Archive for the ‘Treatment’ Category

From Cat Scratch Disease to Bartonellosis

https://www.galaxydx.com/new-educational-resource-on-human-bartonella-infections/

From Cat Scratch Disease to Bartonellosis

Bartonellosis is a term used to encompass all infections caused by pathogenic Bartonella species. Bartonella are emerging, flea-borne bacteria that are highly adapted to living in mammalian hosts and are implicated in a wide spectrum of diseases in humans and animals.

The Parasite Guy Podcast

A Conversation With the Parasite Guy, Dr. Todd Watts

Todd-Watts

Cindy Kennedy, FNP, is joined by Dr. Todd Watts, a chiropractor and functional wellness practitioner from Idaho. Many know him as the “Parasite Guy,” but he also has extensive knowledge of functional blood chemistry, biochemistry and in helping those with chronic illness overcome their struggles to restore their health.

Dr. Watts is the co-founder of Microbe Formulas and CellCore Biosciences and loves to research to formulate products which will change the world.

Dr. Watts was the first to bring Mimosa Pudica seed to the general health market in the United States. He has an amazing health journey which has led him to be able to help others.

 Approx. 17 Min.

Dr. Watts’ Story
Dr. Watts had both Lyme and parasites.

https://drtoddwatts.com

For more:  https://madisonarealymesupportgroup.com/2017/10/03/removing-parasites-to-fix-lyme-chronic-illnesses-dr-jay-davidson/

 

Mother’s Appeal After Boy Diagnosed With Autism When He Just Needed Antibiotics

https://www.bbc.com/news/uk-scotland-edinburgh-east-fife-46989099

Mother’s appeal after boy diagnosed with autism when he just needed antibiotics

25 January 2019

‘Overnight, something went very wrong’

https://www.bbc.com/news/uk-scotland-edinburgh-east-fife-46989099  (News Video in Link)

A mother is calling for greater awareness of a little-known condition she believes changed her easy-going son overnight.

Alison Maclaine fears some children are being misdiagnosed with autism and mental health issues when they are really suffering an infection which can be treated simply with antibiotics.

Her eight-year-old son Jack suffered distressing personality changes and “lost a year of his life”.

And she said she was left “in despair” that she and her family had “no quality of life”.

Now Alison believes he was suffering from Paediatric Acute-onset Neuropsychiatric Syndrome (PANDAS), triggered by a streptococcal infection – a condition that can be treated with simple antibiotics and anti-inflammatories.

Something wrong

Jack went to bed one Friday in January last year, looking forward to a football tournament he was playing in the next day.

But on arrival at the venue on Saturday morning he became overwhelmed with anxiety. After several attempts, he was unable to enter the building.

At home in Dumfries, Alison realised something was very wrong.

She told the BBC: “He started to repeatedly apologise. He said he didn’t deserve to have fun, didn’t deserve to have friends, didn’t deserve to have nice things, didn’t deserve to play football.

Alison Maclaine
Alison Maclaine knew her son’s diagnosis was not right and did her own research into his symptoms

“That eventually led to ‘I don’t deserve to live, when I get home I am just going to sit outside until I freeze to death’.”

When it came to bedtime, Jack refused to have covers and pillows and started to repeat that he needed to die, until he fell asleep.

The following day saw his behaviour sink further.

Alison said: “One of the worst things in the world must be listening to your child telling you he wanted to die and asking you to help him.”


What is PANS/PANDAS?

According to the charity PANS PANDAS UK, PANS (Paediatric Acute-onset Neuropsychiatric Syndrome) is a neuropsychiatric condition which is triggered by a misdirected immune response which results in an inflammation of a child’s brain.

PANDAS is a subset of PANS, triggered by a misdirected immune response to a streptococcal infection which results in an inflammation of a child’s brain.

Happening very quickly, this can cause a child to exhibit symptoms including anxiety, aggressive behaviour, depression, clumsiness, insomnia and the onset of obsessive-compulsive disorder.

It was first recognised in the United States in 1998 where PANS PANDAS charities estimate as many as one in 200 children could be affected.

In 2018, the World Health Organisation recognised the condition, but in the UK it is not widely known.

There is no clear test for the condition so doctors often have to rule out psychiatric conditions. The immediate response to antibiotic or anti-inflammatory treatment is often what confirms the condition.

The charity PANS PANDAS UK said a failure to understand the condition in the UK means that children are regularly wrongly referred to Child and Adolescent Mental Health Services (CAMHS).


‘Absolute despair’

Jack then became aggressive and withdrew from his beloved younger sister Cara. He would become irritable and angry and started to regress, playing with baby toys.

Over the next several months he was repeatedly diagnosed as having autism and severe anxiety.

But Alison, herself a psychiatrist, disagreed.

She said: “It got to the point where I really felt absolute despair.

