Since
hospitalization on May 8th I’ve been too focused on adapting,
recovering, whatever. In a sense running scared.
Yeah I’ve
read about the side effects of brain radiation therapy but 40% through it was
time to press myself. My brain is more than precious to me and with the
metastasis hopefully in retreat I needed to get it busy being my brain.
My
loving ‘care nazi’ still will not let me drive.
So I mowed the lawn 5500 sq ft (510.97m²). A week ago my daughter’s assistance
was needed to cut half. Today I cut it myself motivated by my daughter’s quip, ‘hey
after all the lawn mower is kind of like a walker’. J Plus if
you let go of the bar, I can hear if you fall.
Stubbornly
I waited until the hottest most humid part of the day to wrestle with the lawn.
No problemo, stamina was good, breathing good, I could follow lines and
complete the task - physical check OK
I
checked fatigue and confusion by working on line and/or phone entire day and
early evening keeping up and getting ahead of my cancer book (actually a 2”
binder and growing of copies of every test, result, procedure and more). My
voice is getting raspy.
Inspiration
can too soon become platitudes. Bottom line health care whether mine or anyone else
is about information and what you control.
Yes I
could multi-task attentions and do it well when abruptly my self-check was dwarfed
by the horrific news out of Oklahoma. Too many times over the years I find myself
watching TV in disbelief at news.
My brain’s
memory was right in sink as I found myself pausing to remember and give thanks
for the three of us the day a F3 tornado with winds of 200 mph suddenly dropped from the heavens into College Park, MD late one afternoon in September 2001 (yes,that same September 2001 only two weeks after terrorist attacks) killing two, injuring 50, and throwing vehicles and house parts helter-skelter
for 10 miles. Our neighbors told us they
watched it skipped directly over our home sparing myself, Megan, and most of
all Patti. Forces of nature are NEVER disability friendly.
… and a vivid
reminder that the next moment in time is never guaranteed. So hug or at least
tell those you love every day that you love them.
When and
if possible stop to smell the flowers. My lung cancer will be
there in the morning. in the meantime, our yard features 4 lilac bushes and my radiated but
successfully self-checked brain finished the day by harvesting a bowl of fragrance
to perfume the home.
A sprig with its flower I break."
"Stands the lilac-bush tall-growing with heart-shaped leaves of rich green,
With many a pointed blossom rising delicate, with the perfume strong I love,
With every leaf a miracle—and from this bush in the dooryard,
With delicate-color’d blossoms and heart-shaped leaves of rich green,
When Lilacs Last in the Dooryard Bloom’d by Walt Whitman
Patrick Leer
Health Activist:
Caregivingly Yours, MS Caregiver @ http://caregivinglyyours.blogspot.com/
My Lung Cancer Odyssey @ http://lung-cancer-survivor.blogspot.com/
Technorati Tags: brain metastasis
We have a lilac bush that peaked a few weeks ago - the scent in the house was heavenly!
ReplyDeleteIt was actually your Dad who advised me to "stop and smell the roses" - I haven't heard that reminder in a while.
Welcome back from the left coast!
DeleteDearest Patrick, I have been blessed reading your blog and they have really brought some peace and strenghth to me. I had written before anon. Yesterday I attempted another and got hung up on URL, etc. Not very computer knowlegeable. I have a 4 cm thing in the left lower lobe. The PET scan showed "some activity". Since I am leaving for Israel the 10th of June to see a new grandchild be born, I will be scheduled for a wedge resection shortly after I return on July 15. After looking at the wedge in the lab I hope they have enough info to do the lobectomy left lower node.Or, that the thing is not a cancer???I feel very frustrated with the thoracic surgeon-I like to visualize what will happen-he is not a candidate for best patient communicator but I guess I don't want to be his best friend. He just needs to do his part. First step after weeks of hiding this from my kids was telling them yesterday. I think they'll make it.Why did I ever try to hide this? I taught them to be strong independent people. Patrick my prayers are with you and your family, my church members have you on our prayer list and I am just so grateful for your writings-I thought for a while I was loosing my mind. Your words comforted and I know know what I will need to get through this. I.m off the pity pot and ready to roar. Gayle Pard Edmonton Alberta Canada
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