New Morgellons Order
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Chris Beasley

United States

#1 Aug 15, 2006
I provide this post to all. I hope that everybody may look into the Morgellons that has had much news media coverage of late. The following will explain the support and understanding that people with Morgellons need at this time:

Letter from Dr. Smith
DEAR COLLEAGUE:
I appreciate your taking this information and hope you find it informative. It is my purpose to inform you of what I think is a rapidly emerging infectious disease. I have seen patients with this disease in my practice. Whether or not you know it, you do as well.....

the rest of the letter can be found at: http://www.cherokeechas.com/gregs.htm

Please read the following letter also:

Letter sent to the CDC from Senator Dianne Feinstein : http://www.cherokeechas.com/df-cdc01.jpg

Letter to Doctors from Randy S. Wymore, Ph.D. and Rhonda Casey, D.O. Courtesy of OSU's :

http://healthsciences.okstate.edu/morgellons/...

All of the above support and letters can be found at the New Morgellons Order:

http://www.cherokeechas.com website.

Please take the time to look into Morgellons with an open mind that there "is" a new disease that needs the research and support from all Doctors in every medical field.

Thank you for your time
Chris Beasley
New Morgellons Order
[email protected]
paige nuss

AOL

#2 Feb 23, 2007
I am dying of morgellons disease, and our government does not have a clue or even care enough to fund any amount of funds to research this. A disease that we know has been around, what does it take to get the government and FDA, ect. involed !!!!!!
Lance Marshall

South Africa

#3 May 1, 2007
This (Letter from Dr. Smith) is probably the most credible piece of literature which I have read concerning the subject..
I am not a medical professional but a Mechanical Engineer in South Africa and I too have Morgellons.I contracted it from a friend who had returned from a spell in the USA. I had no idea what it was that I had contracted but I knew that it was an unwelcome guest. Long before I did any research on the subject or found the word "Morgellons", I studied this affliction within my own body (for the last 18 months)and without explaining the "how", I have determined physically, pathalogically and to a limited extent chemically)just about all there is to know about this most horrible disease. I have recorded much of my "experimentation" on video or still photography. I have extracetd from my own body and have (in frozen storage) the actual "bugs" (there is more than one variation), It is extremely contagious (at times) and has a number of methods of transfer. It in fact, has a number of "defenses" when it determines that it is threatened within the host. There are very legitimate pathalogical reasons why the host (patient) reports felling "fuzzy" in the head etc. and the reasons for these I have determined.
The skin manifestation is but a fraction of the actual complete picture and merely a confirmation of infection. This symptom has absolutely nothing to do with a dermatological conditio. As I stated earlier, I am not a medical practitioner but I do have sufficient knowledge, appropriate intellect and more than sufficient competent capability, to have conducted these experiments on myself.
Dr. Smith, I am more than willing to share my knowledge under respected conditions with similar-minded individuals. I do not subscribe to conspiracy theories or other such nonsense distractions.

Chris Beasley wrote:
I provide this post to all. I hope that everybody may look into the Morgellons that has had much news media coverage of late. The following will explain the support and understanding that people with Morgellons need at this time:
Letter from Dr. Smith
DEAR COLLEAGUE:
I appreciate your taking this information and hope you find it informative. It is my purpose to inform you of what I think is a rapidly emerging infectious disease. I have seen patients with this disease in my practice. Whether or not you know it, you do as well.....
the rest of the letter can be found at: http://www.cherokeechas.com/gregs.htm
Please read the following letter also:
Letter sent to the CDC from Senator Dianne Feinstein : http://www.cherokeechas.com/df-cdc01.jpg
Letter to Doctors from Randy S. Wymore, Ph.D. and Rhonda Casey, D.O. Courtesy of OSU's :
http://healthsciences.okstate.edu/morgellons/...
All of the above support and letters can be found at the New Morgellons Order:
http://www.cherokeechas.com website.
Please take the time to look into Morgellons with an open mind that there "is" a new disease that needs the research and support from all Doctors in every medical field.
Thank you for your time
Chris Beasley
New Morgellons Order
[email protected]
JNS12

