WHat will be todays newest, WE KNOW WHAT IT IS,

[Baraka Obam]

Here once again I sit, checking my blood once more to see the fast growing black muck in the blood, the MOST LIKELY CAUSE of this malady. I have shown it growing and seen it in others blood. Is it so hard to imagine a disease that LIVES in all our blood. Who really gives a **** how it got there, it is there and everyone is still running around with your heads cut off, its toilet paper, its water, its bugs, its the gobble goon from the moon. They may be part of the infestation but they are not the reason we are easily invaded. Once again I ask some of you to do the right thing and get a CHEAP microscope and look at your blood. You will find the black slime forming in it. I have seen others that have the same exact situation going on. You can buy a good scope like the one I just bought on CRAIGSLIST for $20 usually for less than 50 dollars. Buy some slides on ebay. This is only one of three things I have seen in all my time looking thru the scope that moved, one was a demodex mite, ugly little fellow but not a killer, the blood problem, that is a killer. Get a microscope check your blood and when you find it, bring your scope with you to the infectious disease doctor OR a BLOOD DOCTOR and show him.

[mmarsha]

DETAILS:Two
Culture Development:

BARAKA, CHECK THIS OUT;BLOOD ISSUES INTENSIFY
Cliffohttp://www.morgellons-disease-research.com/Morgellons-Message-Board/newreply.php?do=postreply&t=5554rd E Carnicom (DARN THE PIC'S DIDN'T POST) GO TO THIS SITE AND CHECK THIS OUT. I THINK YOU AND HE ARE ON SAME PG!!!
MMARSHA
iF THIS URL DON'T WORK TRY CLIFF MIKELSON??? YOU KNOW ME AND COMPUTER...


Apr 22 2009


I am not offering any medical advice or diagnosis with the presentation of this information. I am acting solely as an independent researcher providing the results of extended observation and analysis of unusual biological conditions that are evident.

Three independent methods have been established that appear to confirm the presence of developing modified erythrocytes (red blood cells) within cultured dental samples that exhibit the characteristics of the Morgellons condition as previously researched and identified. All individuals tested thus far have produced the dental filamentous materials, regardless of whether visible skin anomalies are present or not. Please see previous research for further clarification on the prevalence of the condition.

The erythrocytic detection methods are:

1. Direct observation under the microscope at relatively high magnification (8000x - 10000x) using developed microscopy techniques.
2. The use of the Kastle-Meyer presumptive test (visual and microscopic, sensitive test) for blood, a method commonly used in forensics for blood identification.
3. The HEMASTIX (TMP) presumptive forensic test (very high sensitivity) commonly used for blood identification.

The tests have been repeated several times to assure consistency in methods, results and controls.

The appearance of the cultured erythrocytic cellular structures, if accepted as properly identified, in and of itself defies all conventional understanding of blood cell development. This appearance also corroborates a long history of research through this site of environmental and biological samples that defy conventional expectations and knowledge with respect to the state of public health and the environment (e.g, refer to Extraordinary Biological Observations, Carnicom, May 2004). Simply put, erythrocytes are not to be grown in the the test tube under the current state of conventional knowledge. To do so, however, is considered to be a holy grail of biological achievement with huge Operations Main Page

Orignal extracted filamentous dental sample in red wine contained and held in a petri dish with lid. This acts as the culture medium of this report. This sample represents a total collection period of nine minutes of gum exposure to the wine solution; three segments of three minutes each, respectively.

After approximately two to four weeks, a filamentous growth form emerges on the surface of the wine (unanimous at this point). This growth form is identical in nature at the micrscopic level to previous dental cultures that have been reported on with the use of an agar medium. A time lapse video of that growth is available on a previous report.

The earlier forms of the filamentous growth are pure white as in this sample. This is identical to previous agar medium cultures that have been developed. At this stage, the growth is approximately two to three days old. The photographs in this collection are taken from more than one culture to demonstrate various stages of growth and development.







The culture growth several days into development. This stage produces greater variation in the surface structure. Additional structure and color is introduced and appears visually to be more of a mold or fungus nature. It is this stage which departs from the previous agar cultures and adds greater complexity to the form. It appears that the nutrients within the wine are eseential to reaching this stage of development,.

Further development of the filamentous form. A convoluted surface is now a characteristic feature. Some structures have been observed to reach approximately one inch in thickness with numerous folds before being constrained by the lid of the petri dish An additional difference between the agar medium and the wine medium is that growth on the agar medium can occur within 24 hours, whereas the wine medium requires approximately two to four weeks to begin the growth process..

The final form of development that has been reached by the culture growth. Total time elapsed at this stage is approximately one to 1 1/2 months after the appearance of the original growth. Total time elapsed is therefore on the order of two to three months after the original collection of the dental sample in the wine medium. The growth form reaches a much greater degree of complexity than with the use of the agar medium. The diameter of the growth is approxiimately three inches and appears to be constrained only by the petri dish boundary and available nutrients. The structure is cohesive. Thus far every dental sample observed has produced this growth form and onlythis growth form after the time lapse of two to three months.
set of partial and mostly fully reconsituted erythrocytic structures.The non-reconstituted form is more typical of early observation in the session; it appears as though additional heat and/or light is responsible for the final reconstitution that takes place. No budding or fission process characteristic of yeast cell reproduction is observed. Biconcavity and size range is a unique identifying characteristic of erythrocytes. If erythrocyte identification is accepted, species of blood remains unidentified. It can also not be be stated that the reconstitution process is entirely complete. Magnification approx. 9000x.
ADDITIONAL I COULD NOT GET IT ALL TO PASTE, SO YOU HAVE TO GO TO THIS SITE. THEY HAVE SOME AWSOME PIC'S OF blood!!!
MM

[Baraka Obam]

This malady can be seen at much 400x to quite well. It is probably the same as these fellows have found, maybe it has morphed to a larger size, I know it can change, that I have also seen, it does this in a blink of an eye. Well, think I will come back to the site and post untill the cows come home, maybe if I keep on people will realize they should do the right thing and get their own microscope especially the ones with the bio film or yellow goo as I call it. harvest some from a lesion, harvest it from the ears when they crack open or develope lesions or get it from where ever you see it. Try it, you will have somthing to show the doctors, between all of us we may find a infectious disease doctor that knows what it is! Most likely that doctor will be from Africa, India, or Asia.

