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The Fiber Disease

Human Anatomy, Physiology, and Medicine. Anything human!

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Postby RANDY » Sat Sep 23, 2006 12:13 am

For all of those that want to help with our effort to establish center for research around the USA that will keep the CDC honest please print this and keep it in your file for future reference.


1) Get several patients who live in each state call a contact person in state government.
2) Someone needs to find individuals willing and able to call, identify the contact person, and give the phone number to the patients asked to call.
3) ID multiple potential obstacles.
4) Get a minimum of 5 or 6 states to take this on. Thus keeping the CDC honest.
5) Target a few states for intensive lobbying at a time.
6) Follow up with calls.
7) Line up a focused group of constituents to actively lobby their state legislators.
8) Call the contact person at the state public health agency.

Added: Send them the outline of what the Georgia program is doing.


So we are going to get one person from each state.

They will ID the person to call and send the Georgia outline to. We are checking now to see if the Georgia person is willing ot talk to different state health departments. We are not talking to local health departments, only state ones.

Then they need to find about 10 people who are willing to follow up with calls and letters from their state.

Once the initial contact has been made and the docs sent to that person the follow up calls and letters, return receipt willl start.

The goal is not to tell your life story but to professionally insist that a similar program is set up so that these program can report their findings to the Board and we can show the CDC what we have found and compare it to the CDC findings in order to keep this honest.

Please write me and /or call me if you want tolead your state.

I need your name and the name of the 10 people in the state that will do the follow up letters and calls.

We are not to yell or compalin. This is a professional effort to get peole to help us and nothing less but professional actions will be tolerated so I need to talk to each and every person and we will be keeping in contact once a week for updates.

Randy (Yaskal)

434-974-7128
cisfl2004@netzero.com

I will be pacling this effort on my web page as the first page starting next week.

http://unknownskindisease.com
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Postby RANDY » Sat Sep 23, 2006 1:12 am

Look up LIGANDS..there is your
culprit.
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just because you say it is does not make it so

Postby Sabrina » Sat Sep 23, 2006 1:49 am

I am not begging Randy and I resent you saying that. I am using polite etiquette and proper language when asking some one to help you. Take notes and learn. I use words such as please and thank you every day to many people. You should try it sometime.

Now, if I thought that begging anyone would get my family members and me some help you better bet your a_s_s I would do it in a heartbeat, no questions asked, no pride! I have literally begged doctors to help me with this condition in the past, to no avail I might add, and if I was begging Tam I would be happy to share that with you as well, however, I have not begged anybody on the internet for anything in my life and if I ever do I will let you know.
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Postby reliefseeker » Sat Sep 23, 2006 3:24 am

HELLO ALL, I have read your postings with much interest and have really enjoyed this site. It is informative and there are people like me who have this dreaded disease. Please allow me to share some information with you: I became aware of this disease when I was a teenager, I went to the theatre when I was about 16 years old, and felt something crawling all over me. When I atttempted to bathe, I could not stop the pruritis, so I went to the hospital and was diagnosed with scabies. Over the course of 30 years, I would become infected, initially it was infrequent and then it became often. And I wondered why other people did not contract it who were with me. But I was always able to manage my disease with a pyrethrins shampoo or elimite (or some sort of scabies lotion). And carpet has been the number one culprit of my getting infected, particularly if it had not been vacuumed and/or just merely swept. BUT my disease progressed this year. I bought a house last year that had the most beautiful beige "plush" carpet that was 7 years old along with the house. I felt something crawling on me from the carpet in the living room, even after I had vacuumed the carpet I would feel something crawling.Pretty soon, the darn things were in the carpet in my study, then they were in my bedroom. I tried to shampoo the carpet to no avail, then I used Pura-Clean, a carpet disinfectant. After my capet dried in the bedroom, I got in the bed and after about 5 minutes, I was attacked by seemingly invisible "pests". Now that was this past May 25, 2006 and I developed a BAD facial parasitic infection...I could feel something actually hatching in my face and my eyes became swimming pools for those "pests". I used Sulfa on my face until it was clear two weekks, and then had amoxicillin prescribed for my sore and painful throat, and I could feel the tickling sensations of the "parasites" in both my nostrils. The next week, I bought some tennis shoes off the sale racks, and those darn critters poured into my ankles. I now have "pockets" around my ankles that peroidically emit eggs that come through the skin, attached to a hair follicle that crawl and bite the crap out of me. A doctor prescribed ivermectin, and a infectious disease doctor prescribed the abendazole. The albenza stopped the chronic joint pain in my left leg. But nothing has stopped the parasites and the "swimmer's itch". So now every doctor is calling me delusional because when I attempted to show them these crittes, they remained hidden even when I sprayed them with a mixture of pure tea tree oil, peppermint enzyme, and olive oil. So now I'm on own and I have to 'clean my feet and legs every 3-4 hours to remove the eggs that hatch and crawl all over my feet and legs and bite like heccccccccccck!!! Please bear with me while I shorten this letter...I started taking sulfur pills and then noticed bumps on my leg and the swimmer's itch was right at the surface...after reading about garlic being an antiviral, antiparasitic and antiviral I started taking gobs of it. None of the oral supplements give me any relief, then I decided to use the 1500 mg concentrated garlic oil on my skin. AFTER 10 minutes, 3 1/2 inch white threaders came out of my left foot, and two came out of the right one, and one came out of my face. When they came out, I felt 50% better and there is very little biting now. But nothing stops the nonstop emiittance of eggs coming up to the surface. And I too have written CDC, my senators and went to CDC last weeK, but was not allowed to talk to Dr. Gerberding, the director of CDC here in Atlanta. All doctors have labeled me as being delusional, so now I can not get a darn prescription. Well, now I know that those "threaders"/white fibers are most likely anerobic as well as aerobic...and when you treat the inside (and push those "threaders" to the surface you can get them out) more than likely you should the treat the outside. Take care everyone
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Postby RANDY » Sat Sep 23, 2006 3:30 am

