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.
Also, just some things to look into or consider:
Calcium and vitamin B12 levels - make sure they're in normal range
Thyroid function- under active thyroid can cause this
Panic Attacks- can cause tingling and numbness, dizziness, loss etc. Very powerful.
Dehydration
One possible link is that I had a major car accident in 1993, and was hit on the left side. So could be residual side effects from that, though it wasn't confirm.
Dehydration may be in cause, but not likely. I know thyroid in not hypo active, as I've been loosing weight, not gaining and it's being checked regularly, as it runs in the family.
I'm also wondering if it may be related to the PEs, since this is new since the PEs.
It went away shortly after I got out of the movie and never came back. For me, probably some sort of weird combination of dehydration (helped along by all the salt in the popcorn) and maybe some anxiety. As it never came back, I just chalked it up under "recovery" and went on with life.
I get really tingly when I'm not drinking enough water, and I started getting a lot of anxiety a month or so after my PE, and experienced a lot of tingling and numbness that I realized was anxiety and stress related. Not saying you dismiss it as that but it's a very plausible explanation as well for a lot of people.
Have they tested you for MS? And many tick borne diseases can cause numbing, although most doctors don't know about them or test for them.
Just two more possible reasons for the numbing you're experiencing. Hope they're neither one---- and I hope they'll the cause and FIX IT!
This is just discussion---- I'm certainly not qualified to suggest that anyone has MS. But these things should be considered by you.
It would depend on many things (if your MRI would have found them), 'things' that I don't know.
I do know, from personal experience, that the type of MRI, the MRI heads used (and how many), the software used and the experience of the radiologist (and what he's told to look for) make a huge difference. Probably the dye also.
For instance---"Conventional pulse sequences at 3 T offers higher lesion detection rates when compared to 1.5 T, particularly in anatomic regions which are important for the diagnosis of patients with MS."
Demyelination of the nerves is tricky to see, especially if there is just partial demyelanation.
Don't ignore the possibility of Lyme disease. It is 'the great imitator' and I know many people who were dx'd with MS and later improved or got cured with antibiotics. The literature is full of those instances also.
I hope you don't have either!!! But a doctor will find what he's looking for----- not something else.