[0] https://experiments.springernature.com/articles/10.1038/npro...
Disease modifiers like methotrexate or stelara will suppress aspects of the immune system, which protects the body from further damage. Ibuprofen on the other hand will mask pain but not modify the underlying issue.
If CBD was effective (for me it doesn't seem to be), then the challenge is in understanding if it is modifying the disease, or just hiding symptoms like ibuprofen would for pain.
Sometimes I read old stuff and think, "wow, I said that?" other times, "I have no idea what point I was trying to make."
>You could really ask the same question about Crohn's or IBS.
No you couldn't. They are clearly auto-immune disorders.
Out of curiosity, do you have any formal training on medicine/physiology or is your knowledge base self-aquired?
Aren't there diseases where someone are caused not by the microbe directly but by the body's immune reaction to it?
> Out of curiosity, do you have any formal training on medicine/physiology or is your knowledge base self-aquired?
Argument from authority (or lack thereof) is pretty contrary to the HN ethos, imo. You're not right because your degree says so, but because the facts do.
There are symptoms that can be caused by that. The characteristic of an autoimmune disorder is that the response never ends( either chronic or with flare ups) or takes way longer than a normal one would.
> Argument from authority (or lack thereof) is pretty contrary to the HN ethos, imo. You're not right because your degree says so, but because the facts do.
What facts did you state then? I'm asking where does your thinking process stems from?
Yep. For example, that's what causes the "cytokine storm" in COVID-19.
An antibody is in some ways similar. They latch onto the bacteria or virus, but instead of invading they glom on and then signal the body to come dispose of this thing.
If your body picks the wrong feature for the pattern, then the antibody could attach to healthy tissue. Maybe one particular type, like insulin cells, or myelin.
My daughter has an auto-immune disorder and it took two years and a brain biopsy for the best pediatricians in Canada to determine it was auto-immune related. Of course you may dismiss that by saying there are no good doctors in Canada because they're not from (wherever you're from), but your casual dismissal of the complexity of these disorders is simply wrong.
And your last sentence is clearly not just "out of curiosity".
And if you look at IBD such as Crohn's or Ulcerative Colitis then sure.
This isn’t an argument that supports your reasoning. It’s just an appeal to authority.
> When an immuno-suppressive is effective at reducing symptoms you know it’s an autoimmune disorder.
Is surgery an autoimmune disorder? A lot of doctors will give a patient steroids to reduce inflammation after surgery.
I know there's a guy, or maybe he represents a group of researchers, who thinks that Chronic Fatigue Syndrome is caused by inflammation in the brain, either due to some undetectable infection, or just a misfiring that is a lingering effect of some other insult (sounds to me like a histamine response aka allergy).
If your body thought you had the flu but you didn't, you'd be knocked on your ass not unlike many people with CFS or Lyme. And if it never stopped you'd be in pretty bad shape a year in.
So. Are we treating microbes that don't culture in a petri dish, or are we solving an autoimmune response gone whacky? You could really ask the same question about Crohn's or IBS.
I recall years ago reading a long story about a consultant who was called in to figure out why this black soot was all over a neighborhood around a brewery. The brewery said it was diesel exhaust. But why only this neighborhood? He heard of a similar problem is some town in the UK. But Petri dish after Petri dish cultured nothing that could explain the black soot. Ergo, it's not microbial.
Our intrepid consultant pours a small amount of distilled spirits onto a sample dish, and gets a bunch of black shit. The 'soot' was feeding off the Angel's Share (evaporative losses from the brewery), and would barely grow without it. Vigorous growth in vivo, negligible growth in vitro.
We've come up with a cure or treatment for so many microbes that we can detect, but how do we know we're detecting them all? People die of cancer not because cancer is getting worse (well, pollution notwithstanding) but because Cancer is patient. There's a lot of space in the middle for new vectors to slip in.