Archive for the ‘Activism’ Category

Live From the CDC Lyme Protest

CDC-pic

For those of us who could not attend the Lyme protest in front of the CDC, you will enjoy these home made videos put up on Facebook and reposted here.  A big thank you to all those who made it and a big thanks to Sally for sending me these.

Rock on.  We will only move this mountain together.

https://www.facebook.com/kristinamb/videos/10213593617413297/  Kristina Petterson Bauer talking about Gestational Lyme.  She has four kids with Gestational Lyme.  Approx. 7 Min

https://www.facebook.com/donna.fanning.7/videos/1768449213200889/  Kathy Nodolf of Truth Cures “There is no cure for Lyme Disease.”  Kathy’s son died of Lyme Disease.  https://www.facebook.com/donna.fanning.7/videos/1768451373200673/  Kathy – Continuation https://www.facebook.com/donna.fanning.7/videos/1768455443200266/  Kathy explains how the testing & vaccines, were fraudulently created.  

https://www.facebook.com/allemonjello/videos/10215187919667948/  Alyson Lumenello has had Lyme for 28 years & went 24 years undiagnosed.  Alyson shows the shoes on the ground of those who have died from Lyme.  

https://www.wsbtv.com/news/local/group-rallies-in-front-of-cdc-over-definition-of-lyme-disease/744476074  (News Story here.  Approx 2.15 Min.)

By: Wendy Halloran

Updated: May 5, 2018 – 4:32 PM

ATLANTA – The Centers for Disease Control and Prevention experts say a new report shows diseases transmitted through ticks, mosquitoes and fleas have more than tripled. Deer tick bites cause Lyme disease.

Channel 2’s Wendy Halloran attended a protest outside of CDC headquarters where nearly on hundred people, many with the disease were vocal about the CDC’s handling of this public health threat.

The protesters call themselves the ‘Lyme Army’ and say they feel they’re not being taken seriously by the CDC.

“This organization is designed to protect the public, not to hinder and harm us and they’re harming us,” said Mirenda Campirano, who attended the rally from Brownsville, Texas.

She and others protested the CDC’s definition of chronic Lyme disease. They say the CDC’s definition of the disease is too hard to meet the requirements to get care.

“Doctors won’t see us, there is no treatment, no cure, no research when you’re too sick to work you lose your home, you get no disability, they’re not helping us at all,” Campirano said.

“If you don’t have the diagnosis in the paperwork then they don’t believe you,” said Kristina Bauer, who also hails from the Lone Star State.

Both women said they passed Lyme disease onto their children when they were pregnant.

“I want my son to know that I fought for him and I did the right thing so if something happens to me, my son will know I died fighting for him because at this point we’re dying from this disease, it’s killing us,“ Campirano said.

Bauer says she’s had success using naturopathic medicine.

“It’s very expensive, everything is out of pocket we’ve spent hundreds of thousands of dollars on treating four children and myself,” Bauer said.

Also at issue, the use of the term ‘chronic Lyme disease.’

“It’s a real denial of science,” Bauer said.

The CDC said it’s been used to describe illnesses in patients with Lyme disease but often those patients have no evidence of a current or past infection.

Because of the confusion, the CDC says experts do not support its use.

“When you go in to see your primary care physician they’ll say we don’t believe in “Chronic Lyme” it doesn’t exist and they don’t believe the patients that they’re sick,” said Enid Haller from Massachusetts.

Haller calls herself a ‘whistleblower.”

“The blood test doesn’t work for Lyme so they say you don’t have Lyme and you must go see a psychologist now because it’s in your head,” she said.

On the CDC’s website it says: “You may have heard that the blood test for Lyme disease is correctly positive only 65% of the time or less. This is misleading information. As with serologic tests for other infectious diseases, the accuracy of the test depends upon the stage of the disease.”.

