Comments on: Delusions and Morgellons http://www.aamjanata.com/2008/08/17/delusions-and-morgellons/ Experiences, perspectives, rights, responsibilities and the opportunity for a better world Thu, 11 Mar 2010 00:09:24 +0000 http://wordpress.org/?v=2.9.2 hourly 1 By: tallcotton http://www.aamjanata.com/2008/08/17/delusions-and-morgellons/comment-page-1/#comment-847 tallcotton Thu, 11 Mar 2010 00:09:24 +0000 http://www.aamjanata.com/janata/?p=199#comment-847 Why is it that there were many reports of Morgellons before the use of silicone or high density polyethylene. It looks to me like Staninger is simply using the suffering of the Morgies to make money and further her personal agenda. Why is it that there were many reports of Morgellons before the use of silicone or high density polyethylene. It looks to me like Staninger is simply using the suffering of the Morgies to make money and further her personal agenda.

]]> By: jules baker http://www.aamjanata.com/2008/08/17/delusions-and-morgellons/comment-page-1/#comment-690 jules baker Mon, 18 Jan 2010 16:39:35 +0000 http://www.aamjanata.com/janata/?p=199#comment-690 Dr. Staninger is the only one who knows what this is. Her main treatment for getting out the fibers which are made of plastic is by using her recommended far infrared saunas and her supplements. For anyone interested in finding out more about her protocol can find it here: http://newageremedies.com/staninger <a href="http://newageremedies.com/staninger" rel="nofollow"> Dr. Staninger protocol information <a href="http://newageremedies.com/staninger" rel="nofollow"> Dr. Staninger is treating people with fibers and lesions in their skin. (The FDA only allows M.D.s to treat morgellons disease so please only refer to the fibers if contacting Dr. Staninger for treatment) Dr. Staninger is the only one who knows what this is. Her main treatment for getting out the fibers which are made of plastic is by using her recommended far infrared saunas and her supplements. For anyone interested in finding out more about her protocol can find it here: http://newageremedies.com/staninger

Dr. Staninger protocol information

Dr. Staninger is treating people with fibers and lesions in their skin. (The FDA only allows M.D.s to treat morgellons disease so please only refer to the fibers if contacting Dr. Staninger for treatment)

]]> By: Vidyut http://www.aamjanata.com/2008/08/17/delusions-and-morgellons/comment-page-1/#comment-303 Vidyut Mon, 01 Sep 2008 08:08:27 +0000 http://www.aamjanata.com/janata/?p=199#comment-303 Hi Maggiemae and Anne, I am really touched that both of you chose to come here and share your feelings on the matter. I can read the honesty in your words, and while I have no clue on "what is right", I can appreciate that both of you have been through and are going through an experience that changes your life deeply. I really hope that we find some light on this subject that can help you and countless others find peace from this pressure. I admire the strength with which you can still go on and remain functional in a judgmental world. Keep strong. Something is bound to evolve in this situation. Vidyut Hi Maggiemae and Anne,

I am really touched that both of you chose to come here and share your feelings on the matter. I can read the honesty in your words, and while I have no clue on “what is right”, I can appreciate that both of you have been through and are going through an experience that changes your life deeply.

I really hope that we find some light on this subject that can help you and countless others find peace from this pressure.

I admire the strength with which you can still go on and remain functional in a judgmental world. Keep strong. Something is bound to evolve in this situation.

