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Signs herpes outbreak is coming

If the above diagnoses are inconclusive or if a treatment regimen has already been started, a biopsy of the affected skin (i.e.
Spray tub and bathroom floor with disinfectant after each use to help prevent reinfection and infection of other household members.
Wash feet, particularly between the toes, with soap and dry thoroughly after bathing or showering. If you have experienced an infection previously, you may want to treat your feet and shoes with over-the-counter drugs.
Dry feet well after showering, paying particular attention to the web space between the toes.
Try to limit the amount that your feet sweat by wearing open-toed shoes or well-ventilated shoes, such as lightweight mesh running shoes. After any physical activity shower with a soap that has both an antibacterial and anti-fungal agent in it. Morgellons Disease Awareness -  Artist and Morgellons sufferer, Ayla, journals her experience with the disease   I'd like to introduce myself, I'm Ayla, a 59year old artist and graphic designer who contracted Morgellons in Jan.
The herpes group of viruses is composed of at least eight human viruses and numerous animal viruses [see 7:XXX1 Viral Zoonoses]. All human herpesviruses have a worldwide distribution [see Sidebar Herpesvirus Information on the Internet]. Humans are the only known natural hosts for HSV, although animals can readily be infected experimentally.
HSV-2 shedding from the genital tract can occur in seropositive persons who have no history of genital HSV infection.5 Thus, transmission occurs frequently, even in the absence of lesions. After the initial replication of the virus in epithelial cells, cytol-ysis and local inflammatory reactions develop, resulting in the characteristic lesion—a superficial vesicle on an inflammatory base. After initial infection, HSV travels along sensory nerve pathways to ganglion cells, the site of latent infection.
In patients younger than 5 years, primary HSV-1 infection is most often asymptomatic; when symptomatic, it presents as gin-givostomatitis or pharyngitis.
Recurrent herpes labialis is a shorter and milder affliction, often heralded by local pain or tingling for a few hours. Extragenital lesions develop during the course of primary infection in 10% to 18% of patients.
Figure 1 Herpes simplex virus genital lesions in men often present as grouped vesicles on the penile shaft. Figure 2 Perianal herpes simplex infections in patients with compromised immunity may be severe and prolonged. Figure 3 Herpetic whitlows, which occur on fingers, are often misdiagnosed as staphylococcal infections. Urinary retention may occasionally complicate primary genital herpes, particularly in women. Recurrent episodes of genital herpes are usually shorter and milder than primary episodes but still affect women more severely than men. Herpetic whitlow Primary finger infections, or whitlows, usually involve one digit and are characterized by intense itching or pain followed by the formation of deep vesicles that may coalesce [see Figure 3].
Neurologic complication Encephalitis, a severe form of HSV infection, is discussed elsewhere [see 11:XVI Acute Viral Central Nervous System Diseases]. Infection in the immunocompromised host Disorders of T cell-mediated immunity are associated with more severe HSV infections. Neonatal infection Between one in 2,500 and one in 10,000 births are complicated by HSV infection, usually HSV-2. A variety of tissue culture systems support the replication of HSV, and virus isolation from specimens collected early in the course of infection is the diagnostic method of choice. The best strategy for the prevention of neonatal herpes may be close physical examination at the time of labor.18 Cesarean section is indicated to prevent perinatal infection when lesions consistent with the diagnosis of genital herpes are noted during labor. Ocular infections, when severe, may lead to decreased vision, blindness, and even loss of the eye. Posterior Ocular Infections are infections that commonly involve the posterior aspect of the eye including vitreous, optic nerve, retina, and blood vessels. The human herpesviruses include herpes simplex virus types 1 and 2 (HSV-1 and HSV-2), varicella-zoster virus (VZV), cytomegalovirus (CMV), Epstein-Barr virus (EBV), and human herpesvirus types 6 (HHV-6), 7 (HHV-7), and 8 (HHV-8, also known as Kaposi sarcoma-associated herpesvirus [KSHV]). Herpesviruses replicate primarily in cell nuclei, and a protein envelope is added as the virus passes through the nuclear membrane.
Members of the group can cause productive lytic infections, in which infectious virus is produced and cells are killed, or nonproductive lytic infections, in which viral DNA persists but complete replication does not occur and cells survive. Considerable efforts are being directed toward the development of vaccines and antiviral agents that will be active against herpesviruses. Restriction enzyme analysis of HSV DNA and other molecular techniques are used to identify individual isolates. HSV-1 primary infection occurs mainly in childhood, whereas HSV-2 infection occurs predominantly in sexually active adolescents and young adults.
