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Post by ruth on Jul 5, 2010 13:36:05 GMT -5
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Post by bannanny on Jul 5, 2010 13:57:03 GMT -5
I have tons of pics that are identical to yours ruthie... and I see the "scratches" in everything this stuff comes into contact with too. I think it has the capability to embed right into any surface and become a permanent part of it. How it does it, who knows... but it definitely does it!
You could even see them embedded in my skin when Dr. Matthews put this scope thing on it. The images showed up right on the puter as he ran it over my skin... it looked just like your images do too.
big hugs ~~ bannanny
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Post by ruth on Jul 5, 2010 19:58:57 GMT -5
hi nan, i posted this because it looks like the nematodes andy coyle presented, but it does not act the same. it has sporatic movements what does dr. matthews think the bottom line is? did he say?
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Post by skylark99 on Jul 6, 2010 7:34:11 GMT -5
It is likely that most of you have seen this: Common Patterns Emerging from Testing Morgellon Sufferers morgellonspgpr.wordpress.com/2010/06/30/common-patterns-emerging-from-testing-morgellon-sufferers/From this information, we can read that Metametrix has found an unidentified ova in all of the Morgellons patients that they have tested. We also see that GPL has found what might be an antigen. My own Lyme doc has seen the parasite in Morgellons patients blood work. It is noteworthy that some communication between doctors and researchers would be helpful. If your doc has any information or seen any type of organism in your blood work or other tests, it may be helpful to ask that they communicate with either or both of the above institutions, or Cliffe or Andy W, or whomever you think would be able to collaborate, based on your current thoughts and theories. There is no denying that multiple- or co-infections are involved in this illness. I have seen some brilliant and outstanding work done on this very site with regard to mycoplasmic bacteria, yeasts/fungi. There are some fine minds posting here, and I thank you for all your hard work and efforts. On another note, this information is also surprising and corresponds with information provided in the above first link. I am sure most of you have seen this, as well, but to compare the two sources of information and the data that is in each of them is worth noting. Ginger Savely Ralph Strickers Documented data published: www.dovepress.com/articles.php?article_id=4431
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Post by bannanny on Jul 9, 2010 16:36:03 GMT -5
I saw Dr. Matthews again yesterday ruth and asked him if I could post his answer to your question above. He said yes, so here's what he thinks... As for my theory of Morgellons: First let me preface by saying that my theory is incomplete because it doesn't account for some unexplained elements, i.e., maybe there are some nanobots but since these are so far outside my area of expertise I can't comment on them. Okay, so first recognizing I'm leaving some things out, I think that Morgellons is an immuno-deficiency syndrome brought on by an unknown factor, possibly a chemical or a parasite and made worse by a deficiency in some essential elements and or pre-existing infections like Lyme disease. This leads to overgrowth of many infectious agents, resulting in the proliferation of biofilms in the body. When the biofilm load crosses a critical threshold, other bugs and parasites begin coming to the body to join the party and a terrible cascade of multiple infections ensues.
My goal is to interrupt the terrible cascade of infections by correcting mineral deficiencies, and targeting some of the known infections. That being said, we may need to remove several elements of the cascade before the patient can observe any benefits.So there you have it! He scoped my skin again too and along with the symptoms I'm having, he thinks my body's starting to fight back and beginning to reject this mess. I have been doin some herxing but nothing I can't handle... and I have to say from looking at before and after scoping pics that've been done, my skin and hair is looking a whole lot better! The one thing I've been experiencing alot tho is those bouts of extreme heat... like a volcano just erupted on my head and the lava starts to flow down my face and body. They don't last long but they've been happening way more than they were. He thinks it's just another good sign that my body is pushing this sh*t out... and I hope he's right! They aren't hot flashes caused by menopause either cuz I'm way over that one... they're different than those were anyway. Hi White Rabbit... I sure agree with what you said and don't know why it doesn't happen. Seems we could find answers alot more quickly if every morg researcher and doctor out there were to correlate their findings. Dr. Matthews has been great tho... one reason being he's got morgs himself. So just the fact that I finally have a doc who wants to learn as much as we do has been a real blessing! He's had to fight the fight not only with morgs too, but also had to fight to keep his practice alive. You know what they try to do to docs who try to help us, but he's still here and all I can say is I thank God he is. hugs ~~ bannanny
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Post by ruth on Jul 10, 2010 11:36:00 GMT -5
thanks nan,
how does dr. matthews look? does he still have the scarred looking skin?
