Frank Talk About Morgellons

Three years of healing Morgellons sufferers, this is a must-watch video

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Morgellons Attacks Teenagers Too; Danny Shares His Story of How He Got His Life Back

Dear fellow Morgellons victims,

Morgellons Lesion

Morgellons Lesion

I’m writing on behalf of all the young people and the elderly with Morgellons who have been shunned, criticized, and outcasted by society thinking we suffers of this horrible disease are crazy. I personally knew absolutely nothing about this disease until I came home from school one day of September 2007 and noticed granule-like crystals on my hands. I also noticed clear fibers that appeared to be coming out of my hands as well. I went to the computer and typed in “black crystals on hands?” or something to that extent. I stumbled upon a few websites that had details of Morgellons symptoms and the blue, black, clear, and red fibers with granules coming out of hands, body, and or hair. I didn’t automatically assume I have this disease after a couple months of thorough personal research I had whatever this bizarre disease was. Every single symptom I had matched everything I read. I had everything from the physical identification of Morgellons right down to all the mental and cognitive disorders of Morgellons; brain fog, I slept constantly, depression, insomnia at night (slept all through the days), lost a lot of weight, everything aliment you could imagine I had. But by far the worst symptoms was the anxiety that would come out of nowhere, it literally felt like I was even in my body at times.

It began to slowly but surely rule my life. I noticed the fibers everywhere in my home, friend’s homes, family member’s homes, these fibers were everywhere but I was one of the only that had symptoms to this extent. My friends and family had the fibers on there body and hair as well. My friends were the only ones who believed me about the fibers and knew I was sick. I tried to express to my mother and stepfather what was going on but surely my mother thought I was loosing my mind which I can completely understand because of how bizarre this disease sounds to the layman. Finally after convincing my mom I had this disease I stumbled upon a website called “NutraSilver”. My mother personally thought I was crazy but my stepfather said “whether its in his head or not we can see if this helps”

So my stepdad bought a bottle of NutraSilver and it came with another for free. The first night I tried the NutraSilver I had to lie down in bed with my mother I trembled so bad. When I woke up the next morning I felt slightly better. I started to use the NutraSilver a couple times a day and just put some drops in my daily routine of drinking water. Everyday progressively got better, I started to forget completely about Morgellons and live my life. It ruled my life, I am an 18 year old male (at the time I was 17). I also stumbled across an amazing doctor and friend named Dr. Susan Kolb. I found her website when I was researching about Morgellons and even though I lived many states away and was very embarrassed I deciding to just call her and tell her what was going on. She talked to my parents, talked to my family and tried to express to them that this is a real disease. Still after all of that they still did not believe. She gave me great tips to get slowly but surely better as well. I slowly started being able to go to school more and focus more on my life. Everyday with NutraSilver and Dr. Kolb’s advice made everyday easier to get through. As last summer came along (2008), I was very confident I was Morgellons-free. I completely forgot about the disease and was able to live my life.

I moved into a new home, had a new life ahead of me and I felt like my life was finally back, unfortunately I ran out of NutraSilver around September of 2008 and was unable to purchase it again with the lack of my finances. I stopped using it all together. Around November or December my symptoms started coming back fully. I had brain fog again, depression, anxiety, fatigue; the fibers were coming out of my skin again. I was once again infected. They were around my new home and in my hair and body once again. I talked to Doctor Kolb at least once a month to keep her updated. With her help I personally discovered some things that helped in the mean time until I could get another credit card to purchase NutraSilver once more. My symptoms got so bad living at my new home I finally ended up moving back into my mother’s house where I first discovered I had Morgellons. I still felt horrible, I discovered something called Trilogy Cardio Essentials in my fridge that mom used to lower her blood pressure and things of that nature. It was recommended by someone who also used silver on a daily basis that ran a herbal store down the street from me. So I took a couple swigs every day unknowing the effect it would have on me. The next day I glanced at my hands after I was out of the shower. I noticed the fibers purging out like I had seen with NutraSilver; it was very scary.

