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Post by violet on Sept 28, 2009 14:26:57 GMT -5
Here's a pic of Mee-aaats-Mee-aaats!! Well..you guys know the saying..'You feed 'em - You keep 'em' ? That's what happened..he sat in front of the door all day long..crying..'meow, meow'..let me in, let me in'..and one morning I was sitting in the dining room and he looked at me with his cute little face through the window and I couldn't resist anymore..he melted my heart..just like that! the little rascal! As I let him in, he jumped onto my lap and purred really loud and made 'biscuits' with his paws..he's so adorable..I wrapped him up in a towel cuz he was a little wet, it was raining, and held him like a baby in my arms as Kammy came and saw this..OH, Boy!!..ut oh..I thought..She got me!.. How cute!!! Don't you just love how they make biscuits? My white kitty, Sophie, must think she is making a very, very large loaf of bread, as hard as she goes to it. It hurts after a very short time! :-) I think this little gray kitty of yours is going to grow into a gorgeous cat...
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Post by violet on Sept 28, 2009 14:28:56 GMT -5
I had two orange creme cats with matching eyes that used to lay in my bathroom sink like that. They were orphaned and my son found them on his birthday.......heavy sigh. \\\ They sound like they were beautiful Frito. Just beautiful.
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Post by kammy on Sept 28, 2009 18:55:07 GMT -5
Mee-aats! You handsome kitty! Cotton, soybean, and corn use a baculovirus: hmmm? tinyurl.com/yaw7yfuSee my article I published today about how I believe that these baculoviral capsids are also known as fullerenes: morgellons1.wordpress.com/
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Post by kammy on Sept 28, 2009 19:14:51 GMT -5
If we do a search on just 'food fullerene' we get: tinyurl.com/ya2a7jfI didn't know that fullerenes were an antioxidant or a free radical scavenger, did you?
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Post by bannanny on Sept 28, 2009 19:27:09 GMT -5
I'm sorry kam... I still don't know the difference between baculovirus, fullerene's, PA, you name it... I'm lost. But I sure know a sweet face when I see it and Mee-aats has one of the best! What a cutie pie! I'd never be able to resist that...
hugs ~~ bannanny
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Post by kammy on Sept 28, 2009 20:10:58 GMT -5
I keep plugging along Banny, waiting on the Material Scientist, Molecular Biologist, or Nanotechie to drop in and say... 'Yeah, that's it! or Naw, you're a mile off!' I saw where the exact metals they used were listed, if some of us could get some analysis done, we're at that point.
Yes, Meee-aats is sweet!
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Post by bannanny on Sept 28, 2009 20:19:55 GMT -5
That's the only reason I post all the pics and what I think here kammy... in hopes someone out there somewhere is reading this board and one day will step in and give us a hand. Helloooooooooo out there!!
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Post by kammy on Sept 28, 2009 20:30:53 GMT -5
We'll get some help someday, Banny... we've just got to believe that someone, somewhere cares about people and humanity?
I thought those photos in my article might be empty carbon cells and emailed some material scientists, etc., a while back and noone responded... I don't think anyone is going to go out of their way to step in our 'do-do'? But, we've got to keep trying.
Maybe, I can find a 'techie' site and get some help that way?
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Post by kammy on Sept 28, 2009 22:17:56 GMT -5
Still looking at the patents under 'food fullerene': ''Water containing fullerenes and method for producing the same'' www.freepatentsonline.com/6833145.html''A method and an apparatus for producing healthy drinking water containing fullerenes, which is excellent as healthy water...'' ---------------------------- Isn't Squalane the agent in the current Swine Flu vaccine that is of concern? ''Squalane containing ultra fine particles of burning residue of carbon and method for producing the same'' www.freepatentsonline.com/y2003/0113315.html'' Squalane, which contains fullerene useful for a complex material with high functionality including effects on improving health, is provided. Squalane in which fullerene as ultrafine particles of carbon combusting residue are floating is produced by combusting mixed gas of oxygen and hydrogen in squalane in a vacuum and heating and combusting carbon with the combustion gas obtained.''
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Post by kammy on Sept 29, 2009 5:05:03 GMT -5
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Post by toni on Sept 29, 2009 7:05:05 GMT -5
Jeany oh how precious, Mee-atts is just as sweet as can be!
Violet, I cracked up about your precious kitty making "a big loaf of bread" ;D instead of biscuits! ;D hhehee too funny! ;D
Which I'd never heard that term (making biscuits till now, and that too is as cute as can be).