AOL

#4 May 13, 2007
Question-question to Morgellons sufferers. Have any of you had a colonic..or a series of colonics? I have and it produced large morgellons. If you have had one or more, I would like to talk with you if possible. If you have not, you probably want to talk with me. Your help by posting whether or not you have had a colonic or not could help everyone. Thanks, JT
Dan

United States

#5 Jun 1, 2007
Lance Marshall wrote:
I am more than willing to share my knowledge under respected conditions with similar-minded individuals. I do not subscribe to conspiracy theories or other such nonsense distractions.
<quoted text>
If this is the case, then why do you only offer your info on a one to one basis. Post it, for all to see, therefore avoiding any speculation or assumptions by any person reading your words. Do not play games. if you have information, then lets read it.
Lance Marshall

South Africa

#6 Jun 4, 2007
Dan wrote:
<quoted text>
If this is the case, then why do you only offer your info on a one to one basis. Post it, for all to see, therefore avoiding any speculation or assumptions by any person reading your words. Do not play games. if you have information, then lets read it.
Greetings Dan
I have no time or interest in playing games. There is much at stake regarding this subject emotively. I do note a slightly agressive tone and perhaps a misunderstanding in your comment. I have an obligation to share what I know, in order to help but I do not have the time to open myself to a wealth of back-and-forth debate with a world-wide audience. The contradiction in your comment is share on a one-on-one basis but you also suggest that at the same time, I post it for all to see. I am seeking to share with the leading researchers on this subject and get to the heart of it as soon as possible. Do not want to deepen the confusion and this is a possibility.

I have tried to find such scientists but believe me it is very difficult. Here in South Africa I am putting together a team because I cannot find leads in the rest of the world who have urgency, neutrality, broad vision and an openness of mind to work with me.
Lance
mundo

Aiea, HI

#7 Aug 14, 2007
I too am dying of this disease. My neighbor died just this past March and the family was so disturbed and shocked, they demanded an autopsy. They would not admit to the Morgellons, as it hasn't been formally categorized, but she did test positive for both Legionaire's and Lyme Disease. Quite a coincidence considering Legionaire's is very rare in Southern California...especially when you consider the fact that So Cal had the driest year in 130 years of rainfall recording.
The cover-up must end. People are dying and I'm too young to die. My daughter is only 16 and I was just beginning to live life. Please do something. Please!
R.R.
mundo

Aiea, HI

#8 Aug 14, 2007
Oh and one more thing, 85% of those woith Morgellons are also testing positive with Lyme disease. eVEN pRES. Bush had Lyme. Why can't we of the middle class receive the same treatment as the elite like Bush?

Scientists seek better tests for Lyme;Bush suffered from Lyme disease
http://news.yahoo.com/s/ap/20070813/ap_on_he_...
Bessie

AOL

#9 Sep 20, 2007
Lance -
We share a most terrifying and isolating condition. I cry almost every day, as the torment of these bites continues and friends, family, and the medical community views us as crazy. I have begged God for answers to why, WHY am I so afflicted? I'm nearly 60 years old and had a successful career supervising & developing mental health and addictions programming. I started getting tired & confused a few years ago, thought it was due to the MS I've had for 40 years. In the last few months I started getting itchy in the groin area, then realized that I had a "colony" of something breeding inside my intestinal tract. As I began an assault on that issue with anti-parasitic treatments, they started attacking me from the outside in.
Some days I get my hopes up as I try different remedies, only to have them dashed with another, far more intense assault. I think about death often, have even started putting my affairs in order.
I graduated Phi Beta Kappa and was beautiful, a professional who taught fitness and aerobics on the side, and an excellent golfer. I had everything going for me. Now I'm a recluse, and can't wait for death.
My next door neighbor, a nurse, worked full time. She suddenly stopped working and her car never moves. The door on her mailbox doesn't stay up, and I can see that she lets it pile up for 2 or 3 days. Just like me. My bedroom window faces her house, with some bushes in-between. I think she has it, too, and we both got it from something in-between our houses.
I am terrified and incredibly alone.
Lance Marshall wrote:
This (Letter from Dr. Smith) is probably the most credible piece of literature which I have read concerning the subject..
I am not a medical professional but a Mechanical Engineer in South Africa and I too have Morgellons.I contracted it from a friend who had returned from a spell in the USA. I had no idea what it was that I had contracted but I knew that it was an unwelcome guest. Long before I did any research on the subject or found the word "Morgellons", I studied this affliction within my own body (for the last 18 months)and without explaining the "how", I have determined physically, pathalogically and to a limited extent chemically)just about all there is to know about this most horrible disease. I have recorded much of my "experimentation" on video or still photography. I have extracetd from my own body and have (in frozen storage) the actual "bugs" (there is more than one variation), It is extremely contagious (at times) and has a number of methods of transfer. It in fact, has a number of "defenses" when it determines that it is threatened within the host. There are very legitimate pathalogical reasons why the host (patient) reports felling "fuzzy" in the head etc. and the reasons for these I have determined.
The skin manifestation is but a fraction of the actual complete picture and merely a confirmation of infection. This symptom has absolutely nothing to do with a dermatological conditio. As I stated earlier, I am not a medical practitioner but I do have sufficient knowledge, appropriate intellect and more than sufficient competent capability, to have conducted these experiments on myself.
Dr. Smith, I am more than willing to share my knowledge under respected conditions with similar-minded individuals. I do not subscribe to conspiracy theories or other such nonsense distractions.
<quoted text>
Romy Geissler

AOL

#10 Nov 15, 2007
I too suffer from this disease.
Although I reside in NC, I have traveled the world, and did live in the Bay area for a number of years, so I could have picked this up anywhere!
I have been laughed at, ridiculed, and even escorted out of a dermatologists office by a police officer, two police dogs, and an ambulance.
I have never felt more humiliated, and devastated in my life.
I went into the office fully prepared for some ridicule.
I had every article, web address, and any and all info on this. I also had an arsenal of photos of the progression of the disease over one years time.
I went from a pretty vivacious woman, who was conscious of my body and practiced yoga,took my vitamins, and thought I was doing fine.
That was until I started breaking out with these huge lesions all over my head , face, feet and legs.
I have also been findind random pieces of hair just coming to the suface of my skin, if I don't get them with tweezers they will go BACK INTO MY SKIN!
Two young med techs at my Dr.s office acctually saw this happen!
The Dr. did not believe them either!
I have tried every kind of cure that anyone has mentioned on these chat rooms for the disease, now after spending my life's savings, and dealing with the fact that I have been bald with no eye brows or lashes for the past 8mos. Then to know that there is no mention from anyone that there may be any glimmer of hope for a cure for this, I must say that I have seriously contemplated suicide OFTEN!
Can anyone offer any hope?
ppy

United States

#11 Nov 17, 2007
hold on . suicide is not the answer though many of us contemplate that very thought. we have a mission. we may not see the benefits of our efforts but we have to fight on for recognition of this disease. if i die from morgellons then i accept that as my fate. i do not accept the pain, humiliation, and isolation suffered as a direct result of the medical communities ignorance. i will do all within my power to insure that others don't suffer a similiar fate. try to find motivation through efforts and actions to help us find answers. it is rewarding and takes some of the pain and frustration out of our situation. if you would like to talk send me an e mail at [email protected]
exposem

Hartford, CT

#12 Dec 6, 2007
salt and vitamin c is working for me. I've had lyme, too.
bill pitt

