Week 12 on the live blood analysis training course

A Typical Live Blood Analysis Case

This is a case study from one of our live blood analysis training courses where we use dark field microscopy as well as bright field microscopy to perform live and dried blood analysis on a client..

The client (female) suffered with recurrent bladder infections that started soon after getting married and had been getting progressively worse over the years.

The infections have involved the kidneys on a few occasions and have not responded to any natural products that she tried.

She follows a fairly healthy diet and lifestyle. She has tried eliminating specific foods from her diet in case they may have been to blame.

Nothing made a significant difference.

This is what showed in her live blood cell analysis:

Protein Linkage: Grade: 3/5

Chain-like formations of lemon-shaped RBCs.
Commonly associated with impaired digestion of dietary protein, from either excess protein intake or low proteolytic enzyme production by the pancreas. Especially associated with difficulty digesting dense animal protein (such as meat & chicken).
Anisocytosis:  Grade: 4/5

RBCs that vary in size, some larger and some smaller than normal.
Most often due to vitamin B12 and/or folic acid deficiency, iron deficiency, trace mineral deficiency and in some cases certain disease states and inherited forms of anemia.
Cloud Patterns:  Grade: 4/5

RBCs with indentations appearing similar to cloud drawings.
These forms indicate the presence of inflammation and are connected to an acidic pH and trace mineral deficiency. May also indicate high homocysteine levels.
Empty WBCs:  Grade: 3/5

WBCs with very sparse cytoplasm forming a thin border around the cell.
This occurs just before rupture of the WBC and is associated with a severely stressed immune system, parasitism and an unbalanced terrain.
Neutrophils – Cohesion:  Grade: 2/5

Two or more neutrophils stuck together.
This occurs due to increased chemostaxis (chemical messaging between neutrophils) and indicates possible infection, inflammation and some disease states
Neutrophils – Count Increased:  Grade: 3/5
The most common cause for an increased neutrophil count is an acute (usually bacterial) infection.Inflammation in the body can also lead to increased neutrophil levels.Excessive stress can also increase neutrophil numbers.A high neutrophil count may also be due to a number of different disease states
Neutrophils – Disrupted:  Grade: 2/5

Disrupted neutrophils is most often indicative of chronic stress on the immune system, parasitism of the WBCs and an unbalanced, acidic terrain.
May also be associated with toxicity and severe allergic reactions.
Neutrophils – Nonviable:  Grade: 3/5

One of the most important assessments to determine the state of the immune system. Neutrophils should move around actively. Round, symmetrical, immobile neutrophils are non-viable and suggest an underactive immune system. It may be caused by: mineral deficiencies, ongoing infections & antibiotics, smoking, alcohol, medication and sugar intake and digestive weakness. Stress, lack of exercise, poor sleeping patterns and yeast overgrowth can also contribute.
Bowel Pattern:  Grade: 4/5

Observed in Layers 4 – 8
A cluster of round white holes in the centre of the sample.
This indicates bowel challenges that may include bowel inflammation (colitis, enteritis), leaky gut syndrome, strictures, diverticula, irritable bowel syndrome and poor tissue integrity. The presence of bowel patterns in more than 3 layers indicates that supporting the digestive system is a high priority.
Dark Centre:  Grade: 4/5
Observed in Layers 4 – 8
The centre of the sample appears significantly darker than the rest of the sample.This is due to bowel toxicity, often coupled with digestive insufficiency and/or Candida. Possible leaky gut syndrome and poor immunity is usually a consequence of bowel toxicity. This implies that the ability of the digestive system to eliminate toxins is compromised and that the intestinal
flora is not balanced.

To find out how this client was helped and see the 2nd appointment conclusion – join us for the Fascinating Live Blood Analysis Online Training Course Starting Tuesday April 3rd 2018 at 7pm!

Read the course outline here:
https://livebloodonline.com/the-training-course/course-content/ Find out about the right microscope for your needs:
https://livebloodonline.com/microscopes/ See some frequently asked questions:
https://livebloodonline.com/q-a/

Don’t forget that you can join the course and acquire your microscope at any time during or after the course. Email us for a complete breakdown of all the costs of setting up in GBP & USD.

Please contact us if you have any questions, would like to enrol or if you would like to know more about choosing the right microscope.

info@livebloodonline.com

Live Blood Analysis Practitioners

Live Blood Analysis Practitioners

What do live blood analysis practitioners do?

Live blood analysis practitioners observe their clients live blood cells on a screen with the use of a high powered specialized blood analysis microscope with camera.

