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Under Scrutiny

OSU biomedical researcher says science, not belief, will prove existence of skin disorder Morgellons


BY JAIME ADAME

Oklahoma State University Associate Professor Randy Wymore chooses his words carefully when describing the latest research into Morgellons, an often self-diagnosed malady involving claims of strange and inexplicable skin sensations.

Sufferers feel something like bugs or parasites constantly crawling on or beneath the body's surface. They also frequently spot oddly-colored fibers poking through their skin. The greater scientific community dismisses these claims as delusions.

Not so Wymore, a trim man who wears a hoop earring. But the biomedical researcher still maintains scientific skepticism when describing research done by others.

In June, the nonprofit Charles E. Holman Foundation -- a major donor to Wymore's research -- praised a study by researchers claiming a possible link between Morgellons fibers and material in cows with a disease called bovine digital dermatitis.

"The new study confirms that Morgellons disease is not a delusional illness, as some in the medical community maintain," the foundation said in a statement. The findings were similar to a 2011 study by the same researchers.

Wymore, however, described the research with decidedly less enthusiasm.

"Those two papers about the cow disease, I mean we wouldn't have published them in that form. It would have to have been way further along," said Wymore, who heads research at OSU into Morgellons. He's quick to add he's attempting to check out some possible links to the bovine disease himself, while also making clear how his work differs.

"There are plenty of doctors who have been able to look at those papers and say, 'Well, what about this, this.' They can go down the list of things," Wymore said. "Our paper just won't be published until those sorts of concerns have already been addressed."

In the vast holdings of research database PubMed, Wymore's name links to 12 scholarly articles -- none of which deal with Morgellons. His early career involved studying cellular biology, with his work published in reputable academic journals like Circulation Research. The peer-reviewed journal ranks fourth out of 117 cardiac and cardiovascular system journals, according to its publisher, in terms of "impact factor," a way to gauge the number of times articles in the journal are cited by other researchers.

This was Wymore's professional life before he began studying Morgellons "as a curiosity" several months after arriving at Oklahoma State University's campus on the west side of town in 2004. He had left a similar post at the University of Tulsa.

"Once I sort of came to the conclusion that, wow, there's something interesting going on here, I knew people were suffering. And I couldn't just say 'Wow, you people have a really weird disease, sorry you're suffering and nobody believes you, good luck,'" said Wymore, crediting his personal philosophy as a Unitarian concerned with community as reinforcing his commitment to studying Morgellons.



Early on, he spoke with people who said they had the disease, later also discussing Morgellons publicly on CNN and the ABC News program Nightline. Wymore, the lone voice with backing from a research university to say Morgellons exists, said he concluded Morgellons is real because "it was just the evidence was slowly building, looking at samples."

About 30 patients complaining of Morgellons were seen over a period of roughly four years by OSU physicians, Wymore said. Most had Morgellons, according to Wymore. No single "a-ha" moment sealed his conviction, though Wymore said a colleague's study of material exhumed from beneath the unbroken skin of a patient meant that Morgellons can't be explained by clothing fibers working their way into an open wound.

Many people adamantly complain online about their Morgellons symptoms, often plaintively and with deep concern for their health. Along with the sensations and fibers, people with Morgellons describe unexplained lesions and fatigue, as well as a mental toll that, whatever its origin, seems to be debilitating. Roughly 10,000 people have registered with OSU as at least potential Morgellons sufferers.

However, Wymore no longer answers his phone in an effort to avoid lengthy and ultimately fruitless conversations with Morgellons sufferers. But he said he gets calls and responds every week to doctors who take Morgellons seriously.

"They do think there is a psychiatric component to it. But what they're willing to say is, the disease is causing the psychiatric component, rather than the disease is purely psychiatric. That's a big distinction there," Wymore said.

Past attempts at scientific collaboration have fizzled, which Wymore blames not on skepticism but the pressures on modern scientists to remain competitive with their peers.

He continues on despite a January study from the well-respected Centers for Disease Control in which researchers failed to find anything like Morgellons in a sample of people who claimed Morgellons-like symptoms.

"We were not able to conclude based on this study whether this unexplained dermopathy represents a new condition, as has been proposed by those who use the term Morgellons, or wider recognition of an existing condition such as delusional infestation, with which it shares a number of clinical and epidemiologic features," researchers wrote, advising psychiatric treatment for people claiming Morgellons.

Wymore, part of a group that examined the experiment's data prior to publication, said the research had fewer than 50 weaknesses, including a small sample size of people who participated in every step of the study.

