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Post by Harry on Dec 8, 2010 21:23:46 GMT -5
Hi Harry --thanks for joining us! Welcome itching4answers, To answer your question: this is actually the main reason for this thread, in that if we can gather people together here, then we can perhaps take it one more step and forms groups within states or regions, with the goal of making decisions on how we do just that: stir this up and get this disease to the forefront and recognized...I believe it is our only option at this point, because if we do nothing, we will all be here spinning our wheels in our silence for years to come. This is not to say that collectively, we have not made great strides in studying this ourselves and many have worked hard to find pieces of the puzzle that have given us invaluable clues to this puzzle; however the more recognition we receive, the less likely the CDC will be able to sweep this under the rug and leave us here to die in our own misery. The other benefit of more recognition is obvious in that we could possibly get more funding for research studies. We don't have to be alone in this battle...coming together produces a positive energy that I believe we all need right about now! I we can just get the momentum going here, I think more and more people will follow suit and join in this step in the right direction. And I think just knowing people within your own state, will give comfort to most of us.. You might want to check out one of the replies here from Jo, who is from the UK. She informed us that they too were forming a grassroots movement and was graciously offering to share what they eventually come up with. So far, I believe the countries/regions she is actively working with are Ireland (North/South), Scotland, Northern England and London [and eventually Wales]. Here is the link to the page she posted her plans so I hope it works for you [3rd page of this thread] lymebusters.proboards.com/index.cgi?board=rash&action=display&thread=14456&page=3You might want to PM her and send her an email to ask if you can involved there too and see what their plan is to get this disease publicly recognized. We are just starting this thread so I am glad you are on board!!! Let's hope it grows in enthusiasm, because I know I am speaking for many, we are fed up suffering in our own small isolated world. It doesn't have to be this way--but no one is going to do this for us...we have to do this for ourselves, not to mention for our loved ones and children! So please hang in there with us and help us get the word out...! There are people from all over the world and I am sure some from Australia will pop in here from time to time too. Hi Silverangel Glad to see your post too...was just wondering if you had any contact with these others from Michigan and if so, could you contact them about this and ask them to sign into this thread? We need ALL morgellons people to get involved, not just the ones who are currently posting!!! Thanks to all and remember, STRENGTH IS IN NUMBERS, so let's keep this topic ongoing and open for discussion, wherever you are posting or talking to someone...! xxoo Pdidit >Hi pdidt,.good to hear from you,.just to run this by you,.would it be easier to make available down loadable petitions,and photo's,.to help educate the public,. so even one person can get a small portable table with a lawn chair to gather signatures at oh,.say like city hall,.subway station,.or at a collage just before classes end ,.and maybe enlist collage student's,.letting them understand they & their Family's could be at risk also??,..and so on..just need a place to send all the petitions and maybe an information center of some kind. Doc Holliday
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Post by Harry on Dec 8, 2010 18:03:12 GMT -5
I believe and understand the natural world we live in...I've seen & heard quite a bit about nano tech,.mad science unleashing things & more,.although this could be true,. .well!! that's not where I'm coming from. I've been an outdoors man for most of my life,.camping,fishing,.just about everywhere,.and yip!,.had some parasites also,.morgellons acts like a parasite from the natural world,.at first most report scabies,.or head lice,.and mite's,. this has been wide spread including myself,..seems the first outbreak of lesions we all get,. in my thoughts!,.a non typical parasite fighting to get a foothold of the human body,.once the parasite establishes it's self,. lesions diminish symptoms wax & wane,.lesions and other symptoms are always in a cycle just as they are in nature,.. science still has no clue about much of the natural world.. I remember the clear cutting of old growth forest all over the world,.. organisms not known to man could very well have been unleashed,. urban sprawl has taken most of the natural habitats for animals,.so now,.we are in very close contact with animals more then ever before,.science still doesn't understand all of the parasites that these same animals carry,.15- 20 years back,.has anyone reported a bear,moose,.and many more wild animals within 10 miles or in a major city,..well, it seems to be an everyday thing now days,.their are also things called extremophile's that science knows almost nothing about,.just something to think about,.the other thing,.once the immune system is triggered by an outside entity,. it can do some unbelievable things. . Harry ,. AKA-Doc Holliday
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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 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 Harry on Dec 8, 2010 7:19:37 GMT -5
Thanks for the link Harry, very informative >you are surly welcome Shelby
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Post by Harry on Dec 8, 2010 7:18:13 GMT -5
Harry, Thank you for posting that link. Best to you, 22122 >your very welcome 2212,.good to be here..and thank you for your kind words. Harry .
