Dr Moulden and www.BrainGuardMD.com team..Hard at work..sample Report from today

[Guest guest]

hen you invent " the microscope " to neurological damage that no one

else has - you can describe and follow a neurological world that no

one else can - but then, for those who wish your help, you can then

share these observations that no one else can see...but then, thoise

you share this with can see it to...

Coincidentally, when you can nbow see the neurological damage from

vaccine induced autism, yu can tell, most clearly, whether a

particular intervention (like chelation), actually stands up to the

alleged claims of " neurological recovery. " As we now see, there are

improvements in behavior and function with chelation, but most

remarkably, we have yet to see any recovery of the core neurological

damage. We sincerely invite anyone who claims recovery from chelation

to the core neurological damage to send us video and pictures from

before and after chelation - if chelation is a cure for autism (at the

neurological and brain level) - then we will see it...

We look forward to validating these so-called " curea " and " recovery "

that p[eople have been promoting for autistic children.

Once again, my open invitation goes out to trest Dr Cutler's methods

and " put them to empirical validation " - if chelation is curing

autism, and if mercury chelation cures the neurological damage we can

now measure -then more power to these methods.

The sad reality now is this: Anyone who claims to have some " new and

improved " technique or method for curing autism - we can tell you

whether you just flushed your money down the drain for yet another

" cure " that has only alleviated symptoms, and not directly addressed

the hard the neurological cause of the autistic features.

Since the kidneys are adversely affected, chelation is helpful to

remove toxins from the body that the kidneys can longer remove on

their own. However,sicne mercury toxicity is NOT the cause of autism,

then this is not a cure but a symptom management intervention.

www.BrainGuardMD.com team

BrainGuardMD.com Neurodevelopmental report and Strategy

Via: email †" October 15th, 2008

Good am XXXXX;

We have been Working on XXXXXX’s images you have uploaded.

Thank-you for your organization and the detailed dates for all the photos.

We definitely see the " MASS " response in XXXXX. The ischemic process

first kicked in (mildly) around two months of age. This process and

the brain injuries were not apparent in the earlier photos.

At 3 months of age, the process was still active, at least in terms of

the micro vascular damage that was occurring. We see this largely in

terms of the right brainstem micro vascular territories being occluded

and affecting neurological functional controls of the XXXXXXX

architecture.

At nine months of age, the micro vascular ischemic " MASS " response,

relative to the brain, remained and it is from this point forward that

neurological damage has remained in terms of the adverse effects on

cognitive, motor, and sensory functions.

Several cranial nerves, in watershed vascular territories, have been

adversely affected. This includes the X,Xth, and X cranial nerves (on

the right).

You may notice that your son likely tilts his head slightly to the

left, more times than not, while he attempts to focus images within

the field of gaze. This is an unconscious adaptive response in order

to align the visual inputs from the eyes to compensate for a slight

vertical gaze palsy stemming largely from the XXXXXX. This

misalignment of the visual inputs, although not immediately

perceptible to yourselves, results from the ischemic damage to the

capillary vascular beds in the brain from the vaccine induced

hypersensitivity response which ultimately has caused multiple areas

of the brain (and other organ systems) to sustain hypoxic (lack of

oxygen) delivery through the end arterial capillary beds.

This MASS response, and ischemic process, is responsible for your

son’s autistic features and inability to speak. The M.A.S.S. (Moulden

Anoxia Spectra Syndrome) response to vaccination has also clipped the

micro vascular capillary beds in other areas of the brain. This, in

turn, has created your son’s inability to produce meaningful, fluent,

speech., affected sensory processing, motor functions, and likely

balance, coordination, and muscle tone.

Please note that much of these adverse effects in terms of brain

function is accounted by the term “disconnection syndromes.â€

Essentially, the connecting white matter tracts between various areas

of the brain have been disconnected from their ultimate destination by

virtue of the ischemic “MASS†process. This is called an expressive

aphasia in neuropsychology. A variation of this phenomena is known as

“isolation of speech syndrome†or ‘transcortical motor aphasia†if

language comprehension and verbal repetition skills remain intact.