[pat]

Put it on a dvd and send it to me.I'll give it to the guy who does the cancer blood tests I told you about.I can't see that in my blood at all.
marsha, baraka has contacted the clifford carnicom site several times and had no reply.

[Jo]

Baraka,

Nickthebuilder on lymebusters is trying to ID the spores in the blood in conjuction with Carnicom. Apparently they are very small less than 1 micron.

LymeBusters - Chitin is right, treatment successful READ THIS

Jo

[Kritters]

Originally Posted by Jo

Baraka,

Nickthebuilder on lymebusters is trying to ID the spores in the blood in conjuction with Carnicom. Apparently they are very small less than 1 micron.

LymeBusters - Chitin is right, treatment successful READ THIS

Jo

This is an aside, I realize, but I posted a few days ago about the biting and stinging coming back on my arm in the same spot as they were last year after I walked 3 miles in the 85 degree sun... and was very sweaty. This is part of a quote of Nick's:

"...The only treatment method would be topical or injection. In my case, (and as hypothesized prior to testing) treating the skin effectively killed 100% of the active lesions, therefor killing the colonies and stopping the systemic spread of the spores to new follicles and sweat glands, through the blood stream.

-Nick"

That could be why.
Kritts

[Baraka Obam]

Kritters this may be true BUT BUT BUT, that would have to be at a very early stage . I saw these things burst apon my skin after several years of the tiny red bleeding dots on my legs. that was WAY before the actual attack of the giant arm and leg colonies. It was the same MUCK, bright red heavy bleeding DOTS, but they were dots then. When I was burned really bad on my arm and the skin slid offthey came out first on the burnt arm and then on the other, almost instantly. They had to be getting out of dodge! The arm that had been burnt had already gone thru loss of muscle, and that took two weeks to go from weight lifting alot to not being able to lift 3 pounds over my head. The muscle was jelly, this was caused by covering the bleeding spot on the arm with antibiotic cream. I have had this attackl me in many different ways, nervous system, Bone spurs, gall bladder, eye, hair, skin, fibramialga, carrple tunnel, high blood pressure, KIDNEYS, almost all of them are under control except KIDNEYS and high blood pressure. They do not spread as a skin rash may, it builds its system slow but sure as it does this I think the fluid the lesions make inside and out allow them easier time developeing. I also believe that this fluid may be the cause for all the other infestations of parasites, either we draw them to us from a smell we give off OR it is just much easier to establish themselves with this fluid controling immune responce. Is the vector carried in the T cells. Who knows, but I do not think I am so far off base. I have watched this malady from the time I got it untill now, unlike many others that let the doctors explain away the situation I knew this was all related to a visit to a country where plage, leprocy, and all other disease is still common.

[posey]

Baraka when I first used the GSE I had a quite long red thing come from back of my ear where I had scraped some of the goo off and drew blood.

At least an inch long if not a little longer, and each end was different in size, resembling blood clots. But these were not clots. This was connected by an inch long thing in length.

Also, and this is going to be a little embarrasing, I had 2 hard bowel movements; round and with a long 2 inch thing from them. This "thing" would resemle that of a tampon string.. I kept them and froze them just incase I ever find a doctor who is interested in all this. Round part was about that of 1.5 golf ball.

Bitters from the sweets

(really hard to describe these things)

posey

[Baraka Obam]

I had the same mess all the way around the ears, I rubbed them out,LOL with a huge amount of work. If you would have had a microscope you could have seen what builds this stuff on a smaller size. If you look at my pictures you can see the very small blood stuff forming up bigger tubes, they go from black to a blue color when they do this and make a pattern of squares. What size was this thing that you removed and froze, by the way, great idea, more of us need to freeze these things. I also had a mess come out of me and they were always captured by a hard mess. These were like string and translucent at first very long then smaller and smaller after ozone infusion. It must choke them to death anyway it worked well. I will have to see if anymore come out when I get home.

[mmarsha]

Originally Posted by Baraka Obam

I had the same mess all the way around the ears, I rubbed them out,LOL with a huge amount of work. If you would have had a microscope you could have seen what builds this stuff on a smaller size. If you look at my pictures you can see the very small blood stuff forming up bigger tubes, they go from black to a blue color when they do this and make a pattern of squares. What size was this thing that you removed and froze, by the way, great idea, more of us need to freeze these things. I also had a mess come out of me and they were always captured by a hard mess. These were like string and translucent at first very long then smaller and smaller after ozone infusion. It must choke them to death anyway it worked well. I will have to see if anymore come out when I get home.

Hey Baraka, I must ask what is ozone infusion?? I have gotten all glue off now I still have a few knotts on backs of ears and I know they are in there!!! I am going to get more GSE tomorrow and see what happens. The Vita-k age spots is wonderful and is still working, THANK YOU GOD!!! But I have to somehow bust these bumps or small nest?? what ever the HRL you call them??? I have to kill or the glue will be back just like the terminater.
mmarsha , Where do you get that 35 peroxide?