is Morgellons a new mutation of Lyme Disease?
I still feel there is a strong link between Lyme’s Disease and Morgellons. I have been reading stuff on Lyme’s in Australia. I have been caught up today going from site to site reading about Lyme Disease, ticks and more …
[http://medent.usyd.edu.au/fact/lyme%20disease.htm#conclu]
‘Conclusions – Australia
There are some major differences between Australia and the endemic areas of the northern hemisphere with respect to the natural history of LD:
No ticks of the I. persulcatus complex, the principal vectors to humans in the northern hemisphere, occur in Australia. In eastern Australia, the logical candidate vector would be I. holocyclus which has a wide host range and is the most common tick biting humans. It was unable to transmit a North American strain of B.burgdorferi but an association with a so far undiscovered Australian spirochaete can not be excluded.
None of the mammal species identified as reservoir hosts in the northern hemisphere are present in Australia. There are reports of spirochaetes in Australian native animals, and a local mammal could be a reservoir host for an indigenous spirochaete that occasionally infects humans through a tick vector and produces a clinical syndrome similar to LD; however, no spirochaete was detected in the 12,000 ticks or animals processed.
The diagnosis of LD outside known endemic areas cannot be based solely on serological tests especially if they fail to conform with internationally accepted criteria, because of the high incidence of false positive results.
A clinical diagnosis in a non-endemic disease area (especially of Stage II or III disease), is difficult to support without isolation of the causative agent from the patient, from other patients with similar illness or from a known vector in the region.
The existence of LD in Australia will remain controversial until an organism is isolated from a local patient and fully characterised, or until a tick-borne organism can be shown to be responsible for the human infection. If it exists it shares few of the epidemiological or clinical characteristics of US or European patterns of LD.’
Ability to transmit diseases (vector competence) [from http://www.tickalert.org.au/ixholdet.htm]
In general terms a vector may simply mechanically transport a pathogen without it replicating, or it may both transmit and replicate a pathogen. Many viruses, bacteria, rickettsia and protozoal organisms are capable of replicating within ticks. This is known as “biological” transmission and this mode of transmission is the one that applies most commonly to ticks.
For hard (Ixodid) ticks it is virtually impossible for mechanical transmission to occur on its own (i.e. without some replication), as they tend to not take multiple blood meals from different hosts in the one stage. Passing an organism between tick stages (trans-stadial transmission) seemingly requires that an organism can also replicate within the host.
In the case of Ixodes holocyclus there is much speculation about transmission of various pathogens, with the exception of the spotted fevers which are now well recognised. Saying that an arthropod is a competent vector (generally) requires several findings:
(1) frequent isolation of the suspected pathogen;
(2) showing that the distribution of the suspected vector overlaps with a diseased population (be it human or animal);
(3) showing that host-seeking and blood-feeding coincide with the disease incidence;
(4) showing that disease incidence varies with host choice; and
(5) showing the capacity for vector competence in the laboratory.
Bacterial Diseases – Rickettsiae
These days there is not much disputing that I. holocyclus is the main vector for R. australis (Rickettsial Spotted Fever). Unfortunately vector competence work is still required to confirm its status. (S. Doggett pers. com.).
Despite the lack of vector competence studies, the paralysis tick (I. holocyclus) is commonly mentioned as a potential vector of Q-fever (caused by the rickettsial organism Coxiella burnetii). The ornate kangaroo/wallaby ticks Amblyomma triguttatum s.l. have also been implicated in Q-fever (Russell and Doggett, 1995).
Spirochaetes
Some vector competence studies have been undertaken on I. holocyclus with respect to the Lyme disease pathogen Borrelia burgdorferi sensu stricto (with a United States strain). These suggested that the tick can not transmit this strain of spirochaete (Piesman and Stone, 1991).
Despite this, there is a strong belief that some kind of Lyme-like spirochaete causes a Lyme-like disease in Australia and that it is carried by the most common tick afflicting humans, Ixodes holocyclus. At the Royal North Shore Hospital in Sydney the Tick-borne Diseases Research Unit continues its study into this issue.
Cases of Lyme-like disease are being diagnosed on the basis of clinical signs (often musculoskeletal, chronic fatigue, neurological and dermatological), exclusion of other infections, serology (which is supportive but not conclusive), and response to antibiotic treatment (initially, antibiotics may cause a worsening of symptoms [the Herxheimer reaction], presumably as spirochaetes are destroyed, and this in part supports the diagnosis).
The Australian form of Lyme-like borreliosis is associated with a different clinical picture from true Lyme disease of North America. See also the Westmead Hospital Dept of Medical Entomology site for their interpretation on the status of an Australian Lyme-like Disease.
For comparison with North American Lyme borreliosis go to healthlinks.washington.edu.
