Archive for the ‘Lyme’ Category

SOT Treatment For Lyme Disease

SOT was created for those with previously untreatable genetic conditions.  In my opinion, Lyme disease is not a genetic condition, it’s an infection(s) and depending upon your exact case, is only one of many potential infections that can be bacterial, fungal, viral, and/or parasitic.  This is my main problem with SOT besides the fact it is a gene-silencing technique that raises questions about long-term effects as well as the fact Bb changes its outer surface protein, is stealthy, and very probably a bioweaponized pathogen(s) created in a lab to be more persistent and transmissible, and to evade the immune system and treatment.

https://www.treatlyme.net/guide/sot-lyme-treatment

SOT for Lyme Image from Marty Ross MD
 
By Marty Ross MD

Supportive Oligonucleotide Therapy (SOT) Background

Supportive Oligonucelotide Therapy (SOT) is a new treatment for Lyme disease. SOT is also called Antisense Oligonucelotide Therapy (ASOT) which is the term used in medical research papers. SOT uses laboratory derived nucleic acids (genetic code) that blocks production of disease causing proteins or even gene expression. These pieces of genetic code are called oligonucleotides. You can think of oligonucleotides as a genetic message.

For example, in Duchenne Muscular Dystrophy (DMD), SOT provides oligonucleotides that direct the correct production of a protein called dystrophin. People with muscular dystrophy are born with DNA that provides the wrong genetic message for dystrophin. SOT correction to the DNA message leads to production of dystrophin. This prevents the muscle damage seen in DMD.

In Lyme disease, a currently available type of SOT produced by RGCC in Greece uses oligonucleotides intended to stop germ growth and replication. Unlike the SOT therapy for Duchenne muscular dystrophy, the Lyme SOT is not a US Food and Drug Administration (FDA) approved drug. To be approved by the FDA, a therapy must have scientific evidence of safety and effectiveness.  (See link for article)

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**Comment**

Dr. Ross is unsure if SOT for Lyme/MSIDS works, and some of his patients using it before seeing him experienced little to no effects, but some of his colleagues state some patients have experienced improvement.  He also reminds readers that there is a placebo effect of 35% on average in clinical trials for drugs.

Also, please read this article on SOT Therapy side effects.

Common side effects: injection site reactions, flu-like symptoms, headaches and fatigue, changes in liver function.

Serious but supposedly rare side effects: thrombocytopenia, changes in kidney function, allergic reactions, neurological effects, potential impact on fertility and pregnancy.

For more on SOT:

For more on the RGCC test:

 

 

 

 

Category:

Lyme, Treatment

Mom Dealing With PANS & Lyme: “2020 is NOT My Worst Year”

https://www.lymedisease.org/from-a-mom-dealing-with-pans-and-lyme-2020-is-not-my-worst-year/

From a mom dealing with PANS and Lyme: “2020 is NOT my worst year”

Lisa Lew

By Lisa Kilion

2020 is NOT my worst year.

“What are you talking about?” you ask. “You have something the rest of us don’t have–like a private island? A cure to COVID-19?”

Nearly everyone is stressed, distressed, depressed. It’s the year of not being able to breathe, from George Floyd to those suffering complications from COVID-19. It’s the year of feeling trapped in our homes, of existing in a dreamlike state of daily repetition.

And for us PANDAS/PANS and Lyme folks, trapped in our lives.

Yep. Trapped in our lives, just like any other year. Only this year, for the first time, the entire world has experienced a whopping scoop of our secret, isolated experiences. And guess what? They’re not savoring it.

2020 is hellish for many people, most especially the people who have lost someone dear or become ill themselves. And my condolences to you. Several of my friends lost parents this year, people who were older but not ready to die and to die alone. Several of my friends/family became quite ill.

Didn’t have to wait for 2020

The fact is, I didn’t have to wait until 2020 to have these horrid experiences.

Years ago, I lost someone dear to me–my happy, healthy child, when nearly overnight, their personality was gone and in its place a ticcing, depressed child with OCD.

