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Post by Harry on Dec 4, 2010 19:43:58 GMT -5
Hi Kmarie,always good to see you,.I'm sure it's too late ,BUT!!.. hello Jane!,just give Bam a slam,that L do.
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Post by skizit on Dec 5, 2010 1:07:38 GMT -5
Hi guys, If you do have a public gathering, everyone needs to bring their DNA test showing they have been compromised with added DNA. That's why you don't see anyone in government trying to help. 18+ countries, NASA, The Genome Project and the US gov do not want you to know they can blow something up your nose and change your DNA and make you sterile. They will have total domination over every person who is changed and total control over whether you procreate or not.
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Post by Harry on Dec 5, 2010 10:58:18 GMT -5
I think a rally is quite impossible for most of us,.that's why I changed my tune or focus,..there is a link that anyone can download,.and folk's can work in groups or by them selves,..the main thing is!,the public needs to be aware of the problem,.for the simple fact, THEY ARE AT RISK,..more & more new people are coming to all of the morgellon social site's every signal day,.& morgellons at first infection is contagious,.I got it from helping a friend that had it,.wish I knew about morgellons then,.heirs a helpful link with basic tools that can help. . www.morgellonsfocusonhealth.com/map_morgellons_awareness_packet .on a personal level, people can copy this info via their pc,.set up a chair & table at a nearby Collage to hand out information,.draw up a short petition to congress to move the C.D.C on a study that makes sense,.and let the public know our numbers are some where over 100,00 and their Family could be at risk,...sorry about being a bit scattered,.but still not well,. take care every one,I'll be by from time to time
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Post by Harry on Dec 5, 2010 11:52:16 GMT -5
follow me on twitter,..need all the help I can get,..you can find me,.just search on twitter Doc_H_Holliday and join in t.y.
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Post by pdidit on Dec 6, 2010 12:24:51 GMT -5
Hi Harry
I hadn't seen this rally thread as I was working on just doing the what state do you live in? thread. So we are essentially wanting the same goal, just going about it differently. Hats off to you if you can pull off a rally!!! I am all for it, especially if it is in DC, since I live close by.
My thought was to start with square one by forming groups to see where people were located, since I feel that many of us are very sick and unable to participate--we are all scattered too and we need to find a way to get the word out, whether it be a rally or something else. And if we had the NUMBERS to show how many of us were suffering, it would be a start to give us credibility and show the world that this is really happening to people. Another plus of gathering people together by state, is that I feel it is comforting just to know there are others close by in proximity that are going through the same experience.
But the ultimate goal of knowing the locations of those who are stricken with this, would be to eventually form task groups to help make decisions on how to move forward with regards to getting this disease recognized...we need organization and it was my only thought on how we could get people motivated and together on this, cuz if we can't all get together on this, I don't see anything happening. NO ONE is going to do it for us...we have to get on the stick and stop the wait and see mentality. So maybe we have to take baby steps first???
I am open to any thoughts or discussions...frankly, I don't care how it is done, but just that SOMETHING be done. But realistically, I am wondering how many are too sick to physically go anywhere, not to mention financially broke...this is one of the problems I see with this debilitating disease. How did the AIDS patients stage a rally??? Think we need to investigate more on who helped them the most and how they pulled their protests off...??
And I agree...forget about the CDC. I think to come in the back way like this, whether we form a rally or otherwise, the CDC will have no choice but to readdress this illness and give it more immediate attention, due to public pressure.
One thing you might be interested in is that in the thread 'what state do you live in?' is a post by a person from the UK...she said they too, were trying to organize a grassroots movement, along with Ireland,Scotland, Wales. She might be a good contact for you as well...she said she would be happy to help us in any way. Have you looked at this thread and signed in where you live? Anyway, all this going on is in my opinion, a step in the right direction...tis all good.
We ALL have to put our heads together for this, so let me / us know your thoughts and whom you have already contacted, where and when you would want this rally to take place etc.
Thanks Pdidit
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Post by bannanny on Dec 6, 2010 14:32:10 GMT -5
Hey Harry... just wanted to tell you pdidit's "What state do you live in" thread is stickied at the top of the board!
