Archive for the ‘Activism’ Category

Interview With Kris Newby, Author of “Bitten –

Episode #98:  ‘Bitten the Secret History of Lyme Disease Biological Weapons’ With Kris Newby

About My Guest

My guest for this episode is Kris Newby. Kris Newby is an award-winning science writer at Stanford University and the senior producer of the Lyme disease documentary, Under Our Skin, which premiered at the Tribeca Film Festival and was a 2010 Oscar semifinalist. She has two degrees in engineering, a Bachelor’s degree from the University of Utah and a Master’s degree from Stanford University. Previously, she was a technology writer for Apple and other Silicon Valley companies. She lives in Palo Alto, CA.

Key Takeaways

  • How did it feel to be a senior producer on “Under Our Skin”?
  • What did Willy Burgdorfer share in the early interviews for the film?
  • How did Willy discover the spirochete that other scientists had missed?
  • What were the goals of the biological weapons program?
  • Is Lyme disease the result of the bioweapons program or a natural occurrence?
  • What organisms were part of the cocktail that Willy was experimenting with?
  • What is the “Swiss Agent” and the role it may play in the Lyme disease epidemic?
  • What is the “Anthrax Hotel” and the “Eight Ball”? What happened to those that were part of the experiments at the “Eight Ball”?
  • What role do viruses and parasites play in Lyme disease?
  • Was Willy a good guy or a bad guy?
  • Did Willy’s own death from Parkinson’s disease potentially result from his own experiments?

Connect With My Guest

http://KrisNewby.com

Interview Date

May 22, 2019

Disclaimer

The content of this show is for informational purposes only and is not intended to diagnose, treat, or cure any illness or medical condition. Nothing in today’s discussion is meant to serve as medical advice or as information to facilitate self-treatment. As always, please discuss any potential health-related decisions with your own personal medical authority.

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Book Review:  https://lymediseaseassociation.org/about-lyme/controversy/conflict-report-sp-560/bitten-book-review/  May 21, 2019

The debate over the prevalence of Lyme disease and whether it exists in a chronic form has raged for decades. Kris Newby’s well researched book provides documented evidence that the suspicions of disease sufferers, their advocates, and treating physicians deserve investigation. The properties of the pathogen itself and its ally, the tick, appear to be part of our nation’s biowarfare studies.

Swiss American scientist Willy Burgdorfer is acclaimed for identifying the spirochetal bacteria which causes Lyme disease. Indeed, the pathogen bears his name, Borrelia burgdorferi. Yet as the author discloses through filmed interviews and archival reviews, there were other aspects to Willy’s research. Employed by the US government and headquartered at Rocky Mountain Laboratories, Burgdorfer was enmeshed in biological warfare projects.  Ms. Newby discusses his work in Switzerland for the American government which led to the identification of a new strain of Ricketttsia, a pathogen if crossed with Borrelia might well complicate treatment and thus be a candidate for biowarfare.  Interviews by Ms. Newby with American researchers on the topic of the Rickettsia, dubbed the Swiss agent by Dr. Burgdorfer, did not shed any light on the mystery pathogen whose existence seems to be buried in the past.

Ms. Newby’s discovery of tick drops and the experimental release of ticks document ongoing biowarfare research and questions the consequences if studies go awry. The prevalence of new diseases and the expansion of tick territories are examined in the context of now revealed government studies.

Ultimately, whatever mix of causes is responsible for the Lyme and other tick-borne diseases epidemic in the US, the solutions, as strongly stated by Kris Newby, lie with better science, advanced research and proper funding.

Click here for YouTube video of Under Our Skin, Director, Andy Abrams and Kris Newby discussing her new book.

Click here to purchase Bitten on amazon.com

Click here for other purchasing options of Bitten on HarperCollins.com

Ironically, Wisconsin’s most experienced Lyme/MSIDS doctor told me he treated patients in the 70’s before it had a name.  He called it a Rickettsial-type disease.  He might have been closer to the mark than he knew.

 

Tick Prevention, Lyme Disease Awareness Are Goals of New Bills – Wisconsin Has Fallen Behind

https://www.channel3000.com/news/tick-prevention-lyme-disease-awareness-are-goals-of-new-bills-wisconsin-has-fallen-behind-1/1082343575  News Story Here

Posted: May 30, 2019 07:48 PM CDT

Tick prevention, Lyme disease awareness are goals of new bills: 'Wisconsin has fallen behind'

There’s a new push to educate people in Wisconsin about ticks and the illnesses they can carry. A group of state lawmakers introduced a package of bills aimed to spread awareness about Lyme disease.