And with this, my family lost even more–my kids lost much of their childhoods, my husband and I lost a normalcy of parenting, as well as outings, vacations, activities. After school football and soccer practices morphed into doctor appointments. Birthday parties morphed into therapy sessions.

Years ago, my own insidious, dormant case of Lyme flared under the stress of saving my child. So this isn’t my worst year, although 2020 is the year of:

  • death
  • illness
  • prejudice
  • isolation
  • depression
  • paranoia of others
  • protecting ourselves against germs
  • not trusting medical advice (hydroxychloroquine–yes or no?)
  • government and social media censorship
  • children being unable to attend school.

If you have a child with a medical illness like PANS/PANDAS/Lyme, then you’ve most likely experienced all of the above already. And I’ll bet this is not the the worst year of your life. I’ll also bet that you’re finding a way to cope.

So for those with P/P and Lyme, here are the boxes to fill in:

Illness?

Check.

Prejudice?

Check for some of us. And for some of us, being a different race or ethnicity makes it even more challenging to receive the proper medical and educational support for these diseases.

Isolation?

Well, sit back down for a long tale.

There is nothing like the isolation of a PANS family living in a world where there is no cure, where people judge your parenting (or your “behavior” if you have PANS yourself), where the social life of your kid is curtailed, never mind your own social life.

There is no isolation like the life of a PANS family when extended family does not understand what is happening, when mainstream doctors don’t believe you, when there is no one treatment and sometimes insurance companies don’t want to cover the costs of the treatments that exist.

There is isolation when your child is too ill to leave with a babysitter, or too at-risk to leave alone even when old enough to drive. There is isolation when one parenting figure must relinquish a job or career to care for the ill child.

Depression?

Us or our kids?

Our kids who are cut off from society, whether from PANS or Lyme or COVID-19, struggle to remain themselves. Our kids who suffer from brain inflammation are submerged in a new world of depression and sink so deeply that their memories of being happy float away like smoke rings. Whether it’s from COVID or PANS, the helplessness over our own situations is all too real.

Paranoia?

Don’t come near me.

Seriously, how many times has a PANDAS parent wondered if another kid in the class has strep? If the dog has strep? If your brother-in-law’s young cousin who came to the family party has a cold which can inflame your child’s brain? (Or, if I myself am carrying it?)

Paranoia is questioning whether you can share the fact that your child has chronic Lyme and is on a cocktail of antibiotics with an emergency room doctor. Paranoia is fearing the doctor who asks why you are using “alternative medicines” and claims that PANDAS isn’t real. It’s retreating into your own worried mind when you hear stories about other PANDAS parents being accused of Munchausen’s.

Paranoid much? Checkcheckcheckcheck.

Protecting ourselves against germs?

This means not showing up to family parties when you hear someone has a “slight” cold, wiping down surfaces (that action did NOT start in the year 2020, folks), imagining the air that others breathe out has a soft gray roundness to it, marking the bacteria. Wearing masks, prior to 2020.

Not trusting medical advice?

This was a hard one for me, as I was brought up to do whatever the doctor ordered (which did help me immensely when working with a LLMD or LLNP and a strict Lyme protocol).

How do you trust when the young doctor tells you that your child’s inability to control air hunger is caused by stress, and then you notice the lab report states your child is positive for Lyme, which the doctor then claims is a false positive?

How do you trust mainstream doctors after the PANDAS/Lyme doctor prescribes medications which completely eradicate the air hunger (caused by Babesia, for those who want to know). And that is only one example.

Media and government censorship?

Why don’t doctors believe in chronic Lyme, again? Why is the IDSA still against it when well over 700 peer-reviewed studies [showing the persistence of Lyme] have been conducted? Why does the government support the IDSA and spend more money on diseases that affect far fewer people? And don’t even go there when it comes to vaccines which children with immune issues are supposed to be exempt from (and protected by herd immunity).

Children unable to attend school?

