Archive for the ‘Lyme’ Category

Pro Figure Skater On Managing Lyme As An Athlete

https://www.globallymealliance.org/blog/a-professional-figure-skater-discusses-managing-lyme-disease-as-an-athlete

It’s not easy living with Lyme disease– especially for athletes who rely on the strength of their bodies to excel in sports.

Imagine this: you’re running late. You hop in your car, and the gas is on empty. There is no time to stop and fill up. So, you spend your entire trip wondering if you’ll have enough fuel to get where you need to go…

Life as an athlete with Lyme disease is a bit like this. We have to be really careful with our fuel– and sometimes we unexpectedly have a lot less than expected. When flu-like lethargy hits, we have to learn to manage.  Sometimes nerves don’t fire that should– which can make everything (especially jumping as a figure skater) very tricky. We have to be mindful of Lyme triggers, our diet, and making sure to plan as best we can to maximize our training without causing a Lyme flareup.

Screen Shot 2023-03-07 at 3.28.59 PMI’m Carolyn, I’m 39-years-old, and I have chronic Lyme disease.  I’m an adult figure skater, aerialist, photographer, actor, wife, and mom.

The first step for me when I was diagnosed, was to find a coach who understood: someone who understood that I was not being lazy when I couldn’t push through on days where I was in a full blown mast cell or Lyme flareup.  Who understood that skating in an older rink wasn’t an option because of mold.

If you’re reading this, and you already have Lyme, you don’t need me to describe the searing sensation of broken glass in your joints, like someone using your connective tissues to put out their lit cigarettes. Adding insult to injury is the incredible amount of inflammation that comes with Lyme– which means shifts in balance, swelling, and pain. It means some days my skates feel three sizes too small, and my balance point is off.

But skating in a Lyme flareup doesn’t just feel like I’m skating in someone else’s missized skates– it feels like I’m skating in someone else’s body.

Why not just quit? Because I am stubborn, and skating is part of me.

Screen Shot 2023-03-07 at 3.28.26 PMI’ve started skating outdoors as much as possible, because older rinks aren’t an option. The mold spores that others might not notice are detrimental for a Lyme patient. I have ice skates and also in-line figure skates, so that I can be outdoors in the fresh air as much as possible.

I’ve incorporated stretching, flexibility work, and off ice work, for the days that I don’t have enough fuel in the tank to skate. On high inflammation days, I focus on edgework over spins and jumps.

Most importantly, I practice self-love and compassion. As a teenager, my goal was to go to the Olympics, and every step away from that goal was a source of shame and self-punishment. Now, I’m grateful to just be able to skate at all. Instead of pounding my body trying to land double and triple jumps, I focus on big beautiful single jumps. I’m grateful to be able to do even that.

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The above material is provided for information purposes only. The material (a) is not nor should be considered, or used as a substitute for, medical advice, diagnosis, or treatment, nor (b) does it necessarily represent endorsement by or an official position of Global Lyme Alliance, Inc. or any of its directors, officers, advisors or volunteers. Advice on the testing, treatment or care of an individual patient should be obtained through consultation with a physician who has examined that patient or is familiar with that patient’s medical history.
GLA Contributor

Carolyn Budreski 

GLA Contributor

*Opinions expressed by contributors are their own. Carolyn is an adult figure skater with late stage Lyme disease. She’s used her skating & coaching in the film industry, where she works as a stand-in and an actor. She also runs a photography business, focusing on weddings, newborns, and content creation. During the pandemic, she was featured on Sports Illustrated’s website advocating for cold water therapy as a treatment for Lyme disease. She’s also an aerialist, polar dipper, wife, and mom.

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I’m Not Crazy, I’m Sick: New Lyme Film

http://imnotcrazyimsick.com/

THE FILM

Lyme Disease is wreaking havoc on millions of lives.

From the award-winning director Elle Brooks-Tao and Oscar-winning cinematographer of Free Solo, Clair Popkin, I’m Not Crazy, I’m Sick is the story of how three families and a former WNBA MVP’s fight for survival against Lyme.

Coming Soon.

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TV Specials on Lyme

LDN For Lyme

https://www.treatlyme.net/guide/low-dose-naltexone-lyme-disease

Updated: 3/21/23

About Low-Dose Naltrexone for Lyme

Low-dose naltrexone (LDN) is very useful in Lyme disease. This low-cost medicine can

  • improve nerve, muscle, and inflammation pain,
  • decrease autoimmune illness triggered by Lyme,
  • improve mast cell activation symptoms,
  • lower cytokine inflammation, and
  • improve immune system function by increasing TRegs to balance Th1 and Th2.

In this article, I review the science and method for how LDN works. I describe how to use it in Lyme disease, and I review potential side effects.  (See link for article & video)

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For more:

Dr. Steven Phillips on Chronic Inflammation

http://  Approx. 1 Hour

March 25, 2023

Dr. Steven Phillips Discusses Chronic Inflammation

Dr. Steven Phillips discusses chronic inflammation and its management, especially in the context of long COVID and “vaccine” injuries.

