Archive for the ‘Psychological Aspects’ Category

Dutch Lyme Patients Accused of Child Abuse

 BVIKZ interview  The sound of the movie is softer than intended, so it is subtitled in both English and Dutch. Click on settings to select your language. 

Published on Mar 17, 2017
Read the English interview on: https://on-lyme.org/en/sufferers/lyme…  by Huib

The BVIKZ, the Interest Group for Intensive Child Care, is doing an ongoing investigation into false claims of child neglect and abuse by the Dutch Child Protection Services. It has now compiled and researched 168 individual cases. Over thirty percent of these cases are about children with Lyme disease.

During the last eight months hundreds of Dutch parents have been contacting the BVIKZ to report what happened to them. They have also received many reports from parents of children with Lyme disease. National media made this into a primetime topic, which was viewed by 1.5 million people. Shortly afterwards the BVIKZ had their third meeting with the Board of the Dutch Child Protection Services called ‘Safe Home’ (SH).

BVIZK chairman Vera Hooglugt agreed to do an exclusive interview for the On Lyme Foundation. We asked her to tell about their general findings of the BVIKZ investigation and specifically about the Lyme cases. The interview took us over three hours.

The BVIKZ has been working intensively to build all cases, scan all files, support the traumatised parents and children, assist in conversations, provide legal help and build up a case to create political impact to fundamentally change the way the whole system is operating. The meetings with SH are absolutely very important for the process.

Hooglugt thinks that they are only just seeing the tip of a much larger iceberg and wants to encourage other parents to be brave and come with their complaints in case of false allegations.

The tipping process

Tips or reporting seem to come from all angles. Tips come from all angles and we have the impression that the ones doing the reporting don’t realise how much impact it can have on the lives of the children and the families.

Almost all of the reports we saw are subjective and most are very suggestive. As an independent organisation we can really be neutral and unbiased enough to look at the claims without prejudice. So we strip all assumptions, subjective ‘gut feelings’ and also check on the motives of the ones doing the reporting.

Too often we see that the child’s best interests in not at stake. We often see divorced husbands reporting on their ex-wives. The system just regards this as an objective fact, worthy of a formal investigation.

Another example is a government official charged with school absence, who had already given the child leave to skip school. When the family moved house, he found what province they had moved to and asked his colleague to assist in filing in a report on ‘child abuse’.

In another case a commercial company was annoyed that they did not get a contract, because the parents did not find the care provided as fitting for their child. The company reported on the parents and SH did a year long investigation, wrecking the social life of this family.

We urged the parents to ask for the original report, which is within their rights. Their request was denied without reason, so we filed a request as their formal representative.

We then received a paper copy, in which a large part of the text was white-washed. Again we requested the original digital version from SH, but were told that it was deleted due to computer problems. Finally we managed to get the original complaint. By comparing the different versions we could see that all subjective remarks were white-washed.

Employees of the Consultation Office, where new parents go to check on their baby’s health and progress, have been reporting them to SH. Simply for not vaccinating their child or wanting to use other services offered by this institution. 

Another poignant case is the one of an adult lady, who suffers from Lyme Disease and who is been taken care of by her old mother. She cannot stand light or sound, so she lives in a darkened room. The mother of a distant acquaintance of their neighbour reported on them, after hearing a gossip story about closed curtains. People like her seem to be influenced by prompting calls in the media.

In this case SH tried to get a psychiatrist to both judge the mother with ‘Munchausen by Proxy’ and proclaim the daughter legally ‘incompetent’ (not having her own will). This would allow them to lock her up in a psychiatric ward and blame the mother. Why would Youth Care deal with someone who is of age? After a change in Dutch policy they now have the function to provide safety in everyone’s life; from zero to hundred.

Although these examples are shocking enough in themselves, we also saw statements of how family doctors state that they were intimidated by SH to testify against their patients. Fortunately they refused to act against their Hippocratic Oath to ‘first not do harm’.”

