Our Kim
Kim Smith
is our daughter-in-law, the wife of our oldest son, Calvin. They live in Roanoke , Virginia .
Their sons are Josh (9) and Jackson (7). Calvin is an attorney. Kim is an
occupational therapist. They are among the families who founded Christ the King
Presbyterian Church. Kim left the hospital and began home hospice care on
Friday, November 2. They began posting on CarePages when Kim was diagnosed with
Stage 4 breast cancer. Calvin has done most of the posting, but Kim has made
some excellent posts, especially during the current year. Below I have
collected some of these, which reveal Kim’s heart. I have provided a very few
notes to give context for Kim’s comments. I have put these in italics within
parentheses.
One
further note: Kim and Calvin are involved with Susan G. Komen. I understand
that some do not want any association with Komen because it provides some funds
to Planned Parenthood. Planned Parenthood does provided abortions. But Komen
does not provide funds to PP for the purpose of funding abortions. It provides
funds for mammograms, which Planned Parenthood does not do but which they can
send patients elsewhere to receive. No doubt the funds are intermingled. But,
there are many organizations, including charitable ones, which are “mixed in
nature” to which Christians give. Komen’s main purpose is to raise and direct funds
for research to find the cure(s) for breast cancer, a cause about which Smiths
care much.
Kim’s Story. On April 2, 2010, I was diagnosed
with breast cancer. We learned about 2 weeks later that it had already metastasized
to my liver. Following 8months of treatments in March 2011 I had a mastectomy.
In April, 2011, we learned that the cancer had now moved into my bones - along
multiple vertebra and ribs. We are continually trying potential chemotherapy
agents and radiation. We continue on a chemo as long as there is some evidence
of its effectiveness. If that evidence does not exist then my oncologist works
with colleagues all over to determine the best next treatment for my cancer. We
are thankful for your prayers, love, and encouragement for myself, my husband
Calvin, and our two sons Josh and Jackson. I have been married to Calvin since
July 1, 2000. The Lord has blessed us with 2 handsome and energetic boys - Josh
and Jackson. I have a wonderful church family at Christ the King Presbyterian.
I work full-time (although a flexible schedule) as an Occupational Therapist,
teaching and coordinating fieldwork education (clinicals).
(This paragraph mentions Laura Black, a member of Briarwood Presbyterian Church in
March 19, 2012. (In March, Calvin and Kim and Josh and Jackson went to Legoland in Florida , a Christmas
gift from Kim’s mother.) My final
walk back through the park was bitter sweet. I remembered the excitement and
joy from earlier, but didn't anticipate I would feel quite this bad. I knew it
would be a tough day for me, but I just thought I would be wiped out afterward,
not having to sleep while there. As I walked behind the boys and watched them,
I could only smile! They had had a day to remember!!! Along with that smile
came a few tears though. I thought I was hiding them through my sunglasses, but
my wonderful husband noticed and asked. Yes, I was crying..... I hated the way
I felt right then, my back hurt, I was miserable, I hated that I could not make
a day at an amusement park with my family, I hated that my boys had to look at
their mom and feel sad for her, I hated that I missed some of their day - a day
they were so excited about, and they knew I missed it, I hated that they looked
at me with sadness because mommy doesn't feel good, I hated that this stupid
cancer and even stupider chemo was making me feel this way. I hate that I will
likely miss so much more! Bittersweet - pleasure alloyed with pain.
Never did we anticipate THIS LONG ROAD TRIP though! As of today, we have been traveling this road for 2 LONG YEARS. One thing that God is working on with us, throughout this road trip, is to learn to enjoy the journey. Wherever it takes us. Our "anxious-to-get-there" selves are stopping to see the sights and finding ways to enjoy even the bumps in the road (and boy have there been bumps, pot holes, detours and dead ends these last 2 years)!
I am so thankful that God has continued to allow me such fullness of life despite the diagnosis and treatment. I try daily to not focus negatively on the prognosis - or to continue my theme, the destination. It can be overwhelming and often a struggle t
I have not said thank you enough to those of you that have provided help through meals, encouragement, prayer, loving on and entertaining Josh and
Continuing this long lasting road trip...
