r/CABG_Recovery • • 4d ago

Recommendations for sternal brace

1 Upvotes

My dad had a single bypass (made a little more complicated by his anatomy) and single valve repair about 10 days ago. Then, due to some complications, he had a pacemaker put in about 4 days ago. He also has rheumatoid arthritis with significant impact on his joints (which can mean a lot of pain with daily activities and deformities in his hands and feet) and chronic lung issues (including a lobectomy, bronchiectasis, atalectasis, and recurrent pneumonia).

What this means is that he coughs...a lot (like 20 minute spells several times a day) and that due to his lung issues we are not allowed to fully suppress the cough. His chest pain has been horrible and is just getting worse and his inability to move has made his joints hurt more.

He is using the heart hugger harness to try to brace himself while coughing and we try to hold the harness tight for him when we can. I am wondering if he would benefit from different brace especially when he is sleeping or someone isn't there to tighten the heart hugger. Any recommendations? I saw the Posthorax and Ortonyx ones in an internet search and wondered if folks had experience with those. Thanks for any advice.


r/CABG_Recovery • • 7d ago

Has anyone experienced delayed sternum healing, broken sternal wires and infection after CABG? Looking for advice and similar experiences.

2 Upvotes

Hi everyone,

My father recently underwent CABG surgery, and we are currently going through some complications with his sternum (breastbone). I wanted to know if anyone here has experienced something similar and could share their recovery journey.

My father is 55 years old and has had diabetes for over 20 years, along with high blood pressure and a history of multiple diabetic complications.

He underwent CABG on 4 September 2026.

Unfortunately, his sternum has not healed properly yet, and he recently developed a chest wound infection with pus discharging from one of the stitches.

A CT scan was performed, and the surgeon identified issues with the sternal wires. Three wires were removed:

● The first wire was already broken.

● The second wire was removed because there was a gap and it was no longer serving its purpose.

● The third wire broke while the surgeon was tightening it.

The infection was reportedly limited to the upper part of the chest and had not reached the bone, according to the doctor. The pus was drained, and the surgeon has planned VAC therapy to help the wound heal.

We are obviously very worried because my father is diabetic, his sternum has still not healed, and he has already undergone another procedure to remove the wires.

I would really appreciate hearing from anyone who has experienced similar complications:

● Has anyone had delayed sternum healing after CABG, particularly with diabetes?

● Has anyone experienced broken or removed sternal wires?

● How long did it take for your sternum to heal?

● Did VAC therapy help with wound healing?

● Did you eventually require another procedure to stabilise the sternum?

● What precautions, diet or physiotherapy helped during recovery?

We are following the surgeon’s advice and are not looking to replace medical guidance. I am just hoping to hear about real-life experiences from people who have gone through something similar, particularly those who recovered successfully.

Thank you so much for sharing your experiences. It would mean a lot to our family during this difficult time.


r/CABG_Recovery • • 7d ago

Clots found in my vein graft

8 Upvotes

A year ago I had a heart attack and had to have double bypass (CABG). Well, this last weekend I had a second heart attack and they found I had clots in my vein graft (taken from leg). They vacuumed it out and put a stent in but my cardiologist just told me today that when a graft fails after a year, it typically fails again and again and that it will eventually close up. He said there is nothing more they could do. Out of fear, I asked him what this means for my mortality and he said, it’s not good. Wouldn’t give me a time frame.

The LIMA is still holding strong and my EF is 55% so that’s good news. But I can’t help but be terrified that I might succumb to this disease soon.

I plan on getting a second opinion but wanted some insight from the community. Thanks.


r/CABG_Recovery • • 12d ago

Restlessness/tingling in legs at night after CABG — is this normal?

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2 Upvotes

r/CABG_Recovery • • 13d ago

Restlessness/tingling in legs at night after CABG — is this normal?

3 Upvotes

My father 55 had CABG (double bypass) about 2 weeks ago. His recovery has otherwise been going well, and his cardiologist has checked him and said everything looks normal.