The foundation of the accusations

In all cases we see how easy it has been made for anyone to report on everyone else. This allows everyone to report, without a proper filter in the system. Even though a ‘code of conduct’ has to be used, we see that happening far too little. Although Dutch Law obliges SH to do ‘truth finding’ or objective research, we don’t see this is organised well enough by the different organsiations involved in this field. Our conclusion is that a legal perspective needs to be added: are there enough facts present to merit an investigation.

SH does work with the ‘Triage Model’, but if you look into it, you see meaningless categories and no expertise to actually judge them. The overall tendency is that the people working at SH are committed to ‘win the game’, no matter what. In our investigation we do a scan on who is doing the reporting.

We have compiled a spreadsheet of what is being used as the basis for the allegations. Concerns for ‘social isolation’, ‘cognitive well-being’, ‘somatic well-being’, ‘emotional well-being’. Not going to school for a few weeks is considered as damaging the ‘cognitive well-being’ of the child and thus framed as ‘child abuse’.

So these definitions used in this Triage model are so broad that any report, no matter how suggestive, automatically leads to a formal investigation. The fact that a child has not been to school for several weeks, is framed as ‘damage to mental mental health’ and later as child abuse.

If you look at how these organisations build their cases, these ‘investigations’ serve one purpose only: to get their way. The result is forced measures that are imposed on the family. In Dutch these are either called OTS (state surveillance) or UHP (placement in a foster home). 

From all the files we have studied, the fosters from almost all these organisations are disastrous for the children. In a case of a girl with Lyme the foster told her that she was faking the disease and that since his contract said he should force her to go the school, that was what he would do. The girl fell asleep within one hour in class out of pure misery.

Reversed proof

Oftentimes we help parents in these cases. From this experience and the 168 cases we have already investigated, we see that SH operates from a predisposed distrust. They are backed up in this attitude by the organizations that are supposed to provide an objective and unbiased check.

Parents are charged under Criminal Law (articles 300 – 304 in Dutch criminal law). What shocked us is that they are forced to cooperate towards their own conviction. In essence this means that parents are convicted upfront, unless they can proof they are innocent, which is hard to do, given the amount of stereotyping. (attorney Richard Korver, who was recently interviewed in Dutch to provide practical information to parents with children with Lyme, suggested that the legal prinpicple of Confidence be used more often. This means to start with the assumption of attitude that most people simply care for their children; unless proven otherwise.)

Often on the same day a child is released, we see SH apply for a fast track procedure in court. Without the needed for any further research, custody is taken away, based solely on the claim that there is ’eminent danger in the home situation’.

Different organizations are supposed to act as an impartial factor, but we basically see copying and pasting. SH copies the subjective tips and frames them into legal language. The Council for Child Protection (RvdK) copies these reports in their independent evaluation. Judges copy these conclusions in their verdicts. The other side is not even heard.

The Lyme cases

“We have now researched over fifty cases; the ones which we have fully assembled. These people came after the On Lyme Foundation and the Dutch Federation for Lyme Patients (NVLP) notified them to our research. We had no idea Lyme was such a problem because of the medical and political controversies around it. 

We have the strong impression that there are many more Lyme parents, who have become victim of SH but who do not yet dare to contact us. Some parents are so traumatized, it takes us ten phone calls to reassure them that their information is really save with us.

We do see some specific differences with other diseases, which have a less disputed status. Apparently national Lyme policies dictate that after a few weeks of treatment, the cause of the disease is suddenly a ‘mental issue’ (called MUS: Medically Unexplained Symptoms). Regardless of the fact that these children are still as ill as before. 

Again and again we hear stories of parents who tried everything to get medical help in the Netherlands, but who had to go abroad to find better help. The SH doctors overrule the decisions of these specialised physicians instead of cooperating with them. 

Suggestions to remedy the system

Some political parties have started to get interested now; however, what they propose is by far not enough to put a stop to this.

If our investigation of these 168 cases is any indication of the general tendency of how the whole chain of Youth Care acts, we are facing a very grave problem. Every day new cases come in and we cannot even keep up with it, since we want to research it meticulously.

In short our recommendations would be:

  • Awareness of the ones doing the reporting & how much impact it can have
  • A better check on the validity of the reports, before the start of a formal investigation
  • Create an independent supervisory system with a Disciplinary Board
  • Stop SH doctors from questioning or interfering with medical care without consulting with the parents and other specialists
  • Judges should have their own check instead of relying on the reports of this system
  • Stop the liberty of SH to order a fast track judgement, with no need for any investigation
  • Provide money for aftercare of the victims, but certainly not by SH itself
  • Have the Inspection perform an investigation into how SH operates

Looking at the stacks of paperwork on their table, BVIKZ concludes: “This is the actual child abuse”.  

A call to parents

The BVIKZ has to limit its investigation to the Netherlands and can hardly deal with the number of complaints now. Still, they encourage Dutch parents to file their complaints with them, so that together they can make a difference and stop the system from traumatising families like this. You can report them by email.

The On Lyme Foundation however would like to get an impression of the number of parents who faced similar situations in other countries. If you are not from the Netherlands, but you had similar experience because your children suffered from Lyme or its many misdiagnoses, you can mail us (also confidentially, of course) with a short description of what happened.

Note from the interviewer

This topic ties into what is recently discovered regarding the role of the World Health Organization (WHO) regarding the international diagnostic codes for Lyme disease. The WHO has not properly updated their ICD-codes to reflect the many conditions caused by Lyme borreliosis.

These outdated codes contribute to children being classified as having ‘non-specific’ illnesses and having treatments that are ‘experimental’. This allows for the allegations towards both parents and their ill children as well as their expert physicians.

Similar abuses can befall anyone, but is it particularly problematic for those who are already vulnerable. The outdated codes contribute to discrimination and marginalization by many institutions against this patient group.

https://on-lyme.org/en/sufferers/lyme-stories/item/250-research-concludes-not-one-single-accusation-of-child-abuse-is-valid

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**Comment**

This topic has hardly even been broached here in the U.S., but abuse allegations are happening regularly to families with Lyme/MSIDS.  This is why I support the Parental Rights Amendment so parents are not forced to comply with the arbitrary U.N. Rights of the Child which effectively imposes international law upon families which is NOT in the best interest of children.  For more:  https://madisonarealymesupportgroup.com/2017/04/20/why-we-need-the-parental-rights-amendment/

https://madisonarealymesupportgroup.com/2017/02/21/parental-rights-in-medical-settings/

https://madisonarealymesupportgroup.com/2017/05/18/first-peer-reviewed-study-of-vaccinated-vs-unvaccinated-children/  For families struggling with Lyme Disease, they are already fighting a system that doesn’t know how to cope with very ill children who often can’t keep up. Their little bodies are in a raging war of epic proportions. They are often bullied and mocked not only by peers but even by teachers and standard medical professionals who believe they are just being lazy. Infected, exhausted parents often don’t have the energy to fight the “mandatory vaccine” regimens being pushed upon them so just go along rather than weighing in their child’s current health issues. The entire system is stacked against them – forcing many to homeschool just to avoid the unbelievable pressure to conform.

Much has to change in Lyme land.

 

 

 

Understanding and Treating Depersonalization and Derealization

https://www.ruschellekhanna.com/blog/2017/8/4/understanding-and-treating-depersonalization-and-derealization

Ruschelle Khanna August 4, 2017

Imagine the feeling of being under water, trapped in a hole, being aware that you are speaking to your loved ones but unable to fully perceive or emotionally connect with them. Imagine living a life where you are fully aware that you used to have emotions but now feel blunted. Combine this with the feeling that you are somehow separate or distant from your experience and/or your own body.

I am a therapist who treats this experience. It’s name: Depersonalization-derealization disorder DPDR. I am also someone who once experienced this due to Lyme disease. I once described it as watching life through a straw. It is one of the more terrifying experiences I have personally ever had in my life.

