On September 9, 1011 I saw the pathology report that came from Mayo Labs that the broncial wash fluid, which had grown on a petrie dish, was identified as Hormographiella Species and a second organism, filamentous fungus, they were unable to identify. No surprise there since they have not been able to identify it for the past several years (and I suspect not working on it very hard either!)
Unfortunately, I was also informed on this date that I have adenocarcinoma in my right lower lung and will be needing to remove it as soon as possible. I am not certain at this time if there are any other areas of my body involved. It has been caught early and the pulmonologist said I have better than a 40% chance to survive.
However, he is not aware of the long time that I have had this fungus and if you look that fungus up online it carries a pretty poor prognosis as well. However, most people who have it are already very ill and immuno compromised such as with AIDS or long term chemotherapy. I have never had anything like that, so one wonders, why would I have this fungus. And how is it associated with these unidentified fibers. This is a very important connection that somehow needs to be made. Do others have this same fungus? I can tell you that the “normal” pathology labs cannot identify it, but they may be able to at least grow it and then send it to a place such as Mayo. This is how my mold growth was able to be identified. My local pathology department grew the mold from my lung wash but after 6 weeks gave up on identifying it so they sent it to Mayo.
I have survived with “it” for 16 years and now I feel better since I began using the PathoGenX Liquid so if I can get rid of the cancer I think I will be able to get rid of the fungus too. The doctors are amazed that I am not really bothered too much by the cancer diagnosis but they do not understand what I have already gone through with the Morgellons. Cancer to me is nothing compared to what I have been fighting for so long. An additional note, many people with Morgellons end up with some type of cancer, so it is no real surprise to me that I have this diagnosis. Cancer runs in my family as well so I was expecting it to pop up at some point.
Here is another thing my doctors think which is SO very wrong. They think that once they take out my lung lobe the fungus will be gone too! I talk and talk and they do not listen. I told Mayo Clinic way back in the spring of 2005 that I was full of fungus and they would not test for it nor listen. I am telling the team of doctors now, this is not just in the lungs it is systemic, and guess what they say: “We can’t be certain of that just because a lung flush came up with it”. God, what does it take for these medical professionals to realize how this works.
I will try to get my tissues into the hands of pathology departments that will have some of the evidence of the two types of fungus on record. If I do not make it my body will also be donated to science to further study this horrific disease.
Treat yourselves people – the doctors, even the best of them, just do not get it.