Bme pain olympics for mobile browser

Persona 5

2017.04.21 08:26 PM_Your_Neko Persona 5

A Persona style Role Playing Game
[link]


2024.05.16 02:57 programmedlearn Python playwright mobile error

I keep getting errors in playwright. Using it with it with purging to scrape and click on websites via Google. There’s a popup in mobile mode that I can’t get passed. It comes up once you open up google. The error I get is timeout 30000ms.
Code:
import re from playwright.sync_api import Playwright, sync_playwright, expect
def run(playwright: Playwright) -> None: iphone_13 = playwright.devices['iPhone 13'] browser = playwright.chromium.launch(headless=False) context = browser.new_context(**iphone_13) page = context.new_page()
page.goto("https://www.google.com/") # Wait for the popup to appear and click the "Continue in Safari" button print("went to google") page.wait_for_selector('button:has-text("Stay in Safari")') # Adjust the selector based on your popup page.click('button:has-text("Stay in Safari")') print("clicked stay in safari") page.fill('input[name="q"]', "query") page.keyboard.press("Enter") # Press Enter to perform the search page.get_by_role("link", name=“Selector”).click()
page.locator("#menu-item-708").get_by_role("link", name=“Query”).click()
print("we made it!")
context.close() browser.close()
with sync_playwright() as playwright: run(playwright)
submitted by programmedlearn to Playwright [link] [comments]


2024.05.16 02:51 grilledcheese27438 not very happy at current university

i've been looking at transferring since the beginning of my second semester (last semester) of college. I'm attending a big 10 university. i feel completely misplaced. most the kids I'm around all the time are like omg I'm just like so bad at school i got a 89 on my exam >:( and treat me like I'm stupid for having to take college algebra. even explaining i went to a super tiny school that didn't have precalc or anything doesn't change it. i feel so insignificant. i could get past the rat race academic culture; but then i got effing disabled. its gotten so bad I'm looking at getting a wheelchair because my body is literally fighting me on everything. the campus is a 30+ minute walk from the dorms to the other side of campus, and there is a really poor bus system (only city buses, no school owned buses, like 200ish seats at MAX at any point in the day for the main campus loop). so I'm stuck walking a lot. and then there's parts of campus that arent even vehicle accessible. the entire thing is not very accessible or disability friendly, even with a ton of accommodations. and then the courses are SO freaking hard. like, i knew college was hard but some courses have average exam rates of like 40-50 percent. is that even normal?? i feel like everyone is either complaining about insanely high grades or flunking left and right. and I'm only going here because i liked campus (when i toured and WASNT struggling with a mobility disorder) and they offered me so much aid it covered everything and left me with $1600 in spending/savings refund each semester. but I'm not feeling like its worth it to feel crummy and have declining mental health and grades...my friends think I'm overexaggerating though. i get that the financial aid is good, but i got good financial aid (almost full coverage) at most schools i applied to senior year of hs. i think i can get good financial aid again as long as i transfer in state. i don't know if I'm just frustrated or if its actually worth it to transfer somewhere else. all i know is I'm literally in constant pain when I'm there because of trying to get to classes and get meals and just FUNCTION. and my grades are suffering, and so is my mental health, because this whole new chronic illness thing is kicking my ass. my friends think im exaggerating and its just because im depressed and that i should stick it out. but i think maybe they just selfishly don't want me to leave? not sure. please tell me what yall think. im completely lost on what to do.
edit: i also cannot currently graduate in the major I'm in in less than 5 years, which undermines the entire point of the full ride financial aid. did not find that out until like, two weeks after disability diagnosis in October. and now I'm going to have to wait until the end of my (next) sophomore year to submit a major change form because i got a D in the class i needed for switching majors because i was physically struggling to get to class. my fault for not studying harder admittedly but now off track in attempts to switch to biology as well.
submitted by grilledcheese27438 to Advice [link] [comments]


2024.05.16 02:47 grilledcheese27438 not very happy at my current university

i've been looking at transferring since the beginning of my second semester (last semester) of college. I'm attending a big 10 university. i feel completely misplaced. most the kids I'm around all the time are like omg I'm just like so bad at school i got a 89 on my exam >:( and treat me like I'm stupid for having to take college algebra. even explaining i went to a super tiny school that didn't have precalc or anything doesn't change it. i feel so insignificant. i could get past the rat race academic culture; but then i got effing disabled. its gotten so bad I'm looking at getting a wheelchair because my body is literally fighting me on everything. the campus is a 30+ minute walk from the dorms to the other side of campus, and there is a really poor bus system (only city buses, no school owned buses, like 200ish seats at MAX at any point in the day for the main campus loop). so I'm stuck walking a lot. and then there's parts of campus that arent even vehicle accessible. the entire thing is not very accessible or disability friendly, even with a ton of accommodations. and then the courses are SO freaking hard. like, i knew college was hard but some courses have average exam rates of like 40-50 percent. is that even normal?? i feel like everyone is either complaining about insanely high grades or flunking left and right. and I'm only going here because i liked campus (when i toured and WASNT struggling with a mobility disorder) and they offered me so much aid it covered everything and left me with $1600 in spending/savings refund each semester. but I'm not feeling like its worth it to feel crummy and have declining mental health and grades...my friends think I'm overexaggerating though. i get that the financial aid is good, but i got good financial aid (almost full coverage) at most schools i applied to senior year of hs. i think i can get good financial aid again as long as i transfer in state. i don't know if I'm just frustrated or if its actually worth it to transfer somewhere else. all i know is I'm literally in constant pain when I'm there because of trying to get to classes and get meals and just FUNCTION. and my grades are suffering, and so is my mental health, because this whole new chronic illness thing is kicking my ass. my friends think im exaggerating and its just because im depressed and that i should stick it out. but i think maybe they just selfishly don't want me to leave? not sure. please tell me what yall think. im completely lost on what to do.
edit: i also cannot currently graduate in the major I'm in in less than 5 years, which undermines the entire point of the full ride financial aid. did not find that out until like, two weeks after disability diagnosis in October. and now I'm going to have to wait until the end of my (next) sophomore year to submit a major change form because i got a D in the class i needed for switching majors because i was physically struggling to get to class. my fault for not studying harder admittedly but now off track in attempts to switch to biology as well.
submitted by grilledcheese27438 to college [link] [comments]


2024.05.16 02:37 fiddlelake Making Mistakes...How common are they?

