To cope with the struggle of living in Canada in 2025, I have simply blacked out anything that's happened after 2018
2025.01.23 19:02 Red_Alert-Red-Alert To cope with the struggle of living in Canada in 2025, I have simply blacked out anything that's happened after 2018
For me, 2018 was the last truly good year....because that was when I discovered the glory of the anime Cat Planet Cuties, and also samurai girls.....so every single day is 2018 to me. It's just like how people yearn for the 80s, which was only 20 years ago (and the 90s were only 10s years ago and don't you ducking say otherwise).
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2025.01.23 19:02 Glustrio42 MITES Semester Application Webinar
Hey everyone! This summer, I participated in MIT’s Introduction to Technology, Engineering and Science (MITES) and many of my Alumni friends wanted to host an “Application Advice” webinar on Zoom for current Juniors applying to the program.
We’ll be answering any questions that current applicants have about the application, and overall MITES experience. We will also give an informational presentation on some key details about the program itself.
We want to do this because 1.) We get asked too many questions and 2.) We wanted to give applicants a chance to learn more about the application and program. Most applicants aren’t aware of the MITES Applicant Discord Server so we want to help as many people as we can who simply haven’t had access to outside help on the application.
So, if you are a current Junior applying to MITES, we strongly encourage you to attend this webinar and ask ANYTHING you’d like to know about MITES. We really want to help y’all make the best applications you can and we want to see MITES continue to grow and evolve.
The event will be this Sunday, January 26th, from 5-7 PM EST. We truly hope to see you there.
The Zoom link to the Webinar will be posted in the MITES Applicant discord server so be sure to join it if you haven’t already! Here is the link: https://discord.gg/KHeeeqJA
Please note that this is NOT an official MITES-hosted webinar, this is just the MITES Alumni community wanting to do something fun and engaging for the applicants.
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2025.01.23 19:02 woozle618 Strut/shock question
Hey all, I’ve searched the sub and didn’t find answers.
Can anyone confirm that the Bilstein 4600 struts and shocks for 2011-2015 will fit a 2018?
-3.6 in both -RockAuto shows some struts and shocks for both years but the Bilsteins only show for 2015
Would any of these be comparable or even better?
Rancho KYB OME
Thanks in advance. Just looking for some quick info and will delete the post.
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2025.01.23 19:02 LogPresent2289 The Braindead ABA Character You're Not Using
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2025.01.23 19:02 Silly_Speed211 Day 1 - 180 mg oxy/day …
Feeling so rough. Please … how do you guys do this and not relapse? I have nothing to help me.
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2025.01.23 19:02 MachineProof2351 selling plab 2 april seat 2025
anyone willing to buy plab 2 29th april 2025 seat? i have some visa issues so im gonna cancel
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2025.01.23 19:02 lss_web_1444 AMA post title 914
AMA post body
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2025.01.23 19:02 Rebulah-Racktool Tesco stores in Northern Ireland will be closed tomorrow
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2025.01.23 19:02 theatlantic A Possible Substitute for Mifepristone Is Already on Pharmacy Shelves
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2025.01.23 19:02 Gonzalez824 Sarah’s look for ‘Paradise’ press day | IG 1-23-25
 | Via @sarahshahi/Instagram submitted by Gonzalez824 to SarahShahi [link] [comments] |
2025.01.23 19:02 kippergee74933 Sons Of Mr Green Genes – The Connolly's Session – Cassette (Mini-Album), 1996 [r3359067] | Discogs
Links related to Cillian,'s band days. The demo record was recorded at the restaurant and music venue called Connolly's of Leap in Cork, Ireland (https://www.facebook.com/share/1AELHNXnH4) in 1996. These links have the track list etc.
Sons Of Mr Green Genes - The Connolly's Session
https://www.discogs.com/release/3359067-Sons-Of-Mr-Green-Genes-The-Connollys-Session
Cillian describes their music: https://youtu.be/X9MNhDg_nOc?si=v2ltQMPXARUhFpIQ/
https://www.discogs.com/release/3359067-The-Connollys-Session/history#latest
https://i.discogs.com/Ml5mpblCIznHJuO5MQ1hUwr1GxD4b93uEZFf9mPgMhQ/rs:fit/g:sm/q:40/h:300/w:300/czM6Ly9kaXNjb2dz/LWRhdGFiYXNlLWlt/YWdlcy9SLTMzNTkw/NjctMTYxMTMzMDIz/MC03MzY0LmpwZWc.jpeg
There is a video .
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2025.01.23 19:02 InsanityXo98 Does anyone know what this light effect is called?
in which the light points turn into circles
https://www.istockphoto.com/photo/traffic-jam-gm465397588-59124498
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2025.01.23 19:02 Titanium6790 Outdoor Day
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2025.01.23 19:02 reddit_lss_1 Test Title 2025-01-23 19:00:56
 | Test body 2025-01-23 19:00:56 submitted by reddit_lss_1 to lssAuto [link] [comments] |
2025.01.23 19:02 lss_web_1444 Text post title 661
Text post body
submitted by lss_web_1444 to automationContentCom [link] [comments]
2025.01.23 19:02 ekkthree front vs rear porting?
with front center, L and R in (not on) a console, how much difference does porting make whether is ported out the front vs the rear? fwiw, the console is partially open in the rear.
for example, the triangle borea br03 vs the svs ultra evo bookshelfs
https://trianglehifi.us/products/enceinte-bibliotheque-hi-fi-borea-br03-paire?variant=42910258921506
https://www.svsound.com/products/ultra-evolution-bookshelf
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2025.01.23 19:02 bunny_jc can i manipulate you?