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Post by bannanny on Jul 11, 2010 11:38:00 GMT -5
Funny you asked ruth... I just told him the other day how great he looks. I didn't notice any scarring on his skin at all and his eyes look lit up to me... like life has brightened his soul ya know? I know for a long time when I was at my worst with all those nightmare cycles my eyes started to look hollow to me. Now even mine look alive again... course Tom has alot to do with that and also me getting my mind right again and not obsessing over this anymore like I used to. Even yesterday when I had the worst day I've had in awhile... I put myself in the most positive place I could reach and everything started to subside again. The mind is powerful and can be the best medicine we've got IMO!
hugs ~~ bannanny
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Post by toni on Jul 11, 2010 12:34:23 GMT -5
Ruth,
Your slide pictures are so incredible, and they look just like mine. To see your pics, are like looking at my slide.
And I sure agree Bannanny, the scratches are ending up where ever, and for no logical reason - except morgs has something to do with it. It etches itself in the bathtub and sinks, and even my glass slides for the scope, and will literally/physically melt itself right into plastic then disappear. We've seen it, and there's not even any logical reason I've found either in reading of what has this type of capacity.
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Post by ruth on Jul 12, 2010 11:06:34 GMT -5
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Post by bannanny on Jul 12, 2010 12:14:39 GMT -5
Incredible pics ruth!!!! You captured everything I see with the naked eye all the time. The sparks, the strands, the colors... everything. Even worse is feeling it all. Like right now my skin and even my jeans feel like they're full of tiny electrical stickers bouncing in and out of me. I so hate this sh*T!!!!!
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Post by skytroll on Jul 14, 2010 11:53:43 GMT -5
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Post by skytroll on Jul 14, 2010 12:00:28 GMT -5
Seems to me the matrix is in the actin cytoskeleton, as seen in Skizits videos. en.wikipedia.org/wiki/LamellipodiaNotice the reference to mDia? is one of the formins. cat.inist.fr/?aModele=afficheN&cpsidt=18327023this from vaccinia virus: * Summary * Microtubules play an important role in the transport of viral pathogens during the establishment of their infection cycles. The microtubule cytoskeleton also facilitates efficient release of newly assembled progeny at later stages of infection. However, the precise effects of viral infection on microtubule dynamics are not understood. Using live-cell imaging, we show that vaccinia virus stimulates increases in peripheral microtubule dynamics at 8 hr postinfection. Infection also increases the frequency with which microtubule tips reach the cell cortex and reduces the acetylation of peripheral microtubules consistent with their increased dynamics. These virus-induced changes in peripheral microtubule dynamics are independent of the GTPases Rac and Cdc42, which are known stimulators of microtubule dynamics in uninfected cells. They do, however, require F11L-mediated inhibition of signaling via the GTPase RhoA and its effector, mDia. We suggest that increases in peripheral microtubule dynamics and cortical targeting contribute to enhanced virus release. www.cell.com/cell-host-microbe/abstract/S1931-3128%2807%2900073-XThis Cdc42 is related to cytoskeleton rearrangement. skytroll
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Post by skytroll on Jul 14, 2010 12:02:44 GMT -5
The lamellipodium (plural lamellipodia) is a cytoskeletal protein actin projection on the mobile edge of the cell. It contains a quasi-two-dimensional actin mesh; the whole structure propels the cell across a substrate (Alberts, et al., 2002). Within the lamellipodia are ribs of actin called microspikes, which, when they spread beyond the lamellipodium frontier, are called filopodia (Small, et al., 2002). The lamellipodium is born of actin nucleation in the plasma membrane of the cell (Alberts, et al., 2002) and is the primary area of actin incorporation or microfilament formation of the cell. en.wikipedia.org/wiki/Lamellipodiaskytroll
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Post by ruth on Jul 16, 2010 11:20:46 GMT -5