How common are small mistakes? I have been a new for 3 years but only 4 months into an acute care setting.
For example, I have personally discovered 3 med errors by other nurses. 2 have been when I checked the bag that was infusing and both were wrong doses. One was a IV antibiotic that was hung and never spiked. All different nurses. All very experienced.
There have been a couple times where I have not unclamped the secondary. Both of these were realized shortly after. I also forgot to change the TPN bag within the 24-hour window. Done a couple other things not up to "policy".
However, I made my first true med error last week, have a PRN pain med at the 5-hour mark. It was supposed to be Q6hrs. My first incident report on myself.
Another time I walked in on my patient at shift change who was tied, yes TIED, to a chair with 2 gaitbelts. This patient was nonverbal and had limited mobility. The night nurse said she did this so the patient wouldn't fall out of the chair. The manager also saw. I'm not sure if anything came of it.
On day when I was feeling bad about my mistakes, my manager told me she forgot to lock a bed when she was transferring a patient and they hit the floor and broke bones and had other injuries. She said everyone makes them.
I haven't received discipline for my mistakes. I talk to my manager a if I feel like I couldve done something differently or could improve, which is a lot. I feel like a new nurse all over again switching to acute care. I feel like one day I'm gonna walk in and get fired. I compare myself to my co-workers, I didn't drop a patient or tie someone to a chair so I think I'll be okay. Those nurses still work there.
submitted by fiddlelake to nursing [link] [comments]


2024.05.16 02:30 James007_2023 Seeking ANY way to share Garmin Training Plan and Workouts with others

Has anyone figured out how to share a Training Plan, or even a workout, with others?
Looking at the Garmin-provided training plans, they obviously have a way to "package" a Training Plan, create a template, allow others to use them by varying the plan based on variables of the plan (e.g. cycling training plans can be based on heart rate or power). However, there does not appear to be a way to even reuse your own prior plans. I would think the professional racers, and the personal trainer market would be screaming for this.
I have about 30 cycling Workouts. I'm on my second year of organizing those workouts into a 3-month Training Plan. Others are asking me to "share my plan" —and frankly—I'd like someone to train with using the same plans. Even more important, others can help me find and fix errors. Salt in the wound—I had to recreate the Training plan from scratch, on a specific day, because I could not reuse my own work from last year. Painful.
There is no "Share" button, or "Send" or "provide public access." The only way I can see right now is to find a way to Print each workout, and then print the Calendar pages because Garmin does not provide a way to see the entire Training Plan at one time. But also, Garmin does not provide any way to Print Workouts, either, so you are at the mercy of your browser and or screen clips.
Using the Cycling Training Plans on Garmin Edge bike computers is fabulous. My gym workouts I access from my watch and this is also great. However, beyond using the Garmin-provided plans, you have to create your own, and that is brutal. This has been discussed in this Subreddit in the past, and in other places. How can I do this?
submitted by James007_2023 to Garmin [link] [comments]


2024.05.16 02:10 Wide_Echo2810 Help with bills after injury

Hi, I'm posting here hoping to get some help after my fiance fell and hurt his leg. He fell last Friday and broke his tibial plateau as well as tearing his ACL and meniscus. He is going to need surgery and will be out of work at least 8 weeks. He doesn't have insurance or short term disability, and this isn't a workman's comp injury, so we will have to cover the medical bills and regular bills without help.
Unfortunately he is our main breadwinner. We have two kids with disabilities at home and I can only work part time because of their needs. My youngest daughter is 10 and she needs medical care around the clock. With the nursing shortage, I have been filling in 20+ hours a week caring for her as well as working, and now I'm caring for my fiance too. His mobility is extremely limited and he's in a lot of pain, so on top of needing my help, he can't help out with her care either.
We are already drowning, as the rent itself is $1900, and he's been seen in the ER, plus the orthopedic doctor, plus xrays, CAT scans, and an MRI. Surgery is going to be expensive and he will probably need physical therapy afterwards.
Anything you can do to help is greatly appreciated, even sharing the fundraising link to family and friends on social would be an immense help.
https://www.gofundme.com/f/support-awols-recovery-and-medical-bills?attribution_id=sl:51e3e740-dc5c-4ce8-8667-c85df35afa70&utm_campaign=p_lico+share-sheet-task&utm_medium=social&utm_source=facebook
Oh, and this is an alt account. I didn't want to out my main account.
submitted by Wide_Echo2810 to gofundme4everyone [link] [comments]


2024.05.16 01:23 nyumuny Weeks ? Months ? End of life cancer advice

My dad (64) was diagnosed with lung cancer that had spread to his shoulder bone about a month ago. It was only pain in his shoulder which he thought was his arthritis that made him go to the doctors.
Since the diagnosis, his decline has been so, so fast. He’s gone from a working, active, bulky man to a shell of his former self.
He was prescribed slow release and oral morphine to manage the pain. We still don’t know at this stage what the treatment plan might look like as the process has been excruciatingly slow.
In less than a month (maybe 3 weeks at most), he’s physically shrunk, he’s lost A LOT of weight, his appetite is really weak and he’s lost quite a bit of mobility (needs help dressing himself, feeding himself, washing himself, etc). All of a sudden, he has really dry eyes, swelling in his lower legs/ankles and redness, he’s very sleepy (needs at least 2 naps during the day) and in gradually more and more pain that the morphine doesn’t seem to help with. He seems disinterested and tired all the time, and constantly complains of being in pain. I just desperately wish I could take it all away from him.
He seems to need a lot more sleep now, and I’m just trying my best to keep him eating regularly and good amounts everyday. He can barely keep his eyes open a lot of the time and every word or every slight movement seems to take so much energy from him.
I don’t know what to do, or what to expect. I’m just utterly heartbroken. The initial time scale that was given to me by the oncologist was 6 months to 2-3 years depending on how agressive the cancer was. At this stage, I’m really fearing that that was probably far too optimistic and that things are heading in a downward spiral far too quickly. He seemed fine just a few weeks ago and now I’m seeing signs of end of life. I’m terrified. Are these end of life signs ? Should I be thinking in weeks or months ?
I live abroad, and I’m thinking of just moving here for the foreseeable future right now. The guilt of not being able to be with him to help (although he does have my brother who can help) all the time is killing me and I’m worried sick this might be his final weeks.
I lost my mum at 12 years old from amyloidosis and being faced with watching my dad progressively fade away and loosing him is tearing me apart. I’m only 22 now and don’t feel like I’m coping too well, so any insight or advice would be immensely appreciated.
submitted by nyumuny to hospice [link] [comments]


2024.05.16 01:12 kadangamzer Any ideas?

