Looking for others with Pulmonary embolisms

I believe that over time the clots can damage your lungs. I read that somewhere

The last few days I’ve been experiencing shortness of breath more than usual and tightness in my chest. Is it worth going to my gp? I mean what can they do other than keep me on blood thinners?

I am so sorry to hear your problem is continuing. I think it is important to find out what is causing the shortness of breath it can be many different things If you are having an embolism, they can give you medication to breakup the clot, and some oxygen to help with the shortness of breath. If you are having an occulusion, they can break up the occulusion and perhaps place a stent, if you are having Atreial Fibrillation, they can give you medication for this problem. As you can see this is only a small number of reasons for your problem, and they all have medications to help the problem. Please seriously consider seeing your doctor tomorrow.
Gina5009

I would agree. Please go in and get seen. I hope they find nothing.

I had sudden onset in July 2020 - fainted so went to ER and the clots were in lungs and the saddle area between. I’m lucky to be alive. ICU w heparin 3 days, another 4 in hospital- on elloquis for life. They told me the clots had to have been in my groin or hips or legs then traveled to lungs. I never felt any symptoms of clots before they hit my lungs. I do have 2 blood mutations - factor 5 Leiden and Prothrombin.

My husband collapsed on Thursday after a triple heart bypass 8 days earlier. He's had X2 PEs one in each lung, apparently quite significant we've been told. He's on injections whilst in hospital,been told he'll be on medication for at least 6 months . Just wondering if anyone has had something similar happen following heart surgery. How do they monitor the Clots after discharge,can you live a normal life. Asking lots of questions but answers are not forthcoming.
Thank you

I was sitting with my husband when his electrocardiogram suddenly went straight up and straight down. I told the nurse something bad was happening and she called the code. They gave my husband two jolts with the electrodes and converted his EKG to some type of normal and took him off to the Cath Lab with no promises. It was found he could not swallow 3 days following surgery. The doctor later stated they thought he might have had a small stroke.It became necessary for them to surgically insert a tube into his stomach to feed him and then began the rehab to teach him how to swallow again. It took about 3 months for him to fully regain his ability to swallow and have the tube removed. They taught him how to avoid water or food going down his windpipe. He never had an embolism, but they had him on a full aspirin for some time and then on baby aspirin after that. They also started him on Warfrin, but this was just too much for him to monitor and office visits regularly. His life was pretty normal. Watchful but otherwise very normal. He was at home, he had his grandkids visits and pretty much enjoyed life.
Gina5009

Hi I just got diagnosed with PE on Thursday 05/25/23 and I’m frightened

All I can think is I’m going to die. I started Eliquis and it scares me. I’m just scared and feel alone and I don’t want to leave my family and pass away. I know nothing about Eliquis or what it’s supposed to do. I know not much about PE. Just heard about it a few days ago.

I went to the gp and he wasn’t concerned so I’ll just carry on. A pharmacist at work did some sort of training on line and found that my hrt patch maybe the cause even though my specialist said he couldn’t find any evidence so I’ll show him what she screenshot to me

Go to a pulmonologist!! You should have received education from you doc about your blood thinner. It does not sound as if you are getting good medical care.