Dr. Steven Phillips’ bio: Steven Phillips, MD is a well published, Yale-trained physician, researcher, and bestselling author, whose focus of medical practice and research is that chronic and autoimmune illness can be caused by underlying infections.

Dr. Phillips’ substack: https://zerospin.substack.com/

Amazon.com: Chronic: The Hidden Cause of the Autoimmune Pandemic and How to Get Healthy Again (Audible Audio Edition): Steven Phillips MD, Dana Parish, Teri Schnaubelt, Thomas Allen, Brilliance Audio: Books https://www.amazon.com/Chronic-Hidden…

http://

Dr. Steven Phillips Discusses Chronic Diseases (Lyme & COVID)

Steven Phillips, M.D. is a renowned Yale-trained physician, author, international lecturer, and media go-to expert. Well-published in the medical literature, he has treated over 20,000 patients with complex, chronic illness from nearly 20 countries. Phillips experienced firsthand the nightmare of an undiagnosed, serious infection after nearly dying from his own “mystery illness,” and having to save his own life when 25 doctors could not.

Here are the questions we will ask Dr. Phillips:

  • What is Lyme+?
  • What is your own story of Lyme?
  • You say that many infections are categorized as Lyme, how do we separate them
  • Are there good tests for Lyme+?
  • Is it treatable?
  • Is there hope for hundreds of thousands of patients of Lyme+?
  • How can an infection cause autoimmune disorders?
  • What is the role of Th1 and Th2 system in this context?
  • Why does it become chronic?
  • Do I have a vector borne infection?
  • We are seeing the same issue with COVID – Is COVID becoming similarly mismanaged?
  • How should patients approach their chronic Lyme+?
  • Is there hope?
  • How do people get help from you?
  • Do you train other doctors with your protocol?
  • Do they reach out to you?
  • On page 63 you write: Despite my repeatedly negative brucellosis testing at U.S. labs, I shared with my Lyme doctor my ideas for an aggressive combination antibiotic treatment against this infection. Nothing else was working, so my doctor agreed to the plan, and by the second month of treatment I started to improve.
  • Tell us about Jarish-Hexheimer reaction
  • Before we go, tell us how can people find you?

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Hospital payments include:

  • A “free” required PCR test in the Emergency Room or upon admission for every patient, with government-paid fee to hospital.  This test, like Lyme testing, is an utter farce.
  • Added bonus payment for each positive COVID-19 diagnosis, based on a worthless test.
  • Another bonus for a COVID-19 admission to the hospital, based on a worthless test.
  • A 20% “boost” bonus payment from Medicare on the entire hospital bill for use of remdesivir instead of medicines such as Ivermectin, all based on a worthless test.
  • Another and larger bonus payment to the hospital if a COVID-19 patient is mechanically ventilated, all based on a worthless test.
  • More money to the hospital if cause of death is listed as COVID-19, even if patient did not die directly of COVID-19, which is all based on a worthless test.
  • A COVID-19 diagnosis also provides extra payments to coroners, all based on a worthless test.

CMS implemented “value-based” payment programs that track data such as how many workers at a healthcare facility receive a COVID-19 “vaccine.Now we see why many hospitals implemented COVID-19 vaccine mandates. They are paid more.  Source

For those paying attention, COVID is a replay of Lyme and many of the same tactics have been deployed.

More Window Dressing: Blumenthal Announces New Federal Funding For Tick Research

https://www.wshu.org/connecticut-news/2023-03-24/blumenthal-announces-new-federal-funding-for-tick-research

Blumenthal announces new federal funding for tick research

Blumenthal

Molly Ingram/WSHU  U.S. Senator Richard Blumenthal holds a tick, swollen from drinking blood.

U.S. Senator Richard Blumenthal (D-CT) has announced millions of dollars in funding for research into tick-borne diseases.

Diseases caused by ticks have more than doubled in the last ten years across the Northeast.

The Connecticut Agricultural Experiment Station, located in New Haven, will receive $200,000.

Blumenthal said the money will fund vital research at the nationally recognized facility.

(See link for article)

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SUMMARY:

  • Money to New Haven will be used to hire staff for testing ticks
  • $26 Million will go to the corrupt CDC to study Lyme disease
  • $7 Million will go to the complicit DOD‘s Tick-borne Disease Research Program

In the words of Willy Burgdorfer, the “discoverer” of Lyme:

“The controversy in Lyme Disease research is a shameful affair.  I say that because the whole thing is politically tainted.  Money goes to people that have for the past 30 years produced the same thing.  Nothing.” ~ Dr. Willy Burgdorferi

Money lining the pockets of the same people in corrupt agencies will come to nothing.
Mark my words.

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