several months ago, i was having problems with 'stuff' in my hair so i shaved my head. this video was prepared two days after i shaved. i did not know there was this much 'stuff ' on me. i had viewed myself under black-light lighting and my hair looked like a jungle. under normal lighting, day or night, i look fine. under black lighting, i look like i am covered with a sort of fiber or lint.
i have watched this stuff form in a controlled environment to rule out everyday normal contact my skin might ordiarily have. in the video, you can see it on my scalp growing in stages, from bright tips budding from where a follicle should be, to longer strands and shapes eventually connecting.
this was prepared after showering. i 'air dried' so that my skin would not come in contact with any towels, clothing, fabric, etc.
i tried to see a dermatologist for this and other skin related ailments. i tried to show him my skin under the black light, but he took a glance and immediately shrugged his shoulders saying, "what's the matter? you have a little lint on you." i tried to show him that it was coming from me but he would not look. when i told him i have witnessed it and scratched from beneath my skin, he said i was having delusions and hallucinating.
he recommended some pyschotic drug or some such stuff to calm me down. well i wasn't excited until this dipshit refused to look at what i was showing him. he said that everyone had this covering on them. well i don't know about you guys, but from the times i remembered being under a fluorescent light in the past, i do not remember being covered with a invisible fiber coat.
so, i said to him, "ok, fine. can we look at your skin? like, your arm, under the black light to show me that's true" ? he refused, saying it would not do me any good. further saying, in fact, if he did look it would make my mental condition worse. ? at the time, i did not know i had a mental condition. although his ignorance and smug attitude was starting to drive me crazy :)
he said all of this without once examining my scalp or any portion of my skin in general. what if i had had some nasty skin infection or contagious fungus. how could anyone make such a quick determination and diagnosis by casual observation during conversation? he didn't touch or look at my skin with magnification or even just with the naked eye close up. had he done so, he would have found more than whats in the video. i have some sort of fibers under and on my skin. i produce pea-size like tennis balls of fiber all tightly wrapped. they will cling to hair shafts. i think they grow with some hair shafts and follicles. they range in size from microscopic to 3 to 4 inch bundles to date. i have wormy little wires that are on me at all times. they connect hairs under and above skin level. many times they look like they are supposed to be shaped like a bug.
i have these and other symptoms common with the condition referred to as morgellons.
does anyone else have this on their skin routinely, at anytime, day or night? i am constantly emitting this and it just is not right.
I have the exact same thing. I was also angry when the dermatologist gave a mental diagnosis after doing NO tests. I read blacklight is a tool used by dermatologists, and I got one to show my family I wasn't delusional. I think collagen is involved, as the stuff has a plasticy feel to it. penny_asbury@yahoo.com please write to me.
What's worse is not having support from your family. They see you suffering, they see what you go through each day and they know something is wrong. Yet, it is easier for them to shrug it off like the Doctors, Derma's and other medical professionals. Yes, I get the same looks and the same responses from doctors.....all of what is said here I have experienced. I feel alone and abandoned by everyone. It is a full time job and I am hoping by the grace of God that I get through it. For all who suffer, my prayers are with you. Please pray for me too. Take care.
unfortunately i came down with the same symptoms approx two years ago but more severe-the sores became so bad that my scalp and the back of my head are now permanantly disfigured resulting in scarring caused by the"burning" and extreme itching.To my horror not only did this horrible disease spread to allover my body but i also received similar responses from not only the doctors but sadly my family as well.just when i thought things could not get any worse-the symptoms -the constant itching
I didn't know what was wrong with me with depression and many other symptoms that started 2 years ago until April when I began to feel something crawling under the skin on my back. Like many many others I am self diagnosed and using natural meds, and going through hell. The thing that bothers me the most is my hair. It "attacks" my face and I constantly have to wear it up and now it's starting to fall out, but the worst is feeling it move ALL DAY LONG.... IT'S DRIVING ME CRAZY!!!!!!!! Can someone tell me if there's ANYTHING, ANY KIND OF TREATMENT that will help me to at least kill this wiry "pseudo" hair? PLEASE PLEASE SOMEONE HELP ME...
