Do you guys also think this is getting weird that they are trying so hard to discredit this disease? There's too much misinformation.
Absolutely.
The amount of effort that goes into discrediting it is astounding.
The Dr I saw this week was so angry and agitated just at the first 2 minutes of seeing Lyme disease, cdc positive in my folder. Before I even spoke a word. I literally wasn’t going to mention me cfs chronic Lyme nothing. My lips were sealed. He saw that one test and hospitalizations and went off.
This is obviously much larger that we realize. I believe the cabal trains their medical schools to exactly what they want put out there. To the point that these doctors become emotionally triggered, as many of them are trained, when seeing cases like ours. They don’t want their colleagues knowing they have ‘head cases’ like ours that can’t be fixed with PT and SsRI’s. They don’t want to get in trouble for prescribing non traditional treatments that would actual help us if any of these people had once sense of sanity.
I wish it wasn’t so but it very obviously is. Too many of us are being hurt or worse and there is a systematic effort to not get proper tests or assistance for us. For instance, I’ve been told by multiple nurses and private pay long distance doctors, O2 would greatly assist me, but there is zero effort to even address this. 6 years in now. I’m told laying flat with a 89 O2 is normal and to knock it off and sit up.
It’s so surreal and insane.
Thank you for letting me vent on this thread.
Sorry, it’s just….so overwhelming at times the coordinated effort to mock and silence us.