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Post by Harry on Dec 6, 2010 17:16:31 GMT -5
Hi Harry I hadn't seen this rally thread as I was working on just doing the what state do you live in? thread. So we are essentially wanting the same goal, just going about it differently. Hats off to you if you can pull off a rally!!! I am all for it, especially if it is in DC, since I live close by. My thought was to start with square one by forming groups to see where people were located, since I feel that many of us are very sick and unable to participate--we are all scattered too and we need to find a way to get the word out, whether it be a rally or something else. And if we had the NUMBERS to show how many of us were suffering, it would be a start to give us credibility and show the world that this is really happening to people. Another plus of gathering people together by state, is that I feel it is comforting just to know there are others close by in proximity that are going through the same experience. But the ultimate goal of knowing the locations of those who are stricken with this, would be to eventually form task groups to help make decisions on how to move forward with regards to getting this disease recognized...we need organization and it was my only thought on how we could get people motivated and together on this, cuz if we can't all get together on this, I don't see anything happening. NO ONE is going to do it for us...we have to get on the stick and stop the wait and see mentality. So maybe we have to take baby steps first??? I am open to any thoughts or discussions...frankly, I don't care how it is done, but just that SOMETHING be done. But realistically, I am wondering how many are too sick to physically go anywhere, not to mention financially broke...this is one of the problems I see with this debilitating disease. How did the AIDS patients stage a rally??? Think we need to investigate more on who helped them the most and how they pulled their protests off...?? And I agree...forget about the CDC. I think to come in the back way like this, whether we form a rally or otherwise, the CDC will have no choice but to readdress this illness and give it more immediate attention, due to public pressure. One thing you might be interested in is that in the thread 'what state do you live in?' is a post by a person from the UK...she said they too, were trying to organize a grassroots movement, along with Ireland,Scotland, Wales. She might be a good contact for you as well...she said she would be happy to help us in any way. Have you looked at this thread and signed in where you live? Anyway, all this going on is in my opinion, a step in the right direction...tis all good. We ALL have to put our heads together for this, so let me / us know your thoughts and whom you have already contacted, where and when you would want this rally to take place etc. Thanks Pdidit >>Hi pdidt,.the Rally post is an old one,.I rethought the whole thing many times,.because so many of us are so sick,.their are site's with downloadable pamphlets,.and information for use like the one I put a link up for,.it may be much easier if this can be done via computer,.But for me, I haven't come up with anything,.could be some one with much better internet skills could do a better job,.and possibly use site's like utube as a platform,. and a I petition for the public to sign ,.and bring about public awareness,..get the public involved in great numbers that are healthy,.because they are at RISK,,and should understand their Family's can get this Disease also,..check this one out,....... www.youtube.com/watch?v=scmVlm01E_w&feature=related .,,,,,,,,.if we can get the public involved in great numbers,.this might move the Government to really do something positive,..this should be looked at as a public health issue also,..more & more folk's are getting it,. seems every time I get better I get worse,..by the way my state is listed just below my post count under ny name,..if this isn't making sense,.it's because I'm going down hill as I write. take care & thank you,. Sincerely: Harry
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Post by Harry on Dec 6, 2010 17:20:06 GMT -5
Hey Harry... just wanted to tell you pdidit's "What state do you live in" thread is stickied at the top of the board! .thank you Banannnay,..sorry,.have a brain deficit,...my state in below my name & post count,...take care & be well
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Post by bannanny on Dec 7, 2010 16:12:05 GMT -5
It's ok Harry... I so know the lack of brain function these days! I sometimes think it may have been a big part of this morg plan... to purposely get us to a point where we CAN'T think well enough to do what we need to do. But the one thing that wasn't taken into consideration was that we're some incredibly strong people with some very strong wills... and hearts that won't stop no matter what.
Got you in my prayers my friend... and hope you soon get to feeling better again.
big hugs ~~ bannanny
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Post by ruth on Dec 7, 2010 16:29:31 GMT -5
harry, i will be ready to 'fight' should the cdc's unexplained dermopathy report be contestable. then it will have to be done in a court of law as a class-action lawsuit where we will need to participate as a group. while i enjoy your video's, i caution against blanket statements like the dictyostelium remark you made. i have never seen any evidence to support the slime mold theory, nor do i see evidence of it within my own tissues. where is your proof? (yes, i have read all of jan smiths' work and not seen any proof there, either)
when i state i have qd's within my tissue, it is because i can film them blink colors. other 'things' can be infected and those qd's filmed as well. there is no other 'microbe' that does the molecular exchanges, that follows quantum theory and scientific procress is satisfied.
only one person has stepped up to send samples to see if their tissues also has the qd's, and if you cannot see this, how can the public? i for one am excited as this person lives far from me. i will post the vids when i receive the sample.
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Post by bannanny on Dec 7, 2010 16:54:15 GMT -5
It's on it's way ruthie...
