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Post by violet on May 6, 2012 22:29:14 GMT -5
violet, Thank you so much for speaking up. We would all be so much worse off if not for these folks carrying the torch. The research has to start somewhere, and theories developed or disproved. It sure can't be easy to put themselves out there like that. They do it for all of us. Yes, and many who are often themselves so very sick.I was interviewed for 3 days by a film crew from London almost 2 years ago. I dread the day that the story airs on Discovery (if it ever does). I live in a small community where I already am not accepted because I wasn't born here. These folks are going to have their noses even higher in the air than before. I did it for all of us in the morg community, but it will be hell on me and my family. I'm so sorry, bb. Thanks for having taken a very vulnerable step in being interviewed. Just remember that eventually something will more than likely be found out, and then those who have not been very nice to morgies should drag their noses on the ground!
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Post by itchin4answers on May 7, 2012 1:27:10 GMT -5
Dr Peter Mayne became a Dermatologist in 2005. Maybe reading about Morgellons led him to do the training. I am only guessing, I didn't have that opportunity to ask him during our one hour consultation at the end of February 2012. Unfortunately for me, the doctor never examined my skin. It is good to have a Dermatologist on board with this, however I've met him and he is currently making a complete mess of my treatment. So I'm not feeling very confident about him at all. Sorry, not wanting to put a downer, just telling the truth. I did say in a post somewhere after seeing this doctor and getting a diagnosis that he did touch my skin. Yes, he touched my face because I made him. I said the fiber infestation in my face was beyond bearable. I mentioned Morgone Gel and the F6/7 to break down the cellulose fibers. He was adamant that the fibers were not cellulose. He said that the fibers were Keratin and that the spirochete sits at the base of the hair follicle and makes Keratin fibers. A person feels movement because this fiber has no where to go and can not push through the skin. Sounds ok in theory for those of us with Lyme. It doesn't explain anything for those that do not have Lyme. It doesn't explain the coloured fibers I have had and it doesn't explain the fibers in my face, neck and scalp that run along my face in all directions. I am a little peeved to say the least as I do believe "this" is all about money and accolade. I have no concerns saying that here because I did tell the doctor that in a letter not so long ago when I was complaining about his fees and what did I have to show for it? nothing. I paid a fortune for a phone consult to be given directions about treatment, which I could not remember. My GP got all the directions in a letter to him which took over a week to arrive. I was supposed to take 1/2 (150mg) of Rimycin when in fact I followed the directions on the bottle by the dispensing chemist. So I ended up taking 4 times more than I should of done. Any wonder I felt unwell. Besides, the doctor has prescribed capsules and how does he expect me to 1/2 a capsule? Need I say more. Itchie, thanks for catching us up on this guy. Did I read correctly in one of the articles that reported on the research meeting in Texas that "eminent" was placed before many of the docs' names? I didn't think it appropriate at all. Was stretching things a wee bit too much, think I. And I'm right with you on the face issue--trails/tunnels going from main lesion in neck to all over the face. It's awful, and there is very little stopping it short of tearing the face apart to scratch out all the granules. It does prevent more fibers from growing, which is helpful, but what a mess--and so much scaring. Hi violet, I'm just telling you guys what happened with me as a patient of his. I can not comment on anything else because I do not know enough. I did work in health care for many years and I do get most upset with losing my career. I get very frustrated when I see so many errors in health care with doctors and a like and think back to how I was such an admired worker once upon a time...when my life was normal. I didn't find the "eminent" comment, though I agree with you. Whoever cracks the code of Morgellons and frees us all from this living hell will be eminent in my book. itchin
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Post by violet on May 7, 2012 10:30:52 GMT -5
Itchie, thanks for catching us up on this guy. Did I read correctly in one of the articles that reported on the research meeting in Texas that "eminent" was placed before many of the docs' names? I didn't think it appropriate at all. Was stretching things a wee bit too much, think I. And I'm right with you on the face issue--trails/tunnels going from main lesion in neck to all over the face. It's awful, and there is very little stopping it short of tearing the face apart to scratch out all the granules. It does prevent more fibers from growing, which is helpful, but what a mess--and so much scaring. Hi violet, I'm just telling you guys what happened with me as a patient of his. I can not comment on anything else because I do not know enough. I did work in health care for many years and I do get most upset with losing my career. I get very frustrated when I see so many errors in health care with doctors and a like and think back to how I was such an admired worker once upon a time...when my life was normal. I didn't find the "eminent" comment, though I agree with you. Whoever cracks the code of Morgellons and frees us all from this living hell will be eminent in my book. itchin Itch (and everyone), you couldn't find "eminent" because I don't think it was there. :-) I think I goofed. I must have been thinking of something else, and I want to be sure to correct myself to everyone! Very, very sorry for the mistake and comment.
