Post by Admin on Nov 29, 2006 11:06:46 GMT -5
THE MORGELLONS COMM. HAS MUCH TO LEARN FROM LYME!
« Thread Started on Today at 10:20am »
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Greetings to All:
I received the below email as a forward from Ginger Savely.
We in the Morgellons community would do well to take a chapter from the book being actively written here by the Lyme community.
The Lyme community appears to be somewhat more politically sophisticated and organized than is the Morgellons community.
Both communities have enormous stakes at risk in the struggle we find ourselves thrown into. In other words, we are all in the same boat together. I believe the Morgellons community needs to follow the lead of the Lyme community and to become much more individually and collectively pro-active.
It's time to leave our former passivity behind unless we are all simply content to go away somewhere and die....Because, my friends,....That is exactly what will happen if we do not organize and begin to sieze control of our own destiny. You can count on it.
We would do well to remember that when it comes to inflicted afflictions such as Morgellons and Lyme, the "meek" do indeed inherit the earth. The only problem is that the portion they generally inherit is usually six feet under. Keep that fact in the forefront of your awareness. Personally, I prefer to go down fighting the good fight.
The Morgellons community should consider applying the wisdom expounded herein (by Ginger) to our own cause. There are great benefits to be had by working in tandem with the Lyme community to bring further public attention to our cause.
It is time to sieze the moment. Do or Die. It's that simple. No one is going to blow our horn for us. We need to do our very own "Joshua" if we want the hostile walls of the medical establishment to come tumbling down. Peaceful petition for redress is a Constitutional right. The failure to address such petition is one of the definitions of tyranny. The failure to attempt such a petition is one of the definitions of slavery. It's our choice here. And...It's time to choose!
-Cliff Mickelson
***
(Enclosure forwarded from Ginger Savely re: Lyme)
Dear Lyme patients:
We all know how hard it is for us to participate in a rally. We're either too busy or too sick or don't have the money to travel to New York
All of us need to support the Lyme Rights Rally. And there is a way that we can do so. There are dedicated people who are willing to make lime green UN-smiley faces that represent each us who are unhappy about the Infectious Diseases Society of America (IDSA) Treatment Guidfelines.
To wrap it up in a nutzhell, the people who wrote these guidelines have sentenced us to the PRISON FOR THE CHRONICALLY ILL, because they don't encourage early diagnosis or adequate treatment.
We need to fight these powerful people!! They view us as little puppets whose strings they enjoy pulling. We must show them that we are still able to make our own decisions regarding our practices and healthcare!
Please do not be afraid!
This is the United States of America, and we have the right to free speech and to publicly object to these guidelines that cause damage to patients. Send your name and state to Sheila Statlender at SStatlende@aol.com so you can be counted among the people who are able to physicallly attend the Lyme Rights Rally! Add your name to the list of "proxy" lime green UN-smiley faces to be held up at the Lyme Rights Rally on THIS Thursday, November 30, 2006.
There is only 1 day left FOR US TO BE COUNTED at this Rally! I encourage everyone to have your names shown on a lime green UN-smiley face on Thursday! It will make a powerful statement to IDSA and to the media about the many people who are too sick to attend and wiped out financially to pay for the trip.
The members of the Lyme Rights Rally Committee are willing to take their time to make these lime green UN-smiley faces to represent us at the rally. Please email your name and state today!
Thank you for your listening ears. We can bring these people to their knees for their misdeeds if we band together!
-Tina Garcia ; Lyme education and awareness, Pheonix AZ.
« Thread Started on Today at 10:20am »
--------------------------------------------------------------------------------
Greetings to All:
I received the below email as a forward from Ginger Savely.
We in the Morgellons community would do well to take a chapter from the book being actively written here by the Lyme community.
The Lyme community appears to be somewhat more politically sophisticated and organized than is the Morgellons community.
Both communities have enormous stakes at risk in the struggle we find ourselves thrown into. In other words, we are all in the same boat together. I believe the Morgellons community needs to follow the lead of the Lyme community and to become much more individually and collectively pro-active.
It's time to leave our former passivity behind unless we are all simply content to go away somewhere and die....Because, my friends,....That is exactly what will happen if we do not organize and begin to sieze control of our own destiny. You can count on it.
We would do well to remember that when it comes to inflicted afflictions such as Morgellons and Lyme, the "meek" do indeed inherit the earth. The only problem is that the portion they generally inherit is usually six feet under. Keep that fact in the forefront of your awareness. Personally, I prefer to go down fighting the good fight.
The Morgellons community should consider applying the wisdom expounded herein (by Ginger) to our own cause. There are great benefits to be had by working in tandem with the Lyme community to bring further public attention to our cause.
It is time to sieze the moment. Do or Die. It's that simple. No one is going to blow our horn for us. We need to do our very own "Joshua" if we want the hostile walls of the medical establishment to come tumbling down. Peaceful petition for redress is a Constitutional right. The failure to address such petition is one of the definitions of tyranny. The failure to attempt such a petition is one of the definitions of slavery. It's our choice here. And...It's time to choose!
-Cliff Mickelson
***
(Enclosure forwarded from Ginger Savely re: Lyme)
Dear Lyme patients:
We all know how hard it is for us to participate in a rally. We're either too busy or too sick or don't have the money to travel to New York
All of us need to support the Lyme Rights Rally. And there is a way that we can do so. There are dedicated people who are willing to make lime green UN-smiley faces that represent each us who are unhappy about the Infectious Diseases Society of America (IDSA) Treatment Guidfelines.
To wrap it up in a nutzhell, the people who wrote these guidelines have sentenced us to the PRISON FOR THE CHRONICALLY ILL, because they don't encourage early diagnosis or adequate treatment.
We need to fight these powerful people!! They view us as little puppets whose strings they enjoy pulling. We must show them that we are still able to make our own decisions regarding our practices and healthcare!
Please do not be afraid!
This is the United States of America, and we have the right to free speech and to publicly object to these guidelines that cause damage to patients. Send your name and state to Sheila Statlender at SStatlende@aol.com so you can be counted among the people who are able to physicallly attend the Lyme Rights Rally! Add your name to the list of "proxy" lime green UN-smiley faces to be held up at the Lyme Rights Rally on THIS Thursday, November 30, 2006.
There is only 1 day left FOR US TO BE COUNTED at this Rally! I encourage everyone to have your names shown on a lime green UN-smiley face on Thursday! It will make a powerful statement to IDSA and to the media about the many people who are too sick to attend and wiped out financially to pay for the trip.
The members of the Lyme Rights Rally Committee are willing to take their time to make these lime green UN-smiley faces to represent us at the rally. Please email your name and state today!
Thank you for your listening ears. We can bring these people to their knees for their misdeeds if we band together!
-Tina Garcia ; Lyme education and awareness, Pheonix AZ.