You’ve likely heard of the hotly contested California mandate that was signed into law this year requiring the vaccination of all children in the state in order to attend public school. (no exemptions, religious or otherwise)
It established a terribly alarming precedent that will surely be followed by more bold attempts at forced medical procedures and drug interventions on everyday citizens.
It’s happening right now as hospitals to force employees to receive the infamous flu vaccination, often at the threat of losing their job.
I am amazed by the solidarity these strong willed people have shown.
Read the full article below.
A New Jersey social service agency has followed through with its threat to fire three office workers over their refusal to get a flu shot or, as an alternative, wear a surgical mask while in the company’s Burlington Township headquarters, an attorney for the women said.
Alanda Watson, Megan Duncan and Denise Mercurius, who worked in the accounting and billing departments at Lutheran Social Ministries of New Jersey, were suspended without pay last month for failing to follow the flu-prevention protocol, which went into effect in June.
The lies need to stop. We talk about evidence-based practice, so let’s look at what the evidence says.
As of today’s date there are 322,014,008 people living in the USA. http://www.census.gov/popclock/
The CDC says that
During September 28, 2014–May 23, 2015, World Health Organization (WHO) and National Respiratory and Enteric Virus Surveillance System collaborating laboratories in the United States tested 691,952 specimens for influenza viruses; 125,462 (18.1%) were positive.
So there were only 125,462 cases of confirmed influenza for last year’s flu season in the United States. Out of 322,014,008 people, this accounts for 0.0004% of the population that actually had confirmed influenza and not just flu-like illness.
Furthermore, the CDC states that out of these 125,462 cases,
17,911 total hospitalizations resulting from influenza during October 1, 2014–April 30, 2015
So, if only 17,911 people are hospitalized, how on earth can 30,000 people be dead of the US of influenza?
And among the adults that were hospitalized, most had other conditions that also contributed to their hospitalization as…
A mother who claims her daughter suffered “horrendous adverse effects” after receiving the HPV vaccine against cervical cancer has brought legal proceedings.
Fiona Kirby, Kilbeggan, Co Westmeath, is a member of a parents support group, REGRET (Reaction and Effects of Gardasil Resulting in Extreme Trauma), for those who claim their teenage girls became ill after getting the vaccine.
Ms Kirby, a nurse, is seeking a High Court order for the withdrawal of the license given for the Gardasil HPV vaccine, currently being offered to the parents of 11-16 year old girls as a possible cervical cancer preventative.
An order restraining the Health ProductsRegulatory Authority(HPRA), which monitors health products in Ireland, proceeding with use of Gardasil in any vaccine programme is also sought.
The vaccine has been offered to teenage girls in Ireland since May 2010 as part of the schools vaccination programme and is recommended by the World Health Organsiation.
I am a labor and delivery nurse at Scottsdale Osborn, and studying to become a nurse practitioner. My daughter was born on December 6, 1999. She was approximately 14 years, and 2 months old when she first suffered an adverse reaction to a vaccine.
J.G. was a happy, very healthy, normal, teenage girl. All that changed when the doctor in her pediatrics office recommended she receive Gardasil as prevention against cervical cancer.
As a mother and an informed registered nurse, I was confident in the vaccination and willing to allow J.G. to be vaccinated. On January 7, 2012, J.G. received her first dose of Gardasil at East Valley Pediatrics in Arizona. She progressed normally over the next few months, showing no apparent signs of an adverse reaction to the vaccination.
On July 26, 2012, J.G. received the second shot of Gardasil at East Valley Pediatrics in Arizona. She again progressed normally, still showing no apparent signs of adverse reaction.
On January 23, 2013, J.G. received her third and final injection of Gardasil at East Valley Pediatrics.
By March of 2013, I noticed that J.G. was bruising relatively easily, but thought she was a normal teen with maybe a low iron deficiency. After all, she was growing normally and she had just started menstruating. However, J.G. had never bruised like this before, and I had never seen the bruises shaped like this before. I was concerned, but chalked it up to her being an active, growing teenager. Being a nurse, I did not see any reason for immediate concern.
However, my concern increased in July of 2013 during a vacation to Hawaii. J.G. was playing like a normal kid would and was pushed off the boat, hitting her hip against the side.
The next day, the bruise that developed looked like she had been hit super hard, almost as if someone had taken a baseball bat to her hip. I remember asking her, “How hard did you hit the boat?”
She replied, “Not that hard, I guess it’s low iron like you suggest.”
Despite my nursing background, I still did not think anything was seriously wrong.
Ultimately, at the end of January of 2014, J.G. and I went to see her primary care doctor, Dr. Chapman, for a well-child check-up. We reported to her that J.G. was bruising a lot and had been for months. We thought she needed her iron level checked.
Dr. Chapman sent her for labs. That afternoon, we had her labs drawn.
The next morning, we received a phone call. Dr. Chapman told us J.G.’s platelets were low (I believe at 23k), and she needed to see a hematology doctor A.S.A.P.
