Comments for Morgellons http://www.morgellons-disease-research.com morgellons disease Thu, 26 Jan 2012 23:11:34 +0000 hourly 1 http://wordpress.org/?v=3.3.1 Comment on Morgellons Pictures by sinjin http://www.morgellons-disease-research.com/morgellons-pictures/comment-page-1/#comment-744 sinjin Thu, 26 Jan 2012 23:11:34 +0000 http://www.morgellons-disease-research.com/?p=71#comment-744 i know there are many illnesses the doctors are saying is psychosamatic or all in a patients mind its always good to know that nothing was really done to research it until some person in congress got it and those in congress spent almost a million dollars on it and still they havnt found out anything they claim its all in a persons mind how would you feel if you went to your dr. and said its no disease it all in your mind ??????????????? i know there are many illnesses the doctors are saying is psychosamatic or all in a patients mind its always good to know that nothing was really done to research it until some person in congress got it and those in congress spent almost a million dollars on it and still they havnt found out anything they claim its all in a persons mind how would you feel if you went to your dr. and said its no disease it all in your mind ???????????????

]]> Comment on Morgellons Pictures by Celeste Ezell http://www.morgellons-disease-research.com/morgellons-pictures/comment-page-1/#comment-625 Celeste Ezell Sat, 21 Jan 2012 16:21:42 +0000 http://www.morgellons-disease-research.com/?p=71#comment-625 @ Rach, Sulfur sounds like a logical 'remedy' to try..... so ..... off I go on a 'sulfur hunt" ! Thank you for sharing your information. @ Rach, Sulfur sounds like a logical ‘remedy’ to try….. so ….. off I go on a ‘sulfur hunt” ! Thank you for sharing your information.