"You make known to me the path of life; in your presence there is fullness of joy; at your right hand are pleasures forevermore." Psalm 16:11
June 19, 2012. (In June the family took a trip to Destin, stopping on the way in
June 29, 2012. "You have granted me life and steadfast love, and your care has preserved my spirit." Job 10:12
Several mornings while sitting on the balcony at the beach and taking it all in, I spent time in the book of Job. Throughout all of the struggles, devastation, loss, and grief I must continue to recall God's blessings and promises. It can be so easy to focus on the negatives and the curses, but truly I am blessed and the Lord has preserved my spirit (for now and for eternity)!! How can I not be thankful!
This week has continued to be up and down as I reflect on Laura's death. I was in the car yesterday singing Oh Love That Will Not Let Me Go and as the verse mentioned "I trace the rainbow through the rain and feel the promise is not vain" I just burst out in tears. Laura always reminded friends of God's promise made to Noah and the sign of the rainbow... I will never look at a rainbow without thinking of her. "That morn shall tearless be!" Calvin and I still have not told Josh and Jackson about her death. We know that we need to - they were just with her and her kids less than 2 weeks ago - but I am really scared to do so. Please pray with us about this.
Well as for my next treatment, I have been approved for the next clinical trial and was randomized to the experimental chemotherapy (NKTR 102). I will receive my first treatment on Thursday of next week. The infusion time is listed as 90 minutes, so with the blood work on the day of treatment as well as meeting with doc and researcher and then treatment it will probably be about a 2 1/2 to 3 hour day at the center.
As of yesterday I have not had chemo in 7 weeks (last chemo treatment was May 10) so since having a scan on Monday, I have been curious about the potential growth of tumors in that time. According to the researcher, the results state that things remain stable in the chest - which is still a very good sign. As for the liver, the radiologist's report did not give actual measurements this time. It states that they have "progressed and that they are coalescing and difficult to measure". Now the researcher didn't know exactly what that means and my doc is out this week. Even though I teach medical terminology I was not familiar with that term so I looked it up. Sure enough it means "to grow together, to unite into a whole". That is what the researcher suspected. We don't know to what degree and will hopefully find out more from the doc. So you all can be praying about that progression. Hopefully the trial will prove some success in decreasing liver tumors while providing limited side effects for me.
Well, that pretty much covers things for now. Thanks for your prayers and encouragement.
August 8. 2012. Since being on this new clinical trial, I have never really felt like myself. The title above pretty well sums up how I have felt physically and emotionally over the last 6 weeks. I get a little stronger and then the next day I feel like crawling in a hole again.
On Saturday I had the blessing of going to a women's bible study and fellowship with my mom and ladies from my church. It lasted about half the day. When I returned home I slept. It was wonderful to be in the presence of my sisters in Christ - the conversations were very good for my soul (I need to have them more often!).
Sunday I slowly got ready for church but was only able to stay about 30 minutes as I began to feel sucked of energy and if the world was closing in. Later that afternoon I got sick and continued to sleep the day away. That evening my 3 boys were able to enjoy an evening with good friends and I was saddened that I just could not go.
Monday, the joy of my day was having an all out tickle fight with
Tuesday I felt pretty strong so I spent several hours at the office preparing for fall semester (it is coming soon). After a good day at the office, I took the boys to the dentist and helped mom prepare a delicious dinner. I still can't eat very much at times, but I tried!
Today was another day of no energy. To go out for Zaxby's chicken at lunch completely wiped me out!
Today I am meditating on Psalm 23. It is one we almost know so well that we tend to gloss over the depth of it.
The LORD is my shepherd, I shall not want.
He makes me lie down in green pastures.
He leads me beside still waters. He restores my soul.
He leads me in paths of righteousness for his name's sake.
Even though I walk through the valley of the shadow of death, I will fear no evil, for you are with me;
your rod and staff, they comfort me.