Vidyut

]]> By: Anne http://www.aamjanata.com/2008/08/17/delusions-and-morgellons/comment-page-1/#comment-292 Anne Mon, 18 Aug 2008 22:57:10 +0000 http://www.aamjanata.com/janata/?p=199#comment-292 I Really dont leave comments anymore but your unique blog really pulled on some heartstrings for me. A couple of years back my husband was hospitalized for sudden muscle loss, confusion and burning rash that covered his upper torso and head. Prior to this E.R. visit we were told that he had ALS and the cognitive change I had seen in him was just depression and I was just searching. Now because I had other family members with me to verify the rapid change in him they hospitalized him with infectious disease work up and neuro-psych. monitoring his case. This doctor also was a behavioral scientist who spent many days observing and testing to in fact prove that there were both frontal and temporal cognitive changes. Extensive testing was done and then repeated after he was treated with albendazole for the parasitic antibodies that were triggered on his blood work. The second set of test showed significant improvement in all cognitive areas. His personality was back- not that flat stare..(I now have that). He also gained muscle strength and could walk and feed himself again after a month of therapy. We had hope. After returning home he did decline again but our infectious disease doctor moved out of state and the Neuro-Psych Dr. was advised by the hospital not to comment on our case. This is where i thought your article was a little ironic. I then took him to the Mayo Clinic emergency department on advice from another doctor who felt something was there it was just beyond his practice. Mayo Clinic was the worst experience for us. They would not even try to contact the other hospital to confirm what I was telling them. I was told that with neuro-disease rashes are common and I was not accepting his diagnosis. They did not want to hear about my familys similar symptoms and told me so. Meanwhile we all have rashes, platelets dropped, headaches for months, vision changes, weight gain and lossses. CFS, muscle atrophy. Oh and yes the CDC is supposedly doing some kind of research. This they would promise after any publicity we did trying to raise awareness and here we are several years later. With the loss of my husband and my Father from this disease and now I am loosing the ablility to walk and still have severe sores on my head with cronic pain. I try to ignore and go on because I dont want to waste any time begging someone to listen any more. It has been years since I looked under the microscope. I dont like to look at it any more. I already know something is there- Thanks again for your objectives!! I Really dont leave comments anymore but your unique blog really pulled on some heartstrings for me. A couple of years back my husband was hospitalized for sudden muscle loss, confusion and burning rash that covered his upper torso and head. Prior to this E.R. visit we were told that he had ALS and the cognitive change I had seen in him was just depression and I was just searching.

Now because I had other family members with me to verify the rapid change in him they hospitalized him with infectious disease work up and neuro-psych. monitoring his case. This doctor also was a behavioral scientist who spent many days observing and testing to in fact prove that there were both frontal and temporal cognitive changes. Extensive testing was done and then repeated after he was treated with albendazole for the parasitic antibodies that were triggered on his blood work. The second set of test showed significant improvement in all cognitive areas. His personality was back- not that flat stare..(I now have that). He also gained muscle strength and could walk and feed himself again after a month of
therapy. We had hope.

After returning home he did decline again but our infectious disease doctor moved out of state and the Neuro-Psych Dr. was advised by the hospital not to comment on our case.

This is where i thought your article was a little ironic. I then took him to the Mayo Clinic emergency department on advice from another doctor who felt something was there it was just beyond his practice. Mayo Clinic was the worst experience for us. They would not even try to contact the other hospital to confirm what I was telling them. I was told that with neuro-disease rashes are common and I was not accepting his diagnosis. They did not want to hear about my familys similar symptoms and told me so. Meanwhile we all have rashes, platelets dropped, headaches for months, vision changes, weight gain and lossses. CFS, muscle atrophy.

Oh and yes the CDC is supposedly doing some kind of research. This they would promise after any publicity we did trying to raise awareness and here we are several years later. With the loss of my husband and my Father from this disease and now I am loosing the ablility to walk and still have severe sores on my head with cronic pain. I try to ignore and go on because I dont want to waste any time begging someone to listen any more.

It has been years since I looked under the microscope. I dont like to look at it any more. I already know something is there-

Thanks again for your objectives!!

