Friday January 18, 2008
Dr. Harvey's Latest Statements Re Morgellons and Mutant Worms
The latest Washington Post article on Morgellons has interesting statements from Dr. Harvey as followup to my previous post.
Posted by Niels P. Mayer in Medicine at 20080118 Comments[11]
William Harvey, 70, who serves as chairman of the MRF board, has taken those theories one step farther. He says he became interested in Morgellons research after successfully battling chronic fatigue syndrome and made it his mission to find cures for such unexplained illnesses.He wouldn't be specific, explaining that he first wants the results of his research to appear in a top-notch, peer-reviewed journal such as the Lancet. "This may be the story of the century," he says. A semi-retired doctor in Colorado Springs who spent most of his career working in space medicine for the Johnson Space Center, Harvey says he may have found not only why Morgellons patients would both scratch and act strange, but also what could be the "genesis of probably most chronic human illnesses," such as autism, obesity, chronic fatigue and bipolar disorder.
It all boils down to this: mutant worms.
Harvey hypothesizes that a type of nematode, a wormlike parasite that lives in the soil as well as in the guts or lungs of about half the animals on the planet, mutated somewhere in the 1970s in Southeast Asia and jumped from animals to humans. The parasite is easily spread through the fecal-oral route if someone, for example, is out working in the garden, fails to wash his or her hands thoroughly and then eats an orange. Or it gets into the lungs by inhaling sputum or by kissing. The worm then takes up residence in the colon, Harvey theorizes, and the body's immune system holds it in check.
But when the immune system falters, the worms swarm in the body. That's what happens, Harvey hypothesizes, after a human is infected with a strain of bacteria first reported in 1986, Chlamydophila pneumonia. These bacteria like to live in immune cells, Harvey says, and they feast on those cells' energy. With the host's immune system compromised, the mutant nematodes begin reproducing exponentially, Harvey suspects. They burrow a hole in the wall of the colon, then usually travel at night through the bloodstream or the lymphatic system or crawl in hordes between the layers of the skin, like other species of nematodes are known to do, to the parts of the body with the most blood flow: the face, head and nose. There, a cranial nerve leads right into the brain. A pileup of worms could jam blood and oxygen flow to the brain, Harvey says. "That may explain the psychological symptoms," including the hallucinations, he says.
It may explain why Pam Winkler took herself to the emergency room recently. She said that a huge bump had appeared on the side of her skull in the middle of the night. By morning, she said, the bump was gone, but she could feel crawling all over her face. She wasn't making it up, she swore. And she put her stepsister, with whom she's been living since she got out of the state hospital, on the phone. "I can see them. They're moving down from her head to her eye," said Karen DeWeese. "They're about one and a half inches long and a half-inch wide. They look like bubbles under the skin." The ER doctor later found nothing.
The fibers, according to Harvey's theory, are really the hard shells, which he calls cuticles, that these worms shed at five stages as they grow from egg to larvae to adult. The red fibers are the males, he says. Blue fibers are female. "Using a 2,000-power microscope, you can see inside them," he says. "They look like little stovepipes to me. I can tell the blue ones are female because there's a kink in the middle for the sexual organs and some kind of pouch. And we have pictures of them laying thousands of eggs."
"If you write this theory, it's probably going to sound like someone's come from the mental institution," Harvey says. "But the fact is that this is a real disease, and it appears to be growing."
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Posted by Deborah Doctor on January 21, 2008 at 09:16 AM PST #
I've noticed a lot more blue than red so one would conclude there are more females than males if Harvey's color assumption is correct.
One thing which flies in the face of logic is this. I've seen four inch long cutile/fiber. If this were in fact using the lymph or blood stream, people with this would be having strokes left and right. I know it remains in soft tissue because I have seen it, but if it were as thick in blood stream, then more of us would die wouldn't we?
On another note. This assumption of the cuticle would also explain the "fibers" not matching any textile or fabric on the crime lab data base. That database probably doesn't have worm cuticles. Many a doctor have seen these but just could not identify.
I really do wish Dr. Harvey would share his images of these things laying thousands of eggs with his high powered scope with the CDC.
Posted by Grace on January 25, 2008 at 09:58 PM PST #
I have specimens from all over the world
that have been sent to me. I am meeting with a Doctor of Entomology out of USF
Next Friday.
I live very close to Hernando and live in Hernando County.
If you have names of patients and Doctors that these poor people have seen you can send it to my email. commonsensescience@yahoo.com
Thank You,
Trisha
Posted by Trisha Springstead RN on February 21, 2008 at 07:52 AM PST #
ivermectin, which is interesting because many sufferers are finding ivermectin to be only partially curative; many more seem to be finding significant improvements from fenbendazole, moxidectin (myself), or praziquantel (people other than myself). It is interesting to note that the world health organization has found ivermectin to be ineffective as well, which is why clinical trials on Moxidectin and others are underway ( http://lymebusters.proboards39.com/v45index.cgi?board=rash&action=display&thread=3219&page=2#39887 ).
A few quotes to summarize http://www.cpnhelp.org/microfilariae_more_body_s
"My LLMD has been involved in the work of a research team in USA headed by Dr William Harvey with professors in Colorado, Texas and New York investigating the causes of chronic auto-immunei illnesses and fatigue disorders. They have identified how bacteria, viruses and parasites interact to produce these illnesses, finding that the unbalancing of the immune system is at the root of many problems. The herpes viruses in particular are troublesome and also (quelle surprise!) chlamydia pneumoniae which enables many other organisms to take hold. "
"As well as borrelia and actinomyces they've also indentified microfilariae...these microscopic worms clog the blood vessels and lymph system, essential for immune function as most of the defense activity takes place in this system. They also infect the capillaries so impair the nervous system, aggravating many neurological signs and symptoms."
