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what symptoms made you realize something was actually wrong

Family · · 3,567 views
So my dad didn't think anything of it at first. He was just short of breath doing yard work in April, figured it was age and being out of shape. Then the cough started, this persistent dry thing that wouldn't go away even with OTC stuff. By summer he was getting chest pain on one side and his primary care doc kept saying it was bronchitis or allergies because he had no fever.

I'm a nurse practitioner so I was pushing harder on it. The shortness of breath kept getting worse and he started noticing he couldn't do his usual stuff without getting exhausted. That's when I made him get imaging done and that's when they found the fluid in his pleural space.

I think what gets people is that a lot of these symptoms look like nothing. Cough, fatigue, mild chest discomfort. My dad would have waited months longer if I hadn't been checking in on him. The pleural effusion is what finally showed up on the CT and that led to the biopsy.

If anyone here has a persistent cough that's not responding to usual stuff, or you're getting winded doing things you used to do easily, don't let it slide. Especially if there's any history of exposure. I know everyone says that but I'm saying it as someone who sees patients and also as someone whose dad got diagnosed at stage IV in March.

What made you all go get checked out?

10 Replies

Patient
I'm dealing with almost the exact same progression right now, actually. Persistent cough starting last spring, then the shortness of breath crept in, and my doctor kept dismissing it until I pushed for imaging myself. Got my peritoneal diagnosis in November after they found fluid, so catching it earlier than your dad is something I'm grateful for even if stage II still feels surreal.
Family
Joe's was almost like a slow fade, you know? He'd come home from work tired but that's normal, then one day in like July he mentioned his back was sore on the left side. We thought maybe he slept wrong or something. But then the shortness of breath showed up doing things he'd done a thousand times, like taking the trash cans to the curb, and that's when I got worried. The cough came later, maybe August, and that's what finally made him call the doctor. I think because I spent 35 years in classrooms noticing when kids were actually sick versus just complaining, I know the difference between "eh I'm getting older" and "something is actually wrong here." His primary care doc didn't push hard enough at first either, kept saying it was stress related, so we went to pulmonology ourselves without waiting for a referral. Got the CT in October and there it was. Started immunotherapy in November at Moffitt Cancer Center here in Tampa.

What's wild is how much I replay those months wishing we'd pushed sooner, but honestly? Some doctors just don't think mesothelioma because it's rare. How's your dad doing now with treatment?
Medical Expert Response
Your dad's presentation is textbook, and that's actually the hardest part to explain to people. There's a 2018 paper in the Annals of Oncology that found the median time from first symptom to mesothelioma diagnosis was around 6 months, and almost all of that delay happened at the primary care level because the symptoms genuinely look like a dozen other things.

The pleural effusion (fluid accumulation around the lung) is so often what finally gets people imaged properly. I had a patient last year who'd been told it was GERD for four months before a chest x-ray picked up significant fluid on the right side. He'd had 30 years of shipyard work in his history and nobody had connected it.

What you did matters. Knowing to push for imaging when symptoms aren't resolving the way they should, that's what moved the timeline. And I know at stage IV that feels complicated to say, but earlier imaging changes what options are on the table.

The dry cough plus unilateral (one-sided) chest discomfort plus progressive exertion intolerance... that combination with any asbestos exposure history really does warrant imaging. Not an inhaler prescription.

Please make sure his team includes a thoracic oncologist who sees mesothelioma specifically, not just generally. It changes the treatment conversation in ways that matter. Talk to his oncologist about what clinical trials are currently open at NCI-designated centers, because that's where the real movement is happening right now.
3 found this helpful
Attorney Expert Response
Your dad's timeline is unfortunately one I've seen play out many times over 20 years of asbestos cases. The insidious thing about mesothelioma is that the latency period can run 20 to 50 years from initial exposure, so by the time symptoms appear, most people reasonably assume it's something age-related or minor. The pleural effusion being the thing that finally triggers imaging... that's a pattern I hear constantly.

From a legal standpoint, the delay in diagnosis actually matters quite a bit depending on jurisdiction. Most states have a statute of limitations that starts running from the date of diagnosis or the date someone reasonably should have known about the diagnosis, not from the exposure itself. So the April to March timeline your family experienced could be relevant if you're considering any kind of claim.

One thing I'd mention, we had a client years back whose primary care doc documented "bronchitis" four times before anyone ordered imaging, and that documentation trail ended up being significant in the litigation. Medical records from that pre-diagnosis period are worth preserving carefully.

I'm sorry you're going through this as both a clinician and a daughter. That's a hard position to be in, knowing enough to push but also knowing what you're looking at once the imaging comes back.