Viral Diseases
So far, no viruses have been isolated from I. holocyclus (Russell and Doggett, 1995). This does not however exclude the possibility that such diseases may be found in the future.
Protozoal Diseases
So far no protozoa have been isolated from I. holocyclus. This does not however exclude the possibility that such organisms may be found in the future.
Morgellons Attacks Teenagers Too;
Danny Shares His Story of How He Got His Life Back
Dear fellow Morgellons victims,
I’m writing on behalf of all the young people and the elderly with Morgellons who have been shunned, criticized, and outcasted by society thinking we suffers of this horrible disease are crazy. I personally knew absolutely nothing about this disease until I came home from school one day of September 2007 and noticed granule-like crystals on my hands. I also noticed clear fibers that appeared to be coming out of my hands as well. I went to the computer and typed in “black crystals on hands?” or something to that extent. I stumbled upon a few websites that had details of Morgellons symptoms and the blue, black, clear, and red fibers with granules coming out of hands, body, and or hair. I didn’t automatically assume I have this disease after a couple months of thorough personal research I had whatever this bizarre disease was. Every single symptom I had matched everything I read. I had everything from the physical identification of Morgellons right down to all the mental and cognitive disorders of Morgellons; brain fog, I slept constantly, depression, insomnia at night (slept all through the days), lost a lot of weight, everything aliment you could imagine I had. But by far the worst symptoms was the anxiety that would come out of nowhere, it literally felt like I was even in my body at times.
It began to slowly but surely rule my life. I noticed the fibers everywhere in my home, friend’s homes, family member’s homes, these fibers were everywhere but I was one of the only that had symptoms to this extent. My friends and family had the fibers on there body and hair as well. My friends were the only ones who believed me about the fibers and knew I was sick. I tried to express to my mother and stepfather what was going on but surely my mother thought I was loosing my mind which I can completely understand because of how bizarre this disease sounds to the layman. Finally after convincing my mom I had this disease I stumbled upon a website called “NutraSilver”. My mother personally thought I was crazy but my stepfather said “whether its in his head or not we can see if this helps”
So my stepdad bought a bottle of NutraSilver and it came with another for free. The first night I tried the NutraSilver I had to lie down in bed with my mother I trembled so bad. When I woke up the next morning I felt slightly better. I started to use the NutraSilver a couple times a day and just put some drops in my daily routine of drinking water. Everyday progressively got better, I started to forget completely about Morgellons and live my life. It ruled my life, I am an 18 year old male (at the time I was 17). I also stumbled across an amazing doctor and friend named Dr. Susan Kolb. I found her website when I was researching about Morgellons and even though I lived many states away and was very embarrassed I deciding to just call her and tell her what was going on. She talked to my parents, talked to my family and tried to express to them that this is a real disease. Still after all of that they still did not believe. She gave me great tips to get slowly but surely better as well. I slowly started being able to go to school more and focus more on my life. Everyday with NutraSilver and Dr. Kolb’s advice made everyday easier to get through. As last summer came along (2008), I was very confident I was Morgellons-free. I completely forgot about the disease and was able to live my life.
I moved into a new home, had a new life ahead of me and I felt like my life was finally back, unfortunately I ran out of NutraSilver around September of 2008 and was unable to purchase it again with the lack of my finances. I stopped using it all together. Around November or December my symptoms started coming back fully. I had brain fog again, depression, anxiety, fatigue; the fibers were coming out of my skin again. I was once again infected. They were around my new home and in my hair and body once again. I talked to Doctor Kolb at least once a month to keep her updated. With her help I personally discovered some things that helped in the mean time until I could get another credit card to purchase NutraSilver once more. My symptoms got so bad living at my new home I finally ended up moving back into my mother’s house where I first discovered I had Morgellons. I still felt horrible, I discovered something called Trilogy Cardio Essentials in my fridge that mom used to lower her blood pressure and things of that nature. It was recommended by someone who also used silver on a daily basis that ran a herbal store down the street from me. So I took a couple swigs every day unknowing the effect it would have on me. The next day I glanced at my hands after I was out of the shower. I noticed the fibers purging out like I had seen with NutraSilver; it was very scary.
I am still drinking it and it helps just as NutraSilver has. I have used many things to help with this horrific disease but I can honestly say NutraSilver, Dr. Bronners, and Trilogy Cardio Essentials has helped the most by far.
I’m sick of people ignoring this disease; even doctors are ignoring it. I know there are so many people that are struggling with this disease everyday, and I truly desire for them to live their life and again and take back what’s rightfully theirs.