"This reseach will be published very soon but the treatments being recommended are antibioticsi as well as the anti-parasitic agent Ivermectin. My doc wants me to take a course of this as an addition to the Wheldon protocol. He's finding that once these little wrigglers are killed off and the lymph system is functioning properly people feel generally much better and he says the CAP will be more effective."
"the schedule is 4 x 3mg [of Ivermectin] tablets on day one, day seven and day thirteen."
"I took a once daily dose of 12mg of Stromectol (I am @ 165 lbs) for 14 days. We followed this up with 2 weeks of a single 12mg dose once a week to be sure to kill any offspring (demodex have a 2 week lifecycle as I understand). I kept a list of my reactions during treatment, and I've always wondered, given some of my reactions, if it wasn't actually killing something in addition to the demodex."
"... the evidence that microfiariae are found in chronic fatigue is about to be published in mainstream journals. My doctor has been sending videos of the blood of his ME/CFSi patients to Dr Harvey's team in America, they are looking at fatigue disorders. I don't have any pictures but there are references in Pubmed to findings of microfilariae in the CNS, brain cysts, breast cysts and most other areas of the body http://tinyurl.com/2xrkez and of microfilariae involved in other conditions http://tinyurl.com/2hfhka"
Posted by Niels on April 13, 2008 at 04:36 PM PDT #
Posted by ADELE FANTOZZI on September 18, 2008 at 06:41 AM PDT #
I am 47 years old, born and raised in Concord, MA, with frequent trips to the beach (Plum Island, MA and Cape Cod, where we still spend several weeks every summer). I went to medical school at Southwestern in Dallas and now practice psychiatry and neurology in the suburban and rural areas around Philadelphia PA.
I have been told all my life that I have eczema, but at age 12 or so, it suddenly got severely worse, with a lot of scalp involvement. I had growths under my eyelids and bull's-eye type rashes on my legs. Nobody knew for sure what it was, and assumed it was ringworm. Over time, the symptoms gradually improved and abated somewhat, but the "eczema" symptoms never disappeared.
I'm running out of steam, but will summarize that I had a major arthritis attack after presumptively treating Giardia, acquired in St. Petersburg, Russia, about a year ago with Flagyl. My positive ANA led me to a rheumatologist, who insisted I couldn't have Lyme disease due to my incomplete response to a monthlong course of doxycycline, and inconclusive blood tests. Connective tissue diseases have been present in several generations of my family, and we chalked it up to that. I began taking Plaquenil and Etodolac with partial relief, but still significant arthritis in the left ankle, with a lot of swelling.
Then I began to be awake all night with itching. The horrendous rashes, with an apparent "trail", made me think I had scabies, but multiple permethrin and stromectol treatments only seemed to keep it "at bay". I still have multiple skin lesions and horrific scarring. I extruded huge amounts of black and blue fibers for several months.
A dermatologist diagnosed me with Lyme disease and opportunistic scabies, and I started Doxycycline for a 3 month course (which she feels cured her Lyme meningitis). Symptoms improved a bit, but with the ankle and foot swelling still significant. That has receded somewhat with the addition of Zithromax for the past 2 months. The peripheral neuropathy remains bad, though.
My 11 year old son has symptoms of severe itching, and other symptoms consistent with chronic Lyme, ADD, etc. I have not seen any fibers extrude from his skin, though.
Cindy Casey was able to visualize the fibrous material under my skin with the dematoscope here at the conference. I am not sure what to do next, except to gather as much information as I can, and offer to help in any way possible.
This illness is so bizarre, even L Ron Hubbard could not have made it up. I'm very worried about the long term outcome for me and my family......all input is welcome. Thank you for your time in reading this.
Sincerely, Amelia Withington MD
Posted by Amelia Withington MD on October 19, 2008 at 05:28 PM PDT #
Posted by Karen on November 06, 2008 at 06:54 PM PST #
Posted by ADELE FANTOZZI on December 06, 2008 at 12:25 PM PST #
Posted by mary kay wojciechowski on January 28, 2009 at 08:29 AM PST #
One way to search a list by zip code is to go to the site "www.lymepa.org", register, then access the link for LLMD search. Register at that site, and you can see all of the docs who enroll to treat such infections. It is not a huge leap for an LLMD to acknowledge that Morgellons exists (in my humble opinion).
Be sure to go to the web site "www.howicuredmorgellons.com", sponsored by Mel Friedman, who was featured in the Reno news this past March 9. While I doubt that exact protocol would work for everyone, it does have elements of treatment that make sense, such as products which support the immune system, and inflammation control. Some elements of his approach might be able to be customized for individual people....
Thank you for the support, and don't give up! The radio program "Coast to Coast AM" is planning a 3 hour show on Morgellons from 10pm to 1am Pacific time, April 14 (I guess that's the 15th from 1-4am East Coast time--gulp), and I as well as some other familiar names from the Morgellons online and conference/research communities will be participating.
I should note that there have been some changes to my treatment since my post in October, and much more relief (though not resolution) of intensity of symptoms. Hang in there, and keep looking for answers that make sense to you--I do believe that there is relief out there for each person. I also am now seeing twice as many people in my medical practice who have it, and fully expect that I shall soon see more......let's keep talking, and we'll keep coming up with better and better strategies for relief! Cheers, AW
PS: Mary Kay, if your friend can't track down a doc with the strategies above, write back here and I will make inquiries. :>)
Posted by Amelia M Withington on March 19, 2009 at 08:33 PM PDT #
Please try to contact Dr. Harvey in Colorado.His address is 3010 N.Circle Dr., Suite 120, Colorado Springs, Co 80909
fax:1-719-234-0024
Best wishes!
Posted by Terrie Stone on March 23, 2009 at 12:25 PM PDT #