HSV-1 oral-labial lesions recur more often than HSV-2 oral-labial le-sions.3 Vesicles appear most often on the vermilion border and are painful. Primary infections may present as unilateral follicular conjunctivitis, blepharitis, or corneal epithelial opacities. After an incubation period of 2 to 7 days, fever, malaise, and inguinal adenopathy develop; these symptoms are associated with the appearance of vesicular lesions. Aseptic meningitis is not uncommon during primary genital herpes, particularly in women, and in rare instances, herpetic sacral radiculomyelitis occurs.
Pain, itching, tenesmus, discharge, fever, chills, sacral paresthesias, headache, and difficulty in urinating may all occur.
Among the general public, whitlows are most often caused by HSV-2, whereas among medical and dental personnel, HSV-1 is the principal culprit. In clinical settings such as organ transplantation, lym-phoreticular neoplasm, or AIDS, HSV infection is often slow to heal and may disseminate cutaneously or to visceral organs.
HSV neonatal infection can be localized or disseminated and results from transmission of the virus to the infant at the time of delivery, either by ascending infection after premature membrane rupture or by passage of the infant through an infected genital tract. Newborns often present with vesicles or conjunctivitis, or a syndrome resembling neonatal sepsis may be evident. The characteristic cytopathic effect of the virus is often detectable within a period of 24 to 48 hours.
For instance, the use of condoms may prevent sexual transmission when either sexual partner has a history of genital HSV infection. If primary genital herpes is detected during the third trimester of pregnancy, acyclovir in conventional doses should be considered for the mother during the peripartum period and for the newborn post partum [see Treatment, below]. Bacteria may gain entrance into the eye during intraocular surgery (including eye injections). Treatment requires the injection of antibiotics into the eye, and sometimes surgery to remove the infected vitreous. I've been moved to create awareness tools that help educate healthcare practitioners and the public about Morgellons Disease (see Awareness Poster) as well as share what I've learned from this experience.Many of the skin photos in the photo galleries are mine. After acute lytic infections, herpesviruses often persist in a latent form for years; periodic reactivations are followed by recurrent lytic infections. The prevalence of HSV-2-specific antibodies in the United States increases from less than 6% in those younger than 19 years to more than 25% in those older than 30 years.2 In older age groups, changes in prevalence are negligible.
Although virus titers are higher and transmission is more likely when lesions are present, asymptomatic excretion of the virus is common. Subsequent lymphatic spread to regional nodes and viremic spread to other organs may occur, depending on the immune competence of the host.
After reactivation, the virus reverses its course and spreads peripherally by sensory nerve pathways.
In men, lesions are often on the glans penis or penile shaft [see Figure 1]; in women, lesions may involve the vulva, perineum, buttocks, cervix, or vagina.
The lesions gradually resolve in 2 to 3 weeks, unless they are mistakenly incised, in which case healing may be delayed by secondary bacterial infection.
Certain skin conditions, such as eczema and burns, are associated with cutaneous but not visceral dissemination. The risk of transmission is increased in premature births, after prolonged membrane rupture, and with the use of fetal scalp monitor electrodes. Neurologic signs such as seizures, cranial nerve palsies, and lethargy often predominate and are accompanied by cerebrospinal fluid pleocytosis.
Typing of isolates can be accomplished most readily by immunofluorescence with monoclonal antibodies directed against type-specific antigens. Application of sunscreens to susceptible skin areas before exposure to ultraviolet light can prevent reactivation of HSV.
Acyclovir in late pregnancy may also be useful in women with recurrent genital HSV infections; placebo-controlled trials have shown that 400 mg three times daily reduced lesions and HSV excretion at delivery. Sites of latency vary: HSV and VZV persist in neural ganglion cells, EBV persists in B cells, and CMV probably remains latent in many cell types. Viremia can be demonstrated in malnourished children, in certain adults with depressed T cell-mediated immunity, and, occasionally, in immunocompe-tent persons.