My life is finally coming into view again, and I literally owe my life to a man named Russell at NutraSilver and a wonder Doctor by the name of Susan Kolb. I have never met a person so dedicated to seeing their patients or customers get better than Dr. Kolb
Without their help, guidance, and advice I’m not too sure how long I could have held out with all the depression and anxiety.
My final advice to any man, women or child with Morgellons is get NutraSilver, have a positive mind-set and lives your life again; I don’t want anyone to go through what I have been through with anxiety and depression.
Sincerely,
Daniel W.
I will list my personal protocol for Morgellons;
NutraSilver
Dr. Bronners Lemon Castile Soap ( you can use it for toothpaste, hair, body, lotion anything you can think of even laundry)
Acai berry
flaxseeds
Borax laundry detergent.
Air Filter
Trilogy Cardio Essentials.
careman - April 22, 2009 at 23:17
I just don’t have the energy nor the finances to follow such a regime … but we do what we can
pixiemb - January 17, 2010 at 22:02
hello,
does any one know if joel did his story for the abc.
my wife & i hav e had this desease for 7 years of hell.
we could write a book on it. the stages , changes, cycles,
effects on the body & inviroment. the fibres, hair like things,
glitters & black specs, that come out of our bodies
the dust & tiny dandruff like flakes that come shed constantly
from our bodies & it is nearly impossible to be rid of it.
and unfortunately. researchers are going down the wrong path.
it is not a fungus, although the fungus can co habbit with these things.
we saw the adult stage of these things, back when we first contracted it.
they are like a tiny strait stick. or a 2mm fine hair, tan to black in colour,
with a slightly darker head, imagine a really tiny burnt matchstick.
these things move by flicking, if they land on you or your cloths or
even through your shoes, they will penetrate right through a shoe,
into your foot. i saw 1 go into my hand, they just seem to melt into
your skin, within a second, & they are in,
& not as 1 st reported.. it is not just a irratating skin condition &
harmless, adults once in you burrow deep & settle along or in the bones
& dont ever leave,
all the things that come of us, is different stages of there life cycle,
that keep being produced coming out & reinfecting ourselfs & others.
by ingestestion, breathed in, or semi adult. burrow in through the skin
without you feeling it. but happening constantly
over time the more they reproduce, the more you get infected, & overun.
the immune system gets compremised,
then comes fatiuge, aches, pains. joints sieze up. fevers, itching,
crawling feelings restlessness, depression, brain fog.
they are not just a nusance. or a skin desease
they eat cartlidge, destroy joints, eat away flesh under the skin
leaving big suncken old briuse type scares on your body. maily legs & arms
they block small veins & capilaries. & take over areas of your body, buid
up thick layers of skin, holes they make show up as freckles or small moles
they get into the head, cause head aches, tooth aches, ear aches, even
borrow into & out of the eye ball.
into the jaw bone, gums, & live in your tounge, they are a horrid evil curse
they are found and thrive in meat, especially meat on bone
there are stages that are mpossible to kill, or get rid off.
i could go on & on but i wont. im sure the do have a uniquice spiratite associated with them, like the one associated with syphalis, which also burrows in & eats cartledge and destoys joints & eventually disfigures & leaves one crippled.
p.s you hardly feel them go in.. when you feel a sharp prick, check the area, thats them comming out. normally white tiny balls, which if you check is a tiny mass of 100s of dust size minuture fibres. when they fall off you. those tiny balls eventually break up & get air born by even the breeze you make walking. & settles with the dust. or stuck in your clothes, eventually back in you or others
around you
givait - November 10, 2011 at 00:42
hi
yes Joel did the piece and you can possibly still read the transcript or listen at abc.net – radio national – health report. It was quite good.
we too have endured life for 7+ years now. we use a lot of natural stuff eg lemon myrtle soap & shampoo. we are lucky to live in the bush and thus away from most pollutants. we agree if a fungus is involved then it is some symbiotic link and that it is actually an insect. the spring is amazing thing to see! I have only very mild infection which only flares when I am overly stressed or fatigued. Peter still has legs that have the lower parts covered in lesions, a few on his head, arms and shoulders. He is positive that this has to be in the brain as it clearly attaches to the blood source; just like a tick!
hard to eat and hard to cook for such; both of our eyesight has deteriorated drastically; Peter is covered in white spots. Note: I was told this early on that this was common in Sydney around 20 years ago (now closer to 30 years ago) and is called Sydney White Spot! In Queensland it is called ‘Forester’s Itch’. These stories only reinforce my believe that this is a morph of Lyme’s which by the way according to the Australian Dept of Health does not exist in Australia !! morons. we have a local apothecary that make a homoeopathic tincture from the local ticks which works amazingly on the poisonous reaction.