]]> Comment on Morgellons Pictures by Celeste Ezell http://www.morgellons-disease-research.com/morgellons-pictures/comment-page-1/#comment-624 Celeste Ezell Sat, 21 Jan 2012 16:01:54 +0000 http://www.morgellons-disease-research.com/?p=71#comment-624 I have to my surprise been reading recently about other sufferers for this bizarre, painful, embarrassing, disfiguring disease...which primarily affects my skin, mouth, lips and even fingernails... things like what Jeri said re clapping her hands and 'stuff' popping out. If some of this disgusting debris comes out of intact skin, in typically doesnt hurt other than possibly a quick sharp pain or intense itch (an itch that can only be described as "from the inside out") The weird debris exiting from lesions can be very painful....from sharp and intense to a slow burning sensation. I, too, suffered the emotional pain, feelings of helplessness and embarrassment after consulting a horrible, 'holier than thou', dermatologist who basically accused me of being some sort of drug addict mutilating myself. The 'stuff' that exits my skin is in several forms, but never varies from those now very recognizable forms. My first symptoms showed up in about the year 2000, literally overnight, were very severe and very scary. I lived with that misery for about 3 years when it started clearing up for reasons unknown to me....tho leaving me with covered with white scars of varying shapes, mostly roundish, but some long and very thin. I hated those ugly scars, especially those on my face. I'd never had a 'skin' condition before in my life. However, relieved to be rid of the painful sores that would take up to a year to heal, I learned to deal with the scars. Then about 6 years after I thought I was "healed", it popped up again and I've been having to go thru the frustrating misery of dealing with the sores and debris, the itching and burning and pain. It is my opinion, after much research and observation, that this horrifying condition is somehow related to some sort of living organism.....something akin to a mold, fungus or bacterium with properties similar to fungus. I know how crazy this sounds, but from the very beginning, I had the feeling/notion that 'something' was actually growing in/under my skin.....like using me for a growing medium. With my first traumatic experiences, I didn't visually notice the 'fibers' but much of the time had a sensation of having run into a spiderweb. The sort of thing that primarily presents itself (after exiting) is varying sizes of something black and hard and rather sharp, additionally some black material is very flat and is at times white/pale green on the opposite side, some flat and green similar to the lichen that grow on tree bark. Sometimes the debris is dry and at times exits 'wet' which definitely give it the appearance of plant material...sort of like sea weed. Some black material is very tiny and with some difficulty can be brushed off my skin or tweezed away as it at times still under the very outer layer of skin cells. If I use a sterile tweezers and try to grasp the tiny black thing I can much of the time audibly hear a crunching sound...it seems that coming along with the tiny black 'things' seems to be a crunchy clear crystal-like material......which will adhere itself to my hair...and won't come off unless 'scraped' off....although it seems to get removed from my hair when I color my hair....I keep my hair blonde. The chemicals in the haircolor seem to dissolve the 'crap' that sticks to my hair. Another very odd thing I noticed from the beginning (and only now reading that others are noticing the same thing) is that the crystal-like stuff that sticks to my hair, seems to have some sort of magnetic charge...If there is a glittery crystal thing (really tiny) shining on my face (which i think mite be adhering to facial hair), certain hairs from my head begin to wave around and move toward the crystal thing and finally stick to it. I can feel the hair touch my skin, pull out the strand from the root on my head and the end still sticks to my face...when I pull the hair away from my face it appears to "pop" loose from something.....and one feels a very fine, for lack of a better word, 'spray', on the skin which has that cobweb sensation. Mostly I notice the bigger particles/debris, but on close observation it is obvious that most of whatever this crap is, is really really small...almost invisible to the naked eye. I could go on and on and on.....this is so disgusting. One more thing I do want to mention is that after my first 'attack', the hair on my arms totally changed. I had many many lesions on my arms. Prior to being afflicted with this, the hair on my arms grew smooth and soft, all the same direction, lying down relatively flat next to my skin. Now the hair on my arms looks sort of wiry, breaks easily and sticks up, around and every which direction. Recently a rather large piece of green looking material came flying out of the tip of my nose after I tweezed out (with great difficulty), what looked like a small piece of white dry skin. I inspected this green 'thing' closely. To the naked eye, it looked much like a tiny leaf or piece of a leaf, but on closer inspection with magnification, it, tho in the shape of a tiny leaf, it was a conglomeration of some kind of somewhat hardened 'goo' filled with black specs and covered in a few places with a sticky looking whitish yellow substance. This is just way too wierd and I simply cannot understand why a laboratory cannot identify the makeup of some of this debris. After all, if science can identify the composition of distant stars, asteroids, and meteorites, WHY CAN'T THEY IDENTIFY THIS STUFF? Even if they don't know what "the blob" is exactly, there's no logical reason why the components of said "blob" can't be identified. This is maddening, depressing, frustrating and life altering.....and then the medical community passes one off as a ''mental case''.....treating people with unacceptable disrespect. Imagine a person with untreated leprosy being told that there's really nothing wrong with them and they should just go on with their lives and quit obsessing about their fingers or the end of their nose falling off. There's so much I could say about this *%#**# condition. I guess I need to start a blog. Thanks for listening. ? Blessings and comfort to all of you going thru this misery. I have to my surprise been reading recently about other sufferers for this bizarre, painful, embarrassing, disfiguring disease…which primarily affects my skin, mouth, lips and even fingernails… things like what Jeri said re clapping her hands and ‘stuff’ popping out. If some of this disgusting debris comes out of intact skin, in typically doesnt hurt other than possibly a quick sharp pain or intense itch (an itch that can only be described as “from the inside out”) The weird debris exiting from lesions can be very painful….from sharp and intense to a slow burning sensation. I, too, suffered the emotional pain, feelings of helplessness and embarrassment after consulting a horrible, ‘holier than thou’, dermatologist who basically accused me of being some sort of drug addict mutilating myself. The ‘stuff’ that exits my skin is in several forms, but never varies from those now very recognizable forms. My first symptoms showed up in about the year 2000, literally overnight, were very severe and very scary. I lived with that misery for about 3 years when it started clearing up for reasons unknown to me….tho leaving me with covered with white scars of varying shapes, mostly roundish, but some long and very thin. I hated those ugly scars, especially those on my face. I’d never had a ‘skin’ condition before in my life. However, relieved to be rid of the painful sores that would take up to a year to heal, I learned to deal with the scars. Then about 6 years after I thought I was “healed”, it popped up again and I’ve been having to go thru the frustrating misery of dealing with the sores and debris, the itching and burning and pain. It is my opinion, after much research and observation, that this horrifying condition is somehow related to some sort of living organism…..something akin to a mold, fungus or bacterium with properties similar to fungus. I know how crazy this sounds, but from the very beginning, I had the feeling/notion that ‘something’ was actually growing in/under my skin…..like using me for a growing medium. With my first traumatic experiences, I didn’t visually notice the ‘fibers’ but much of the time had a sensation of having run into a spiderweb. The sort of thing that primarily presents itself (after exiting) is varying sizes of something black and hard and rather sharp, additionally some black material is very flat and is at times white/pale green on the opposite side, some flat and green similar to the lichen that grow on tree bark. Sometimes the debris is dry and at times exits ‘wet’ which definitely give it the appearance of plant material…sort of like sea weed. Some black material is very tiny and with some difficulty can be brushed off my skin or tweezed away as it at times still under the very outer layer of skin cells. If I use a sterile tweezers and try to grasp the tiny black thing I can much of the time audibly hear a crunching sound…it seems that coming along with the tiny black ‘things’ seems to be a crunchy clear crystal-like material……which will adhere itself to my hair…and won’t come off unless ‘scraped’ off….although it seems to get removed from my hair when I color my hair….I keep my hair blonde. The chemicals in the haircolor seem to dissolve the ‘crap’ that sticks to my hair. Another very odd thing I noticed from the beginning (and only now reading that others are noticing the same thing) is that the crystal-like stuff that sticks to my hair, seems to have some sort of magnetic charge…If there is a glittery crystal thing (really tiny) shining on my face (which i think mite be adhering to facial hair), certain hairs from my head begin to wave around and move toward the crystal thing and finally stick to it. I can feel the hair touch my skin, pull out the strand from the root on my head and the end still sticks to my face…when I pull the hair away from my face it appears to “pop” loose from something…..and one feels a very fine, for lack of a better word, ‘spray’, on the skin which has that cobweb sensation. Mostly I notice the bigger particles/debris, but on close observation it is obvious that most of whatever this crap is, is really really small…almost invisible to the naked eye. I could go on and on and on…..this is so disgusting. One more thing I do want to mention is that after my first ‘attack’, the hair on my arms totally changed. I had many many lesions on my arms. Prior to being afflicted with this, the hair on my arms grew smooth and soft, all the same direction, lying down relatively flat next to my skin. Now the hair on my arms looks sort of wiry, breaks easily and sticks up, around and every which direction. Recently a rather large piece of green looking material came flying out of the tip of my nose after I tweezed out (with great difficulty), what looked like a small piece of white dry skin. I inspected this green ‘thing’ closely. To the naked eye, it looked much like a tiny leaf or piece of a leaf, but on closer inspection with magnification, it, tho in the shape of a tiny leaf, it was a conglomeration of some kind of somewhat hardened ‘goo’ filled with black specs and covered in a few places with a sticky looking whitish yellow substance. This is just way too wierd and I simply cannot understand why a laboratory cannot identify the makeup of some of this debris. After all, if science can identify the composition of distant stars, asteroids, and meteorites, WHY CAN’T THEY IDENTIFY THIS STUFF? Even if they don’t know what “the blob” is exactly, there’s no logical reason why the components of said “blob” can’t be identified. This is maddening, depressing, frustrating and life altering…..and then the medical community passes one off as a ”mental case”…..treating people with unacceptable disrespect. Imagine a person with untreated leprosy being told that there’s really nothing wrong with them and they should just go on with their lives and quit obsessing about their fingers or the end of their nose falling off. There’s so much I could say about this *%#**# condition. I guess I need to start a blog. Thanks for listening. ? Blessings and comfort to all of you going thru this misery.