Marc's cream, the guy from Germany..it works to kill the eggs.
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Postby Skytroll » Sat Sep 23, 2006 5:40 am

Some news that might wake some up.


http://tinyurl.com/q9hel
http://tinyurl.com/n87hw

Especially the part about healthcare.

Another take on it:

http://tinyurl.com/ky7hu

Here is the Corridor:
http://www.nascocorridor.com/add_a_map.html

Drugs can have a straight run back and forth right through the Heartland.

I am excited, aren't you?




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ok

Postby RANDY » Sat Sep 23, 2006 6:15 am

You all need to check out the role of Ligands in our disease. It is a molecule that attaches to a larger molecule by a force and thus cuases that molecule not to do what it is suppose to do in the body.

It is involved with Sarcoidosis, lyme and parasitic diseases and MRSA.

It is one peace of this holy grail for the Messanger RNA piece of the puzzle that I was thinking came from a mutated DNA causing a bad copy of the RNA .well..check out Ligands in biochemistry and look up what you have wrong with you other than this with this disease and you will see the connection.

Randy
Last edited by RANDY on Sat Sep 23, 2006 8:54 am, edited 1 time in total.
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Postby RANDY » Sat Sep 23, 2006 8:52 am

BTW: I was not putting anyone down about asking or begging..that was not my intention. I was stating the fact that you had to ask and ask and ask again, still with no answer was a show of how inhuman and how little he cares for us and you. Not that you were doing anything wrong. It showed his character and not yours.

Randy
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Postby Skytroll » Sat Sep 23, 2006 2:56 pm

EPA not useful anymore? Or is it to cover what they are or are not doing? Or maybe they actually have found that nanofibers are causing the disease of the 21st Century. The aerosol experiment worked, didn't it? When EPA, DOE joined forces, I think the EPA knew their cover was being ruffled. Now, they are insignificant, and the history suppressed. Are we to keep letting these agencies and their misguided leaders follow this protocol?
Will the scientific truths of scientists works be buried again?

If we do not speak now, and start this movement we will never know what hit us. Because, slowly all of the free info as Systemic says will not be free or available. So, my job is to expose this the best I can.

I think a lot is a stake here for the American people, including, and first our health. Are we to let the MIC and the UN control our very movements upon this earth?

Here is one story about the big lie, that has governed the EPA, global warming, climate change,
evolutionary projects to ease us into chimeric transformations:

http://www.foxnews.com/story/0,2933,215084,00.html

and another to take our Voices out of Hearing range:

"The U.S. Environmental Protection Agency is moving ahead this summer to shut down libraries, end public access to research materials and box up unique collections on the assumption that Congress will not reverse President Bush's proposed budget reductions, according to agency documents released today by Public Employees for Environmental Responsibility (PEER). At the same time, EPA's own scientists are stepping up protests against closures on the grounds that it will make their work more difficult by impeding research, enforcement and emergency response capabilities.

In an August 15, 2006 document entitled "EPA FY 2007 Library Plan," agency management indicates that it will begin immediately implementing President Bush's proposed budget cuts for the next fiscal year, which begins in October, without waiting for Congress to act. The memo describes what EPA terms "deaccessioning procedures" (defined as "the removal of library materials from the physical collection") for its network of 26 technical libraries. Under the plan—"

http://www.yubanet.com/artman/publish/a ... 0955.shtml

Rearranging the chairs on the Titanic.

