45 Comments

  2. Not always a BullsEye mark and there is a small percentage shown to also have Lyme but do not believe we have confirmed all Morgellons also has Lyme. Still looking for root cause but majority of medical community writes off as Paratosis Psychosis. There is deeper root cause still to be discovered. Nocardia? Candida Auris?
    Skin Deep: The Battle Over Morgellons a good documentary m

  3. I strongly agree. I am a technological engineer. I have researched and studied about it. With the advances thus far made with micro-computing fostered by AI technology is where the threat lies. Once it’s perfected? Even the normal house fly should cause you suspicion. Period.

  4. I have morgellons disease but I remember having the same spots since I was 12. I had a biopsy done at OHSU and it's double DNA, confused DNA hair and nail and in addition to the fibres which I rarely get I mostly get big chunks of what looks like cartilage or nail basically out of my skin. And until I remove all of it they don't go away. So extraction is the only cure and the doctors will not help with it. But my doctor did apologize about saying that it was all in our heads back in the day, that needs to be removed from all morgellons disease information. It's definitely not in our heads and people saying that will make us even crazier than the lesions themselves. There's a lot of anxiety and depression around whether they will heal or what they're going to do, the pain and being able to survive. Just be acknowledged as a sane person with a disability is really hard. Just don't get me going

  5. Also a lot of people have Lyme disease and they don’t know it. The bulls eye rash only occurs in less than half of the patients with Lyme disease. The tests are also very unreliable, there is a lab in California called Igenex that is really reliable but it costs more money then the standard fda approved test that is very inaccurate

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