I picked up J.G. from school and kept her home until her appointment in 2 days. When we arrived to the office at Phoenix Children’s Hospital, they took more blood samples, 14 tubes, I believe, to double-check the labs and verify the diagnosis. She was again low – at approximately 24k platelets. They then asked how long we had noticed symptoms, and if we had seen bloody noses or spots on her skin. She had not at this time, just bruising.
Phoenix Children’s Hospital decided to refer J.G. to a rheumatologist named Dr. Ede and have her follow up with Dr. Shah, the hematologist. The plan was to send her labs and watch her to see what her body will do.
Dr. Ede told us during our appointment that J.G. did not meet the guidelines for Lupus, and her urine was negative for any indication of kidney damage that is present with kids with Lupus.
He did tell us that her labs were positive for something called Anti-phospholipid antibodies. This meant she was at high risk for clots. He wanted to follow her case, but felt she was not going to be a Lupus patient. He also asked that her labs be run again prior to any treatment for low platelets, such as Immunoglobulin therapy (“IGG”) to recheck the ANA and Double Stranded DNA.
J.G. was diagnosed on February 11, 2014, with immune thrombocytopenic purpura, ITP.
Dr. Shah told us J.G. would probably remain in the 30k platelet range for a few months, and would likely need intervention therapy such as IGG, Rituximab, or steroids.
The antiphospholipid issue was explained as being a possible positive as an auto immune response. The physicians could not say for sure which autoimmune condition came first, antiphospholipid antibody syndrome or thrombocytopenia.
They also said her labs were all negative for virus or other causes of ITP, and decided it was more likely a chronic immune thrombocytopenia. For several months, J.G. did stay at around 35K platelets.
Then, in May of 2014, J.G. experienced a seriously heavy period, nose bleeds twice in one day that would not stop, and little red dots all over her arms and legs. We took her to the Phoenix Children’s Hospital urgent care and they found J.G.’s platelets were 14K. (Note: a normal platelet count ranges from 150,000 to 450,000)
Dr. Williams, a hematologist with Dr. Shah, began seeing J.G. They told us to come back in the morning first thing for her first round of IGG. She was admitted all day for the infusion. They ran her blood for labs that Dr. Ede requested and started the infusion. These labs showed her ANA and double stranded DNA were both negative now. Dr. Ede decided to continue to follow her case, but did not need to see her anymore, because she does not meet the guidelines for Lupus.
J.G. came back to Phoenix Children’s Hospital for labs again to check her platelets a few days later. Her levels were around 75K. However, they quickly fell to 10K again, and she was then admitted again for another dose of IGG. Her levels rose again to 100k then fell down again to 23K.
Dr. Williams decided it would be best to start her on a medication called Rituximab to try to reverse the effects of her immune system’s response by resetting her B cells that cause her body to mark her platelets for destruction.
That night, J.G. started with bleeding of the nose again, small red marks all over her body, including her bottom, and heavy, irregular menstrual bleeding. She went to urgent care again and was told she had a 4k platelet count. The physician on call reported to the hematologist who then decided to admit her again for a high dose of steroids known as dexamethasone.
She took a super high dose of steroids for a few days to try to give her a boost while the Rituximab did its job. The steroids made J.G. very ill, with a stomach ache, headache, and racing heart. She gained some weight, too. She started the infusions of Rituximab, which is given in 4 doses for 4 weeks.
J.G. was admitted outpatient all day for those infusions and tolerated it well. She was to continue the lower dose steroids for several weeks so her platelet levels would stay above 25k. She did remain around 30K for many weeks. Then in August of 2014, her platelets jumped to over 150k. She was doing great and responding well to the treatment. She was removed from steroids. She officially completed Rituximab on June 24, 2014, and had a complete response with normal platelet count since July of 2014.
We have spent numerous hours and dollars fighting J.G.’s illness, all brought about by the Gardasil vaccination.
Worse yet, J.G. has lost her teenage years due to her debilitating condition, and cannot live a normal life. The fear of bruising and her potentially low platelet count dominates her mind wherever she goes.
J.G. continues to remain in remission, and continues to be seen by Dr. Williams every few months. During her last visit in January of 2015, her labs were rerun to show a negative DNA and slightly positive ANA and positive antiphospholipid antibodies.
Dr. Williams has said he thinks that the antiphospholipid antibodies and ANA should go away in time. However, she is still at a high risk for chronic ITP due to her age, her history of bruising post-vaccination, and the presence of other antibodies.
Her labs have continued to remain positive and her court expert Dr. Shoenfeld thinks she will remain APS positive for life. It will never go away. She will have high clot risk and the risk of return of blood related disorders and high pregnancy risk. Unfortunately it won’t go away. But so far so good. She’s still healthy.
No child should have to go through what my daughter has experienced.
This article in it’s entirety, is compliments of www.SaneVax.org
Tara and J.G., my heart aches for what you have been through. I am so sorry you have been through such a trauma and live with the anxiety brought on by an unnecessary shot.