For More:  https://madisonarealymesupportgroup.com/2019/05/30/newscasts-on-proposed-lyme-bills-tonight-at-6-9-pm-wisconsin/  Bills are included in this link as well as a letter of concerns sent to all sponsors of the bill.

Please contact your representatives with feedback on the bills after reading the letter of concerns.

Letter to Wisconsin Lyme Bill Sponsors

 

Newscasts on Proposed Lyme Bills Tonight at 6 & 9 PM – Wisconsin

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Tonight, May 30, 2019 there will be news coverage of the 5 proposed Lyme bills in Wisconsin.

 

  • The 6:00pm newscast is Channel 3 (3000). For me this is actually channel 603. Make sure and find out what channel it is for you in your location.

 

  • The 9:00pm newscast is on Fox47, which may be an abbreviated story.  For me this is channel 617. Also check to determine the station in your location.
I will post the link to this story as soon as it’s available.

I’m including the letter with concerns I sent to each of the sponsors of the proposed bills Letter to Wisconsin Lyme Bill Sponsors

I encourage all Wisconsin residents to let let your voices be heard about this.

For the actual proposed bills:  https://madisonarealymesupportgroup.com/wp-content/uploads/2019/05/time-to-bite-back-against-lyme-disease-05-23-19.pdf

For the Fox 11 news story:   https://madisonarealymesupportgroup.com/2019/05/29/lawmakers-create-bills-to-bite-back-against-lyme-disease-wisconsin/

The bill of particular concern in #5 in that it:  “Establishes a sixteen-member Tick-Borne Disease Study Committee to create a report for the legislature on consensus-based recommendations for policy changes on awareness, prevention, surveillance, diagnosis, reporting, and treatment of Lyme Disease.”

As you can read from my letter above, nothing about Lyme/MSIDS is agreed upon except the fact early detection and treatment is imperative.  If this 16 member committee is only filled with CDC/IDSA believers, patients and the doctors who dare to treat them are doomed as it will be business as usual. Chronically infected patients need representation by qualified ILADS trained practitioners who understand the complexity of diagnosis, testing, and treatment.

 

Why Lyme Disease Is Causing a Mental Health Crisis

https://globallymealliance.org/lyme-disease-causing-mental-health-crisis-heres/?

By Kerry Heckman

Note: This post discusses self-harm and suicide. If you feel suicidal or a danger to yourself or others, PLEASE call the National Suicide Prevention Lifeline: 1-800-273 TALK (8255),or text “HOME” to 741741 to reach the Crisis Text Line. You can also call 911, or go to your nearest hospital emergency room. YOU ARE NOT IN THIS FIGHT ALONE.

May is Lyme Disease Awareness Month and Mental Health Awareness month. These matters are inextricably linked because there is now a mental health crisis among those with tick-borne diseases. As Dr. Robert C. Bransfield writes,

“Lyme and other tick-borne diseases contributes to causing a significant number of previously unexplained suicides and is associated with immune-mediated and metabolic changes resulting in psychiatric and other symptoms.”[i]

If you’ve been in this circle for even a short while, you most likely have heard about a fellow Lyme warrior who died by suicide. You may have even known the person or have once called them your friend. Sadly, it happens far too often.

Statistically, those with any chronic illness are more likely to die by their own hand than those the general population, but for those with Lyme and other tick-borne diseases the risk is even greater. The reason for this is complex, but here are three  important factors to consider:

1. Living with Lyme disease is hard.

The fatigue, the aching joints and muscles, the headaches, the brain fog and other symptoms of Lyme disease are constant and debilitating. Moreover, most Lyme patients have insomnia and rarely get a break from the barrage of symptoms. This means the patient also has to cope with a great deal of uncertainty (anxiety) over his or her health— a very heavy burden.

2. Lyme disease treatment is notoriously challenging for a variety of reasons, all of which it helps the Lyme patient to be aware of.

First, because Lyme and other tick-borne diseases are not accepted by the mainstream medical community, the psychiatric ramifications of such illnesses generally go unconsidered by most doctors. Second, because treatment is often long term, painful, and the patient may get worse before he or she getsbetter. Third, Lyme disease treatment is expensive and rarely covered by health insurance, even though patients are often unable to work while undergoing the process.

