Ask Lemmy

26701 readers

2735 users here now

A Fediverse community for open-ended, thought provoking questions

Please don't post about US Politics.

Rules: (interactive)

1) Be nice and; have fun

Doxxing, trolling, sealioning, racism, and toxicity are not welcomed in AskLemmy. Remember what your mother said: if you can't say something nice, don't say anything at all. In addition, the site-wide Lemmy.world terms of service also apply here. Please familiarize yourself with them

2) All posts must end with a '?'

This is sort of like Jeopardy. Please phrase all post titles in the form of a proper question ending with ?

3) No spam

Please do not flood the community with nonsense. Actual suspected spammers will be banned on site. No astroturfing.

4) NSFW is okay, within reason

Just remember to tag posts with either a content warning or a [NSFW] tag. Overtly sexual posts are not allowed, please direct them to either [email protected] or [email protected]. NSFW comments should be restricted to posts tagged [NSFW].

5) This is not a support community.

It is not a place for 'how do I?', type questions. If you have any questions regarding the site itself or would like to report a community, please direct them to Lemmy.world Support or email [email protected]. For other questions check our partnered communities list, or use the search function.

Reminder: The terms of service apply here too.

Partnered Communities:

Logo design credit goes to: tubbadu

founded 1 year ago

MODERATORS

[email protected]

To people who had pneumothorax surgery, How are you doing now? (slrpnk.net)

submitted 11 months ago by [email protected] to c/[email protected]

14 comments fedilink hide all child comments

Just had my 2nd lung collapse almost a year after the first . The doctors are recommending me to get a VATS surgery but I'm not sure what to expect post surgery. I have an appointment tomorrow to finalize my decision and I could ask them but I also want to know the experiences of people who had it done.

Do you regret doing it?

Are there any persistent pain even years after the surgery?

Were you able to return to normal life after, like swimming, lifting weights etc?

you are viewing a single comment's thread
view the rest of the comments

[–] [email protected] 7 points 11 months ago

I’ve had VATS twice now. One in 2019 and one in 2021. Both were for a pleurodesis as the pneumothoraxes I experienced refused to self resolve. Zero regrets on both, but I didn’t have a choice, really.

Only pain I was left with is slight discomfort in my left upper chest region if I inhale too deeply while reaching up for things, and some nerve damage that results in a localized burning numbness that extends slightly into my armpit if I press above my right breast. Nerve damage came from the second.

I did have nerve damage from the first that left me numb in a candy bar shape right under my ribs on my left side for a year or so. The numb burning above my breast comes and goes in severity but the severe end has been weakened more and more with time.

I was able to return to normal life. Exercise isn’t an issue as long as I avoid over extending my arms upward. Basically no straining to reach stuff on my left side. I haven’t been swimming in many years, but I can imagine large, powerful strokes could cause me some discomfort.

Life is back to normal for me now, but I do have some anxiety that crops up with chest pains. The worst part of it all in my experience was the chest tubes.

Hope this helps.