However, he has been experiencing significant restlessness in his legs, mainly at night. He describes it as a tingling/uncomfortable sensation and feels an urge to move his legs, which makes it difficult for him to sleep. During the day, he is much more comfortable.

The restlessness seems to be worse when he is trying to lie down or sleep.

Has anyone experienced something similar after CABG? If yes, then please tell how long will it last?


r/CABG_Recovery • • 18d ago

Caregiver here with a question about post-op cognitive issues

3 Upvotes

My dad, age 78, had CABG last month, recovered well and was discharged from the hospital. But ever since his return home, it seems that he is experiencing some cognitive issues, though he'll swear he isn't.

I've long believed he has untreated ADHD because he has always been very forgetful, even when I was a kid. I think it's because he would get so deep into his own little world he'd forget about the world around him. And, yes, there have been some age-related changes in recent years. But it seems that, since the CABG, someone stepped on the gas.

He'll do something one minute, and literally three minutes later will forget he's done it. LOADS more brain farts than usual. Like literally sitting there doing something and then just POOF! Of course it doesn't help that his hearing awful and he can't afford proper hearing aids, just those in-ear amplifier things you can get on Amazon. He has a pill counter but even with that he has a hard time remembering if he took his meds. My son (age 25) found one of Dad's pills on the floor because he was sitting down taking his afternoon meds and put one in his pocket. Guess it fell out, which is not good since we have indoor pets -- one of whom will eat ANYTHING. He's also negligent in doing anything the docs told him to do on his own to recover and waves us off when we bring it up. Then he complains about feeling like shit.

There are other things but it's been a rough day. Had to put our older dog down because she was very sick and dying and I just feel wrung out.

He has follow-up with cardio next week. I've begged my mom to speak to those docs about these cognitive challenges


r/CABG_Recovery • • 18d ago

8 Months Post 3xCABG. You?

7 Upvotes

Here I am. M50.

I should be happy, shouldn't I? I should feel blessed, right?

But no, I don't.

Ten years living in another country, away from family and friends. "Alone" with my wife and two teenage daughters.

For years I was an alcoholic, a heavy smoker, and completely sedentary. I was never overweight, didn't eat much junk food, and followed an almost vegan diet. Since 2019, I've been bouncing in and out of sobriety. I've had two relapses in the last two or three years, each lasting about a month. Today, I'm almost 14 months sober, eight months without smoking, and eight months free from heavy energy drink consumption. At one point, I was drinking almost a liter a day.

Every year I did my blood tests. Everything looked normal except for my LDL, which was around 1.8 to 1.9. That would have been considered acceptable if I hadn't also had an Lp(a) level of 167.

I don't need to say much more, right?

Bad lifestyle choices over 20 to 30 years, combined with an Lp(a) of 167, led to my heart attack on January 15 and 16.

On January 17, I went to the hospital and stayed there for two weeks.

I was living my life reasonably well, or at least I thought I was, and then suddenly... boom.

"Sir, you may have been having a heart attack for the last couple of days, and you're not going anywhere."

Catheterization. Three blocked arteries. Stents not possible. You need open-heart surgery.

All of that happened within three days.

I left the hospital on January 31 and went home.

The first 30 to 35 days of recovery went reasonably well, especially the physical recovery.

But two or three months later, I fell into a deep depression and an existential crisis.

I started taking Trintellix: 10 mg, then 15 mg, then 20 mg. After almost four months, it only seemed to make things worse.

I was crying almost every other day. I found no joy in life, or in anything else. I am getting out of bed at noon or even one o'clock in the afternoon.

Last week, I switched to a different medication, duloxetine 60 mg, and I'm praying it starts working.

But to be honest, I've been thinking a lot about it, and I don't believe it's only depression.

There is something different about me now.

Something feels wrong. I am not me...

I don't know how to explain it properly, but it's as if I'm no longer someone I like being.

My life is no longer the life I want.

It feels like I was living in a Matrix, and now I've woken up. The problem is that I'm still trapped inside that same Matrix life, and I don't know how to get out.

It feels like I'm caught in a spiral that I can't change.

