Archive for the ‘Lyme’ Category

5 Things to Know About Chronic Inflammatory Demyelinating Polyneuropathy (The 6th Thing is Lyme Can Cause It)

https://www.medscape.com/viewarticle/918480?

5 Things to Know About Chronic Inflammatory Demyelinating Polyneuropathy

By Ariel Harsinay

September 20, 2019

Chronic inflammatory demyelinating polyneuropathy (CIDP) may be a rare disease, but it is one of the most common forms of neuropathy and the most common form of chronic autoimmune neuropathy. Roughly 30,000 Americans are currently diagnosed with CIDP. Unlike many other neuropathies, CIDP is treatable, but its similarities with other nerve disorders often make it extremely difficult to diagnose. Here are five things to know about CIDP.

1. CIDP is an autoimmune disorder that attacks the peripheral nervous system.

CIDP is an autoimmune, neurologic condition in which the myelin sheath surrounding the axons of neurons is attacked by the immune system, causing demyelination. Myelin normally serves as axonal insulation, allowing neurons to rapidly transmit action potentials and communicate with neighboring neurons. The demyelination seen in CIDP impairs this process, resulting in motor impairment, numbness, difficulty walking, and general weakness and fatigue.

The immune response causing CIDP involves the activation of T cells as well as the expression of cytokines, tumor necrosis factor, interferons, and interleukins. Immunoglobulin and complement are also implicated in CIDP pathogenesis.

2. CIDP presentation can vary considerably.

Fifty to sixty percent of CIDP cases are so-called “typical,” presenting with symmetric symptoms of both proximal and distal limbs in which motor impairment is more prominent than sensory symptoms. A diagnosis requires that a patient’s symptoms have progressed gradually for at least 8 weeks, although some patients present with either acute or relapsing-remitting forms of the disease. While CIDP symptoms can usually be managed throughout life, long-term disability is not uncommon.

Some 20%-30% of CIDP cases are idiopathic, although it is frequently seen in conjunction with a variety of other illnesses, including HIV, diabetes, lupus, hepatitis, lymphatic cancer, and restless legs syndrome. It also may present as a comorbidity of infection or as a side effect of various cancer and HIV drugs.

CIDP can affect anyone but is most commonly diagnosed in individuals in their 50s and 60s and is twice as common in men. The global yearly incidence of the disorder is 1.5-3.6 million, with around 30,000 people affected in the United States at any given time. In patients with type 2 diabetes the incidence rises to over 26%.

3. A variety of tests can confirm a CIDP diagnosis.

Nerve conduction studies and electromyography are diagnostic standards in CIDP they; can reveal the demyelination and resulting slowed neuromuscular transmission characteristic of disease. Nerve biopsy can also be helpful, providing pathologic evidence of nerve damage and inflammation.

Often physicians will also order a lumbar puncture in suspected CIDP cases, looking for elevated spinal fluid protein without elevated white cells. In atypical cases, in which electrophysiologic tests may be inconclusive, MRI can help confirm a diagnosis. Blood tests may also be used to detect common comorbidities such as diabetes and lupus.

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**Comment**

And, Dr. Cameron has written how one woman with CIDP actually had Lyme disease:  https://danielcameronmd.com/chronic-inflammatory-demyelinating-polyneuropathy-cidp-case-resolved-antibiotics/

Excerpt:

Lyme disease has been ruled out in other conditions based on negative serologic tests only to seroconvert to positive serologies on follow-up. [1,2] This was demonstrated in the case of a 41-year-old woman with chronic inflammatory demyelinating polyneuropathy (CIDP), according to Perronne from the Infectious Diseases Unit, University Hospital Raymond Poincaré, APHP, Versailles Saint Quentin University, Garches, France.

The woman, who was then treated successfully with 6 weeks of doxycycline and hydroxychloroquine, showed “a dramatic clinical improvement” with a complete disappearance of neurologic signs, according to Perronne.

The authors advised against automatically ruling out Lyme disease based on negative serologic tests.

The woman presented with asthenia (loss of strength), weakness, and diffuse paresthesias (abnormal skin sensations). All of which are hallmark Lyme symptoms.

For more on CIDP:  https://30g7el1b4b1n28kgpr414nuu-wpengine.netdna-ssl.com/wp-content/uploads/2012/01/CIDP.pdf

A word of warning, however.  The pdf mentions the success of corticosteroids, but Lyme literate doctors have discovered this to be counter productive unless antimicrobials are used concurrently as catabolic steroids depress the immune system allowing the infection(s) to proliferate.  

