Author lists reads like a Who's Who at the IDSA Lyme school. Makes sense it would since they're revisiting the arthritis white whale.
They can propose all they like. Wish they'd move away from the arthritis obsession, though. That it's - by some - felt to be a forced fit perhaps attributed to...
:(
I would suggest the way forward and out from this is the development of readily available diagnostics that will unequivocally confirm or disprove active infection.
Anything less has time and time again proven to destroy lives - irrespective of how one perceives Lyme.
Sometimes I wish researchers and advocates would be more careful with wording, as well intentioned as they may be. It can have a misleading effect. There are no generally effective therapies and few are really looking, current scientific findings are all over the place, and clinical experience...
I know this isn't what you were speaking to, @Mij , but lest anyone think I don't deserve my ME/CFS diagnoses, I received them from no less than six clinicians, four of whom were all prominent ME/CFS researchers. Each one would be recognizable to most on this forum - and each was well acquainted...
This is still widely underappreciated. Fortunately, awareness is slowly gaining traction, as is the novel(!) concept that some of these pathogens can cause neurological problems via infecting the brain, including babesiosis. Th babs brain connection should have been on the map in a big way years...
I hear you. But that's not the way it works. It's not the real world.
I had an embedded tick removed in the center of a bulls-eye. But I'd been infected long before that. That was almost 20 years ago. Since then I've tested positive on the 2T and the C6 and the MTTT - all FDA aprroved and...
Sure you can. PEM aside, tell me the difference between Lyme symptoms and ME/CFS symptoms. They can be identical. It's easy to appreciate how doctors can confuse one for the other. Compound that with dismal diagnostic protocols and solutions, and one's own immune abrogating Lyme responses.
It's...
I did. I do.
Why? Did the Lyme kill off the ME/CFS? Does that mean I need never worry about getting cancer as Lyme will eradicate it?
People can have more than one disease at the same time. I've three at least right now. Four.
Oh dear.
In the US, in North Carolina, many CDC-approved and FDA-approved tests for Lyme were positive for patients, and later recommended to be discounted because someone maintained there weren't enough of the right kinds of ticks in NC. Which is just silly. This blade swings both ways.
Who...
Can you, if you stick to FDA-approved? Although there are gougers for sure, I'm not clear on how large this specific problem is. Lyme patients aren't all rubes; people know how to research, and now more than ever before, they do.
Period. Here is the real problem. This is a two-sided coin. Show...
There are some genetic tests. Not many.
There are a handful of neurologists that might make a clinical call.
Sorry, I don't remember in general how testing is done. I know only one rare type, and it's a genetic one. I think testing sodium/potassium/calcium levels while episodic might be a way...
It's like trying to share the gravity of ME/CFS to not just healthy people, but to other chronically ill - you have to live with a channelopathy, or live with someone who has one, to grok it.
While it's great to sorta admit there are long-term intractable problems with some infections, and it's great to unite infection sufferers under a kind of support group/banner, and yes, there's power in numbers - I still cannot help feeling "one step forward, two steps back".
How'd direct CDC...
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