A tiny pinprick of blood is put on to a glass slide and then viewed on the screen.

The blood analysis microscope and camera project a picture of the live blood cells onto a screen to be seen by the live blood analysis practitioner and client together, allowing the pictures and videos to be recorded.

In live blood analysis, the blood is not dried or stained beforehand, so the blood elements can be seen in their living state.

The live blood analysis practitioners and client look at the variations in the size, shape, ratio, and fine structure of the red blood cells, white blood cells, platelets, and other blood structures.

The insights gained from the live blood analysis, correlated with other clinical data, enables live blood analysis practitioners to understand their clients individual state of health on a much deeper level.

As a result, an appropriate course of natural treatment and lifestyle/dietary interventions can be formulated and furthermore, the effectiveness of various treatment combinations can be tested and progress can be monitored by observation of changes through further live blood analysis.

Nutritional microscopy uses live blood analysis to achieve optimum health naturally through diet and nutrition.

Dried blood analysis or The Oxidative Stress Test is another very valuable test in live blood cell analysis. The Oxidative Stress Test (Dry Blood Analysis) allows live blood analysis practitioners to view the level of free radical damage/oxidative stress and toxins in the body.

Many clients will not follow the advice that their live blood analysis practitioners give them and need visual proof that their unnatural habits are having a negative impact on their health.

Live blood analysis allows live blood analysis practitioners to do just that.

Dried Blood Analysis

Dry Blood Rings

Dried Blood Analysis

Dried Blood Analysis or the Oxidative Stress Test (OST) was developed in Europe in the 1920’s and has since been used by medical practitioners and naturopaths in many countries across the world.

In the 1930’s NATO physicians, Dr Heitan and Dr La Garde, introduced Dried Blood Analysis to Dr Bowlen (head of surgery at Massachusetts General Hospital in Boston in the 1930’s), and later Robert Bradford (of American Biologics Hospital in Tijuana, Mexico).

For this reason Dried Blood Analysis is also referred to as the HLB test (Heitan, La Garde, Bradford).

In essence the Dried Blood Analysis test is an evaluation of a patient’s coagulation morphology. There is a very distinct difference between the dried blood sample of a healthy individual and that of a chronically ill patient. The healthy sample is a solid mat of pinkish-red dried blood with a strong, well-interconnected fibrin network. 

In the presence of degeneration, toxins and other imbalances, the dried blood sample shows white areas, called polymerized protein puddles (PPPs) and other abnormalities that can be indicative of certain systemic conditions.

As the blood dries on the slide, there is a natural centrifugal activity whereby the different elements in the blood spin out into rings, depending on their specific gravity. Organs near the centre of the body create light PPPs that don’t spin out very far, whereas heavier PPPs are created by lymph and skin conditions that spin out around the outside of the layer. The size and shape of the PPPs is also suggestive of the nature of the condition, which we cover in the live and dry blood analysis training  course https://livebloodonline.com/the-training-course/

The PPPs observed in the dried blood test are believed by some researchers to be caused by the presence of Disseminated Intravascular Coagulation (DIC) and the presence of water-soluble fragments of the extracellular matrix.

This theory is supported by some emerging research and we look at the mechanisms of DIC and degradation of the extracellular matrix in the live and dry blood analysis training course.

A healthy dry blood sample shows a healthy, even red colour, no white open areas and a distinct, interconnected fibrin network.

Copyright Dr Okker R. Botha, Johannesburg, South Africa, 2009

Week 8 on the Live Blood Analysis Training Course

We are on week 8 of the live blood analysis training course and now starting to study dried blood cell analysis which is also referred to as the Oxidative Stress Test (OST).

In dry blood test analysis (or dried blood analysis), we leave 8 layers (spots) of blood to dry naturally on a slide, we then observe the anomalies seen.

We are looking at anomalies that could be signs of allergies, adrenal stress, psychological stress and intestinal irritation as well as reproductive organ, bowel, vital organ, lymphatic and thyroid imbalances.

Heavy metal toxicity anomaly as seen above.

Appearance:

Heavy metal toxicity appears as black points at the edge of the layer, or as a dark shore or waves.

Cause & Interventions:

Strongly indicative of heavy metal toxicity, this can be from the environment (pollution, contaminated food, water or air, smoking and passive smoking) and also amalgams.

Points at the edge of the layer usually indicate the presence of lead and/or amalgams.