Regarding treatment for CIDP, the pdf states that “up to eighty percent of CIDP patients respond to one or more therapies that modulate the immune system. Treatments shown to work in clinical trials include prescribing corticosteroids, blood plasma exchange or plasmapheresis, and intravenous immunoglobulin or IVIG. All three treatments are highly effective and lead to improved strength and function in CIDP patients. Each treatment has its advantages and disadvantages that should be discussed with the physician.”

If you’ve been diagnosed with CIDP but suspect tick borne illness, please share this with your medical practitioner.  Also, point out the initial seronegativity on Lyme tests by patients with CIDP who were found to seroconvert later.  

Is Prolonged Treatment For Lyme Disease The New Norm?

https://danielcameronmd.com/is-prolonged-treatment-for-lyme-disease-the-new-norm/

IS PROLONGED TREATMENT FOR LYME DISEASE THE NEW NORM?

The Infectious Diseases Society of America (IDSA) guidelines recommend a 3- to 4-week course of antibiotics for the treatment of Lyme disease. But a new study by the Centers for Disease Control and Prevention (CDC) indicates that nearly 2 out of every 3 patients with Lyme disease are treated longer than 4 weeks.

According to an annual, cross-sectional, nationwide survey,

  • 20.3% were treated for 5 to 8 weeks, while
  • 35.6% were treated for more than 8 weeks.
The CDC authors were surprised at the number of Lyme disease (LD) cases being treated with prolonged therapy.

“A surprisingly large proportion of respondents reported receiving more than 8 weeks of antibiotic treatment for LD,” writes Hook in the journal Ticks and Tick-borne Diseases.

Prolonged therapy for Lyme disease is not new. “Many respondents reporting receiving prolonged therapy is concordant with other reports of providers’ non-adherence to or unfamiliarity with LD treatment guidelines,” writes Hook.

The CDC authors were not able to address the rationale for extended treatment without having access to the attending physician or patient charts. Instead, they cited the familiar dogma regarding Lyme disease treatment.

  • “There is no scientific evidence of clinical benefit from antibiotic treatment longer than current guidelines recommend.”
  • “In patients with persistent symptoms and a history of LD, several controlled trials showed no benefit in prolonged antibiotic therapy.”

The authors postulate that prolonged therapy for Lyme disease could be stopped with education.

“Our results indicate that providers in LD endemic areas may benefit from education regarding the duration of therapy needed, especially in light of the risk of antibiotic-related complications and development of resistance.”

Editor’s note: I find that most doctors are well aware of the IDSA and CDC opposition to more than a 4-week course of antibiotics. The evidence behind the IDSA and CDC recommendations is flawed. I am an author of the International Lyme and Associated Diseases Society (ILADS) guidelines, which recommend prolonged therapy for Lyme disease if needed.

References:
  1. Hook SA, Nelson CA, Mead PS. U.S. public’s experience with ticks and tick-borne diseases: Results from national HealthStyles surveys. Ticks Tick Borne Dis. 2015 Jun;6(4):483-8.

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**Comment**

All I can say is “THANK GOD FOR ILADS!”

To understand the shady biased back story on why we are in the straits we are in:  https://madisonarealymesupportgroup.com/2019/02/22/why-mainstream-lyme-msids-research-remains-in-the-dark-ages/

Also worth noting are the severe conflicts of interest within the CDC, the very people making treatment guidelines:

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ConflictReport  Go to part III

I just posted this excellent article on the backstory of the Lymerix vaccine which also uncovers shady dealings, dishonesty, and conflicts of interest:  https://madisonarealymesupportgroup.com/2020/02/10/the-bitter-feud-over-lymerix/

 

A Vote Against Lyme Disease

https://now.tufts.edu/articles/vote-against-lyme-disease

A Vote Against Lyme Disease

Cast your ballot for the best new ideas in fighting a growing health problem
A deer tick lurking on a grass stem. Tufts students are competing to find the best new ideas for fighting the tick-borne illness Lyme disease.
Participants in the challenge have come up with some creative ways to keep deer ticks like this one from spreading illness. Photo: Shutterstock
By Julie Flaherty
January 9, 2020

In the video, Kobe the German Shepherd is getting his check-up at the veterinarian’s office. His owner says the dog is doing well, but she does mention,

“We’re starting to see a lot of ticks on him after his walks.”

