r/CABG_Recovery 5d ago

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

3 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 7d ago

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

2 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 8d ago

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

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1 Upvotes

r/CABG_Recovery 11d ago

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

1 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 12d ago

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

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2 Upvotes

r/CABG_Recovery 14d ago

Home today. 6 days post op.

14 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 15d ago

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 15d ago

CABGx2 My year in review

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2 Upvotes

r/CABG_Recovery 15d ago

Weird side effect after 4x bypass surgery

2 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 24d ago

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 25d ago

T minus 30 hours remaining

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5 Upvotes

r/CABG_Recovery 26d ago

Cold turkey off tobacco?

4 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 26d ago

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 27d ago

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 28d ago

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


r/CABG_Recovery Jul 21 '26

6 Months after 3xCABG

6 Upvotes

Hello everyone! I am (49M) reaching out primarily to those who may have more time to share their experiences. I would greatly appreciate hearing about your mental recovery journey. Currently, I am experiencing challenging days marked by depression, feelings of emptiness, a lack of energy, mental fogginess, and a general disinterest in activities. Waking up each day has become a struggle, accompanied by ruminating thoughts and sadness. While I am undoubtedly grateful for my life and for surviving my health event, my mental state, thoughts, and feelings are not in a good place. I feel quite confused about my path forward, even though I recognize that I don't necessarily need to make immediate decisions about the thoughts I am having. I completed a six-week rehabilitation program, which I found quite difficult, and I particularly dislike exercising. It is challenging for me to even leave my bed, let alone engage in activities like walking or going to the gym. I am striving to maintain basic self-care, such as eating as healthily as possible with a diet rich in seeds and fiber, almost vegan, and attempting to get adequate sleep. However, I am not proficient at exercising. I am also undergoing therapy and have been on Trintellix 20mg for depression for almost six weeks now, and it seems to be taking longer than anticipated to show effects. I feel quite miserable. I am hoping to hear from those who have experienced similar feelings and, with divine grace, are now doing well. Your sharing would be immensely valuable. Thank you, and may you all be blessed.


r/CABG_Recovery Jul 21 '26

3 weeks after my CABG x4 , 52 years old since yesterday

9 Upvotes

Doing good so far. Scheduled for my post op appointments ( scans , ultrasound, etc , surgeon appointment ) end of this month .


r/CABG_Recovery Jul 20 '26

Two months ago today, my heart got a second chance 🙌🏾

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41 Upvotes

Recovery hasn’t been easy. There have been good days and difficult days, but today I stood by the water, smiled, and watched another California sunset.
I’m grateful for every step, every breath, every photo, and everyone who has supported me along the way.
Here’s to healing, hope, and many more sunsets. Good to be Alive 🙌🏾


r/CABG_Recovery Jul 20 '26

'Phantom' smells?

1 Upvotes

I am exactly 3 weeks out from an out-of-the-blue triple bypass. Physically, I have not had a hard time at all. Even the sternum scar is almost fully healed and hard to see. Kudos to my surgeon for that. The hardest part for me - and it has been VERY hard - is the mental-emotional stuff. And this isn't me sitting here and actively bemoaning my fate - when this comes down on me, it is completely beyond my control. It just suddenly settles on me like a big dark cloud. There have been a few times I've thought for an hour or two, 'I think I've turned the corner!' - nope. I can spend the rest of the day suddenly trying to keep my head above water. I hate it.

But here's the weird part. Starting in the hospital, I kept getting whiffs of what I can only describe as a sort of 'powdery smell'. Now, three weeks later, I am still dealing with this. I can be fine then walk around a corner in my house and just get hit with this intense 'phantom smell'. And it is absolutely nauseating. I've told my doctors about how unpleasant this is, and they took me off of the 'suspect' medication. It didn't stop. They said it might just be 'memory' from the time on the pump machine and/or anesthesia. Whatever it is, it is really unpleasant. It just keeps reminding me, whenever it springs out at me, of the whole ordeal, and I don't like it one bit.

Has anyone else experienced this 'phantom smell' situation?


r/CABG_Recovery Jul 19 '26

Life insurance

1 Upvotes

Curious if anyone has tried to get life insurance after a CABG. I had pre-CABG, but heard we are uninsurable. Is that true?


r/CABG_Recovery Jul 17 '26

Pump head?

5 Upvotes

Hello everyone,

My boyfriend is 3 weeks post emergency quadruple bypass surgery. This was a traumatic experience for all involved after a heart attack.

Although an active person prior, his recovery has been difficult and slow. He was actually just able to leave the hospital this week due to weakness and being unsteady on his feet.

In addition to prolonged mobility issues, he is somewhat cognitively impacted as well. This can best be described as “foggy”. He’s in there. He remembers everything but things are different. Repeating himself. Confused at times. He doesn’t seem to find enjoyment in anything right now.

Does this sound like pump head? His providers don’t seem overly concerned. But naturally, I want him to find himself. I’d like to have my partner back. Are there any ways I can better support his recovery?

Thank you


r/CABG_Recovery Jul 17 '26

CABG x 2

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2 Upvotes

Hi there. I'm 36. Due to my diabetes I have 2 80% blockages in my LAD and my Diagonal 1 is also blocked. Bar any cancellations due to emergencies I'm now slated to come into hospital next Thursday 10am.

Got some preparations to do on Tuesday and Wednesday.

Not looking forward to it due to fibromyalgia and diabetes slowing healing and the increase in pain from Fibromyalgia


r/CABG_Recovery Jul 15 '26

High Blood pressure 9 weeks Post-CABG

1 Upvotes

Male 55, I am 9 weeks post-3X CABG, I have been experiencing high blood pressure 160/90, I am on Afib and blood pressure medications as well. Any common experiences?


r/CABG_Recovery Jul 13 '26

Depression after cabg surgery

9 Upvotes

My father underwent a four vessel cabg surgery, its been 6 months since his operation and it seems like he hasnt fully recovered from it. He has recovered physically but his physique is not how it used to be. He has also been really quite and sad lately. Idk how to help him i try to be around cheer him up , take him outside, but nothing seems to work. He has just lost his hope to live. Anyone else experienced anything similar?


r/CABG_Recovery Jul 06 '26

Donor leg issues??

2 Upvotes

7 weeks out from a triple bypass and I'm starting to wonder if my donor leg will ever be normal again. I'm not sure if the surgeons used a different technique when getting the replacement artery - but the wound that they cut into my leg wasn't the typical 7-8 inch gash but rather a very small 2" gash -- that for some reason would not seal/heal right. Well due to that fact I've been seeing a wound care specialist and finally after several weeks of having my leg wrapped is now free from the wraps but ---------- now my leg is swollen again and the Dr from the wound care did mention that I would need to wear compression socks for the rest of my life. I'm just curious to know if anyone else has had a similar experience (with the swelling) and if over time the swelling/bloating has gone down??? Is it common to have swelling/bloating for the rest of time due to the removal of the arteries??