[Mz]

I have a form of cystic fibrosis. I have made a long list of dietary and lifestyle changes. The current best source of information about that is a blog called Mic Eats.

In a nutshell, people with CF misprocess fats, wind up excessively acid and wind up with serious malnutrition. I got very picky about the fats I consume, aggressively addressed the nutrient deficiencies until my body worked more normally, and I eat a diet that compensates for my body's tendency to become way too acid.

I also avoid chemicals that bother me, avoid exposure to germs, etc.

I look fairly ordinary these days. It isn't obvious to other people that my entire life revolves around this. It is sort of like being a kosher Jew who eats only approved foods and so forth.

[ShannonAlther]

Since you actually have CF, it would be trite to point out (but I will anyways for the peanut gallery) that the mutation in the CFTR gene causes secreted mucous to be much thicker than necessary. In the lungs, this causes difficulty breathing, rampant infections, and death by the age of 50 at the optimistic. Lifestyle interventions are not as helpful as you think in the general case, and the only reason you didn't die in your crib is because of aggressive antibiotics use.

[Mz]

Lifestyle interventions are not as helpful as you think in the general case

Because of people like you treating me like absolute shit on CF lists, I left all of them some years back. Then someone with classical CF in their 30s whose number was up tracked me down because they didn't want to die. They follow my blog and private message me occasionally and thank me profusely for helping them get healthier (instead of, you know, DYING).

So, like, that's just your opinion, man.

[ShannonAlther]

I don't believe I've accused you of anything except being wrong, Mz, and furthermore your blog notes that you have a rare CFTR mutation, a milder form of the disease (I only briefly scanned so I may be wrong). That's awesome! Your quality of life is probably really high compared to the average CF patient!

But the only intervention that's lifestyle-y that I know of is chest physiotherapy. I'm glad that the person you found now feels better, but the data does not support your claim.

[Mz]

I claim I am doing something groundbreaking. Your claim amounts to refuting the idea that anything new can be done, that the outcomes we currently have is as good as it gets.

Despite various publications of results where hand washing reduced mortality to below 1%, Semmelweis's observations conflicted with the established scientific and medical opinions of the time and his ideas were rejected by the medical community. Semmelweis could offer no acceptable scientific explanation for his findings, and some doctors were offended at the suggestion that they should wash their hands. Semmelweis's practice earned widespread acceptance only years after his death, when Louis Pasteur confirmed the germ theory and Joseph Lister, acting on the French microbiologist's research, practiced and operated, using hygienic methods, with great success. In 1865, Semmelweis was committed to an asylum, where he died at age 47 of pyaemia, after being beaten by the guards, only 14 days after he was committed.

https://en.wikipedia.org/wiki/Ignaz_Semmelweis

Hand washing. What a silly idea. Let's just put this guy in a loony bin for how completely insane he is.

Edit: Also, the person found me. I didn't find them.

[ShannonAlther]

> Your claim amounts to refuting the idea that anything new can be done, that the outcomes we currently have is as good as it gets.

Poppycock. The Wikipedia page lists a small handful of promising technologies[0], and there are others not listed there: improvements in organ transplantation and/or cloning would do wonders. I'm particularly fond of the idea of synthetic chloride channels that do the work of the CFTR protein.

But the reason that cystic fibrosis is lethal is because of the mucous. The lethality of the mucous is unrelated to your lifestyle choices, since the lungs of a CF patient are colonized by bacteria that prefer the different type of mucous. This sort of thing is exacerbated by fraternizing with other people who have CF, since they're likely to infect one another.

Over time, the bacteria become resistant to the antibiotics used to treat the disease. So more antibiotics are definitely in order, although that's not the be-all end-all. Again, I'm just saying that lifestyle interventions are almost certainly not effective (I can't even see how).

But there's a critical point in here: sure, Ignaz Semmelweis was laughed at for positing an unusual theory. But so were tens of thousands of others who came up with actually crazy ideas, too many to list. All I'm saying is, just because people disagree with you doesn't mean they're wrong.

[0]https://en.wikipedia.org/wiki/Cystic_fibrosis#Research

[Mz]

You are quoting Wikipedia at someone who HAS CF? Is your knowledge of CF based completely on reading crap online? Because mine absolutely is not.

All I'm saying is, just because people disagree with you doesn't mean they're wrong.

And all I am saying is I have heard this kind of dismissive crap from the "peanut gallery" before. It isn't anything new or novel for people to treat me in a completely disrespectful, dismissive fashion.

So if that is all you have to bring to this discussion, then I think I am done. Because it isn't a good faith tactic At All and I have wasted enough of my life on assholes on the internet who are sure that I am crazy because REASONS, none of which are at all actually logical or scientific, though that is what they are typically claiming as justification for just crapping all over me gratuitously.