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2025.01.23 19:02 EMPwarriorn00b What are the advantages of administrative, feudal and range governments?
I just managed to adopt centralized administration, but I noticed that I still have decisions that would allow me to switch to either a feudal or a range government. Is there going to be any advantage to switching away from an administrative government to either of these government types?
submitted by EMPwarriorn00b to AfterTheEndFanFork [link] [comments]
2025.01.23 19:02 _ABlaine Tips for crib training?
My 7 month old and I co sleep but I would love any advice to get him in his crib. I’m happy to continue to co sleep at night or do a combo of crib sleeping and co sleeping. But, for my own sanity, I need some independent sleep.
From when he was born to now, he has been a very dependent sleeper and heavily prefers sleeping with me than with dad (dad helps with some naps but we follow safe sleep 7 so only I sleep with the baby at night).
The longest he’s slept in his crib is about 20 minutes, I’ve been trying for about a month and he won’t go past that.
I have tried drowsy but awake, fully fed and lay down awake, asleep but wake him a bit in transition, fully asleep. I’ve bought the lullavibe (he hated that), we’ve tried different sleep sacks, and we’ve heated the bed, and we’ve slept with his sleep sacks and sheet so our scent is there.
I’m really tired and desperate. Please share any advice or tips.
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2025.01.23 19:02 electronzapdotcom Simple Test Of Voltage Boost Converter That Is Potentially Dangerous
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2025.01.23 19:02 donofdebt Fitzgerald Advisors - Post
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2025.01.23 19:02 bevscomics Meet Articuno!! [OC]
![Meet Articuno!! [OC]](https://preview.redd.it/riz3r4i8ksee1.jpeg?width=640&crop=smart&auto=webp&s=0c80ba8e386724e0bdf8583bbcf0cfff57959306 "Meet Articuno!! [OC]") | submitted by bevscomics to comic [link] [comments] |
2025.01.23 19:02 stitchinthyme9 Mother newly diagnosed
TL;DR: My mother, who lives alone, was diagnosed with Alzheimer's yesterday. Where do we go from here?
Quick background: I'm an only child who was raised by my single mother; she has two sisters who are much younger than her, one of whom she's close to. She was very neglectful of me when I was a kid, so I have never felt close to her, and as an adult I have been in fairly low contact -- I live 200 miles away from her, see her a few times a year, and talk on the phone as infrequently as I can get away with. We do text sometimes, as well.
Just before Christmas, my mother's ex, with whom she has remained friends, emailed me to alert me to some concerns he had about her memory and cognition. She seemed mostly normal when I visited her for Christmas, so I thought he might be exaggerating a bit, but he suggested that I contact my aunt, who sees her a lot. (I hadn't been in touch with this aunt in many years for reasons unrelated to any of this.)
So, I took his suggestion and talked to my aunt, and what she told me was seriously concerning. For instance, my mother had told her that "a man and a woman" were going to be visiting her and she wasn't sure who they were -- that was me and my husband. Also, she'd been in a minor car accident last summer (which I did know about), and my aunt shared the police report with me, which said my mother had tried to make a right turn from the middle lane and hit a car in the right lane, and that she didn't seem to recall events leading up to the accident. For the first time in my life, she didn't remember when my birthday was. She also didn't recognize her other sister (the one she's not as close to) at Thanksgiving, or remember exactly how many sisters she has. This level of her symptoms started around last summer according to my aunt, but I didn't notice anything unusual when I visited her in August.
I talked to my mother about her memory problems when I was there at Christmas, and she seemed receptive, so I told her that I was going to call her doctor and see about getting her in for some tests -- I told her I would even go up there personally to take her for them, and she agreed. Her doctor ordered an MRI and some bloodwork, and her ex took her for those; they didn't show anything abnormal, so the doctor referred her to a neurologist and called them personally to get them to take her this week.
When they called her to confirm that appointment she nearly canceled it, but my aunt and I talked her down and I took her there yesterday. They gave her a cognitive assessment and she scored 10 out of 30. Diagnosis: Alzheimer's. I did a little research online and based on her symptoms, my inexpert opinion is that she's probably around stage 4 (defined as "moderate cognitive decline/mild dementia"). The doctor said the only medication available is probably not a great idea because the side effects will likely outweigh any benefit.
After the appointment, I asked my mother if she heard or understood anything the doctor was saying to me, as she was in the room the whole time. She didn't; she just kept saying there's nothing wrong with her and we all think she's crazy but she's not. She doesn't know about the diagnosis and probably won't believe it if we try to tell her -- she's likely to just say the doctor is an idiot. We're still trying to work out the best way to ease her into it, but I'm honestly not sure she even has the capacity to understand it now.