"No one was observed to have had fibers emerging from the skin, and so my feeling is that, just by default, they did not have a Morgellons population," Wymore said.

Of course, if such fibers don't exist in the way Wymore says he's observed them, the finding would make perfect sense. CDC researchers stated that fibers from biopsy specimens were "compatible with cotton fibers."

Funding hasn't noticeable dropped off since the CDC report, according to Wymore, and it includes enough money for a lab technician. Notably, if tax-deductible donations to OSU's Morgellons research foundation reach $50,000, it's eligible for a $100,000 grant from an endowment fund set up by T. Boone Pickens upon Pickens' death, Wymore said.

So Wymore stays in the lab, Morgellons his full-time research topic, though he has other university duties. He conducts broad sweeps of samples to search for a connection between Morgellons and a particular fungi or bacteria. "Is there anything different we see about a Morgellons patient from the control, unaffected population as far as bacteria on the skin?" Wymore said, describing one question he's trying to answer.

He's also working on a case study of a Morgellons patient, which could be complete within the next six months.

"We're going to go for the highest-profile journal we can," Wymore said.

Wymore said he sees colleagues doing interesting, less controversial research and sometimes longs to participate. But his immediate future lies with Morgellons.

"My goal has pretty much always been that I will keep doing this Morgellons research until other labs better suited to it completely just get involved and quickly make progress and I'm not necessary, that would be one condition. Or we, or someone else, figures out the cause of this," Wymore said. "So I guess, in either case, I'll keep doing this until I'm not necessary."

Send all comments and feedback regarding City to jadame@urbantulsa.com



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COMMENTS
9 comments posted for this article
gmoreno
 4/17/2013 - 12:14am
   Dr.Randy Wymore soy de Chile necesito comunicarme con usted, por favor deme su correo le enviare mis observaciones, que he realizado por 3 años. Aquí en Chile he consultado a varios dermatólogos y no saben nada sobre estas investigaciones de morgellons. Mi email gmoreno8867@gmail.com
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denisemontanino
 3/ 8/2013 - 3:39pm
   Dr.Wymore, Thank you for all your hard work. I have been to a de doctors but according to them I'm crazy. I live in Aledo Tx west of Ft Worth if you know of any doctors in this area could you please send me there named and location. I really to find someone to tell me I have this disease.
   
   Thank you so much
   denise.montanino@yahoo.com
   817-965-4633
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Paul Von
 3/ 8/2013 - 9:58am
   I have concluded I have the Lyme/Morgellon composite disease, and am now taking Levofloxacin antibiotic at 500 mg per day along with Artemisia absinthium (wormwood), which slows cellular efflux mechanisms. Wormwood is an important adjunct to antibiotic products, as these types of bacterial organisms tend to pump antibiotic elements out of the affected cell- rendering many antibiotics ineffective. There is also strong evidence that biofilms and cysts may be formed by this disease, which makes it quite intractable and difficult to eradicate.
   It is important to continue any antibiotic regimens for a significant period of time (at least 6 months), as this disease is a composite disease that often carries a number of other bacterial co-infections. There should be regular prescription changes made to antibiotic regimens, as this disease often becomes resistant to antibiotics in a very short period of time.
   Levofloxacin can be followed by a high-dose regimen of Doxycycline for a minimum of six weeks, then followed by other products such as Vancomycin or similar.
   Herbal remedies are fools gold, and not recommended in any competent studies. Avoid any metals products such as Colloidal Silver, and avoid oral doses of magnesium or zinc, as these materials feed the organisms. Avoid electromagnetic fields from cell phone, wi-fi, or wireless technologies, as these technologies significantly impair autoimmune functions.
   For a brief description of the Lyme/Morgellons composite disease, please refer to the link below, and good luck.
   http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544355/
   Also see this important page.
   http://morgellonswatch.com/2007/08/28/a-history-of-the-fiber-disease/
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linbartlett
 2/ 4/2013 - 5:56pm
   I Am in Virginia also, my home too is as Efarkash has described. Emmerte too describes the all too familar symptoms. Whatever this stuff is morph's into many different forms.
    Interestingly I have found some reddish twig-like material most everywhere in our house. With curiosity I got a magnifying glass to examine a piece and was in awe to see a beautiful clear red iridescent filament rhythmically waving away from and towards the main structure. After a few minutes it broke away from the main structure and became the "fiber" we all talk about.
   
