Post by ctbarb on Jan 6, 2010 21:33:00 GMT -5
Hi Folks,
I've been quite sick these last few weeks, and after speaking with specialists in Boston on the phone, if you look and recognize any of these photos, please let me know - PLEASE!
I have these organisms coming from my mouth, nose, lungs and stomach (coughed up and vomited up), in my stool and urine (although only certain species are in urine, and NOT this particular one), are emerging from my body. They are also in my skin, and have emerged from sores, and ears. This is not the norm.
I found today photos that I took more than a year ago, that match exactly what I am still seeing today, although these photos are much better in quality, I think.
I know that there are more than one type of organism living inside of me, these are the ones that are causing havoc in my body...and perhaps in yours too. I've been told now for more than four years that "You can't get that here!", as I've mentioned on this board previously. I'm here to tell you, that you CAN! This disease is not endemic in the USA, nor any adjacent countries, so how did they get here? And, how did I get them? The mystery is about to unfold, here on Lymebusters. Hopefully, it will be confirmed at the end of January when I visit a world expert in Boston. I am being seen by a specialist of emergency medicine (called an intensivist) at the direction of the Chief of Medicine and Infectious Disease of a major world class medical facility. The doctor that I will see first, has indicated that he has recognized at least one of the organisms, but cannot discuss in detail until he personally meets with me as a patient. I can understand the ramifications of this request; therefore, I am not disclosing his name or the specific facility, I hope you can honor my wishes.
If this disease is confirmed, you will be the first to hear it. That I promise you. If you should have any of these photos in your collections, please let me know and I will keep them confidential and submit them to these specialists only with your approval. If more than one of us has this RARE disease in this country, then we will know that something is happening that should not be, and will be investigated, and if it is not, then we can take appropriate action. I do not believe that they will ignore these findings. I know we've been disappointed before many times, and so have I, but I am adamant of what I am seeing and have documented in digital photographs, the progression of this disease. They are amazed at the due diligence that I have done, and little do they know, of the due diligence done by so many of you too! We are NOT DOP, in any sense of the word!
Remember, just try to match the photos as closely as you can, then contact me here or by PM, and we will go from there. If I can collect more than 25 photos that are a match to mine, from different people, (any one of them), then we have a RARE disease within the boundaries of the United States, that should not be here! And, as I've been told so many times - [glow=red,2,300]YOU CAN'T GET THAT HERE!!![/glow]
I will post a series of photos, that I feel are the most common in their lifecycle...look carefully at your photos for a close match.
Thank you, I hope this works and we can prove that we have indeed, a disease that needs to be investigated in a proven, recognized, world class institution!
Please give me a little time and I will publish each photo as I find them, there will be many.
Love and prayers,
ctbarb
I've been quite sick these last few weeks, and after speaking with specialists in Boston on the phone, if you look and recognize any of these photos, please let me know - PLEASE!
I have these organisms coming from my mouth, nose, lungs and stomach (coughed up and vomited up), in my stool and urine (although only certain species are in urine, and NOT this particular one), are emerging from my body. They are also in my skin, and have emerged from sores, and ears. This is not the norm.
I found today photos that I took more than a year ago, that match exactly what I am still seeing today, although these photos are much better in quality, I think.
I know that there are more than one type of organism living inside of me, these are the ones that are causing havoc in my body...and perhaps in yours too. I've been told now for more than four years that "You can't get that here!", as I've mentioned on this board previously. I'm here to tell you, that you CAN! This disease is not endemic in the USA, nor any adjacent countries, so how did they get here? And, how did I get them? The mystery is about to unfold, here on Lymebusters. Hopefully, it will be confirmed at the end of January when I visit a world expert in Boston. I am being seen by a specialist of emergency medicine (called an intensivist) at the direction of the Chief of Medicine and Infectious Disease of a major world class medical facility. The doctor that I will see first, has indicated that he has recognized at least one of the organisms, but cannot discuss in detail until he personally meets with me as a patient. I can understand the ramifications of this request; therefore, I am not disclosing his name or the specific facility, I hope you can honor my wishes.
If this disease is confirmed, you will be the first to hear it. That I promise you. If you should have any of these photos in your collections, please let me know and I will keep them confidential and submit them to these specialists only with your approval. If more than one of us has this RARE disease in this country, then we will know that something is happening that should not be, and will be investigated, and if it is not, then we can take appropriate action. I do not believe that they will ignore these findings. I know we've been disappointed before many times, and so have I, but I am adamant of what I am seeing and have documented in digital photographs, the progression of this disease. They are amazed at the due diligence that I have done, and little do they know, of the due diligence done by so many of you too! We are NOT DOP, in any sense of the word!
Remember, just try to match the photos as closely as you can, then contact me here or by PM, and we will go from there. If I can collect more than 25 photos that are a match to mine, from different people, (any one of them), then we have a RARE disease within the boundaries of the United States, that should not be here! And, as I've been told so many times - [glow=red,2,300]YOU CAN'T GET THAT HERE!!![/glow]
I will post a series of photos, that I feel are the most common in their lifecycle...look carefully at your photos for a close match.
Thank you, I hope this works and we can prove that we have indeed, a disease that needs to be investigated in a proven, recognized, world class institution!
Please give me a little time and I will publish each photo as I find them, there will be many.
Love and prayers,
ctbarb