“I felt that he had no quality of life, we had no quality of life. There were times when I contemplated things.”

Jack Maclaine
His family feels that Jack is “back”

That despair led to Alison doing her own research and the discovery of PANS and PANDAS.

Alison said reading the symptoms was like reading a description of her son and his behavioural changes.

Jack was finally diagnosed privately by a consultant paediatrician in England and treated with simple antibiotics.

They worked overnight and Alison had her son back.

She said: “Jack responded dramatically to the treatment. He hadn’t left the street in five months except for school. After two days on antibiotics he wanted to come to Morrisons with me and Cara. It felt like Jack was back.”

Dr Tim Ubhi

Dr. Tim Ubhi finally diagnosed PANDAS in Jack

 

Alison is frustrated now, believing if Jack had been given got antibiotics when he first presented to the GP in January, the outcome would have been different.

She said: “It is so frustrating knowing the treatment was so simple. Now I hate to think there are other children in the situation that they have this disorder that has not been picked up on and have been sent down a mental health/psychological route which can’t fix the problem.”

Dr Tim Ubhi, who diagnosed Jack’s condition, said: “The problem here is if we do not recognise this condition and we ignore it, potentially there are children out there who are suffering who could actually get treated and actually improve their symptoms.

“So we have a responsibility as physicians to think about this as a condition and do the work to actually create an awareness of what the condition is doing in the UK.”

A Scottish government spokeswoman said: “We appreciate that watching any loved one suffer is heartbreaking, even more so when it is a child.

“We are working together with partners to improve the outcomes and support for adults and children with rare conditions, and ensure that everyone receives the appropriate treatment.

“Ministers are unable to make or influence clinical decisions or definitions, and it would not be appropriate for them to do so.”

If you, or someone you know, have been affected by mental health issues, these organisations may be able to help.

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**Comment**

These stories are repeated over and over worldwide.  Time for doctors to get on board and learn about it so they can recognize and treat this.

Please take note of the plethora of symptoms and the tandem workings of PANDAS/PANS with Lyme/MSIDS. A highly respected LLMD here in Wisconsin has found that 80% of his PANS kids also have Lyme/MSIDS (borrelia and other coinfections).  

For more:  https://madisonarealymesupportgroup.com/2018/07/28/stories-of-pandas/

https://madisonarealymesupportgroup.com/2018/01/05/scary-side-of-childhood-strep/

https://madisonarealymesupportgroup.com/2019/01/27/pans-pandas-autoimmune-encephalitis-rickert-hong/

https://madisonarealymesupportgroup.com/2017/06/30/child-with-lymemsidspans-told-by-doctors-she-made-it-all-up/

https://madisonarealymesupportgroup.com/2018/12/17/my-kid-is-not-crazy-study-shows-1-3-kids-with-pans-have-hallucinations/

Vaccines can also be triggers:  https://madisonarealymesupportgroup.com/2017/09/21/aluminum-flawed-assumptions-fueling-autoimmune-disease-and-lyme/

https://madisonarealymesupportgroup.com/2017/12/02/scottish-doctor-gives-insight-on-lyme-msids/  He has also successfully treated a number of young women who fell ill after their HPV vaccination, which seems to have stimulated a latent Lyme infection to reactivate.

https://madisonarealymesupportgroup.com/2016/04/24/gardasil-and-bartonella/  Asymptomatic girls after receiving Gardasil activated dormant Bartonella which was confirmed by testing.

 

 

Erratic Eye Jerks in Child with Lyme

https://www.ncbi.nlm.nih.gov/pubmed/30655046

2019 Jan 14. pii: S0929-693X(18)30263-X. doi: 10.1016/j.arcped.2018.11.013. [Epub ahead of print]

Opsoclonus in a child with neuroborreliosis: Case report and review of the literature.

Abstract

Opsoclonus consists of massive erratic rapid eye jerks. They may occur in isolation or in association with myoclonus and ataxia, i.e., opsoclonus-myoclonus syndrome (OMS). We report the case of a 9-year-old girl who suffered from headaches for several days and was shown to have opsoclonus and left peripheral facial palsy. Work-up excluded the diagnosis of neuroblastoma, but CSF analysis showed aseptic meningitis, and serology for Borrelia burgdorferi (Lyme) was positive. The outcome was favorable with complete regression of symptoms after treatment with ceftriaxone 2g/day for 3 weeks. Although rare, the diagnosis of Lyme neuroborreliosis must be raised in the presence of isolated opsoclonus, particularly if the clinical picture is incomplete and if other features, such as peripheral facial palsy and pleocytosis in the CSF, are present.

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**Comment**

To see what Opsoclonus looks like:

Again, researchers shouldn’t be writing that this manifestation is “rare,” because nobody’s truly keeping track of this.  For decades folks have been undiagnosed due to horrifically abysmal testing that misses half of all cases.  

