Posted 4/20/2020 12:31 PM (GMT 0)
Many people with bartonella have some or many forms of skin manifestations including scratches that come and go, stretch marks and/or striae which may appear more permanent but vary in color due to herxing/flares.
LLMD’s have to know this. Why is this important symptom picture not published data in medical journals? Why is bartonella not confirmed to be transferred by ticks? Why did the material presented by the TBD Working Group mysteriously not mention much, if anything, about bartonella?
For those who have bartonella, the symptoms can be debilitating; the disease can be extremely difficult to eradicate and recover from; and treatment can be unbearable. WHY is bartonella being hidden in a closet by LLMD’s instead of being pushed to the forefront with documented case record reports published in medical journals by every LLMD?
This makes me angry. When I google bartonella striae or stretch marks, all I find are reports that it’s false information that patients get off the internet. Makes my blood boil. WHY are the LLMD’s who see these clinical presentations over and over again not publishing this information? Why has there not been medically accepted proof that ticks transmit bartonella?