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.
Did a doctor suggest that it might be thoracic outlet syndrome which 'might' be an anatomic abnormality?
http://emedicine.medscape.com/article/462166-overview
It doesn't have to mean that, but I found it curious.
"Thoracic outlet syndrome (TOS) has been an important clinical entity for more than a century. In 1821, Sir Astley Cooper first described axillarysubclavian artery symptoms due to compression from a cervical rib. In 1875, James Paget described the clinical symptoms resulting from subclavian vein thrombosis (eg, arm swelling, pain).
In 1884, von Schroetter correctly attributed these upper extremity venous symptoms to thrombosis or compression of the subclavian vein at the thoracic outlet. Consequently, venous thrombosis at the thoracic outlet is known as venous TOS or Paget-Schroetter syndrome."
Bee------ that was a savvy acupuncturist you had!
I think I remember reading that a massage therapist developed it because of her position (bending over a patient). Maybe I ought to be checked out, come to think of it---- I was a dental hygienist for 17 years and you know how they sit (and apply pressure) 8 hours a day!
My brother's clot occurred after surgery on his shoulder. His doc thinks that the strap they used to mobilize his arm may have been too tight. But when my brother mentioned my history, his doc thought it may be a genetic component despite all my genetic testing coming back normal. He's on warfarin. As most hematologists say, there may be genetic clotting issues that scientists aren't even aware of, or for which there is no test. So there could be an unknown genetic component I'm sure.
But I do doubt either of us has TOS.
My brother had cancer in his early 20s, and also has a specific chromosomal syndrome which can make him prone to clots, I just read, and with me having ulcerative colitis, well, we both are sort of genetic misfits, so who knows. For me, at this point, it doesn't matter why I clot, as I'm multi clotter and therefore, on the warfarin train for life.
I don't know that I believe only 1%-2% of DVT clots are in the arm, but maybe that's true. But I do know that arm DVTs are less than leg DVTs to break off and travel to the lungs. Not saying it doesn't happen. Just saying the percentage is lower for that happening.
You said:
***I don't know that I believe only 1%-2% of DVT clots are in the arm****
I don't either----- If something isn't looked for it isn't found. (grin) Like Lyme disease is a 'rare' disease. Snort!!! Poppycock!!!
My symptoms was pain in my arm and chest for about a week, then my arm started getting pain and tingling, what finally made me go the ER, was my arm turning a red/purple color, and extreme pain.
If anyone thinks they have a DVT in their arm, or anywhere for that matter, you aught to get it confirmed via an ultrasound, rather than just speculate. My 2 cents.