3. Lyme disease bacteria can infect the brain.

Neurological Lyme disease affects thinking and behavior. Thoughts can become distorted and hopeless and often rise to traumatic levels. It’s said that “depression lies,” because people’s nervous systems send them messages that they are worthless or a burden to others in their life. Lyme disease lies, too, since it fosters depression and its woes.

What’s important to remember is that you are not alone in this fight. There are millions of people living with Lyme and also people in remission who stay connected to the Lyme community in the hope of helping others.

Naturally, as a therapist, I encourage everyone with Lyme disease to consider therapy. Ideally, you should make sureyour therapist understands chronic illnesses and medical trauma. However, simply having an empathetic ear to listen to your story can be  transformative. Often our friends and family don’t understand how difficult it is to live with this disease, so a therapist can be a necessary support in this fight.

But what if regular therapy isn’t enough. What if you are in crisis right now and need help?

How To Tell if You Are in a Mental Health Crisis:

1. Self-harming behaviors.

Self-harming behaviors have many manifestations. They may look like self-injury, such as cutting or burning or they may manifest as the patient purposely not taking important medis, or taking too much of something that can be harmful.

2. Suicidal thoughts.

Thoughts about suicide are a sign of something very serious taking place and require immediate attention. Take note if your thoughts are increasing in frequency and intensity—If the trend is on the rise this can determine the level of intervention you  need. Feelings of suicide should never be ignored.

3. Suicidal plans or behaviors.

Having a plan to complete suicide or engaging in behaviors, such as saying goodbye to loved ones or giving away possessions is a medical EMERGENCY. Call 911 or go straight to your nearest emergency room and tell them what is happening.

4. Your intuition.

Do you feel like you need immediate mental health care? Therapists, outpatient, and inpatient programs are all more accessible than ever before. With tele-health becoming more popular, you may even be able to see a psychiatrist or therapist through a secure video chat platform.

What To Do in a Mental Health Crisis?

1. Call 911 or go directly to the nearest emergency room.

People who survived suicide attempts report that the time between considering suicide and making an attempt is only about an hour. That’s a very small window. Seek help at once.

Many of us who have Lyme also have negative perceptions of emergency rooms, but during a mental health crisis the focus is not on treating the Lyme disease. Doctors need to observe you and assess your suicidality. Most importantly is that you are in safe and contained place where you can get help.

2. Call or text a suicide hotline.

Suicide hotlines, such as the National Suicide Prevention Lifeline are free, anonymous, and available 24/7. These hotlines can also help you find information about local suicide crisis resources, such as voluntary inpatient and outpatient programs.

National Suicide Prevention Lifeline: 1-800-273-TALK(8255)

Crisis Text Line: Text “HOME” to 741741

3. Reach out to a trusted loved one.

Opening up about mental health can make one feel ill at ease and vulnerable, but talking to such a loved one can help you immediately. Ask this this person to help you get the care you need.

How To  Prepare Yourself for a Mental Health Emergency

  1. Remove firearms from your home and lock up lethal medications
  2. Make a contact list of crisis phone numbers, local resources, and trusted friends or family members. It’s a good idea to let these people know in advance that they are on this list, so they can be prepared to rise to the occasion if necessary.
  3. Print this article out, fold it up and keep it with you always. You never know when you may need to consult it.

Always keep in mind, you don’t have to go through Lyme disease all alone. If no one sympathetic is near, search the internet in your area for Lyme or chronic illness support groups. If you can’t find such a community where you live, please dig deeper. There are thousands of people creating safe spaces and raising Lyme-suicide awareness online.

You deserve to heal. You deserve a life free of Lyme and its many debilitating symptoms. You deserve to be seen and heard. You deserve to be treated with dignity and respect in your illness. The world needs you and you need the world.


[i]Bransfield RC. Suicide and Lyme and associated diseases.Neuropsychiatric Disease and Treatment,2017; 13:1575-1587.


kerry heckmanOpinions expressed by contributors are their own.

Kerry J. Heckman is a licensed therapist and author of the healing and wellness blog Words Heal. She was diagnosed with chronic Lyme disease in 2016

For a great article for on-line therapy:

 

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For more:  https://madisonarealymesupportgroup.com/2019/05/27/have-you-been-told-its-all-in-your-head-the-new-biology-of-mental-illness/

https://madisonarealymesupportgroup.com/2019/05/27/uk-woman-isolated-pumped-full-of-anti-psychotics-told-its-all-in-her-head-until-finally-diagnosed-with-lyme/

https://madisonarealymesupportgroup.com/2018/07/05/suicide-poses-a-complicated-risk-in-those-with-infectious-diseases/

https://madisonarealymesupportgroup.com/2018/06/14/depression-the-radical-theory-linking-it-to-inflammation/  Accepting that some cases of depression result from infections and other inflammation-causing disorders of the body could lead to much-needed new treatments, he argues.

https://madisonarealymesupportgroup.com/2018/01/18/depression-not-caused-by-chemical-imbalance/

https://madisonarealymesupportgroup.com/2018/03/09/aggressiveness-violence-homicidality-homicide-lyme-disease/

https://madisonarealymesupportgroup.com/2018/04/12/psychiatric-drugs-create-violence-suicide-school-shootings-other-acts-of-senseless-violence/

https://madisonarealymesupportgroup.com/2019/02/16/lyme-is-all-in-your-head-a-wake-up-call-to-mental-health-professionals/

https://madisonarealymesupportgroup.com/2017/08/07/understanding-and-treating-depersonalization-and-derealization/

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/

 

 

 

Man Shares His Story About Dealing With Lyme Disease

https://www.wsaz.com/content/news/Man-shares-his-story-about-dealing-with-Lyme-Disease-510295481.html  News Story in Link

Man shares his story about dealing with Lyme disease

Man makes it his mission to raise awareness about Lyme Disease
By Taylor Eaton

ELLIOTT COUNTY, Ky. (WSAZ) — In 2006, Patrick White says his life really started changing.

May is Lyme Disease Awareness Month, and a man from Kentucky shares his experience with the disease.

“The first sign that something wasn’t right was 2006,” said White. “I remember the date because it was my wife’s birthday. I slept all day on her birthday, which was totally odd. That was the first sign. There were other things. Bone pain, odd bone pain. I’m 44, and this started when I was in my early 30s. It was odd to have that pain. I always worked in construction, was in the Marine Corps but never experienced this type of pain.”

White developed a lot of different health issues.

“The mood swings. Rage was the worst part of it,” White said. “I’d get so angry over some of the smallest things. From there, it started to kind of spiral. Depression started. I got really depressed.”

He was left in the dark for years though, not knowing what was causing all of his problems. It was one misdiagnosis after another for him because his symptoms mimicked a lot of other illnesses.

“I had no idea what was going on,” White said. “I just knew I was in so much pain. It got to the point when I would walk, it felt like my bones were like glass and they were going to snap and break. It was through my whole body.”

It wasn’t until around 2014 when one of his doctors brought up the possibility of Lyme disease. White was tested and it came back positive.

“I didn’t know anything about Lyme at that time,” White said. “It wasn’t even a thought in our head that could happen.”

Lyme disease is a bacterial infection that is transmitted through the bite of an infected deer tick. Typically, a rash will develop around the site of the bite, called a bulls-eye rash. Aside from that symptom, there are no other symptoms specific to Lyme disease.

However, White says he didn’t develop a rash.

Other common symptoms include fever, chills, fatigue, and body aches.

“I never saw the bulls-eye rash,” White said. “I can’t remember getting flu-like symptoms. I can’t ever remember getting sick like that.”

Many times, Lyme disease isn’t diagnosed immediately because people don’t realize they have been bitten. If it’s not diagnosed immediately, the bacteria can spread throughout the body and cause a number of different health issues.

However, many of those symptoms can mimic other diseases and infections, which is why Lyme disease can be difficult to diagnose.

White says after his diagnosis, he finally felt he had some answers. He still doesn’t know exactly when he was bitten.

Typically, Lyme disease is treated with antibiotics if it is caught early.

However, White received a late diagnosis and is still feeling the effects of it.

“I still have seizures,” White said. “I still have memory loss. But, I am able to get out walking now and can help around the house.”

He is undergoing a treatment now called immunotherapy. He credits the treatment for giving him a big part of his life back.

“Where I am at now, I am extremely happy,” White said. “It feels good. I feel like I have my life back.”

White has now turned to art and support groups to help him on his journey forward. He is making it his mission to raise awareness about Lyme disease.

“Since I have started getting better, I really push this awareness because I don’t want to see anyone go through this,” White said. “I am petrified of ticks now. I am constantly on the lookout when we go in the woods. I know that little thing that is the size of a poppy seed will change and destroy your life. You have to be diligent with your body checks. You have to check yourself constantly.”

May is Lyme Disease Awareness Month.