PANDAS and Lyme can result in:

  • separation anxiety
  • inability to think or focus
  • constant bathroom runs/ need to urinate
  • decline in math ability
  • blurriness which affects reading
  • handwriting
  • impulsivity
  • emotional control
  • sweats
  • joint pains
  • fatigue
  • insomnia

Oh, we tried, years ago, for our child to connect with a class via a computer. But the world was not ready for it. And then 2020 happened and we went virtual overnight (I know, I’m a teacher and it’s been a job x 1,000). But it’s possible.

Checkmate.

So if this isn’t my worst year, what was?

Maybe it was the year my healthy, happy child became ill and no one could accurately diagnose the issue.

Maybe it was the year we HAD to get an attorney to deal with the school system and withdrew $10,000 from our now nearly extinguished savings account, to pay for said lawyer.

Maybe my worst year was when we had to weigh options for a child at risk–why is there a schism between medical and psychiatric support when it comes to hospitalization? What do you do when a medical issue causes severe depression? Why won’t anyone out there help?

Maybe my worst year was when my marriage was dragging along like a bottom feeder. (Note: we are much stronger and happier now.)

Maybe my worst year was when I discovered my other child had Lyme also. At the same time I discovered I did as well, and most likely gave it to my kids when pregnant.

Maybe my worst year was when I was too sick to take my daughter to the swimming class she begged for, when no one at my job knew that I could barely walk down the hall due to dizziness and fatigue, when I gave the best of me to my students and not to my own kids, when I’d collapse on my bed at home after work while my husband cooked dinner, only to listen as conversations drifted upstairs.

But….

But that was also the year I became involved with the Lyme Disease Challenge. That was the year I wrote many articles about PANDAS, PANS and Lyme. That was the year I continued to connect with others and to learn from these new communities. That was the year I understood on a deeper level the pain my kids endured. And that was the year, like all the other years, that I rubbed my child’s back until they fell asleep.

I have learned multiple lessons from these worst years
  • A truly horrendous year does not mean that I am immune from more horrendous years. There’s no such thing as paying my dues. Life does not owe me a good year.
  • Get it all out. Write. Cry. Weep over your laptop, sob beneath your sunglasses in the parking lot of supermarket, pound your pillows. Bicycle or run as hard as you can.
  • Then, do something for someone else. Get out of yourself. Text a friend to check up on them. Sign up to advocate for Lyme, PANS, or anything else that needs your support.
  • Connect. My husband and I have been cycling through this year. We have close friends who bicycle with us. I have a friend with whom I walk (socially distanced). I text with my colleagues, my cousins, my siblings. I’m not usually a fan of Zoom gatherings as I spend all day on Google Meets with my own students. Get on social media and respond with positivity and inspiration to someone else’s cry for help.
  • Avoid social media except when you’re using it for a calculated reason–for me, that means joining writing groups, teaching groups and Lyme, PANS groups. But avoid negativity and posts that show off on FakeBook. It hurts to see kids achieving and fancy famiy vacations (not this year!) when we hang out in the jungle of medical mishigas [craziness].
  • Set new goals. Maybe going to college directly from high school–with high honors–isn’t the path for everyone. Maybe the fact that my kid is willing to continue undergoing medical treatment is worthy of an award. Maybe getting through each day and smiling at a cashier is an achievement.
  • Recognize character. There is much love, caring, resilience and perseverance among the parents in the PANS and Lyme support groups. We are on both sides of the street politically, yet we come together in our quest to save our children. As an adult, it is astonishing to see the strength of the love of so many parents.
  • Exercise! Now this can be a hard one if you’re physically incapacitated or have young children or kids who cannot be left alone. When my husband was very ill, we got him an “under desk pedal exerciser.” Do ANYTHING! At my sickest, which wasn’t as sick as some who suffer from Lyme, I could manage only 14 miles on my bicycle, and that was with energy gels. I’d have to rest the day after. I’d have to rest after showering. Now exercise is my mindfulness activity; it’s one of my keys to mental health.
  • Stay balanced. This one is hard. I’ve been trying to step back from the decisions that my teenagers make, since I have no control, focusing instead on presenting data and options and, lastly, bringing my focus back to myself and what I actually can do. I don’t have much control over my teens. I can show love. And impatience, sometimes. I can guide. I can teach through example. I can be my most-fulfilled self.
  • Practice gratitude. I am thankful for our doctors, for certain individuals at the schools who have been extremely responsive and helpful. I am so grateful for my husband. And my doggies. Friends, both in and out of the PANDAS/LYME world. My bicycle. My computer. My hands, which now have arthritis from Lyme, but which still work for me. My legs, which are strong. My brain, which is back after floating with unicorns for a short while. And I’m grateful that my kids continue to fight and have turned into warm, creative people who can express themselves.