WHAT DPDR LOOKS LIKE

An individual suffering from depersonalization may experience:

Detachment from emotions
Distorted body image
Difficulty recognizing their own reflection
Loss of sensation in parts of the body
Feeling unreal or like a spectator in their own lives
Sufferers of derealization may experience:

Feeling detached from their surroundings
Feeling that general life events are unreal
Perceiving objects as changing in shape, size or color
Feeling that people they know are strangers
Feeling that environments they know are unfamiliar(1)

WHAT THE RESEARCH SAYS ABOUT DPDR

There isn’t a ton of research exclusively done on DPDR. This is because mental health providers believe it is a symptom of another mental or physical illness such as anxiety or brain injury like epilepsy. There is no single known cause of DPDR, however it is generally understood that periods of severe stress or trauma as well as substance abuse can trigger DPDR.(2)

The National Association of Mental Health (NAMI) states:

Dissociative disorders usually develop as a way of dealing with trauma. Dissociative disorders most often form in children exposed to long-term physical, sexual or emotional abuse. Natural disasters and combat can also cause dissociative disorders.

AVAILABLE TREATMENT OPTIONS

Psychotherapy

The literature tells us that there basically is no known, consistent , effective treatment for DPDR. However, there have been some examples of things that have worked for some people. The best tools therapists have to work with and treat DPDR revolve around the possibility the scenario in which DPDR is brought on by severe anxiety and trauma. In this case, there has been some success with Trauma Focused Cognitive Behavioral Therapy (TF-CBT). This involves taking a look at and slowing down the thoughts, feelings and emotions we are having on a daily basis that could be keeping us in a place of elevated stress.

Another option is assisting those who have chronic DPDR to live with the experience, much like chronic pain. Treatment like this includes mindfulness based interventions including breathing, meditation, journaling, and body oriented therapies such as yoga therapy and creative therapies.

Medications

The literature on effective medications for DPDR is also pretty inconsistent. I am generally not a practitioner that advocates for the use of pharmaceuticals right away, however, if someone has struggled with DPDR, I find that testing medications can be an indication of which direction to go in all aspects of treatment.

A small study conducted on 14 clients showed a reduction in symptoms of DPDR in in 4 patients with the use of Naltrexone.(3) There has also been some evidence that Lamictol as an addition to therapy couldreduce symptoms of DPDR.(4) It may be helpful to find a therapist and psychiatrist who are willing to experiment with some combination of medications and therapies.

Finding answers to complex medical and mental health issues can be very frustrating, overwhelming and leave us feeling defeated. I propose we take a step back, find a way to find relief right now, in the moment, with DPDR or not, then put together a plan to continue searching for answers. I fully understand if this were something I lived with on a daily basis it would probably be impossible to just say I could not recover. I would want answers and I would keep trying. However, just like chronic pain, I would not want to deprive myself of the present moment just because it’s there.

If you are seeking answers to DPDR or other chronic mental pain, please contact a healthcare provider today. Some options:

In need of emergency support: National Suicide Prevention Hotline 1.800.273.8255

A little Relief from DPDR: YouTube Video “Tapping to Reduce Depersonalization” – https://www.youtube.com/watch?v=4ANHr_T7GpA

Ongoing Therapy in NYC or Online Counseling in New York State: My office 347.994.9301

References:

1. Theravive. https://www.theravive.com/therapedia/depersonalization-or-derealization-disorder-dsm–5-300.6(f48.1)

2. Simeon, D. Depersonalisation disorder: a contemporary overview. CNS Drugs. 2004;18(6):343-54. Cited at: https://www.ncbi.nlm.nih.gov/pubmed?term=15089102 Date Accessed: 04/01/2017

3. Simeon D, Knutelska M. An open trial of naltrexone in the treatment of depersonalization disorder. J Clin Psychopharmacol. 2005;25(3):267-70.

4. Sierra M, Baker D, Medford N, et al. Lamotrigine as an add-on treatment for depersonalization disorder: a retrospective study of 32 cases. Clin Neuropharmacol. 2006;29(5):253-8.

