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My current room I actually found through this very subreddit and honestly was a great find until the past few weeks. A sudden water leak, and very slow fixing by the contractors means I'm in need of finding a new place.
Currently looking on all the usual listing portals, FB Marketplace and housing groups, UofT rentals website.
However, it worked once, and maybe it will work a second (and not have a huge water leak this time)? Either way, I appreciate any comments and recommendations.

We’ve used coldwell banker agents through the entirety of our search.
During this time they’ve:

1. Encouraged us to buy a home with massive termites nests, asbestos, and leaks in the ceilings. 100k under our budget and told us to bid 60k over ask. The home isn’t even livable.
   
2. During reviewing homes they have scheduled showings then move our showing literally during it so that they can show it to brokers.
   
3. They’ve lied about what offers are on houses so that we can’t throw an offer at ask that and sat on the market in and we come to find out almost every instance of working with this agent there’s dual agency going on. Meanwhile the listing agent is putting offers in herself on a house while asking potential buyers at the open house what they wish to put in as an offer.
   
4. They have NOT presented our offers to clients we had to call the listing agent directly to which we’re told “there was never an offer we knew about.”
   
5. Discouraged us from putting offers in on homes not within their group.
   

*the one office we were using has been a nightmare of them manipulating listings and the market as well as lying to both home sellers and potential owners. We are now working with a friend that has been great and honest but please vet your agents we thought we did.

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Checked my coolant levels before going for a drive , it was within normal and closer to the max line..After about an hour drive, coolant levels are really low, below the minimum level even..car didnt overheat...I saw some of the coolant in the bonnet of the car..not much but you can see there was a coolant leak..unfortunately the check engine light came on during the drive, saw a bit of smoke from my tail pipe too ..read the CEL and saw P0420 ( catalytic efficiency below threshold bank 1) ..
It's a 2011 citreon exclusive 1.6l petrol engine.
what could be wrong?

Hi so I have been leaking for months. But these past month has been extreme with urinary frequency and urgency. Non stop needing to pee after I just did
I ruled out any bacterial infection and masses/tumors with tests. They think it’s OAB.
I have been struggling so much lately and I think I have myself a hemorrhoid because of it. I have been prescribed meds and I’ll start taking them today based off of people’s reactions in here. I start a new job next week and I’m soooo effing nervous. It’s on a farm and I’m so scared I won’t be able to work with this OAB.
Does anyone have any suggestions and natural remedies that may help?

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[worker0] internal there are remaining allocations on the jobtempalloc, this is a leak and will impact performance.
[worker0] to debug, run app with-diag - job temp memory leak validation cmd line argument. This will output the callstacks of the leak allocations
is it something i should worry about?? and how do i fix it

The newly installed water valve for the kitchen faucet was leaking unnoticed for a month, it was a small leak, when I opened the lower kitchen cabinet for the first time after the installation I saw this.
The water was leaking in the small space between the brick wall and the thin wood sheet.
The small black line in the lower half is white scraping off the wet wood sheet after I tried cleaning it.
The dots in the upper half were easily removed by vinegar.
​
It smelt bad, but I stopped the leak dried the space as much as I could but the smell kept persisting, so I cut off the thin wood sheet, and it revealed some mold on the surface of the brick wall which cleaned easily after spraying with vinegar and wiping, this is how the space looks now.
After waiting a while for the smell to disappear, it didn't and then I also noticed small surface mold in the interior of the nearby cabinets to this one, which kept reappearing after cleaning them but in different spots.
Which leads me to believe that there is more mold behind which I can't see or easily access.
Luckily the lower cabinets are raised off the floor about 8 inches by metal legs, so the bottom of the wood cabinets didn't touch the water directly and the floor underneath is ceramic.
The lower portion is covered by black plastic baseboards you see in this picture. Which aren't removable but I am willing to break them to reveal the floor if necessary.
The top of the cabinets is cultured marble which is caulked to the wall and glued to other marble pieces, which makes it very hard to move the lower cabinets.
​
I am in the middle east as per the sub rules, I tried searching online for mold services but couldn't find any.
​
How can I solve this? any input is appreciated.
​
TLDR: Leaky valve in lower kitchen cabinets between the wall and cabinets and into the floor - mold most likely grew in places hard to access - what is the procedure in this situation?

Welcome to MTVChallenge's Daily Discussion Thread. ☀️
Comments can be about The Challenge...or not! You've entered the MTVChallenge pub where anything goes. The only rule for these threads is **NO unaired spoilers**!!
Leaks from the set of Ride or Dies can be seen right here and discussed on any of the TMI Tea-sday threads or 💣Spoiled🌋 episode threads.