]]> Comment on Morgellons Fibers by Kailyn http://www.morgellons-disease-research.com/morgellons-fibers/comment-page-1/#comment-492 Kailyn Tue, 22 Nov 2011 19:42:23 +0000 http://www.morgellons-disease-research.com/?p=41#comment-492 Geez, that's unbelivebale. Kudos and such. Geez, that’s unbelivebale. Kudos and such.

]]> Comment on Morgellons Disease by Elliander Eldridge http://www.morgellons-disease-research.com/morgellons-disease/comment-page-1/#comment-482 Elliander Eldridge Wed, 16 Nov 2011 09:39:01 +0000 http://www.morgellons-disease-research.com/?p=7#comment-482 How exactly does one have a psychiatric condition when there is an observable physical cause? One does not say one has a psychiatric condition when, say, they are itchy due to the chicken pox or flea bites. We say they are experiencing physical symptoms only. Even if they become irritable from said symptoms it is not psychiatric. Unless we allege that crazy people can conjure multicolored threads, but I know of no physical law which would allow such a thing. I find it particularly annoying that everywhere we look the patient is described as crazy first and then the facts evaluated. It's sickening. How exactly does one have a psychiatric condition when there is an observable physical cause? One does not say one has a psychiatric condition when, say, they are itchy due to the chicken pox or flea bites. We say they are experiencing physical symptoms only. Even if they become irritable from said symptoms it is not psychiatric. Unless we allege that crazy people can conjure multicolored threads, but I know of no physical law which would allow such a thing.

I find it particularly annoying that everywhere we look the patient is described as crazy first and then the facts evaluated. It’s sickening.

