#mri test

[precisionimagingcenters]

Full Body MRI Test: Things You Should Know

A Full Body MRI Test provides detailed imaging of internal organs, muscles, and tissues. It helps detect potential health issues early. Understand the procedure, benefits, and potential risks before scheduling. For more details click here.

[patho123]

Patho World, located in Bopal, Ahmedabad, is a top diagnostic facility with a focus on magnetic resonance imaging (MRI) scans. Patho World, a renowned modern facility, has the newest MRI technology, guaranteeing high-resolution images that help with precise diagnosis. Experienced radiologists and technicians dedicated to delivering accurate and trustworthy results work at the center.Go to https://www.pathoworld.in/pathology-lab-in-bopal-ahmedabad.php to schedule your appointment right now.

[xoxoemynn]

Hello, have a sleepy Daphne. She has a very big week this week and has requested extra loving and who am I to deny her anything?

[prince-liest]

Night shift in the hospital on Christmas week is so delightfully boring, hahaha. It's my first time covering nights on inpatient and I was relatively nervous about it at first because it involves covering nearly 30 patients alone (well, normally alone; this is a "practice" nights week for me so I have a senior with me)... but unlike day shift, you're not generally managing actual patient care at night, you're just fielding calls from the night nurses in case they need something that an MD/DO has to order. It's also generally day team's job to be like, "Hey, we anticipate X might happen with this patient. If that happens, do Y or Z."

So far it's been a couple of shifts and they've been quite delightfully boring, which is how I like it. Come in at 6pm, take signout from the two teams we're covering, admit anywhere from 0 to 3 patients and staff them with the night attending (admissions done by 10pm, he leaves at midnight), scour the emergency department tracking shell a few times to see if we're going to have to do any admissions after that (we're required to do admissions for any residency clinic patients - so far we haven't needed to), waffle around and finish our notes until it seems like a reasonable time to get a move on, have midnight lunch, and then retire to the call rooms until our alarms ring at 5:45am and we do sign out at 6.

Throughout this, we also get calls for things like "Can this patient have a melatonin?" and follow up on anything that was pending overnight (day team usually tries to make sure we don't need to but sometimes it can't be avoided - usually it's been trending troponins or hemoglobin), and on one occasion yesterday we went to a mildly funny rapid response that occurred because someone freaked out about a patient's pre-existing neurological deficits (she was super stable; not sure what the rapid team was, like, meant to do in that situation, lol).

Anyway, I've been sleeping from somewhere between midnight and 1am until 5:45am so far which has been great. The mattress in my call room is absolutely horrific, though, lol. It's like 4 inches thick and somehow has springs in there. Better me than my senior, though - she's got the slightly nicer mattress but still gets less sleep than me because I'm pretty good at just knocking out.

Today will be my first day taking calls independently, so fingers crossed it goes as boring as yesterday! I brought a couple fancy mini-bundt cakes for me and my senior because we both deserve something for working night shift on fucking Christmas, haha.

[darkfalcone]

Anywayyy I need sofia to kidnap me to take me away from stress

[skunkes]

your art is such an inspiration in every way but it also got me over my crazytown fear of selfship with ocs and in having the most fun ive ever had in my life. Hanging out with him in my mind (also your linear burn lineart trick helped so much?? all of my sketches feel so complete now. i love it!!)

oc selfship cope is the only thing keeping me alive and sane rn so if i can spread that knowledge/courage/ability/etc im happy ^_^ yippee

[marc--chilton]

(mgv) the ducklings succumbing to societal expectations/norms and going to wilson when house is bein silly (medical malpractice) to like try to "control" him sorta. because they never challenged their perception of relationships and "defaulted" to An Alpha Can And Should Keep Their Omega On A Leash. like a fake stupid harmful "hierarchy" of the secondary sexes. and wilson ends up scolding him because for one he's not house's alpha, rude to assume that, and even if he WAS he doesn't like. own him. just because house listens to his Alpha Voice doesn't mean wilson can use it against him, that's fucked up

[tj-crochets]

Just got a new prescription filled, and it might be the new funniest prescription packaging I've ever received (the previous winner, of course, being the time they stuck the manufacturer's bottle in a GIANT orange plastic prescription bottle)

It's a single pill, three cents, and for some reason I do not understand they put this single tiny pill in the size large (but not sized giant) prescription bottle. Absolutely ridiculous ratio of bottle to pill lol

[atomiccryptid]

if any of you have had to get an mri before can you tell me what it was like? i have a 45 minute one next week and i am. not looking forward to it.