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I had a lap in 2021 and never had an ultrasound since then. My hospital sucks and endo care is lacking. But I can't go anywhere else unfortunately. I live in Europe, I'm 38 and only have 2 hospitals nearby that have endo specialsts. So in my hospital there's currently only 1 specialst available cause the other one is burned out.
I have stage 4 endo and adeno with kissing ovaries, uterus/bowel adhesions, bowel is in a weird loop because of this and my ovaries are also stuck to my uterus. My ovaries are weak and all they've done in 2021 was drain the right ovary and excising the left one. So it was a matter of time before the right one would return. They didn't do anything else, they didn't handle the adhesions because I was told to try ivf, and then get another surgery if necessary. I couldn't try ivf cause I also suffer other illnesses and couldn't do it.
They kinda knew I would prob need a hysterectomy and a bowel resection in the future so it was our plan to do only the necesarry to keep fertility and minimal damage. Colorectal surgeon attended and said that it's safe and bowel looks ok. Bowel is in a weird loop but looked ok. There was no sign of deep endo in my bowel. Just a nodule on top of it. Idk why they didn't care to remove that nodule. I guess because I wasn't in any bowel pain back in 2021.
Since a week ago I'm in daily ovary pain and the last few days it's very sharp stabbing pain. Especially when sitting down. It feels like it's being pulled when I sit. And it radiated to the inside of my leg and also my calf. At night in bed it's the worst cause I can't sleep on my side because of it. My hip and leg, and buttock also started to hurt and feels like sciatica. I've had that before 2021 as well. That's kinda what led me to endo diagnosis.
Hospital told me waiting lists to see the doctor are huge and I tried going to another hospital. But waiting lists are 120 days there as well. That's just not ok. So Im sticking to my current hospital.
I wonder when it's time to go to urgent care? I can't wait for an appointment for 4 months with this pain. They already see me as this demanding patient cause I speak my mind. I've seen multiple hospitals in 2021 because I doubted their expertise. And they felt so offended by it back then. I ended up getting surgery with them after all, cause it was closeby. The hospital that doesn't really seem to care about their endo patients cause time is money here. It is really bad. The gyno is so stressed out. We don't have specialsts who just handle endo here. They're all gynos with endo interest. I absolutely hope that will change in the near future. (this popular TV programme is giving endo attention today so I'm Def going to watch it tonight)
The other hospitals I've gone to had the exact same horrible endo care as my current one. And it was close by. None of them ever listened to my pain, none of them listened when I told them hormones are making me sick and I have other stuff going on. It feels like a full time job to handle the interactions, side effects and other chronic illnesses I have. And I have a few.
I suspect MCAS and/or Lupus. Saw a rheum last year who did ANA. No auto immune disease, according to her. But I'm getting worse by the day. Gp isn't helping anymore. She said she's done whatever she could and I've seen all the specialsts. I haven't. But oh well.
Anyway.. When do you visit urgent care? When is it legit? My hospital has a gynochology urgent care number, mainly used for pregnant women, offcourse. And I've rang them several times in the past. But they looked at me like my pain is no big deal. And had me wait 3 hours. Turned out the endometrioma was leaking and they thought that was normal. I was losing tiny bits of dark old blood everyday. And there's a lot of discharge again. But no old blood. They were convinced it wouldn't rupture cause it was too adhered and couldn't move.
I doubt myself heavily. Tell myself it's no big deal. But my periods are changing. The last 3 times I've had a cycle of 41 days. Normally they're 26 days. I told them this but still the same response. They have waiting lists and I have to wait, it's not urgent. I'm in a lot of pain, 24/7. That right ovary is stabbing heavily and I feel like I'm about to get a period every day. It's out of the ordinary for me. I can still walk, but my hip and leg are so painful. Pins and needles, sciatica is back.
I just don't want to be a burden to them. They will prob throw pills at me and they know I don't want to take them. I have developed nsaids allergies and hives. And I can't. I can't take codeïne because of interaction with other meds I take. And I don't want to try oxycodone. So stuck with Tylenol. And when I tell them all of this they see it as a sign that I'm not in a lot of pain because I refuse to take them. 'nsaids have given me stomach ulcers and I took so many of them that I've damaged my stomach. And I break out in severe hives when I take them now.
It's like they don't hear this. Cause ppl in pain take all they can get. Offcourse, I get that. I can still get up, get a shower but. I can't work. I can't run my household. I can't go out because standing up for long amounts of time brings me to tears. When is the right time to stop telling myself I should suck it up? I feel like such a burden. I developed medical PTD because I've been gaslighted for 20 years. I knew I had endo and was literally made out to be crazy. And even going near a hospital gives me great anxiety.
I feel Ive had a break from endo for nearly 2 years. It was still excruciatingly painful. But it wasn't daily anymore. It is now.
Do you guys feel like a burden when it comes down to hospital visits? I see those sarcastic faces of my doctor in my dreams. I've had therapy for this. In hospital, so that was very stressful. And this gave me more ptsd, cause the last thing the therapist told me was: I don't know what to do with you, I cannot help you. And she sighed. Whenever I told her about endo pain she kept saying she doesn't know anything about the disease. On my last visit I told her.. Do you tell someone who's battling cancer to just live a happy life and don't worry too much? And I walked out.
I feel pretty alone.

We just moved to Wilton and have not had great experiences with our water provider (Norwalk First District). Water pressure measured outside the house is ~25 PSI which is the bare minimum they're required to provide to us so they refuse to do anything about it. The water is also very hard and previous owners have had issues with leaking service pipes in the front yard (2 times). When I had a plumber come take a look he seemed pretty appalled at the service.
We're first time homeowners so I'm not sure if this is normal and just "part of homeownership" but we're trying to figure out what our options are. Ultimately, we can have a softener and pressure system installed but at this point I'm wondering if it's worth it just converting back to a well.
I've contacted Connecticut PURA but they said since Norwalk First District is a municipal utility system they are not under the jurisdiction of the Public Utilities Regulatory Authority.
Does anyone have any suggestions? Is it possible to switch water providers?

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