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.
mewshep
Hi everyone
Firstly, thank you to everyone on here for being so supportive. This is a great forum and I am not sure what I would do without it.
Ever since my PE back in December I have had problems with my GI tract. The day of my first PE I was retching and same the next day when I went to hospital. 4 months later (and lost of changes of medication) and I am still nauseus, hardly able to eat, no appetite, weak and in pain. I am now on loads of medication and investigations for all that. They have done scans, endoscopy, blood tests...they were about to do a colonoscopy yesterday but when they tested my INR levels it was 5 so they refused. Trouble is my INR is never stable - it's either 1. something or above 4 or 5. Very frustrating. I am anxious with all my stomach problems that there is something else they are not finding. I am probably being a worry-wart but my dad had DVT and PE and the medication didn't work. He kept keeling over and eventually became quadraplegic and died last year. I am worried I might be the same.
Anyway, thanks for listening everyone. Don't you just feel alone sometimes?
Firstly, thank you to everyone on here for being so supportive. This is a great forum and I am not sure what I would do without it.
Ever since my PE back in December I have had problems with my GI tract. The day of my first PE I was retching and same the next day when I went to hospital. 4 months later (and lost of changes of medication) and I am still nauseus, hardly able to eat, no appetite, weak and in pain. I am now on loads of medication and investigations for all that. They have done scans, endoscopy, blood tests...they were about to do a colonoscopy yesterday but when they tested my INR levels it was 5 so they refused. Trouble is my INR is never stable - it's either 1. something or above 4 or 5. Very frustrating. I am anxious with all my stomach problems that there is something else they are not finding. I am probably being a worry-wart but my dad had DVT and PE and the medication didn't work. He kept keeling over and eventually became quadraplegic and died last year. I am worried I might be the same.
Anyway, thanks for listening everyone. Don't you just feel alone sometimes?
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