I am still drinking it and it helps just as NutraSilver has. I have used many things to help with this horrific disease but I can honestly say NutraSilver, Dr. Bronners, and Trilogy Cardio Essentials has helped the most by far.

Worried male doctor

M.D. trying to "figure out" Morgellons Disease

I’m sick of people ignoring this disease; even doctors are ignoring it. I know there are so many people that are struggling with this disease everyday, and I truly desire for them to live their life and again and take back what’s rightfully theirs.
My life is finally coming into view again, and I literally owe my life to a man named Russell at NutraSilver and a wonder Doctor by the name of Susan Kolb. I have never met a person so dedicated to seeing their patients or customers get better than Dr. Kolb

Without their help, guidance, and advice I’m not too sure how long I could have held out with all the depression and anxiety.

My final advice to any man, women or child with Morgellons is get NutraSilver, have a positive mind-set and lives your life again; I don’t want anyone to go through what I have been through with anxiety and depression.

Sincerely,
Daniel W.

I will list my personal protocol for Morgellons;
NutraSilver
Dr. Bronners Lemon Castile Soap ( you can use it for toothpaste, hair, body, lotion anything you can think of even laundry)
Acai berry
flaxseeds
Borax laundry detergent.
Air Filter
Trilogy Cardio Essentials.


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Morgellons Economics; Who Wins and Who Looses?

I have spoken to well over 1,000 Morgellons sufferers in the past 3 years during my direct involvement with Morgellons Disease. Most are ordinary people from every walk of life while some are medical professionals themselves infected with this disease or care for those who suffer.

Morgellons Disease is characterized by these symptoms: non-healing lesions, ‘brain fog’, depression often leading to suicide, multi-colored fibers growing from their skin and most disconcerting, the relentless sensation of being bitten on and under their skin. The Morgellons Research Foundation, located on the campus of Oklahoma State University, states that there are approximately 93 typical symptoms and each individual with Morgellons has some but not all of these symptoms.

Most Morgellons victims tell the same story; they are diagnosed with Delusions of Parasitosis (DOP) and labeled permanently in their medical record as having ‘Mental Health Issues”. Most doctors will not even look at the lesions and tell their patients to “stop scratching yourself.” Those who are prescribed medication through misdiagnosis spend a great deal on medications that effectively do nothing for them. Many follow the message boards on the Internet and desperately chase lotions, potions, chemical and herbal remedies only to experience no improvement. Those who suffer the longest often tell me of how the medical profession takes their money and all they get is worse.

Many Morgellons victims tell the story of how they have lost their jobs, homes, savings, and family and just about everything else trying to get relief. They feel alone and isolated and often ‘cocoon’ in their homes. I hear this far too often. Some call me crying out of desperation and loneliness; it breaks my heart.

Most medical practitioners seem to be into Morgellons treatment just for the money. There is a PhD in Los Angeles who knows of an effective treatment but does not use it because she does not make any money on it. There is a Nurse-Practioner from Texas whose medical license was suspended by the Texas Medical Board for prescribing antibiotics too frequently who now commutes to San Francisco under a California license to treat Morgellons patients. She continues to administer antibiotics to Morgellons patients with no results. She charges $500 for the initial visit. All the Morgellons patients received for their hard-earned money is they get worse.

Imagine, over 40 US Senators and Congresspersons have written to the US Centers for Disease Control (CDC) requesting them to conduct an investigation into Morgellons. It only took six years for them to begin their investigation in Oakland, California at Kaiser-Permanente Hospital with funding of a mere $338,000. That amount of money is barely enough money to begin an investigation yet alone complete one. Their investigative conclusions are due in May, 2009.