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Post by itchin4answers on May 7, 2012 20:28:54 GMT -5
Hi violet, I'm just telling you guys what happened with me as a patient of his. I can not comment on anything else because I do not know enough. I did work in health care for many years and I do get most upset with losing my career. I get very frustrated when I see so many errors in health care with doctors and a like and think back to how I was such an admired worker once upon a time...when my life was normal. I didn't find the "eminent" comment, though I agree with you. Whoever cracks the code of Morgellons and frees us all from this living hell will be eminent in my book. itchin Itch (and everyone), you couldn't find "eminent" because I don't think it was there. :-) I think I goofed. I must have been thinking of something else, and I want to be sure to correct myself to everyone! Very, very sorry for the mistake and comment.Hi violet, We all goof (well I do!). I wrote that I was "frustrated", no the word I was looking for is BITTER I am very very bitter. I have one more test pending which I will have this week and then I will be looking for a Lawyer. My son keeps saying he wants me to sue the Government, well you know I just might try!! itchin
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Post by simone on May 8, 2012 19:47:23 GMT -5
I also hope researchers and doctors also look at people who make video's on this like skizit and many others. To learn... What better information to see from someone looking at this 24-7. meaning US that see it.. video it.. feel it.. I can only hope good doctors see our video.
Right now I'm arguing with a young uk doc. regarding one of my vids and it's gone to other vid's. To him we're delussional but he's looking more into it because he seems to comment alot. Telling me what pub med. published. yada yada... He's trying so hard to discredit us.
I think this condition is a very slowing healing process and I have a feeling the same will be with this condition being accepted and acknowledged in the medical field.
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Post by itchin4answers on May 10, 2012 2:43:09 GMT -5
The evidence is mounting up.
I am positive for Mycoplasma Fermentans.
My doctor called this afternoon and said "we've struck the jackpot you have Gulf War Syndrome and that was released by the US Army in Iraq".
My doctor wants to start treatment immediately so we'll chat tomorrow.
I was over the moon to get a positive result because my research from way way back like 8-9 years ago - Gulf War Syndrome is where I started and then Lyme. I don't feel so dense after all...LOL
I spoke to my mum and she was shocked, I said she can tell dad that his daughter has GWS and she didn't even enrol for the Army.
I'm gob smacked to say the least, all these years of suffering and of course not to mention "delusional" and all your physical pain is all in your head! grrr.....
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Post by Lynn on May 10, 2012 12:04:43 GMT -5
Hi Itchen
Love this and now I want to some how go to a Dr. and see if I can find a similar diagnosis. I still would try to solve the problem with diet and herbs, but it would be nice to have family know there are real issues involved that are not just skin problems or mental problems.
