HHS Tick-Borne Diseases Working Group (TBDWG) Meeting News
Lyme patient advocate Monica White, President, Colorado Tick-Borne Disease Awareness Association (COTBBAA), had verbal comments accepted at the July 2020 meeting of the HHS Tick-Borne Diseases Working Group:
“My name is Monica White. I’m president/co-founder of Colorado Tick-Borne Disease Awareness Association. I’ve lived with chronic Lyme, co-infections & conditions for nearly 16 years due to lack of an early diagnosis & treatment. Formally a fully functional wildlife biologist & wildland firefighter for the US Forest Service, I am functional now only with repeated courses of combined antibiotics, antimicrobial, & immune therapies.
I recently relapsed with tick-borne illness after a period of no treatment. And again, even with current positive lab results in hand, I was met with dismissal from mainstream medicine.
With an enlarged liver and spleen during another extended hospital stay, the infectious disease doctor wrote in my report… and I quote…”I highly doubt this is in anyway related to either Lyme disease or babesiosis.” I again left hospital care without a diagnosis…and I’ve again made improvements in my health only with retreatment for TBDs. This dismissal of TBDs in the differential diagnosis is commonplace for TBD patients, especially those with chronic or persistent disease.
Though persistence of pathogens is shown in multiple studies conducted by respected researchers in the community, some on this panel….and is found in both animals and humans, findings have thus far been ignored or disputed by many members of this panel each year. It is past time to settle the science on this issue for…
- patients that don’t get early accurate diagnosis and treatment.
- patients that fail short course single antibiotic/antimicrobial therapies;
- patients thatare overlooked for have co-infections or tick-borne conditions,
- and patients that do not respond to currently available therapies.
Maternal-fetal transmission of many TBDs is a fact, but research is lacking in diagnostics and treatment before irreparable damage has occurred. My own children acquired Lyme and co-infections congenitally, and both suffered from delayed diagnosis and treatment, as well as from multiple relapses of disease.
The resources available to patients have been… and continue to be…. INADEQUATE. Our medical system is failing these patients, and this has ramifications that go so far beyond my individual story.
We should not have to fight as hard as we have… for as long as we have…to get government funded reliable direct diagnostics & curative treatments for acute & persistent disease!
Individuals…families…OUR children have been losing EVERYTHING for DECADES due to the lack of attention to the seriousness and the debilitation that Lyme, other TBDs & conditions has on those infected or exposed.
There is no excuse for patients having to spend months, years, or decades seeking accurate diagnosis and treatment, with crippling physical health, mental health, financial burdens, loss of careers, & relationship stresses beyond what many families can endure.
No one should suffer the way I have suffered…the way my children have suffered… and the way that the patients I share a voice for…have suffered.
“Patient’s needs MUST be the priority of the WG for this final phase of the panel!” Thank you!”
To find written comments submitted by the public including Monica White that are on the TBDWG site released for the July 2020 TBDWG meeting:
To find many LDA articles about the first two terms of the TBDWG: