Pulmonary Embolism Support Group
By far the most common form of pulmonary embolism is a thromboembolism, which occurs when a blood clot, generally a venous thrombus, becomes dislodged from its site of formation and embolizes to the arterial blood supply of one of the lungs. Symptoms may include difficulty breathing, pain during breathing, and more rarely circulatory instability and death.
TossNTurn
I'm curious. When I was diagnosed with my PEs, I had almost no pain at all. A little twinge (1 on a scale of 1 to 10) every so often in my breastbone, probably a result of my coughing that day. The first few weeks of recovery were also pretty much pain-free. After reading this board, I know how rare that probably is and I know it was my lack of pain that made getting to the PE diagnosis that much harder.
Now, at four weeks post-diagnosis, I'm starting to experience some more intense pains (3-4 on a scale of 1 to 10) not just in my breastbone but all over my ribcage and shoulders and even along my backbone. The pain isn't constant but when it is there it is uncomfortable and the twinges seem to be getting more frequent and staying longer. I know 3-4 on a scale of 1 to 10 is totally tolerable, but it is three times the pain I had when I was diagnosed, so it tends to set off my anxiety triggers.
My doctor thinks the pain is just part of my recovery process, but I'm curious about the pain trajectory for the rest of you. Did you start off with no pain and then develop more as the healing process went along? Or was it terrible at first and got better over time? Did it come and go? How bad did it get? Anyone have no pain at all?
Now, at four weeks post-diagnosis, I'm starting to experience some more intense pains (3-4 on a scale of 1 to 10) not just in my breastbone but all over my ribcage and shoulders and even along my backbone. The pain isn't constant but when it is there it is uncomfortable and the twinges seem to be getting more frequent and staying longer. I know 3-4 on a scale of 1 to 10 is totally tolerable, but it is three times the pain I had when I was diagnosed, so it tends to set off my anxiety triggers.
My doctor thinks the pain is just part of my recovery process, but I'm curious about the pain trajectory for the rest of you. Did you start off with no pain and then develop more as the healing process went along? Or was it terrible at first and got better over time? Did it come and go? How bad did it get? Anyone have no pain at all?
Posts You May Be Interested In
-
Look at what my best friend did with my picture!
-
We all have 24 hours in a day. How we spend these hours is important. Watching a little bit of a video about how sitting affects us made me aware of how much sitting and laying down I do. Gonna have to work on that.Your turn. Tell me another truth.
sternum near the bottom. It started to ease up
about two weeks after being released from
the hospital. It comes back every now and
then. Pain was my only symptom.
Within 2 days almost all pain was gone
Chris
In the 6 weeks since I got out of the hospital, my pain has been all over the place (mostly 3 or higher, often 9), and almost always worse than when it all started. My doctors think it's weird but not totally abnormal.
So anyway, I I had pretty bad pain, it is down to a two in the patches.
The other two times, there was no pain. The reason I went to Urgent Care both times is because I had shortness of breath upon exertion that got worse daily until I could barely walk across the room...but no pain.
Leslie
I only experienced pain after diagnosis.
What interesting lives we live now, huh?
Others may have had pain in the lead-up, or other variations for how and when it came and how long it lasted.