**Comment**

I want to encourage any of you out there in Lyme-land that are experiencing this.  In my experience this horrible psychological phenomenon typically goes away with proper treatment for Lyme/MSIDS. Think of it as a passing symptom you will eventually conquer.  (This is true and often possible for nearly every symptom in the book)

I also caution you in regards to psychiatric medications as they often have unintended consequences in people with a pathogen invasion such as Lyme and coinfections.  I’ve known of many patients whose symptoms worsened or they developed new ones after taking these meds.  If they are truly needed – take them!  Many have to take sleep aids, anti-anxiety meds, and meds for depression.  Please, always work closely with a medical professional trained in this area – particularly in regard to Lyme/MSIDS.  

I must also give a plug for support groups at this juncture.  They have been a life-line to many as you can unabashedly share what you are going through and receive true understanding and acceptance.  Sometimes just knowing you are not alone or crazy can do more than any medication!  From the support group can spawn many meaningful relationships that blossom.  Many in my group meet together for coffee and other things as they have found true companionship with folks on a similar journey.

And as always, be kind, gentle, and understanding to the sickie (you!).  Find simple things you enjoy and do them – even if it’s a nap!  Find beauty and dwell on it.  In essence, stop and smell the roses.  The most helpful advice to me came from a patient who had made it to the other side of health when I was at my worst.  He said, “Don’t get depressed about being depressed.”  That may seem strange but many of us struggle with this new darkness that seems to cloud our lives and we feel guilty about it.  Personally, I found this depression went hand in hand with how I felt physically.  The worse I felt physically, the worse I felt emotionally.

You can overcome this.

It will take time, but you can overcome!

For more on psychiatric Lyme & other helps:

For a great article for on-line therapy:  https://www.ruschellekhanna.com/onlinetherapy

https://madisonarealymesupportgroup.com/2015/10/18/psychiatric-lymemsids/

https://madisonarealymesupportgroup.com/2017/01/17/lymemsids-and-psychiatric-illness/

https://madisonarealymesupportgroup.com/2017/07/26/can-lyme-steal-your-mind/

https://madisonarealymesupportgroup.com/2015/09/16/bizarre-symptoms-msids/

https://madisonarealymesupportgroup.com/2017/01/11/sick-shaming-of-lymemsids-patients/

https://madisonarealymesupportgroup.com/2017/01/11/bug-that-hijacked-my-mind-part-1/

 

FREE: View “Under Our Skin” Best Primer on Lyme Disease

http://www.veoh.com/watch/v21055812yWtmpgB8  Approx. One hour forty five minutes.

If you have not watched the incredible documentary, “Under Our Skin,” please do so.  It reveals what patients and the doctors who dare to treat them go through.  It reveals the controversy up front and personally.  You will learn that Lyme is congenital, very probably a STD, and devastating.

The documentary covers so much ground but unfortunately doesn’t talk about the coinfections that typically come with Lyme (borrelia).

Can Lyme Steal Your Mind?

http://www.amenclinics.com/blog/can-lyme-steal-your-mind/?trk_msg=RV5QQ65CCVI4R57CV8PGKSB054&trk_contact=25HN640GN6IROQPP74BMQNTCPG&trk_sid=S1OO3ABQL8T30RUK21RS5028SG

Can Lyme Steal Your Mind?

can lyme steal your mindAdrianne was normal until the age of 16 when she went on a mountain vacation with her family. When they arrived at the cabin near Yosemite they were surrounded by 6 deer. It was a beautiful moment.

Ten days later Adrianna became agitated and started having auditory hallucinations. Her family brought her to a psychiatrist who diagnosed her as psychotic and prescribed medications, which didn’t help. The next 3 months were a torturous road of different doctors, multiple medications, and a cost near $100,000. Adrianna had become a shadow of her former self.

Desperate, her parents brought her to Amen Clinics for a scan. Her scan showed areas of unusually decreased activity. It caused our physician to look deeper at the potential causes of Adrianna’s symptoms, such as an infection or toxicity. It turned out she had Lyme Disease. After antibiotics, she got her life back.