I have finally beaten all of the bosses on acended, did the path of pain, and 112% the game plus I did p5 and I got all the achievements. (All on mobile) And I still love the game after 300 hrs in, and I want to play it more until silksong comes out and I need suggestions for something more to do in the game (excluding radiant bosses cuz they're almost impossible on mobile).
submitted by kadangamzer to HollowKnight [link] [comments]


2024.05.16 00:36 Mer_Moh I'M BACK AND I'M FEELING LIKE A GOD

So I'm M29 started swimming back in 2003 non stop till 2012 then got back in 2018/19, I had to stop for many reasons mainly logistical and financial, Today i had my 1st session since 2019 in a local semi-olympic pool and I'm feeling indestructible, i forgot how much i loved swimming and how much it's been a core part of my childhood, i felt like i was finally home. I was too excited and forced myself a bit (didn't do any physical workout since 2021), i was just happy to be swimming again and soon i learned my athletic limits lol and I'm okay with them, now i know relatively what my goals will be. I swam a total of 650m: 200m freestyle, 100 backstroke, 150m breaststroke and the rest with a swimming board between my legs and swam only with my hands back and freestyle (the last two were to release back pain). I'm gonna do 2 sessions of 1h30 a week and i can't wait for the next session even tho the subscription makes 10% of my salary. I'm so happy till the point I'm sharing this with you guys even tho I'm a passive scroller, I'm open to all advices and tips from you guys about what to eat and stuff like this. Sorry for the long post.
TL;DR: I'M BACK TO SWIMMING AFTER 5 YEARS AND I'M SO HAPPY ABOUT IT.
submitted by Mer_Moh to Swimming [link] [comments]


2024.05.16 00:36 Odd-Fill-321 DMG experience

I have,had painful severe treatment resistant depression.after along trial journey in now on a maoi for three years that's performing miracles I still enjoy discussing reading learning substances how they affect the bran and basically pharmacology
I think back and remember the time frustrated I went the all natural route and the tons of stuff I tried
I rember how almost everything has a great amazing profile but never really lived up to it most had subtle effects if any.there were exceptions like kava for example,one exception though unlike kava was definatly strong but unlike kava for me was horrible I rember DMG if get the main brand can't rember the name but like a green and white box? Anyeay I rember it was made to be sublingual and after putting DMG under my tongue like a prescription med the effect was robust fast and potent I kept using it for a while because A it was something that actually worked B wasn't quite sure how I felt about it effects then I learned just how strong it was,the INSOMNIA.the insombia from dmg was so intense i mean i coulf not sleep a wink upon taking just a singular sublingual tab.iknew it wasn't just me as I tricked my brother into taking one and he immediately came and yelled at me ,what the hell did you give me I haven't slept in days ? Not sleeping allowede time to really evaluate DMG and. I was finally certain I hated hated it's effects they were extreme potent and depressing!
I. Also know it wasn't me because I'm not positive but I believe it in fact is named from the Olympics and almost in general altogether.
I'm just curious if anyone else messed with sublingual DMG . A had insomnia B noticed it had potent robust fast acting effects C felt it's effects were not pleasant At all ? Ty for reading and in advance for any reply !
submitted by Odd-Fill-321 to Supplements [link] [comments]


2024.05.16 00:13 ObjectiveSample2643 Lunasstrasshole can litterally eat shit out of her own litterbox ffs

Meant to take a break from Rise's endgame and give a little more attention to World since I'd hit kind of a roadblock and got burnt out from it. World has been fantastic so far... Until this fucking pile of steaming hot garbage showed her fucking face
Teostra was a literal pushover for me : sure he hits hard and he's fast, moves a lot, and starts heat damage if you stay close for too long,but guarding in front of his face when he aggros you and then attacking depending on the available opening was a pretty reliable strategy, and made for a rather fun fight still. Teostra is a fair fight, it's an endgame elder dragon so it makes sense that it's punishing
But then the devs wondered "What if we took this perfectly good fight, and took away everything that made it fair and fun?" And thus that fucking blue haired Karen saw the light of day it never should have.
Where do I even start ? She will never fucking stop attacking and covering half the arena with her fucking clown vomit! You can't even make good use of a guarding weapon like (gun)lance to learn her patterns because the fucking area hazard spam would deal the same fucking damage as if you'd just stand there and took it up the ass! At least Bazelgueuse and Uragaan leave pretty visible chunks that light up as they are about to explode, at least Vaal Hazak leaves a clear trail that does take some time before it affects you, but with lunastra, you can't even get close to her without burning alive!
Speaking of burning alive, why not mention her instant, half invisible gusts of flames ?! Who the FUCK thought it was a good idea to have a hitbox so fucking large have so little visibility/windup ? She can litterally do it out of any fucking move and it just goes so fucking far if she misses, the hitbox goes around the fucking earth and hits you again somehow. Just flaps her wing and ta-da! There goes 80% of your health bar. What about the remaining 20% you ask ? Well you can try to retreat and dring a potion of course ! Unless she decides to hit the 379217863th attack string in her godforsaken pattern!
"Oh well just don't immediately get up when knocked down, just wait for an opening to get up, run and heal" WHAT FUCKING OPENING ? Playing passively only nets you a slap on the back of the head, except you can't even learn from it because you can't fucking tell what this cunt's about to pull out of her ass the instand your I-frames wear off. And run WHERE EXACTLY ?! Into the fucking continent's worth of surface she's infected with her fucking trashfire, of the only quarter of the area that isn't lego riddled floorboards where she's definitely not about to jump to, trust me :}
Also can we talk about the fact that you only have 15 MINUTES FOR SOME UNKOWN FUCKING REASON ? Like the monster isn't already hard enough to keep up with, let's just add an arbitrary time limit because fuck you, that's why. "Well this is your cue to play aggressively!" And get instantly punished because I went for a flinch instead of retreating/guarding ? Sure, be my guest then!
All that and I still haven't gotten into the worst part yet : the fucking microwave oven attack. Asshole really just stands there, sets 90% of the fucking New World on fire and periodically farts out nukes. What do you even fucking do against that ? Guard ? The fire will kill you. Sheathe and dodge ? The time it takes for you to sheath is longer than the interval between shockwaves ? Superman dive ? Again, the time you take to get back up and a second shockwave has hit the hunter. Preemptive positionning ? The only safe place is at the other end of the fucking arena, where even HBG's are out of range, god forbid you're a blademaster. And unlike Teostra's supernova, there is little to no windup for a screenwide wipe you can't block.
Capcom really just took Kushala's area denial, Anjanath's aggressiveness, Uragaan's lack of a fucking bell and casually sprinkled a bit of the oh so special hitbox cancer, threw it into a blender, drank the stuff, vomited it out into the toilet, fushed it down and collected the sewage to create this gasoline pissing piece of shit!
Oh and you wanna know the best part ? The side characters giving you "advice" : Handler : "Don't be afraid to use the SOS flare to call for help!" Yeah sure buddy, jacking up the monster's HP while I wait during the 7 remaining minutes for potential help to arrive is bound to yield fantastic results I'm sure. But the game doesn't respect you so neither will I Field Team Leader : "Knowledge is your best weapon and defense. Read your monster field guide" SHUT THE FUCK UP FIELD TEAM LOSER I DON'T HAVE THE FUCKING ENTRY BECAUSE IT'S MY FIRST TIME HUNTING THE DAMN THING! Doesn't help this is their reaction to me carting because I made the regrettable decision of retreating and drinking a potion when my health was low.
Lunastra is just plain unfair, between area denial that punishes slow weapons just for existing, instant attacks that will catch even mobile weapons off-guard constantly jumping at a range where even ranged weapons/slinger (if you can even get ammo for it) will struggle to deal good damage while she can casually melt your healthbar off by breathing in your general direction (oops, my mistake, there was one flame particle in the air so that means it's the hitbox and damage of a Valstrax divebomb)
Ah, and I didn't even mention my third cart in the span of 10 minutes, while she was just casually camping near the entrance and fucking blasted me into The Elder Scrolls IV for at least trying to get more intel on her patterns while I painstakingly wait for time to run out. I've got no qualms with the fight being difficult, it's a post-game boss after all, so It's normal to have trouble against it. But between the insta-low hps, the area hazards spam and constantly jumping around, it just doesn't feel fair or fun at all.
Between this and the pain in the ass that was Leshen, I'm like one bad monster away from quitting world entirely. Fuck Iceborne, fuck the post game, if it's gonna be filled with shit like this why would I even fucking bother ?
Fuck you Lunastra, I'd tell you to burn in hell but that's where you come from you fucking lion cunt.
submitted by ObjectiveSample2643 to monsterhunterrage [link] [comments]


