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Morgellons disease.

Mysterious disease in which different-colored fibers pop out of the afflicted person’s skin.

Post date: Friday, May 12th, 2006.

Tags: Deadly Disease Unexplained.

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50 Responses to “Morgellons disease.”

  1. At 8:29 pm on May 23rd, 2006, M wrote: #

    I had the same symptoms described for Morgellons disease and my doctor prescribed Hydroxyzine HCL 10 MG. and Clobetasol Propionate ointment 0.05% The symptoms of itching and burning disappeared in 10 days.

  2. At 3:42 pm on July 12th, 2006, Anonymous wrote: #

    Update for May23,2006 on prescription of Hydroxyzine HCL 10 MG. and Clobetasol Propionate ointment 0.05%.Here it is July12 ,2006 and I am getting small symptoms after being off medication since May 23.I am keeping the disease from reoccuring with the same medication.I will keep you posted.

  3. At 5:02 am on August 17th, 2006, Alcuin Bramerton wrote: #

    The questions being asked about Morgellons disease are disturbing. Is it the result of covert bioterrorism? Is it a new stress-induced, psychosomatic epidemic? Is it a spiritual disease? Is it being brought on by fear? Is Morgellons disease a physical epiphenomenon of war-on-terror paranoia? Why is it peculiarly American? And why is it specifically clustered in Texas, California and Florida?

  4. At 3:54 am on October 24th, 2006, Tania wrote: #

    My name is tania and I have suffered from this disease for 2 years now, both my daughters and my husband have this as well but they dont have the lesions like me. I live in a small country town in Victoria Australia and I worked in a Pharmacy and I have seen a lot of people with this same thing. THis thing is very contagious if you ask me and very frightening.I think it is all over the world but unless you have the lesions you probably dont know you have it.Something really stange is going on. If it wasnt for the internet I probably would have killed myself by now.

  5. At 2:56 am on November 10th, 2006, Gillian wrote: #

    My name is Gillian, I live in Melbourne Australia. I have suffered the symptoms of Morgellons for a few years now.

    Tania I am so sorry to hear that your daughters have this. I do not have children.

    It is now 2 years since I learned about Morgellons (which explained my terrible symptoms, particularly the hair/fibers). I have tried my heart out during this 2 year period to have Morgellons exposed, either via media or whatever means. 18 months ago I was on a talk back radio show in Western Australia – talking about Morgellons, but since then nothing further.

    I have never been given a diagnosis of DOP (Delusions of Parasitosis). I did have Rickettsia/Spotted Fever Group and have drank a river of antibiotics, but my “morgies” symptoms will not go away, and the psychological distress involved with this is awful. Medical mistreatment by the medical community is yet another topic of debate!!

  6. At 8:29 pm on November 28th, 2006, Prichard wrote: #

    If you are interested in Morgellons Disease or experience Morgellons symptoms, I would like to invite you to participate in the Morgellons Disease Information Community and Message Board at http://www.morgellonsite.com

  7. At 10:35 pm on December 3rd, 2006, joseph wrote: #

    I had morgellons in 1993 and 1994.I cured myself using pine oil on skin everyday for
    a really long time.It took a long time for
    results.I kept at it.I have been fiber free for 12 years.
    It also helps to shave your head.Keep your
    environment superclean,so you don’t reinfect yourself.I cleaned with pinesol.
    I don’t know if the disease has evolved the past 12 years.American Indians used
    pine.
    Other treatments probably work.The important things are clean environment
    and build up your immune system.
    If I could beat it on my own,others can
    do it with support.

  8. At 8:49 am on December 5th, 2006, joseph wrote: #

    I’m asking everyone to petition the Google
    foundation to research Morgellons.Does anybody want to run with that idea?

  9. At 2:45 am on December 23rd, 2006, Lyle Hut wrote: #

    for morgellons disease information and support check out http://www.morgellonsite.com

  10. At 7:05 pm on February 28th, 2007, Smileykins wrote: #

    Considering that the CDC’s task force is trying to look into how this situation developed, all the “independent scientific research” needs hard, hard, scrutiny, and whatever course of action neccessary, applied from the people who are in these patients’ lives. Due to their notable problems with cognitive skills, “morgellons disease” patients aren’t in a position to recognize scientific misconduct.

  11. At 6:11 am on March 9th, 2007, Sean wrote: #

    Thank God that i am not the only one. I thought I was loosing my mind. I have had ALL of the symptoms associated with this ds order for almost 4 years now. Life has been almost unbarible. Everyone I try to talk to about it thinks I am insane. Early on I bounced from doctor to doctor with no little to no results. The reaction I get leaves me feeling depressed and more helpless. I have gone from being an popular extrovert that exuded self-confidence and optimism to a shell of a man, depressed, isolated and continuously doubting sanity. I know that I have a mental psycosis, but it a a result of my phsical aliments. I started web searches last year and until tonight I thought I was alone and possibly insane. My condition has been pretty cyclical. Symptoms usually last for 4-5 months and when the sores heal, I get scars that look red, swollen and infected (the scar are tender and hideous). The symptoms remain dormant for a few weeks and then it starts again. The scars become pustuiles, resembling extra-large pimples, boils or abcesses. Everytime it reoccurs it gets worse and worse. It spread, one becomes two and the sore seen to fallow my viens/arteries. What was once confined to my thighs, has now propegated allover my body. And finally, it has moved to my face and scalp. I had tried countless remedies, medical, home and psychiatridc. NOTHING works. I have almost given up. I don’t tell people anymore, I stay home as much as possible and I am pretty sure that whatever the hell this is, it is slowly and steadily killing me. I don’t sleep, I have no appetite, I can’t work, my teeth are falling out, I am scarred (scared, too), My skin crawl and hurts all the time. Sure it’s MENTAL, but trust me it is DEFINITLY PHYSICAL and until tonight I thought I was the only one that was suffering the crippling effects of this disease/parasite. I feel like after 4 years someone finally understands. So if I am CRAZY, and this imagined disorder has consumed my entire being with no remedy save death, at least I am not alone…
    I want HELP, I need HELP. I am TERRIFFIED, DESPARATE and will to try ANYTHING. But can I do if my family, friends and doctors dismiss me as a psychotic skin-picker. I feel like I am already DEAD, only my body is still hanging on. I am just waiting for it to catch up, and at this rate it will be sooner than later.