A terrible crime by the pharmaceutical industry and government agencies that allow it.
I am so happy you are maintaining well at this time. Sounds like a lot of hoops and tests to get to this point.
You have no doubt been guided and blessed.
Stick with the guidance of the Lord and he will continue to carry you when you need it.
J.G. you are a brave girl and so positive.
Always let the Lord be your constant guide and you will always have the best possible response.
Thank you for sharing your story. Just know that another girl will be able to avoid what you have been through because of it.
There are physicians with expertise in healing from Gardasil/Cervarix/Silgard injuries.
The battle rages on in the United States as citizen’s fight to keep vaccine exemptions on a slippery slope pointed away from medical freedom. Pharmaceutical funded lobbyists are making no effort to conceal their agenda as they coat senate committees like wet blankets covering truth. The trend is moving fast away from public power as senators misrepresent their voters. In California and Vermont, it has been confirmed that the community, because of its strong opposition, is simply no longer able to testify on record. Any whisper of the possibility of endlessly stacked parents rejecting votes sees immediate postponement of committee meetings to remove such options.
It is clear that certain topics are off limits and conversation is controlled by pharmaceutical interests. The term is called astroturfing and it can be witnessed in full force at any state capital currently voting to take away medical freedom and vaccine exemptions. In a recent interview with Sharyl Attkisson, Dr. Joseph Mercola asked the question, “What other currently health related issues might be happening right now that you believe investigative journalists and the media are not reporting on. Or could do a better job if they weren’t being suppressed by the people who authorize the release of that information? Attkinson, a five-time Emmy Award winning investigative journalist and author of the book, “Stonewalled: My Fight for Truth Against the Forces of Obstruction, Intimidation, and Harassment in Obama’s Washington.”, gave the following reply:
“If people were simply covering in terms of news value, facts, and fairness we’d be giving way more coverage to vaccine side effects, autism, ADD, and all the immune disorders that have emerged in the past and been made untouchable by this environment that I’ve discussed with you (referring to astroturfing.)
WASHINGTON – When Phoenix nurse Tarah Gramza realized that her daughter’s autoimmune disorder may have been caused by a vaccine, she looked into suing the vaccine manufacturer.
Then she learned that the government won’t let her.
Instead, Gramza is beginning what could be a years-long legal battle with the U.S. government, trying to get an infinitesimal slice of the $3.5 billion fund set aside to compensate people who have adverse reactions to vaccines.
Gramza, like most Americans, had never heard of the National Vaccine Injury Compensation Program – the trust fund that’s financed by a 75-cent tax on each dose of vaccines that the Centers for Disease Control and Prevention recommends for children.
The program started in the 1980s after a number of vaccine manufacturers threatened to pull out of the United States in the face of a growing number of lawsuits.
In order to protect the vaccine supply, and keep the majority of Americans immune to possibly devastating disease, Congress pledged to protect the manufacturers from lawsuits.
But some say that solution – the National Vaccine Injury Compensation Program – is not living up to its promises. It’s complicated, litigious and time-consuming – and often ends without any compensation at all.
“There’s no part of it that’s easy,” said Renee Gentry, president of the Vaccine Injured Petitioners Bar Association. “It’s knock-down, drag-out fighting at every step.”…
You may be a bit stunned and left speechless by the clip below.
Doesn’t the surgeon general’s position include health safety?
Did he mention anything about the risks when getting a vaccine if ill? Did he mention anything about the vaccine insert warnings? How about the risks of “vaccine cocktails”?
Maybe part II could include the friendly vaccine ingredients.
I bet little children would be fascinated about how the formaldehyde surrounding dead frogs, in their science classrooms, is included in vaccines or maybe the colorful blue and pink antifreeze that sprays on their daddy’s windshield is also in the “helpful” shot.
This clip is nothing short of embarrassing and I can’t help but think that the repetitive laughing, tickle-me-Elmo would have been a better puppet in this scene.
The Morning Call of Lehigh Valley Pennsylvania is now reporting that one nurse’s aide has been awarded $11.6 million for being paralyzed with GBS after receiving a flu shot. This is newsworthy, because pharmaceutical companies cannot be sued in civil court for damages due to vaccines. Congress gave them total immunity to such lawsuits in 1986 and that law was upheld by the pro-Pharma Supreme Court in 2011. Sales of vaccines include a tax that is paid to fund a special court where government attorneys fight for the U.S. government to prevent paying out damages due to vaccines. It is a long and difficult process, so settled cases represent only a tiny fraction of the amount of vaccine damaged people in our society…
Sarah Behie’s symptoms started nearly three weeks after she got a flu shot.
The nurse’s aide at Lehigh Valley Hospital noticed that her knees and arms hurt and that her limbs felt weak.
As the pain and weakness grew worse, the 20-year-old was admitted to the hospital and later diagnosed with Guillain-Barre syndrome, a rare neurological condition that would leave her partially paralyzed and living in hospitals and nursing homes for nearly four years…
