Category Archives: Healing & Recovery Room

Update on Amish teen who fled from judge’s ruling to get forced chemotherapy

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Background:  When Sarah was diagnosed with cancer in 2013, her parents, Andy and Anna Hershberger, initially agreed to chemotherapy treatments. However, they opted to end such treatments when Sarah’s condition grew worse, fearing that the treatments themselves might eventually lead to her death.

As is typical in today’s post-constitutional America, officials at Akron Children’s Hospital responded with a legal attempt to strip Sarah’s parents of their right to choose their own daughter’s medical treatment. The hospital sought court permission to obtain “limited guardianship” over her, thereby giving them the authority over medical decisions pertaining to her. Doctors testified she would not make it six months without chemotherapy.

Initially, Probate Judge John L. Lohn — since retired — ruled that Sarah’s parents were competent enough to make medical decisions on their daughter’s behalf. Eventually, however, a higher court ordered him to appoint a guardian.

The family responded by fleeing the country, choosing instead to seek alternative medical treatment in Mexico and Canada. Months thereafter, the hospital decided to relinquish guardianship, seeing no point in pursuing the matter further.

Update:  Sarah has had MRIs and blood work, and the judge over the last year helped facilitate at least one trip to the Cleveland Clinic. The MRIs did not show any cancer, Her family is continuing to treat her with less invasive alternative medicine.  The court formally terminated Sarah’s guardianship on September 24. The judge acknowledged that Sarah, who will turn 13 in November, showed no symptoms of cancer and that she appeared to be healthy.”Read more…

ABSOLUTELY RIVETING: FDA/Cancer Cabal heavy handed 200 counts against Dr. Burzinski

A very rich, powerful, prominent and highly politically connected family seeks FDA approval to work with Dr. Burzinski’s and his cancer treatments on the husband’s (Charlie) absolutely inoperable tumor. This interview with Charlie’s wife is the most candid, riveting, shocking story about the FDA irrational attack on Dr. Burzinski and the American people who seek a choice other than that offered by the Cancer cabal. Jaw dropping! This is the real deal on the FDA. Hold on to your composure!

Lyme Disease – Bioweapon and cure

Excerpt from posts: Following is how we have alleviated many of the symptoms of Lyme Disease. Tea: Burdock Root, Marshamallow, Rose Hips, Dandylion Root, Bitter Wormwood. Sea Weed: 207-565-2907, Citricare 800-622-8664. Immusist 888-702-3315.

VLA comment:  For those who are not the new age generation, you may be turned off with his alluding to Crystal and Indigo children. And that he calls it Lymes disease instead of Lyme. (So what!) However, he is right about Lyme disease being a bioweapon.  And I certainly would add his protocol to yours. And hopefully yours is the SALT CURE.  Most importantly, I have facilitated, many times,  the cure for Lyme disease by the Salt Cure.  See:  www.LymePhotos.com I recommend you watch UNDER OUR SKIN to see how pervasive this epidemic really is:
http://www.underourskin.com/film/

Lyme Disease: The Plague, denied!

 

I’m 24 and Have Lived with Lyme Disease for 16 Years

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Allie Cashel at age 7, when she was diagnosed with Lyme disease for the first time. (Photo courtesy of Allie Cashel)

 

 

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Allie Cashel is the cofounder of sufferingthesilence.com, an online community for people living with chronic disease.

VLA Comment:  Riveting story

I have cured Lyme Disease and the numerous entities associated with it with one easy cure.  It is called the “Salt Cure”.  Salt has always been a revered element.  With this cure the body become infused with salt.  These bioweapon entities can not live in salt.  And since the salt pervades all the tissues, they can’t hide either.  Anti biotics not only don’t work and suppress the symptoms but it radically disturbs the gut microbiome which leads to a host of immunological diseases.  Go to:  www.LymePhotos.com

 

Cytochrome P450 testing covered by Health policies

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Read Wellmark policy

10% of Caucasians are “non metabolizers”.  This means that they cannot metabolize more than 50% of today’s drugs such as adderall, and other SSRIS.  It is suspected that the heinous trend of school shootings and suicides are caused by non metabolizers who are given psychiatric drugs without first being tested for their ability to metabolize them.  Because this test is not standard of care hospitals and doctors who destroy lives by giving counter indicated medication can not be successfully sued.  There is a movement to make this test standard of care but it is being thwarted by the invested pharmacuetical companies who would stand to lose billions of dollars if the public knew.