  12. At 9:58 am on May 1st, 2007, Gracie wrote: #

    Hi all. I don’t have this disease but have one that took ME 50 years to diagnose. Most doctors had never heard of my genetic disease! I am sorry to say but seems our worst enemy beyond the disease itself are doctors. Good luck in finding one that does not think you are a hypochondriac or just there for drugs.

    I looked up the drugs Hydroxyzine HCL and Clobetasol Propionate ointment and found these are merely useful to treat symptoms and not to eradicate the underlying cause. Its pretty apparent that this disease is caused by parasites, most likely several at the same time. Some doctors report successful outcomes with the Lyme disease treatment for Morgellons. The pine oil sounds promising but you all need to remember that antibiotics are not healthy. Make sure whatever treatment you choose, you do a total body cleanse, especially the colon. While usually summed up as (something) in his weight loss book, Kevin Trudeau approaches most of what ails the common person as the result of modern living and how to combat it. IF interested in that, get a cheaper used copy on Amazon. What he says is for real even if his presentation is that of a dishonest salesman. I am wondering how tea tree oil would work as it has mixed properties, but don’t drink it as it can cause neurological damage.

    Good luck to you all and I am planning on incorporating this disease in my next book! I hope it sheds some light on the problem.

  13. At 2:22 am on May 15th, 2007, LOLITA wrote: #

    I have had…Morgellons, as has my husband, for 3 years now. We have been called crazy, drug addicted, you name it. By family, “friends”, strangers. I have over 400 lesions all over my body. Where I once earned a living as a professional model I now hide, shop and run errands late at night and fight the depression, pain, shame and lack of answers in an ever more secluded world. I think I can safely speak for most of us who suffer from this dread nightmare when I say I’d much rather have the truth, some answers, even the faintest of hopes that whoever/whatever is responsible for this recognizes their mistake and will disclose anything that might help us rather than seeking to sue,etc.life is worth more than money!

  14. At 10:54 am on May 25th, 2007, carl leach wrote: #

    I have had Morgellons ever since 1985. At that time I lived in the Pittsburgh area. I through the whole “its your imagination routine” many years with the doctors until I was at the point of taking a gun and shoot the next doctor – dermatologist in the kneecap, and when he screamed out in pain, I was going to ask him, “What’s wrong?” and when he would say, “You just shot me in my leg!”, I was going to tell him it was his imagination. Today the movie “Bug” comes out, with Ashley Judd and I want to see if they tie it in with Morgellons or if the purpose of this is to debunk the awareness of Morgellons. I now live in the DC area and if I knew of a way to pass it on to the congressmen, they would get the ball rolling, before this would reach epedemic proportions (just a joke – I think),

  15. At 7:58 pm on November 13th, 2007, roy wrote: #

    I believe morgellons is related to lymphatic filariasis. I successfully treated the parasites with paraclear from sweetsunnah.com. Its a combination of about 19 herbs effective against parasites. I was also drinking a lot of pau d’arco tea at the time. Another very important product is carnivora (venus flytrap extract). Currently, I am dealing with the bacteria has a symbiotic relationship with the parasites. You can email me at rwilson@mymed411.com

  16. At 12:21 pm on December 11th, 2007, perri ann wrote: #

    please help me i am so sick i have had moegellons for 2 yrs i live in ny and cant find any doctor to help me(845)-216-4262

  17. At 9:36 pm on January 16th, 2008, Tom wrote: #

    I saw pictures of this at http://www.timesocket.com/disease/morgellons-disease-pictures-and-story/

  18. At 9:40 pm on January 25th, 2008, Anonymous wrote: #

    I have had this condition for several years. I seem to have all rhe symptoms. I only learned about it the other day when Kaiser California announced a plan to study it. I have been to a couple of doctors but after the fibromyalgia episode I refuse to put myself in that kind of a position.

    I lived in San Francisco in the 80′ late 90′ I spent three years in Vancouver BC. I am a nurse and it seems they are the number one sufferers.

    I have tried various self treatments. The disease is mainly confined to my scalp. The amazing thing is I suffer from the nightmares,insomnia and was also diagnosed with ADHD. These symptoms are worse for me than the skin problem.
    E.

  19. At 5:40 am on March 23rd, 2008, Sean wrote: #

    Hi there,

    I am a Filmmaker from Sydney, Australia and would like to help in getting the message out there.

    Regards,

    Sean

  20. At 10:56 pm on April 13th, 2008, Mary wrote: #

    Hi Sean , My name is Mary a Naturopath in Qld . I have been suffering M for 2 years now . It finally hit home @ Xmas ‘07 and realized it was M so I have used my Frequency Specific Microcuurent for 2 months now ,Jan amd Feb. Found tremendous releif and may have broken it reproductive cycle . This last month March took Homeoopathic Silica 30C to rid the body of the invader ,let it run it coarse,just about gone now , and last week I recieved my sulphur soap from America and use it as a preventitive caution, since I think this “blight” is in the environment.
    I am now asisting another suffer in Australia , and another friend of mine I have seen may have it to …suspect got iot thru tattooing.
    You can contatc me : runes@ozemail.com.au
    I hope to hear from you , as I feel I have made a major thru in eradicting this sci -fi type nightmare in short order after trying just about everything under the sun in the past with no avail .
    Cheers Mary

  21. At 6:01 am on April 27th, 2008, Marie wrote: #

    Hi Im in New Zealand. was shocked to stumble across this disease on the web 2wks ago!! i have been suffering with most of these symptoms for 7yrs. tried everything natural medicines, para herbs, colon cleanses and with a good gp and dermatologist, steroids, antibiotics etc..this organism? is incredibly prolific. my worst symptom has always been insomnia due to itching. recently my dermat told me to try peanut oil after all else failed, he said it used to be used in england for skin probs.i have had amazing results at clearing lesions in 3 days with applying peanut butter at night,i leave on all night and use old clothes. it is anti-pruritic. he says it is controlling my problem but not curing. but im sleeping and have more energy and can now venture outside. i was pre-school teacher.seems diff things work for diff people. this is cheap and natural. thank god for internet.i wd have expected some prelim results by now from CDC study??

