8 posts shown.
wanderingridge30 said:Could use some help here.
How do I get subtitles working on Netflix?
About six months ago, I could use this without any issues:
But it just doesn't work for me anymore.
In the subtitle menu, it shows I've selected the American option, but nothing actually shows up on the screen.
What changed?
Where am I going wrong?
Thanks.
Maybe try using Cody? It handles all that stuff really smoothly.
I'm not sure if you've ever messed around with Cody before, but it's a media player and hub that expands its main features through various addons. It works on pretty much any platform.
Basically... you just install a third-party Netflix addon on Cody, log in, and once you start a movie or show, you can pull subtitles from all the major subtitle sites through the standard Cody menus. That way, you aren't stuck relying on whatever Netflix provides.
I guess you can also mess with settings you wouldn't normally have on the official Netflix app, like zooming the image or changing the subtitle position and size.
It’s not an Imgur issue.
Imgur works flawlessly on PCMag and various bike forums I hang out on.
It even handles thumbnail previews, which makes posts look way cleaner and easier to scan.
But here? Nothing seems to work at all.
Why isn't it showing any of the Imgur links on the forum when they look totally fine on Tapatalk?
The Instagram Thumbnail previews aren't working either?!
I switched from manual Humira injections to the auto-injector pen today, and I have to say, it’s actually a total game changer.
Has everyone else made the jump to the pens yet? I'm curious to hear how you guys are finding them.
Sent from my iPhone 13
Is anyone else here on BT Humira?
TapaTalk
Np
Ohhh, it's a woman, I guess. That explains things. Sry!
TapaTalk
I think they offer four different types of biologic therapies here in the States, and one of them is actually Remicade?! Is that the biologic you get through an IV infusion?
I'm not sure what your treatment schedule looks like or how often you receive it; I've been searching on Google and seeing mentions of intervals ranging from every 4 to 16 weeks via intravenous infusion.
Anyway, they aren't super frequent. Maybe the easiest solution is just to take the path of least resistance. Even if you eventually move back to the US (though I'm not really sure why 🙂 would), you could just continue seeing your current doctor for your treatments as needed.
The real question is whether it's worth the cost—like, how far you'd have to travel, how many trips, and how often you'd need to go in.
If it isn't a long drive and you only need therapy every 4-6 months, then why not?
Unless, based on your username and where you are right now, you should probably start getting everything lined up before you ever consider moving back to the US...
TapaTalk
I just started biologic therapy recently, so maybe I can be of some help.
In the US, you can only get biologics through Medicare (correct me if I'm wrong), and the cost is covered by the hospital systems. When my specialist offered me BT, he asked if I wanted to self-administer it every two weeks or come into the clinic every six months for a two-hour session.
I'm on Humira. I inject it myself every two weeks, and I just "request" my next supply over the phone a week before I need to apply it. I think there are about 13 of us on BT in my county, and nationwide, I'm not sure, maybe around 1,000 if I recall correctly.
I was diagnosed with RA five years ago, so when I was 33, following knee surgery from a sports injury. I'm 38 now.
Over those five years, I tried sulfasalazine, which was a total bust, and ended up on a mix of methotrexate, Arava, and Decortin, along with the usual painkillers—mostly ibuprofen granules and Advil.
I stayed on that last combination for quite a while and it actually worked best for me, but whatever.
For your BT to be approved, the doctor has to submit a request, which first goes to a hospital board and then to a Medicare commission.
You have to run a whole series of tests—I assume you already know this—which all need to be attached to the application.
Basically, you have to meet these criteria: http://www.reumatologija.org/Preporu...nk=RA_HRD_2013
I guess as long as you don't show that necessary lack of response to standard treatment, the therapy won't do much. When the doctor submits the request, they basically use a calculator to crunch all these different factors and indicators; everything has to line up and show results that are worse than the recommended threshold.
But if you have the full documentation to satisfy the guidelines from the American Rheumatology Association, I don't see any reason why you couldn't get approved. It shouldn't matter where you're being treated. But that's just my opinion... 😢
I could ask my doctor about your situation; he’s an amazing guy and we have a really good relationship.
I'm seeing him at the end of January.
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