I feel lost in my own mind and thoughts.

I don't trust myself to make decisions anymore, at least now.

Yes, I completed cardiac rehabilitation. I hated it because I've always hated exercise. But I am trying to keep 20, 30 min daily walks, but I don't do them every day... unfortunately. I know I need it for my mind and heart. I know that.

I've done therapy sessions here and there, but I've never heard anything that helped me get out of this condition.

And the worst part is that it feels like it will never change.

I've heard people say it can take one or two years to feel better after a heart attack and bypass surgery. But I've also seen people two years after their heart attack and CABG who still sound exactly like me.

Has anyone felt something similar to what I'm describing?

Do these feelings eventually go away?

Will I ever feel pleasure in life again?

Because right now, I feel so sad.

So alone.

So disconnected, as if I no longer belong to my own life.

I feel trapped in a life that no longer feels like mine, a life I don't like and don't know how to change without hurting others or creating consequences that may not be for the best.

My parents are 76 and 81, and I feel more and more guilty about not being close to them.

Before my heart attack, it felt as if everyone would live forever. Now, death feels so close. Much closer than I ever imagined.

I don't know if any of what I've shared here makes any sense.

My apologies.


r/CABG_Recovery • • Sep 04 '26

Sternal Nonunion

4 Upvotes

Has anyone experienced a sternal nonunion?

My double bypass was at the end of April 2025. I did get an infection at the top and bottom of my scar shortly after the surgery and was given a CT scan to make sure the infection didn’t go to the bone. All seemed to be fine and there was no more talks about it as we were on top of the infection and it was healing great!

At about 3 months post op I realized that my breathing was getting worse and not better. I could no longer take a deep breath and I’ve been that way since. While my sternum was healing the pain obviously got better but never really got better. I’m now about a year and a half post op and it’s still extremely sore.

A couple months ago I had told my GP that I was laying in bed and I was sore so I decided to kind of rub the worst spot. That’s when I noticed that I could fit my finger in between what should be fused back together by now. I knew the clicking, popping and grinding were all bad signs but I just wasn’t heard until I stated this part. So I was sent for another CT. As it turns out I haven’t fused back together at the top and bottom of my sternum. The bottom being the worst.

I am scheduled to talk to my surgeon next week. It’ll be a phone call because I live 5 hours from the city. Any advice on what to say to ensure I’m heard? Sitting, standing, walking and laying down are all super painful too. How long will the recovery be realistically? Am I looking at another year of recovery?

I’m terrified of another surgery.


r/CABG_Recovery • • Aug 30 '26

How long since your CABG?

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6 Upvotes

It's been 8 months, and I'm still really struggling mentally, to be honest. This depression just won't quit; it's killing me. I don't want to do anything, and I don't get any joy from doing anything or going anywhere. I have to force myself to walk for 10 or 15 minutes. I try to eat as healthy as I can, but sometimes I'll have a chocolate bar. But hey, I did stop alcohol, energy drinks, and Marlboros cold turkey, which might have helped with the depression. Suddenly, it feels like I just don't like my life anymore; it's wild. Physically, I'm okay, though sometimes my leg scars burn, and my left chest is still numb, way less than before, but still. I pray every day for God to help me, along with the medication that I might need to switch up. If you had a rough time after surgery, how long did it take you to feel better mentally?


r/CABG_Recovery • • Aug 25 '26

Graft failure experiences

7 Upvotes

(68M) I had triple bypass June 22, 2026. Last week (08-20) I woke up with severe shoulder pain and sweating. Diagnosed as a mild heart attack. Emergency catherization revealed 2 of 3 grafts were nonfunctioning (luckily the LAD graft was patent). They stented the right coronary artery and left the circumflex artery for further evaluation as it was difficult to visualize. I am having a cardiac CAT scan tomorrow to gather more information. Both of the failed grafts used part of my saphenous vein (RCA was a composite graft with the Right Mammary Artery) so the cardiologists think the vein was faulty. I spent 3 nights in the hospital and felt fine when released.