Facial palsy and aseptic meningitis are huge clues for Lyme

Aseptic meningitis is when the lining of the brain becomes inflamed.  In this case, due to a Borrelia burgdorferi (Bb) infection.  This explains the headaches.

577px-Brain_and_Nearby_StructuresBy Alan Hoofring  https://visualsonline.cancer.gov/details.cfm?imageid=4279, Public Domain, https://commons.wikimedia.org/w/index.php?curid=34938301

As the picture shows, the meninges cover the entire brain so the headache caused by this is going to cover the entire head.  This is what I personally had that took years of antibiotics to rid.  I wondered if there would ever be a day without this type of headache.

I’ve spoken with many Lyme/MSIDS patients who have had exactly the same thing.  It is not rare.  The pain is unbelievable, and ONLY treatment took it away.  Ibuprophen will not touch this Mother one little bit.  CBD, systemic enzymes, NOTHING will touch this if you have a Bb infection.  The infection must be dealt with first.

For those of you with this presentation, please also consider Chiari, especially if you’ve had this type of headache for some time:  https://madisonarealymesupportgroup.com/2016/04/02/chiari/  Within a week I met numerous Lyme/MSIDS patients with a Chiari diagnosis.

Lyme/MSIDS can cause numerous other eye issues:

https://madisonarealymesupportgroup.com/2017/07/21/growing-list-of-eye-problems-in-lyme-disease/  The authors described patients with tick-transmitted diseases presenting with the following ophthalmologic findings:

  • Follicular conjunctivitis
  • Periorbital edema and mild photophobia
  • Bell’s palsy, cranial nerve palsies and Horner syndrome
  • Argyll Robertson pupil
  • Keratitis
  • Optic neuritis, papilledema, papillitis and neuroretinitis
  • Myositis of extraocular muscles and dacryoadenitis
  • Episcleritis, anterior and posterior scleritis
  • Anterior, intermediate, posterior and panuveitis
  • Retinal vasculitis, cotton wool spots and choroiditis
  • Retinitis, macular edema and endophthalmitis
Now add Opsoclonus to this growing list

https://madisonarealymesupportgroup.com/2015/09/16/bizarre-symptoms-msids/

https://madisonarealymesupportgroup.com/2018/08/08/dr-jay-davidson-video-on-nematodes-in-the-eye/

 

 

 

 

Nova Scotia’s Top Doctor Takes Heat Over Retweet Dismissing Chronic Lyme Disease

https://www.thechronicleherald.ca/news/local/strang-retweet-raises-ire-of-sufferers-279636/

Nova Scotia’s top doctor takes heat over retweet dismissing chronic Lyme disease

Dr. Robert Strang, Nova Scotia’s chief medical officer of health, retweeted a tweet that called into question the existence of chronic Lyme disease.
Dr. Robert Strang, Nova Scotia’s chief medical officer of health, retweeted a tweet that called into question the existence of chronic Lyme disease. – Contributed

HALIFAX, N.S. – A recent retweet by the province’s top doctor dismissing chronic Lyme disease as a condition based on pseudoscience and supported by a chronic Lyme cult, is being met with sharp criticism by one of Canada’s top tick experts.

“There are a lot of people who are sick and belittling them publicly is trivializing their illness and their suffering, so it’s deeply unfortunate given all of the science work and medical work that needs to be done around Lyme disease,” said Vett Lloyd, a biology professor at Mount Allison University. She also leads the university’s Lyme Research Network. “Chronic Lyme disease is not a cult. It’s not a myth.”

On Wednesday, Dr. Robert Strang, the province’s chief medical officer of health, retweeted the anonymous tweet from an account named LymeScience.

“As a former victim of the chronic Lyme cult, I feel it’s pretty important that they stop controlling the narrative around Lyme disease with their pseudoscience and misinformation,” read the opening line of the tweet.

“They’ve been called a threat to public health for good reason. But it would help to remember not everyone who falls for it is an idiot. The cult is well-funded and only growing. I’d hope most people can see more needs to be done to stop this anti-science movement.”

The Twitter account is linked to the website LymeScience.org, which offers a slew of information attempting to debunk chronic Lyme disease. But the website is not affiliated to any particular person or group.

The Chronicle Herald attempted to reach Strang to find out his motivation behind the retweet, but he declined comment.

Besides calling the statements false and inflammatory, Lloyd also said she was confused by the tweet because chronic Lyme has a couple of different meanings. She says chronic Lyme could refer to advanced untreated cases of Lyme disease or cases of the illness where the bacteria persists after treatment and the person still has infection symptoms. It’s more likely that Strang’s retweet is taking aim at the latter category, says Lloyd.

Strang told the Herald last September that the standard short-term antibiotic treatment for Lyme in the province is effective. He declined to say chronic Lyme exists and that bacteria could persist after a short course of antibiotics. But he said in some cases people have residual symptoms after being treated.