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Postby Sabrina » Sat Sep 23, 2006 4:30 pm

RANDY wrote:I was stating the fact that you had to ask and ask and ask again, still with no answer was a show of how inhuman and how little he cares for us and you. Randy



Dear Randy, Your perception is a bit warped and your reading comprehension a bit lacking to say the least.

I asked for Tam to share the letter ONE freaking time. Please reread my post, and then reread it again, and perhaps once or twice again after that.

I cannot help it if you have a problem with Tamtam. You always have and probably always will. This is YOUR problem. Please keep your personal problems with him off of this board. I would like to make it clear that I am not begging you to do this since I used the word “please”, I am just being polite. :)

Now if you want to talk about who is being inhumane then you may want to use an appropriate example such as our government agencies that are supposed to be doing their jobs and doctors that see this crap eating my flesh and tell me to get out of their office and not to come back. No phyc. referral is ever given so it does not matter if they think your nuts or not. THEY REFUSE TO TREAT REGUARDLESS IF THEY SEE THIS AND BELIEVE IT OR NOT! I have seen animals get treated better!

I had an ER visit in July. I had to go because I had yellowish puss coming out of my lesions that I have had all over my legs for at least a year now. I could not take the pain any longer and went to the ER to beg for some type of relief from the increasing and severe pain. Do you think I could get even one lousy pain pill? NO, they would not give me a damn thing for pain. I guess that oozing puss coming from open year old lesions did not look painful to them.

The doctor actually had the nerve to get mad at me for asking him why he was not addressing the black excrement and fibers that were in my lesions when he diagnosed me as having foliculitus. I told him that I was unaware of any type of foliculitus that produced such symptoms and that I believe that he may have misdiagnosed my condition. I asked him why he was refusing to address the fibers and black stuff. He actually got angry and told me to leave and that “we are done here” and I was begging for his help. He gave me no answers and nothing for the severe pain, just the boot.

That is my definition of inhumane. Tam owes nobody anything. Remember that.

Tons of people every day lay claim to knowing what this is. London is a perfect example of that. I do not see you attacking them. Why so personal with what Tamtam claims?

I had and still have about sixty or more lesions on my right calf alone. I cannot afford the luxury of trying out anyone’s “cream” for them either since I am broke as H-E-L-L!!! I have managed to get rid of the oozing puss since a fellow Morgie took pity on me and mailed me some antibiotics. The lesions, with new fibers daily, still remain and bleed daily.

Another example and better yet, how about the I.D. Doctor named Marion Michaels from Children’s hospital in Pittsburgh that said, “I did not treat the first little boy with Morgellons and I will not treat the second one.” How Freaking humane is that?

Last point, I fail to see why I should have to beg any doctor who is taking my money to help in the first place. I have paid Tam nothing.

On this note and in honor of the physicians spoken about above, I would like to start a doctor hall of shame on this thread. At least we will know who not to go to so our money is not continually wasted on inhumane treatment.

Doctor hall of shame coming soon on the first page of this thread. STAY TUNED!

Peace,
Sabrina


P.S.

Dear Reliefseeker,

Welcome to biology online, sorry you suffer.
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Postby Foxy Lady » Sat Sep 23, 2006 6:22 pm

Hello, all. I do not have the disease but am very interested and have searched many sites and seen many pictures, especially Anne Dill's and Jan Smith's. What a pity Anne Dill withdrew from the forum.

By coincidence I was on the CoastToCoast website and saw the report of a guest called Charles Ostman. This man's into some serious nano-syntho-bio technology.

Please have a look. It may be nothing. Go to coasttocoastam.com and look in the September shows for this man's name. There are six slides. Go to slide 6. At the bottom is a picture of exactly the type of multicoloured tangled fibres that both Anne Dill and Jan Smith have shown.

Thank you.
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Postby Foxy Lady » Sat Sep 23, 2006 6:23 pm

Hello, all. I do not have the disease but am very interested and have searched many sites and seen many pictures, especially Anne Dill's and Jan Smith's. What a pity Anne Dill withdrew from the forum.

By coincidence I was on the CoastToCoast website and saw the report of a guest called Charles Ostman. This man's into some serious nano-syntho-bio technology.

Please have a look. It may be nothing. Go to coasttocoastam.com and look in the September shows for this man's name. There are six slides. Go to slide 6. At the bottom is a picture of exactly the type of multicoloured tangled fibres that both Anne Dill and Jan Smith have shown.

Thank you.
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