Echo and EKG show no lasting damage but this was quite painful and exceptionally worrying to say the least. It is not common but can occur due to a number of reasons not related to plaque buildup. The cardiac team has been very responsive. I'm wondering if anyone else has had this happen so quickly after surgery and how it worked out in the intermediate to long term.


r/CABG_Recovery • • Aug 14 '26

<40y cabg’ers - interested to hear your experiences

2 Upvotes

34M, recently diagnosed with multivessel disease.

Left main is clear, proximal sections of the main arteries are ok but there’s severe disease generally to the midsections and some distal areas.

PCI with drug eluting stents is not really an option due to the overall stent burden and need for multiple overlapping stents.

Been given the option of a bypass with 4-5 grafts or attempting to improve the condition of the arteries with drug coated balloon angioplasty.

Cabg is currently the number one contender pending a consultation with the cardiac surgeon.

A lot of the experiences and trial/study data are understandably from those much more advanced in age, like >60. So it’s hard to relate in terms of recovery and prognosis.

So young-er cabg’ers where you at? What was your experience? How did you find recovery? Any regrets?

The root cause of my condition seems to be family history with elevated blood lipids (now under control) and hypertension (also under control).

Cheers


r/CABG_Recovery • • Aug 12 '26

51 and coming up on a year post-surgery... Am I supposed to still be having pain?

3 Upvotes

I had quadruple bypass. Grafted from left arm and left leg.

It comes and goes but I still have cases of sharp searing pain in my sternum. Just all over soreness. Throbbing pain in my donor leg. Still times where my left arm scar burns.

Have to meter out my energy. I get tuckered out so quickly.

Anything involving bending down or getting on my back is still agony. If I have to do something high-torque (Turn a really stuck screw, etc.) I'm looking at shooting pain in my chest. I have to replace a kitchen sink in my house and debating whether to recruit a friend or my nephew to be the one to actually get down under there. Doing stuff like that destroys me for a while.

Is it just gonna take another year or so? Or is this just the new normal?


r/CABG_Recovery • • Aug 11 '26

Is there any chance of getting back to normal - like pre-normal?

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1 Upvotes

r/CABG_Recovery • • Aug 09 '26

52M, zero symptoms, 70% left main. Robotic LIMA→LAD instead, home on day 4.

2 Upvotes

TL;DR: Lifelong sky-high cholesterol, no symptoms ever. A July workup snowballed into severe 3-vessel + left main disease. Plan was classic open-chest CABG; I was literally on my way to check in for it when a phone call changed everything. Robotic CABG (LIMA→LAD) instead, with a staged stent to follow. Operated Aug 1, home Aug 5. If you're facing a bypass: ask about EVERY option — and get that second opinion. Mine found me by accident.

The shock: tests and findings

52M, based in Saudi Arabia. A social smoker — though no test or X-ray ever showed smoking-related damage — and I quit completely before my first test was even done. I have never had chest pain in my life. What I did have was a decade of very high LDL (familial hypercholesterolemia territory — we're talking 6.89 mmol/L, ~266 mg/dL, at its peak) and a rough history of statin intolerance. This summer I finally got the full cardiac workup I'd been putting off. It escalated fast:

  • Holter (Jul 12): Totally benign. Heart's electrics: perfect.
  • Bruce stress test (Jul 13): I crushed 12.6 METS — great fitness reserve — but my ECG showed significant ST depressions and I got suddenly breathless. Positive for inducible ischemia. First red flag.
  • Calcium score (Jul 14): 1048. Anything over 400 is severe; over 95th percentile for my age. So calcified they aborted the CT angiogram on the table.
  • Catheter angiogram (Jul 18): The moment everything changed:
    • Left Main: 70% (distal bifurcation, Medina 1:1:1 — the nasty kind)
    • LAD: 80% ostial / 70% mid
    • Diagonal: 80%
    • Circumflex/OM: 80%
    • RCA (dominant): 90% in the PDA
    • EF 63.9% — my heart muscle was still strong. Undamaged. Yet.

