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what made me finally go to the doc - weird stuff i was feeling

Patient · · 3,145 views
so i kept coughing for like 6 months, thought it was just getting old and smoking too much back in the day. then i started getting this sharp pain in my chest when i'd breathe deep, like someone was poking me with a wrench. my wife kept saying go see somebody and i kept blowing it off because i felt fine otherwise.

then about a year ago i noticed i was getting tired way faster than normal. used to be able to work on cars all day no problem, but suddenly i'm winded just walking up the driveway. and this weird fluid feeling in my lungs, like something was sloshing around in there when i'd lay down at night.

went to my regular doc in detroit, told him about the cough and the pain and being so tired all the time. he did a chest xray and that's when things got real. they found fluid around my lung and sent me to a specialist. got a ct scan, then a biopsy, and boom. meso diagnosis in december 2025.

so yeah, if you're coughing alot and getting chest pain when you breathe and just feeling worn out all the time, get it checked. i wish i'd gone sooner instead of waiting a year thinking it was nothing.

9 Replies

Patient
Yeah man, the chest pain when breathing deep is what got me too. Glad you finally went in and caught it early like you did, that's huge.
Attorney Expert Response
Thank you for posting this. What you're describing, especially that fluid buildup around the lung, is something I've seen in hundreds of cases over the years and it's almost always what finally gets people through the door.

December 2025 is very recent so you're likely still in the middle of figuring out treatment options and next steps. One thing I'd say from the legal side is that a December diagnosis starts a clock in Michigan. The state has a specific statute of limitations for mesothelioma claims and it typically runs from the date of diagnosis, not from when you were actually exposed. Missing that window could affect your options significantly.

Working on cars in Detroit, that's a detail that matters more than people realize. Brake pads, gaskets, clutch components, a lot of those parts through the 70s and 80s contained asbestos. We've had clients who had no idea their daily work was the source until we started pulling product records.

The legal process, when someone does decide to pursue it, typically involves identifying the manufacturers of the products you worked with, then determining which companies may still have legal liability or trust fund assets set aside for exactly this situation. There are asbestos bankruptcy trusts that collectively hold billions specifically for mesothelioma claimants.

Please consult an attorney for your specific situation, especially given the recent diagnosis and Michigan's filing deadlines.
3 found this helpful
Patient
Man, that chest pain thing really hits home. I had the same exact deal - sharp stabbing when I'd take a deep breath, and I kept thinking it was just my back acting up from all those years bent over engine blocks. The tired part got me too. I remember my wife practically dragging me to my doc in Feb after I couldn't even make it through a morning without needing a nap.

The fluid sloshing around is what finally got me moving. Felt like I had water in my lungs when I'd lay back in my recliner, real weird sensation. Soon as they did my chest xray they found the effusion right away. Got my diagnosis about a month before you did, went through the EPP surgery in February and honestly it wasn't as bad as I thought it'd be. Recovery was solid. Doc said getting it early really helped.

Your wife was smart pushing you to get checked. Mine did the same thing and I'm glad she did because yeah, early catch makes a real difference. The cough thing people blow off too much. Six months of coughing ain't normal no matter how much you smoked back in the day.

How you doing after your diagnosis? You looking at surgery or you on a different game plan?
Medical Expert Response
Thank you for writing this out so clearly, because the symptom pattern you described is almost textbook for pleural mesothelioma and a lot of people on here need to read exactly this.

The fluid you felt "sloshing around" is called a pleural effusion, which is fluid accumulating in the space between the lung and the chest wall. It's actually one of the most common presenting symptoms we see, and it's also one of the reasons people get so winded so fast. Your lungs literally have less room to expand. The SEER database puts median time from first symptom to diagnosis at somewhere around 3 to 6 months for most patients, so a year of dismissing it, while completely understandable, is something I hear from almost everyone who comes through.

The thing that gets me every time is the "I felt fine otherwise" part. Mesothelioma is sneaky that way. Patients are often genuinely functional until the effusion gets large enough to cause that shortness of breath on exertion, and by then it's already been growing for a while. You're not unusual for waiting, you're actually the norm, which says something about how we need to change how people think about persistent respiratory symptoms after occupational asbestos exposure.

A December 2025 diagnosis means you're very early in this process. There have been some genuinely promising developments lately, the DREAM3R trial results on immunotherapy combinations come to mind, and your oncology team should be discussing where you fall in terms of staging and what options look right for your specific situation.