2020…

2020 is the year that I have bicycled more than 3,000 miles. It is the year that my oldest takes his disease seriously and pushes forward with treatment, submitting himself to monthly IVIGs that give him nausea and headaches. 2020 is the year that I am totally in love with my husband of 22 years, the year that my dogs are always happy to see me (that’s every year), my daughter becomes a social media genius who helps my son’s band get 100,000 views in one week.

My goal has been to reach beyond the trappings of PANS and Lyme–and now COVID-19 also–and find my life again. I’m out there, cycling, straight through frigid winter months as long as the ground isn’t coated in ice. I’m working on my writing, my novels, my dreams.

2020 is NOT my worst year, but I am forever changed by the worst years I have survived.

Lisa Kilion lives in New York. This post was originally published on her blog PANS Life.

Related Posts:
  1. Letter to grandparents of a child with PANS/PANDAS
  2. COVID-19’s daunting challenges for families with Lyme and PANS/PANDAS
  3. TOUCHED BY LYME: 20-year-old’s advice to her 14-year-old self: “You gotta have hope”
  4. Why therapy isn’t enough when you have OCD and PANS/PANDAS

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For more:  https://madisonarealymesupportgroup.com/2020/07/25/what-is-pans-pandas-and-why-are-cases-on-the-rise/

Category:

Lyme, PANS, Psychological Aspects, vaccines

Symptomatic High-Grade AV Block & Phase 4 Right Bundle Branch Block – A Previously Unreported Manifestation in Lyme Carditis

https://www.heartrhythmcasereports.com/article/S2214-0271(20)30263-3/fulltext#secsectitle0020

Phase 4 Block of the Right Bundle Branch Suggesting His-Purkinje System Involvement in Lyme Carditis

Open AccessPublished: December 01, 2020DOI:https://doi.org/10.1016/j.hrcr.2020.11.017
We describe an adolescent with symptomatic high-grade AV block and evidence of phase 4 right bundle branch block, a previously unreported manifestation of infra-nodal conduction system involvement in LC.

A previously healthy 14-year-old boy presented via emergency medical services in mid-summer because of syncope (fainting).

Interesting findings:

  • Patient frequently hunts and fishes in wooded, Lyme-endemic region 
  • Didn’t remember tick bites or EM rash
  • Two weeks prior to ER visit patient had a runny nose, cough, abdominal pain, followed by headache and nausea.
  • In the ER he had bradycardia, altered mental status, headache, and vomiting.
  • Initial ECG showed complete heart block
  • He was given 2,000mg of IV Ceftriaxone every 24 hours
  • Testing supported clinical suspicion of Lyme
  • He was given a temporary pace-maker which was removed after 5 days of IV antibiotics and he was switched to oral doxycycline to complete a total of 21 days of antibiotics
  • After being monitored in hospital for 7 days, he was discharged with an auto-detecting wireless monitor until a follow-up appointment and stress test
  • Follow-up appointment patient was well with normal ECG

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**Comment*

Case study states: 

Significant AV block due to LC occurs in about 1% of LD cases.

I believe this statistic is premature considering many do not test positive and therefore are undiagnosed. I’ve posted numerous articles where patients are sent packing even when they present with positive test results three times in a row! We will never know how many patients with AV block have an underlying tick-borne illness due to abysmal testing and the lack of training and experience of most doctors with tick-borne illness.