When Halloran asked the CDC to respond to the criticisms. They sent the following statement:

Lyme disease is a serious illness that affects hundreds of thousands of people each year in the United States and tragically some experience long lasting debilitating consequences from their infection. As the nation’s health protection agency, CDC saves lives and protects people from health threats including Lyme disease by basing all public health decisions on the highest quality scientific data that is derived openly and objectively. The agency continues to raise awareness about the growing threat of Lyme and other tickborne diseases and just released this report on the problem:  https://www.cdc.gov/vitalsigns/vector-borne/

 

 

 

Fox News: Bartonella is the New Lyme Disease

 Approx. 4:45 min Fox News

April, 2018

Lyme Disease expert Dr. Tania Dempsey, Founder of Armonk Integrative Medicine talks about why Bartonella is the new Lyme Disease.

_______________

**Comment**

So thankful for this timely interview reminding us that Lyme is the rock star we all know by name but that there are many more wanna-be’s in the sidelines that are just as destructive as Lyme.  More are being discovered all the time.  https://madisonarealymesupportgroup.com/2017/07/01/one-tick-bite-could-put-you-at-risk-for-at-least-6-different-diseases/  (The current number is actually 16 diseases)

So far, mainstream medicine is only talking about an extremely limited version of Lyme – the kind that causes a little fatigue and joint pain.  First off, borrelia is pleomorphic and shape shifts necessitating numerous types of antimicrobials to deal with each stage:  https://madisonarealymesupportgroup.com/2016/02/13/lyme-disease-treatment/  Many experts are concerned that mainstream’s insistence on the mono-therapy of doxycycline is setting patients up for dementia/Alzheimer’s later on:  https://madisonarealymesupportgroup.com/2017/06/10/the-coming-pandemic-of-lyme-dementia/  (Please read my comment at the end of the article)

https://madisonarealymesupportgroup.com/2018/03/28/dementia-and-lyme-disease-with-dr-cameron/

https://madisonarealymesupportgroup.com/2018/03/25/a-brief-history-of-neuroborreliosis-research-dementia-an-inside-look-at-two-researchers/  Dr. Judith Miklossy that showed the presence of Borrelia burgdorferi in the brains of 13 consecutive Alzheimer’s patients in Switzerland……Pathologist Alan McDonnald sectioned and stained hundreds of samples and found some amazing things that I have listed below.
• Borrelia often forms biofilms within the human Alzheimer’s brain
• More than one species of Borrelia is involved
• The spirochetes either attract amyloid or helps produce it as the bacteria biofilms are found interspersed inside the amyloid plaques
• Nematode worms are sometimes seen in the diseased brain of both MS and Alzheimer’s patients
• The nematode gut stains positive by DNA probes for Borrelia
• The nematodes destroy brain tissue and deposits feces and eggs in the brain
• Borrelia biofilms are seen in fatal glioblastoma tumors
• Both Borrelia burgdorferi and Borrelia mayonii have been found within the testicle of one patient
• In severe dementia, amyloid can sometimes be detected in the blood using amyloid stains, this might be a blood test for Alzheimer’s?

Then there’s the open can of worms of coinfections as ticks are filled with numerous pathogens and can transmit them to humans:  https://madisonarealymesupportgroup.com/2016/01/16/babesia-treatment/

https://madisonarealymesupportgroup.com/2016/01/03/bartonella-treatment/

https://madisonarealymesupportgroup.com/2016/02/07/mycoplasma-treatment/

https://madisonarealymesupportgroup.com/2016/03/28/combating-viruses/  (Lyme/MSIDS patients often have viral involvement)

Nearly every patient I work with has Bartonella.  So far experts are denying ticks transmit it; however, I’ve read in numerous places that many believe they can and with the preponderance of patients with it – one has to consider the very real possibility.  Dr. Dempsey obviously believes this and also points out most cats carry it as well as many other insects making Bartonella a widely transmitted pathogen that’s hardly getting any media coverage.