I have a very loving Aunt who just sent me the latest from the Mayo clinic on what to do for my condition. Which one of the items listed was to maybe seek professional help for the delusions. I feel helpless that they do not remember or recall all the other problems I had before the total outbreak. How even when the outbreak did happen the Dr. had look at samples and told me I had four stages of some kind of bug and he used the words I am guessing fleas. When I tried to get him to do lab work on my samples he said there were no labs available to him to diagnoses my samples. I took them back home and found they never looked anything like stages of a flea. So I just started researching all kinds of bugs and found they resembled mites. I keep telling family members it is not a skin condition. That is like telling a diabetic their sores from their disease is just a skin condition. Oh lets tell the Aids victims that their sores are just a skin condition and that they were delusional and accused of putting the sores there themselves. Unfortunately they did go through that for quite a few years. I know for sure 10 years, but probably twice that, because if I remember right the Dr.s or scientist who put Aides on the map took ten years to get it established with medicine.
Hope what ever treatment you get will help and I hope this gets documented enough to throw at the faces of those who had your child taken away. Maybe get a lawyer some day to threaten a lawsuit for your pain and suffering and ex-sponge your records. Some how some day some one has to pay for letting us go without real medical help to fight a disease that is ruining our health. It might as well be the medical or government people who took away more of your chances for help by taking your kid. They forced you down a trail deep and further from real help causing you to not be able to get real help for a real disease. They are partly responsible for your still being ill. I hope they get back what they gave and you get restitution. Hope I used the right word there.
Itchen I wanted to barrow your post to let the moderators know there are some of us who can not access the forum. The only way I got to read this post was to click on your name and click on your post in the area provided when you search a member and hit the reply button from there. Another member who also can not get to the forum part of the board told me how to do this so I could read some post.
I bet the board is so quite because some of us can not get on board. I sent a private message to administrator for help with the issue. Hope others that can not get on board will do the same so they will know how many are having the same problem. We get a message that tells us the forum URL has change and provide a link to click on and you click on it and takes you to the front page of the forum board and then when you click on recent it takes you right back to the same message about the URL being changed. Thank you.
In Light Lynn/TorpedoLynn
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Post by toni on May 10, 2012 16:53:21 GMT -5
Hi Itchin, I'm so glad you got a positive on something, because you as well as all of us (knows) there IS something horrible happening. And I'm very sorry it's Mycoplasma Fermentans. But now they can see (everyone) who ever doubted anything. Keep strong. And hi Lynn, Yes, I too cannot get to the board, and the only way I could was by clicking on "most recent posts" and then clicking on Itchins name to "get where I am on this thread". The site is saying it re-directed with the link, yet it doesn't work right. Take care all.
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Post by bb on May 10, 2012 17:39:52 GMT -5
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Post by itchin4answers on May 10, 2012 19:23:10 GMT -5
Hi Lynn, toni and bb, Thank you for your posts. This morning the reality has hit me like a lead balloon. Disbelieve, hurt and my eyes fill with tears. I am having trouble grasping all that is going on, how are my family supposed to understand? So very hard for all. To say to friends and family I am a walking bioweapon is going to raise concerns with them. All of this sounds far fetched but it's true. I was right from the start and my research began with the Gulf War Veterans website. This is their website today; www.gulfwarvets.com/Great source of information from Dr Garth Nicholson and others. It is true - everything starts where it ends. bb, thank you for bringing that link to my attention. I found the exact same link for Tony last December as he had the Mycoplasma pneumonia. I think it was around 2006 that I phoned National Security one day to report "Morgellons"...that's how scared and sick I was. I had been programmed well, bioterror preparedness. So like a good citizen I placed a call, gave all my personal details and I was given a reference number. The lady on the other end of the phone was very nice and offered to send a police officer over to my home to sit with me. I said I would be ok and she needn't do that. So from that day on National Security had free rein to look through all my personal information because I said it was ok. I knew back then that something terrible was going on. I was given the gift of fear for a reason. I feel like I'm standing outside of myself once again...WHY...is all I can think about. Mum doesn't understand how I have contracted this M.Fermentans. I said possibly