#packaging and testing

[semimediapress]

Tata Electronics eyes Malaysia semiconductor deal to boost ATMP operations

June 4, 2025 /SemiMedia/ — Tata Electronics is in advanced talks to acquire a semiconductor plant in Malaysia as part of its strategy to strengthen its assembly, testing, marking and packaging (ATMP) capabilities. The company is evaluating multiple candidates, including SilTerra, a wafer foundry owned by Dagang NeXchange Berhad (DNeX), as well as OSAT operations of Globetronics and assets from…

[picatchu]

(in the voice of my cat) ahh so you're in a bag... immense violence NOW

[theshitpostcalligrapher]

no minecraft stream today folks i woke up and seem to have the flu

[mitamicah]

My secret santa gift for @sepetajmikolikomehoces in the Bojere fanbook discord 🥹💗

[kreachvera]

does anyone else know the kuro ky phenomenon . lets all consider shiro sol as well. smile.

[amidtheglitz]

bitching on main idec.

MY POWER IS STILL OUT. IT HAS BEEN 5 DAYS.

[cloudellesims]

successfully converted my fav cloud replacements from ts4 to ts3 *and they're seamless*🥳🎉

more random pics

i realised i probably picked the wrong time of day to take these screenshots but oh well, you get the idea!

[tj-crochets]

Hey y'all! Weird question time, this time about hives. I have to get into some detail in my description of the hives, so it's going below a read more

So I used to get hives all the time. Like, a few every now and then through winter, gearing up to get bad mid-April, and then late June/early July they'd tip over into anaphylaxis, I'd go to urgent care for steroids, and then I'd a month or two of no hives before going into the slowly ramping up low level hives mode again until the next year. I'm pretty sure I have MCAS, I have like all the symptoms of severe allergies and have even been able to pin them down to specific foods but test negative for all IgE allergy testing (besides dust and cockroaches). Since I've been on higher-than-normal doses of daily antihistamines, I almost never get hives anymore My question: do I have the definition of hives right? Are these how hives go for you? My hives were: - raised, red/pink, and noticeably hotter to the touch than surrounding skin - most were about quarter sized, the smallest maybe the size of a pencil eraser, the biggest the size of a handprint - they had clearly visible edges - the ones on my fingers and toes were sometimes severe enough that the swelling of the hive prevented me from bending the joint - extremely itchy - each individual hive lasted about 24 hours, but I had a constant rotating cast of hives - larger hives turned into yellow bruises when the hive went down - they almost always formed on joints first and only spread to non-joints if I was having a bad flareup (hips and wrists first, then backs of knees, fingers, toes, elbows, and ankles, then eyes and ears, then everywhere else, but almost never my chest, back, or stomach) My endocrinologist seems convinced the joints-first hive pattern is indicative of an autoimmune issue, but I have zero issues with my joints* and test negative for RA like three different ways *well. I have mild scoliosis (maybe) and almost definitely dislocated a rib at least once, but those are not really autoimmune related? I also sometimes have joint pain but only when my muscles are so tight they are hauling on my bones and like...that's not the joint's fault pretty much every doc I've seen is just like "yeah you do electrolytes wrong muscles don't like that :/"

[destinationtoast]

Well, it's been a hell of a couple of weeks, and one of many things that happened is that I ended up coming home from Urgent Care looking rather like fruit being packed up for long distance shipping.

I got pretty scraped up when I fell while hiking nearly a month ago. Then I got significantly better... and then I got a whole lot worse.

If you would like to avoid some truly disgusting and painful wounds, you should know that you are likely to develop an allergy to Neosporin if you use it for multiple weeks (and probably the same goes for other brands of over-the-counter antibiotic ointments, I'm guessing).

[swinging-stars-from-satellites]

forgot about college breaks and all my friends are going home in 10 days so I am now hurrying up to get their Christmas presents together sjsjsjdjfbd

[ladyohdeath]

holy fuck guys i haven’t been this sick in ages. the amount of fevers ive had in the past three days is in the double digits

[missinglaterals]

oughhh it's all coming together now that I got the cat textures in there.

[allbeendonebefore]

every day on this site "DM me" okay prove you are literate.

[heatlightning-mp3]

its like yeah maybe this is autoimmune fuckery but if thats the case then like maybe do a little more testing? please? because these symptoms, while now chronic, are still acute and like imo its just neglect atp

they see the older tests and just dont bother to check again and its lazy as hell, as much as we avoid that word. we're gonna have to tell them tomorrow that we do not feel comfortable getting discharged without another cbc with diff and cmp and honestly if they try to say no we might just like refuse to be discharged until they do bc like. we actually have a right to do that anyways and we are trying to document as much as possible atm

we always worry that pushing this kind of stuff will change the way we're treated / make them retaliate but the thing is is that like 😭 some doctors always act rude and dismissive these days and like that was true in the past but has only gotten worse. it seems like most of these doctors have reached the same fucked up conclusion and im pretty sure its bc they all share an electronic health record but like

if i am already viewed in this way, and i can tell i am, its not paranoia, i guess i don't have much to lose by being firm since im already labeled "anxious" and potentially "difficult" though the records i see have never said that and only stated that i am logical, well-versed in managing / understanding of my conditions, and "pleasant" even when i push back

but like essentially what i am trying to say is that i think just shutting down and letting them do whatever they want in order to avoid a bad reputation or something doesnt really matter anymore. being seen as a "hypochondriac" is so much better than being dead and it seems like the only way to survive thru all this atp. rolling over and taking it has not ever done us any favors and, quite frankly, a huge reason why we are in this position

and likeeee part of me wants to just try and listen to what they say but um thats made us really sick recently. seems like the only option atp is to be more firm and less willing to budge on what we feel is right because fawning and trying to make sure we arent labeled in certain ways doesnt seem to make a different atp and health shit is too dire to not keep fighting unless we want to like. die. lol

[applejee]

my favourite sparkling water company has stopped selling my beloved tangerine flavour in supermarkets in favour of peach. a peach flavour THAT ISNT EVEN FUCKING GOOD!!!!!!!!!!

[lesbianstarlightglimmer]

Wow the way I just want to run into traffic rn is insaaaane :D