2024.05.16 00:02 teamdokifanclub_off Strange red rash on my legs

14M, I don't really remember my height and weight, White.
After being outside for 4 hours during Special Olympics track meet, I developed a red rash on my legs. I thought that this rash was a sunburn. The rash had a stinging sensation, no unbearable pain. I had a good deal of sun exposure during the event.
Don't take medications, and don't drink, smoke, or use recreational drugs at all.
submitted by teamdokifanclub_off to AskDocs [link] [comments]


2024.05.15 23:57 jephthai PT Seminar For Our BJJ School

TL;DR -> We brought in a doctor of physical therapy to do a seminar on injury resistance, working out, staying healthy, assessing weaknesses and injury potential, and understanding the world of diagnosis, triage, treatment, and recovery. It was great, and I think more BJJ schools should do stuff like this.
This isn't medical advice; I'm telling you what we did and learned, but if you want the medical detail get your own PT to do your own seminar :-)
I have been meaning to post this, and was recently reminded by discussion with u/Historical-Pen-7484 and u/viszlat, so here it is.
Our school recently did something I don't think I've heard anyone else do. Instead of hosting a coral belt or famous competitor for a seminar, we invited a local physical therapist that some of us had worked with. We called it a "PT Seminar", and it was a pretty neat time.
The premise was: the PT will watch us roll for an hour to observe BJJ in action, and then take an hour (and a bit more...) to speak to a host of relevant topics.
I preloaded him with a bunch of questions that BJJ people often ask -- stuff like, "How can I become injury resistant?" or, "How long should I stay off the mat when I'm injured?" etc.
The results were pretty awesome. We got some input from him on how we should adjust or adapt our warmups and mobility / flexibility work in class, and what we should be doing outside of class to maximize our longevity in BJJ. He took us through some diagnostic tests to evaluate for major mobility issues or weaknesses (which was fascinating), and gave some recommendations for working on some of the gaps he observed. Finally, he took a number of questions, which turned into some real back and forth. We learned a lot about our fellow students' aches and pains, and gained some insight on a lot of topics.

Detailed review:
Becoming Injury Resistant
His main recommendation was (of course?) to add two days a week of resistance and mobility training. The advice was to do moderate intensity on all the major muscle groups, emphasizing free weight compound movements to develop and maintain stability in the joints. He wasn't saying we should become body builders or power lifters, but that we needed something that isn't functionality equivalent to BJJ to round everything out. He said more than two hours a week would be another hobby, and not to get sucked more deeply than necessary into the workout crowd (unless we want to).
Warmups and Stretches
I talked with him ahead of time about different ideas in BJJ about warmups and stretches. He talked through what the medical / sports-science benefit of the warmup and stretches actually are, and used that as a basis for some recommendations for our class structure.
He advocated a minimal warmup -- that its purpose is to raise body temperature and heart rate, lubricate the joints, and psychologically prepare for physical activity. So he said it should never take more than a few minutes to warm up. He said 5 minutes is too long, and crossing over the boundary with strength and conditioning.
On the S&C point, he asked if our classes are supposed to include S&C, or if people are expected to do that on their own. Our class was more or less unanimous that we look to do BJJ during paid class time, and he suggested we should think of S&C as something we do on our own time outside of class.
Regarding stretching, he suggested avoiding static stretches during class, and he cited some research results that show static stretching actually sets you up for injury (though stretching for mobility and flexibility should include static stretches, and should just be thier own thing, he said). He took us through some examples of the kind of dynamic and active stretching he thought would be a better fit, given our functional performance goals in BJJ.
Injury Identification and Response
We had a lot of discussion about how to know when you're injured, when to decide it's a bad one, and when to invoke medical expertise. He remained pretty open minded, speaking to when a doctor should be involved, and where he thought PT fits in to maximize recovery. His main suggestion was that injuries that are healing get steadily better, and things should get attention when they flat-line or get worse over time.
Some of our students had a lot of questions about what makes a good PT, so he went into that. Just like BJJ schools have red flags, he said there are better and worse PTs out there. He said that if you go to a place that gives you a list of exercises based on your doctor's diagnosis, and has you do the same thing for awhile, it's not as good. He prefers a PT approach that applies more analysis, and makes frequent changes to the workload to accommodate changes during recovery and adapt to what is experienced by the patient.
He seemed to advocate a pretty nuanced approach to time off and return to activity. His basic logic was that the longer you spend not doing your activity, the more you atrophy, compensate with changed behavior, and settle into a worse condition. Of course, that is balanced by returning too quickly and too much, re-injuring, or aggravating your body and extending recovery.
So he kind of recommended careful re-introduction of activity, perhaps under supervision of a PT (of course), and finding as many ways to do things as you can without aggravating the injury so you don't fall behind.
I don't want to risk this seeming like a medical advice post, so I won't go into more detail. Go find your own PT and get advice from him so it's legit :-). I will just say that this was extremely valuable, and helped a lot of us frame our thinking about the next time we are hurt and how we will approach return to the mats.
Assessing Weaknesses and Problem Spots
Our PT took the group through a bunch of his basic triage / diagnostic exercises. It was very interesting -- for example, he said we were all surprisingly good on upper core strength, but most of us failed the lower core strength tests. This led to some fascinating conjecture as to why, and he spoke to how that manifests as increased risk of injury in some ways.
He did a few different tests, for mobility, strength, etc., and gave a lot of recommendations on specific details of exercises and what expectations we should have of our bodies. Some people remarked that they didn't know this or that were below normal, and it gave a bunch of us some side-goals about where we want to take our bodies in the future. Again, this is very close to medical advice, so I won't repeat a lot of it here.
Diagnosis and Q&A
Finally, he took a lot of questions, and people came out of the woodwork! Back issues, historical injuries, morphological oddities... we learned a lot about our fellow students. But we also got to see how he would inspect, and reason through what might be wrong. In some cases, he spoke to appropriate pros and cons of surgical solutions vs living with something -- all very helpful stuff!
Conclusion
It was really all I had hoped it to be. I had worked with this PT through a major injury (torn hamstring and glute), and been so impressed, I wanted to share him with the school. The end result was really excellent.
If you want to do the same thing (and I think I would recommend it for any BJJ school), it may not be that hard. I tried really hard to pay him, and when he refused money, I tried to suggest a gift in kind like an iPad or something. He said some things about professional requirements to do community outreach, etc., etc., so it turned out to be a pretty good deal. We asked attendees to throw in a couple bucks, and we took him out to eat, and that was it.
I do believe that he actually picked up four patients out of it (at least, three told me they have been to see him a time or two, and one said he was going to). We worked hard not to make it a sales pitch, and our guy was very professional about the whole thing; but nevertheless, if you want to get something similar worked out, the potential for bringing in some business might help tip the scales as you talk to your local PTs.
Someone asked if we'll do it again, and I think we will. Or might mix it up and bring in an orthopedist. Could even think about a nutritionist, sports scientist, etc.
There are so many topics that BJJ instructors or students pretend to know a lot about, but it sure makes a difference when you bring in a real expert in some domain and pepper them with questions!
submitted by jephthai to bjj [link] [comments]


