hi, John:
Congratulations on your slow but steady recovery.
You really
do deserve a month off (from work) that you can enjoy a bit, having gone through therapy, not to mention an 8 cm AN removal. I thought my 4.5 was large but I feel like a pipsqueak compared to you. That's O.K. I willingly cede that distinction.
I also ignored symptoms, such as a steady decline in the ability to hear in one ear. Finally; intermittent, stabbing head pain on one side, a noticeable loss of equilibrium, a pronounced lack of appetite due to diminished sense of taste (I lost 30 pounds), weakness and unaccustomed lethargy combined to motivate me enough to consult with my PCP. After ruling out a suspected thyroid condition, he ordered an MRI scan, with contrast. Using my lack of appetite as a clue, he suspected and was looking for a sinus problem but the MRI found the AN, instead, prompting a personal, evening call, direct from my doctor's home phone. I was both impressed and concerned. My PCP and the neurosurgeon I eventually selected were alarmed at it's size and placement, pushing on the brainstem to the point that my brain had been pushed as far to one side of my skull as it could go. I underwent microsurgery (retrosigmoid) less than a month later. Then, three months following the surgery, FSR treatments (26) to kill the remaining tumor. So far, so good, as I note in my signature. I was fortunate not to suffer any serious complications and am doing well, now.
I regret that you've had a long road to full recovery but at least you can now see 'the light at the end of the tunnel', as it were.
I wish you continued success in your recovery and an enjoyable autumn as your 'issues' steadily improve.
Be sure to try and keep us informed of your progress.
Jim