After sharing some tips on keeping Kobe tick-free, the veterinarian adds:

“Do you think about doing tick checks on yourself?” It’s a good practice, the vet says, along with wearing insect repellant and treating clothes and shoes with the pesticide permethrin.

Dog owners already talk with vets about preventing ticks on their pets, so why not have vets share some info on protecting the rest of the family from tick bites?

The short video is one of four proposals that students developed as part of the Tufts Lyme Disease Challenge. The competition, the brainchild of Tufts trustee Hugh Roome, A74, F77, AG74, FG80, FG80, A11P, F15P, A18P, seeks to build on Tufts University’s long history of leadership in Lyme disease research. It draws on the broad scope of research at Tufts to develop novel approaches to preventing, diagnosing, treating and eradicating one of the fastest growing infectious diseases in the United States. Each year, an estimated 300,000 new cases are diagnosed.

Check out the video proposals and vote for your favorites. The top vote-getting team will receive $1,000.

The competition kicked off on November 1 with expert talks, panel discussions and brainstorming sessions to discuss what’s most needed in the fight against Lyme, from educational outreach to basic knowledge of the bacteria that causes the disease. Over 100 Tufts students, post-doctoral fellows, faculty and staff participated in the half-day event commented,

“It was great to have so much energy in the room and hear so many terrific ideas,” said Linden Hu, a Lyme disease researcher at Tufts University School of Medicine. “The goal now is to keep the momentum going and really have Tufts make a difference in eradicating Lyme disease.”

Since the event, smaller teams of students have worked with Lyme disease researchers at Tufts to develop their proposals. The four students from Cummings School of Veterinary Medicine at Tufts who submitted the Kobe video say that well visits with the vet could be a new way to spread education about Lyme Disease prevention.

In another video, a group of medical and biomedical engineering students propose a way to prevent tick bites from turning into disease. Lyme bacteria are amazingly cagey in their ability to avoid detection by the immune system. The students propose using nanoparticle infused therapeutics to boost a person’s immunity, essentially preventing the bacteria that cause Lyme Disease from starting a full-blown infection in the body.

The videos are impressive in their wide range of approaches. A group of biomedical engineering students suggest using the power of pheromones to create a tick-attracting trap; the first step would be enhancing tick pheromones so they last longer and can spread over a larger area.

The fourth video aims at one of the significant gaps in Lyme research: a thorough understanding of Borrelia, the bacteria that causes it. Borrelia is difficult to grow in a lab. One solution, the video offers, is to use a drug printing robot to make dozens of growth media with different combinations of nutrients, to quickly see which recipe is the best for culturing the bacteria.

You can vote once per email per day. Voting closes at midnight on February 24.

Julie Flaherty can be reached at julie.flaherty@tufts.edu.

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**Comment**

When you click onto the link called “Video Proposals,” you will be sent to a page where four videos explain the different research topics.

They include:

  • Vets Against Lyme: Combating Lyme Disease by harnessing the human animal bond

 

  • Team Diamond: Finding a growth media for borrelia & high throughput screening techniques  To me this appears very important because if researchers can’t culture Bb, nothing else really matters.

 

  • Team HMK: Nanoparticle and immunotherapy: Paradigm shifting Lyme treatments.  Please be aware that the researchers claim 70% of patients get the EM rash, which is untrue.  It varies from 25-80% and may even be lower than that. Research to date has required patients to test positive on antibody testing that misses over half of all cases and have the EM rash, despite many never getting the rash. They also only mention the Bull’s eye rash when many patients have a variety of rashes. They also push the PTLDS paradigm (post treatment Lyme disease syndrome) but at least present the two opposing viewpoints (hay-wire immune system vs. persistent infection)

 

  • Sour to Sweet: Tick prevention – using pheromone to attract ticks so they can be killed. I appreciate the presenter’s statement that ticks can fall out of trees.  This is denied by most authorities, yet patients commonly report becoming infected this way.

6 Traits to Look For in A Therapist When You Have Chronic Lyme

https://rawlsmd.com/health-articles/6-traits-to-look-for-in-a-therapist-when-you-have-chronic-lyme?