]]> By: Maggiemae http://www.aamjanata.com/2008/08/17/delusions-and-morgellons/comment-page-1/#comment-291 Maggiemae Mon, 18 Aug 2008 02:39:06 +0000 http://www.aamjanata.com/janata/?p=199#comment-291 I wanted to personally thank you for your kind words regarding my blog site. I find it very refreshing and it altered my mood from funk to neutral, which all things considered is a good day for me. I was not schizoprenic 14 years ago. I actually had the world in my hands. I now have two distinct personalities which were thrust upon me once I came down with the lesions. Behavior? I am a model citizen. I have a clean record, have never been arrested, and raised two very talented and intellectual children. I have been successful in just about everything I have put my hands to. Being forced to mask this hedious and life-stealing affliction has generated the two personalities. I can not go out in public without looking like a freakshow. The looks, the lack of contact (no hugs from my daughter-in-law) and the fear of being outed, has left me a shell. I barely look someone straight in the eye for fear they will see the lesions under all the makeup and give me "that" look. I have been forced to alter who I am - behavior modification? This psychologically is more painful than the actual affliction's affect in the body! In this world I have learned never to "assume" anything....or discount anything, either! This affliction has the "star" spot with it's own schill website (Morgwatch - who's funding it?) and posters that make the rounds bashing, discrediting, and debunking. Have you ever known of another affliction that warrants this? Try Lou Gherig's or Parkinsons, or Lupus, or....get my point? Why only THIS one? Because it is a big coverup, big money involved, big lawsuits to ward off...I am certain. There are too many brilliant minds that deal with ebola, hunta, leishmaniasis, bacteria from the stone ages, separating photons, lab on a chip...on a daily basis. The fact that all of us have white bleached out scars is just one common aspect. In 58 years I have accidentally cut myself numerous times, wounds healed, even with a tan, the melanin returned after time. Not so here. The fibers that twirl and move and "strike" at you are not 50,000 peoples or more, universal delusion. These fibers are everywhere. Pull your nice clean shirt or sweater down tight. At an angle, you can see them growing. The handles and edges of your purse, steering wheel, makeup bag...there they are, growing. That is only part 1 of a two-part affliction. There are various types of sensors, chips, and nanotech (buckyball bundles) that are also along for the ride. My take? To monitor us in the field. They HAVE got it down to an art. Look up stencils (Alfred Mann Institute) and take it a step further. The "applications" for this is endless and I resent being a guinea pig so someone else can have the Lexus and 5 bathroom home at our expense. It's major money to be made (or lost) - and my wish? That some scientist that finds himself "terminal" will have the kahonas to expose this without fear of being terminated, knowing he or she righted a very bad wrong and resisted being owned. The PTB can justify anything, twist thoughts, words, so that the meak conscience they possess will be passified. They are the delusional. Quantum everything. Waves rolling, over, around, through....and laws that govern them. Karma exists, Newton proved it. I get some satisfaction knowing that. Thanks for your open and "kind" mind. You will never know how welcome that is! Mm I wanted to personally thank you for your kind words regarding my blog site. I find it very refreshing and it altered my mood from funk to neutral, which all things considered is a good day for me. I was not schizoprenic 14 years ago. I actually had the world in my hands. I now have two distinct personalities which were thrust upon me once I came down with the lesions. Behavior? I am a model citizen. I have a clean record, have never been arrested, and raised two very talented and intellectual children. I have been successful in just about everything I have put my hands to. Being forced to mask this hedious and life-stealing affliction has generated the two personalities. I can not go out in public without looking like a freakshow. The looks, the lack of contact (no hugs from my daughter-in-law) and the fear of being outed, has left me a shell. I barely look someone straight in the eye for fear they will see the lesions under all the makeup and give me “that” look. I have been forced to alter who I am – behavior modification? This psychologically is more painful than the actual affliction’s affect in the body! In this world I have learned never to “assume” anything….or discount anything, either! This affliction has the “star” spot with it’s own schill website (Morgwatch – who’s funding it?) and posters that make the rounds bashing, discrediting, and debunking. Have you ever known of another affliction that warrants this? Try Lou Gherig’s or Parkinsons, or Lupus, or….get my point? Why only THIS one? Because it is a big coverup, big money involved, big lawsuits to ward off…I am certain. There are too many brilliant minds that deal with ebola, hunta, leishmaniasis, bacteria from the stone ages, separating photons, lab on a chip…on a daily basis. The fact that all of us have white bleached out scars is just one common aspect. In 58 years I have accidentally cut myself numerous times, wounds healed, even with a tan, the melanin returned after time. Not so here. The fibers that twirl and move and “strike” at you are not 50,000 peoples or more, universal delusion. These fibers are everywhere. Pull your nice clean shirt or sweater down tight. At an angle, you can see them growing. The handles and edges of your purse, steering wheel, makeup bag…there they are, growing. That is only part 1 of a two-part affliction. There are various types of sensors, chips, and nanotech (buckyball bundles) that are also along for the ride. My take? To monitor us in the field. They HAVE got it down to an art. Look up stencils (Alfred Mann Institute) and take it a step further. The “applications” for this is endless and I resent being a guinea pig so someone else can have the Lexus and 5 bathroom home at our expense. It’s major money to be made (or lost) – and my wish? That some scientist that finds himself “terminal” will have the kahonas to expose this without fear of being terminated, knowing he or she righted a very bad wrong and resisted being owned. The PTB can justify anything, twist thoughts, words, so that the meak conscience they possess will be passified. They are the delusional. Quantum everything. Waves rolling, over, around, through….and laws that govern them. Karma exists, Newton proved it. I get some satisfaction knowing that. Thanks for your open and “kind” mind. You will never know how welcome that is!
Mm

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