   I have had some very very sci-fi symptoms I've not heard addressed anywhere.
   Some of the lesions will start spontaneously weeping clear fluid and I can feel volumes of fluid moving through my body - I get extreme edema in my lower legs.
   Prior to any lesion appearing small bruises with hard lumps appear in the area of the soon to be lesion. I have dozens and dozens of these bruises constantly.
   Many horrifying unbelievable phenomena have occured after I contracted what I believe to be Morgellons.
   I have been "zapped" or shocked when picking up some of the fuzz balls.. being so startled I screamed and immediately dropped the fuzz ball.
   On occasion I have rolled the fuzz balls between my fingers and fibers have shot out from the fuzz ball. One fiber was a couple inches long and similar to fishing line.
   I can feel a sticky substance on parts of my skin.. when bathing and rubbing those areas what appears to be hair from my head comes out of my skin. This also happened when I was receiving a professional massage at a Cancer Center (I also have stage IV Breast Cancer).
    I've had fluke-like matter drop off my body numerous times.. all approximately 1"-1 1/2" in size.
   Early on, my sinuses were acting up, so I used something similar to a neti pot for nasal irrigation, allowing the water to flow into a partially full sink. Out from my nose came two white fluke-like things.. definately alive.. swimming in the water. I picked them up and they would flip off my finger - I had no sensation of the move. One fell to the floor and immediately turned deep black.
   One lesion was bleeding, I removed what I thought was coagulated blood with my finger and the blood adhered to my finger.. since I was on my way to the doctor's anyway I asked the doctor to remove it.. they couldn't get it off, saying it needed to be surgically removed.. bit by bit I scraped it off.
   Again early on in this "battle" I was in the shower and watched in horror as this mucous-like amoeba-like "thing" emerged from my thigh.. I quickly grabbed tissue paper and blotted it off. Within a short period of time it crystalized on the paper. Again about an inch or more in size.
   My soaps had white yin-yang shaped matter on them after I washed. When placed in the shower soap dish the next day I would find they crawled out of the dish and up the wall.
   
   I took a bath with 4 cups of epson salts..the bottom of the tub was black with hundreds/thousands of grain like stuff and fibers. The next two days I thought I had the flu.. but was actually a horrible Herxheimer Reaction, throwing up, too dizzy to move.. no fever.. no respiratory problems.
   There is plenty more.. but it gets really gross so I'll stop here..
   Please.. Please.. PLEASE find a treatment.!!!
   
   THANKS DOC !
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efarkash
 12/21/2012 - 11:41am
   I am in Virginia and have the same symptoms as the first comment emmerte. I have black like specks that drop off and turn into these bug like things that stick to the surface oif what they fall on and then another type that turns into a little red worm which then mate and turn into this sticky mess of crystalized stuff that speads these egg, gnit type stuff around the house. I have a family and grandchildren and am constantly cleaning after my walking path because these fall off from I doi not know where and spread everywhere! I have them eliminating from me and my white blood cell count is high and my glucose. I have been laughed out of the hospital w/o even getting passed triage, my primary care physician told me I was bringing debris into him and did not have time for me the farthest I got wasd w/ a nurse from the dermotologist office. That is who gave me the results of blood work but what do I do w/ those rresults? It does show in my home like you would not believe, my husband has nott been to work for two weeks because he is constantly cleaning behind me from these things multiplying everywhere and we are not sure if it is contagious to my kids and gtandchildren. This is new to us andf do not know what to do. My hair is alive and when a strand is removed starts moving around liked a snake. Someone please help me w/ any suggestions on what meds moght relieve some of these symptoms. I am not delusional. My family is witness to this disgusting thing that I have taking over our home. I am leaving my number knowing that I might get some bad peoipl,e calling but hope I might get one person to give me a good suggetion, I AM DESPERATE! 804-874-6360.
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emmerte
 10/ 1/2012 - 5:34pm
   Dr. Wymore, Thank you for the work you do! It is particularly hard to suffer these symptoms and then deal with the disbelief of non-sufferers. But these symptoms are unbelievable- such as the morphing of tiny black specks into nymph-like things, then into slender rod-like needles, and then into a partially formed, almost grasshopper-shaped insect. Most unbelieveable is experiencing the appearance in the mouth, after eating, of a tiny insect followed shortly thereafter by tiny eggs, one at a time. Specks of fuzz found on clothing upon examination have tiny black things in their center. One wonders how the researchers account for these phenomena? Good luck with your work!
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