Lloyd, a Lyme disease survivor, says there’s ample evidence showing chronic Lyme is real and that short-term antibiotic treatment doesn’t always work. Lloyd was forced to travel to the U.S. to seek long-term antibiotic treatment after her standard treatment at home failed to work.

“There’s quite a bit evidence that you can have bacterial persistence after short-term treatment. My experience was that the standard treatment was not enough to return me to health.

“I required longer-term treatment to recover my health outside of Canada. I spent many years in Canada being diagnosed with everything under the sun and getting sicker and sicker but when I was treated for Lyme disease in the U.S. I got better in short order.”

She says Strang should be working to bring people on both sides of the chronic Lyme debate together instead of furthering the divide by resorting to name-calling.

Dr. Richard Dubocq, a Maine-based doctor currently treating 140 Lyme patients from Canada with long-term antibiotics, says about half of his Lyme patients live in Nova Scotia. Like Lloyd, he says he was shocked by Strang’s retweet, calling it irresponsible and an attempt to raise fear and paranoia.

“I’m just surprised that he’s allowed to send this out on the airwaves because on so many different levels it delivers false information,” said Dubocq.

Dubocq follows treatment guidelines set down by the International Lyme and Associated Diseases Society (ILADS). But those guidelines that recommend long-term antibiotic treatment in chronic or persistent cases of Lyme are not widely accepted by the North American medical community. Mainstream doctors, including in Nova Scotia, follow the standard Infectious Diseases Society of America (IDSA) guidelines for the treatment of Lyme.

Donna Lugar, the Nova Scotia representative for the advocacy group the Canadian Lyme Disease Foundation, says hundreds, if not thousands, of people are struggling in Nova Scotia with a tick-borne disease.
Donna Lugar, the Nova Scotia representative for the advocacy group the Canadian Lyme Disease Foundation, says hundreds, if not thousands, of people are struggling in Nova Scotia with a tick-borne disease.

But in recent years several U.S. states have passed doctor-protection laws that fall in line with ILADS guidelines, allowing physicians to treat Lyme more aggressively with longer-term antibiotics. No such laws exist in Canada.

“I recently attended the 19th annual ILADS conference in Chicago attended by over 1,000 health-care providers from around the word,” said Dubocq. “The quality of data was impeccable.”

Health Minister Randy Delorey would not make himself available for an interview but in an email statement said people should consult the department’s official Twitter account for information about Lyme disease. He did not weigh in on Strang’s retweet or offer his stance on chronic Lyme disease.

“The department reminds Nova Scotians that our clinical guidelines for the testing and treatment of Lyme disease are evidence-based and derived from national clinical guidelines,” said Delorey.

Donna Lugar, the Nova Scotia representative for the advocacy group the Canadian Lyme Disease Foundation, said Strang’s retweet is inexcusable.

“Hundreds, if not thousands, of people are struggling in this province with a chronic illness,” said Lugar. “What are we ill with, if not Lyme and/or other tick-borne diseases? Are we all mentally ill, as some doctors would suggest?”

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For more:  https://madisonarealymesupportgroup.com/2018/04/17/persistent-borrelia-infection-in-patients-with-ongoing-symptoms-of-lyme-disease/  Conclusions: Using multiple corroborative detection methods, we showed that patients with persistent Lyme disease symptoms may have ongoing spirochetal infection despite antibiotic treatment, similar to findings in non-human primates. The optimal treatment for persistent Borrelia infection remains to be determined.

https://madisonarealymesupportgroup.com/2019/01/16/study-shows-diminished-pathogen-specific-antibody-production-in-coinfected-mice-contributing-to-persistent-infection/

https://madisonarealymesupportgroup.com/2018/10/30/study-shows-lyme-msids-patients-infected-with-many-pathogens-and-explains-why-we-are-so-sick/  For the first time, Garg et al. show a 85% probability for multiple infectionsincluding not only tick-borne pathogens but also opportunistic microbes such as EBV and other viruses….In addition to tick-borne co-infections and non-tick-borne opportunistic infections, pleomorphic Borrelia persistent forms may induce distinct immune responses in patients by having different antigenic properties compared to typical spirochetes32,33,34,35. Nonetheless, current LD diagnostic tools do not include Borrelia persistent forms, tick-borne co-infections, and non-tick-borne opportunistic infections.

http://norvect.no/230-peer-reviewed-studies-show-evidence-of-persistent-lyme-disease/

http://lymerick.net/persistent-borreliosis.htm  Microscopy, Culture or PCR-verified cases of persistent [seronegative] Lyme Borreliosis

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

https://madisonarealymesupportgroup.com/2018/07/23/exploring-the-controversial-concept-of-chronic-lyme-disease/