Do note that despite your best efforts, expressive language functions,

as well as varied neuromotor and sensory functions, will not recover

until the body (and liver) is properly healed such that these vascular

beds can re-form. These micro vascular end-artery beds are required

for the white matter tracts to “plug-in†to the varied brain regions

required to complete the circuits necessary for several functions that

have been hampered for XXXXX, one of which is expressive language

skills. Do note that micro vascular territories in the kidney have

likely been adversely affected by the MASS response and this, in turn,

may contribute to the inability to excrete various toxins and heavy

metals without help (i.e. chelation).

The MASS process affects not only the brain (autism), but also the

liver, the kidneys, the bowel, the pancreas, and other organ systems.

The is large variability between individuals as to the degree to which

functional deficits in any particular organ system, including the

brain, exists.

Please note that the neurological damage XXXXXl suffered at 2 to 3

months of age, remained through 9 months of age, with a partial

(albeit incomplete) recovery by twelve months of age. There appears to

have been another significant ischemic MASS response that was further

exacerbated by the 18 month period with further neurological

compromise †" the effects of which remain to this day. Please note that

microvascular territories that have been previously compromised by

MASS renders the same tissue area uniquely susceptible to further

“hits†when the MASS hypersensitivity response is re-activated by

subsequent vaccinations and immune challenges.

It appears that the MMR and Varivax vaccinations at 13 months of age

triggered the MASS response again and this, in turn, has caused

further damage to the micro vascular trees, and ultimately

neurocognitive functions for XXXX.

BrainGuardMD detects a significant change in neurological functioning

in the transition from the 18 month to 20 month photos with marked

flattening of facial animation, increasing asymmetry in facial

architecture (once again the right brainstem being preferentially

affected) photo at 20 months of age, including measures of

neurological dysfunction that remain proprietary to BrainGuardMD.com.

By 44 months, the neurological damage is readily apparent and once

again this is most marked for the micro vascular territories of the

right brainstem. These same areas were initially compromised at two

months of age. Do note that the MASS response, upon repetitive

environmental triggers by (vaccination, infectious disease, toxins

etc..) or and/or residual vaccine adjutants (aluminum) and

preservatives (mercury) will preferentially affect the tissue areas

that have previously been compromised in terms of their breadth and

redundancy of micro vascular arborization. It is for this reason that

we see a cumulative and preferential decompensation in neurological

functionality specific to the right brainstem as imaged using our

BrainGuardMD technologies.

Do note that this “Right Brainstem†area is simply a window to what is

happening in clinically silent ways to other areas in the nervous

system and body that have also had their micro vascular trees

“clipped†by the “MASS†response to vaccination.

Do note that the neurological damage we see has remained relatively

constant between the photos from seven years of age up to the most

recent photo at ten years of age. There has been some slight increase

in the degree of ischemic damage to the right brainstem as detected in

one of our BraingGuardMD.com measures over the past three years.

The bottom line is this: although you may have been using and trying a

multitude of “interventions†over the years †" Nothing you have done,

to this point, has reversed the core neurological damage we can see

that began as around two months of age. This is important information

for you to have as it demonstrates that, despite good intentions, and

funds yu have spent in good will, the interventions have used up to

this point have not recovered the core neurological impediments that

have been adversely affected by the MASS response †" to vaccination, in

your child.

You are dealing with a stroke rehabilitation individual in terms of

your attempts to help XXXXX recover lost functionality and language

skills. Anything that is accepted as beneficial in the stroke rehab

literature will presumptively be helpful for XXXXX. Anything you have

tried, supplements or otherwise, up until this point, has NOT reversed

the core neurological damage we can now see and measure.

BrainGuardMD.com and AMassNetwork.com Solutions

We are interested in helping your child recover & measure this

recovery with our Techniques:

We are interested in moving forward with our intervention protocol

with XXXXXl. Please note that this protocol involves out tailor making

a solution for XXXXX specific to his physiology as we delineate from

the blood work parameters we assess. And will require you to obtain.

The protocol involves:

1) We require a current 30 second video clip of XXXXX tracking an

object through extremes of horizontal and vertical gaze (looking left,

looking right, looking up, looking down, smiling etc…). This can be

uploaded to our BrainGuardMD.com site.