due to travelling so much, my exposures etc. I have been bitten by every bug known to man since I was very little. I can not help but think there is a link to my disease and my home UK. Yes, this disease IS a continuation of the World War II experiments in Nazi Germany, these days though they do the experiments in the comfort of your own home. Lynn, yes, restitution is the right word. Someone has to take responsibility for this, if the AU Government want to point the finger at the USA fine by me, they could at least compensate those of us who have suffered beyond comprehension. I often think about people who have this and never come to the internet and don't have anyone to talk to. There are no words to describe the loneliness and isolation. I'm not so worried about myself so much, it's my son and the doctor who diagnosed me DOP when I was pregnant needs a good slapping around the head, idiot. I've printed up this blurb to give to my Dad (he's a book worm) in the hope he will look to read this book. Project Day LilyBy:Garth L. Nicolson, Ph.D and Nancy L. Nicolson, Ph.D. The Institute for Molecular Medicine www.immed.orgProject Day Lily chronicles the events surrounding the "Gulf War Syndrome” suffered by over 150,000 veterans (and tens of thousands dead) without proper acknowledgment or treatment to keep secret the origin of their illnesses. Were our Armed Forces exposed to chemical and biological toxins that were supplied, in part, by a sinister network of rogue bureaucrats, intelligence operatives and scientists? This is the story of how one of these biological agents was found by two American scientists as part of a massive testing program and how various academic and government employees did everything in their power to keep this information secret. Project Day Lily is based on a true story. The authors wrote Project Day Lily in order to shed light on a crisis facing our country and the world. A fictional format was used to maximize dramatic content; the events described are true, and the scientific principles discussed in the book have been documented in the authors’ publications, reports and sworn testimony to Presidential Commissions and committees of the U. S. Congress. Project Day Lily is dedicated to the memory of Dr. Fred Conrad (Colonel, USAF, retired) and five other academic colleagues who died under mysterious circumstances while investigating aspects of the alleged illegal testing of Biological Weapons in Texas hospitals, nursing homes and prisons. This book is also dedicated to the men and women of our Armed Services and their family members who were put in harm’s way and were never properly warned about the dangers of Biological Weapons, and to the Texas Department of Criminal Justice personnel and its prisoners and to the people of the Great State of Texas who were betrayed and lost their health and loved ones to a vicious agenda in the name of ‘National Security’. www.projectdaylily.com/I'll check back with you all later, and thank you for supporting me. itchin
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Post by itchin4answers on May 11, 2012 5:55:56 GMT -5
I'm not having trouble getting to the board, rather my email account, Facebook also. That little lock in the browser becomes open with a big red cross through it. Annoys me more than anything. I can not see how my personal information would be of any interest to anyone. I spoke with Dr Mayne and I like the man, he knows what he is doing. He found the missing link - M.Fermentans - and he said that is why I am not getting better. He said M.Fermentans causes ALS. What is ALS? www.alsa.org/about-als/what-is-als.htmland brain infections. I don't want either. Starting treatment next week with Ciproxin. tinyurl.com/84trvgjThis is not on the Pharmaceutical Benefits Scheme. Treatment will be for about 4 months at $75 a month. I do get a pharmaceutical allowance with my disability pension, though that wouldn't cover the price of a roll of toilet paper, just under $6 is what the Government give to help with paying for medicine. I gave my parents the document provided by bb and I read the first page to them. My parents had been working out that where I had travelled to in 1992 put me right in the "down wind" of all that had happened in the Gulf. I know of another girl in Melbourne who started with Morgellons after holidaying in Greece. I felt sorry for my dad, I could see it on his face and in his eyes. Dad asked me if M.Fermentans was man made - I said "yes, engineered". Dad then disappeared to another room to lose himself in something else. Mum tried to search Gulf War Syndrome on the internet last night and said she got totally confused as she is only new to the net. So thanks again bb for that link as I had forgotten all about it. All these years later my family can not grasp the enormity. Maybe they will grasp how bad things are if my brain continues to deteriorate and my body. Body pain is bad, particularly my back and yes I'm a little scared. I don't want to suffer any more. If anyone is interested I would like to think about finding a Lawyer, for all of us if possible. Just throwing ideas around, thinking aloud. I can not and will not let go what has happened. The Australian and Victorian governments are committed to several international human rights agreements that recognise everyone’s right to the highest possible standard of physical and mental health. They recognise your