395 karma · joined June 5, 2014
[1] https://torrentfreak.com/rarbg-over-267000-movie-tv-show-mag...
I also wonder if Forte' Agent still works? Does Newsguy still exist? /s
edit: found the answer to my question
1) Harley's with open pipes 2) cars without any exhaust (common) 3) after market exhaust on import cars (thanks Fast & Furious) 4) garbage trucks, gas powered gardening equipment, 4x4's/big trucks, new muscle cars 5) scooters, mopeds, gas powered bicycles, motocross motorcycles (I get sideshows/giant groups driving up/down my street to the next location), enduro & regular motorcycles
The thing is is that there are already laws in place to deal with most of those..
I know Anhingas as sacred Water Birds of the Native American Church [1].
Also, do people get titles (Political Director Abundant SF) for entities that don't exist? https://www.linkedin.com/in/todd-david-7998473
white flight = moving out of city because of fear, cost, crappy schools, etc. is flight. A white person moving to the boondocks because they want to homestead or live off grid is not "flight".
gentrifier = higher income person/family moving into a city or neighborhood, raising the housing costs by doing so, causing the long time residents to leave because of said costs and changing the culture of said area because the old families don't live there anymore.
What?!
https://sfstandard.com/politics/tech-families-abundant-sf-mi...
Also, from dmonitor: >genuinely confused how the author/illustrator can include that sentence under their depiction of a black person. the lack of awareness is incredible.
It was 1937. I was born in the 60's and Song of the South regularly played on the Sunday night Disney show. Racism was blatent back in the day, but also considered normal.
After a long time (during covid) I was finally able to see my PC who sent me to an audiologist for a hearing test. The audiologist only found slight hearing loss at high frequencies in my left ear (the ear closest to the CNC machines I used to work with). She said she didn't see anything else abnormal & asked if I wanted an MRI to see if it could find anything. I agreed. The MRI found nothing wrong with my ear or eustachian tube.
I've reported it to VAERS and have been sort of following Gregory Poland, MD [1](director of Mayo Clinic Vaccine Research Group), who also got tinnitus from his first mRNA covid shot. The issue definitely needs research.
Dr Poland, along with others, have recently released a couple of reports [2,3] saying that we need a new roadmap for covid vaccines. I agree!
Also, I used that tone generator site that someone else posted and it seems that my jet engine screams at about 18000 Hz.
[1] https://en.wikipedia.org/wiki/Gregory_Poland [2] https://www.sciencedirect.com/science/article/pii/S0264410X2... [3] https://www.cidrap.umn.edu/covid-19/cidrap-unveils-roadmap-a...
Edit to add VAERS website. If you suspect you got tinnitus from an mRNA vaccine please report it here: https://vaers.hhs.gov/reportevent.html
Interesting that you say this after our progressive DA was recalled & our mayor is trying to supplement the SFPD budget by $27.6M.
Also interesting, I have lived in SF since 1972 and only been mugged once, in my 1st yr there (I was 7 & mugged by kids across the street in the projects for my Mickey M watch and about $0.50). I will freely and safely walk anywhere in the City at any time of day or night. And I'm an older guy.. This ongoing discourse is tiring.
You know, there's a good Ari Daivari, Slim J & Jeeves K joke in here somewhere..
>Companies are very interested in unexpected events, particularly bad ones (called “adverse events” in the jargon). Viagra was “discovered” because of an unanticipated side effect of a drug being tested for a heart disorder.
Tell that to Moderna and Pfizer. They, nor the FDA, have shown any interest in adverse events reported by both patients and doctors to VAERS [1], unless whatever hypothetical minimum number of people report it. I've had, as well as Dr. Greg Poland [2], a pretty severe adverse reaction to the mRNA vaccines but our problems remain unaddressed because not enough people have reported it, science knows little about our reaction, or it doesn't monetarily benefit anyone (liability or profit). As for the Viagra discovery, it was a monetary benefit.
Scientists and researchers in the medical field need to realize everyone is different and we have different reactions to various drugs. I guarantee you that carbamazepine was causing my apnea problems. It also caused two other adverse reactions that are not listed as side effects.
Now that I think about it, your entire comment screams pharmaceutical marketing to me.
[1] https://vaers.hhs.gov/ [2] https://www.mayo.edu/research/faculty/poland-gregory-a-m-d/b...
edit: mRNA
I am a thin guy with very low body fat. As soon as I told my doctor that I had woken up 2-3 times with my soft pallet dry & semi-collapsed, also that I would wake up regularly with a dry mouth, he immediately sent me for a sleep test. I went and did the test and the results were that I had mild sleep apnea. The sleep doctor told me that they were ordering a CPAP machine for me. I asked why I needed it for mild apnea and also told them I wouldn't use it. They ordered it anyway and told me to take the issue up with my doctor.
While all this was going on I was in the process of reducing the amount of meds I took (bad accident in 2010). I also started reading up on & studying sleep apnea. One of the first things I learned, and that worked, was keeping my mouth shut during sleep (many ways to accomplish that). The other thing I learned is that Big Pharma/FDA does a horrible job of listing medication side effects. I say that because "causes sleep apnea" was not on the list of side effects for carbamazeine (used for my peripheral neuropathy). As soon as I stopped the carbamazepine the apnea symptoms vanished. I have no need for a CPAP, it was ordered and I've received many calls about it, but there it sits at the sleep doctor's office..
Anyway, yes, bloodletting (properly called phlebotomy) is really the only way to deal with it. The first 3 years after my diagnosis my hematologist and I tried out quite a few things to help control it, including diet modifications and different time intervals between phlebotomies. We ended up settling on phlebo every 6 weeks and eat whatever I want.