went for the thyroid nodule biopsy yesterday...
it was fascinating!
once again... i got to lie on my back and watch the whole thing on the ultrasound monitor... seeing the needle go in for the 6 passes it took to get enough tissue to make a diagnosis... each time amazed with how close it came to my pulsating carotid artery. yikes! doc... are you sure that student is ready to be practicing on me???
truly fascinating!
i'll hear results later this week.
then a trip up to the clinic resulted in hearing that i've been placed in arm/group 1 of the clinical study... which means i'll get the same treatment emma got when she had her melanoma 5 years ago (interferon).
bummer. i was hoping for group 2... but since we have been asking G*D to put us in the group that would be best for my condition... now we have to walk in faith that he did indeed do that.
faith is always so much easier when G*D answers our prayers the way we thought he should answer them.
anyway... on monday i'll head over to ann arbor... have a midline installed in my arm that will last for the entire month... and get the first of monday-friday infusions. i'll have the weekends off. and after the month... i'll give myself shots at home on monday, wednesday & fridays... for 48 weeks.
i should be off work for at least 6 weeks. they say that by that time i'll have a pretty good idea of how i'm going to respond to the injections. most people are able to go back to work at that time. i'm hoping and praying that will be true for me.
of course they'll watch me closely along the way... and if my liver goes wacky... they'll give me a break.
since beth is heavy into her new job... we're lining up people who live in jackson and work in ann arbor to drop me off at the hospital on their way in... then beth or someone can pick me up after my infusion which takes 3 hours each day. that way beth can keep things somewhat normal with work.
of course... westwinds is being great about it all. and emma is already coaching me on what to expect. and i have an incredible family. what more could i ask for?
yesterday... when i was at the u of m... i was walking down the big corridor behind a young lady pushing a wheelchair. she had a bad case of scoliosis and as i passed her, i noticed she was pushing her oxygen tank in the wheelchair.
wow... a quick reminder that my situation is nothing compared to what so many have to deal with every day of their entire life.
beth said her dad used to always say... "be kind... everyone is fighting a battle."
good words.