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Post by bessie on Jun 8, 2009 10:30:15 GMT -5
www.scienceblog.com/cms/blog/4006-its-june-2009-morgellons-time-21842.htmlIt's June, 2009 Morgellons Time June 6, 2009 First, there is no cure for this, and I would suggest reading ALL my blogs on this topic~ www.scienceblog.com/cms/blog/maggiemaeYou may be able to lesson the outbreaks but only temporarily. I would be very very wary of any claims to cure and of anything nano. There is not enough evidence to show it is really safe, and a lot more evidence to show it is harmful. Google article "US Experts Call For Tighter Controls on Nanotechnology" quip "Speaking after the US Environmental Protection Agency took its first step to regulate a nanomaterial -- near atomic-sized particles of silver being used as pesticide in products from shoes to a washing machine -- experts told AFP that nanotechnology is already producing materials that can harm the environment and human health. "There are some very serious concerns about potential health consequences," said Patrice Simms of the US Natural Resources Defense Council (NRDC). "We know next to nothing about their potential health effects," said Simms." I ask everyone to contact the CDC and all the Congresspeople AGAIN, reminding them we are still waiting and they are still stalling...... Does it not seem strange to you that the CDC can identify a rouge virus that consists of part human, part avian, 2 part swine from different continents and they can't identify (won't) what organisms are causing our HORRIFIC suffering? People, please don't be complacent about this. You realize we were told the flu virus will most likely mutate in the Fall - hummmm, Stephen King's "The Stand" comes to mind. The officials are still stalling - still covering some entity butt - still buying time....for what? Is there a game plan being put into play?? If they can identify the freaken mutant flu virus in a nanosecond, do you still have doubts they can't identify this?? Truly! The CDC has not been our friend, has been covering and stalling and is a FIBER lint Bucky ball in some evil, dark, DEEP pocket, doing their bidding. Greed and corruption has always been the reason evil exists. Speak up, shout, be PROVOCATIVE...contact Mr. Dan Rutz and whomever the new head is, and Washington DC - ask them again, for the truth. Thank you, Mm
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Post by toni on Jun 8, 2009 11:45:05 GMT -5
Keep pounding I sure agree!
I write them all the time, as long as I'm with Morgellons, I don't quit - that to me would be saying I GIVE UP MY LIFE to this and accept it being nothing but purely trying to survive-and living with yogurt and milk on top my head the rest of my insane life that it is anymore.
Thank you Bessie for bring this up, cause we sure do need to write. I had to blow off some smoke there above.
[glow=red,2,300]And if ANYONE or many at the same time will do a TV news interview I WILL do my best to get you the media.
LET ME KNOW, because we need to get this out there on TV again...
How CDC is DRAGGING their ARCES while we die off one at a time.[/glow]
Thank you.
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Post by lilsissy on Jun 8, 2009 11:53:05 GMT -5
WOW THIS IS HITTING IT SQUARE !!!! YES.... YES ......YES....... THE CILIA, these are artificial cilia. The little hairs I have been talking about in incomplete cystic fibrosis. These little hairs are supposed to move in unison like grass in the wind. You have these in your nose , ears, ovaries. They clear foreign substances and mucus from our bodies. If they are not lined up properly the mucus and bacteria , viruses get stuck. They have created artificial cilia and I bet this is in the chem trails so it is haphazardly lining up jamming our body's secretions. I bet they have turned to existing biology to create a living form of these artificial cilia. ami.usc.edu/projects/ami/projects/sencil/#cut from above but you must see the pictures, The biosensor device (Sencil, Figure 1) is comprised of an optical fiber that extends through the patient's skin and a biosensor element attached to the end of the fiber that is inserted percutaneously to sample interstitial fluid. We call this a Sencil, for “ sensory cilium”. The external end of the fiber will be attached to a photonic analyzer by means of a connector that accepts the free end of the fiber. The analyzer sends excitation light through the fiber to reach the biosensor element and receives returning fluorescent emissions from the biosensing element through the same fiber.I have felt for sometime FRET sensors would be involved because this is the what they use to be able to read the brains of mice. We are the mice!! On the C.D.C. , Rock them to SLEEP.......... the old MAFIA SAYING,
THE C.D.C. has BEEN ROCKING US TO SLEEP!!!