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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 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 16:13:10 GMT -5
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Post by Harry on Dec 6, 2010 17:44:32 GMT -5
25 mins. north of Boston,...Bless you too shelby .
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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 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 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 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 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 Harry on Dec 4, 2010 16:36:56 GMT -5
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Post by Harry on Jun 2, 2010 12:49:20 GMT -5
Hello everyone,...we have been planing a Rally of a sort,..... a person using the screen name, Silvermaran . left a message at MDR to the effect,.... he or she represents a Lyme Rally before November,.. due to the U.S. Elections,...I belong to 3 site's that are feed up also... I would suggest two strategics's points,...1. mass awareness to the General Public in understanding both facts of these Disease's,..many with Morgs have Lyme also. 2 the General Public is at RISK in contracting theses disease's. 3. enlisting the great young minds of University's & Collage's to get involved,... they are at risk also.,and is their Right....two artist's at MDR are involved in the design of flyer's & leaflet's,.....we can always make changes,....this information would be available via P.C. round the would,...again this is a Public Safety Issues. Thank you ....Harry ...... .Doc Holliday at MDR
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Post by Harry on Jun 2, 2010 12:43:24 GMT -5
Hello everyone,...we at MDR have been planing a Rally of a sort,..and the Sanctum is also been active,..but on their own,... a person using the screen name, Silvermaran,. left a message to the effect,.... he or she represents a Lyme Rally before November,.. due to the U.S. Elections,...I belong to 3 site's that are feed up also... I would suggest two strategics's points,...1. mass awareness to the General Public in understanding both facts of these Disease's,..many with Morgs. have Lyme also. 2 the General Public is at RISK in contracting theses disease's. 3. enlisting the great young minds of University's & Collage's to get involved,... they are at risk also.,and is their Right....two artist's at MDR are involved in the design of flyer's & leaflet's,.....we can always make changes,....this information would be available via P.C. round the would,...again this is a Public Safety Issues. Thank you ....Harry ...... .Doc Holliday at MDR
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Post by Harry on May 25, 2010 10:57:32 GMT -5
Hi everyone,...I am so sorry folk's,..I've been very sick,..and trying to do to much while almost delirious,.... thinking has not been good at all,....my bad!......the Public doesn't understand the Beast!,.. I call Morgellons Disease,...and how it is destroying the lives of people as they once knew it,...how could General Pubic know about something,..while Doctor's seem to be suppressing information via outrageous Diagnosis,. delusional of parasitos,.....how ridiculous can some mind's be??,....while these Doctor's see some of the sickest people,...with lesion's on there face,... that would make topnotch marine shriek,...the same Doctor's look at them with no alarm what so ever,...why??,...how could they ever in all humanity,.. come up such diagnosis,..that is way beyond the realm of common sense,...how is it possibly 20,000 plus people have the same symptom's,... Scientist would never make such a claim with out proof,...or their fellow scientist would bitterly object,....Scientist in a most humbling way will explain their understanding of that fact,.. ,..millions of Galaxy's exists,..that is true by today's standards,...and Billions of stars exists via new technology,......how can the all know Doctor's of today ever make such a claim or diagnosis with out the fact,...that should be laughable,..but it's not because of the thousands of people that suffer every single day,..with one of the most horrifying disease's called mogellos,......Harry sorry if all seems off,..it's me,..I to crrect this later t y
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Post by Harry on May 24, 2010 23:33:44 GMT -5
things sure change,....we now have 24 well committed people to help,....thank all of you,...please hang in,..still have lots of work,...thank ya'll ....Harry
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