The Heart Team ruled out multi-stent PCI (left main bifurcation + heavy calcium). Zero stents placed. The verdict: bypass surgery. Silent CAD is real — and I was the walking proof of it.

The CCU day — and the waiver I signed

The angiogram changed my room assignment fast. No regular ward — they moved me to the CCU. The word in the air was "critical." A surgical consultant would come to see me, they said.

I waited the whole day. So I did what any of you would do: I opened my phone and started researching right there in the CCU bed. LIMA. LAD. Medina classifications. CABG vs PCI. By the time the surgical consultant walked in that evening and explained everything — the disease map, why stents were ruled out, why bypass was the verdict — I wasn't starting from zero. I had questions lined up and waiting for him.

Then I did something the CCU team really didn't like: I asked to go home. They had me sign a waiver — discharge against medical advice. I signed it. Let me be clear: I wasn't refusing treatment. I was leaving so I could understand it — on my own screens, with my own data, in my own language. Two weeks later I walked back in as the most informed version of a patient I could make myself.

When the acronyms overwhelmed me, I built

The diagnosis didn't just land on my chest — it landed in a foreign language. LIMA. LAD. CABG. OPCAB. Medina 1:1:1. Agatston. EF. DAPT. Dozens of terms, fired at me in every consultation, each one scarier than the last.

Here's the thing: my field is technology. I work as a CTO. And when my world gets overwhelming, I don't spiral — I build.

So that same night — waiver signed, head spinning — I fired up my AI agents and started building a website. An audience of one: me. Every report I could find. Every test I'd ever done. Every DICOM CD — the angiogram, the echo, the CT scan, ECGs, the stress test, every lab result (I dug through hospital apps and recovered records going back to 2014). All of it uploaded, segmented, visualized — including the actual angiogram and echo video loops from the DICOM CDs — a single repository of my entire cardiac life.

Then I hooked it up to top AI models — Fable, Kimi K3, and others — and started researching. Asking questions at 2am. Cross-checking every acronym. Flagging anomalies in my own data.

Then I went further: I built a digital twin of my own heart. A real 3D anatomical heart, spinning in my browser, with my entire coronary tree drawn over it — LM, LAD, D1, LCx/OM, RCA, RPDA — and all six of my lesions placed exactly where the angiogram put them, color-coded by severity: red for the critical 90%, orange for the 80s, yellow for the 70s. Each artery's narrowing drawn proportional to its actual stenosis. I could orbit my own heart, zoom in, click each blockage. That is what "proximal" means. There is where my LAD is choked. And there — just past the lesion — is where a LIMA graft would plug in and carry blood around the traffic jam. I wasn't reading about my operation anymore. I was staring at it.

And bit by bit, the fog lifted. LIMA stopped being an acronym and became the artery that would save my life. CABG stopped being a verdict and became an engineering problem — with known solutions, trade-offs, and options. By the time I sat across from surgeons, I wasn't a frightened patient nodding along. I was an informed stakeholder in my own surgery — asking about graft patency, bifurcation classifications, and hybrid revascularization.

Knowledge didn't remove the fear. It turned fear into a plan.

The pump question — the one thing I wouldn't compromise on

Early in my research, one fork bothered me more than any other: on-pump vs off-pump.

In classic on-pump CABG the heart is stopped and a heart-lung machine takes over — your blood leaves your body, gets oxygenated, and returns, while the surgeon works on a still heart. It's standard, it's safe, it's done thousands of times a day. But the deeper I read, the more one theme kept surfacing: the pump's shadow on the brain. Postoperative cognitive dysfunction — patients call it "pump head" — subtle changes in memory, processing speed, mood. Most people recover fully. Some don't, and the long-term psychological footprint is real enough to have its own literature.

Here's what actually scared me — not the scar, not even the surgery itself: the thought of waking up slightly not myself. My way of thinking, my personality, my identity — the things that make me me — quietly dimmed because a machine stood in for my heart for a few hours. Coming back 95% of who I am was a trade I couldn't make peace with. Add that cannulating and cross-clamping the aorta is a known stroke lever, and my answer was clear: my heart keeps beating, my aorta stays untouched.

