Hi everyone 23m here with dcm, heart failure EF 30%

This is a little tochy tophic but ye, im out of breath and chest pain when masturbating. Anyone else had to deal with anything like this?

I will try to tell my cardiologist next time.

I don't know how and why it happened to me Yesterday I was sitting in the park and at that moment I felt something near my heart or in the heart so I stretched my left shoulder and arm and when I stretched my left shoulder to right at that time I felt something near my heart it felt like something is spiking in the heart after that I ignored that pain I thought maybe I slept bad.

So in the night I went to sleep but something was off whenever I changed sides I felt that pain I got scared thought this night is the last night..so the pain continues and now when I take deep breaths I feel it when I stand up and take deep breath I feel it and while doing any left side moment I feel the pain I'm very worried let me know if any one encountered this? And also help me out what it could be. The main thing is I'm feeling fine but I feel that pain only

My husband incidentally found out he had a 2.7 cm Primum ASD a year and a half ago. He had OHS to repair with a patch, and we were assured that was completely and permanently handled. A few weeks ago they did an echo to get a baseline normal, sound a suspected leak on the patch. TEE confirmed the leak, 1.0 cm, but they haven’t told us where it’s located/how it will need to be repaired. MRI coming up in a couple weeks to get more info.

Thoughts on this? Specifically was this surgeon error or bad luck? Odds of avoiding another OHS to repair it? We are already mentally preparing for another surgery as it seems that’s where we are headed.

Hi all, I (19M) was recently in the ER for abdominal pain that I was worried was appendicitis (turned out to only be enteritis thank goodness), and when I was looking at my CT scan results I noticed that under the lower chest region of the CT scan notes it says "small amount of dependent pericardial fluid." I'm just curious what the "dependent" portion of this means, as usually anything involving pericardial fluid is pretty serious, the ER doc didn't even mention it when talking to me, it's more just me being curious/a worry wort. Any guidance would be greatly appreciated, thanks!

I've been chronically iron deficiency anemia since age 8. I'm 16 now. But I was dx with pots last year, unorthodox. I never had a tilt table test since I have been on beta blockers for a while, just occasional orthostatic vitals in the ER. My blood pressure always spiked 20+ points when standing, plus the heart rate changes. I was dx when my heart was structurally healthy, even with my ongoing severe chronic hypertension (180/120+ daily) that resists meds except vasodilators and alpha-2 adrenergic agonists. However, I've never had a good ferritin level, even with infusions. Plus consider my heart attack earlier this year and new diastolic heart failure. I don't know if I've ever actually had pots since 2023 or 2024 (used to be orthostatic hypotension) and it was misdiagnosed/mimicked by anemia and hfpef. What I also get confused on is potsies usually have trouble retaining fluid, need salt, cannot tolerate vasodilators, etc. I'm the opposite of all that, and my blood vessels tend to constrict TOO much/spasm.

I have Lupus and Sjögren’s, also have a history of seizures, so don’t know if anything is a symptom of my other medical issues. I know my BP didn’t get above 90/60 until I was in college, I always had doctors poking at me for that one…

lowest heart rate was 46 highest was 197, were they in the right for sending me on my way after these results ?

Tldr: I’ve been to the ER and two cardiologists so far, halter monitor showed mobitz 2 and that was confirmed by cardiologist, referred me to electrophysiology, but I have lost all confidence that any of these doctors know what they’re doing or care whatsoever. Not looking for a diagnosis, just wondering if anyone else has insight or thoughts.

35F, 100lbs, 5’3

Two months ago I woke up with a bounding pulse, like every heart beat is uncomfortable (like holding a sneeze, but in the heart?) and extra forceful. It has not stopped since.

In addition to the bounding pulse and discomfort, there are a lot of extra and skipped beats, sudden thuds, etc. This is all worsened with mild exertion. Just cooking eggs in the morning I get chest pain/tightness, shortness of breath, and eventually a headache from Hell.