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Post by kammy on Sept 29, 2009 11:00:42 GMT -5
Buckyballs made safer for humans www.newscientist.com/article/dn6458-buckyballs-made-safer-for-humans.htmlThe soccer-ball-shaped carbon nanoparticles were shown to cause brain damage in fish and kill water fleas in a study in March 2004. But now a team at Rice University in Houston, Texas, US, has come close to understanding how buckyballs - more formally known as fullerenes - kill cells and how their toxicity can be lowered in human cells. Although the toxic nature of the carbon-60 nanoparticles may be useful in medicine, for example in fighting cancer, there are concerns that their potentially widespread use in fuel cells, drug delivery and cosmetics could mean they find their way into the environment, and so into animals and humans. "There are a couple of different manufacturers that will, and are, mass producing fullerenes," says Christie Sayes, one of the team. "They could make it into consumer based products: fuel cells and batteries or make-up," she says. Ruptured cells The team, led by Vicki Colvin, looked at the effects of buckyballs on human cells. They found that even at quite low concentrations in water the buckyballs killed human skin cells. However, when they attached chemical groups such as hydroxyl groups to the buckyballs, their toxicity was greatly reduced.The higher the number of groups that were attached, the less toxic the fullerenes became, so that a buckyball with 24 hydroxyl groups attached showed a toxicity seven orders of magnitude lower than the original buckyball. The researchers believe the buckyball is toxic because in water it leads to the formation of an oxygen free radical which reacts with lipid molecules forming the cell membrane surrounding a cell. This causes the lipid molecules in turn to become free radicals - and when these try to interact with the water outside the cell, the membrane ruptures leading to cell death. Eva Oberdõrster at Southern Methodist University in Dallas, Texas, who led the buckyball study in fish, called the new work "an excellent first step" in reducing the toxicity of buckyballs.
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Post by kammy on Sept 29, 2009 11:03:56 GMT -5
Finally, a definite 'OH' to attach to the 'HO' to stop the chain reaction!! This is too funny that the compound I've been looking for is the chemical symbol 'OH', when I told someone that was what I was looking for months ago! (Nevermind, inside chemistry joke.) Theoretically, hydroxyls should help with our lesions. Hydroxyl group en.wikipedia.org/wiki/HydroxylIn chemistry, hydroxyl is composed of molecules consisting of an oxygen atom and a hydrogen atom connected by a covalent bond (single bond). The neutral form is a hydroxyl radical. The hydroxyl anion (OH−) is called hydroxide; it is a diatomic ion with a charge of negative one. When linked to a larger molecule the hydroxyl group is a functional group (–OH). Hydroxyl group The term hydroxyl group is used to describe the functional group –OH when it is a substituent in an organic compound. Organic molecules containing a hydroxyl group are known as alcohols (the simplest of which have the formula CnH2n+1–OH). Hydroxyl radical The hydroxyl radical, ·OH, is the neutral form of the hydroxide ion. Hydroxyl radicals are highly reactive and, as a consequence, short-lived; however, they form an important part of radical chemistry.
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Post by kammy on Sept 29, 2009 11:51:08 GMT -5
Did you understand that the CDC has a hand in making this swine flu vaccine and promoting it that has fullerenes in it? That either I am wayyyyyyyyyy off base with my findings or the CDC has not looked at baculovirus/fullerenes as a cause to our disease and is unaware of the effects on humans that they can create a disease such as ours?
If the CDC is not aware because of possible lack of research, then you can almost bet that this upcoming report is NOT going to address our issues.
I want to state that I do not believe that all baculovirus expressions are necessarily fullerenes, unless the technology has come to that? As per what they are supposed to be made out of was laid out earlier in this thread. However, I believe that the ones that I am viewing in Morgellons human samples are fullerenes, as per my blog article showing and stating why I think so. We just need confirmation.
BTW. Banny, baculovirus/fullerenes are the 'black specks'... has anyone had a large lesion that at times when you worked it, you got black stuff under your fingernails?
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Post by bannanny on Sept 29, 2009 15:29:54 GMT -5
Here's a couple different looking black specs of mine kammy. Toni and I have identical pics of this one below (being mine)... This one being toni's (next to a salt granule)... If you look closely, you can see the "folded arm-like extensions" on mine too at the top of the pic. Then this one looks like it has strands coming out of the corners... (bottom lighting) (top lighting) I don't know if any of that will help you out... but all I understand is pics as you know! To lighten it up a bit again, here's a good pic of violet's beautiful "Sophie"... hugs ~~ bannanny
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Post by violet on Sept 30, 2009 11:38:42 GMT -5
Dear Kat and Kammy:
More pictures of your precious little furry children, please!!!!!! We LOVE them! :-) (And it sure gives a nice, relaxing break from our anxst!!!!)