And then there’s that nagging concern about long-term effects and if 21 days of antibiotics were enough for his patient. It often isn’t.

Please see:

https://madisonarealymesupportgroup.com/2020/11/25/what-makes-a-doctor-lyme-literate/

Category:

Heart Issues, Lyme, research, Testing, Treatment

Risk of Development of Chronic Kidney Disease After Exposure to Borrelia Burgdorferi and Anaplasma spp

https://pubmed.ncbi.nlm.nih.gov/33152525/

Risk of Development of Chronic Kidney Disease After Exposure to Borrelia burgdorferi and Anaplasma spp

Corie Drake 1, Michael Coyne 2, Donald J McCrann 1, Jesse Buch 1, Rebekah Mack 1

PMID: 33152525

DOI: 10.1016/j.tcam.2020.100491

Free article

Abstract

Lyme disease is a multi-faceted illness caused by infection due to Borrelia burgdorferi. Acute kidney damage secondary to Lyme disease is well described but less so as a chronic event. The role of Anaplasma spp. and secondary kidney dysfunction is not known. A retrospective cohort study was performed to determine if dogs within a defined Lyme disease and anaplasmosis region with B. burgdorferi or Anaplasma spp. antibodies had an increased risk of chronic kidney disease (CKD). Patient exposure was defined as having a B. burgdorferi or Anaplasma spp. antibody positive result recorded at any point in the available patient history. CKD was defined as concurrent increased symmetric dimethylarginine and creatinine (Cr) for a minimum of 25 days with inappropriate urine specific gravity (USG). Patients were matched using propensity scoring to control for age, region, and breed. Contingency tables were used to compare dogs seropositive and not seropositive to B. burgdorferi and Anaplasma spp. and CKD outcome. For each comparison that was performed, statistical significance was defined by a P-value of <.025. The risk ratio of CKD for patients exposed to B. burgdorferi and Anaplasma spp. were found to be 1.43 (95% confidence interval [CI, 1.27, 1.61], P < .0001) and 1.04, (95% CI [0.87, 1.24], P = .6485), respectively.

Results suggest in this cohort no increased risk for developing CKD when exposed to Anaplasma spp. but a significant increase in risk for developing CKD with exposure to B. burgdorferi.

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For more:  https://madisonarealymesupportgroup.com/2019/03/08/lyme-nephritis-in-humans-physio-pathological-bases-spectrum-of-kidney-lesions/

https://madisonarealymesupportgroup.com/2020/12/15/lyme-disease-is-a-small-vessel-disease-dr-klemann/

Category:

Lyme, research

Interactions Between Borrelia Burgdorferi & Ticks

https://pubmed.ncbi.nlm.nih.gov/32651470/

Interactions between Borrelia burgdorferi and ticks

Cheyne Kurokawa 1, Geoffrey E Lynn 1, Joao H F Pedra 2, Utpal Pal 3 4, Sukanya Narasimhan 1, Erol Fikrig 5 6

    Free PMC article

    Abstract

    Borrelia burgdorferi is the causative agent of Lyme disease and is transmitted to vertebrate hosts by Ixodes spp. ticks. The spirochaete relies heavily on its arthropod host for basic metabolic functions and has developed complex interactions with ticks to successfully colonize, persist and, at the optimal time, exit the tick. For example, proteins shield spirochaetes from immune factors in the bloodmeal and facilitate the transition between vertebrate and arthropod environments. On infection, B. burgdorferi induces selected tick proteins that modulate the vector gut microbiota towards an environment that favours colonization by the spirochaete. Additionally, the recent sequencing of the Ixodes scapularis genome and characterization of tick immune defence pathways, such as the JAK-STAT, immune deficiency and cross-species interferon-γ pathways, have advanced our understanding of factors that are important for B. burgdorferi persistence in the tick. In this Review, we summarize interactions between B. burgdorferi and I. scapularis during infection, as well as interactions with tick gut and salivary gland proteins important for establishing infection and transmission to the vertebrate host.

    Category:

    Lyme, research, Ticks