteering “medcial” oversight.
I know of people who had Lyme and got well using an alternative device
called a Beamray. You may want to look into it. This film does a great job
of exposing how Lyme is looked at by conventional medical world. Another
film like this is called the Burzynski movie, but about cancer. A must
watch film.
http://rense.com/general85/morgnan.htm
Its been five years since I contracted lyme disease, how the disease realy
affected me was it earased my identity. In the first year after being
diagnosed and treated with doxyclonine I was basically drooling on my self,
most of the time I couldnt recall my own. Ownly in recent times i have been
able to recall and rember my past before lyme disease. This documentary is
the only that helps me feel not alone and shows too me how lucky i am to
walk away from lyme with only the symptons i have.
This should be require viewing. I know several people diagnosed w/Lyme’s,
but several other with Lou Gerigs or Parkinson’s or MS. What I don’t
understand is the resistance to treatment for long term Lyme’s and the
persecution of these physicians. Let’s get this info out to people- lots
out there suffering in silence.
one of the designer viruses the CIA unleashed on the population
The order of the system of a mercury-sensitve person is disturbed by chronic daily exposure with traces of mercury by ingestion, inhalation and skin penetration. The infection with Borrelia can not be correctly counteracted and faught by the disturbed immunesystem, and the burden of the Borrelia infection and unknowing new daily exposure of mercury weakens the body even further. The flair ups of the disease can only be explained by the incidence and level of new mercury exposure, the level of borrelia can not change from one hour to the next, like the symptoms do. All patients feel better with… Read more »
I just got done watching this documentary, what a great piece! I had some
tears fall when Dr. Jones was being interrogated about his honest practice
and those who were on the mend. What evil entities that control our society
and rights!
My bro in law has Lyme’s and has had it for 4 years+ but misdiag’ed after
all those years. He is going through the hurxing process. If anyone here
can please help me to help him, I would appreciate it. I found this video
due to people posting on Debbie Gibson’s article of coming out with Lyme’s
disease and mentioning, “Under Our Skin.”
Death panels, indeed. Insurance companies are driving treatment regimens,
and no deviation will be tolerated.
Very powerful film. Thank you so much. God bless all the brave people who
have suffered from this disease, and the good doctors who dare to treat
them.
my father is a physician specializing in treatment of chronic Lyme… a
disease the entire medical community, except for a handful of brave
physicians, has shit on for reasons of money and power.
for those suffering… i feel you. you aren’t faking, arent lying, don’t
have Fibromyalgia, you don’t have arthritis…
Chronic Lyme will be defined one day, and it will be done.
Until then, keep fighting!
Important to watch – for many, many reasons. Please take the time. It is
part of understanding how political climate, insurance companies, and
profiteering cost lives and practices of competent practitioners.
My 23 kd, and 41 kd came up positive, after having years of horrible symptoms, just be told we don’t see anything wrong. This also being told I have abnormal brisk reflexes, tremors, uncontrollable muscles movements, abnormal gait, still nothing wrong?!? I was bitten by a black legged tick several years ago, when I discovered it was on the back of my head. I had flu like symptoms, I was dizzy and had bad headache. But was told Lyme does not exist in Florida. So there you go, according to who I have seen so far there’s nothing wrong with… Read more »
Never knew how disastrous the disease can be.
Thank you for posting. Very educational.
I wonder what effect combining the anti-biotics and
fully supporting the flora of the intestines would have on the body.
And could a strict, healthy diet restore the immune system contributing to
a faster recovery?
Great informative video on Lyme Disease ~ March 2014 I was told / informed
from my Feb 2014 lyme blood test that I have most likely had this for 10,
20 or 30 years. . . Yet, another gift from Virginia ~ Chronic Lyme Disease
. . . SADLY, AND FOR U WHO WATCH THIS VIDEO ~ U WILL NO LONGER TAKE WALKS
IN THE WOODS OR CAMP EVERY AGAIN!!!! BEACHES ARE SAFE THOUGH! 🙂
Im currently undergoing testing… effing ticks.. never again will i go
into the woods. my life is hell now. when i seen this, i ran back to the
doctor right away. ive been being treated for lupus out of nowhere, after
this tick bite. so now i want to make sure im treating the right thing.