As this infection continues to spread globally, little scientific attention is being paid to those who have Morgellons and suffer with no hope and no help from the established medical and scientific communities. Apparently, there are not enough people who suffer Morgellons for scientific research to make research financially beneficial to fund the research. Today, only a very small handful of individuals and small organizations have attempted to discover the cause(s) and methods of disease contraction and transmittal of this mysterious disease. When I ask a half dozen scientists what Morgellons is, I get 6 different answers suggesting that no one really knows very much about this horrific disease.

Although every major US television network has reported on Morgellons, 99% of the medical profession and the general public have not heard of Morgellons.

This is exactly what happened 30 years ago when patients presented with symptoms also classified as ‘Delusional’ but is now well-known as AIDS/HIV. Those early victims endured the same neglect and abuse as Morgellons victims do today; denial, labels of being delusional and general neglect. Until enough people were infected, they were ignored by the mainstream medical community.

So what do Morgellons sufferers do to eliminate their suffering? They commit suicide as one of my friends did yesterday. We all have a responsibility to take care of each other. Until enough people suffer from Morgellons, it will remain “unprofitable” to conduct real scientific research into this horrible pandemic disease. Clearly, the Winners are the suppliers of medical goods and services and the Losers are the Morgellons sufferers.

Morgellons Lesions before treatmentMorgellons Lesions

Morgellons Suffers Need a “Poster Child Celebrity” To Tell This Amazing Story

Since Morgellons Disease was reported in the mainstream media in 2005, there has been no real progress made in discovering the cause, how Morgellons is contracted and transmitted, if it is contagious or if it is directly responsible for deaths other than suicides. Deaths are increasing exponentially and so is the level of infection in the global population.

The symptoms are right out of a science fiction novel: ‘brain fog’ (confusion like ADHD), severe depression, deep bone and muscle ache just like fibromyalgia, severe chronic fatigue just like Chronic Fatigue Syndrome (Morgellons victims sleep 10 to 16 hours a day and are still exhausted), multi-colored fibers growing from their skin that are coated in high-density polyurethane that will not burn until 1,400 degrees Fahrenheit, and most bizarre, they experience animals that relentlessly move and bite the victim under their skin 24/7.

Morgellons victims loose their lives to this disease; MD’s and Dermatologist dismiss the symptoms as Delusions of Parasitosis (DOP), a subset of schizophrenia. The Medical Community treat their Morgellons patients much like HIV/AIDS patients were treated 30 years ago when that disease was new. These victims are shunned by family and employers and are left alone without support and eventually become severely depressed, hopeless and suicidal.

Over forty US Senators and Congressmen has written letters to the Centers for Disease Control requesting an investigation into this bizarre disease. The CDC began its investigation in Oakland, California at the Kaiser-Permanente Hospital in January, 2008 and is expected to release its finding in May 2009. The funding was a mere $338,000; barely enough to set up the investigation. Inside sources say that the remainder of the funding comes from the US Army.

In the past 5 years, there has been little funding to scientifically explore the cause(s) and treatments to help the Morgellons suffers begin to ‘get their lives back’. There are small pockets of individuals who are conducting their own Morgellons investigation with little or no funding. The Morgellons Research Foundation, located at Oklahoma State University, is severely underfunded and has expressed no interest in finding any relief for Morgellons victims, but rather focuses on discovering the cause of this mysterious new disease. Meanwhile, Morgellons victims search relentlessly on the Internet for some clue as to how to eliminate their suffering.

Worse, there is no spokesperson to bring to the public eye the incredible torment Morgellons victim’s experience. The scientists that are willing to discuss Morgellons at all say that there are at least 10,000 new Morgellons victims a day in the USA alone. Most will not get diagnosed correctly and will be given a DOP label to labeled in their medical record for life as mental patients. Included in this number of new Morgellons victims are celebrities, Senators and Congressmen and other public figures. Until one or more of them steps up and shares their Morgellons suffering with the world, the rest of us will remain asleep to Morgellons until each of us becomes the next Morgellons sufferer. Until a celebrity has the courage and conviction to publicly announce their Morgellons disease and encourage mainstream science to fund and investigate Morgellons disease, the silent suffering will continue.

 

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