Copyright M-R-O ABOUT M-R-O  (2007)
Regarding myself, I was formerly an electronics and IT specialist, and now I am in my fifties and on disability after my life changed in 2005. I became infected after an one-night-stand with, what is known as "Morgellons", and "Lyme" disease. So I know very well that this new disease is highly contagious, even by skin to skin contact!

Both diseases are controversial, and not accepted by most of the medical professionals worldwide. Anyway, after 6 months of the unbelievable horror and pain, real, and emotional, and usual ignorance of doctors and their incorrect medications, I decided to start my own investigations about this disease.

At the time, there was not much information available about this new kind of disease caused from colored fibers. Only a few articles on the Internet described an epidemic situation in Texas, Florida and California. People were taking microscopic slides of unusual parasites to entomologists, etc. showing their horrendous cavernous scars, that would not heal, and still being told that they were delusional, and inflicting their own wounds.

Also, the Morgellons foundation from Mary Laitao was documenting for the first time in 2002/2003 about an unknown "fiber" infection. They deserve credit, but after many years of focusing only on fibers, without new information or treatment options, no help was given to me or the other sufferers who were waiting for a cure and more help and information.

Therefore, I started the first site (Morgellons-Research.Org) myself in the spring of 2006, with a bit more information about this disease. Also, to give "Morgellons" afflicted, more hope and support to handle this horrible condition. Before I found my own helpful remedies to fight this condition, I went through a very hard time like all sufferers, with no relief from bites, open lesions, Lyme and chronic fatigue, and everything associated with this disease. The loneliness and isolation associated with this ailment is unbearable. 

I spent months of long days and nights of microscopic research, and investigation in different areas. I experimented with many substances and did a lot of work on my German and English websites. I contacted WHO, the CDC, local authorities, doctors, professors, parasitologists, and universities, etc.

Not much help was forthcoming. They only come forward when the work is done, to get credit and accept money for it. Anyway, after my appearance on the Morgellons scene, I realized that the thousands of sufferers that visited my website, had hope again, and new directions. I have had many credits, as well as many critics since then.

My website explains how the infestation is spread via the fibers in nature and among humans and animals. I described, as well, for the first time, the infection process and the location of the fibers and biofilm on the skin and hairs, in the lymph system, the blood, the GI tract, and how to reduce the infestation with meticulous hygiene and internal and external medication.

If one of these 3 steps is missing, no progress toward healing can take place. I also presented information for protecting a good immune system, the effects of hormonal influences, and the need for a higher vitamin, protein and mineral intake. It took an enormous effort for me to continue the years of constant work involved, and to provide emotional support for "Morgellons" victims. I had many episodes of burn-out.

Although I am feeling physically better now, the suffering that goes along with this disease continues for me daily, from dawn to dusk. Also because the supporting of the other worldwide sufferers has attributed to more mental depression, due to the daily misery that others go through and report to me.

It is better to be crucified than to have this disease. Nobody, not even the most evil animal on earth deserves this kind of existence and suffering. Actually, my time is very limited and there is so much work to be done with "Morgellons". I am doing all I can, and, sometimes, I feel I am doing it alone. What more can a normal man do to fight this disease, and at the end even being blamed and attacked on the Internet for my efforts. Who, with any right or a white coat should throw the first stone against me? Is it wrong to take care about desperate human beings and showing the truth? 

Left alone and ignored by society, and neglected by the the medical community with this disease, many sufferers have already committed suicide. This despicable, painful, disgusting, humiliating condition, is against the dignity of man. 

What is the medical comunity actually doing to help us? Physicians should begin, now, to provide medical care for the sufferers, like they promised when they took the Hippocratic Oath. Otherwise, their disregard of the medical needs of the "Morgellons" sufferers is due to ignorance, money, or avoiding the inadequate rules and regulations of the medical insurance companies. Their attitude is just inhuman and not in consensus with ethical aspects.

Nonetheless, I feel it is necessary to postulate again now that the "Morgellons" situation is getting worse and the scientific community is still taking too long to wake up. The infection rate is still increasing and many people all over the world are contacting me, because they and all members of their family are newly infected and it could not be avoided because they were not aware of such a disease. This situation is also due to the miserable information policy and ignorance of all CDC`s, politicians, and mainly the WHO.


I agree that some of the findings about "Morgellons" may appear extraterrestrial, and sound like science fiction as it was never known before. But now is the time that we must go further, by investigating the DNA of invasive filamentous fungi, protozoa, bacteria and surely some involved viruses. The subcutaneous, invasive infestation can be described in terms of a spider web; integrated into the human skin. If no measures have been taken, within 3-6 months to stop these life forms, they expand more and more in the human body.

It resembles slimy nerve fibers that are connected together, each over a glassy, slimy tubule which can expand. In addition they metabolize with their exo-enzymes (protease, liptase, keratinase) the proteins, lipids and mostly collagen at a subcutaneous skin level. Thus, after a certain period of time, the skin will become thinner and more transparent and will hang down (collagenosis) and lose its tone and elasticity too.

This point must be made clear. It takes a long time to make improvements. It takes until the last small fiber is washed out from the clothing or cleaned up from the environment and body. Before you give up, you must know that healing is possible only with hard work. As soon as you recognize that there is no magic pill from the pharmacy, you can try to make this go away, the sooner you begin to fight this unbelievable conditon with patience. This is not a game with break-times between! If you give up, then good luck to you...

Just thinking, you can handle these few pustules on the skin with essential oils etc., would be a fallacy, because the real grade of an infestation/infection is mostly invisibile to us. For an infected person, each day counts in order to fight against the total invasion of their own body. The external skin manifestations are just the tip of an Iceberg. The "Morgellons syndrome" is not a skin disease, the skin symptoms are just one expression of it.

Many people have taken over some of my work and expanded and improved upon it. This is okay and a deep recompense to me anyway. Now there are numerous Internet sites and on many of them one can find my ideas, work and their COPY INVESTIGATIONS. They benefit from my and others- efforts, but don't do any of their own reseach. Believe it or not!

Anyway, I want to say thanks at this point to all worldwide members of my organization who helped me in supporting my work. Also I want to name all Morgellons afflicted and websites, as well as many blog and board writers who have done good investigative work, they deserve credits and thanks for their efforts and amazing work what they have done over the years, in order to find out more about this disease.

My own documentary site should not be considered just as the "Rocky Horror Picture Show", but today and for many years, this disease is the naked reality in the USA and in many other countries. I just tried to show to the world - the enormous suffering of each "Morgellons" afflicted person, which is incomparable to any other disease, including every bad life circumstances which comes along with having this disease.

Right now I do not have any Morgellons or great Lyme symptoms, but I still have lung problems with cough and emphysemas, but gladly I do not have any malignant cancer right now!! I do not know how long I am going  to be clear, re-infection from the environment can happen almost daily but right now I am quite fine, otherwise I could not do all this daily work over years now!

My Message to all sufferers: Please, don`t give up, and fight for your life and rights as a human being (especially in the USA). It`s worth doing so!! This disease is fightable even if it takes a long time, but you will have at least a supportable remission from it. Everything that has a beginning must have an end, too...

Stay tuned...

Sincerly Marc Neumann



"All truth passes through three stages. First, it is ignored and ridiculed, second it is violently opposed, and third, it is accepted as self-evident." 

- Arthur Schopenhauer, German philosopher -

(At this moment we are in the second stage)