Delurking.
HA is a horrible, debilitating, isolating condition.
Mine began in March, and I've done my best, but I'm seeing my GP on Tues to see what medication options there are - it cannot be a coincidence that this all began a few months after stopping citalopram (I thought I was well enough to stop).
It began with worrying about whether or not I have a type of tumour called a pheochromocytoma. This is not as outlandish as it sounds since I have a genetic mutation which causes it - I am screened annually. Anyway, this year, my scan had to be postponed as the York MRI scanner has to be made compatible with my new-ish cochlear implant.
Since then, I think I've managed to induce some of the same symptoms! I get quite a few pvc's (I have always had these but they are increasing), and go about feeling like I am about to drop down dead of a heart attack. I've had horrible panic attacks, developed pulsatile tinnitus (so this is obviously a sign of a tumour in the head and nothing at all to do with having had surgery in the affected ear .... in fact, the implant centre said it was all normal), dizziness. Familiar complaints, I'm sure.
I've joined a PVC support group, seem to spend hours on the net diagnosing myself with things like supraventicular tachycardia. I have hidden in bed checking my pulse, and afraid to actually go to bed as that's when I notice the skips more.
The ridiculous thing? I get maybe 20-30 a day, and I'm sure 95% of those are caused by this anxiety. I had various heart tests before my surgery two years ago and was deemed athletic! I doubt I've developed some awful disease in the interim. So ... the pvc happens, which generates fear, which generates more, and on it goes. I need to break the cycle as I'm becoming a nervous wreck!!
Not looking for advice as such .... I'd say it's good to know others are having similar experiences, and that I'm not going mad.