Lyme Disease is on the Rise

The Lyme disease (LD) infection rate is increasing. It is the most commonly reported tick-borne illness in the United States.

Public health officials report between 30,000 and 36,000 cases of the disease a year. According to the Center for Disease Control, LD is now present in nearly half of U.S. counties in 43 states, a leap of nearly 45% since 1998.

What is Lyme Disease?

According to the CDC, “Lyme disease is caused by the bacterium Borrelia burgdorferi and is transmitted to humans through the bite of infected black legged ticks.” These ticks are mostly found in the Northeast and Mid-Atlantic states, the northern Midwest and the West Coast, and are often found on white-footed mice and white-tailed deer living in woods and high grass areas. Interestingly enough, Lyme disease was named after Lyme, Connecticut in 1975, the town where it was first identified.

Lyme disease can be effectively treated and cured

Doctors faced with treating the disease in early stages can successfully cure it with the use of antibiotics. Unfortunately, LD can be misdiagnosed because some doctors are not familiar with it. For those who feel they may have the disease, it is best to be diagnosed and treated by a Lyme Literate Medical Doctor that may likely to be a member of ILADS, the International Lyme and Associated Disease Society.

Symptoms may start with flu-like feelings such as fever, chills, sweats, possibly muscle aches, fatigue, nausea or joint pain. Physical symptoms often begin with what may look like a bull’s eye rash and in some cases even Bell’s Palsy (facial drooping). An even bigger problem, there may be no indication of a bite at all, which is a reason why Lyme disease may not be suspected. See some of our research on LD, click here.

Lyme disease is hard to detect

The disease has a way of manipulating the brain into thinking you’re not sick, as it slowly starts to work on neurological functions. LD is known as the great imitator because it can mimic various disorders such as Arthritis, Chronic Fatigue Syndrome, Fibromyalgia, ALS, ADHD, and Alzheimer’s disease, just to name a few.

Even in later stages of the illness, LD can be treated. However, some may have symptoms that can linger for months or even years following treatment. In some instances, people experience memory loss, depression, anxiety, trouble focusing, emotional tantrums, or personality changes. Many find themselves suffering, not understanding why they can’t seem to get better until they are finally properly diagnosed and get the treatment needed to become healthy.

How to protect yourself from Lyme disease

Protect yourself, children and pets against LD by avoiding areas where deer tick live, such as wooded bushy areas with long grass. You can also decrease your chances of getting LD by covering up, using insect repellant, clear brush or tick enticing areas, and remove ticks immediately with tweezers. The ticks are most active in May, June, and early July.

Parents may have concerns because children are affected with the disease more often than adults, but neurological symptoms of late-stage Lyme disease are found to be rare in children.

The first step in any healing process is an accurate diagnosis. If you or someone you know may be experiencing symptoms of Lyme disease, call us today at (888) 288-9834 or visit our website to schedule visit and find out more about how we can help.

 **Comment**
I am so thankful that the psychological/psychiatric issues of Lyme/MSIDS are being discussed much more of late.  Unfortunately, many doctors and therefore the public believe that this complex illness is nothing more than a little fatigue and joint pain.  While some may present that way, there are many more that present with neurological, gynecological, cardiac, muscular, vision, psychiatric, GI, and tendon issues (and more I’m forgetting).  Probably the least talked about is the psychiatric aspects – which is probably the reason these patients in the past were told they were delusional and making things up.  The symptoms are so unbelievable that I like to tell folks,
“You don’t get Lyme until you GET Lyme.”
Confession time:  Before I became infected I viewed my husband through a different lens.  My workaholic, type A, responsible, strong husband cried frequently, sat on the couch for hours playing “Candy Crush,” and limped.  He started drinking vodka secretively at night to get to sleep.  He was flushed all the time and slept most of the day and roamed the house like a zombie at night.  His speech was slurred.  He heard voices.  Once, he opened his mouth to speak and complete gibberish came out.  He developed rage and could not handle any sort of stress.
Then I started with symptoms.  My lens shifted as I finally understood as it was happening to me.
If your spouse, loved one, friend, or patient opens up and starts telling you bizarre symptoms, please don’t write them off.  It is my belief that many commit suicide after years of being marginalized.  They aren’t listened to, believed and validated.  They become isolated and deal with anxiety.  Some are so afraid, they take hours to work up the courage to go to the grocery store.
https://madisonarealymesupportgroup.com/2015/10/18/psychiatric-lymemsids/ An in-depth article on psychiatric symptoms.  Dr. Bransfield is an expert in this area.  Dr. Marke has done wonderful work as well.
https://madisonarealymesupportgroup.com/2017/01/17/lymemsids-and-psychiatric-illness/  Dr. Marke gives a lecture to psychiatrists which I highlight.
https://madisonarealymesupportgroup.com/2017/07/12/suicide-and-chronic-lyme-disease/  A therapist speaks who specializes in helping those with chronic Lyme/MSIDS.