Dark waves deeper into the layer indicate that metals are being held in the fatty tissues, brain and nervous system, which is associated with an increased risk of Alzheimer’s, Parkinson’s, Multiple Sclerosis (MS).

 

Join us on the next live and dry blood analysis training course here.

 

Copyright Dr Okker R. Botha, Johannesburg, South Africa, 2009

Week 5 on the Live Blood Online Training Course- white blood cell viability

We are on week 5 of the Live Blood Online Training Course and looking at white blood cell (neutrophil) anomalies.

Neutrophil viability is one of the most important assessments used to determine the state of the immune system.

The main criteria used for determining the viability of a neutrophil include size, condition and activity.

A neutrophil should be approximately twice as big as a red blood cell (RBC), approximately 14 microns in diameter. The main determinants in assessing the condition of a neutrophil are the condition of the cell’s border and segmentation. The border should be fairly smooth and regular and the neutrophil should not be hypersegmented nor macrocytic.

The most important factor to observe when assessing neutrophil viability is activity.

Here we look at the granules within the cell’s cytoplasm. Ideally, there should be many of them actively streaming within the cell.

The cell itself should also be stretching out its membrane in irregular shapes to move around actively in the plasma. Typically, neutrophil viability should be at least 75{0ad5881c2192913025db5bf2180b2e0b17ede26560c7c351a451156c0b06bc98}.

Non-viable neutrophils are often round, symmetrical and immobile.   

Implications:

Poor neutrophil viability may be caused by many factors – please join the Live Blood Online Training Course to find out more.

pH of urine and blood

pH of urine and blood

The pH of urine and blood is extremely important and is now, more and more, being considered an important indicator of one’s health.

In The pH Miracle: Balance Your Diet, Reclaim Your Health by Robert O. Young, Ph.D. & Shelly Redford Young, we find this statement: “the single measurement most important to your health is the pH of your blood and tissues – how acidic or alkaline it is.” Tracking your pH of your urine is easy to do, and takes very little time.

You will need a box of pH test strips and a journal to track your progress.

Most health practitioners recommend doing a daily pH test for 30 days to give a general idea of your alkaline/acid measurements.

Keeping track of your ‘numbers’ will measure your levels and monitor your progress over time to determine if you need to make changes or not and to see if what you are doing is working.

The pH of blood must be tightly regulated in a very narrow range between 7.35 and 7.45. Below or above this range means symptoms and disease. Death is associated with blood pH imbalances of 7.80 and above or 7.0 and below.

Testing your urine pH can give you an early indication and warning that your body is over acidic.

What the pH of urine and blood can tell you

The pH of urine indicates how the body is working to maintain the proper pH of the blood. The pH of urine indicates the efforts of the body via the kidneys, adrenals, lungs and gonads to regulate pH through the buffering system.

This can provide a fairly accurate picture of body chemistry, because the kidneys filter out the buffer salts of pH regulation and provide values based on what the body is eliminating.

Urine pH can vary from around 4.5 to 9.0 for its extremes, but the ideal range is 5.8 to 7.2.

First pH of urine Test in the morning:

Test your first urine of the morning before eating or drinking, this is the urine that has been stored in your bladder during the night and will usually be more acidic.

Briefly place the pH strip in the urine mid-stream and wait 15 seconds to read your pH.

The pH number of the morning reading should be 6.8 – 7.2

If your pH of urine is below 6.8, you could be overly acidic and low in alkaline buffers.

To increase your alkalinity you may want to source a more alkaline water, and introduce organic greens high in the minerals calcium, magnesium and potassium into your diet.

If your pH of urine are 7.2 or higher, you have a healthy reading and you appear to have the alkaline buffers needed to neutralize acidity in your diet and lifestyle.

Second Morning pH of urine Test:

Take this second urine pH test after drinking water or a green drink but before eating any food.

Repeat Daily for Thirty Days (and more).

Take the first and second urine of the day and record the average of them both. This is the number you will use when you track your trend over 30 days.

This will enable you to see the trend over time and help you to measure how alkaline you are.

These tests are able to indicate how effective our digestive system was able to deal with what we drank and ate the previous night/day.

When we are eating an acidic diet, these numbers will tend to be low.

When we start alkalizing the numbers will start to increase and over time, will begin to sustain themselves.

Your second morning urine should always be better than your first morning urine, ideally between 7.2 – 7.4.

Live blood analysis training

Live blood analysis training

There are a limited number of places for Live Blood Analysis training around the world, at Live Blood Online we offer live blood analysis training online via interactive webinars.