Once HSV reaches cutaneous sites, cell-to-cell spread occurs until host immune mechanisms limit further dissemination. Recurrences may take the form of keratitis (more than 90% of cases are unilateral), blepharitis, or keratocon-junctivitis. The differential diagnosis includes syphilis, chancroid, Behcet syndrome, erythema multiforme, and can-didiasis. Recurrent whitlows commonly appear and are sometimes associated with severe local neuralgia. In rare instances, HSV infection during pregnancy or in the elderly is complicated by visceral dissemination, particularly to the liver.
About 40% to 50% of infants born to mothers with primary infections are at risk for the development of severe disease, whereas fewer than 8% of those born to women with recurrent herpes are at risk for severe disease.1,13 Maternal infection is often asymptomatic at the time of delivery, and asymptomatic shedding may occur in women with no known history of genital herpes.
Scrapings or tissue specimens can sometimes be tested directly for herpesvirus antigens by immunofluorescence or immunohistochemistry. Medical and dental personnel who treat HSV-positive patients should wear gloves to prevent contact with infected areas. The amount of visual improvement is affected by the duration of the infection, therefor prompt evaluation is recommended if endophthalmitis is suspected.
The sites of latency for HHV-6 and HHV-7 have not been identified, although both herpesviruses have been detected in salivary glands. Various mechanisms are engaged in host responses to HSV, including T cell and natural killer cell cytotox-icity, macrophage activation, production of antibody, and production of interferon. In adolescents and young adults, posterior pharyngitis and tonsillitis may be the primary problem. Branching dendritic ulcers, usually detected by fluo-rescein staining, are virtually diagnostic and are often associated with diminished visual acuity. In women, lesions rapidly ulcerate and become covered with exudate, with resultant vaginal discharge.
Intubation or catheterization of debilitated patients may facilitate the spread of infection; for instance, herpes esophagitis often complicates long-term use of nasogastric tubes.


In women with a history of genital HSV infection, genital HSV can be detected at delivery in approximately 2% by use of tissue culture and in 14% by use of polymerase chain reaction (PCR) techniques.
If untreated, disseminated or central nervous system infection is fatal in more than 70% of patients, whereas localized disease is generally self-limited.
Alternatively, scrapings may be prepared by Giemsa or Wright stain and examined for the presence of multinucleated giant cells, which indicates infection with HSV or VZV. Like most, I panicked bought a lot of unnecessary products—some toxic, then managed to pull myself back from the brink of actually hurting myself.
Recurrences are frequent with both HSV-1 and HSV-2 infections, usually as a result of endogenous reactivation. The differential diagnosis includes streptococcal pharyngitis, aphthous stomatitis, Stevens-Johnson syndrome, herpangina, and infectious mononucleosis. Deep stromal involvement may result in scarring, corneal thinning, and abnormal vasculariza-tion, with resultant blindness or rupture of the globe. Treatment has greatly reduced the mortality from severe infection [see 11:XVI Acute Viral Central Nervous System Diseases].
Serologic techniques that accurately differentiate HSV-1 from HSV-2 infections are now commercially available.
Symptoms and signs often persist for 10 to 21 days, and autoinocula-tion to other sites, such as fingers and eyes, is common. Signs and symptoms of primary genital herpes often persist for several weeks before complete healing. Such tests can be used to confirm a diagnosis of primary HSV infection, but they are seldom helpful in diagnosing recurrences.
Always wary of doctors, I tried to stay out of that loop but finally caved when my beloved ones pressured me to seek help. Precipitating factors are sunlight, wind, local trauma, fever, menstruation, and emotional stress.
Previous infection with HSV-1 may reduce the severity and duration of a first episode of genital herpes caused by HSV-2.
Serologic techniques can also establish a diagnosis in patients with atypical complaints, identify asymptomatic carriers, and identify persons at risk.15 PCR detection of HSV DNA in CSF has become the standard means of diagnosing HSV encephalitis.
A dermatologist gave me Ivermectin which caused a Herxheimer (die-off) reaction and many of the black particles I'd been seeing with a scope surfaced. Ocular herpes is present in about 5% of all patients seen at ophthalmology clinics; 25% to 50% of ocular HSV infections recur within 2 years.
This gave me great relief from the discomfort of what felt like fiberglass embedded in my skin. Of all the primary cases of genital herpes in the United States each year, 60% to 80% will recur.