  22. At 7:29 am on April 27th, 2008, Janet Appleyard (&Steve) wrote: #

    Dear Sean, and also Mary,

    My name is Janet Appleyard. I live in Perth, Western Australia
    My husband (Steve) found this blog. We both have Morgellons – contracted about October last year. (I got it from him.) I would be willing to help in any way I could with awareness/promotional stuff.

    My doctor has a long shared history with me- she believed me – well she saw stuff come out of my hands when i used Aquim alcohol-based cleanser.

    Both my husband and I are scientists by training. I have been working in a variety of other jobs for at least 15years. Currently unable to work – psychologically(contagion issues plus anxiety). Steve is still working.

    I really feel the isolation and would like to meet fellow suffers from Perth. You know – discuss treatment, strategies etc. However E-mail would be great for a start.

    Just to know that I am not alone is uplifting. I really felt we were the only two. I am 44 y.o. my husband is 51. He is definintely non-social, but has a brilliant brain (which has helped so much)and has always disliked doctors.

    What about a support group?
    My E-mail: appleyrd@ozemail.com.au

    Regards, Janet Appleyard
    Perth Western Australia.

  23. At 7:32 pm on May 26th, 2008, Cindy wrote: #

    This is the start of my 4th year with Morgellon’s. Today i have screamed and cried most of the day…. Sick of the pain, and all else that goes with this ulgy disease. Friday i took samples from a lovely chemtrail floating down, not our firs. The pictures from under our microscope would make anyone scream with terror….We have been exposed to something without our consent, they don’t even do that to criminals on death row!!!! I was a caregiver for years and now I can barely care for myself….

  24. At 10:11 am on June 8th, 2008, Renae M wrote: #

    Janet, Hello to you, dear fellow Human Being (Occupied). I am in Kalamunda/ hills district and would dearly love the chance to delve further into our mutual “affliction” and god willing, help bring about an understanding and an end to this hideousness.
    Am 38yo f, same contractual period as you and likewise not working OMG 6mnths
    It is terrible for you & Steve to both have it but you can, at least, confide your fear/loathing and try to rationalise what you’re experiencing with your partner.
    Hope I dont sound too desperate but (I am) eager to nut this out with someone and maybe even get together sometime for a face-off ?…. some humour helps I find.

  25. At 8:34 pm on June 16th, 2008, Leigh wrote: #

    Hi everyone,

    I am not sure if I have this disease or not… i suddenly broke out with some pimples on my jaw line and neck and was diagnosed with acne. I should say here that I am 34 years old. I do believe those to be acne, but I am concerned about the ones coming on my back… they look different – big sores; a lot of inflammation; and they don’t heal easily. I have tried variousantibiotic creams; some seem to be drying them out, so hopefully they will go away. A big portion of my back is covered – when one does go away, more arise in close vicinity to it… i have never seen acne like this before. However, there are no fibres – so all lesions exude vibres?

    However, I have been researching Morgellons online, and found the following cure:

    A morgellons sufferer put some colour fast bleech in the bath (just a little bit), a little bit of washing powder, to have a bath in. Without her knowledge, her cat knocked over a bottle of alfalfa tablets, and about 25 of these ended up in the bath.

    She noticed something amazing happening as the was in the bath: everything morgellons leaving her body in droves!!! she soaked for about an hour, and had another bath later on, getting rid of the last of it. Apparently it cured it completely, not just the symptoms…

    It’s got something to do with the alkaline environment it provides – apparently the bacteria can’t survive in it. I am not sure what happened to the nematodes carrying the bacteria – but she clearly states that ‘everything Morgellons’ left her body.

    Anyway, I am thinking of doing this even if I am not sure that I have the disease… rather safe than sorry. I also bought the tablets yesterday, and am taking a smallish dose (2) each day, even although you can take 6. It apparently boosts your immune system greatly, and helps for energy… another suffer who didn’t bath in the stuff but is taking the pills says there has been an improvement, although it didn’t cure her. 11 other people also bathed in it (you can bath in the grass seeds) and are all cured…

    If any of you try it, please will you let us know the results?

    Thanks,

    Leigh

  26. At 8:37 pm on June 16th, 2008, Leigh wrote: #

    Hi again,

    I also wanted to mention that I live in Auckland, New Zealand. Do you know of many people living in New Zealand that has this disease? We are originally from South Africa – apparently it is there as well…

  27. At 6:19 am on August 13th, 2008, david wrote: #

    A little research turns up a disease called Chronic Melioidosis, which causes itching and ulcerated weeping lesions. The crawling sensations are Springtails, who detect dying flesh and avail themselves.
    Unfortunately Melioidosis is related to a disease called Glanders (which was announced to be eradicated around 1900).
    However it was not eradicated. It was tweaked by bio-warfare amoral scientists.
    It was dropped by German planes on Russian army in WWI, to infect the horses which were in use at that time in wars. The Russians retaliated by dropping it on German units.
    The scientists noted that it also infected the soldiers, so the tweaking was carried on after the war.
    In the 30’s, Japan dropped it on China, causing a condition called Rotten leg syndrome. There are still people in China who have this disease, as some of the dropped cannisters did not break open when lan ding in rice paddies, but gradually released their wretched cargo, when the cannisters rusted.
    The US military bought the Japanese biological weapons program from Japan in exchange for not prosecuting the head of Japans bio-weapon programme.

    They then in turn dropped Glanders on N. Korea, and China, during the Korean Conflict. And God only knows how many times it has been used since.