2024.05.15 23:52 SicilianEggplant As of today, Reddit is displaying in desktop/mobile view by default.

It appears to load as old Reddit (white page, no dark mode resembling regular browser view). -Went to “Fix Old Reddit” and it seemed to adjust for mobile screen. -Redirect options were all off. When I check “Always load new Reddit”. this shows “sh.reddit.com” when that never appeared before, but appears to resemble how it did look.
edit: “forcing new Reddit” seems to allow promoted posts to show after trying to quit/reopen Safari (which would previously fix it if it happened)
I guess “always load new Reddit” is fine, but it wasn’t required for me before today. Did something change?
submitted by SicilianEggplant to SinkIt [link] [comments]


2024.05.15 23:45 jennasmithy0984 Statistics Course Help Reddit Online Helper for Data Analyst, Biostatistician, Data Scientist, Statistician, Research Analyst, Quantitative Analyst, Operations Research Analyst, Market Research Analyst courses class assignment Test quiz homework help Reddit take my stat class exam test reddit

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submitted by jennasmithy0984 to Statisticshelpers_ [link] [comments]


2024.05.15 23:37 toesucker_68 parents wont let me get a mobility aid

For context, i have both POTS and May Thurner Syndrome which causes lots of blood pooling in my legs on top of the pots (i don't faint with my pots, but i do tend to get dizzy). I would like to try a mobility aid because every time i go out, its painful for me to walk due to the blood pooling. If i don't sit down periodically, i tend to get very out of breath, have a racing heart, nausea, a headache and weird leg spasms. The problem is my parents, they don't think i need a mobility aid because they don't think I'm "sick enough" for one. They say they don't want myself to think I'm "disabled" and that i need exercise and that i can walk around a store. How can i convince them i feel a mobility aid will help me?
submitted by toesucker_68 to POTS [link] [comments]


2024.05.15 23:23 Brilliant-Lychee-518 Flexafen

What Is Flexafen™?

Flexafen is incredible supplement is specifically designed to provide temporary relief for those occasional aches and pains that can hold us back. With Flexafen, you can experience unrestricted movement and enjoy life to the fullest!
What sets Flexafen apart from other supplements on the market is its unique synergistic blend of nutrients. This powerful combination of ingredients works together to create a truly remarkable effect. Each nutrient in Flexafen is carefully selected for its individual benefits, but when combined, they work in harmony to provide maximum relief and support for your body.

How Does Flexafen Work?

Each capsule of Flexafen contains a combination of active substances. However, the peacemaker protein, a form of collagen linked to joint health, is the most significant active component of Flexafen.

The most prevalent connective protein in the human body is collagen. It helps to support the region around your joints. It provides your skin with organic elasticity and support.
However, as you age, your collagen levels fall, which causes joint pain. Some individuals use collagen supplements as a defence. As a result, the immune system in your body is continually attacking your joints.
Causing tissue damage to the bones, surrounding organs, and all of your cartilage. As long as these assaults continue, you will be in continual discomfort and, very frequently, in excruciating pain.
Thus, the six essential nutrients in this formula encourage prompt relief from various aches and pains. It was created to quickly ease pain, as well as to lessen stiffness and inflammation.
The unusual ingredients in this remedy help you restore control of your body without producing any unfavorable side effects.
This supplements contribution to joint flexibility improvement makes possible more fluid and unrestricted mobility. Minimizing wear and tear problems keeps your body overall functioning at a healthier rate.
This supplements main goal is to prevent Leaky Joint Syndrome and to improve motion. It preserves the collagen strands that make up the cartilage tissue in your body.
Your body instantly absorbs the nutrients in this supplement, which strengthens your immune system and helps control the production of free radicals. You can stop your body from deteriorating its joints in just 7 seconds by taking Flexafen daily.

Flexafen Active Ingredients

Flexafen contains the highest-quality, REAL research-backed ingredients, from some of the most trustworthy suppliers on the planet.

Inside each capsule of Flexafen, you will find:
  1. Collavant n2 Undenatured Type II Collagen: Collavant n2, which was previously called b-2Cool, is a type 2 collagen that is sourced from chicken sternum. It is undenatured, which means that it is a protein that hasnt gone through structural deformation. It comes from the cartilage of the chicken, and it hasnt been overly processed. However, it helps consumers to strengthen their own cartilage, which offers support and flexibility in the joints. Since collagen and cartilage both diminish with constant movement and exposure to toxins, restoring it is an important step to improving pain.
  2. Boswellia Serrata Extract: A patented synergistic blend of proprietary extracts that come from the sacred Boswellia plant, AprèsFlex has been shown in THREE separate, double-blind, placebo-controlled clinical studies. To reduce pain, stiffness, and inflammation and provide life-altering results in as quickly as 5 days.
  3. MSM: The most potent ingredient that consumers will get from the Flexafen formula is MSM, or Methylsulfonylmethane. MSM is used for a multitude of concerns, but it is especially helpful for anyone with arthritis, joint pain, or post-exercise muscle soreness. The main reason that it has such a positive effect is because of the organic sulfur that it uses. This ingredient is crucial for the building of healthy bones and joints, and it even supports the immune system with its increased production of immunoglobulins. These effects can lead to relief from allergies for some consumers.
  4. Sodium Hyaluronate: Sodium Hyaluronate is one of the most common ingredients to find in anti-aging remedies because of the profound moisture support that it provides. When the body loses its ability to effectively maintain collagen in the joints, it is almost certain that it is also seen in the skin at the same time. Collagen makes it possible for the skin to hold onto moisture as well, so introducing an ingredient that can restore what it has lost instantly improves the youthful appearance of users.
  5. White Willow Bark Extract 4:1: The white willow is a type of European willow that is also found in many parts of Asia. The name comes from the underside of the leaves, which are a stark white contrast to the vibrant green topside. In Flexafen, consumers get the support of an extract that is sourced from the bark, which contains salicin.
  6. Boron: Boron is the last ingredient of this compilation, but it is quite important to healing the joints. This chemical is only needed in small amounts, helping users to reduce their risk of joint pain and bone injuries. However, when the body doesnt get enough of it, the growth and regeneration of bone tissue can be detrimentally impacted.