Although most genital recurrences represent reactivation, exogenous reinfection can also occur. There were NO fibers visible in my skin in the previous months before taking the medication. Within two days of taking the Ivermectin, I watched in horror as fibers started to rise to the surface of my skin. That plus coming off the tail-end of the pharmaceutical seemed to stop all the symptoms of itching, biting and crawling for approximately the next 4 months. The only thing that hadn't cleared up was the hyper-sensitivity to my skin which I thought I was stuck with for the rest of my life, an unfortunate consequence of having Morgellons. Had I not been actively using a microscope to look at my skin during this period, I might have presumed I was well. The skin however, doesn't lie and told a whole other story for under it's surface, fibers and particles were clearly still present—multitudes of them. Early on, I'd heard about the testing that Pam Crane of Morgellons Focus On Health (site no longer active) was championing and felt that it was probably the way to go. My only problem with moving forward was a lack of practitioner, as I felt having the best testing in the world wouldn't mean anything unless someone was up to the task of decoding it's contents into a meaningful protocol, sort of like buying a Cadillac that arrives without the key. I wanted to have a conversation with whatever doctor I was going to see and to hear them speak about their philosophy of healthcare. Just try to get a physician on the phone before actually making an appointment and you will find it is an impossible task (especially the high-end specialists).
She talked about The Great Plains Labs and why the testing used in Functional Medicine is so important for our community. She sounded like she knew how to do her job well and was more than capable, indeed she had impressed me as understanding how to approach the disease in a holistic manner that aligned with my own healthcare philosophies. I believe my first words to her were, "Where do I sign the dotted line?" (While focusonhealth has been taken down, here is another radio show with Nancy speaking with Pam. Let me remind you that I felt fine when I first contacted Nancy, but the emerging fibers showed me I was not. Nancy forewarned me that treatment would kick up all the initial symptoms I had when first ill with Morgellons, such as itching and stinging and that I might experience more fatigue with die-off, possibly even get lesions although I hadn't had many lesions previously. Within a week and a half of beginning this new protocol all the discomforts she mentioned came back.
Black particles began coming out from the skin, sand-like crystals were suddenly pushing from the scalp, I was itchy and uncomfortable but this time around it was at a much lower volume then at onset.
I have experienced some lesions, in the form of 'papercuts' and blood spots appearing on the skin. They were tiny and healed quickly. It took close to 3 months for the symptoms of this detox to disappear, lessening with each week.
We added in another few products to my protocol fine-tuning the process. Once all my symptoms had abated I was ready to move on to the next step and do a colon cleanse. I used supplements for one month that gently cleansed the colon (Colon Cleanse by DaVinci Labs??). After that, I began with chelation therapy (Chelex by Xymogen) to remove heavy metals. Nancy has taken me through this journey with constant support through email. The fact that she is able to tell me what I can expect and interpret what I am going through is invaluable. Having gone through the early treatment phases and emerging symptom-free, makes me feel that I did indeed work through something—hopefully clearing biofilm. So where am I right now and what are the changes that happened over these few months of treatment?My skin cleared of many of black particles, although I still have them (my great lament was that I didn't have a camera back when I first got sick, because my skin was so saturated it was alarming!).
Actually, I feel spry and 10 years younger than my 55 years of age (at the time this was written), an unexpected and very welcome gift.
Still, they are here and I am monitoring them carefully. I am convinced of the value of the Great Plains and Metametrix testing. It just makes sense that one would want to know the particular weaknesses of their body before embarking on a journey of healing.
Getting the labwork done and seeing Nancy are the two smartest things I did throughout my ordeal. Morgellons for me is like that impossible teacher I had in my youth. But it has also left me savoring hard-won battles and set me straight on how to live more in balance. Therefore, I try not to rail against the unfairness of the experience, but to look at how much I learned and the ways in which it has stretched me as a human being.
Yes it has been a miserable teacher, but by it's hand I have been become an attentive student.I wish you all full recovery.
AylaWhile I am not comfortable sharing my protocol as it is specific to my lab results, I will outline what I feel are the bare-bones minimum I'd look to take if I were building a protocol.
This would be a good probiotic (I use 3 different kinds throughout the day as was indicated by the results of my testing).
FOS, according to Nancy can promote yeast growth so I'd stay away from a probiotic that includes it. I'd include a biofilm buster which breaks down the cellular matrix in the gut that inhibits absorption of necessary nutrients.
