VATS approach for lung nodule surgery: How was your recovery? Pain?

Posted by marylb @marylb, Dec 17, 2025

I'm 71 years old and I have a 15mm ground glass nodular opacity in my RUL, toward the surface, not deep in my lung. I'm scheduled for surgical treatment with wedge resection VATS in 2-1/2 weeks. My thoracic surgeon told me surgery one day and discharge the next day after the drainage (chest) tube removal. He also said no chemotherapy, no radiation and very little pulmonary rehabilitation will be needed. I'm, of course, terrified about the surgery. Has anybody had this type of surgery? How was the pain after? How was your recovery? Did you need chemotherapy and/or radiation? Thank you for any help you can give me!

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Profile picture for chubby55 @chubby55

Hi Yes I recently had this type of surgery RLL. Had robot assisted procedure to remove malignant tumor Sclc early stage. 6 hours in theatre 3 days hospital came home with drain.. Im post op 6 months still pain as described by consultant and was expected. My last scan was no spread don't need further treatment obviously further scans for the future to keep an eye on things... Managing pain bit swings and roundabouts to be fair. But managing can take up to 12 months I was told. Hope this helps good luck for surgery hope all goes well.

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@chubby55 Thank you for the reply, yes it helps. Wow, 6- hours, that’s a long time. Glad your last scan was good and continue to be.

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Hi Yes I recently had this type of surgery RLL. Had robot assisted procedure to remove malignant tumor Sclc early stage. 6 hours in theatre 3 days hospital came home with drain.. Im post op 6 months still pain as described by consultant and was expected. My last scan was no spread don't need further treatment obviously further scans for the future to keep an eye on things... Managing pain bit swings and roundabouts to be fair. But managing can take up to 12 months I was told. Hope this helps good luck for surgery hope all goes well.

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Me....Surgery was easy
the road to recovery was simple//
keep using the breathing measuring apparatus
Probably forever and stay Warm

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Profile picture for magwriter @magwriter

Hi @marylb. I had a similar surgery this past August. The surgeon did a wedge biopsy in my upper right lobe, it was identified as malignant and so they carried on and did a lobectomy. I was discharged after two days. I had more pain than the others above, athough a couple of things may have contributed to that including previous surgeries and an allergic reaction to the adhesive dressing. I used Tramadol for the pain for about three weeks and am still using Lyrica for nerve pain. I agree with the tight band around my middle and can't wear a regular bra. Get a cotton sports bra (Fruit of the Loom makes a simple one, like a short cami that's super comfortable) and wear loose tops. I'm 68 and slowly getting back to my usual activities. You can do it. I think. you will be surprised.

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@magwriter Thank you!

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Profile picture for rcerwin3 @rcerwin3

Thank you! Looking into this.

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@rcerwin3 you're most welcome - let me know how it goes. Merry Christmas!

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Profile picture for marylb @marylb

@raffi Thank you for the encouraging words! Glad you’re doing well. I’m not familiar with the acronym NED, could you explain it please? Thanks.

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@marylb NED means No Evidence of Disease. In other words, the cancer has not reoccurred as of that scan. Yay!

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Profile picture for EllaB @raffi

@kenhorse
I had the same experience with two rats (robotic surgery) six weeks apart. The second surgery took a little longer recovery but overall just over the counter painkillers. NED from 2023 (2 and half years 😜)

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@raffi Thank you for the encouraging words! Glad you’re doing well. I’m not familiar with the acronym NED, could you explain it please? Thanks.

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Profile picture for rcerwin3 @rcerwin3

My Dad, his Dad, his Sister and his brother all died of lung cancer but I am older and they died at 69, 70, 67 and 65. I was diagnosed at 66. We have no way of knowing what KIND of lung cancer theirs was but it would sure be nice to know where this came from. I have never smoked and just at the end of my yearly physical asked for a chest x-ray because I knew I was inching toward the age my Dad was when he died. Mine was 2.3 centimeters so it had been growing awhile. Do you have to know the type of cancers all of your family members had to participate in this study? I would do ANYTHING to not fear I would pass this on to my children.

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@rcerwin3 that is a lot of loss - sending you hugs! And good for you for asking for a chest x-ray - truly. For the study, you don't have to know the type of cancer. They have a screening questionnaire on their website. With so many family members having lung cancer, I think you qualify. You fill out the screening form - and then they email and call you if you've been accepted. If you have, they'll send a phlebotomist to your house and do genetic testing (for free). It takes a few weeks and then a counselor from their team will call and go over the results. If your results are positive, they'll also offer to test your family for free.

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My Dad, his Dad, his Sister and his brother all died of lung cancer but I am older and they died at 69, 70, 67 and 65. I was diagnosed at 66. We have no way of knowing what KIND of lung cancer theirs was but it would sure be nice to know where this came from. I have never smoked and just at the end of my yearly physical asked for a chest x-ray because I knew I was inching toward the age my Dad was when he died. Mine was 2.3 centimeters so it had been growing awhile. Do you have to know the type of cancers all of your family members had to participate in this study? I would do ANYTHING to not fear I would pass this on to my children.

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