6 Traits to Look for in a Therapist When You Have Chronic Lyme

6 Traits to Look for in a Therapist When You Have Chronic Lyme

by Jenny Lelwica Buttaccio
Posted 1/23/20

There are times when the mental weight of dealing with chronic Lyme diseasebecomes too much to handle. Severe symptoms, mounting medical bills, and social isolation can leave you feeling overwhelmed and discouraged. Talking to friends or family can lighten the mental load, but sometimes, you need the help of trained professionals to cope, implement positive or more productive habits, or provide emotional support.

However, choosing a therapist when you’re chronically ill can be an added challenge. Many mental health professionals aren’t aware of the possible mental and emotional toll of tick-borne infections like Borrelia, Bartonella, Babesia. You need a trust-based relationship with your therapist, and the absence of that can hinder your ability to make progress with the stressful circumstances in your life. So how do you find a professional you can trust?

We reached out to two experts, one therapist with an extensive background in Lyme disease and another who doesn’t have any, to find out what characteristics might be helpful when choosing a mental health professional. Here are the six qualities they recommend you look for.

#1 A Familiarity with Lyme Disease

Sandy Berenbaum, LCSW,, has been working with clients who have Lyme disease for more than 28 years. A Lyme-literate psychotherapist and social worker in Connecticut, Berenbaum has also battled Lyme herself since 1984, but she didn’t receive a proper diagnosis until 1990 — and many of her symptoms were psychiatric.

After her diagnosis, Berenbaum sprang into action and began attending Lyme conferences to learn as much as she could about the illness. Even as a social worker, she was unaware that tick-borne diseases could cause mental health issues like depression and anxiety, bipolar mood disorder, psychosis, and more. “I’d been to about three Lyme conferences when it occurred to me that it could be Lyme that’s causing these symptoms,” she recalls.

group of students walking down college campus steps, sun shining over buildings

Berenbaum recalls the story of a young teenage boy, a former honor student, who had been referred to her practice for psychosis and paranoia in 1991. The teenager was on the brink of being admitted to a psychiatric hospital, but then he disclosed to Berenbaum that he had previously participated in volunteer work at a nature center in a Lyme-endemic part of New York. Berenbaum spoke to his mother about the possibility of a Lyme infection and its connection with mental illness, who took her advice to investigate whether or not Lyme disease could be a contributing factor in the decline of her son’s mental health.

“I recommended a doctor who was very Lyme literate. He started treatment, and it was a rocky road because it was just around the time when the doctors were starting to figure out that there were coinfections,” says Berenbaum. “But he was getting better, and when he went on Babesia treatment, he started getting better faster.” Today that 15-year-old teenager is grown up and has a family and a demanding career as a lawyer.

That experience became the catalyst for Berenbaum to dig deeper into the root cause of why people might present with behavioral problems or other mental health problems. Of course, not every incidence of mental health is caused by Lyme. Still, a sudden onset of symptoms, ones that don’t go away with the usual treatments, or multiple psychiatric diagnosis could indicate exposure to Lyme disease or Lyme coinfections.

“When a therapist doesn’t have familiarity with Lyme, they won’t really understand how tremendously fatiguing the illness is,” says Berenbaum. That could lead to a patient feeling lonely, misunderstood, and unsupported, and they can become soured on therapy at a time when they need it most.

#2 A Willingness to Learn

While it would be great to only work with a Lyme-knowledgeable mental health practitioner, the reality is that not everyone has access to one. Instead, many of us have to use the resources that are within reach for reasons such as insurance reimbursement, the urgency of the matter, or proximity. Fortunately, that doesn’t mean you’re out of luck.

Amanda Stephenson, LCSW, a licensed clinical social worker in Lombard, Illinois, doesn’t have a history of working with clients with acute or chronic Lyme disease, however, she strongly feels that any therapist who’s trying to build a therapeutic rapport would benefit from doing some research when treating someone with the illness. It starts with being open to a new patient’s explanation of Lyme disease, she notes — but that also requires you, the patient, to show up prepared to do some friendly educating.

therapist holding medical chart, discussing it with patient, zoomed in on hands

“I would recommend bringing resources on Lyme to the first session, because any initial session is primarily information gathering and assessment,” Stephenson says. “When patients can provide as much background information as possible, it is helpful to the therapist in understanding their needs.”

Stephenson also suggests explaining your current treatment plan for Lyme and any mental health side effects you might have already identified. For instance, if you’ve noticed you feel depressed or anxious after taking a particular medication or treatment, information about Herxheimer reactions or detoxification strategies could be useful information to share. That way, the therapist can begin to learn how Lyme symptoms can ebb and flow from one day to the next.