More on Bartonella:

https://madisonarealymesupportgroup.com/2016/08/09/a-bartonella-story/

https://madisonarealymesupportgroup.com/2016/12/29/cardinal-state-bartonella/

https://madisonarealymesupportgroup.com/2018/02/07/finally-rt-pcr-detected-bartonella-henselae-dna-on-tissue-valve/

https://madisonarealymesupportgroup.com/2017/05/11/bartonella-henselae-in-children-with-congenital-heart-disease/

https://madisonarealymesupportgroup.com/2017/01/04/endocarditis-consider-bartonella/

https://madisonarealymesupportgroup.com/2018/03/15/risk-of-transmission-of-bartonella-via-blood-transfusion-chile/

https://madisonarealymesupportgroup.com/2016/02/08/new-bartonella-species/

https://madisonarealymesupportgroup.com/2018/04/03/encephalopathy-in-adult-with-cat-scratch-disease/

https://madisonarealymesupportgroup.com/2016/11/29/bartonella-seizures/

https://madisonarealymesupportgroup.com/2017/10/23/opthalmic-manifestations-of-bartonella-infection/

https://madisonarealymesupportgroup.com/2018/03/09/bartonella-outbreak-in-homeless/

https://madisonarealymesupportgroup.com/2018/04/07/pathogens-from-ticks-in-uk-cats/  Of 540 ticks, 19 (3.5%) contained DNA from one of the tick-borne pathogens evaluated. Pathogens detected were: A. phagocytophilum (n = 5; 0.9%), Bartonella spp. (n = 7; 1.3%) [including Bartonella henselae (n = 3; 0.6%) and Bartonella clarridgeiae (n = 1; 0.2%)]…..

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Midcoast Lyme Draws Crowd: HHS Working Group Slides Available From HHS V. Chair

Midcoast Lyme Draws Crowd: HHS Working Group Slides Available From HHS V. Chair

May 2018

Hundreds of people came out to hear about Lyme disease at the 4th Annual Midcoast Lyme Disease Support & Education Conference in Augusta, Maine, on April 28th, 2018. Over thirty experts spoke, including LDA President Pat Smith, Drs. Brian Fallon, Neil Spector, Lee Cowden and Kristen Honey, PhD, PMP, Vice Chair of the HHS Tick-Borne Disease Working Group. Dr. Honey is also a Lyme survivor. Her presentation titled Lyme Innovation, provided an overview of the TBD Working group– it’s background, responsibilities, including details of operation, reporting and timelines. CLICK HERE TO VIEW SLIDE PRESENTATION:  http://www.mldse.org/

Working Group meetings are open to the public, and minutes, reports, expenses and related documents are stored in a searchable database that is available to the public.

Vanila Singh
Bio – Kristen Honey, PhD, PMP (Vice-Chair, HHS Tick-Borne Disease Working Group)

Senior Policy Analyst, Office of Management and Budget,
Office of the Federal Chief Information Officer
Executive Office of the President;
Senior Research Scholar, Stanford University;
Member, Stanford University Lyme Disease Working Group

Dr. Honey is a Senior Policy Analyst in the White House Office of Management and Budget, Executive Office of the President, Washington D.C. She is also a Senior Research Scholar at Stanford University and member of the Stanford University Lyme Disease Working Group. As a broadly trained biologist and ecologist with a passion for real-world challenges, she gravitates to “wicked problems” like tick-borne diseases. She transforms scientific methods through open data, open science, open source, and open innovation (e.g., crowdsourcing, citizen science, prizes, challenges, and public-private collaborations). In 2015 to 2016, Dr. Honey co-founded Lyme Innovation and led data-driven innovations for invisible illness, mental health, and suicide prevention from the White House Office of Science and Technology Policy. She was a 2013–2015 Science and Technology Policy Fellow with the American Association for the Advancement of Science.

Dr. Honey earned her Ph.D. at Stanford University in the Emmett Interdisciplinary Program in the Environment and Resources, School of Earth Sciences, while simultaneously earning a Ph.D. minor in Civil and Environmental Engineering. She holds an M.A. in Environmental Studies from the University of California, Santa Cruz, and a B.A. in Human Biology with Honors from Stanford University. She is originally from Portland, Maine, and the small island town of Long Island in Casco Bay, Maine, and is a late-stage Lyme disease survivor.

In Her Own Words: “I am a late-stage Lyme disease survivor. My personal Lyme healing journey is one of grit, courage, and inspiring recovery.”