    That is why no doctor or lab will even test tissue for gram negative Burkholderia Mallei,(Glanders), nor Burkholderia Pseudomallei (Pseudo Glanders AKA Melioidosis)

    Opening up that can of worms would result in massive lawsuits, and no medical practioner wants to get drawn into something like that.

  28. At 4:26 am on August 22nd, 2008, web wrote: #

    Hi All,
    for what is is worth…here goes. Yes, I contracted Morgellons, several times I came close to curing myself, but certain foods seem to bring it back with a vengence! Stay away from sugar! Instead use Pure Stevia, Kal Brand is best.

    Stay away from cakes, candies, icream, anything with hidden sugar and all corn/products that are not organically grown.

    Itching: Put 1/8 cup of Borax in a bath tub of hot water and pour in 2 8oz bottles of peroxide and soak for a minimum of a half an hour. Be sure to have a mirror and do not get upset if the worms start coming out.

    Be aware Borax in high dosages can be toxic so do be careful and realize some people can use more, other need much less. I do not know if Borax can build up in the blood stream, but is VERY affective and helps to heal sore wounds!

    Wash clothes in a Chlorine detergent and ad about a table spoon of Borax.

    Spray your bed with a diluted solution of Borax to keep from being eatten alive at night while sleeping. It is wonderful.

    Be aware that itching ears, nose and scalp can be helped by rinsing with a .05% dilution of Hydrogen Peroxide before bed time to aford a better nights sleep. I have used .05% Peroxide dipped on a soft cloth and have wiped the interior of my ears, nose and scalp with very good effect.

    Do use a menthol salve like Vicks vapor rub on itchy areas. It gives temporary releaf.

    Diomatious Earth: I pour this into 00 gel caps and take two a day. 1 AM/1 PM

    Borax: I have taken 1 capsule of Borax every three to 4 days depending on how I feel and my bodies reaction.

    Finally, get yourself a book of Greys Anatomy and purchase a small Tens unit.
    Most recently I have been using the unit to disrupt the disease and it appears to be working.
    http://www.google.com/search?hl=en&q=tens+unit

    Once you are on the mend do take 1,100 PPM Collidal Silver! It helps to prevent reinfection.

    Animals: I keep them on Collidal Silver as a prvention.

    Clean House: I wash my floors, alturnating with Diamatious Earth and Borax and some Mentholy like Eucaliptus Oil or T-Tree Oil.

    For some of you, you may find that you still have a yeast problem as I do. I am still working on this, but again for the 4th time I am at the threshold of feeling like this thing might be in remission. We seem to play this dance of on again off again, but I am starving it to death (no sugars) and attacking it as a parasite with Herbs.

    Also, for I take an antihistamine to reduce swelling and to keep my body from over reacting to the bugs.

    Also, for the fortunate few with a good doctor, have them monitor your blood for toxicity when using the Borax and to see what vitamins you are low on and you will be! This bug weakens you by taking what your body needs to survive. You will be low in D for sure.

    I take Vita C 4,000 mg per day and Sea Salt 2-4 00 gel caps and take C-Q10 for your mental agility…it works.

    Yes, I really do all this….and it has made life much better.

  29. At 10:37 pm on October 26th, 2008, Gillian wrote: #

    The National Health & Medical Research Council (Australian Government) acknowledges Morgellons disease.

    Ph: (02) 6217 9000
    Email: nhmrc@nhmrc.gov.au

  30. At 10:02 pm on November 1st, 2008, Mary Lynn wrote: #

    With no adequate tests to positively diagnose Morgellons and with no doctors at Kaiser Permanente, in California, Orange County, to acknowledge they have ever heard of Morgellons puts me in limbo status for help. Five yrs now and am currently using 9volt zapper and lots of garlic. Do you think chemo or radiation could kill this? Good news re Australia gov. I live on the edge of a golf course where chemical sprays are used and believe I was infected when an 85ft Euculyptus tree fell into my house 6 yrs ago. Chronic fatigue came before the sores and other symptoms but this bacterium, parasite, nanotechworm or whatever is morphing into a stonger bug that is wrecking havoc on my total body. I pray help will come soon for all suffering from this affliction!!! Mary Lynn

  31. At 10:40 pm on November 21st, 2008, Leanne wrote: #

    Thank god – whoever he is – your here. I have been suffering M for 18 years now, i still cannot get a Dr to listen and am currently diagnosed with relapsing remitting Multiple Sclerosis and “pockets of glass” from a car accident i had when i was 7. I am now 43. I am going absolutely nuts. I am so glad to have found this page. I am in the midst of much brain fog trying to get all my symptoms, history and story onto paper. I will certainly be back…in the meantime i wont give up trying. I am living near Lismore :) if anybody is close by or wants to contact me my email is clarityhealth@hotmail.com

    Thankyou for being here and all the best to all of you xx

  32. At 1:36 am on November 24th, 2008, Leanne wrote: #

    I called the National Health & Medical Research phone number above…AS USUAL i got the same replies…”can u spell that please”, “no im sorry we do not have any informaton on that, let me check our records”, “no im sorry, we cant help you, here is a number to call Health Direct 1800 022 222″, “the lady who made that post no longer works here”!!!!

  33. At 12:14 am on December 16th, 2008, Alan wrote: #

    Hi Marie! I’m a 36y r old New Zealand sufferer of this terrible disease! I’ve had it for around 6 years and was feeling “nutty” until I typed my symptoms into Google a few weeks ago and BINGO! I was quite excited (sic!) to find another kiwi sharing my problem. Would love to share stories some time. I’m going to try the Peanut butter tonight!!! Will let you know how it goes. Thanks! Alan Barlow alan@proworkflow.com

  34. At 3:22 am on December 17th, 2008, Pixie wrote: #

    hi to fellow sufferers of Morgellons. my husband and myself have had it for ? 3years but who knows how long before the lesions one actually has the disease.

    we researched and reseached got as far as sub-cutaneous migrains and systemic mycosis Then I found the morgellons.org site and we Knew that was the answer.

    we have been fairly active in our local area to spread the word; a recent article in our local free monthly paper – Nimbin Good Times (you can read it online) has put us in contact with several others who also have Morgellons.

