The really offensive aspect of the immunity debt conversation for me personally, is the implication that disease is a burden we all share, which requires a cost from each of us.
When it could not be more blatant that the cost of disease falls most heavily on the most vulnerable with the least impact on the affluent.
Whose immunity is getting paid off?
@Curiousfoolish I have End Stage Chronic Lyme disease. I’m in a state full of ticks, where most doctors swear #lymedisease doesn’t exist. It infuriates me. Insurance doesn’t cover late stage, undiagnosed Lyme so it’s all cash. Disgusting.
@OfficiallyPatty hi, what kind of borrelia do you have? it's very important to know because trust me treatments are not the same for each borrelia. have you got coinfections too? if yes, which one ?
for me it's borrelia myamotoi with babesia, toxoplasma CMV EBV candida.
@sp1r4l_99 I have several. It’s been years - 27 drs and 10 different states. It went undiagnosed for such a long period that by the time they diagnose it it had already spread to several organs and other parts of my body. I’m functioning fine now, but that could vary on the day.
@OfficiallyPatty i was make all antibiotics treatments, 6x 3 months each but don't work (i stop it). i tried alternatives treatments like colloidal silver, dr buhner protocol ....(in 3 years, the cost was 7000€ and all my money disappear). At this time, i kepp only fentanyl 100 for pain but evolution of disease will go to the bad. Walking was finished since 1 month and i'm using Wheelchair and my fingers will become more and more rigid with full pain