Description: 

The cytochrome p450 (CYP450) family is involved in the metabolism of a significant proportion of currently administered drugs, and genetic variants in cytochrome p450 are associated with altered metabolism of many drugs. It is proposed that genetic testing for cytochrome p450 variants may assist in selecting and dosing drugs that are impacted by these genetic variants.

Drug efficacy and toxicity vary substantially between individuals.  Because drugs and doses are typically adjusted to meet individual requirements as needed by using trial and error, clinical consequences may include a prolonged time to optimal therapy and serious adverse events.

Various factors may influence the variability of drug effects, including age, liver function, concomitant diseases, nutrition, smoking, and drug-drug interactions. Inherited (germline) DNA sequence variation (polymorphisms) in genes coding for drug metabolizing enzymes, drug receptors, drug transporters, and molecules involved signal transduction pathways also may have major effects on the activity of those molecules and also on the efficacy and toxicity of the drug.

Pharmacogenomics is the study of how an individual’s genetic inheritance affects the body’s response to drugs. It may be possible to predict therapeutic failures or severe adverse drug reactions in individual patients by testing for important DNA polymorphisms (genotyping) in genes related to the metabolic pathway (pharmacokinetics) or single transduction pathway (pharmacodynamics) of the drug. Potentially, test results could be used to optimize drug choice and/or dose for more effective therapy, avoid serious adverse effects and decrease medical costs.

Some CYP450 enzyme genes are highly polymorphic, resulting in some enzyme variants that have variable metabolic capacities among individuals, and some with little to no impact on activity.

Individuals with a lack of function activity in these enzymes (CYP2C19, CYP2D6, CYP2C9, etc.) can be classified according to how fast they metabolize medications:

  • Poor metabolizers (PMs): lack active enzyme gene alleles, they will process a certain drug more slowly than normal because of the missing enzyme(s), the medication can build up in their system which can increase the likelihood that it will cause side effects. The individual might still be able to benefit from the medication, but at lower dosages.
  • Intermediate metabolizers (IMs): have one active and one inactive enzyme gene allele, these individuals have a reduced enzyme function in processing drugs, they may not process some medications as well as a normal metabolizer would. This can increase risk of side effects and drug interactions.
  • Normal metabolizers (extensive metabolizers Ems): these individuals have 2 copies (alleles) of the most common (wild type) DNA sequence of a particular CYP450 enzyme gene resulting in an active molecule and are termed extensive metabolizers. Medications are processed normally, these individuals are more likely to benefit from treatment and have fewer side effects than people who don’t process the same medication(s) as well.
  • Ultra-rapid metabolizers (UMs): individuals with more than 2 alleles of an active enzyme gene, which cause the medications to leave the body too quickly and often before they have had a chance to work properly. These individuals will likely need a higher than usual dose of medications.

US patents on Cannibas

 

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Patents Related To The Dietary And Medicinal Study And Use Of Cannabis

US Patent 6,630,507 (pdf-120KB)
“Cannabinoids as Antioxidants and Neuroprotectants” Assigned to the United States of America, it provides guidelines for relevant medical conditions and dosage schedules for CBD. Review LOG notes on the use of vaporization to separate CBD from THC
Medicinal Acidic Cannabinoids / US 7,807,711 B2 (pdf-120KB)
Invention relates to an acidic cannabinoid, the method for extracting and preparing.
Pharmaceutical Compositions For The Treatment Of Chronic Obstructive Pulmonary Disease US 2009 / 0197941 A1 Aug. 6, 2009 (pdf-132KB)
Discusses the preferred ratio of CBD to THC being 1:1
Anti-nausea And Anti-vomiting Activity Of Cannabidiol Compounds / US 2003 0225156 A1 Dec. 4, 2003 (pdf-64KB)
Inventor: Raphael Mechoulam. The applied dose can be adjusted based on the relative bioavailability and potency of the administered compound. Adjusting the dose to achieve maximal efficacy…
Combination Of Cannabinoids For The Treatment Of Peripheral Neuropathic Pain US 2010/0035978 A1 Feb 11, 2010 (pdf-1.5MB)
This patent identifies “the ratio of CBD:THC by weight is between 10:1 to 1:10.”
US Patent 6,410,588 B1 (pdf-1.5MB)
Feldmann, et al. “Use of Cannabinoids as Anti-inflammatory Agents”
US 2007/0099987 A1 (pdf-1.4MB)
Weiss, et al. “Treating or Preventing Diabetes with Cannabidiol”
US Patent 6,946,150 B27 (pdf-2.7MB)
Brian Whittle. “Pharmaceutical Formulation.” Using a pump action spray to administer cannabinoids via the mucosal surfaces

HPV vaccine (Gardasil/Cervarix) Orthomolecular Treatment Protocol

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Severity of side effects

When other health experts re-evaluated those cases, they determined 1,112 (44%) to be serious. The initial onset of symptoms occurred several weeks to a year after the HPV vaccine was given. They included: headache, dizziness, muscle weakness and pain, nausea, hypersomnia, learning difficulty, impaired writing, photophobia, tremors of arms, feet and fingers, joint pain, irregular menstruation, gait disturbance, memory loss, skin eczema and acne.

Girls who had adverse effects from the HPV vaccine were variously diagnosed with:

  1. Higher brain dysfunction
  2. Guillain-Barré syndrome
  3. Multiple sclerosis
  4. ADEM: acute disseminated encephalomyelitis
  5. SSPE: subacute sclerosing panencephalitis
  6. CRPS: Complex regional pain syndrome
  7. POTS: Postural orthostatic tachycardia syndrome
  8. Anti-phospholipid antibody syndrome
  9. SLE: systemic lupus erythematosus
  10. Rheumatoid arthritis
  11. Chronic fatigue syndrome
  12. Fibromyalgia
  13. Cushing’s syndrome (exposure to high level of cortisol)
  14. Hashimoto’s disease (immune system attacks the thyroid)
  15. Hyperprolactinemia (high prolactin, induces breast development and lactation)

Laboratory findings included:

  1. Normal blood chemistry
  2. No inflammatory finding in the blood
  3. Increased pro-inflammatory cytokines in the spinal fluid (IL-2, IL-10, TNF-à)
  4. Reduced brain blood flow by perfusion scintigraphy
  5. High leukocyte sensitivity against aluminum.

 

HPV vaccine contains toxic aluminum

Vaccines often contain an adjuvant, which is an additional chemical added to provoke the body’s immune response to the vaccine. The HPV vaccines contained an adjuvant that consisted of an aluminum compound, amorphous aluminum hydroxyphosphate sulfate (AAHS).

Current research strongly implicates aluminum adjuvants in various inflammatory neurological and autoimmune disorders in both humans and animals. For example, a recent research paper explained that nanomaterials such as this aluminum adjuvant can be transported by immune system cells first into the blood, lymph nodes, and spleen, and in some cases may penetrate into the brain. [1] This type of access throughout the body is potentially life-threatening. The brain symptoms are often the most delayed because of the time the aluminum takes to travel from the blood through the blood-brain-barrier into the brain.

Aluminum accumulates in neurons in the brain, and it is toxic to neurons, causing a variety of pathological conditions. It inhibits uptake of dopamine and serotonin, which are important neurotransmitters in the brain. Aluminum toxicity is a known factor in Alzheimer’s disease, and may contribute symptoms of Parkinson’s disease. Dementia resulting from kidney dialysis is related to aluminum and results in memory loss, loss of coordination, confusion and disorientation. In animal experiments, rabbits given aluminum showed difficulty in memory retention and difficulty in learning.

ORTHOMOLECULAR PROTOCOL