Wisconsin – 117% Increase in Human Version of Mad Cow Disease

In a recent article by Dr. Mercola,  http://articles.mercola.com/sites/articles/archive/2017/07/25/chronic-wasting-disease.aspx?utm_source=dnl&utm_medium=email&utm_content=art3&utm_campaign=20170725Z1_UCM&et_cid=DM152228&et_rid=2092836335,  statistics reveal there is a a 117% increase in Wisconsin and an 85% increase in the U.S. of the human version of mad cow disease, Creutzfeldt-Jakob, which is a contagious neurological disease caused by eating beef contaminated with brain, spinal cord or other central nervous system tissue from infected cattle.

Now the Canadian Government is warning that chronic wasting disease (CWD), a similar disease found in the deer family may jump to humans as well.  Both mad cow disease and chronic wasting disease cause transmissible spongiform encephalopathies (TSE).

The deer family is also known to pick up hitchhiking ticks and carry them long distances.

This warning is due to a study which found CWD was transmitted to three out of five macaque monkeys infected with white tail deer meat.  There is also a systematic literature review showing CWD could also be transmitted to squirrel monkeys.

There is a potential for transmission to humans exposed to deer through diet, health products containing antler velvet, slaughter, velvet harvest, field dressing, preparing trophies and hunting lures.

The state of Wisconsin offers free CWD testing to hunters.

The Milwaukee Journal Sentinel states,

“Wisconsin Department of Natural Resources (DNR)] figures show that tens of thousands of hunters are killing deer in areas where CWD is prevalent and are not submitting them for testing. In 2016, in a CWD-prone area that the DNR describes as the southern farmland zone, 442 deer tested positive for disease out of 3,760 samples. More than 65,000 deer were killed in that zone and were not tested, according to DNR figures.”

Animals infected with CWD shed prions in saliva and urine and remain contagious for life and contaminate land and water.

Similar to Chronic Lyme Disease, CWD does not evoke a detectable immune response or inflammatory reaction. It is different; however, in that it is smaller than most viruses.  It also persists in the environment which is why animals raised in captivity are more likely to infect each other.  Avoid meat from those who force natural herbivores to eat animal parts (routine in concentrated feeding operations).

Researchers have also found an infectious protein (TDP-43) in Alzheimer’s patients is quite similar to prions in mad cow disease and CWD and was found in 200 of 340 autopsied brains of Alzheimer’s patients.  Patients with TDP-43 are 10 times more likely to have been cognitively impaired at death.

A 2005 study published in the journal Medical Hypotheses, stated:

“In the opinion of experts, ample justification exists for considering a similar pathogenesis for Alzheimer’s, Creutzfeldt-Jakob and the other spongiform encephalopathies such as Mad Cow disease. In fact, Creutzfeldt-Jakob and Alzheimer’s often coexist and at this point are thought to differ merely by time-dependent physical changes. A recent study links up to 13 percent of all ‘Alzheimer’s’ victims as really having Creutzfeldt-Jakob disease.”

**Please have your meat tested.  It’s free and it may save your life.**