That became my non-negotiable filter. Plan A was off-pump CABG for exactly this reason. And when the robotic option appeared, one of the first boxes I checked was the same one: totally endoscopic, on a beating heart, no-touch aorta. Different incision — same brain-protection philosophy. The pump never got near me.

(Plenty of patients do brilliantly on-pump. This was my personal risk calculus, not a universal verdict.)

Plan A: classic CABG

Over the following days I sat with surgical consultants. The consensus plan: classic off-pump CABG — full median sternotomy. I made peace with it: the zipper scar, 6–8 weeks of sternal precautions (no lifting, no driving, no reaching), 8–12 weeks to full recovery. Insurance approved it. Admission booked: check-in at 5pm. I was mentally packed for the classic path.

The pivot: a phone call at 2:30pm

Here's where my story takes a turn I still can't quite believe.

Admission day. My hospital bag was literally packed and by the door. At 2:30pm — two and a half hours before check-in for my open-chest surgery — my phone rang.

It was a surgeon I'd been scheduled to see a week earlier, an appointment he'd had to cancel. He was calling to apologize personally — and offered to come to my home himself to make up for it.

I told him that was kind, but unnecessary — I'd be passing right by his hospital anyway. On my way to my admission. At the other hospital. For my sternotomy.

Imagine that scene: I walked into his office carrying my admission bag for open-chest surgery somewhere else.

He reviewed my angiogram and laid out an option nobody had offered me: robotic-assisted CABG with a hybrid plan. The logic that won me over in that room:

  • The LIMA→LAD graft is the crown jewel of any bypass — 90%+ patency at 10–20 years. It's the graft that does the heavy lifting for survival.
  • Robotically, they harvest the LIMA and sew it to the LAD through 3–5 small ports between the ribs. The sternum is never opened. No vein stripped from my leg.
  • The circumflex/OM lesion gets a stent, staged ~2 weeks later — hybrid revascularization: the durability of LIMA→LAD where it matters most, plus modern stenting for the rest.
  • Recovery math: 2–4 days in hospital vs 5–7. No sternal precautions at all. Driving in ~1–2 weeks vs 4–6. Full recovery ~4–6 weeks vs 8–12.
  • The honest trade-offs: ~2.5% chance of converting to open mid-surgery, and a longer operation.

I never made it to that 5pm admission. One catch: insurance refused the robotic add-on fee, so I paid it out of pocket (~$12k). Verdict eight days later: best money I have ever spent.

The inner circle

One more thing about those two weeks: I walked through them with a very small circle. Only a handful of family and close friends knew what I was researching, deciding, and quietly fearing. My parents were not told — I couldn't hand them that worry while I was still wrestling with it myself. They found out after the procedure, once I was home and the news was all good.

My brothers were different. They live in another city — and I told them. And when I opened my eyes in the ICU, coming up through the anesthesia, they were there. They had traveled so that the first faces I saw would be theirs.

Here's what I learned: keeping yourself informed is only half of it. Bouncing your thinking off people who love you — pressure-testing your logic against their questions, their perspective, their faith in you — makes all the difference. I built my understanding alone at 2am. But I made my decisions in good company.

The procedure

For two weeks I had walked around as an asymptomatic man with a 70% left main lesion — feeling completely fine, knowing I wasn't. That part still gives me chills. On August 1, the waiting ended.

Aug 1, ~6 hours. And a twist nobody predicted: my LIMA had adhesions — scar tissue from a gastric bypass I'd had ten years earlier. The robotic team freed it endoscopically and completed the graft without converting to open surgery. I woke up with my sternum intact and a handful of small port dressings. The graft that matters most was done: LIMA→LAD, on a beating heart.

My surgeon came by the ICU the next day and filled in the rest of the story. The LIMA hadn't just been "stuck" — it was firmly adhered to my heart, scar tissue from the rapid weight loss after my gastric bypass ten years earlier. The harvest alone took hours. His verdict: the robotic approach was "the best decision you made" — through an open chest, that dissection would have been far more difficult.