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Post by jeany on Sept 30, 2009 11:39:40 GMT -5
Finally, a definite 'OH' to attach to the 'HO' to stop the chain reaction!! This is too funny that the compound I've been looking for is the chemical symbol 'OH', when I told someone that was what I was looking for months ago! (Nevermind, inside chemistry joke.) Theoretically, hydroxyls should help with our lesions. Hydroxyl group en.wikipedia.org/wiki/HydroxylIn chemistry, hydroxyl is composed of molecules consisting of an oxygen atom and a hydrogen atom connected by a covalent bond (single bond). The neutral form is a hydroxyl radical. The hydroxyl anion (OH−) is called hydroxide; it is a diatomic ion with a charge of negative one. When linked to a larger molecule the hydroxyl group is a functional group (–OH). Hydroxyl group The term hydroxyl group is used to describe the functional group –OH when it is a substituent in an organic compound. Organic molecules containing a hydroxyl group are known as alcohols (the simplest of which have the formula CnH2n+1–OH). Hydroxyl radical The hydroxyl radical, ·OH, is the neutral form of the hydroxide ion. Hydroxyl radicals are highly reactive and, as a consequence, short-lived; however, they form an important part of radical chemistry. Excellent research Kam!! Of course I just had to know what that Hydroxyl is all about and looked it up. I found a german website where it said that Hydroxyl is a form of fruit acid Alpha-Hydroxy-Acid or short AHA. Ergo Hydroxyl is found in fruits...and especially in bananas. That' the reason why some Morgies report that putting a banana peel on their lesions helped to clear them up? The main source according the german website is sugar cane juice. Here's a site according the Hydroxyl in bananas. I think the bananas should be quite ripe to have the highest effects.. Effect of hydroxyl radical on the scission of cellular wall polysaccharides in vitro of banana fruit at various ripening stagesFruit ripening is generally attributed to disassembly of cellular wall, particularly due to solubilisation and depolymerisation of pectin and hemicellulose. Effects of ·OH induced by the Fenton reaction on the scission of pectin and hemicellulose in vitro were investigated. As fruit ripening progressed, the sugar components of the WSP, HC1 and HC2 attacked by ·OH showed obvious molecular-mass downshifts. OH production in pulp tissues increased significantly as banana fruit ripened, which further help account for the role of ·OH in accelerated fruit ripening. Jeany
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Post by jeany on Sept 30, 2009 12:02:41 GMT -5
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Post by jeany on Sept 30, 2009 12:07:19 GMT -5
completeskincaretherapy.blogspot.com/2009/08/understanding-alpha-and-beta-hydroxyl.htmlAlpha and beta hydroxyl acids are similar to a microdermabrasion or exfoliate treatment. They slough off the top layers of the skin thus promoting new skin cell growth. Additionally they claim to stimulate the production of collagen and elasticity in the skin. Alpha hydroxyl acids are derived from fruit, milk and sugars. They are represented on skin care labeling as: Glycolic acid - sugar cane Lactic acid - milk Malic acid - apples and pears Citric acid- oranges and lemons Tartaric acid - grapesBeta hydroxyl acid is salicylic acid which is derived from aspirin and is oil soluble. Beta hydroxyl acid is best for oily skin that is prone to breakouts, blackheads and whiteheads. The acid is able to penetrate deep into the pores to exfoliate and clean. Furthermore, because Beta-hydroxyl acids are derived from aspirin they retain anti-inflammatory properties. ** how 'bout mixing some Aspirin in to the paste??? Jeany
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Post by jeany on Sept 30, 2009 12:13:45 GMT -5
How to make AHA easily yourself at home using fruits!! www.care2.com/greenliving/homemade-fruit-acid-skin-care.html#Alpha-hydroxy Acid (AHA) fruit acid skin care products are easy to make at home. Fruit acids loosen the “glue” between dead skin cells, and the cells fall away, leaving your face very smooth and soft. Here are three simple plant acids examples to use for your skin: 1. Lemon juice. 2. Strawberries. 3. Grapes. MORE HYDROXY ACIDS Malic acid ( apples, vinegar, applesauce, cider); lactic acid ( buttermilk, yogurt, powdered skim milk, sour cream, blackberries, tomatoes); tartaric acid ( grapes, grape juice, wine, cream of tartar); citric acid (citrus fruits such as lemons, limes, grapefruit, and orange); or glycolic acid ( sugar cane). A german site mentioned also Papaya.Just dab some of the liquid on your face with your fingertips, let set for ten minutes or so, then rinse. Note, too, that your skin can get sunburned more easily when you use fruit acids, so make certain to use sunscreen. Jeany
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