    LS has been a huge motivator for me and I have set up an Australian Morgellons Support Mob site. also with a Wordpress blog. I hope you can all use this site as a central place for us all to pool resources of knowledge, contacts etc.
    http://www.morgellonsaustralia.bravehost.com/

    I will be phoning the NRMRC tomorrow and try to find out the latest from them but am off to their site to see if there is anything as I am sure many of you have since reading Gillians post :)

    I hope you don’t mind Mary & Janet, I have added your names to my mailing list. I will put a ‘join mailing list’ function on the page if there is the need for that. Please let me know what you think of the site and if it will do for a support site? suggestions please? It has been wonderful to share information with those around here so hopefully the forum will provide the same feeling for other sufferers.

    I am very pro natural treatment but have relented and we both take a drug – itraconazole 300mg/day and we take worming tablets – mebenzadole – for three days each month; we use peroxide on the lesions; shower with coal tar wash; use condies crystals; take multivitamin, zinc, magnesium and a dose of alkalizer daily. I drink either water, chai or green tea & no dairy. tried another billion ;) things lol. There is a full natural treatment listed at the support site – it comes from the New Morgellons Order site.

    my email is pixiemb@gmail.com
    please contact me if you would like to be added to the Morgellons mailing list.

    I am sure all sufferers would be interested in hearing from anyone who has been researching or will research Morgellons Disease.

    There is a movie called ‘Invasion’ {I think} with Nicole Kidman & Daniel Craig. After the movie there is an interview with Dr Randy Wymore on Morgellons.

    peace to all
    pixie

  35. At 2:43 am on December 25th, 2008, james wrote: #

    MORGELLON’S DISEASE – AN INSTANT CURE FOR MORGELLON’S DISEASE???
    Thu, 05/15/2008 – 00:20 — Arthur Cristian AN INSTANT CURE FOR MORGELLON’S DISEASE???
    Forwarded from Oxyp…@yahoogroups.com Sunday, 22 April 2007, 11:09 a.m.
    http://mms-central.com/MMS-stories.htm
    . . the Morgellon’s disease of today is a totally NEW disease. The fibers are red, blue, white and other colors. These fibers DON’T BURN AT 1400 DEGREES F !.
    We now know that Morgellon’s disease is caused by some kind of nanotechnology. The fibers are grown by miniature machines. Maybe they escaped from some laboratory. (See article by Dr. Hildegarde Staninger)
    Have a Bath with Sun powdered laundry detergent with Colorsafe Bleach PLUS Alfalfa tablets.
    These seem to combine to produce something that is lethal to the machines. This cure for Morgellon’s disease was discovered by accident.
    This testimonial is from the person who discovered this cure: (Daisy Baleen) Posted on Health and Healing @ Yahoogroups.com
    I have been Morgellons sufferer for over ten years. Recently, I discovered, quite by accident, something that is literally making it disappear from my BODY. I have experimented with various “super baths,” filling the tub with hot water and putting in things like lemons, baking soda, dish detergent, laundry detergent, alcohol, etc. Well, one day about four months ago, I was filling the bath and I was pretty dirty from housecleaning so I put some Sun powdered laundry detergent with colorsafe bleach into the water, just a tad, because it really cleans the skin.
    Anyway, I left the bathroom for a minute or two and heard a crash that sounded like one of my cats getting into something. When I returned nothing seemed amiss, so I slid into the water for a soak.
    Everything seemed normal until the bubbles parted, and I got the sight of a morgellons sufferers’ lifetime dream: those black and grey specks MIGRATING OUT OF MY SKIN AS FAST AS THEY COULD IN DROVES BY THE HUNDREDS FROM EVERY SQUARE INCH OF MY BODY!!
    And even as I saw that, I also noticed several large oblong things “dissolving” in the bottom of the tub. I picked one up, and it was an alfalfa tablet. Then I noticed the bottle on the counter next to the tub was overturned, and about 25 of them had fallen into the water! They were the cause of the migration of all things Morgellon out of my skin in a fantastic migration for about an hour!
    Brown flecks, black specks, fibers, white patches of fibers drifted off the surface of my skin like No Problema, see ya later, something I had NEVER BEEN ABLE TO ACCOMPLISH WITH ANY OTHER TOPICAL AGENT.
    THE MIGHTY ALFALFA HAS SINCE CONQUERED MORGELLONS IN MY BODY. The scabs are gone, the fibers are history, the patches of fibers are all taped to a piece of wax paper and about to be sent off to a research lab that has requested them.
    I am sending you my testimonial in hopes that other sufferers will at least know some relief from the scourge of the skin.
    Dandelion the Flame Point Siamese must be credited with this miraculous discovery. He is only three years old, but he’s a hero to his long-suffering Mommy!
    I’ve done a little research on the mighty alfalfa, and apparently it creates an alkaline environment in the body in which things like CANCER and other diseases cannot survive. So, taking it internally can only be a good thing, also; but it’s the BATHS that made all the difference in the world for me.
    I also tried putting St. Johns Wort in the bath along with it, with even better results. And for some reason, using the Sun powdered laundry detergent with colorsafe bleach also helps facilitate the migration of the specks.
    God, I really hope this helps even one person as it has helped me. It has cleared up my symptoms so completely that I kept forgetting to post this information on the morgellons websites!!!!
    Thank you to God for this wonderful, freak discovery! Please spread this information far and wide.
    ———
    Editor’s note: The primary ingredient in this discovery was the laundry detergent with color-safe bleach. The bleach is an oxidizer similar to MMS. The boost from the alfalfa is not easily understood but clearly was helpful. Nano-bodies carried in the blood stream would be perfect targets for chlorine dioxide gas to destroy so a four-drop dose of MMS taken internally would be a perfect compliment for this bathing process. Note also that MMS can be used in swimming pools and also safely in a bath tub. MMS is a water purifier first and foremost. For a tub one might mix a 40 drop dose of MMS for bathing (not drinking). Other Morgellons testimonials will be forthcoming.)
    ——————–

  36. At 7:31 am on March 17th, 2009, Danser wrote: #

    There is a highly effective treatment for Morgellons and you can see proof of it here:
    http://brandytwirl.multiply.com/photos/album/1/Morgellons_Pictures_Before_and_After_Treatment

    You can also see a video here: http://www.morgellonshope.com/content/view/690/46/

    If you have Morgellons, it is time to end your suffering.

