Archive for the ‘Lyme’ Category

Morgellons NOT Associated With Fungus

  Approx. 1 Hour 15 Min.

Morgellons NOT Associated With Fungus

May 17, 2020

Interview with microbiologist Marianne Middleveen.

For more:  https://madisonarealymesupportgroup.com/2020/02/24/classification-staging-of-morgellons-disease-lessons-from-syphilis/

What a Difference a Year Makes

https://globallymealliance.org/what-a-difference-a-year-makes/

by Jennifer Crystal

When I was little, my grandmother used to sing the Dinah Washington song, “What a difference a day makes, twenty-four little hours…” Later, memories of her singing those lyrics carried me through some of my toughest days of tick-borne illness. They remind me even today that I just need to get through the next hour, the next minute, because things could be better tomorrow.

Sometimes they were better. A Herxheimer reaction might settle, a solid night’s sleep might lower my emotional temperature, or my actual fever might go down. And sometimes, the tomorrows weren’t much better. When I first started intravenous antibiotics, I felt horrible for six weeks before noticing any improvement. Often the next day was worse than the last. I learned that while I could coach myself to survive each minute or second, I had to wait longer to really live again and even longer to thrive, which was my desire. For that type of progress, it was better to chart my improvement over months, if not years. Check here for an overview of some of my long-term recovery strategies.

Birthdays are always a nice time to reflect on the year passed, and this has been especially true since I’ve been sick with chronic Lyme, two tick-borne co-infections—babesia, ehrlichia—and Epstein-Barr virus. A lot can happen in a year, both good and bad. We never know what joys or sorrows await us. Lyme patients don’t know how they’ll respond to treatment or how long it will take them to feel better. For many, though, they can see real progress—with dips and valleys—over a year or more.

I was thinking back to my 29th birthday recently, when I was in the midst of a relapse. Sick and exhausted, I wondered if I could endure further treatment. I struggled with my self-esteem. Frankly, there didn’t seem to be much to celebrate.

But flash forward a year to my 30th birthday party. I worea pretty pink dress. I was surrounded by friends and family. I was smiling, my cheeks glowing, with much to celebrate: a return to remission, to independent living and the resumption of freelance work. However, improvement over that year was by no means linear. I had many bad days, sometimes weeks. But when I considered the headway I made between my 29th and 30th birthdays, all I could think was, “What a difference a year makes.”

When I blew out the candles that year, I wished for continued health, for my life to keep blossoming—and it did. A couple years later, I moved to Boston and started graduate school. In the decade since, I’ve written two books and forged a teaching career. I have gotten back on my skis. I have also wrestled brief flare-ups of my illnesses, grieved the death of loved ones and mourned the loss of love. Those have been my low points, but when I see how many gains I’ve made over the last decade—and how much my stamina has improved—I want to pinch myself. I can hardly believe it.

As I blew out my candles last year, I never could have imagined the world would be in the midst of a global pandemic by my next birthday. But I also couldn’t have imagined all of the good things that have happened to me this year, including landing a literary agent, surviving COVID-19 despite my underlying health conditions. And thus, I hold onto hope—for me, for you, for the Lyme community, for our world.

When I blow out my birthday candles this week I’ll wish for a healthier year for all of us. I hope that by this time next year, I’ll be able to celebrate that wish coming true.


jennifer crystal_2

Opinions expressed by contributors are their own.

Jennifer Crystal is a writer and educator in Boston. Her memoir about her medical journey is forthcoming. Contact her at lymewarriorjennifercrystal@gmail.com.

 

 

Well, that made my day!  I love to see patients improve. If you are having a rough day, month, or year – hang tight.  It will get better in time.  

More Ticks, Risk of Lyme Disease in Wisconsin

https://waow.com/2020/04/30/more-ticks-risk-of-lyme-disease-in-wisconsin/ (News Video Here)

More ticks, risk of Lyme disease in Wisconsin

WAUSAU, Wis. (WAOW) — A mild winter combined with a larger population of deer in Wisconsin this year could mean more ticks to look out for.

Experts at the Tick-Borne Illness Center of Excellence in Woodruff treat people from across the country, but they say Northern Wisconsin stands out.

“It is a highly prevalent area for wood tick diseases and deer tick diseases,” said center manager Kathy McCaughan.

This year, experts say they’re seeing the impact of a mild winter.

“The ticks really don’t go away in the winter they just go underneath the leaves and the snow kind of insulates them and the first tick that we had reported here was the beginning of March already,” said Clinic Program Director Connie Campbell.

Combine that with a higher deer population and more people outside, there could be a higher risk of spreading lyme disease.

“Now with COVID, everyone is out and about a little bit trying to get fresh air, just kinda be vigilant,” said Campbell. “You wear light-colored clothing so that you can spot them really easily, deet helps but you don’t spray it on your skin you spray it on your clothes.”

The Centers for Disease Control and Prevention also says to tuck your pants into your socks when you’re going out and perform a tick check when you get back home.

You can learn more about Lyme disease on the State’s Health Department Website.

You can also download an app from UW-Madison to track ticks and learn about removal/prevention.

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**Comment**

We really have no idea why there are more ticks. Blaming the weather isn’t prudent considering ticks are ecoadaptive and survive about anything but fire. Research shows it’s migrating birds and photoperiod (light required for ticks to molt) that propagates ticks and the diseases they carry: https://madisonarealymesupportgroup.com/2018/11/07/ticks-on-the-move-due-to-migrating-birds-and-photoperiod-not-climate-change/ (research conducted by an independent researcher)

But this doesn’t fit the climate change narrative that keeps being pushed upon us. Right now, climate change is a popular topic so if researchers want grant money they put that moniker in their work so they obtain money.  Even if it’s untrue.