Honolulu, HI

#13 Dec 15, 2007
my father died due to what is now called morgellons.I have had the condition all my life,i'am 59 yrs old and i was just 5 when became aware that i was never alone. I have spent my entire life fighting to rid myself of this sub species,i was close to death in 2005 today i'am alive thanks to the few Drs out there that are willing to step outside the box.SPECIMENS I HAVE DONATED TO RESEARCH HAVE NEVER BEEN MADE PUBLIC there is a secure un-web site where research info is controled by the CDC and Homeland Security.is it sinking in yet?
sonja-lennox

South Africa

#14 Oct 14, 2008
I'm staying in Cape Town, South Africa and is also suffering from morgellons disease. I'm the 1st patient in our government hospital that was diagnosed with morgellons. No one here seems to believe or regonise morgellons disease. Who can I contact in South Africa that actually knows more about morgellons.
E-mail: [email protected]
Donna Mae

Rancho Cucamonga, CA

#15 Oct 22, 2008
Please help me [email protected]
I cant take it anymore
Chris Beasley wrote:
I provide this post to all. I hope that everybody may look into the Morgellons that has had much news media coverage of late. The following will explain the support and understanding that people with Morgellons need at this time:
Letter from Dr. Smith
DEAR COLLEAGUE:
I appreciate your taking this information and hope you find it informative. It is my purpose to inform you of what I think is a rapidly emerging infectious disease. I have seen patients with this disease in my practice. Whether or not you know it, you do as well.....
the rest of the letter can be found at: http://www.cherokeechas.com/gregs.htm
Please read the following letter also:
Letter sent to the CDC from Senator Dianne Feinstein : http://www.cherokeechas.com/df-cdc01.jpg
Letter to Doctors from Randy S. Wymore, Ph.D. and Rhonda Casey, D.O. Courtesy of OSU's :
http://healthsciences.okstate.edu/morgellons/...
All of the above support and letters can be found at the New Morgellons Order:
http://www.cherokeechas.com website.
Please take the time to look into Morgellons with an open mind that there "is" a new disease that needs the research and support from all Doctors in every medical field.
Thank you for your time
Chris Beasley
New Morgellons Order
[email protected]
Donna Mae

Rancho Cucamonga, CA

#16 Oct 22, 2008
I have suffered and tried all,..please help me [email protected]
Donna Mae

Rancho Cucamonga, CA

#17 Oct 22, 2008
Please tell me what you are using I am desperate cant stop it,..
[email protected]
exposem wrote:
salt and vitamin c is working for me. I've had lyme, too.
zulu magic4u

Ann Arbor, MI

#18 Feb 26, 2009
I've been looking at my morgellon fibers under a microscope and by accident I looked at my toilet tissue and my paper towel under the microscope and I saw fibers that look like a morgellon clone I also saw the black specks, a blue fiber and the gel like stuff and I've seen bug pieces and bodies weaved into the toilet tissue and also in the paper towel. I truly believe the source of the morgellon fibers is these paper products. I also wonder about the nose tissue.. I use cottonelle toilet tissue and I used spartan brand paper towels.. I will be changing these brands. I will be looking at the new brands under the microscope until I find something that not buggy. Please check out my findings for your self. They really look like the morgellon fibers and black specks. And I'm also infected and I've been fighting it for 3yrs now. And for the last 3yrs I've tried over and over to convence my Doctor that I'm not crazy and he still don't believe me. I have all the symtoms escept the open lesions. Thank God.
PATRICK VAN NIEKERK

South Africa

#19 Apr 19, 2009
I live in Johannesburg. I have been a sufferer from Morgellon's for almost ten years. I would like someone to contact me i.c.w. the group that is forming here in SA. I am not crazy or delusional. This is a serious matter which requires intense effort worldwide. Thank you
Pat Van Niekerk
PATRICK VAN NIEKERK

Bryanston, South Africa

#20 Apr 19, 2009
Could Lance Marshall and Sonja Lennox please contact me on [email protected] I live in Johannesburg and would like to be part of some sort of discussion or action/lobby group.

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