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Post by Harry on Dec 7, 2010 17:12:23 GMT -5
all you folk's are very nice,.....so far!,..just messing,.you all are,..ya!,. I think your so right with that bannanny,..but in the days we're in now,.a whole lot of people are toughing it out,.lost homes,jobs,floods,fires,oh my,..hmm,. sound more like Dorthy from the wiz of OZ,. Ruth!,how do we proceed with that kind of move??,.I would have thought we would need to get Congress to move again,.NO?,.if so this was what I was trying to say,,to get the General Public involved by having them sign petitions,.and let them understand they and their Family's are st risk also,.their is power in numbers,.. how does one get a photo for an avatar??,.take care & be well,...bye y áll
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Post by Harry on Dec 7, 2010 17:24:36 GMT -5
Hi guys, If you do have a public gathering, everyone needs to bring their DNA test showing they have been compromised with added DNA. That's why you don't see anyone in government trying to help. 18+ countries, NASA, The Genome Project and the US gov do not want you to know they can blow something up your nose and change your DNA and make you sterile. They will have total domination over every person who is changed and total control over whether you procreate or not. Hmm.,..I think I get it skizit,..sorta like ZOMBIE'S
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Post by skizit on Dec 7, 2010 19:24:33 GMT -5
Harry, What did you say about dictyostelium? I'm not familiar with your video.
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Post by Harry on Dec 8, 2010 10:30:51 GMT -5
Harry, What did you say about dictyostelium? I'm not familiar with your video. .not sure what you mean skiz,.not sure I mentioned dictyostelium?? .the video!,..just a bit of interest for morgellons suffer's,.it's not mine,.it was on the net.
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Post by ruth on Dec 8, 2010 13:48:14 GMT -5
hey guys, i wonder if i got 2 threads crossed as i am not seeing the video where it says all M sufferers have dicty?? i am just seeing jim croce come up. i'll see if i can locate it and direct you guys to this issue.
blanket statements could be used against us, and i wonder who these people actually are that leads us in the wrong direction to keep the confusion going.... some will not respond to me and my research.......... (red flag!)
however, the director of nanotechnology risk assessment actually called me and said he was sorry that i am an acceptable risk of this technology!
we will eventually have to present our case to the supreme court since we are being fought by the establishment to keep this quiet.
which will only happen when we have the document to challenge.
when i get the members' sample and if it lights up with the qd's, then it will be to our advantage for others to get their tissue (ear wax is best to use) with the qd's filmed and then we can unite and have direction from knowing what 'it' is. the many grants from the govmt for this technology and quantum dot corporation who has fought in court for ownership, will be the ones who will be forced to share their trillions of dollars with us!!
anyways, i think that is why the report is delayed coming out, as it will be the path to OUR recourse. they know we are going to fight for transparency with this issue.
anytime anyone offered anything to me (relative to M) i took it. yet only one person wants to know if they have quantum dots which makes me wonder about who the people on this forum really are.
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Post by bannanny on Dec 8, 2010 15:01:17 GMT -5
Let's see what mine show and go from there ruth... and we WILL get there too my friend. Just takes time (which we all know!)
love you guys ~~ bannanny
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Post by Harry on Dec 8, 2010 16:20:09 GMT -5
harry, i will be ready to 'fight' should the cdc's unexplained dermopathy report be contestable. then it will have to be done in a court of law as a class-action lawsuit where we will need to participate as a group. while i enjoy your video's, i caution against blanket statements like the dictyostelium remark you made. i have never seen any evidence to support the slime mold theory, nor do i see evidence of it within my own tissues. where is your proof? (yes, i have read all of jan smiths' work and not seen any proof there, either) when i state i have qd's within my tissue, it is because i can film them blink colors. other 'things' can be infected and those qd's filmed as well. there is no other 'microbe' that does the molecular exchanges, that follows quantum theory and scientific procress is satisfied. only one person has stepped up to send samples to see if their tissues also has the qd's, and if you cannot see this, how can the public? i for one am excited as this person lives far from me. i will post the vids when i receive the sample. ..Ruth!,..do me a favor please,.do me a copy paste where I mention this dictyostelium!!! ,& slime,. this is the second time someone mentioned this,.and I don't believe I ever said that,.. so I'm a bit confused. .Harry
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Post by ruth on Dec 10, 2010 13:57:21 GMT -5
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Post by Harry on Dec 10, 2010 16:48:16 GMT -5
>that's fine Ruth,.someone else said the same,,weird,...but the other day I clicked on a thread link that did a roundabout,..and I got confused, dizzy too,.could be a glitch on the thread also,.I've had that happen, .take care .xx harry
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