I used Interfase Plus and Wobenzym at different times (there are different kinds of Wobenzyme. I've used Carlson's liquid D3 which is lipid based, but recently have switched because of assimilation issues with fats to a dry encapsulated D3 (Prothera brand 5,000 I.Us a day). Certain of the B's can become depleted when the body is fighting infection, so a good B-complex seems necessary. Also, Mr. Common Sense and now Clifford Carnicom have written about NAC and it's benefits along with vitamin C in helping quell the symptoms of our condition. I'd look into this as a close friend from the community began taking both high amounts of Vitamin C and NAC and her symptoms disappeared. She was taking 3,000-5,000 mg of C spread throughout the day and 600 mg 2x's a day of NAC both in the morning and at night. She eventually reduced it to 2,000 mg of vitamin C and 600 mg of NAC because the NAC was giving her headaches. The lesser dosage has been fine for keeping her symptoms of crawling, biting and stinging away. When she went off the protocol symptoms came back and when she again resumed, they went away. I might mention, that my protocol has always called for 1000 mg of vitamin C, three times a day.
While I was not on NAC as a separate supplement, it is in another product I take daily ?(Liver Protect by Xymogen). Nancy has stated that the clients she sees that do this first make themselves much worse and take longer to get better. If I am going to do this right, I want to know what my baseline toxic load is so I can measure my progress over time.
The results arrived right after I finished my third week of chelation. My total toxic representation was OFF the chart with high levels of antimony, silver, cadmium, tin and magnesium.
I have a host of other metals as well, they just were at lower levels than those mentioned above. Once Nancy reviewed my test results and knew how I was responding to the treatment she modified my protocol to include a liver support, and the addition of 3-4 new products that would also help balance me out.
I keep an ongoing visual journal using photos which I share with her so she can see any new developments. During chelation I was more tired, needing to take naps and sleep longer on most days. I also had some tiny red spots appear on the skin without breaking through.Red spots appear on the skin. Based on what was going, on Nancy pulled back on the chelation so that the process is even slower and gentler until my body can adapt. Using shea butter and coconut oil mixture as a moisturizer seems to draw fibers and black particles from my skin if left on for 3-4 hours.
Most are not readily apparent unless you really look for them. Hair The Morgellons has moved into my hair. An acupuncturist, pointed out after looking at my hair photos, that there were multiple "hairs" emerging from one follicle. This is probably why my hair feels thicker even though it has been brittle, weak and falling out.
Helicobacter pylori, the bacteria I had with high levels the first time I was tested, is completely gone.
There was a new bacteria that showed up on this round of testing that wasn't on the previous. Nancy feels that this is something that could have morphed, or, could have been present all along, but like peeling an onion back, was hidden under layers. She is adding seven new supplements to my protocol to address adrenal support as sleep has become fitful and I feel somehow too 'plugged in.' Fight or flight mode. I'll be taking a prebiotic to address the new bacteria as well as some new products from Xymogen to open detox pathways. I'm excited to be moving in a new direction. Every time we do a new test, I see the value of this approach.


Randomly throwing supplements at the body without being tested, with the hope that something might work, seems a dangerous practice. Not terrible full-blown itchy, just enough to let me know that I was reinfected or maybe this is an allergic flare-up. This episode might have lasted longer than necessary had I immediately washed all my clothes but I got lazy and didn't wash them for a few days. Was not constantly itchy, but found I'd get itchy at odd intervals, sometimes once a day, sometimes not for days at a time and sometimes for a mere few seconds or so.
I am putting a garden in upstate and often have my hands in the soil (without gloves) and have found that I am fine. The only itching I've got is from the occasional mosquito bite (and yes, these are real mosquitoes). Now, instead of direct application of GSE I brush my teeth twice, once with toothpaste and once with a clean brush that has two drops of GSE on it.
Note that I have been letting my supplements run out in the last few months because I needed a break from taking approx.
I wonder if the return to itchiness had something to do with my letting down my guard and not watching my pH.
After the first day of swimming, I noticed small circular red blotches appear under the skin of my calves and thought, uh-oh, here comes trouble.
I FINALLY have a microscope again (it was replaced after more than 7 months at the manufacturer!). I had a few breakthrough 'papercut lesions' on the hands which I don't know what to make of.