synthetic biology tinyurl.com/2fcrfxrOf all the tested analogues L-4-fluorotryptophan, L-6-fluorotryptophan and L-p-fluorophenylalanine effectively and irreversibly inhibited cell growth Figure 1. Oxidation of methionine residues and conformation of the prion protein. In spite of the huge amount of literature on prion proteins available to date little is known about the initial event leading to its misfolding. The moderately hydrophobic canonical amino acid methionine usually stabilizes á-helices in proteins. However its oxidized form, methionine-sulfoxide is hydrophilic and has a higher preference for â-sheets. If the oxidative stress within the cell is sufficiently high to oxidize certain methionine side chains within the prion protein, at least one portion of protein's á-helices is converted into â-sheet structures. Figure 2. Chemical model to study the nature of á-helix to â-sheet conversion in prion protein structure. By expanding the genetic code of the AUG triplet with extremely hydrophobic norleucine and extermely hydrophilic metoxinine it is possible to arrest physiologically and pathologically relevant conformational states of the prion protein. In this way we have a kind of Yin and Yang states reflecting two extreme conditions: One prion that mimics the stable, reduced form and one in which all methionine side chains are oxidized. The norleucine variant resulted in an á-helix rich protein that lacks the in vitro aggregation of the parent protein. In contrast, the methoxinine variant resulted in a â-sheet rich protein with strong aggregation tendency.
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Post by ruth on Jul 16, 2010 12:08:41 GMT -5
www.michaeljournal.org/syntheticbio.htm"They include sequences that that turn genes on or off, transmit signals, change colors." this is how i see it under the scope. the balls emit colors and are drawn towards the same and as they connect they form a filament of that color. i've seen the balls 'jump' to connect. i found this out by using black paper for a slide.
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Post by ruth on Jul 16, 2010 12:11:48 GMT -5
Francis Crick, co-discoverer of the DNA double-helix writes; "DNA makes RNA, RNA makes proteins, and proteins make us." The building blocks for proteins are amino acids. Codons (chemical bases) determine which amino acids will be produced within the cell, which is added to the protein under construction.
There are 64 codons but only 24 amino acids. Synthetic biologists work below the level of the gene, at the codon level, to rearrange codons to build new sets of biological instructions. For example, one codon might work better in plants, another codon might work better in bacteria. So they are created
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Post by ruth on Jul 16, 2010 12:20:36 GMT -5
Chris Voigt at UCSF (University of California in San Francisco) has re-engineered a strain of salmonella to produce the precursor to spider silk. DuPont has added genetic networks to the cellular machinery of E coli which, when mixed with corn syrup, produce a key component in Sorona, a spandex-like fibre. DuPont and Tate & Lyle are building a $100 million dollar factory in Tennessee to produce this. They expect it to cause as much fuss as the introduction of nylon in the 1930s. 5. Expanding Earth’s Genetic System – alien genetics Steven Benner of the Westheimer Institute for Science is creating new biological modules that can be chemically synthesized so that they reproduce and pass on their genetic inheritance in the same way that DNA does.He has created new nucleotide bases, adding to the four natural DNA bases. He states: "In five years or so, the artificial genetic systems that we have developed will be supporting an artificial life-form that can reproduce, evolve, learn and respond to environmental change." Eric Kool of Stanford has created a new molecule and states, "One day his xDNA could be the genetic materials for a new form of life, maybe here or on another planet." using bacterias that infect humans open up the dna to be reproduced by that bacteria infection? ? i wonder how many people that were infected by salmonella and e coli went on to develope morgellons??
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Post by ruth on Jul 16, 2010 12:36:53 GMT -5
looks like venter is taking all the credit for synthetic life, he should be the one to build a vaccine with a suicide gene that will infect our infection.........then stop it? i wrote him once, but he did not write back. maybe i'll appeal to his curiosity again. www.jcvi.org/cms/research/groups/
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Post by skytroll on Jul 17, 2010 3:11:47 GMT -5
Ruth,
He is planning or is out on his ship the Sorcerer II, investigating more abiotic material from under the sea.
Bet, he is prepared when people really wake up and see what he has created!
His arse will be sparse! We will make him eat MORGELLONS, fiberballs in all!
Skyship
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