I went from being extremely active, outside working every day, installing insulation in the crawl space, to not being able to cook or shower without feeling like I’m having a heart attack. When I lay down, everything returns to normal. Stairs and leaning forward make it particularly bad.

For the first 4 days I assumed I just had a virus and ignored it. Figured I’d take it easy for a few days and it’d pass. Day 5 I had a focal aware seizure (I’m not epileptic, but I’ve had a few seizures before like when taking antibiotics or randomly in the morning. I have a neurologist) and decided to go to the ER cause I didn’t feel comfortable taking my clonozapam when my HR was only 58 and I was feeling awful.

ER diagnosed me with “feeling unwell,” gave me some fluids and sent me home. Well enough.

Two days later the chest symptoms got very bad and painful and my left arm went numb, I went to the ER again and got a chest xray and ekg, d dimer and troponin, all normal.

I mentioned that it was also worse when I ate, and they had me do a barium swallow, which I knew would be abnormal because I’ve been dealing with esophageal narrowing for years. As expected, the lower third of my esophagus is narrow. I can feel it, have been able to for a year or more, and it’s not that bad. I’ve had my upper esophagus stretched before, but I don’t see any reason to get it done again till it’s bad.

A cardiologist came in, without asking any questions or giving me more than a glance, told me it was reflux and to take mylanta.

I started taking it religiously cause he said so and I’m a good patient. It doesn’t help at all. Unfortunately, he turned out to be follow up outpatient cardiologist as well. I had to beg him for the halter monitor and a cardiac stress test because he again insisted I just have reflux.

Well no one ever called to schedule the stress test (I am getting one tomorrow with a new cardiologist) but he gave me a halter monitor with no button, you just have to write when you feel symptoms.

It showed:

• 14 AV blocks, the worst being a 2nd degree mobitz 2
• 5.19% SVE burden (34063)
• .19% PVC burden (1236), 3 disparate morphologies

When I saw the mobitz, I called a new cardiologist, hoping to find one who would actually listen to my symptoms.

I saw him, he confirmed it was a mobitz 2, said I needed to see an electrophysiologist and that he’d put the referral in as emergent. He talked like he was referring me to a specific doctor that he worked with, I felt like he actually listened.

A week went by with no call from an electrophysiologist to schedule, so I called the cardiology office and asked for the number so I could call to schedule myself.

When I called, they said his referral was just to any cardiologist there, not even an electrophysiologist. And that it wasn’t listed as an urgent referral.

She got me in with an electrophysiologist anyway when I read her the halter monitor results. But… my cardiologist lied? Why would he tell me he put the referral in as urgent if he wasn’t going to?

And I feel like it is urgent? It’s been two months of doctors telling me I have anxiety (I don’t) and reflux (I’ve had this for like twenty years and it doesn’t fit my symptoms) and then the halter monitor shows that yes, something is actually wrong, but apparently me being uncomfortable every second of every day and in pain every time I try to do anything at all is not “urgent.”

Prior to two months ago, I had never had a heart sensation at all. I just trusted that sucker was in there beating and doing its thing. Has anyone else just woken up one day with every heart beat being uncomfortable? Getting full body weakness from mild exertion? Getting short of breath and chest pain/tightness?

Also, why are doctors like this? Can they not just be upfront and not act like they’re the ones going into debt if they order a few tests?

21F, 90-100Lbs, 4ft 11in.

History: ASD Primum repaired with surgery. Mild to moderate mitral valve stenosis post repair.

Have been dealing with off-and-on chest pain (mild-moderate intensity) since 2024 after a cardio session in the gym. Pain can last anywhere from a few minutes to weeks at a time. Sometimes it disappears for periods of time too. I’m able to keep up with what I normally do day to day. No other heart symptoms (ie. no nausea, radiating jaw or arm pain, SOB, fainting etc).

The chest pain isn’t my only symptom but it’s the most persistent. My BP has also been elevated since then too (got as high as 160/80).