right to health care and to other services essential to health, including safe water, housing and health-related education. In Victoria, publicly-funded healthcare services must legally comply with the Victorian Charter of Human Rights and Responsibilities Act 2006, which protects a range of human rights, a number of which are relevant to people seeking or receiving health care. Consumers, patients and providers Consumers are people who are current or potential users of health services, including hospital patients. This includes children, women and men; people living with a disability; people from diverse cultural backgrounds and faiths, socioeconomic status and social circumstances, sexual orientations and health conditions. The healthcare provider is the trained health professional providing your care. The healthcare service is the organisation responsible for providing healthcare services. Your rights in the Australian Charter of Healthcare Rights Access – a right to access health care. Safety – a right to receive safe and high quality health care. Respect – a right to be shown respect, and to be treated with dignity and consideration. Communication – a right to be informed about services, treatment, options and costs in a clear and open way. Participation – a right to be included in decisions and to make choices about your health care. Privacy – a right to privacy and confidentiality of your personal information. Comment – a right to comment on your health care, and to have your concerns addressed. health.vic.gov.au/patientcharter/victoria/index.htm
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Post by itchin4answers on May 11, 2012 17:58:14 GMT -5
Dear itchin, I would love to hear what Prof. Nicolson has to say about so-called "Morgellons". I have sent him an email. I printed and read that entire article, then told my husband he may have it since he tested positive for Lyme. He has a pretty positive attitude about it, considering. He is an exterminator who will be continually contracting Lyme (or Stari in Texas) and he is pretty unhealthy. He recently began seeing an accupuncturist who told him he is her most challenging patient ever and she is very concerned about him. She is doing blood workup, but doesn't see any point in testing for Lyme at this point. She is helping me to detox, etc. She said his profession is aging him too fast. I wish I could share his attitude! Hang in there, you are not alone! Hi bb, I finally read that entire article on the Mycoplasma, it was very well written. Your husband, so sorry to hear he is not well, sounds just like my Tony (very unwell). I think that my personality helps to balance things between us, as I am the one a little more determined and won't let people get to me (though they do). There are some YouTube with Dr Garth Nicholson talking about Morgellons. I listened to them last year, sorry I haven't looked for them again, but they should be there. Dr Nicholson sounds, and looks like a very sincere man, and he has been put through hell too. Hi ginna, I have to agree with what you said (your comment below); I am really starting to think that morgellons may not anymore be it's 'own' disease, but instead a process of acquiring and the blending of other infections. (I wanted to highlight your comment though I can not get it to work, I can not get smiley faces to work either, another computer glitch maybe)
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caroltrew
New Member
My dogs have Morgellons too!
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Post by caroltrew on May 12, 2012 6:39:31 GMT -5
Hi Itchin, I too have just last week been dianoiased with Mycoplasma, I am looking at my lab work now and they are calling it Mycoplasma Pheumoniae Antibodies. M Pheumoniae as IGG. EIA. Mycoplasma Pheumoniae Antibody detected. 1.57 H Reference Range <0.90 IRS. I'm being treated with Azthromycin 500 mg. This is my 3rd. week of a 7 day treatment. Being treated by Dr. Neeland Uppal in Pinnallis Fl. My Pain Management Dr. just yesterday saw these results and from what I gather it would not be his personal peferred treatment. The Pharmacy told me that this med. stays in your system for two weeks after taking it, so if there was a problem with the insurance covering it back to back (saying too soon for refills) I would still have it in my system. So we will see. Pain mangement Dr. is very UP on Morgs. and everything and has helped me more than anyone to this point. He said also a dianosis of M. Pheumoniae ment that there was a underlying infection, and that was what we had to get to. Dr. Uppal (infectious desiese Dr.) also ordered further testing of Antimitochroudrial Ab and Antismooth muscle Ab, after looking at past lab work done by my pain management Dr. My pain mamagement Dr. said lets wait for thse results and take it from there, that she was suppose to be the Infectious Disease Dr. I hate the diffrence in opinion, it's not very encourgeing. At least like you say we have found something to work on, and go from there. It's funny tho, not either Dr. mentioned a word about it being Gulf War Sysdrom. I'll speak to them next visit (for Sure) on that. In the mean time thanks for all the info on it and I'll read up on it and please keep us posted on your treatment and condition, and any new news on Gulf War Systrom
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caroltrew
New Member
My dogs have Morgellons too!