I stopped the Ormus because I wanted to document F-6, which has gotten quite a buzz in the Morgellons community. I still have 1.5 bottles left and intend to take it in a few months feeling I didn't give it a proper shot. For now, I want to concentrate on doing one therapy at a time, so I can really be sure what each does. October 17, 2011: Began using F-6 and have started a new link documenting that experience including photos showing what is emerging from the skin. I'm going to take it slow with this product as I don't want to have any major herxheimer episodes. Caroline Carter, A healthcare worker that has Morgellons and works with ozone therapy (and who made her Morgellons worse with ozone saunas) said she cannot even be around it anymore.
I have since talked with another person that had strong outbreaks from doing an ozone sauna. Ozone therapy is typically great for cancer, AIDS and herpes, but for this disease might make us worse. There seems to be improvement to the hair which feels stronger and seems to be falling out less. A lot of "debris" is coming up through the skin, fibers, black particles, granules and many more fibers then ever seen before. A week and a half later I ate some quinoa with my lunch and two hours later had 3 oatmeal cookies (oatmeal, walnuts, carob chips, baking soda, vanilla).
This forage into complex carbs was unusual for me.While eating the cookies I started to itch.
By the third cookie, I was having full-blown symptoms of itching, stinging and biting sensations (no crawling, thank God!).
The fact that it came on with such force and was related to food, makes me think that Morgellons counts among it's causes a hyper-allergic reaction to food. In this case, I don't really know what specific ingredient triggered the reaction.By eliminating carbs again, symptoms quieted down. I am noticing flare-ups of the arthritis in my foot which had so improved at the beginning of my treatment (but I kill my feet dancing one night a week, so that could play into this). The ones I can visually see without a scope are bigger then I've had before but there is no increase in the amount I generally see with my scope in the skin.
Will keep you posted of new developments.I've noticed that when it's very hot (93-97 degrees) and my skin is exposed to the air, I have more sensations on my arms.
It's not unusual to feel a single pin prick sensation on my left upper arm, often I'll feel the same type of prick mirrored in the same spot on right arm sometime later, as if they were somehow linked.The other day on my bike I felt as if I hot poker were being pressed momentarily to my arm.
When I looked down, there were three distinct tract marks in that spot, about a half, to an inch long that hadn't been there before.
Since having Morgellons, it feels like the skin is no longer a reliable friend but is capable of erratic changes suddenly.
They took about 5 days to disappear.?September 27, 2012 • Live blood microscopyJust posted a new link with photos of my recent session with Rick Panson, a microbiologist and healthy body coach who did a live blood and dried blood microscopy and gave me additional guidance for my health. It's a bird's eye view into the system, giving a fuller, deeper understanding of what's going on  then just looking at lab results—although lab tests have their place! In the next two weeks I get more testing done so will post those results when in. There were many problems with the blood. We are in a seasonal shift and my fingers have had a few tiny papercut lesions since the change began.Started the protocol Oct. Beginning with one pill a day of capyrilic acid with one pill olive leaf extract and 1 tsp.
The L-glutamine is supposed to strengthen the gut lining and prevent leaky gut syndrome caused by the yeast die-off. Will stay on this for a few days and slowly double the dosage, then determine where to go from there.
16, 2012 Went back to Rick Panson for another live blood analysis and posted the photos under my last blood microscopy. This is encouraging for all of you who wonder how long it will take to knock back candida and even if our protocols are working. Rick recommended Candex and Nancy told me she loved the product except now they are adding corn to Candex (and it's unknown if it's GMO corn), so she is no longer recommending it. Adrenal system had a number of markers indicating a lot of stress to the system, very low levels of vitamins C and B's, four different pathogenic bacteria showed up—Helicobacter Pylori was high, Clostridia, E. Kreb cycle needs support. Heavy metals hair test—all toxic metals were down except arsenic which went up with cadmium.
Lead which was extremely high on my first test showed a considerable decrease as well as silver but lots more chelation ahead. It's been 2 years since I started using supplements to pull the metals out and I think it will take a couple more years of work.