Benefits of Flexafen Supplement

According to the manufacturer, taking Flexafen on a regular basis will help you achieve the following health benefits:-

submitted by Brilliant-Lychee-518 to u/Brilliant-Lychee-518 [link] [comments]


2024.05.15 23:17 gossamer_gubble54 Undiagnosed EDS and *rare* inflammatory kidney disease

I haven't been able to get an EDS diagnosis as, although all the markers are there (and some of Marfan) my bloods didn't have the correct indicators.
I have a diagnosis of HSD (which is quite bad) but also of a chronic inflammation disease of the kidneys which I've had since birth. I also had a kidney removed about 5 years ago owing to excruciating pain and ill health for a year that was seemingly undiagnosable - despite the diagnosed "disease"??! Don't even get my started on how stupid it all was, it was medical gaslighting and negligence.. however the kidney (singular) failure also did not show up in my bloodwork, or look obscure (any more obscure than usual) in the ultrasounds. Although there was visible and explainable reasons for the pain outlined by the histology report following surgery.
I therefore believe and operate under the assumption that I do have EDS.. and that my inflammation of the kidneys is also a complication of my connective tissue. I could go and get a second opinion, and I could also get genetic testing to discover if there's an issue there. For the time being, the rheumatologist did confirm there is a connective tissue problem and that's what I attempt to manage.
I struggle with my energy and mobility to a certain degree but am very lucky that I can mostly manage day to day life with some accommodations and if I go slower, bring snacks, take rests etc. It gets harder as time goes on.. and I will, at some point, go back to a rheumatologist but I kind of can't be bothered right now..
I feel as though I'm at the tipping point of my health in that, I can no longer keep up fully and I'm trying to find a new balance and find the right support. But often when I ask for help, I seem fine and get dismissed.! I am aiming to have an appointment with my new GP soon and think she's helpful and kind so will ask there too but would like to be prepared.
I'm not on any medications. I take vitamin D and sometimes magnesium and turmeric with black pepper. I'm trying to get stronger again also. Was very sad I had to give up sports, but the recovery time is just not worth it. Trying to get stronger again through exercises and hypermobile friendly stretches. I've also done a significant amount of grounding and balancing of my nervous system. I have also been tested for PCOS through several ultrasounds and do not have this.
I have four areas I'd like advice:
I've been told all my life to keep a low sodium diet for my kidneys.. and for the most part I do. But there's days I crave salt or find that I need it for physical strength (possibly POTs). I'll eat chips or salted crackers or drink pickle juice (!) if I feel like I need a quick boost or electrolytes. I've tried eating a banana or some other low salt replacement, but I really feel like I need the salt. Otherwise, I don't add salt to my food, I naturally don't like things that have too much salt. I would love to see if taking electrolytes or adding protein powder will help me feel physically stronger, but I am worried about my kidney health. Does anyone have any advice.. or can recommend what kind of diet to follow? Most doctors don't know how to help or think I'm being *dramatic* (when often I underplay how much I struggle cause hello internalised ableism). Unfortunately also my kidney specialist I had when I was a kid passed away.. and my case was too complicated for the nutritionist I saw, although he did say for the most part my diet seemed healthy.
I've been getting more flare ups recently after overexerting myself. There are a couple of factors that I can pinpoint (like drinking beer or sitting on the ground outside unsupported for too long) that can trigger a flare, but sometimes I can't tell why. Again this could be diet related, could be due to not making better accommodations on a given day or could be not resting sufficiently, dehydration etc. Does anyone know how to figure out what the triggers can be? Or if it's more related to the inflammation or EDS so can know what to manage better? Some days I seem to manage perfectly, and others I mess up and have no idea why.
Does anyone have experience getting an EDS diagnosis without the blood work markers and can offer recommendations? Long shot, but does anyone know any specialist doctors that might be interested in my case?
For whatever reason I haven't been able to get financial benefits in Ireland, even when I was severely ill and had surgery (owing to the negligence of my GP) mostly due to the complicated nature of my illness. Again - I have a diagnosed "rare" disease, that affects all my insurance, but doesn't qualify me for care or benefits?! Is there anyone in Ireland who receives benefits due to EDS and how did you go about getting this/ what process?
I can still work but can't do 40+ hours unless it's mostly remote and I can work in bed. I also can't work on my feet anymore unless it's like 1/ 2 days a week and I spend the next day in bed. I really want to work (and would, in another life, be working outdoors/ with kids and camping all the time) but am limited by my options. I'm looking for a new job now but scared of being at work 40 hours a week and asleep or in bed for the remaining time.
Sorry it's so long, any help or advice appreciated :)
submitted by gossamer_gubble54 to IrishWomensHealth [link] [comments]


2024.05.15 23:13 thelug Unifi Access First impressions

We have a small / medium setup that just went live. We have 14 cameras on Unifi Protect, 2 wireless AP’s, 8 Doors with the Enterprise Door Hub Controller, 2 G2 Pro readers, 6 G2 regular readers. UNVR, Dream Machine Pro SE, 2 Unifi Switches, & Unifi LTE Backup pro. Other than the Access system the rest of the setup has been being installed slowly over the last year.
The install and setup on the Access hub, readers, new magnets, existing magnets, latches etc. was very easy, straight forward, and a breath of fresh air. Setup and integrations that would have saved me time.
While I installed the Access system, I also moved from the internal DMPSE drive for Protect to the UNVR. The transfer process for this to the UNVR was easy and seamless. When I setup the new Access install, I initially set it up on the DMPSE not thinking that I would need / want the system to be on the UNVR. I then realized the UNVR & DMPSE don’t cross talk for video storage (That is really annoying btw that I must have multiple console entries in the drop down for one location. If I have a DMPSE & another UNVR or Cloud Key it should intelligently integrate. When I realized I needed the Access app moved to the UNVR as well I discovered the process was time consuming and not as easy. There was no transfer process. I had to press the reset button on the Enterprise Hub, and every reader, then re-adopt on the UNVR. Luckily, I caught this before anything was really setup and configured.
Next step was adding about 1200 users… ugh… so we made the hard decision and decided to not import any old data and do it fresh, there were some pain points. The Unifi Access system has very limited data entry points. Just first name, last name, email, and employee ID. Very disappointing that we couldn’t add more fields like phone number, address etc. When adding users via the web browser there is no ability to send an Identity email invitation. You must open the Access phone app to send the invite. The Access phone app also doesn’t allow you to enter the email address when creating a new user. So, you are stuck with using the browser and the phone to send Identity invites.
TLDR: The Not So Good:
Things below that need to be better are mainly the interface of the apps.
No ability to send Identity app invite from web browser on computer.
No ability to add email on Access phone app.
Limited data fields for user accounts in access.
Having a Dream Machine Pro SE & UNVR forces 2 separate console interfaces. If I had access and protect installed on the DMPSE I would only have one console. Adding another console like a UNVR should just extend the features, storage etc.
It would be nice to be able to have continuous recording from the G2 Pro Readers and treat them like an additional IP Camera. The Doorbell Pro does this already.
No ability to set an expiration date to regular accounts only visitor accounts.
The good:
Plug n Play easy setup Integration was great with other Unifi products (except the one complaint above about multiple consoles)
System is fast and easy to use for users and admins.
Phone app feature is great for user that don’t want a FOB or a Key Card.
Minimal hardware needed mounted in the closet.
G2 Pro reader is very nice just a little pricey.
Happy to answer questions on the setup. Also, welcome suggestions.
submitted by thelug to Ubiquiti [link] [comments]