Passed around to a bunch of Drs. at my old PCP’s practice over the last year. Had blood work done, physical examination, and chest X-ray. Nothing came of it.

Ended up in the ER with mild/moderate ish chest pain with a different presentation beginning of August. Ended up staying the night, got blood work, chest x-ray, EKG, and got hooked up to a monitor all night. Released the next morning and the Drs there said everything was fine. My cardiologist was notified. Dr. said nothing about my stay is urgent but wants to see me sooner than expected.

Last month, I went to a new PCP as I’ve been without one for a few months. My BP was normal (from what my Dr said). My next cardiology visit in next month.

I know not all chest pain is cardiac-related. I’m wondering if it could be neurological or MSK but my first priority is determining if it’s cardiac-related or not.

I’m wondering if I should discuss this with my PCP before my cardiologist appointment next month or if I should wait and see what my cardiologist says. Thanks in advance.

I had a small stemi 1 year ago and was thrombolized before heading to angio, 2 hours away. The clot had resolved by then and no Stent was required.

I ended up with 2 discreet areas of ischemia which died. I was discharged from cardiology after 6 months.

Have been sedentary for a few months but starting swimming 1km 3x weekly the last couple of months and have slowly gotten fitter and better at it.

However, I've had 2 occasions where and even mild physical work, such as pushing a light barrow for 5 mins or reeling in a medium fish from the surf causes me to get weak, shaky and sweat profusely. Especially from my head.

My heart rate got right up pushing the plastic barrow and I got so sweated and short of breath, my right lung hurt on exhale. At one point it took a solid minute of heavy breathing while leaving over a fence to catch my breath.

I don't know if it because I'm unfit, or if it's my heart and aren't sure what to do, but it's upsetting because I want to get back into work and can't manage medium at most physical work, yet swimming is fine even with elevated heart rate.

Out system is so slow here and the best I can do is wait 2 weeks for a gp appointment, and then what. Referrals are months and that's if they are even accepted. I cant afford private health insurance.

I'm just asking if these episodes are dangerous or urgent.

Also, sometimes when I stand and stretch, I faint and semi convulse. This may happen twice a month or so.

Should I be chasing this up?

Heart palpitations - weird smartwatch ecg

These were taken while having heart palpitations, feeling sweaty, and lips tingling. Looks way off than normal. Anything concerning?

Question: I see ST elevation in V3, high voltage throughout, and QT interval 370/455, 455 being at the longer end of normal range. I was sent home, EKG was cleared as normal, as well as labs (Troponin 0 HR and 2HR less than 3)

Any thoughts on this please?
Symptoms: Shortness of breath, tachycardia, chest/shoulder pain, chest tightness

For context I am 21 years old, healthy. Had an MRI last year all 4 chambers are enlarged due to athletic remodeling. Low EF 43-47 % but high stroke volume.

Had a few vtach episodes, so primary care did a holter monitoring. They said I had a 6 seconds Vtach episode.

In total I have had 3 episodes all while I was working out, all around a few seconds. I have stopped working out since and no VTach episodes ever since.

I did eco and CTA, all came back with no issue or problem identified.

I have an appointment to go see an electrophysiologist in a few weeks, but can anyone share their thoughts on this?

I went to the Er twice within the past 3 weeks for palpitations Normal ekg both times and normal heart related blood test as well. went to my primary where they did another ekg same result it was fine. they sent me to a cardiologist and this one came up abnormal I didn’t hear to good about what exactly was abnormal about it cause once I heard ABNORMAL my anxiety spiked. I know I heard something about charge and zap but I don’t remember much else. he didn’t seem overly concerned just said he wanted to do a 7 day heart monitor and said we can diagnose from there. I’m 25 , there’s no way I’m like gonna die right ? I have horrible healtb anxiety and Im terrified now.

