Don’t worry, we are nearing the end of the story of my SVC syndrome from blood clots and the related hospital stay! If you will, come back to early fall when I was in the hospital trying desperately to get home to my girls again (you can see the previous posts here under Detour – SVC Syndrome).
We are now at the seventh day of my stay and I awoke anxious, ready to have my port taken out. During the morning, the doctors came around and I found out that if I had the procedure done that day, I could go home the next day (spoiler, doctors are not always right). If Interventional Radiology couldn’t get it done that day, I would be scheduled for the next day and go home the following. This had me concerned since we were headed into a weekend and it seems pretty obvious that much of the hospital would be operating on a limited type staffing through a weekend and, rightfully so, working on emergency patients first. With how quickly they had been able to get my care started when I arrived the week prior on a weekend, I don’t have a problem with that. Once the port was removed, they would need to get my Heparin (short term blood thinner I had through IV) numbers back to level, then switch me over to Lovenox (more long term blood thinner injected). My activity was to be limited once I was home. The original plan was to take it easy for 10 days with lots of rest and only going to doctor appointments. I was not to be left alone with my girls or drive anyone anywhere for the same time, until I was seen.

