I sincerely hope that this collaboration also includes education about medical misogyny, medical trauma and medical gaslighting. One of the biggest obstacles patients face is not being believed, especially women.
My Infectious Disease Doctors are as closed-minded as anyone I have ever known. They give my conditions names but cannot explain what causes them. When I make suggestions, over and over I have heard them say, "Well, it can't be that. It must be something else." So, What Else and Why? When doctors become closed off from ongoing research because it doesn't fit in their (preconceived) medical system, then we are in deep trouble and the systems in which they work are doomed to ultimately fail. Politics gets involved and when the national systems of Status-Quo Medicine (CDC, NIH, etc.), Pharmaceutical Monopolies (We have to recover costs of our patented research) and Monolithic Insurance (No, we never pay for that) get in bed together, they have very hideous microcephalic progeny as a result. Is there a Real Doctor in the house?
👍🏾💯👏🏾🙌🏽 Best comment. I've been saying the same thing. Forbid you say you looked a symptom up online they lose it but dismiss what you're telling them because they don't know how to help you.
Thank you for trying to help those of us get better but are constantly being told with western medicine that’s it all in our heads. I want to be apart of making a change or helping others through my struggle and pain. How do I connect with your guys?
Medicine is highly siloed authoritarian profession so I hope this workshop will include independent microbiologists and researchers. Shareholder preferences now control medicine and it has lost its way; no one is looking for the root cause of chronic diseases. Historically infection was usually found to be the cause of inflammation but the paradigm of modern medicine is to provide treatments that provide life-time annuities to the pharmaceutical industry. No pharmaceutical industry would want to develop a cure for autoimmune disease because that would not be profitable. In medicine the dead shall speak to the living but autopsies are expensive and seldom done anymore. There are too few doing the fine tissue microscopic studies using advanced lab techniques. In the case of ME/CFS they don’t know what they are looking for and looking in the wrong places. Some of these infections such as Ebola are now believed to persist in tissue reservoirs only to become reactivated later. The CDC acts like a quasi-government and before they knew what they were dealing with, gave Lyme disease and all the procedures around it to the private 13,000-member IDSA organization. Medicine is supposed to be based on science until it becomes inconvenient as in the case of Lyme. The problem is the long-term disability insurance industry doesn’t want to underwrite the costs of complex-disseminated [chronic] Lyme and TBDs. They have managed to define the disease, not by the symptoms but with a test they developed. It’s the test that got us into all this trouble and it has to be scrapped.
There are so many currently available therapies that can be directed by looking at commonly-usex lab test differently, that is to say, through a different lens. Why are someone's white blood cell counts chronically low? What underlying viral/bacterial infections might be down-regulating the immune system, and let's identify what readily-available tools are out there to bring the immune system back into homeostasis? From IV vitamin C to peptides to IViG, let's identify the low-hanging fruit type tools available now to practitioners are share the knowledge on how/when to deploy them. Lyme disease practitioners already have their own Go-To's, let's share those ideas, create lists that can drive an individualized protocol, then go from there. I think being able to clearly lay this stuff out will enable us to clearly be able to think and map out, ”Okay, what are the next steps? What's needed now that we've exhausted all the tools at our disposal, currently?” These are the beginning steps as I see it. But the question to practitioners is the same as what we ask of researchers: are you willing to share what you know? ? Unselfishness, Altruism need to be at play. Are we big enough people to be able to give what we know without making a profit somewhere? (Looking at you, big pharma.) Can we move forward with the focus-on-the-greater-good being enough?
Will viewer questions be adressed during/after the workshop? What would be the benefit for a debilitated patient to spend precious energy and focus to attend? Thanks for your response!
Says the person with the username "Jesus Heals". 🙄 FFS man.. your people don't even believe IN science. mRNA has saved a lot of lives and will continue to do so. As will many other vaccines.
I sincerely hope that this collaboration also includes education about medical misogyny, medical trauma and medical gaslighting. One of the biggest obstacles patients face is not being believed, especially women.