Posts: 5
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Post by caroltrew on May 12, 2012 7:17:44 GMT -5
This is great bb I will diffently read this. He is right about the co infections, that's just what my dr. said. Another strage thing that is showing up im Morgs. (which they have also found in me) is the presence of cytoplasmic fluorenscence on the HEp-2 slide, other reactivities (e.g., antimitochondreal antibodies or anti- smooth muscle fluorencence) may be responsible for this fluorescence. That is why they are further testing for Antimitochroudria Abs., and Antismooth muscle Abs. Dr. sasid all these positive test in this area lead back to one thing (underlying infection, not detected. Does that mean that this cytoplasmis flourenscence (for this showed up first) leads back to the Mycoplasma? an infection? in brain body where?
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Post by Lynn on May 12, 2012 8:01:52 GMT -5
Hi BB
I clicked your link and get a nice DNA stand to the upper left and a bunch of little oblong boxes with a ghostly file imprinted into each one. There are over a dozen to choose from. Are all of them the answer from Dr. Nickleson?
Thank you. In Light Lynn/TorpedoLynn
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Post by violet on May 12, 2012 9:14:45 GMT -5
I spoke with Dr Mayne and I like the man, he knows what he is doing. He found the missing link - M.Fermentans - Starting treatment next week with Ciproxin. tinyurl.com/84trvgjHi, Itchin. I'm so glad you have a diagnosis. I can sense your relief in that. I just want to send you a BIG warning, though, about using Cipro. It has recently been found to cause some side effects that you want to be sure to be aware of if you decide to proceed. It can cause retinal detachment. It can also cause problems with tendons. I've had the retinal involvement (a sudden influx of floaters instead of detachment, fortunately) and tendon issues from using it. The tendon issues seem to have resolved themselves, which I'm very thankful for, as that is not always the case. My internist said her husband took Cipro recently and has had serious tendon issues from it. Please be sure to do an on-line search to consider the potential for serious side effects before using it, okay? I feel really bad having to send you this information, Itch. But it is what it is, and it's better to know there may be complications from using it before you proceed. Update: It was retinal detachment that her husband suffered--not tendon issues. It is a very serious situation in that detachment of the retina can quickly cause blindness if not attended to right away by an opthalmologist.
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Post by toni on May 12, 2012 10:03:39 GMT -5
First time I'd ever taken Cipro was in 1990 for brochitis. That was in fact the first time I'd ever had bronchitis - which I wonder about "today" if that's what it was back then, because Cipro is not the first line of defense for treating bronchitis either. Sure gets me wondering now "why" that doc prescribed that.
Anyways, long story short, on my 2nd or 3rd day of taking it, I almost passed out at work, it had me so lightheaded, I had to hang onto my desk to remain upright, and I popped out in allergic hives.
I went home, took an antihistamine, and a cold shower and called my doc, which he said I did the right thing and to discontinue it.
I'm only expressing this info too so that IF you take that med and have any "oddball reactions" it's probably the drug, so please just keep a real good eye out for "adverse reactions" because (the side effects might not be a herx reaction) but rather a serious reaction.