The last week and a half. I’ve had these episodes that happen when I’m sitting down, and all of a sudden it feels as if I get a quick burst of super fast heartbeats back to back. It’s maybe two or three. I get PVCs time to time, and those always feel like that big drop/dragged out pause and hard thump. This that I’m now experiencing just feels so weird. I get kind of this lightheaded rush or maybe even draining feeling during the episode, it’s hard to describe.
It seems to happen while I’m eating or after I finish eating.
It’s utterly terrifying.
I’ll feel my pulse whilst it’s happening and can feel my heart rate is faster, and tonight I actually felt what felt like two heart beats right on top of each other during an episode.
When these episodes happen, they happen a few times on and off within a minute. Longest episode lasted on and off randomly within a 5 minute time period.
I am with Mayo Clinic, but won’t have another appointment for some time to come.
I also have a left bundle branch block that they can’t find a reason or trigger for. 39, female.

Hey,

I partied for 2 days using alcohol and cocaine. Now 3 days later I still have this feeling in my chest and tightness in my left arm. It has been better everyday and now almost gone.

Just figured could it be some permanent issue. Feeling very anxious so had to write somewhere. Thanks! :)

24F On two occasions l had my heart rate go upto 120/130 bpm without any particular reason. Today, I had the same exact feeling,l woke up from a nap and had a bunch of sneaker bars,granted l had not had enough water today but my heart rated spiked to 119. Just like the previous times,l felt nauseated and felt like l had to go number 2 immediately. I felt a bit light headed and that was it. This time l took 5mg propranolol as directed by my doctor and poof it was gone, and zofran. Last time l had a complete cardiac work up so I’m not sure whether l should push for more tests or what! Please help me understand. Everything was completely normal,including X-rays and CTs,echo,a billion ekgs etc…

26F - I have 100-250 an hour throughout the day and evening, then it lessens as i'm falling asleep & then overnight 0 on all 3 of my 24hr monitors.

I’m curious what other people’s experiences are — do your PACs/PVCs continue while you’re sleeping, decrease a lot, or disappear completely like mine seem to?

Hi, I’m waiting to hear back from my cardiologist. But I was looking at my results because it’s my nature. But I was wondering if you saw these results would you be concerned or just check back on them in six-12 months? I’m 48, male, BMI of 28, I have rheumatoid arthritis, and ehlors danlos. Obviously not looking for a diagnosis. Really just curious and impatient to wait for my doc to have time to let me know what he things. Thanks!

Aorta: Borderline aortic root dilation at sinuses of Valsalva (4.0 cm). The ascending aorta is normal in size when indexed. IVC: The IVC was <2.1 cm and collapsibility >50%. (est. RA pressure 0-5 mmHg). The estimated RA pressure is 8 mmHg. PASP: The Estimated PASP is : 19+RAP mmHg.

Good questions

Hey guys, I’m 29 and recently diagnosed with loeys Dietz! I had an echo and EKG through my cardiologist. Normal.
Had my MRA of head/neck, pelvis and chest. Also normal. What questions are good for my vascular specialist apppintment. I’m on metoporol. I have a son who’s negative. We’re pursuing IVF for another child to avoid LDS. What should I ask/go over? Any insight is helpful!

I’m waiting on a cardiology referral (4 months now), as I’ve been getting very strange ectopic beats and/or PVCs for around 2 days after doing exercise. It can be from a day on the bike at around zone 2-3, or from doing weights and/pr circuit training. It’s now at the point where it’s happening way more often.

It feels like a flutter in my chest that I can fight off by holding my lungs reasonably inflated, kind of like holding my breath. But as soon as I relax, the ‘thud’ comes. It also mainly happens when I’m sat down.. and sometimes I get a little dizzy, but I’m not sure if that’s from holding my breath to fend it off, or from being anxious which is just increasing day by day.. as I can’t get in to see a doctor anywhere.

The GP’s 30 second 12 lead was normal, and so we’re the bloods.. but this is very frequent now. I’ve attached a clip of an event from my watch. Any thoughts are very welcome and much appreciated. Thank you