To head scalp person. I had Morgellon's, same experiences with Doctors. I cured myself with a very stiff loofa and SELSUN BLUE, the original one. Shower three times a day with that from head to toe and do that for at least three weeks.
Hello, I suffer from the same freakish disease I use to have perfect skin now I'm covered in sores from digging them out. I don't know what's worse having this disease or you family, friends, and doctors thinking your crazy. I found hope when morgellons was on Dr. Phill and I then decided to tell my new doctor about my skin she researched it and told me ur not crazy morgellons is real. It was dated back in the 1800's I think you can find it on morgellons reasearch sites. She thinks it's due to having a low immune system I will find out once I get my blood work results in. She thinks it has to due with cell death and the cells finding their way thru the skin. They move though so that can't explain it. If you put two of them next to eachother they will move closer together. I do alot of research it really helps keep my mind sain and having a doctor who is also researching it by following a doc in Texas really gives me hope and security. I'm on alot of vitamins which helps.
Many many people are suffering similarly with the same lack of medical care. Come to: http://groups.yahoo.com/critterscience and to: http://groups.yahoo.com/bodybugs
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I have the exact same thing. I was also angry when the dermatologist gave a mental diagnosis after doing NO tests. I read blacklight is a tool used by dermatologists, and I got one to show my family I wasn't delusional. I think collagen is involved, as the stuff has a plasticy feel to it. penny_asbury@yahoo.com please write to me.
What's worse is not having support from your family. They see you suffering, they see what you go through each day and they know something is wrong. Yet, it is easier for them to shrug it off like the Doctors, Derma's and other medical professionals. Yes, I get the same looks and the same responses from doctors.....all of what is said here I have experienced. I feel alone and abandoned by everyone. It is a full time job and I am hoping by the grace of God that I get through it. For all who suffer, my prayers are with you. Please pray for me too. Take care.
unfortunately i came down with the same symptoms approx two years ago but more severe-the sores became so bad that my scalp and the back of my head are now permanantly disfigured resulting in scarring caused by the"burning" and extreme itching.To my horror not only did this horrible disease spread to allover my body but i also received similar responses from not only the doctors but sadly my family as well.just when i thought things could not get any worse-the symptoms -the constant itching
I didn't know what was wrong with me with depression and many other symptoms that started 2 years ago until April when I began to feel something crawling under the skin on my back. Like many many others I am self diagnosed and using natural meds, and going through hell. The thing that bothers me the most is my hair. It "attacks" my face and I constantly have to wear it up and now it's starting to fall out, but the worst is feeling it move ALL DAY LONG.... IT'S DRIVING ME CRAZY!!!!!!!! Can someone tell me if there's ANYTHING, ANY KIND OF TREATMENT that will help me to at least kill this wiry "pseudo" hair? PLEASE PLEASE SOMEONE HELP ME...
To head scalp person. I had Morgellon's, same experiences with Doctors. I cured myself with a very stiff loofa and SELSUN BLUE, the original one. Shower three times a day with that from head to toe and do that for at least three weeks.
Hello, I suffer from the same freakish disease I use to have perfect skin now I'm covered in sores from digging them out. I don't know what's worse having this disease or you family, friends, and doctors thinking your crazy. I found hope when morgellons was on Dr. Phill and I then decided to tell my new doctor about my skin she researched it and told me ur not crazy morgellons is real. It was dated back in the 1800's I think you can find it on morgellons reasearch sites. She thinks it's due to having a low immune system I will find out once I get my blood work results in. She thinks it has to due with cell death and the cells finding their way thru the skin. They move though so that can't explain it. If you put two of them next to eachother they will move closer together. I do alot of research it really helps keep my mind sain and having a doctor who is also researching it by following a doc in Texas really gives me hope and security. I'm on alot of vitamins which helps.
Many many people are suffering similarly with the same lack of medical care. Come to: http://groups.yahoo.com/critterscience and to: http://groups.yahoo.com/bodybugs