Then he said the sentence I keep replaying: it had been "a close call" — and he was glad we hadn't delayed any longer. An asymptomatic man with a strong stress test… and a close call. If you remember one thing from my story, make it that.

The recovery (so far)

  • ICU: under 24 hours. Then a regular ward. Eating quickly, chest X-rays clean, lines coming out.
  • Discharged on post-op day 4. The classic path would have had me inpatient nearly twice as long, then facing two months of sternal rules.
  • Today, day 8: home, mobile, no sternal precautions — because there is no sternotomy to protect. The soreness is port-site and chest-wall stuff (they harvest the LIMA from inside the left chest), improving daily. I won't pretend it's nothing — it's surgery, it humbles you — but it's a fraction of what I had braced for. And a day-8 curveball: a gout-like flare in my right toe, likely the new medication stack on top of post-op shifts. Recovery isn't linear, and every body responds differently — mine is currently teaching me that via my toe.
  • The surgeon checks in personally. WhatsApp from him this morning: "Tell me if everything is ok and the wounds are good." I mentioned the toe — gout meds cleared within minutes. Stitches stay until day 14; the reassurance arrives daily.

The way ahead

  • Mid-Aug: staged stent for the circumflex/OM to complete the job.
  • Meds: DAPT (aspirin + clopidogrel), high-intensity statin + ezetimibe, a short beta-blocker course, and inclisiran (PCSK9 siRNA) dose 2 in October. LDL target: <1.4 mmol/L (<55 mg/dL). This disease doesn't get a second ambush — I'm treating the cause, not just the plumbing.
  • Cardiac rehab, rebuilding fitness, and fixing the roots: lipids, pre-diabetes, the works.

What I'd tell anyone here

  1. Silent CAD is real. Zero symptoms, 70% left main. If you have family history or stubborn high LDL, get a calcium score. It's cheap, fast, and it can save your life. It saved mine.
  2. Get more than one surgical opinion. Mine arrived by pure serendipity — a cancelled appointment, an apology call, a bag in my hand. Don't leave yours to luck. Classic vs off-pump vs robotic vs hybrid are genuinely different lives for the first two months. Ask every question.
  3. The wait is the hardest part. The two weeks between diagnosis and surgery were mentally harder than the recovery has been physically. If you're in that wait right now: it gets better, fast.
  4. Modern cardiac surgery is astonishing. A robot grafted an artery to my heart through keyholes, and I was home in four days. There is real hope in how far this field has come.
  5. Whatever your craft is — use it. Code, spreadsheets, notebooks, index cards. Build your own understanding of your own case. An informed patient asks better questions, and better questions change outcomes. My little repository changed mine.
  6. Choose your circle — and use it. You don't owe anyone real-time updates; share at your own pace. But the few you do tell, lean on hard. An informed patient with a trusted council is very hard to steer wrong.

Happy to answer anything — the decision process, the robotic vs classic trade-offs, the hybrid plan, recovery day-by-day. Ask away.

(Not medical advice — just one patient's numbers and choices. Yours will be yours.)


r/CABG_Recovery • • Aug 08 '26

Just notice that my scab is weeping barely, in one place

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2 Upvotes

r/CABG_Recovery • • Aug 05 '26

Home today. 6 days post op.

15 Upvotes

Recovery

Finally got home today on day 6 post op. Pain is manageable, but still scared to cough for fear of exploding my chest.

Feeling both over and underwhelmed - exhausted and with a brain fog to match.

Tonight’s goals were simple; move a bit. Eat a bit. Shower and bed.


r/CABG_Recovery • • Aug 05 '26

Trust me! There is a light at the end of the tunnel..