#3 Offers a Preliminary Phone Consultation

You’ve probably been through many different kinds of treatments and seen several doctors in the process, so no doubt the idea of relaying an extensive medical historyto someone new who might not be open to hearing it is exhausting. So before you have your first official session, ask about a free phone consultation — the majority of therapists offer them — to get a feel for whether they are a good match for you and your needs.

zoomed in photo on women hands dialing on a cell phone

“I do a half-hour to 45-minute phone intake that I don’t charge for; I want to make sure that it’s a good fit between the person that’s calling and me,” says Berenbaum. “And by good fit I mean, am I going to be able to help this person? And how are they going to know, before they decide to start with me, that there’s a good chance I’m going to be able to help?”

During the phone consultation, Berenbaum gathers some basic information, explains her problem-solving approach to working with patients, and helps them understand that she and the patient work together as a team to define the problems. Typically, phone consults are informal and won’t serve as a therapy session. But it’s a way for you to get a sense for a therapist’s knowledge of Lyme and willingness to learn before investing your time and money.

#4 Sympathy Toward Invisible Illnesses

For most people with Lyme disease, their symptoms and suffering might not show on the exterior, and that invisibility can result in disbelief and skepticism among peers, family members, and the medical community. Indeed, it’s not uncommon for doctors or other healthcare professionals to question whether the illness is real, or if it’s all in a patient’s head.

The ramifications of this doubt can be risky for patients’ well-being. Primarily, they may be less likely to seek help for mental health services at all because they’ve come to mistrust the very systems that offer them. Is there a way through it all?

Blurred portrait of psychiatrist consulting patient, focus on hourglass in foreground

“I think it’s important to voice this concern upfront with the therapist. Exploring previous negative experiences is imperative in establishing a positive therapeutic relationship with any provider,” says Stephenson. “Therapy, particularly from a social work perspective, is supposed to be a helping relationship, so the clients are considered to be equal partners in the process.”

Stephenson adds that it would be helpful to sign a HIPPA release form, allowing the therapist to talk with the medical providers who are involved in your treatment process to gain insights into what you have been through.

#5 Has A Network of Referrals

Sometimes mental health doesn’t improve quickly or significantly enough with therapy alone, and there may come a time when you need a referral to a psychiatrist with prescribing powers. For that reason, when you choose a therapist, it’s beneficial to pick one who has trusted relationships with at least a couple of psychiatrists. You might never take advantage of those relationships, but you don’t want a lack of them to ever become an obstacle to your healing process.

“A lot of Lyme patients can’t find a psychiatrist or a psychiatric nurse practitioner who knows Lyme or will treat them with psychopharmacology,” says Berenbaum.. “I’m not saying psychopharmacology is for everybody, but if you decide you need it, you’ll want to know who to go to,” explains Berenbaum. She has a ready list of psychiatrists she can recommend who she knows are amenable to Lyme patients’ needs and are knowledgeable about the range of treatment options.

#6 A Flexible Cancellation Policy

Sometimes, the unpredictable nature of Lyme is such that you don’t always know how you’re going to feel on the day of an appointment. Due to symptoms beyond your control, you may have to cancel with super-short notice — a move that can cost you a cancellation fee or even the full price of a session at most therapists’ offices.

Because of her familiarity with Lyme, Berenbaum doesn’t charge a cancellation fee of any kind, though she appreciates when a patient can provide her with at least 45 minutes notice. “I have chosen to work with a whole population of sick people, so I think it would be wrong of me to charge for cancellation when you’ve had a bad night or your brain isn’t working well,” she says.

Black woman with a headache, placing a hand on her head while resting on the couch

Berenbaum might seem like a unicorn in this matter, but there are other therapists out there with flexible cancellation policies. For instance, one therapist in Illinois who works with chronically ill patients told us she allows her patients to text a cancellation notice by 7 PM the evening before the scheduled session without a fee. (Most therapists require 24-48 hours or more of advance notice.) Those few additional hours allows patients to see how their symptoms wax and wane and guageif keeping their next-day appointment might be feasible after all.

Of course, it’s important to be respectful of a mental health professional’s time and livelihood, and to consider the other patients who might benefit from your open time slot. But it doesn’t hurt to explain your situation and how your symptoms fluctuate from day-to-day, and to ask about the possibility of a flexible cancellation policy. You might find that some people are more accommodating than others.