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Post by bessie on Jun 8, 2009 12:46:52 GMT -5
This should probably be a separate thread, but the videos on this website explain much of artificial life issue by scientists: blueskysunshine.org/blog/?p=1586Bessie
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Post by imblownaway on Jun 8, 2009 13:04:43 GMT -5
O.M.G.
I just happen to be having one of those mornings. The brain fog is so intense. (like I never fully shake off the slumber) I have become aware of the fact that when this happens to me all I have to do is go outside and sure enough. I look up at the sky and yep lines and lines above me. I am not imagining this. they are always there when I feel like this.
Oh forgot to say good thread. ;D
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Post by imblownaway on Jun 8, 2009 13:12:57 GMT -5
Did you see this toni? there is also a video. from lilsissy link above
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Post by toni on Jun 8, 2009 14:20:00 GMT -5
Imblownaway,
Yes, I looked at that video.
That small hair-like implant" to monitor different activity in the body reminded me of like a tiny thermometer to keep an eye on what's going on in the persons blood. Looks like an accurate way to keep an eye on themselves...like a diabetic having to poke their skin and use that drop of blood, but that "thermometer" (sencil) will do it without having to use blood outside the body.
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Post by bessie on Jun 8, 2009 14:47:23 GMT -5
kmarie - Yes, it is disgusting....at the same time that they are talking about population explosion, and this year - for the first time - there is a global food shortage. Yet how to create more people, instead of the "old fashioned way". Is it simply a case of one hand not knowing what the other is doing? Do we really need people to live twice as long as they are already? It doesn't even make sense! About 10 years ago my mother said "I don't know why I am here. My husband died 30 years ago, most of my friends and relatives are gone, I'm mostly blind and can't walk. I've done enough living." Now, at 92, she is in a nursing home asking the same question.
Bessie
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Post by lilsissy on Jun 9, 2009 0:42:54 GMT -5
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Post by lilsissy on Jun 9, 2009 1:28:44 GMT -5
looks like our hair servs as the building blocks for these sensors, United States Patent Application 20080072683 Kind Code A1 Liu; Chang ; et al. March 27, 2008
-------------------------------------------------------------------------------- Micromachined artificial haircell
Abstract A micromachined artificial sensor comprises a support coupled to and movable with respect to a substrate. A polymer, high-aspect ratio cilia-like structure is disposed on and extends out-of-plane from the support. A strain detector is disposed with respect to the support to detect movement of the support.
Inventors: Liu; Chang; (Wimetka, IL) ; Engel; Jonathan; (Minneapolis, MN) ; Chen; Nannan; (Urbama, IL) ; Chen; Jack; (Fremont, CA) Correspondence Name and Address: GREER, BURNS & CRAIN 300 S WACKER DR 25TH FLOOR CHICAGO IL 60606 US
Assignee Name and Adress: The Board of Trustees of the University of Illinois
Serial No.: 809523 Series Code: 11 Filed: June 1, 2007
U.S. Current Class: 73/774 U.S. Class at Publication: 073/774 Intern'l Class:
Near the end of this patent is the kicker,
[0043] Haircells according to example embodiments provide a simple receptor that may serve as a modular building block for a variety of sensors, thus providing multi-modal sensing, including applications beyond flow sensing and simple mechanical sensing, if desired. Such various types of sensors may be provided, for example, by varying one or more features of the preferred haircell. For example, haircells according to example embodiments may be used as an acoustic sensor, vibration sensor (1-3 axes), equilibrium sensor, magnetic sensor, airflow sensor (1-3 axes), waterflow sensor (1-3 axes), tactile sensor, accelerometer (e.g., via direct vibration), chemical, biological, or biochemical sensor, and other types of sensors. Cilia operating, for example, as ear hairs may be used to provide a microphone-like device.