2024.05.15 22:55 gossamer_gubble54 Undiagnosed EDS and *rare* inflammatory kidney disease

I haven't been able to get an EDS diagnosis as, although all the markers are there (and some of Marfan) my bloods didn't have the correct indicators.
I have a diagnosis of HSD (which is quite bad) but also of a chronic inflammation disease of the kidneys which I've had since birth. I also had a kidney removed about 5 years ago owing to excruciating pain and ill health for a year that was seemingly undiagnosable - despite the diagnosed "disease"??! Don't even get my started on how stupid it all was, it was medical gaslighting and negligence.. however the kidney (singular) failure also did not show up in my bloodwork, or look obscure (any more obscure than usual) in the ultrasounds. Although there was visible and explainable reasons for the pain outlined by the histology report.
I therefore believe and operate under the assumption that I do have EDS.. and that my inflammation of the kidneys is also a complication of my connective tissue. I could go and get a second opinion, and I could also get genetic testing to discover if there's an issue there. For the time being, the rheumatologist did confirm there is a connective tissue problem and that's what I attempt to manage.
I struggle with my energy and mobility to a certain degree but am very lucky that I can mostly manage day to day life with some accommodations and if I go slower, bring snacks, take rests etc. It gets harder as time goes on.. and I will, at some point, go back to a rheumatologist but I kind of can't be bothered right now..
I feel as though I'm at the tipping point of my health in that, I can no longer keep up fully and I'm trying to find a new balance and find the right support. But often when I ask for help, I seem fine and get dismissed.! I am aiming to have an appointment with my new GP soon and think she's helpful and kind so will ask there too but would like to be prepared.
I'm not on any medications. I take vitamin D and sometimes magnesium and turmeric with black pepper. I'm trying to get stronger again also. Was very sad I had to give up sports, but the recovery time is just not worth it. Trying to get stronger again through exercises and hypermobile friendly stretches.
I have four areas I'd like advice:
I've been told all my life to keep a low sodium diet for my kidneys.. and for the most part I do. But there's days I crave salt or find that I need it for physical strength (possibly POTs). I'll eat chips or salted crackers or drink pickle juice (!) if I feel like I need a quick boost or electrolytes. I've tried eating a banana or some other low salt replacement, but I really feel like I need the salt. Otherwise, I don't add salt to my food, I naturally don't like things that have too much salt. I would love to see if taking electrolytes or adding protein powder will help me feel physically stronger, but I am worried about my kidney health. Does anyone have any advice.. or can recommend what kind of diet to follow? Most doctors don't know how to help or think I'm being *dramatic* (when often I underplay how much I struggle cause hello internalised ableism). Unfortunately also my kidney specialist I had when I was a kid passed away.. and my case was too complicated for the nutritionist I saw, although he did say for the most part my diet seemed healthy.
I've been getting more flare ups recently after overexerting myself. There are a couple of factors that I can pinpoint (like drinking beer or sitting on the ground outside unsupported for too long) that can trigger a flare, but sometimes I can't tell why. Again this could be diet related, could be due to not making better accommodations on a given day or could be not resting sufficiently, dehydration etc. Does anyone know how to figure out what the triggers can be? Or if it's more related to the inflammation or EDS so can know what to manage better? Some days I seem to manage perfectly, and others I mess up and have no idea why.
Does anyone have experience getting an EDS diagnosis without the blood work markers and can offer recommendations? Long shot, but does anyone know any specialist doctors that might be interested in my case?
For whatever reason I haven't been able to get financial benefits, even when I was severely ill and had surgery (owing to the negligence of my GP) mostly due to the complicated nature of my illness. Again - I have a diagnosed "rare" disease, that affects all my insurance, but doesn't qualify me for care or benefits?! Is there anyone in Ireland who receives benefits due to EDS and how did you go about getting this/ what process?
I can still work but can't do 40+ hours unless it's mostly remote and I can work in bed. I also can't work on my feet anymore unless it's like 1/ 2 days a week and I spend the next day in bed. I really want to work (and would, in another life, be working outdoors/ with kids and camping all the time) but am limited by my options. I'm looking for a new job now but scared of being at work 40 hours a week and asleep or in bed for the remaining time.
Sorry it's so long, any help or advice appreciated :)
submitted by gossamer_gubble54 to eds [link] [comments]


2024.05.15 22:22 AnybodyOk1528 Sensitive gums post op: gum cap?

Hi y’all! I’ve been browsing around this thread during my recovery and wanted to share my concerns.
For a lil context: I’m 7 days post-op, got my 4 teeth out on local anesthesia. Got 3 stitches (2 on the left side and 1 on the right). I overall feel good, and haven’t swollen to much on the right side, and I can eat with no disconfort or pain. On the left side, my mobility is more limited and I’m still a lil chubby (this side really swelled up compared to my right side).
Anyways, my concerns is about my gums on the left side. The gum in between my cheek and molar « grew upwards » and doesn’t seem to go down. It is sensitive, red, and « floppy » I guess, kinda like a gum cap (not sure?): I can move it to access my teeth but it’s still attached and sensitive so I try not to.
Have any of you experienced the same thing ? I couldn’t find anything like this and don’t know if it has a name or anything.
Apologies for the gross photo but I feel like it’s more explicit this way.
submitted by AnybodyOk1528 to wisdomteeth [link] [comments]


2024.05.15 22:21 Next_Relative_1230 [Here's Way To Watch]* tyson Fury vs Oleksandr Usyk Full Fight Live Streams, Free ON TV Channels

There's only a few days until the biggest fight of 2024.
The long-awaited fight is almost upon us.