it is all we can do and endure and strive to make the most of our lives while we live with this disease. I hope you have friend support for both of you 
Yes most definitely I believe it is just natural mutation of ticks just as we see with mosquitoes as new defences are developed. Less chemicals improves the impact so we do not take any chemical medications; the disease just feeds on them! Peter has now lost all his teeth and is waiting for lower dentures
The brain fog still sucks; the rest we just deal with and try to ignore.
keep sane givait
peace & happiness
pixiemb - November 13, 2011 at 14:13
Delusions of Delusions of Parasitosis (DDOP)
Mr. Common Sense | July 1, 2011 at 8:52 am
This MD believes he can make a psychiatric diagnosis; only Psychiatrists can make such a diagnosis
Delusions of delusions of parasitosis (sometimes known as DODOP or DDP) is a poorly understood but increasingly common condition, most frequently seen amongst dermatologists, although it can affect physicians of any specialty.
Sufferers of delusions of delusions of parasitosis present with a fixed conviction that a patient (and in severe cases multiple patients) are suffering from delusions of parasitosis. This belief remains firmly held by the afflicted physician, despite being presented with clear evidence of somatic pathology in his or her patient(s). Affected physicians will appear otherwise rationale and rarely display psychiatric co-morbidities.
A characteristic sign of delusions of delusions of parasitosis is a refusal for the physician to conduct more than a cursory examination of patients presenting with
This is too hard. I don’t know what this is; time to blame the patient….
symptoms of parasitical infestation. In the most extreme cases the physician will also refuse to engage in a professional doctor/patient dialogue.
Whilst the etiology of delusions of delusions of parasitosis remains unknown, there exist several hypotheses as to it’s origin.
One such hypothesis states that delusions of delusions of parasitosis is in fact a ‘meme’, commonly taught to vulnerable physicians in training. Once this belief takes hold, it is extremely difficult for the sufferer to free themselves of this conviction and it becomes increasingly difficult – if not impossible – for the sufferer to approach unfamiliar cases of parasitical infestation without diagnosing delusions of parasitosis.
A modern variant of this hypothesis states that delusions of delusions of parasitosis is an ‘internet disease’ – whereby physicians inadvertently reinforce each others delusions of delusions by reading about them online.
When pressed, sufferers will classically cite flawed, poorly researched and dated medical
Diagnosis of DoP is for a lifetime….
literature in an attempt to justify their beliefs. They will then go on to transfer their belief system to younger physicians who become similarly deluded. It is thought such cycles have served to perpetuate this condition amongst the medical community – where it has believed to have existed, to a greater or lesser extent, for some 75 years.
The prevalence of delusions of delusions of parasitosis is unknown, and case studies in the literature are few. Some have estimated that over 90% of dermatologists in the UK alone suffer from delusions of delusions of parasitosis. In recent years reports of delusions of delusions of parasitosis have displayed a worrying upward trend.
Treatment of delusions of delusions of parasitosis is troublesome. It is sometimes recommended that the patient attempt to strike up a ‘rapport’ with the physician, in order to gain their trust, and perhaps open their mind to the possibility of explanations other than delusions in patients presenting with symptoms of unfamiliar parasitical-like infestation. However this approach is difficult and is thought to have a fairly low success rate. The physician’s delusions of delusions are frequently firm and will remain in place despite the most striking and rationale evidence to the contrary.
Many doctors are this open-minded
If directly confronted, afflicted physicians may even respond by accusing the patient of suffering from delusions of delusions of delusions of parasitosis, although evidence for this advanced phenomena is beyond the scope of this review and will not be discussed here.
In any case, no randomized controlled trials into the treatment of delusions of delusions of parasitosis have been conducted, and currently it is recommended that it be managed on a case by basis.
Strategies to overcome delusions of delusions of parasitosis in the medical community have been proposed. One such strategy is for patients to apply continued pressure on government bodies to properly investigate increasing reports of parasitical-like conditions in their populations. It is hoped that this approach, whilst by no means a ‘quick fix’, will yield a gradual improvement, and – it is at least hoped – bring some relief to the thousands of physicians currently believed to be suffering from this debilitating illness.
____________________________________________________
This article, written by Mr. Common Sense, is a wonderful perspective on how ridiculous doctors must feel when they blindly label a Morgellons sufferer with a Delusions of Parasistosis diagnosis while not undermining the horrific suffering Morgellons victims endure. There currently is no cure for Morgellons Disease, even though it is still not recognized by the so-called Medical Community as a disease.
If you or someone you love or care about has Morgellons, please tell them they no longer need to suffer; there is a way to eliminate their symptoms so they can return to their lives without brain fog, fatigue, biting and scratching and in some cases, open, weeping non-healing lesions. Watch this warm and compassionate women explain how she eliminated her Morgellons symptoms nearly 5 years ago.
Russell Altman - November 13, 2011 at 14:56