CLICK HERE FOR INFO/REGISTER FOR 4TH MEETING OF THE TBD WORKING GROUP – MAY 10, 2018 https://lymediseaseassociation.org/govt/govt-agencies-a-policy/hhs-tbd-working-group/1854-tick-borne-disease-working-group-4th-meeting-may-10-online-and-open-for-comment

CLICK HERE FOR INFO/REGISTRATION FOR 5TH MEETING OF THE TBD WORKING GROUP – MAY 15-16, 2018  https://www.hhs.gov/ash/advisory-committees/tickbornedisease/meetings/2018-05-15/index.html

 

 

 

 

 

 

 

Gender & Lyme: Is Tick-Borne Disease Different For Women?

https://globallymealliance.org/is-lyme-disease-different-for-women/

MAY 5, 2018

GENDER AND LYME: IS TICK-BORNE DISEASE DIFFERENT FOR WOMEN?

by Jennifer Crystal

Every Thursday evening, three girl friends come over to eat ice cream with me and watch Grey’s Anatomy. Yes, that show is still on! Despite the fact that it’s been running for 14 seasons, it often makes some commentary on current social issues. In one recent episode, the Chief of Surgery, Dr. Bailey, checks herself in to the hospital because she believes she is having a heart attack. But because her tests initially come back clean—she suffers from Obsessive Compulsive Disorder (OCD) and is under tremendous stress— she grows increasingly upset when her male doctors won’t listen to her, and her symptoms are written off as psychosomatic.

Does this scenario sound at all familiar?

Dr. Bailey’s experience is one that too many female patients go through—not just women with Lyme, but women with any illness. In her March 2013 New York Times article, “The Gender Gap in Pain”, award-winning health writer Laurie Edwards cites several studies that prove that women’s complaints of pain are much more likely to be dismissed than men’s. For Lyme patients, the complaints are not just about pain, but also about brain fog, word reiteration, forgetfulness, heart palpitations, insomnia, and that particularly nebulous one, fatigue. Because Lyme symptoms can seem idiopathic—meaning they arise spontaneously from unknown causes— and do sometimes encompass a psychological component, it’s easy for doctors to write them off as “all in someone’s head.”This especially occurs when faulty diagnostic tests can’t support what a patient knows to be true: that she is physically ill with an all too real pathogen. Women who appear in doctor’s offices wearing makeup or hairstyles that mask how awful they really feel are often told, “But you don’t look sick!”

If women are louder with their complaints, it’s only because they’re not being heard. A patient recently wrote to me to ask if Lyme is more common in women, because all of the other patients in the waiting room of a doctor she recently visited were female. Perhaps those females had legitimate tick-borne illnesses that had been dismissed longer than their male counterparts’, and they had finally made their way to a Lyme Literate Medical Doctor (LLMD). Whatever the reason, medical research demonstrates that more men than women test positive for Lyme disease. A study by Dr. John Aucott of Johns Hopkins University found that when testing for Lyme—with tests that are, admittedly, less than 60% accurate—women’s and men’s antibody responses were different, and more men than women tested positive.

Does this mean more men than women actually have Lyme disease? That’s hard to know, since the tests are so unreliable. What it does mean though is that men have a greater chance of having their symptoms confirmed by clinical tests, while women face a greater uphill battle in getting accurately diagnosed. Some have to wander around for years—it took me eight years, battling both male and female doctors—to be taken seriously. Even on Grey’s Anatomy, the fictional Dr. Bailey had to collapse on the hospital floor before her doctors would admit she might actually be suffering a heart attack, and whisked her in to surgery.

In addition to more men than women being diagnosed with Lyme disease, women face different challenges from the illness. My own symptoms always increase during menstruation, when the hormones progesterone and estrogen diminish. I have a higher chance of getting a migraine than a male, and my fatigue and sleep disturbances are worse during those few days. Doctors and patients alike agree that many, many women say the same thing. Women also have to contend with the possibility of yeast infections from antibiotic treatment for Lyme. Yeast overgrowth can be a problem for any gender, as antibiotics not countered by probiotics and a special diet can cause intestinal yeast overgrowth, but women also have the added potential of vaginal yeast infection.  And of course, women who contract Lyme while pregnant must work with their doctors to manage their own health while trying to avoid passing the Lyme bacterium to the fetus; women who already have Lyme and become pregnant have similar concerns.