If anyone in a situation like this wants to understand their legal options, please consult an attorney who handles asbestos cases specifically, because the procedural rules vary a lot state to state.
3 found this helpful
Medical Expert Response
Patricia, that dismissal cycle you're describing is so common and it's genuinely one of the harder things to watch as a clinician. What I want to add to what's been said here is that pleural effusion (fluid building up around the lung) is often the first objective finding that finally gets taken seriously, but by then you've usually got months of symptom history behind you. There's actually a study out of the Brigham and Women's thoracic group that looked at diagnostic delay in pleural mesothelioma and found patients saw an average of 3.2 providers before getting appropriate imaging. Three point two. And the OP's dad was lucky to have someone in the family who knew to push for that CT.

The other piece nobody's mentioned yet is the fluid itself. A lot of patients and families hear "fluid on the lung" and think it sounds manageable, almost minor. But the character of that fluid, whether it's exudative (protein-rich, which signals something more serious than a simple infection), is a key early signal. That distinction can be made from a thoracentesis (a procedure to sample the fluid) before you even have biopsy results back.

Anyway, talk to your own oncologist or pulmonologist about what your specific imaging is showing. Every case reads differently.
3 found this helpful
Family
Yeah, that diagnostic delay piece is exactly what we're dealing with. My dad's primary care doc wasn't ordering imaging for months because the presentation was so nonspecific on paper. It wasn't until I basically said "we need a CT now" that anything changed. And you're right about the pleural effusion being the wake-up call, but by that point his cancer was already advanced. I'd be curious about that Brigham study if you have a link, honestly. Are you seeing patients pushing back harder on their doctors now after cases like his, or does the same dismissal still happen?
Patient
Man, reading your dad's story hits different because I went through something similar but kinda backwards. I had the shortness of breath first back in like September 2025, figured it was just getting older and not moving around enough since I retired. Thought maybe I needed to get back in the garage tinkering with engines, you know, get my lungs working again. But then that dry cough showed up and wouldn't quit, and I remember thinking "this is weird, I'm not sick but I can't shake this thing." Went to my doc in November and he said probably dust from the old house renovation work we did back in 2015, maybe some mold. Didn't even mention the brake pad dust from all those years working on cars. Got the CT in December and boom, there it was. The pleural effusion was already there, I just wasn't paying attention to how tired I was getting. Had my EPP surgery in February and honestly the recovery went smoother than I expected, like the body's a lot tougher than you think once you get the bad parts out. What I wish I'd done is pushed harder earlier instead of assuming every ache and shortness of breath was just the price of getting old. Your dad was lucky to have someone in the medical field pushing on it.
Family
The backwards timeline thing is interesting because honestly the order doesn't matter as much as people think, but it does make diagnosis harder. Your instinct about getting back to the garage is so common and it makes sense, but yeah once that persistent cough showed up that should've been the red flag. Did your doctor eventually connect the dots or did you have to push for imaging like my dad did?
Veteran
Mine came up during a routine VA screening in June, which honestly saved my life. I was feeling fine, maybe a little winded climbing stairs but figured that's what happens when you hit 70. The radiologist caught something on the chest x-ray and ordered a CT. Pleural effusion, just like your dad. Had the pleurectomy done in August and I'm recovering solid now, three months out.

What gets me is I spent twenty years in the Navy on the Oriskany working as a hull tech. Asbestos was everywhere back then, nobody said squat about it. I didn't even connect the dots until the VA doc mentioned my service record and started asking about exposure. So here's the thing that might help Patricia and anyone else reading: if you're a vet and you're getting respiratory stuff that doesn't make sense, push the VA hard to look at your service years. Don't wait for symptoms to get worse. The screening caught mine early enough that we had options. Your primary care doctor isn't gonna know what you were exposed to in 1975 on a carrier.
Veteran
Same story here man, except I was the stubborn one not listening to my wife. Persistent cough starting around August last year, figured it was just the usual dust from living in San Diego and getting older. She kept saying go to the doctor, I kept saying it's nothing, I've been through worse. Then the shortness of breath kicked in during my morning runs and that's when I couldn't BS my way through it anymore.

Got the initial chest X-ray in September, they saw something, CT scan in early October confirmed pleural effusion. Biopsy came back positive for mesothelioma in late October. Stage II, so I was luckier than your dad but the whole thing moved fast once they actually looked.

What pisses me off is I spent 78 to 82 at Camp Lejeune and served on the Iwo Jima, both places loaded with asbestos insulation in the barracks and ship compartments. Nobody ever said anything about it back then. Wasn't until way later you hear about all the exposure guys got. Filed my VA claim in November, still waiting on that decision while I've already had surgery in December. The VA moves slower than a broken down truck.

My surgeon at UC San Diego said the cough and shortness of breath are usually the wake up call but people dismiss them because they're so common. Your dad's lucky he had you pushing on it. A lot of us don't have someone in the medical field catching this stuff. Tell your dad to get that pleural effusion drained if they haven't already, it helps with the breathing.

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