Please see:  https://madisonarealymesupportgroup.com/2019/06/17/ontario-public-health-officials-called-out-on-shoddy-biased-research-utilizing-an-erroneous-climate-change-model-to-program-a-futuristic-tick-problem/

This is just another example of how finances dictate the science being done.  Sad but true.

“For blacklegged ticks, climate change is an apocryphal issue.” -John Scott

Chronic Neurological Lyme Disease Or Co-Morbid Conditions?

https://danielcameronmd.com/chronic-neurological-lyme-disease-dismissed-for-co-morbid-conditions/

CHRONIC NEUROLOGICAL LYME DISEASE OR CO-MORBID CONDITIONS?

man with fatigue holding head

Some patients with chronic neurological Lyme disease continue to have persistent, debilitating symptoms following treatment.

A recent study confirmed the severity of chronic symptoms in this patient population but unfortunately dismissed the symptoms, attributing them to various co-morbid conditions, rather than Lyme disease. [1]

 

The study, “Patient-reported outcome after treatment for definite Lyme neuroborreliosis” by Eikeland and colleagues, describes 258 patients treated for definite Neurologic Lyme disease. Many of them remained symptomatic an average of 5 years after their initial treatment.

According to the authors, a higher proportion of their chronic neurological Lyme disease patients reported severe fatigue. Furthermore, “Mental health-related quality of life was poorer among [neuroborreliosis] NB-treated patients than in normative data.”

Although many of the patients’ symptoms are consistent with those found in chronic neurological Lyme disease, the authors attributed the symptoms to co-morbid illnesses, based on a retrospective review of the medical records.

READ MORE: Six cases of neuroinvasive Lyme disease

The symptoms included: radiating pain, general pain, fatigue, facial palsy, malaise, dizziness and/or unsteadiness, headache, numbness in arm and/or leg, memory and/or concentration problems, paresis in arm and/or leg, and diplopia.

Symptoms due to chronic neurological Lyme disease or co-morbid conditions? CLICK TO TWEET 

Co-morbid conditions listed for these patients included: fibromyalgia, allergies, depression or anxiety, multiple sclerosis, systemic disease sarcoidosis, systemic lupus erythematosus, Sjögren’s syndrome, rheumatoid arthritis, chronic fatigue syndrome, Parkinson’s disease, thyroid dysfunctions, and cancer.

Note: The study was not designed to assess whether the patient, in fact, had the co-morbidity listed in their records or instead had complications of chronic neurological Lyme disease.
References:
  1. Eikeland R, Ljostad U, Helgeland G, et al. Patient-reported outcome after treatment for definite Lyme neuroborreliosis. Brain Behav. 2020:e01595.

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**Comment**

Another worthless study to add to the ever increasing pile of trash.

These poor, sick people were given all sorts of labels: fibromyalgia, lupus, Sjogren’s, RA, CFS, Parkinson’s, cancer – the typical “bad guys,” but ALL were infected with Lyme disease which can cause symptoms indicative of those labels.

It’s very interesting that with Lyme disease, “authorities” want to blame anything other than a persistent borrelia infection, but with COVID-19, those same “authorities” want to blame everything on COVID-19.  This should smell bad to you.  This is not science – it’s biased, narrative-driven propaganda.

For more: Peer-Reviewed Evidence of Persistence of Lyme:MSIDS copy

https://madisonarealymesupportgroup.com/2020/03/09/the-long-term-persistence-of-borrelia-burgdorferi-antigens-dna-in-the-tissues-of-lyme-disease-patient/

https://madisonarealymesupportgroup.com/2017/05/10/body-of-research-showing-borrelia-persists/

https://madisonarealymesupportgroup.com/2020/04/08/how-do-lyme-disease-symptoms-persist-long-term/

https://madisonarealymesupportgroup.com/2019/07/31/post-lyme-disease-syndrome-vs-chronic-lyme-disease-syndrome/

https://madisonarealymesupportgroup.com/2018/04/13/chronic-lyme-post-mortem-study-needed-to-end-the-lyme-wars/

 

Lyme Disease Awareness Month: Kris Kristofferson Was Misdiagnosed With Alzheimer’s, Memory Loss Was Due to Ticks

https://meaww.com/kris-kristofferson-lyme-disease-awareness-misdiagnosed-with-alzheimers-memory-loss-ticks-symptoms

Lyme Disease Awareness Month: Kris Kristofferson was misdiagnosed with Alzheimer’s, memory loss was due to ticks

Kris had been complaining to doctors about memory loss said his wife Lisa Meyers in 2016, ‘That was a big clue to me that maybe it was not really Alzheimer’s’


                            Lyme Disease Awareness Month: Kris Kristofferson was misdiagnosed with Alzheimer's, memory loss was due to ticksKris Kristofferson (Getty Images)

 

The tick-borne illness affects many people but isn’t easily or efficiently diagnosed, with its array of symptoms, it can also be misdiagnosed.

Renowned songwriter and actor and country legend Kris Kristofferson contracted the disease and it went undiagnosed for years. Kristofferson is known for his roles as Rudy Martin in ‘Fast Food Nation’ and songs like ‘Me and Bobby McGee,’ and his suffering shocked many people. (See link for article)

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**Comment**

Kristofferson had a laundry-list of symptoms indicative of tick-borne illness.

What’s truly unfortunate is that there are plenty more out there suffering from the exact same thing to this day who could get better but doctors are woefully ignorant.

For more: