I have only two sessions left set for tomorrow and Wednesday and then
my therapy will be over. It has gone by so fast. Am very thankful that
the short-term effects have been relatively mild compared to what could
have been. Hoping that it will be the same case with the delayed
long-term effects.
After my last appointment, my first follow-up appointment with Dr.
Selch is scheduled for July 17, about six months from now. It will also
include an MRI. This is supposedly a good sign because if it wasn’t, my
follow-up appointment would have been scheduled for April, i.e., the
3-month cycle. Normally after treatment, it takes a bit of time to
measure how effective the treatment was. If I am lucky, the MRI will
show some shrinkage of the tumor. However, I do have an appointment with
Dr. Lai at the end of this month along with the 3-month MRI cycle that
he has me on.
Being hopeful that the insurance issue between Blue Shield of
California and the UC health system will be worked out soon. My
continuity of care services applications, which would allow me to
continue to receive care up at UCLA from both Dr. Selch and Dr. Lai are
currently under review by Blue Shield and I should get a determination
sometime this week. All indications show that both applications should
be approved, but in the event that they are not, then I will need to go
find another neuro-oncologist if Blue Shield and the UC health system do
not come to a new agreement soon. So hoping for the best.
Lastly, I am set to return to work on February 6. I will be starting
out about 30 hours a week (M-F) to see how it goes. It’s hard to believe
that it will have been six months when I return. Seems that a lot has
changed since I left (e.g., moved to new office building, new staff have been hired, reorganization of the company after merger) maybe not, maybe the change is just me, or rather
my perception, who knows…but this will be another step towards my new
normal…
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