  37. At 1:07 pm on March 29th, 2009, Danser wrote: #

    A Challenge to Celebrities Who Quietly Suffer From Morgellons Disease

    I have a challenge to Celebrities around the world that are silently and privately suffering from Morgellons Disease; when your symptoms have been reduced or eliminated, who among you will become the “Spokesperson for Morgellons?”

    Morgellons disease is just as real as HIV was 30 years ago. The only difference is 30 years of research and study by the medical community that has gone in HIV. This will only occur when Morgellons hits a certain ‘plateau’ of patients and research attention.

    What is truly needed now is a celebrity who has Morgellons and is willing to tell the world about this horrific disease. This will only work if the celebrity has Morgellons and has eliminated their symptoms to the point where they can really function in this capacity.

    Let’s tell the truth here; 99.99% of the medical profession has never even heard the word ‘Morgellons’ yet alone has been willing to open their minds to the possibility that it might even exist. Only those who have experienced Morgellons can truly ‘know’ what this is unless they are living with some one who suffers every waking moment of their lives with this terrible disease on their minds. How could they not? The feeling of biting and scratching 24/7 will certainly draw anyone’s attention.

    The author of this post deals with Morgellons victims daily, hundreds each month as this pandemic explodes across our planet. He hears their cries of pain and suffering, the loneliness and isolation they experience and most horrific is the way the medical community is quick to diagnose Delusions of Parasitosis (DOP) without the benefit of an exam or lab tests (to date all known lab test result in nothing being found).

    What the MD’s have forgotten is that in order to have DOP, the patient must be schizophrenic because DOP is a sub-set of schizophrenia BEFORE they can be diagnosed with DOP. If their patient is not schizophrenic, DOP is not possible.

    What is missing here is public awareness. To date 40 US Senators have written to the US CDC requesting an investigation. It took 6 years for the CDC to begin their investigation into this new disease. It has now been nearly a year and a half since the CDC began the investigation and their conclusions are expected in May of 2009. The question to the reader is: What sort of conclusion might you expect if you funded such an investigation if you only funded it to the tune of $338,000? You decide.

    There is a safe and effective way for Morgellons victims to reduce or eliminate their Morgellons symptoms; Nutrasilver. This natural mineral has proven in thousands of cases to eliminate most, if not all cognitive and lesion symptoms within a few short weeks. Although not a cure, Nutrasilver has an amazing ability to push this disease out of the body from the inside rather than treating with lotions and potions. This can be very frightening, but the good news is that it is coming out of the body.

    I am aware of several Celebrities who have become “symptom-free” from Morgellons disease using Nutrasilver and I challenge them to step forward and become the “Poster-child” of this grass-roots movement of Morgellons suffers. There are obvious personal benefits to doing this, but the most important thing a Celebrity can do for the Morgellons movement is to step up and make the world aware of this life-stealing disease and let Morgellons victims know they can get their lives back using Nutrasilver. http://www.nutrasilver.com

    To see proof of how Nutrasilver affects Morgellons victims, please click here: http://morgellonstreatment.blogspot.com/ Caution; this site is NOT for the faint-of-heart.

  38. At 6:12 am on April 4th, 2009, marie wrote: #

    Hi Alan. havnt heard of many NZ sufferers yet. I also tried colloidal silver and nutra silver for a period and although they helped relieve some symptoms they havnt been nearly as effective as peanut oil or p.butter.mainly because peanut seems to stop the itch which greatly helps the insomnia and it also heals the lesions which makes me confident to go out in public and lead a fairly normal life. but the disease definitely is not cured and in fact has been terrible during the southern summer when i have been sweating thick black sweat and had an increase in hairlike fibres from my body.the heat seems to greatly aggravate this organism. i can see an increase in suffering coming in the northern summer.
    i think if anyone who had actual morgellons had been totally cured of the disease they would have been quick to advertise the fact on the net. maybe some people have very mild cases or catch it very early.

  39. At 1:50 pm on April 11th, 2009, Danser wrote: #

    Dear Marie,

    If you take Nutrasilver as directed, you will see you cognitive symptoms gone in 2 weeks and your lesions gone in 3 weeks. You have to follow the protocol included in the package. there is a money-back guarantee, so please do not stop taking it.

  40. At 7:04 am on June 30th, 2009, Lisa wrote: #

    I am really quite irritated and even angry at these ‘advertisements’ of cures..please stop posting about Nutrasilver and Alfalfa as cure-alls. The scientific community that is actively researching this disease has not once, not ever, agreed with these claims. Stop selling your snake oil to vunerable folks..i beg you. Just think..if it were true..Morgellons would be dead in it’s tracks… you only hear about this from … whom?

    To date..there is no known cure for morgellons..only hypothesis and conjecture.. take care of yourselves as best you can..try different protocols and be good to yourself.. go to rense.com.. seems to be an open source of info with NO selling of cures..just common sense information.

    I am a sufferer, I have all of the symptoms, and lately, as one poster stated, i am having the intense tooth pain and no appetite whatsoever. I don’t know what or why or how.. i just know that it is, and that i am def not delusional. i go to the forums when i am feeling particularly alone with this..sometimes i feel worse, sometimes better.. but at least i know i am not alone

    i am with you all in this fight..wherever it takes us

  41. At 5:53 pm on August 28th, 2009, mollie wrote: #

    I suffered for 5 years with Morgellons. I contracted it in Belize. I finally rid myself of this disease despite all the Doctors not helping me. Have gone through every possible thing a person can with Morgellons.