Tyson Fury vs Oleksandr Usyk- Reddit Live Stream

Tyson Fury vs Oleksandr Usyk- Reddit Live Stream

Tyson Fury, the WBC champion, and unified heavyweight champ Oleksandr Usyk, meet on Saturday in Saudi Arabia.
The winner will become the first undisputed heavyweight champion of the world in the four-belt era.
Before then, there's a stacked undercard, shown live on DAZN PPV.
Here's everything you need to know ahead of Fury vs. Usyk.
Fury vs. Usyk fight date, start time
Date: Saturday, May 18
Time: 5 p.m. UK / 2 p.m. ET
Main event ringwalks (approx): 11:05 p.m. UK / 6:05 p.m. ET
The Fury vs. Usyk ringwalks are scheduled for 11:05 p.m. UK / 6:05 p.m. ET with the main card set to begin at 5 p.m. UK / 2 p.m. ET. These timings are subject to change.
Can I watch Fury vs. Usyk on DAZN?
Fury vs. Usyk will be available on DAZN PPV in over 200 countries across the globe. You can sign up and purchase here.
Full details of the PPV prices can be found here.
What devices are supported by DAZN?
DAZN has apps available for all of the following platforms: Apple TV, Chromecast, Amazon Fire TV, Amazon Fire Stick, Amazon Fire Tablet, Android Phone & Tablet, iPhone & iPad, Android TV, LG, Smart TV, Panasonic Smart TV, Samsung Smart TV, Sony Smart TV, SmartCast, Xbox One, Xbox Series XS, PlayStation 4, PlayStation 5 and Roku.
Here is a full list of the devices where DAZN is available, in addition to web browsers on DAZN.com (if you are in Argentina, Chile and Colombia you must download the DAZN app from the Apple App Store or Android Google Play store and then sign up from there, rather than via web browser):
Mobile Devices TV & Streaming Devices Game Consoles
iPhone, iPad Amazon Fire TV Stick PlayStation 4
Android phones, tablets Android TV PlayStation 5
Amazon Fire tablet Apple TV XBox One
Google Chromecast XBox Series X S
Hisense
LG Smart TV, Smartcast
Panasonic, Samsung & Sony Smart TV
Philips, Roku
Vestel
Vizio
Where is the Fury vs. Usyk fight?
The fight will take place at the Kingdom Arena in Riyadh, Saudi Arabia.
Fury vs. Usyk odds
Tyson Fury: -120
Oleksandr Usyk: +100
Odds are correct as of Monday, May 13 and are supplied by DraftKings.

Tyson Fury record and bio
Nationality: British
Date of birth: August 12, 1988
Height: 6' 9"
Reach: 85"
Total fights: 35
Record: 34-0-1 (24 KOs)
Oleksandr Usyk record and bio
Nationality: Ukrainian
Date of birth: January 17, 1987
Height: 6' 3"
Reach: 78"
Total fights: 21
Record: 21-0 (14 KOs)
Fury vs. Usyk fight card
Tyson Fury vs. Oleksandr Usyk: For the IBF, WBA, WBC and WBO heavyweight titles
Jai Opetaia vs. Mairis Briedis; For the vacant IBF cruiserweight title
Joe Cordina vs. Anthony Cacace; For Cordina's IBF super featherweight title
Frank Sanchez vs. Agit Kabayel; Heavyweight
Moses Itauma vs. Ilija Mezencev; Heavyweight
Mark Chamberlain vs. Joshua Wahab; Lightweight
Sergey Kovalev vs. Robin Sirawn Safar; Light heavyweight
Daniel Lapin vs. Octavio Pudivtr; Light heavyweight
David Nyika vs. Michael Seitz; Cruiserweight
Isaac Lowe vs. Hasibullah Ahmadi; Featherweight
The heavyweight rivals have been on a collision course for more than a year having initially been pencilled in to clash at Wembley last April. Terms could not be agreed on that occasion and the fight was pushed back until two days before Christmas, only for Fury's life-and-death fight with Francis Ngannou to put a spanner in the works.
Fury and Usyk agreed to push their meeting back until February 17 only for the Brit to suffer a cut above his eye in one of his final sparring sessions. A new date was quickly agreed with both men now in Saudi Arabia ahead of Saturday night's showdown. Here is everything you need to know about the clash...
What UK time will Tyson Fury vs Oleksandr Usyk fight start?
Tyson Fury and Oleksandr Usyk will likely walk to the ring at around 11pm UK time on Saturday night, which will be 1am in Riyadh, Saudi Arabia. But as fans experienced when Anthony Joshua fought Francis Ngannou in March, the first bell could ring after midnight in the UK, meaning a late night for fight fans. The ultimate start time will depend on how long the undercard fights take to complete. The first fights of the day will start at around 2.45pm in the UK with the official undercard kicking off at 5pm.
How to watch Tyson Fury vs Oleksandr Usyk fight via TV channel and live stream
This article contains affiliate links, we will receive a commission on any sales we generate from it. Learn more
Watch Tyson Fury vs Oleksandr Usyk
Watch Tyson Fury vs Oleksander Usyk live on DAZN
PPV is £24.99 and includes one month of a DAZN subscription.
Tyson Fury and Oleksandr Usyk are set to lock horns in a huge bout on May 18 with each fighter attempting to etch their name in boxing history as the first undisputed heavyweight champion since 1999. The stakes couldn't be higher as the pair will go head to head for the prestigious WBC, WBA, WBO, and IBF titles.
DAZN
Get it here
Tyson Fury vs Oleksandr Usyk will be available on DAZN, TNT Sports Box Office and Sky Sports Box Office. Click the link above to watch on DAZN or visit TNT Sports' website to watch their coverage. Fury v Usyk on TNT Sports Box Office costs £24.99 in the UK and can be watched on discovery+, EE TV, Virgin Media TV and Prime Video. You do not need to be a TNT Sports subscriber to buy this event.
Full fight card and undercard
Oleksandr Usyk vs Tyson Fury
Tyson Fury will throw his world title up in the air along with Oleksandr Usyk's three belts with the winner of their undisputed fight becoming the first man in the division's history to hold all four belts at one time.
Fury vs. Usyk fight date, start time
Date: Saturday, May 18
Time: 5 p.m. UK / 2 p.m. ET
Main event ringwalks (approx): 11:05 p.m. UK / 6:05 p.m. ET
The Fury vs. Usyk ringwalks are scheduled for 11:05 p.m. UK / 6:05 p.m. ET with the main card set to begin at 5 p.m. UK / 2 p.m. ET. These timings are subject to change.
Can I watch Fury vs. Usyk on DAZN?
Fury vs. Usyk will be available on DAZN PPV in over 200 countries across the globe. You can sign up and purchase here.
Full details of the PPV prices can be found here.
What devices are supported by DAZN?
DAZN has apps available for all of the following platforms: Apple TV, Chromecast, Amazon Fire TV, Amazon Fire Stick, Amazon Fire Tablet, Android Phone & Tablet, iPhone & iPad, Android TV, LG, Smart TV, Panasonic Smart TV, Samsung Smart TV, Sony Smart TV, SmartCast, Xbox One, Xbox Series XS, PlayStation 4, PlayStation 5 and Roku.
Here is a full list of the devices where DAZN is available, in addition to web browsers on DAZN.com (if you are in Argentina, Chile and Colombia you must download the DAZN app from the Apple App Store or Android Google Play store and then sign up from there, rather than via web browser):
submitted by Next_Relative_1230 to GranTurismohdfr [link] [comments]


http://rodzice.org/