The Live Blood Online Live blood analysis training course can be taken at your leisure, anywhere in the world where there is an internet connection – this offers a huge saving on expensive travel and accommodation.

  •  The Live blood Online live blood analysis training course is presented via 12 interactive and interesting weekly webinars with GoToWebinar. All of the lessons are recorded for your future reference. This is a HUGE advantage as this enables you to repeat the recording of the lessons as many times as you need. Many Live blood analysis training courses leave you with a microscope and manual with no help, support or back up.
  •  The study material can be referred to whenever you require at your convenience, you can join anytime and study at your own pace.
  • Manuals, study material, reference charts and photos are all provided.
  • A certificate is sent on completion of the Live blood analysis training and course and submission of 2 test cases.
  • Your live blood analysis training tutor is a registered homeopathic doctor who has established himself as a leader in Live and Dry Blood Analysis and has been successfully teaching Live Blood Analysis for 16 years.
  • Live Blood Online live blood analysis training provides ongoing support to help you with everything you need to get started and practicing live blood analysis with confidence and proficiency.
  • Questions are answered throughout the live weekly webinars. Help and support is provided through a private Facebook Page support Forum where attendees can, post, comment, compare notes and help & support each other.
  • An online traing centre is alsp provided where you will find your 500+ page manual and a library of pictures & videos to help you along with lots of useful information to help you in your practice.

The Live Blood Online live blood analysis training courses are held every 3 months and continue for 12 weeks.

They can be joined at any time.

Practitioners certified by Live Blood Online have been trained to a very high standard and level of proficiency

Live blood analysis microscope

Live blood analysis microscope

Not all microscopes are created equally. For optimal performance your live blood analysis microscope specifications need to be suited to its particular application.

Naturopathic microscopy involves the analysis of live and dry blood samples in brightfield and darkfield, each with its own set of unique microscope requirements.

Although most microscopes essentially work on similar principles, there is a great degree of variation in optical configurations, illumination and ultimately image quality. Live blood analysis microscopy in darkfield and brightfield is a highly specialised technique, requiring a very particular set of specifications.

A suitable optical and illumination assembly must be in place to ensure the best results in viewing live blood in darkfield and brightfield.

Any compromise in the setup of the system will result in an inferior image and the user not being able to detect all the important anomalies.

Many suppliers on the internet claim to supply darkfield and brightfield live blood analysis microscopes suitable for live blood analysis but the supplier’s knowledge is limited. Only a specialist will know the requirements for a live blood analysis microscope.

So it is very important to only buy a live blood analysis microscope form a specialist supplier who understands the requirements and specifications for a live blood analysis microscope that will ensure the best results in viewing live blood in darkfield and brightfield.

Many practitioners make the mistake of buying a microscope from a company that claims their microscopes are suitable for live blood analysis microscopy and then find out that this is not the case, they are not able to see many of the anomalies and therefore not able to perform live blood analysis to its full potential.

It is not that the company is deliberately cheating the practitioner, it is more a lack of specialist knowledge.

If your microscope has not been supplied by us, it’s likely that you won’t be able to detect everything that can be seen in the blood.

Don’t let this happen to you if you are looking for a microscope!

At Live Blood Online we know exactly what specifications are needed in a live blood analysis microscope for it to perform optimally as a live blood analysis microscope system.

Don’t buy a microscope until you have seen this video.

We supply the best microscopes for live blood analysis worldwide AND if you buy your microscopes from us you get the interactive 12 week training course for half price! (We are also currently offering free shipping on microscopes)

Week 1 latest on the Live Blood Analysis Online Training Course

Week 1 on the Live Blood Analysis Online Training Course

Week 1 on the Live Blood Analysis Online Training Course

In week 1 of the Live Blood Analysis Online Training Course we are learning how to use the microscope and get a perfect blood sample every time.

Consistency is very important in live blood analysis for for best results.

We are learning a lot about live blood analysis (LBA), especially how valuable and helpful it is as part of a preventative approach

Many of the so-called preventative measures are really just early detection measures.

For example, having a regular blood sugar test is not part of prevention – it will only show an imbalance once the body has failed at all its attempts to regulate the blood sugar.

When you get an abnormal blood sugar reading it is at quite a late stage already and one should really have had preventative measures in place years before the abnormal result.

“LBA detects imbalances that may lead to disease and one can then implement measures to help minimize the likelihood of serious conditions developing in the future.”

One of the questions we often get asked is – “Why is the visual impact of LBA so important?