    For two months I showered from HEAD TO TOE with medicated Selson Blue Shampoo. Changed clothes every day and washed sheets every day. This finally took care of it.

  42. At 6:56 pm on January 4th, 2010, Yourfriend wrote: #

    Hi Guys,
    I’m curing my morgellons too with out a dr.’s help (dr.’s won’t help.) Selsun Blue works, salt water scrubs work (use epsom salt), washing clothes & sheets daily works & today I just tried a generic version of Vicks that I bought from the 99 cents store. I put the Vicks on really thick all over the areas that feel like they are crawling & it stopped the crawling & biting immediatly. For the areas around my eyes I used coconut oil. I heard they coconut oil is good too.

  43. At 10:22 am on January 18th, 2010, Bradley James wrote: #

    The people below used Dr. Staninger’s products. I’ve been on her protocol for 1 year and i’m 85% better. She saved my life..you can read other testimonials below. You can buy her products to help get rid of the fibers and lesions.

    Dr. Staninger products are availible online. DR. Staninger is still taking patients but the FDA doesn’t allow her to say that she treats morgellons disease. If you have symptoms with lesions, itching and fibers her products really help.

    Testimonial 1
    “hi all i’ve been a member here for a long time. as a long time sufferer i have wasted thousands of
    dollars on just about every protocol to be found on the net. some have knocked them back some have made me sicker some no effect at all. well i,ve got to tell all of you, if you are sick of being sick call dr staninger. she knows what this is and how to treat it. no mayonaise v8 juice or motor oil. believe me i have no financial interest my only motivation is to know that i have helped someone get relief” -steve, curezone.org

    Testimonial 2
    “If you have resources, Dr. Staninger’s protocol is the most effective thing around. You also have to have a slew of blood work done. Many people have become symptom-free on her protocol – I have spoken to a few. I am close to it, and have been for about 22 months (I am a patient of hers). The most important aspects of her protocol are Far Inrared treatment. Also, lots of vitamins and minerals as well as several herbs and supplements. Anonymous poster at xxxxxxxxxs-xxxxxxx-research.org

  44. At 9:24 pm on January 20th, 2010, debby wrote: #

    I have suffered with this malady since June 2001, as I write this I cannot stop scratching. I considered suicide a few times, thought
    God hated me etc… but now I just accept it. the only time I did not have a problem is when I had 3 surgeries recently and was on strong anitibiotics.

  45. At 6:52 am on May 5th, 2010, Gillian wrote: #

    60 Minutes (Australian Channel 9 network) are in the process of putting together a story on “Morgellons”, to go to air on Australian Television some time this year.

    Stephen Taylor (Producer) of 60 Minutes would like to hear from other sufferers in Australia.

    Please write to Stephen at: sttaylor@nine.com.au

  46. At 7:49 pm on June 18th, 2010, Sunny wrote: #

    EVERYONE. I FOUND THIS INFO ON THE WEB: Chitin is a biological polymer. Very similar to Cellulose, with the exception of the ends of the molecular chain. Chitin is very much involved in this condition, the pathogen we are talking about, is a fungus, possibly a hybrid that is closer to being a microsporidia.
    The information about this pathogen or fungus being cellulose based is bogus. After coming down with the condition myself (not nearly as serious as most) and with no luck treating it with antibiotics/antifungals topical or internal. In fact, like reported, the antibiotics only seemed to damage my system in the long run and allowed the symptoms to increase heavily after or even during the dosages. And from my readings, I wasn’t even going to attempt taking this to a dermatologist. I was 25 when this started and had NEVER had such a skin condition in my life, I am in great shape, and I refused to believe that this was normal for skin to become so irritated and inflamed.

    I was positive that I traced my exposure to an outdoor area, and soon enough, I found several people including a good friends with the same lesions. That’s when I started my research, and being an amateur mycologist seems to have been my lucky advantage.

    I am very interested in others trying the method of treatment that I developed, even though we are likely continually exposed on a weekly basis, treating the skin is the first step toward killing the spore producing colonies and therefor stopping the spread of the pathogen in the blood to other areas. I’m NOT selling anything, I’m NOT a physician and what I’m about to tell you will only cost you a couple bucks for a large volume of topical treatment.

    The key here is Chitinase. Chitinase is an enzyme used in many biological processes to cleave the glucose bonds of Chitin. It’s produced by many fungus as a building block for biological growth, and it’s produced by some grains, as a means of defense against spores and fungus. In my case, I extracted Chitinase from several sources, including a Trichoderma fungus and Barley. Obviously for the average person, growing and extracting a enzyme from a fungus is not going to be easy, but I had equally effective results from the Barley Chitinase, and it’s much easier to make.

    Here is what you need to do… Find a home beer brewing store, and go there is person. Ask them for the most stripped out and unprocessed Barley that they carry, MAKE SURE IT IS BARLEY and not WHEAT, wheat doesn’t contain the necessary enzymes. In my case, I think the strain was GR 18 or something to that effect. Most strains should work, but Barley is known to vary in enzyme levels. What your looking for is the most unprocessed, lightest color, Barley grain. They should be able to direct you to something close to that if you give them that description. It can not be roasted or otherwise adulterated barley. You shouldn’t need more than a lb to treat the whole body, this should cost around a dollar. If they ask you if you want it milled, you can have this done, but you should then use all the extract that I’m going to describe, as milled barley might lose it’s enzyme potency once it’s sat after being milled. There might also be benefits to soaking the grain in water for several hours NON MILLED prior to making this extract. I had such good results with the milled barley that I’m not sure how how much better the non milled version of this extract would be.