Please make sure you're being seen by someone who specializes in mesothelioma specifically, not just general thoracic oncology. I saw a patient referred to us from a Detroit-area general oncologist in 2023 and the treatment plan changed significantly once a meso specialist got involved.

Talk to your oncologist about all of this, but keep asking questions.
3 found this helpful
Attorney Expert Response
Thank you for sharing this. The symptoms you described, especially that pleural effusion (the fluid feeling), are exactly what we see in the majority of mesothelioma cases that end up in litigation. By the time the fluid shows up on imaging, the disease has typically been developing for 20 to 50 years from the point of initial asbestos exposure.

One thing that matters a lot legally, and I say this because you mentioned working on cars, is that automotive work is a significant source of asbestos exposure that people don't always connect. Brake pads, clutch facings, gaskets. We had a case where a mechanic was diagnosed in March 2019 after 30 years of brake work at a shop in Flint, and the exposure history went back to specific product lines that were still being manufactured with asbestos through the late 80s.

So a few things that tend to matter down the road if you're thinking about your legal options. The specific products you handled, the manufacturers, the job sites, the years. The more detail you can reconstruct now while memory is fresh, the stronger any potential claim could be. Michigan has its own statutes of limitations that could affect your timeline depending on when the exposure occurred.

I can't promise any particular outcome because every case is different and jurisdiction matters enormously. But this type of case may qualify for compensation through asbestos trust funds, which exist separately from traditional lawsuits.

Please consult an attorney for your specific situation, but don't wait too long to make that call.
2 found this helpful
Patient
The chest pain combined with the fluid buildup is what they caught with me too, though mine presented differently since peritoneal hits the abdomen first. I'm glad your wife pushed you to get checked because that delay matters more than people realize. I waited probably longer than I should have, attributed a lot of my symptoms to just getting older and having worked around asbestos decades ago without thinking much about it.

What you're describing with the fatigue and the sloshing sensation, I kept detailed notes on when those symptoms got worse because my oncologist at Cleveland Clinic wanted that timeline. Turns out the fluid accumulation was progressing faster than the initial imaging suggested. They do periodic imaging now to monitor how quickly it's building up, which informs the surgery decision and timing.

One thing that helped me was getting really specific about the pain location and character. I started journaling it in November after my diagnosis and realized the pattern, like certain positions made it worse, certain times of day. When I saw the surgeon about HIPEC options in late December, having that data actually shifted how they approached my case. They were considering a more conservative route initially but the progression notes made them push for surgery sooner rather than later.

Also just want to say the exhaustion piece is real and it doesn't mean you're weak or getting old. That's the tumor burden doing its work on your system. Once I understood it was a medical thing and not me just being out of shape, I stopped beating myself up about it and focused on what I could actually control with my treatment plan.
Patient
Yeah the fatigue thing is wild, nobody warns you about that part. Sounds like your wife did you a solid pushing you to get checked, mine basically dragged me to that first appointment lol. How far along were you when they finally caught it? I'm still kinda amazed they got mine early enough that the EPP surgery was an option.
Family
I'm reading this at like 2am because my dad's been having trouble sleeping and I've been up with him, and this just hits different right now. The fatigue piece you mentioned - that's what I wish someone had flagged for my father earlier. He's a retired teacher and kept attributing his exhaustion to just getting older, but looking back at his timeline, the shortness of breath started showing up about eight months before his diagnosis in March. We caught his at stage IV, so that window of "I feel fine otherwise" cost us.

What I've learned managing his care since October when we transitioned to palliative is that pleural effusion (the fluid sloshing around you described) often gets worse before it gets better, and the cough can actually intensify in certain positions when you're lying down. My dad needed a thoracentesis procedure to drain fluid from around his lung, which gave him maybe three weeks of real relief. I'm a nurse practitioner so I understood the mechanics, but understanding it intellectually and watching your parent struggle with it are completely different things.

The thing I wish I'd pushed harder on earlier is asking his regular doctor about a CT scan instead of just the X-ray. We could've caught more detail sooner. You got to a specialist quickly though, which is huge. How are you doing with the treatment planning now?
Patient
man, i'm really sorry to hear about your dad. that early fatigue thing is sneaky because yeah, you just think oh i'm getting older, my body's slowing down. nobody wants to think it's something serious. the thing that got me was my wife basically dragging me to the doc, so if your dad's got someone like that in his corner pushing him to take it seriously, that's huge. stage iv is rough but there's still stuff they can do these days, way more options than there used to be. how's he doing with treatment right now?

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