]]> Comment on Morgellons by Annie Newman http://www.morgellons-disease-research.com/morgellons/comment-page-1/#comment-445 Annie Newman Thu, 20 Oct 2011 04:14:57 +0000 http://www.morgellons-disease-research.com/?p=12#comment-445 hello, my sons father and my very best friend died in 2001 He had Morgellons. I am trying to find the number to call the research people. I think I have stumbled across the cause or a link to the disease. I have all the signs of Morgellons around my duplex. the red, blue, white fibers, fuzz etc. My place has an unusual infestation of larvae from a carpet Beetle. So either they are causing the similarities or there is some link. these larve have caused sinus infections since I have been here, and rash. they can cause boils on people who are allergic. You can not see them as they are less then 1/8th of an inch. They do grow and shed there skins. I have been itchy as well thinking it was the laundry soap. PLEASE DIRECT me to someone to call. I have to move. i have to leave everything behind that can not be frozen for 2 weeks. The eggs are impervious to chemicals. it makes clear sense to me that this may be the cause They tunnel through soft metal, wool , food, etc even my CD;s This is not a joke. I have an appt with the housing authority. tomorrow to figure out how to deal with the owner who will not tent the house. for skin links google :dermatology and carpet beetle larvae. it is not a well known problem. you will be shocked I have been tunned into these critters because people thought I was going crazy and I had to prove to them I wasnt. The beetles and larvae ( which cause the problems) were identified by the California Agriculture Dept but the guy doesn't know half of what the larvae do. I have lived with them for a year now. its everything you all go through but I have no sores I did get a rash 2c so please email me some phone numbers I am in northern california , Marin County hello, my sons father and my very best friend died in 2001 He had Morgellons. I am trying to find the number to call the research people. I think I have stumbled across the cause or a link to the disease. I have all the signs of Morgellons around my duplex. the red, blue, white fibers, fuzz etc. My place has an unusual infestation of larvae from a carpet Beetle.
So either they are causing the similarities or there is some link. these larve have caused sinus infections since I have been here, and rash. they can cause boils on people who are allergic. You can not see them as they are less then 1/8th of an inch. They do grow and shed there skins. I have been itchy as well thinking it was the laundry soap.
PLEASE DIRECT me to someone to call. I have to move. i have to leave everything behind that can not be frozen for 2 weeks. The eggs are impervious to chemicals. it makes clear sense to me that this may be the cause They tunnel through soft metal, wool , food, etc even my CD;s This is not a joke.
I have an appt with the housing authority.
tomorrow to figure out how to deal with the owner who will not tent the house.
for skin links google :dermatology and carpet beetle larvae. it is not a well known problem. you will be shocked
I have been tunned into these critters because people thought I was going crazy and I had to prove to them I wasnt. The beetles and larvae ( which cause the problems) were identified by the California Agriculture Dept but the guy doesn’t know half of what the larvae do. I have lived with them for a year now. its everything you all go through but I have no sores I did get a rash 2c
so please email me some phone numbers I am in northern california , Marin County

]]> Comment on Morgellons Pictures by julie http://www.morgellons-disease-research.com/morgellons-pictures/comment-page-1/#comment-444 julie Sun, 09 Oct 2011 18:41:12 +0000 http://www.morgellons-disease-research.com/?p=71#comment-444 mite birds mite birds

]]> Comment on Morgellons Pictures by Annie http://www.morgellons-disease-research.com/morgellons-pictures/comment-page-1/#comment-442 Annie Mon, 26 Sep 2011 23:48:19 +0000 http://www.morgellons-disease-research.com/?p=71#comment-442 Hello, Thank you I think I will try it too! Annie Hello,
Thank you I think I will try it too!
Annie

]]> Comment on Morgellons Pictures by Rach http://www.morgellons-disease-research.com/morgellons-pictures/comment-page-1/#comment-436 Rach Sat, 17 Sep 2011 01:08:18 +0000 http://www.morgellons-disease-research.com/?p=71#comment-436 Hi, I have a friend that was diagnosed with this a few months ago..he s using sulfur soap and it seem s to be helping...you can find this type of soap in a botanic,a cvs or walgreens...hope it helps! Hi,
I have a friend that was diagnosed with this a few months ago..he s using sulfur soap and it seem s to be helping…you can find this type of soap in a botanic,a cvs or walgreens…hope it helps!

]]> Comment on Morgellons Pictures by Sophia http://www.morgellons-disease-research.com/morgellons-pictures/comment-page-1/#comment-428 Sophia Thu, 25 Aug 2011 23:44:46 +0000 http://www.morgellons-disease-research.com/?p=71#comment-428 Hey Dave, Sounds like it. I had the same from living in a moldy apartment. Seems best to treat for all the things you've mentioned and rotate treatments, but above check to make certain you remain alkaline. Email if you want. spokeoaholes@gmail.com Best, Sophia Hey Dave,

Sounds like it. I had the same from living in a moldy apartment. Seems best to treat for all the things you’ve mentioned and rotate treatments, but above check to make certain you remain alkaline. Email if you want. spokeoaholes@gmail.com

Best, Sophia

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