The process is slow but steady which is a good thing because I think if the body released too much metal into the system at once there would be negative impact on the health. Nancy pointed out that lead and cadmium are antagonistic to calcium absorption and bone health, so seeing this rise in cadmium and knowing I still have too high levels of lead makes me think that I might have to give up the painting at some point or switch mediums rather than compromise bone health. The heavy metals test also measures "essential and other elements," (minerals) It seems as a consequence of pulling heavy metals out, the minerals have been compromised. Nancy suggested this organism is a pleomorph moving from bacteria to fungus according to favorable conditions in the body. This is the third time it's changed. Feb 3, 2013 Just an acknowledgment that I just passed my 3rd anniversary since getting sick with Morgellons. The only time I really have symptoms is when I really mess up on diet (itchiness will start) or when ?very overheated and sweating from physical exertion like dancing, where it sometimes feels like needle pinpricks are sticking my skin from the INSIDE out, accompanied by itchiness. Thieves is a great oil for preventing flu or when one is coming down with illness, but I am unclear if it can damage beneficial bacterias. Stopped taking thieves after a few weeks but do still take lemon and added in lemongrass and grapefruit to my daily capsule. Itchiness did not return. September 22, 2013 Decided to go on Stephen Buhners herbal protocol for Lyme disease (crafted from his excellent book, Healing Lyme). Although I tested negative for Lyme and feel fine, I don't trust the traditional testing one gets with their regular MD, and even though I don't think I'm dealing with Lyme, I can't discount the fact that so many Morgellons sufferers also have Borrelia and other co-infections that might be related to our disease which seem to improve with Lyme treatment.
Also, his protocol addresses other issues I feel are pertinent to my health (even before Morgellons). Certainly, I see over time that my immune system is weak, and my gut reaction now to coasting is that it could be an eventual time bomb.
I'm taking Cats Claw, Sarsaparilla root (Jamaican—which I grind in my coffee grinder), Eleuthero (Siberian Ginseng), Astragalus, Japanese Knotweed and Andrographis. To his formula I've added in Ashwagandha and Sweet Cinnamon (from Sri Lanka) for the brain, as well as nettles (excellent herb for trace minerals and general support of system) and Pau D'arco (fungal). I take a quarter level teaspoon of each herb (which is roughly the equivalent of one 00 capsule) added to some water and drink it down.
Surprisingly, I did not feel exhausted, although the protocol was pretty intense and caused a lot of flushing through the digestive system. This is not a new symptom and usually happens in the first few weeks of starting any new protocol. As these breakouts have always been so minor and short-lived? (an occasional papercut lesion or what looks like a pin prick), I paid them little mind. In this case, the skin continued to break open for the duration of treatment and I had some long "scratch" marks come up as well. It seemed like the last papercut I got was deeper and for the first time I started to worry that perhaps I was giving myself a lesion problem that I might not be able to turn off. This little spot has bothered me on occasion on and off throughout the years of my Morgellons experience, but during the Buhner protocol, it itched almost constantly. On the plus side, I could tell there was a lot of detoxification going on and all of those bitter herbs were really helpful for quelling sugar cravings. I believe I will revisit this protocol modified in the future, but for now, am taking a rest from it.
Note that when I ceased treatment, the papercut and pinprick lesions stopped, although I recently had a three-inch long "scratch" appear on my leg weeks after stopping his treatment some weeks back.
This was a surprise, since problems usually only show up on my hands and 3 inches is rather a statement!For the first time, the scratch resembled images I've seen for Bartonella.
There is much about it that I think is helpful, and I encourage people to study these herbs and supplements carefully, and decide for themselves if they want to incorporate them. This is a very difficult protocol and for any who have detoxification pathway issues, this could impact their health negatively. The release of toxins in a system that cannot remove them properly can be deadly, so it is important to not rush carelessly forward with something this strong. I did feel like the protocol helped me on many levels, but I could not tolerate the heart issues with pressure on the chest, burning, and breathing difficulties.
The creator of the protocol feels that Bartonella is at the core of the Morgellons infection, and Bartonella likes to set up shop in the endothelial tissue of the heart.
Thinking this was just a severe Herxheimer reaction, I went back on the protocol but was unable to advance more than one drop of each tincture before heart and breathing issues returned with a vengeance. This time, the heart issues did not abate immediately, and it's been some weeks now in which they often come back on a low level. His original protocol (which he posted on Jenna's blog and which is now removed) did not use MSM, or Silver Sol or various other supplements. It also did not include baking soda, which is not inherently a problem, but at 2 teaspoons a day, might become one.



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Comments
  1. VUSALIN_QAQASI 04.09.2013 at 21:19:30
    Back viral shedding, when herpes is most transmissible to sexual the proteins.
  2. WwWwWwWwW 04.09.2013 at 14:20:53
    But it surely did not does not replace typical part of life and folks.