[holocene-sims]

a sneak peek for an upcoming (timeline tbd) update 😊

[sneevil-28]

[flutterbyfairy]

i have a neurologist appointment in about a month that i'm quite nervous about due to previously being dismissed/not having my concerns listened to, so gonna post this to ask for some advice on getting Taken Seriously or if anyone knows things about the type of condition i might have about what i should be asking them to do/test.

might be quite long so putting it under a read more, and tw for medical stuff and doctors being dismissive. also i am So So Tired and therefore not able to think very clearly so apologies if i've messed up any of the medical info about conditions i mention and apologise just generally for the rambliness of my writing.

summary of why i'm going:

bunch of disabling symptoms that have continually progressed over the past 5+ years, including: muscle weakness, fatigue, muscle twitches/small spasms, nerve pain, blurry vision, lack of coordination (have this from autism, however has gotten significantly worse recently so might also be related to neuro stuff). first symptoms were difficulty having my arms over my head (like having to take multiple breaks while putting my hair into a ponytail because i couldn't hold my arms over my head for the like.. three minutes to do a ponytail) and blurry vision (that optometrist has said seems like might be due to a systemic disease because of how variable it is) since i was 13, which was seven years ago. i started getting more impairing symptoms when i was 15, and began needing a wheelchair for anything that required standing or walking for more than 10 - 15 minutes. i'm currently 20 and need my wheelchair whenever i leave the house, i can't leave the house or do things around the house often, i can stand for a max of like four minutes and can't hold my hands above my head for more than like 30 seconds to one minute. pretty much all my symptoms get a lot worse with any exertion.

GP thinks i have myasthenia gravis, but the test for acetylcholine receptor antibodies was negative and he doesn't have the ability to do other tests.

the neurologist has already said he thinks i have functional neurological disorder and that i should do CBT and pysio to improve my functioning (i already know CBT is horrible for me, i'm in other therapy which is good, i've done some psyio before but she just taught me some stretches and that was it, more psyio could be good but it'd have to be with someone who isn't trying to do a graded exercise therapy type thing since i get PEM). he has mentioned doing a spine MRI but this hasn't been done yet. he said he doesn't want to do further testing for myasthenia gravis but i will probably try to get him to agree to doing a repetitive nerve stimulation EMG or something.

i also have scapular winging on the side of my body with worse muscular symptoms which has also caused a lot of nerve pain, and i might also have some sort of spine issues (straightening of cervical lordosis was seen on a CT scan, they said it was probably due to muscle spasms, and i get a lot of neck pain which might be due to that? as well as a ton of back pain along my spine. might have CCI but haven't been tested yet). since it seems like i'm getting some structural changes in areas where i also get a lot of the pain and weakness and spasms i'm hoping if i bring that up the neurologist might maybe look more at organic causes + the state of those structural changes but i dunno.

he did a basic neurological exam in my initial appointment with him and said that i have give way weakness/waxing and waning weakness because when he got me to do the pushing my limbs against resistance i could do okay for a couple seconds but couldn't maintain it. he also said in the letter that i had positive hoovers sign however i am.. very confused by this because from my understanding hoovers sign is mainly looked at when someone has one limb that's at least somewhat "normal" and one that either can't be moved or is very weak, and then the person can't move the weak leg but when asked to push the stronger leg against resistance they push the weak leg down. both my legs are strong enough that i can stand and whilst one leg is a bit weaker they're relatively similar. i lifted and pushed against resistance with both legs so.... i am not sure how hoovers is applicable here? does anyone know why it was applied and if that was correct or if i should be challenging that? he's saying that the give way weakness and positive hoovers are indicators that the problem is "non-organic" and therefore should be treated with CBT and pysio.

i'm not sure what i think is actually going on. i think myasthenia gravis might make sense, but also so could other neuromuscular diseases like a mitochondrial disease or something. also very possible it's myalgic encephalomyelitis (aka chronic fatigue syndrome) but obviously that one is a diagnosis of exclusion so i want to rule other things out if possible. i want to know what's going on so i can have the best chance of being as well as is possible for me. i know CBT is not right for me and whilst some type of pysio could help a bit/prevent some decline (based on past experience i know it won't Cure Me but obviously it can help a bit to build some muscle or maintain range of motion and things like that which are important) if there's other things i can do on top of that i want to.

i've tried to do research to work out the best tests to ask for and i think EMG might be good but also know a normal EMG doesn't typically pick up myasthenia gravis so it needs to also have repetitive nerve stimulation i think?

i can't see a different neurologist at least not anytime soon, so i need to get this neurologist to do as much to help as possible. a social worker from where i get therapy is coming to the appointment to help me so that should be good but i need to work out what the best way to advocate for myself is and what tests are going to be the most useful to ask for.

if anyone has any advice for getting doctors to take you seriously or for any tests i should be advocating for or conditions i should be looking into or anything i would really appreciate it <3 (emoticon description: heart)

[hillbilly---man]

You know those things mechanics can hook up to your car to read the error codes off the computer?

It'd be super cool if they made those for people too

[liebelesbe]

had to get up before 11am to go to a doctors appointment, you know what that means! (nap time)

[rising-above-stars]

I'm going to fucking scream

[floral-hex]

MRI scheduled for next week to look for “abnormalities” in my brain