    Directions: Take the milled barley and put it in a plastic bowl. You really only need a half lb to make plenty enough to treat your whole body. Add spring water or distilled water, just enough to wet the grain evenly, and so that they are all saturated and loosely moving around in the water. You can use tap water if you don’t have the others, but it’s likely that there is a spore count in the water too and it will diminish the life of the enzymes before you even start using them. Now, let the mixture sit for around 4 hours in a cool place, anything under 80 F is fine, you just don’t want it basking and rotting in the sun or heat. Next, get a blender and blend the mixture until it’s very milky and pulverized. If you don’t have a blender, get a pestle or something similar like the end of a metal ice cream scoop and smash the already milled grain until you feel that you have smashed everything a few times over in the contents of the bowl. Now you need a strainer or a piece of screen. Run the mash through the strainer and collect the fluid that results. Shake the mixture up and stir very well before straining so that the milky fluid works well through the screen. Now press the barley through the screen to really juice it. You should put the remaining barley in a piece of cheesecloth or a clean sock with a larger stitch like cheesecloth. Ok, now you have the enzyme/barley mixture finished. If you wanted to try the whole grain approach, soak it just like the milled barley, and you must use a blender with the method, otherwise following the same directions for the milled barley.

    To treat yourself you will need to take off any clothing around the area you are treating, or possible just strip totally naked to avoid making a mess of your clothes. Put the solution in a cereal bowl or shallow bowl, put a plastic spoon in it and stir it every time before dipping your fingers in the bowl just enough to get a decent amount of the liquid on the underside of your fingers. It should be slightly pasty, if not, you might want to make it with less water than you used. Paste it over your lesions lightly so that you provide an even coat without pressing it all away from your skin. Let it sit on the area, and re-coat the area as soon as it feel like its starting to dry, which should take several min.

    Now, don’t be alarmed when you see the area flare up like a horrible allergic reaction, that’s the Chitinase cleaving the fungus’s chitin in your skin, and you will likely see the same broken vessels that we so commonly see after initial infection, only there will be many many more, and it’s likely to sting and prick very notably especially more so if your more heavily infected. Let the remaining chalky residue sit for about an hour, and then go rinse it off or take a shower, or if you want, just leave it there the rest of the day until you do shower, it won’t hurt you because it’s just barley. You can save any leftover extract in the fridge but it won’t keep for much more than a day or two and I would recommend using it fresh for best results.

    One more thing I would like to mention is that I have talked to several of the prominent figured involved with the media’s version of what is going on, several of whom are listed on morgellons organizations sites as professional references with credentials such as Dr. or Microbiologists, several of them whom have also been on Fox news. I won’t mention names but I do want to say that most of these people are either puppets or they are scared, and they aren’t looking for a cure, they are avoiding it. I spent months asking them for their opinion on the issue and it got me nowhere…

    I NOTICED THAT I FEEL BETTER AFTER EATING POTATO & ALSO AVOCADO….I DID SOME RESEARCH & CAME ACROSS THIS:

    …the class I chitinase of avocado, chestnut, and banana, which belong to a family of pathogenesis-related proteins (PR-3), was revealed to be an important cross-reactive allergen for latex-sensitized people. Class I chitinase of plants contains a hevein-like domain in common at the N-terminus. Hevein is one of the most important latex allergens. Thus, the cross-reactivity of latex-allergic patients can be partly ascribed to the shared hevein-related structures. This site closely overlaps the conserved residues indispensable to the chitin-binding property of hevein, which is the root of its anti-fungal activity. On the other hand, patatin has been identified as a major cross-reactive allergen in potato. Patatin is a defense-related protein with lipid acyl-hydrolase or esterase activity, and functions as an important storage protein in potato tuber. Latex allergens (Hev b 7)homologous to patatin have also been found in natural rubber and have been officially registered. As in the case of cross-reactivity between class I chitinase in vegetables and hevein, the structural similarity between patatin and Hev b 7 likely accounts for part of the cross-reactivity of latex-sensitized people….

    ANYWAY -IT WAS A LEAP OF FAITH, BUT I BLENDED AVOCADO AND SPRINGWATER AND APPLIED IT TO MY HAIR,SCALP & SKIN -LET IT DRY…OVERNIGHT, WITH AMAZING RESULTS. I HAVEN’T TRIED THE BARLEY YET BECAUSE I BELIEVE THAT I MAY BE ALMOST CURED USING THE AVOCADO METHOD.

    AVOID PETROLIUM PRODUCTS INCLUDING THE MINUTE QUANTITIES USED AS PRESERVATIVES IN MAKEUP AND CREAMS. THIS PATHOGEN NEEDS IT TO BREED. AVOID SUGAR. I ALSO RECOMMEND THE FOLLOWING FOODS:
    banana, avocado, potato, tomato, kiwi, chestnut, walnut, passion fruit, bell pepper, celery, almond, buckwheat, persimmon, pommegranite, curry, cayenne pepper, lod pressed coconut oil, sunflower oil, olive oil , avocado oil, pau d’arco, capsicum capsules,coffee, honey.

  47. At 8:02 pm on June 18th, 2010, Sunny wrote: #

    ALSO,

    prior to commencing the “avocado treatment” – my scalp was very bad with ‘active’ raised tracks. I was prescribed Bactroban (antibiotic ointment) -It worked reasonably well. My scalp cleared. BUT I was supposed to use an anti-bacterial on my scalp prior to putting on the bactroban -however, since the anti-bacterial had a petrolium product in it, I skipped that step.

  48. At 8:08 pm on June 18th, 2010, Sunny wrote: #

    ALSO, (in my opinion) when this affliction first hits you – eat acid based foods (meat, chicken, peas, corn etc) as this breeds in an alcaline environment in the gut. Tri-plex worming solution worked for me (2 courses of it) to clean out my bowel. Spicy foods helped too.

  49. At 8:20 pm on June 18th, 2010, Sunny wrote: #

    This is what I did when I had sore teeth: I would rub eucalyptus oil on my gums before retiring at night (do not swallow -spit out as much as you can. This was before discovering the benefits of avocado though…

  50. At 6:04 pm on October 4th, 2010, Julia S wrote: #

    Hello can anyone help me, after a months stay in Sri Lanka I have Springtails in my hair – which is very curly. I have tried everything to eradicate them, and am not getting any help from doctors etc. A dermatologist prescribed Ivermectin but this did not help. Julia S

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