Some final words of wisdom: When choosing a therapist, find one you believe can become a source of strength and support for you, as opposed to another source of stress. And if ever you feel invalidated by your therapist, it’s perfectly okay to move on to someone else.

“I believe that my client and I form the beginning of a team,” says Berenbaum. “My first goal is to give the client hope, whether it’s a mother, whether it’s a kid, whether it’s an adult — they need hope.”

Dr. Rawls is a physician who overcame Lyme disease through natural herbal therapy. You can learn more about Lyme disease in Dr. Rawls’ new best selling book, Unlocking Lyme.
You can also learn about Dr. Rawls’ personal journey in overcoming Lyme disease and fibromyalgia in his popular blog post, My Chronic Lyme Journey.

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Excerpt: 

Media outlets recently reported about a 21 year old Ridgefield male who was charged with assault on Friday, November 15.

We have since learned of this man’s plight and offer our apologies for any insensitivity on our part. This 2016 RHS grad has been dealing with the very serious, complicated, and often misunderstood symptoms of Lyme Disease and has been diagnosed with Bartonella and Babesia, both co-infections of the disease. We have also learned that his actions were the direct result of manifestations of this horrific illness. 

Mainstream medicine is still in the Dark Ages and hasn’t a clue about the psychiatric presentations of Lyme/MSIDS.

https://madisonarealymesupportgroup.com/2019/09/17/ignoring-psychiatric-lyme-disease-at-our-peril/

https://madisonarealymesupportgroup.com/2019/08/11/the-unfortunate-connections-between-lyme-disease-mental-illness/

In this claims report, the #1 treatment sought by Lyme patients was psychological care:  https://madisonarealymesupportgroup.com/2019/12/14/trends-and-patterns-in-lyme-disease-an-analysis-of-private-claims-data/

Perthshire Boy’s 11 Year Health Ordeal

https://www.dailyrecord.co.uk/news/local-news/perthshire-boys-11-year-health-21251890

Perthshire boy’s 11 year health ordeal

Son finally returns to classes

By Melanie Bonn 10 JAN 2020

The health problems from Lyme disease have been a nightmare for a teenager like Finlay

A Perthshire mum has revealed the “nightmare” of her teenage son missing over a year of high school because he has been suffering from a condition connected to Lyme disease.

Finlay Trotter (16), from Bankfoot, was all set to play a lead role in Perth Academy’s summer show 19 months ago. But a raft of worrying symptoms doctors could not offer a diagnosis for got the better of him.

With raised glands, reocurring earache and severe pain in his hands and feet, he was unfit to attend school.

Finlay had to drop out of not just the play but all of his studies – and at a crucial time in fourth year. He last went through the school gates in November 2018. Soon after he was diagnosed with Bartonella.

His mum Ruth told the PA: “Just before that, the school had brought it to my attention just how much time Finlay had missed in recent months. They sent an email asking if I realised how often my son was off.

“He wasn’t a kid who messed around, Finlay was serious about his schoolwork.

“He was at the upper end of his classes before he left.”

This week he attempted to go back, with the hope of just getting a couple of subjects under his belt this year.

But this first week of term was not plain sailing, with the teenager needing to return home at lunchtime on Monday, before missing Tuesday altogether.

Finlay’s friends have taken exams in the time he has been away and the promising student now finds himself in the bottom of his maths and English classes when previously he’d been a strong learner.

His mum says since contracting the mystery bacterial infection, it has been “a nightmare for him”.

She says she “honestly doesn’t know about his future”, fearing his life may never be the same.

When things fell apart in November 2018, Finlay’s unexplained pain and tiredness hit his other big interest – street dancing.

He had been part of a squad, achieving countless firsts in competitions performing solo and with friends in his crew, J Squad.

“On what would be his final competition, just before going on with his crew, Finlay told me he couldn’t move his fingers,he said they were agony,” Ruth recalled.

“It was quite scary, he said he was feeling awful, but he pushed through the competition. That would be the last time he danced.

“My youngest son went from dancing four or five hours a week to not being able to get out of bed.”

Since Finlay stopped dancing, the street dance crew has disbanded.

Ruth explained how a walk in the country was the root of her family’s ordeal with Bartonella, a ‘co-infection’ of Lyme disease.

“Eleven years ago in 2008, Finlay was out with me on a walk with his two older brothers. When we got home he had 13 ticks buried in his skin. The other boys didn’t have one. I’m convinced that’s when he got infected.