Don’t forget that ticks do not discriminate. They will bite anyone of any gender. But  women who get tick-borne illness as a result do often face discrimination when it comes to being validated, diagnosed, and treated by physicians. Once accurately diagnosed, women face different complications than men.

For now, women can’t do much about the fact that menses can worsen our symptoms, or that we are more susceptible to yeast infections, or that Lyme can affect pregnancy. We can, however, speak up for ourselves and for our illnesses. We can push back against doctors who won’t listen, or go elsewhere to find better medical care. We can also fight against the psychosomatic write-offs of Lyme sufferers. And we can share our stories, bonding together in a movement to earn validation and respect for all patients.


jennifer crystalOpinions expressed by contributors are their own.

Jennifer Crystal is a writer and educator in Boston. She is working on a memoir about her journey with chronic tick-borne illness. Contact her at jennifercrystalwriter@gmail.com

 

What to do About the Tick Explosion

https://www.outdoorhub.com/news/2018/05/01/experts-warn-tick-explosion-coming-summer-prepare/

Experts Warn Of “Tick Explosion” Coming This Summer; Here’s How to Prepare Yourself

We just spent the last 5-6 months dealing with plummeting temperatures, ice storms, and practically enough snow to gag a polar bear. And now that the weather is finally turning, you bet your boots those of us in the Midwest are anxious to shed our winter coats and soak up the summer sun, but you may still want to keep your skin covered even as it warms up outside. Experts are warning people that a potential “tick explosion” is underway, and the bloodthirsty critters will be crawling around in abundance this summer.

“They’re up and looking for a host hoping something will walk by that they can latch onto,” Dr. Thomas Mather told WHIO.

And before you try and pull the old ‘I’m not going to the woods, so I’m safe’ routine, Kayla Socarras, a microbiology researcher at Drexler University College of Medicine, says not so fast.

Yes, ticks are highly concentrated in rural, woodland type areas, but Socarras says ticks can be found in practically every region of North America.

For this reason, we’ve come up with a few ways you can avoid these creepy creatures this summer:

  1. Wear Enough Clothing- Look we get it, you just spent 5 cold months enduring layers upon layers of heavy coats and itchy sweaters, so the last thing you want is to walk around dripping sweat in more layers of clothing. But long-sleeved shirts and pants really are the best way to avoid picking up any micro-sized hitch-hikers along the way.
    Tick Explosion
    pxhere
  2. Sprays and Repellents- Some days, it truly will be too damn hot to walk around the woods in long sleeves. This presents an opportunity to try out some insect repellents. Your best bet is sticking to the ones that contain DEET, picaridin or oil of lemon eucalyptus – ticks despise these the most, and likely won’t want to stick around for a free ride.
    Tick Explosion
    pxhere
  3. Check Yourself for Ticks… Then Check Again- After any and all outings outdoors, Socarras recommends performing a thorough inspection of your skin for tiny black spots. “Ticks are so small, people sometimes confuse them for a freckle,” she stated. A quick shower is another good idea, as it allows to inspect your more… hidden regions. “They like moist areas, like the groin and under your arms,” Socarras warns.
    Tick Explosion
    pxhere
  4. Don’t Assume You’re Safe in Your Own Yard- Ticks can be found anywhere, and that includes your very own backyard. So don’t get caught with your guard down this summer just because you aren’t making a trip to the woods. Ticks will happily call a city park or a fruit tree in your yard ‘home.’ “In general, you can be bitten by a tick in the most urban places. It’s a common misconception that you can’t get bitten in the city,” Socarras says.

_________________

**Comment**

There’s new stuff in the works, but this link still has some of the best ideas for tick repellents and removal:  https://madisonarealymesupportgroup.com/2017/05/11/tick-prevention-and-removal-2017/