Tin foil wear?
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Fear sells.
I wonder how many people who buy this clothing have a cell phone stuck to their head most of the day?
@Bernard said in Tin foil wear?:
Fear sells.
I wonder how many people who buy this clothing have a cell phone stuck to their head most of the day?
Yes, which, according to the State of California, is dangerous.
It you do it in any other state, it's fine.
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I googled “how much would it cost to build a liveable 3 bedroom 2 bathroom faraday cage.” Google (with all its AI) could not even give me a numerical range; it just tells me that it will be very expensive (with numbers for much smaller/simpler Faraday cages).
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As a migraine struggler, I'll have to admit to looking into whether my headache frequency had any correlation with heightened solar activity. It's part of the whole "your brain is a meat computer" and may be influenced by outside energy sources type of thinking. So these hats did catch my interest...
Still, selling tin foil hats is a bold marketing move to go from silly joke to viable business plan!
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Well...? dang. Placebo?
I went ahead and bought one of the hats. (Migraine folks will understand the willingness to try just about anything) So far this month my need for medication to stop a headache has dropped significantly. Sleeping heavier into the morning too.
Huh.
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Ron, that's great! I was skeptical of using clothing to block EMF radiation but it's definitely a real phenomenon and detrimental. I can tell you there are two benefits to having your RM ruin the electric account in your name and then one in his own. You have a respite from EMF radiation and silence in the form of appliances that can't be used. I wish you well with managing your migraines. I don't have them but hear they're awful.
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My favorite PCP used to reprimand me (gently) by saying, "You do what you need to do to get through life."
I've taken this advice to heart.
The older I get and the worse my health gets the more I find myself using it in ways I never could have imagined when I was 40.
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As a migraine struggler, I'll have to admit to looking into whether my headache frequency had any correlation with heightened solar activity. It's part of the whole "your brain is a meat computer" and may be influenced by outside energy sources type of thinking. So these hats did catch my interest...
Still, selling tin foil hats is a bold marketing move to go from silly joke to viable business plan!
@Rontuner wow! So you’ve just been wearing the hat? All day long or only outside?
I didn’t realize you were a migraine sufferer. What kinds of medicine do you use for them? I started having regular migraines probably around 2006. In late 2022 I switched the new class of migraine medicines (I now take qulipta daily and ubrelvy if I get a headache or migraine). These medicines have been life changing for me, so I always recommend to anyone who hasn’t changed their treatment protocol in a few years that they consult with a physician, because there are now many more migraine-specific treatments than ever before.
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So I wear the hat overnight - bonus, I can pull it over my eyes for darkness but it is cooler than the eye mask I had been using. (I also have that phenomenon that I didn't know was "a thing"- when I close my eyes, I don't see black - more a reddish static) Sometimes I also wear it at the computer or in the car between appointments.
Hey, I'm all for using the placebo effect if it continues working - or maybe there is something to this?
I've had sporadic headaches since high school, but they increased in frequency in the early 2000s. I started with a triptan only in the last 7 years or so to take when I sense one coming which has given me days back - almost always stops it with just one dose, though there is a limit to how many to use/month and I was going over some months. (I used to lose days going back to bed or just suffering through) Started Qulipta about a year ago, but that hasn't changed frequency significantly - also some of the meds are hard on heart, liver or kidneys so trying to keep those numbers in range. Moved on to Botox treatments - had to go through all the other options first. I just had one treatment which they said may not do much. Second treatment is scheduled for the end of the month and that seems to be when most patients notice a reduction in frequency. Migraines? Clusters? I get the sense no one really knows for sure and they just guess and see if something helps.
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