My Infectious Disease Doctors are as closed-minded as anyone I have ever known. They give my conditions names but cannot explain what causes them. When I make suggestions, over and over I have heard them say, "Well, it can't be that. It must be something else." So, What Else and Why? When doctors become closed off from ongoing research because it doesn't fit in their (preconceived) medical system, then we are in deep trouble and the systems in which they work are doomed to ultimately fail. Politics gets involved and when the national systems of Status-Quo Medicine (CDC, NIH, etc.), Pharmaceutical Monopolies (We have to recover costs of our patented research) and Monolithic Insurance (No, we never pay for that) get in bed together, they have very hideous microcephalic progeny as a result. Is there a Real Doctor in the house?
👍🏾💯👏🏾🙌🏽
Best comment. I've been saying the same thing. Forbid you say you looked a symptom up online they lose it but dismiss what you're telling them because they don't know how to help you.
Thank you for trying to help those of us get better but are constantly being told with western medicine that’s it all in our heads. I want to be apart of making a change or helping others through my struggle and pain. How do I connect with your guys?
Medicine is highly siloed authoritarian profession so I hope this workshop will include independent microbiologists and researchers. Shareholder preferences now control medicine and it has lost its way; no one is looking for the root cause of chronic diseases. Historically infection was usually found to be the cause of inflammation but the paradigm of modern medicine is to provide treatments that provide life-time annuities to the pharmaceutical industry. No pharmaceutical industry would want to develop a cure for autoimmune disease because that would not be profitable. In medicine the dead shall speak to the living but autopsies are expensive and seldom done anymore. There are too few doing the fine tissue microscopic studies using advanced lab techniques. In the case of ME/CFS they don’t know what they are looking for and looking in the wrong places. Some of these infections such as Ebola are now believed to persist in tissue reservoirs only to become reactivated later.
The CDC acts like a quasi-government and before they knew what they were dealing with, gave Lyme disease and all the procedures around it to the private 13,000-member IDSA organization. Medicine is supposed to be based on science until it becomes inconvenient as in the case of Lyme. The problem is the long-term disability insurance industry doesn’t want to underwrite the costs of complex-disseminated [chronic] Lyme and TBDs. They have managed to define the disease, not by the symptoms but with a test they developed. It’s the test that got us into all this trouble and it has to be scrapped.
Yes.......110% accurate. Human health and life has been monetized and thats not in line with HEALING,
There are so many currently available therapies that can be directed by looking at commonly-usex lab test differently, that is to say, through a different lens. Why are someone's white blood cell counts chronically low? What underlying viral/bacterial infections might be down-regulating the immune system, and let's identify what readily-available tools are out there to bring the immune system back into homeostasis? From IV vitamin C to peptides to IViG, let's identify the low-hanging fruit type tools available now to practitioners are share the knowledge on how/when to deploy them. Lyme disease practitioners already have their own Go-To's, let's share those ideas, create lists that can drive an individualized protocol, then go from there. I think being able to clearly lay this stuff out will enable us to clearly be able to think and map out, ”Okay, what are the next steps? What's needed now that we've exhausted all the tools at our disposal, currently?” These are the beginning steps as I see it.
But the question to practitioners is the same as what we ask of researchers: are you willing to share what you know? ?
Unselfishness, Altruism need to be at play. Are we big enough people to be able to give what we know without making a profit somewhere? (Looking at you, big pharma.) Can we move forward with the focus-on-the-greater-good being enough?
Will viewer questions be adressed during/after the workshop?
What would be the benefit for a debilitated patient to spend precious energy and focus to attend?
Thanks for your response!
Right away all should renounce the evil-doers suggesting mRNA anything will ever help with 'Lyme' or any other infection...
Says the person with the username "Jesus Heals". 🙄 FFS man.. your people don't even believe IN science. mRNA has saved a lot of lives and will continue to do so. As will many other vaccines.