“The visual impact of LBA is very important. It was shown in a study that people who were given the actual images of their damaged arteries were much more likely to make necessary changes to their diet and lifestyle than those who only saw the images once.”

“Being able to see the impact of poor dietary and lifestyle choices and to refer back to those images has a very powerful effect on keeping us motivated.

More about the Live Blood Analysis Online Training Course:

Join on this fascinating journey!
You don’t need a microscope to join.
We offer a 2 part payment plan.
We provide all the help and back-up needed.
You receive 2 wall charts and a 500+ page manual.
You get recordings of all the lessons to review at your leisure!
This is THE most comprehensive training course in live blood analysis.

Course content – http://livebloodonline.com/the-training-course/

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Enrolment – http://livebloodonline.com/the-training-course/enrolment/

Info pack – http://livebloodonline.com/

What our students are sayinghttp://livebloodonline.com/the-training-course/what-our-students-are-saying/

“I am really enjoying the course, it is just what I wanted. I find the explanations by pictures and videos very helpful. I am not able to attend all the webinars so I can study the recorded webinars and catch up in my own time.” – Pierre Margetides Naturopath, London

Please contact us if you have any questions, would like to enrol or if you would like to know more about choosing the right microscope for you and avoiding any costly mistakes.

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Are There Naturally Occurring Pleomorphic Bacteria in the Blood of Healthy Humans?

    1. Richard W. McLaughlin1,
    1. Hojatollah Vali1,
    1. Peter C. K. Lau2,
    1. Roger G. E. Palfree1,
    1. Angela De Ciccio1,
    1. Marc Sirois3,
    1. Darakhshan Ahmad4,
    1. Richard Villemur5,
    1. Marcel Desrosiers5 and
  1. Eddie C. S. Chan1,*

+ Author Affiliations

    1. Faculties of Dentistry and Medicine, McGill University, Montreal, Quebec H3A 2B4
    1. Biotechnology Research Institute, National Research Council of Canada, Montreal, Quebec H4P 2R2
    1. Departément de Chimie-Biologie, Université du Quebec à Trois-Rivieres, Quebec G9A 5H7
    1. INRS-Institut Armand Frappier, Pointe Claire, Quebec H9R 1G6
  1. INRS-Institut Armand Frappier, Laval, Quebec H7V 1B7, Canada

Dark-field microscopy of blood from healthy individuals revealed the existence of pleomorphic microorganisms. These bacteria exhibited limited growth and susceptibility to antibiotics and could be detected by fluorescent in situ hybridization and flow cytometry. They were further characterized by analysis of their 16S rRNA and gyrB genes.

In our search for spirochetes involved in Alzheimer’s disease (13), we observed pleomorphic bacteria in the blood of healthy human subjects by dark-field microscopy. This was a surprising finding since it is generally acknowledged that the bloodstream in healthy humans is a sterile environment (7) except when there is a breach in the integrity of the tissue membranes (6). However, the concept of the occurrence of bacteria in the blood of healthy humans is now more plausible because of cultivation-independent laboratory approaches. The main techniques employed in such studies include PCR amplification and sequencing of the16S ribosomal DNA (rDNA). These methods have revealed the presence of a wide diversity of microorganisms in the environment, and indeed within the human body (12). In this report we present evidence based on molecular phylogenetic techniques and light and electron microscopy, as well as other conventional microbiological methods, for the existence of a population of bacteria in healthy human blood. In view of the apparent controversial nature of our findings, it was encouraging to note the recent report of Nikkari et al. (14), who detected blood-associated bacterial rDNA sequences by using real-time PCR methods and a probe targeting conserved regions of bacterial 16S rDNA, and an earlier report by Tedeshi et al. (16) on the presence of pleomorphic bacteria as intraerythrocytic parasites in clinically healthy human subjects.

For light microscopic examination, blood samples from 25 healthy volunteers were drawn in a Vacutainer tube with no anticoagulants (Becton Dickinson, Franklin Lakes, N.J.); blood was drawn in the conventional manner involving antisepsis of the skin and avoidance of any introduction of external microorganisms by contamination. (Since external contamination was always a possibility, particular care and precaution were exercised at all times to avoid this. The specific procedures, as well as appropriate controls, are specified throughout the text.) A wet mount of the serum from the clotted blood of each sample, fresh or incubated at 30°C for between 5 to 7 days, was examined by dark-field microscopy (Leitz Dialux 20) for pleomorphic bacteria.

https://jcm.asm.org/content/40/12/4771.long