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Post by violet on May 12, 2012 12:12:45 GMT -5
Thank you bb for sharing this information. I would be very interested in his suggestions to 'manage' this disease. I knew him from Houston, Texas when I was there. He and his wife are good people. Violet and Toni, Yes Cipro has what is called a "black box warning" along with other antibiotics in it's same 'class'. Cipro was prescribed for me for the mycoplasma pneumonia. I had to take them for 3 months. I called the doctor on several occasions because I feared the 'possible permanent consequences'. Thankfully, I got thru the 3 months without problem. (or so I think?) it happened over a year ago. Very good to hear that you escaped (hopefully) any of the serious side effects. Just keep vigilant about noticing any that may come about, as sometimes the side effects happen months after taking the meds... (I realize you probably already know this.) Take care. Violet, I had not known about the "floaters" being a side effect. I have noticed more of them recently and I don't like them and it worries me. They are not constant floaters fro me. Thank you again for pointing this out because it seems to make sense about why I noticed floaters. Dr. Nicholson responded very quickly and said I can share this info. His website is here but I'm not finding his Morgellons info there, it is just FYI: www.immed.org/This is his email: "Although there are bacterial elements to Morgellons disease, it iscertainly more complex than Lyme disease or Mycoplasma (usually aco-infection in Lyme). Morgellons appears to have unusual elements of parasites and perhaps eveninsect elements (the fibers of some Morgellons patients havecharacteristics of chitin, an insect material). Although themicroorganisms involved have not yet been identified, I believe thatMorgellons will ultimately be found to contain a complex array ofdifferent microorganisms (for example, Lyme disease is a complex mix ofco-infections that include Borrelia, Mycoplasma, Babesia, Bartonella,Ehrlichia, etc.). One of the Morgellons co-infections is likely to be Mycoplasma, inparticular Mycoplasma fermentans, because Morgellons patients often have this co-infection, but that is far from the whole story. As other elements are discovered and confirmed, a more rational approach fortreatment will evolve. I have attached some general information on preventing transmission, etc. Prof. Garth Nicolson" Now how do I post a 6 page pdf file from him? It even suggests some things to do to manage this scourge.
Itchin, I sent it to your email address. I tried copying and pasting here but it lost some formatting. I'm headed to a b-day party and don't have time to work on it. Please share it if you can!
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Post by ginna898 on May 12, 2012 12:28:52 GMT -5
Oh NO, From Toni's Link: www.whale.to/m/scott7.htmlI - PATHOGENIC MYCOPLASMA A Common Disease Agent Weaponised There are 200 species of Mycoplasma. Most are innocuous and do no harm; only four or five are pathogenic. Mycoplasma fermentans (incognitus strain) probably comes from the nucleus of the Brucella bacterium. This disease agent is not a bacterium and not a virus; it is a mutated form of the Brucella bacterium, combined with a visna virus, from which the mycoplasma is extracted. The pathogenic Mycoplasma used to be very innocuous, but biological warfare research conducted between 1942 and the present time has resulted in the creation of more deadly and infectious forms of Mycoplasma. Researchers extracted this mycoplasma from the Brucella bacterium and actually reduced the disease to a crystalline form. They "weaponised" it and tested it on an unsuspecting public in North America.
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Post by toni on May 12, 2012 12:57:20 GMT -5
Hi Ginna, And yes, I've been reading about this, and it's quite scary. Here's more about that link and Dr. Scott and Myco/Brucella. Actual Government records are reproduced that reveal plans made in 1969 to create a "new synthetic virus, one which does not naturally exist, and for which no immunity could have been acquired." Other documents reveal that between 1985 and 1989, while publicly labeling Saddam Hussein an evil monster, the United States was secretly selling Iraq hundreds of deadly biological weapons, some of which Hussein employed against the Allied ground attack and stopped that attack dead in its tracks after just 100 hours. A four page Foreword by Dr. Garth Nicolson, one of the world's top microbiological medical researchers, validates the research. www.whale.to/v/scott.html
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