“There is false information going around that ticks need to be attached for 24 hours to pass on bacteria. But they literally just need to be attached, they then bring up the contents of their stomach then wait for fresh blood.

“Whilst not all ticks are deemed to have infections, approximately five per cent do. Three months after that day he got the bites, oval lumps had appeared on his legs. Finlay was ill and we took him to hospital to get tests for leukaemia and cancer.

“I now believe this was the start of his Lyme disease. He was diagnosed with Henoch-Schonlein purpura (HSP), a condition that would mean his immune system was over-fighting an infection. We were sent home with the view he would improve with time.

“It took a frustratingly long time to get the correct diagnosis. At the age of eight he started having hot feet which kept him awake at night.

“After lots of tests through the NHS, the doctor said he’d just have to put up with it as they couldn’t find anything wrong.

“They admitted it was very unusual for a child to have this.

“He had various symptoms over the years, stomach aches, reoccurring ear infections but we became really concerned in November 2018.

“Finlay’s joints were agony, he had stomach aches, earache and swollen glands. They could tell something was a miss by his bloods. Nerve tests proved inconclusive.

“He had scans, saw rheumatology, and was tested four times for Lyme.

“Previously three tests for it came back negative. The GP wasn’t going to get him referred because the tests had said no to Lymes.

“In the UK, the Lyme disease test on the NHS is only approximately 60 per cent correct.

“The infectious diseases clinic in Dundee never even saw him. They just wrote back saying no, they didn’t believe he has Lyme disease. That made me really angry, not to even meet my son.

“So many people report the same thing, that Lyme disease wasn’t picked up and the vital time window to treat it and stop the other stuff that follows was missed.

“The NHS doctor suggested he might have ME or fibromyalgia but, as his mum, I wasn’t convinced as he had so many symptoms.

“It was soul destroying as a parent. If you don’t know exactly what you are dealing with, how can you treat it?

“In January 2019 stretch marks started to appear on his lower back and arms. These marks continued to get worse and more angry-looking, changing on a daily basis.

“I finally read up on something called Bartonella. And that’s what it is.

“The Bartonella henselae bacteria can lead to hot feet, stretch marks and joint pain.

“It’s a bacterial infection usually picked up from a scratch from a cat, but also from a tick bite. It’s known as a ‘coinfection’ of Lyme disease.

“Finlay has Bartonella. He got his diagnosis last April from Armin Labs in Germany.

“Finlay has made improvements lately that have made it possible to reconsider school, but that was only after Annette Montague-Thomas, an alternative therapist who had treated AIDS in South Africa, saw him.

“She’s been absolutely phenomenal. Since Finlay has been on her herbal treatment, he has steadily been getting better.

“Chillingly, Annette said she’d found it easier to treat people with the AIDS virus that those with Lyme’s.

“He’s not out of the woods yet, but there’s been a massive improvement. He has been undergoing biomagnetic therapy which has definitely helped as well.”

Explaining her reasons for sharing Finlay’s story, Ruth said “I’m looking to help spread awareness of Lyme disease.

“The NHS do an amazing job overall, but I believe they need to be a lot more hot on this, they need to take this problem more seriously.

“In February we welcome Lyme Disease GNHCT Scotland to Perth, to help people all over Scotland with Lyme disease.

“They have also found a Lyme link too in people with autism.

“More investigating needs to be done but the results so far are very encouraging.”

The stretch marks on Finlay’s arm are a sign of the Bartonella infection
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**Comment**
Believe it or not authorities are still quibbling over whether ticks can even transmit Bartonella or not.
In my experience, Bartonella is even harder to treat than Lyme disease and that’s saying something.  More and more is coming out on Bartonella’s ability to cause so many different symptoms and yet mainstream medicine doesn’t even have it on their radar, despite many Lyme patients being coinfected with Lyme and Bartonella and even other pathogens.
While this young man was fortunate to have the tell-tale marks on his skin, many are not so lucky and the only way to get diagnosed is due to symptomology.  Testing for Bartonella is just as abysmal as testing for Lyme and many patients fall through the cracks.
For more:  https://madisonarealymesupportgroup.com/2016/01/03/bartonella-treatment/  Besides explaining the pathogen and treatment options, this link has a checklist for you to print out and fill out.  Take this with you to your doctor appointment and be aware of Bartonella symptoms.