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Post by lilsissy on Jun 9, 2009 1:46:08 GMT -5
The straw with in a straw is comprized of cabon nanotube,
-------------------------------------------------------------------------------- United States Patent Application 20090111174 Kind Code A1 Parker; John A. ; et al. April 30, 2009
-------------------------------------------------------------------------------- Biomolecule analyzing system
Abstract A biomolecule analyzing system (10) that provides an expeditious, accurate and reliable method for analyzing a biomolecule (150). The system (10) includes two substrates (12,28) each having an inner edge (14,30), an outer edge (16,32) and an inner surfaces (20,36) from where extends a multiplicity of cilia (22). To the inner edges (14,30) is attached an input tube (82) that is also attached to a biomolecule sample reservoir (90). To the outer edges (16,32) is attached an output tube (106) that is also attached to a sample deposit chamber (120). The tubes (82,106) include a plurality of conductive plates (98) that are applied an electrical charge that causes the biomolecule (150) to traverse through the tubes (82,106). When the biomolecule (150) passes through the cilia (22) signals are produced that are applied to a pair of image capturing devices (40,50). Each device (40,50) produces a signal that is applied to an electronic data processor from where a three-dimensional image of the biomolecule (150) is produced and viewed on a data monitoring device (70).
-------------------------------------------------------------------------------- Inventors: Parker; John A.; (El Monte, CA) ; VanDeMortel; Mike; (Yorba Linda, CA) Correspondence Name and Address: ALBERT O COTA 5460 WHITE OAK AVE, SUITE A-331 ENCINO CA 91316 US
Serial No.: 977679 Series Code: 11 Filed: October 25, 2007
U.S. Current Class: 435/288.7; 977/751 U.S. Class at Publication: 435/288.7; 977/751 Intern'l Class: C12M 1/34 20060101 C12M001/34
--------------------------------------------------------------------------------
Claims
--------------------------------------------------------------------------------
1. A biomolecule analyzing system (BAS) comprising:a) a first substrate and a second substrate, with each substrate having an inner edge, an outer edge, an outer surface and an inner surface, wherefrom the inner surface of said first substrate extends downward a multiplicity of probes, and from said inner surface of said second substrate extends upward a multiplicity of probes, wherein the termini of said probes are spaced apart from each other and are in an anti-parallel configuration.b) a first image capturing device that is attached to said outer surface of said first substrate, and a second image capturing device that is attached to said outer surface of said second substrate, wherein each said device is applied a signal from said respective first and second substrates, thereby causing each of said devices to produce an output,c) an electronic data processor having a duel input that is applied from said two outputs of said first and second image capturing devices, wherein said processor operates in combination with software to control the operation of said BAS,d) a d-c power source having means for supplying the required electrical power levels to said BAS, wherein the outputs from said d-c power source are controlled by said electronic data processor,e) a biomolecule passage track comprising:(1) a non-conductive input tube having an input edge that is attached to a biomolecule sample reservoir, and an output edge that is attached to the inner edges of said first and second substrates, and(2) a non-conductive output tube having an input edge that is attached to the outer edges of said first and second substrates, and an output edge that is attached to a sample deposit chamber, wherein said input and output tubes having means for causing a biomolecule sample applied from said biomolecule sample reservoir to sequentially traverse through said input tube, the space between said multiplicity of probes, through said output tube and terminating at said sample deposit chamber, wherein when the biomolecule passes through the area surrounding said multiplicity of spaced probes, said probes are stimulated, thereby causing a charge to be applied to said first and second substrates, from where a pair of signals are then produced that are applied to said first and second image capturing devices where the input signals are converted to an image that is applied to and processed by said electronic data processor and viewed on a data monitoring device as a three dimensional image.
2. The BAS as specified in claim 1 wherein said first and second substrates are comprised of a piezoelectric substrate having an inner surface, an outer surface and an irregular crystal matrix, and wherein the material for said first and second substrates is selected from the group consisting of GaN, galium compounds and mechanically confined nanocrystals.
3. The BAS as specified in claim 2 wherein said multiplicity of probes are comprised of a multiplicity of cilia, wherein each cilium is further comprised of a single-walled carbon nanotube.
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