2) After we have this, we will quantify XXXXX current neurological

functions based on our BrainGuardMD 12 measure of neurotypicality.

These measures reflect the neurological damage XXXX has already

sustained from vaccine injuries †" re: the ischemic stroke process.

3) We will need you to complete the medical history questionnaire we

provide (lifestyle analysis).

4) We will have you complete the blood work we require at a lab in

your area.

5) We will process the blood work. AFTER we have reviewed the blood

work it is at this point we can definitively state whether or not we

can provide an intervention for XXXXX that he can consume on a three

times a day (30 minutes before meals) schedule. After twelve days we

will need to repeat the blood work. We will be able to show you that

the values are normalizing (these values normalize the same way for

everyone †" as long as the intervention is tailored specific to the

patient’s physiological needs as assessed by the blood work). If these

values are not normalizing as we expect, then we shall reconstitute

and start again.

6) After this second blood work is processed, we will re-constitute

the next phase of intervention (herbal †" all approved as safe for

human consumption) that continues to heal XXXXX’ hepatic functions

which is necessary for healing the bone marrow, immune, and

neurovascular anomalies that have emerged from the MASS response and

vaccine injury.

7) We use repeat 30 second video clips to monitor the improvement in

neurological function with our intervention so as to have quantifiable

measures of the successful response to intervention that are

neurological based reflecting the original neurological damage that

XXXX has sustained from vaccination.

8) Do note that the older the vaccine injured person is, relative to

the vaccine injury, the longer it takes for the body and physiology to

heal. The bottom line is that healing does take place and we will be

able to share this with you in terms of the normalizing metabolic

values from the blood work as well as the neurological features we now

have measured from BrainGuardMD.

Additional Photos would be helpful for our baseline measured for your son:

1. Please send me a picture with XXXXX tilting his head to the right

(30 degrees tilt and one with his right ear touching his right

shoulder while looking direct at the camera).

2. Please send a 30 second video clip of your son wherein he is

looking straight at the camera, tracking an object through visual

space (i.e. have him follow your finger as he looks all the way ;left,

all the way right a few times, as well as looking straight up towards

the ceiling, and straight down towards the floor)

Please feel free to call directly to discuss this report and our

findings. I welcome addressing any questions you and your husband may

have.

There is hope. I recognize this information is rather disconcerting,

Please bear in mind that the first step in solving any problem in

clinical medicine is knowing what the problem is in physiology. With

this knowledge, we are in a position to truly start helping XXXX by

targeting interventions specific to the cause of his neurodevelopment

challenges and vaccine injuries.

Please note that if you have a newborn child, that we can now use

BrainGuardMD to scan, pictures, and video, to identify the MASS

response that will lead to sudden infant death (before the child stops

breathing) and identify the MASS response (a medical emergency) that

is actively causing silent brain damage in the here and now that will

later be diagnosed as autism, learning disabilities, attention deficit

disorders, infantile paralysis, adverse vaccine reaction, or sudden death.

Kind regards,

J. Moulden BA, MA, M.D., Ph.D.

President & CEO CNAPS Medical devices Inc.

1-705-498-6284

In response to this post by Kay:

>

> When I am making a decision to try something new for my son I look

> at many different factors. Some of these may include:

>

> 1. Is there research reports and published scientific evidence to

> support the product/theory?? There is certain scientific evidence

> for autism and mercury poisoning in the literature.

>

> 2. Is there approval by FDA or other government regulatory

> bodies? (DMSA for example is approved by FDA for metal removal)

>

> 3. Is there input from relevant specialists and professionals whom

> have expertise and whose opinions may validate research findings??

> (Andy would be considered an expert on chelation and there are other

> MD's whom support it as well and are considered experts-so therefore

> there are multiple experts that support chelation for autism)

>

> 4. Lastly, would look at antidotal patient/parent information from

> using the product. There are many parents on this site alone that

> have seen improvements or recovery from chelation. There are also

> other sites dedicated to recovery by chelation (as well as diet and

> supplements).

>

>

> So Dr Moulden it looks like you have quite a bit of work to do!!

> Andy has already done lots of work and his work meets my standards!!

>

>

> Kay

>