So now that we have a diagnosis, there are a few immediate problems.
First: The doctor also said she should not be driving, and ordered a driving assessment; since I don't live nearby I hid the order in her house and told my aunt where it is, but I'm still not sure that anyone will be able to get her to actually go. I could go scorched-earth and report her to the DMV in her state, but I'm worried it will completely destroy whatever trust she has in me after she was so mad at me about the neurologist appointment (because she thought I'd scheduled it behind her back, though I had told her about it). Her sister, ex, and I are her entire support system. Her sister does her best to discourage her from driving and takes her out shopping every week, but she still has a car and a valid license. I suspect she's not driving much because she doesn't remember how to get to places, but it's still a worry that she has the car.
Second: I think she has an advance medical directive, but I'm pretty sure she doesn't have a power of attorney. A year ago I could definitely have gotten her to sign one, but I literally spent half of this week's visit to her convincing her that I am, in fact, her daughter. It's like she knows I'm important to her, but she doesn't remember exactly why; she even asked me my name twice. Plus, she has always had a suspicious and distrustful nature, and the dementia is only making it worse. So I'm not 100% sure I could get her to sign a POA. (I wouldn't even care if it was me listed on it; I'm fine with it being her sister instead. But she doesn't trust her sister completely either.)
Third: Her living situation is stable for the moment, but only because her sister helps her a lot. She sees her once a week (to take her shopping), but they talk on the phone multiple times a day, and my aunt has been known to go to her house to check on her if she doesn't answer the phone. She also checks all my mother's bills and helps her pay them, makes sure she's taking her meds correctly, checks on the food in her fridge to make sure nothing is bad...so yeah, I think my mother would be in serious trouble if not for her. She's keeping me informed on how my mother is on a daily basis.
So I'm not sure what, if anything, I should do right now. I do know that when we get to the point where she can't live on her own, I am not going to move her in with me. While I care about what happens to her, I just can't live with her for my own sanity's sake. We've always gotten along a lot better when we're not under the same roof. But there's no way she will ever consent to any sort of community/assisted-living situation without a fight unless her personality changes a lot.
Anyway, I'm still processing all this; I basically went from thinking she was fine to discovering she has Alzheimer's in the space of less than a month. Part of me feels guilty for being so low-contact with her that I never noticed it before this (she's very good at hiding it when you only see her for a short time), but I also believe that my distance from her is largely her own fault -- she had the chance to bond with me when I was growing up and threw it away. But either way, I'm one of the few people she has, and I am not cruel enough to abandon her now.
Not sure what I'm looking for here...advice? Commiseration? Comfort? Maybe a bit of all three.
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2025.01.23 19:02 Mohaimin66 CPAP Leakage
 | Hi everyone , My wife has been using CPAP (Airsense 11) for past 10 days. Here’s the leakage data in the screenshot. We need advice for below queries:
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2025.01.23 19:02 No_Bother3564 Endo not helping after starting levo and feeling awful :(
Hello everyone, I was diagnosed with Hashimoto’s and subclinical hypothyroidism back in November. For the past couple years, my TSH has been around 4.8-5 and my pcp had said it was just mildly elevated but to keep an eye on it. Over the past year or so I have been starting to have symptoms of hypothyroidism so at my most recent annual exam, she recommended that I see an endocrinologist.
At my endocrinologist appointment in November, My TSH was 5 and my thyroid antibodies was 89 so she stated that I definitely have Hashimoto’s and my thyroid level wasn’t super high so I could either wait it out or medicate and see if the medication helped. Since I had been feeling so awful (severe brain fog, fatigue, hair, loss, rashes, acne, irritability, unwarranted anxiety) I decided to try the levothyroxine 25 mg. I never take medicine so I was hesitant but feeling so bad that I decided to give it a try. The first day I tried itc i felt like a brand new person, I had so much energy and I felt great. This lasted for a couple weeks and slowly started to taper off. At my check up with my endocrinologist in December, my TSH was down to 1.8 so she stated that the medicine had been working at this point. I still felt pretty good at that point, however, one month later (now) now I am feeling like I did before I even started the levothyroxine. I am fatigued, irritable, have unwarranted anxiety, my rashes are back. I should also add that since starting levothyroxine I have been constipated where I have never been constipated before and I am also gaining weight and I never have had issues with gaining weight prior to starting the levothyroxine.
I reached out to my endocrinologist stating these symptoms and she said it was not due to my thyroid and then I should check in with my PCP. My PCP then said that it is thyroid related and to reach back out to my endocrinologist. I asked my endocrinologist if I should go off of the levothyroxine and she said that she doesn’t recommend it as my symptoms will most likely get worse, but I could try it for six weeks and see how I feel. Should I try going off of the levothyroxine since my numbers are technically low enough? Should I ask her to try a different medication? I’m so frustrated because I was so hopeful that I would feel better and now I’m worried about making my thyroid worse. Thanks
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