I know you can’t see me but tears are running down my face as I think about you. The following quote comes to mind:
“You is kind. You is smart. You is important.” ― Kathryn Stockett, The Help
Although this was said from a maid to a little girl, we never outgrow the need for affirmation and this is most certainly true if you are a woman chronically infected with tick-borne illness, have a child with tick-borne illness or you are one in the growing army of women who while being infected yourself, care for an infected menagerie at home.
The U.S. Food and Drug Administration has learned that some ranitidine medicines, including some products commonly known as the brand-name drug Zantac, contain a nitrosamine impurity called N-nitrosodimethylamine (NDMA) at low levels. NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables.
The FDA has been investigating NDMA and other nitrosamine impurities in blood pressure and heart failure medicines called Angiotensin II Receptor Blockers (ARBs) since last year. In the case of ARBs, the FDA has recommended numerous recalls as it discovered unacceptable levels of nitrosamines.
When the agency identifies a problem, it takes appropriate action quickly to protect patients. The FDA is evaluating whether the low levels of NDMA in ranitidine pose a risk to patients. FDA will post that information when it is available.
Patients should be able to trust that their medicines are as safe as they can be and that the benefits of taking them outweigh any risk to their health. Although NDMA may cause harm in large amounts, the levels the FDA is finding in ranitidine from preliminary tests barely exceed amounts you might expect to find in common foods.
Ranitidine is an over-the-counter (OTC) and prescription drug. Ranitidine is an H2 (histamine-2) blocker, which decreases the amount of acid created by the stomach. Over-the-counter ranitidine is approved to prevent and relieve heartburn associated with acid ingestion and sour stomach. Prescription ranitidine is approved for multiple indications, including treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease.
The agency is working with international regulators and industry partners to determine the source of this impurity in ranitidine. The agency is examining levels of NDMA in ranitidine and evaluating any possible risk to patients. The FDA will take appropriate measures based on the results of the ongoing investigation. The agency will provide more information as it becomes available.
The FDA is not calling for individuals to stop taking ranitidine at this time; however, patients taking prescription ranitidine who wish to discontinue use should talk to their health care professional about other treatment options. People taking OTC ranitidine could consider using other OTC medicines approved for their condition. There are multiple drugs on the market that are approved for the same or similar uses as ranitidine.
Consumers and health care professionals should report any adverse reactions with ranitidine to the FDA’s MedWatch program to help the agency better understand the scope of the problem:
Download and complete the appropriate form, then submit it via fax at 1-800-FDA-0178
The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.
Dr. Daniel Erickson, owner of seven CA urgent care facilities, was thrown into the spotlight after his press conference on the COVID 19 stirred up enough controversy to get censored by YouTube. Here’s Del’s follow-up interview and this doc’s message is clear: he is not backing down.
Nikki Kent, diagnosed with Lyme disease in the U.S., says she feels failed by the Ontario health care system after being denied treatment. (See link for article)
____________________
**Comment**
An MRI showed Kent had lesions on her brain.
Important points:
Because the Canadian tests would not yield a positive result, the health care system would not treat her for it.
She showed her positive American testing and they still denied her treatment.
The Canadian testing, like mainstream American testing, only tests or confirms a small number of strains of Lyme (borrelia).
In light of COVID-19, which has yet to be isolated (detected) with a subsequent picture from an electron microscope, it also becomes clear that antibody tests for COVID-19 are also useless, as are PCR tests as nucleic acids can not be used as the standard for giving evidence of infection. FYI: HIV, H5N1, SARS, and many other viruses have never, ever been seen by anyone. This should alarm us.
It appears that Bill Gates’ Microsoft file patent for a “body activity data” apparatus involves far more than just tracking vaccines.
Patent #WO2020060606, which is described as a “Cryptocurrency System Using Body Activity Data,” senses body activity of the user.
“Human body activity associated with a task provided to a user(1) may be used in a mining process of a cryptocurrency system. A server may provide a task to a device of a user which is communicatively coupled to the server(2). A sensor communicatively coupled to or comprised in the device(3) of the user may sense body activity of the user. Body activity data may be generated based on the sensed body activity of the user. The cryptocurrency system communicatively coupled to the device of the user may verify if the body activity data satisfies one or more conditions set by the cryptocurrency system(4), and award cryptocurrency to the user whose body activity data is verified.”(5) https://operation-nation.com/bill-gates-microsoft-file-patent-for-dystopian-body-activity-data-implants/
These ‘digital certificates’ are human-implantable ‘QUANTUM-DOT TATTOOS’ that researchers at MIT and Rice University are working on as a way to hold vaccination records. It was last year in December when scientists from the two universities revealed that they were working on these quantum-dot tattoos after Bill Gates approached them about solving the problem of identifying those who have not been vaccinated.
Quote by Gates to the Financial Times:
“You don’t have a choice. Normalcy only returns when we’ve vaccinated the entire global population.”
The implantable mark emits a glowing red X pattern as it delivers the vaccine and what is left behind is capable of data storage and retrieval for years afterwards.Smartphones are implicated:
“Detection of the microdots is possible using specially adapted smartphones that can detect the near-infrared fluorescence. ‘Because these phones offer on-board processing power, camera applications, and inexpensive consumer-grade camera modules, we chose to adapt an existing smartphone to enable NIR imaging rather than build a completely new imaging system,” they wrote. “In addition, we believe that familiarity with the function of these devices will lessen the learning curve for NIR imaging in a field setting.'” https://www.genengnews.com/topics/drug-discovery/quantum-dots-deliver-vaccines-and-invisibly-encode-vaccination-history-in-skin/
Researchers have turned this technology to the COVID-19 virus.
PittCoVacc, short for Pittsburgh Coronavirus Vaccine uses lab-made pieces of viral protein to build immunity, similarly to current flu shots. What’s different is that it utilizes a microneedle array which increases potency. The patch goes on like a Band-Aid and then the needles — which are made entirely of sugar and the protein pieces — simply dissolve into the skin.
“Testing in patients would typically require at least a year and probably longer,” Falo said. “This particular situation is different from anything we’ve ever seen, so we don’t know how long the clinical development process will take. Recently announced revisions to the normal processes suggest we may be able to advance this faster.” https://www.upmc.com/media/news/040220-falo-gambotto-sars-cov2-vaccine
A 2019 MIT study funded by the Gates Foundation describes how “near-infrared quantum dots” can be implanted under the skin along with a vaccine to encode information for “decentralized data storage and bio-sensing.” https://sci-hub.tw/10.1126/scitranslmed.aay7162
All of this stored data needs to have a system big enough to handle it. Enter 5G.
Hopefully it is becoming clearer all the time what COVID-19 is really about.
Madison Area Lyme Support Group 