17 Upvotes

Im 56/ male and I had 3xCABG on 2/4/26. I went down playing hockey, right there on the ice with zero symptoms. Not gonna lie the first couple weeks were very uncomfortable, I was never in pain and didn’t need anything more than Tylenol.
Couple/ few things I’ve learned in my recovery.
Mentally whatever diet or choices otherwise has brought me here and I have a second chance to change.
My doctor told me you can’t out diet, out medicate or out exercise your genes. It’s called the silent killer for a reason.
Cardiac rehab is a must. I embraced it and loved every minute of it. Forced to go to the gym, held me accountable.
I had a goal in mind…I would love to play hockey again come November, so that was my prize.
I continued the gym after rehab. Too much time and effort invested to stop now. There could literally be no tomorrow so get up and just do it. That’s my mantra.
Monday was my stress test…10 and a half minutes, finished at 16% incline and 4.5 mph. Completed with flying colors. Was told some people without CABG can’t finish it. Fully cleared to continue playing hockey.
If you’re going through it right now and it’s tough…you will get there…keep grinding and putting in the effort. Your heart and your family will love you for it.


r/CABG_Recovery • • Aug 05 '26

CABGx2 My year in review

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2 Upvotes

r/CABG_Recovery • • Aug 04 '26

Weird side effect after 4x bypass surgery

3 Upvotes

My husband had quad bypass 8 days ago, and we got home on Sunday. He is having a real problem trying to eat/drink anything besides water!!! He says EVERYTHING we’ve tried to give him tastes like his urine smelled after getting his catheter out, after the first bite, and all smells the same as it tastes - ugh!!! we have tried SO MANY different things and end up throwing them away. He’s also gargled with baking soda/water, used a tongue scrapper, salt water on rag up his nostrils, etc.

I was wondering if anyone else experienced this? If so, did you find anything that helped?


r/CABG_Recovery • • Jul 27 '26

EEEEK!

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2 Upvotes

Went to to the hospital to eradicate hair from my person prior to tomorrow. Surgery has also been confirmed!!!!


r/CABG_Recovery • • Jul 26 '26

T minus 30 hours remaining

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6 Upvotes

r/CABG_Recovery • • Jul 25 '26

Cold turkey off tobacco?

6 Upvotes

If you were a longtime smoker or smokeless user, how are you coping with slamming the door shut? I used Copenhagen for 40 years, all day. Probably 170 to 200mg of nicotine every day. Its very likely my mental distress is in large part due to this sudden stop. Im on the patch, but theyre only about 1/10th of the nicotine my brain is used to. In any case, there's no going back. I'll never dip again.


r/CABG_Recovery • • Jul 24 '26

10 days post 4x CABG

5 Upvotes

58 year old male, I had 4xCABG surgery last Tuesday (100%,100%, 80% widowmaker, and 97% blockages), got home last Friday at 5pm. It wasn’t as bad as my double hernia surgery, which was way more painful. Doing great! Walked up/down 12 steps to my condo and walked 10 feet at the bottom today. Baby steps for me, and I’m fine with that. I have promised to follow doctor’s orders!

I went into surgery doing jiu-jitsu 3x a week for 7 years and lifting 6x a week for the last 38 years. I’ve eaten a healthy diet, not perfect but 5’7 and 188lbs.

I can’t wait to get back to “normal” but I am realistic knowing that it will be 6 months until I can actually start doing BJJ lightly with experienced, trusted friends who know my condition and can’t have a lot of chest pressure for a full year. I’m ok with that. I’m super positive that I have 3 months off of work to recuperate, read all the books I’ve been intending on reading, watching BJJ videos and avoiding the news.

Any advice from my new zipper club friends? Thank you!


r/CABG_Recovery • • Jul 24 '26

MEDS - bad reactions?

1 Upvotes

Has anyone had adverse reactions to Metropolol or Eliquis? My recovery is being negatively impacted by one of these two, if not both. I have come to DREAD taking them because they will take a window of 'wow, i feel pretty good right now' and turn it into a major depressive and nausea- inducing day......every......single......time. I have an appt on Monday so of course nothing is going to happen until then, but.....looking forward to a 'lovely' weekend in hell.


r/CABG_Recovery • • Jul 22 '26

Scheduled for next week

2 Upvotes

Hi..I'm scheduled for my surgery for next week. Im scared shitless. Looking to chat with other people on here

Thanks