You prepare a table before me in the presence of my enemies;
you anoint my head with oil; my cup overflows.
Surely goodness and mercy shall follow me all the days of my life,
and I shall dwell in the house of the LORD forever."
Y'all that is my comfort, that is my strength in this! He is WITH ME! And I will dwell with Him FOREVER!!! Thanks for your continued prayers. Mom is here for just short of one more week and it will be hard when she leaves. We have been blessed... Surely the Lord is with us! Next treatment is Thursday Aug 16 and then scans on Thursday Aug 23.
August 10, 2012. I type this update while hiding behind tears. Josh is upstairs,
I was excited earlier today...got my shower (taxing), put on some makeup (had to sit down), Put on my red dress and heels (then stretched out on the bed). Calvin came home early from work to get changed too. We were heading up to
But when it came down to it, I just could not go. I can't even sit through church these days, much less drive an hour for a reception. There was no guarantee I could survive it so we said "NO" to me going. He pulled off my heels and I walked him downstairs and out the door, then as he drove north I crawled in bed :(
Oh how I wanted to be there. To be with him. I wanted to celebrate with the Judge and his family. You see, they are very dear to us. I wanted to see Calvin and others honor him and his service. And I wanted a night with my husband...just my husband.
September 20, 2012. "Cast your burden on the Lord, and he will sustain you; he will never permit the righteous to be moved." Psalm 55:22
Yeah we are burdened here! But He is sustaining us! I believe that Calvin mentioned in his last post that he has been having some stomach pains and not feeling well. That has worsened over the last few days. Yesterday he went in to see his doctor and had an dray and blood work done. This morning, after I dropped off the boys at school, I had to report for my Brain MRI (Calvin had said Friday but it was today). While waiting to be called back Calvin called to let me know that his doc had called and told him to go to the Emergency Room b/c his lipase enzyme (pancreas) was very high. Thankfully a friend of ours was able to get him to the hospital while I had my mri. He was still in the ER when I got there. Around 3:20 he was finally transferred to a room. The plan is that he will be there a few days to control the pain and try to stabilize his pancreas. At this point they are uncertain of the cause. Some of you may remember this enzyme was high about a year ago as well....today it was much higher.
As you can imagine this news was extremely hard for the boys to hear. "Daddy isn't supposed to be sick, mom that's you." They want daddy home and some sense of normalcy. They were not able to see him but begged to go to the hospital. Tomorrow after school they will get to visit him.
We are tired and burdened from the journey we have been on. But we are well aware that God will sustain us and carry us through this current trial.
Thank you for your prayers. Pray for Calvin's healing, my strength, and for they boys as they try to deal with this.
Friends it has been a rough road for the Smith's. I know that while I desire to spend every moment with Calvin, I MUST take care of me (or else we end up with two patients at Memorial.
October 12, 2012.
Pink, Green, and Blue -
Colorful Musings from a Woman with Stage IV Breast Cancer
Part 1 - Pink
You have to know where I am
starting here... It is October and everywhere we go there is Pink for Breast
Cancer Awareness Month. Last night, I was extremely saddened when I read an
article on today.com about a woman who, like me, has stage IV breast cancer.
She was putting down the pink and stating it was like a slap in the face to
those of us fighting in incurable stage of breast cancer. She doesn't feel
included in the activities of the month because she believes the focus is
mostly on new breast cancer diagnoses, prevention, and early detection. To
quote her, "I was beyond prevention, beyond cure, beyond survivorship,
beyond pink." Yet another woman (with stage III) in the article stated
that she too "can not celebrate because she is not a survivor".
Oh y'all this hurt me deep
down as I read it. I understand the pain, fear, anger and such of this
incurable diagnosis. It is true that I am beyond prevention and beyond a cure
just like this woman. But oh this is not just about ME. Sure we all wish I
didn't have to go through this. I wish this woman didn't have to go through
this either. But it is the portion we have been handed. And as I spoke about at
our Roanoke
race for the Cure last April, survivorship doesn't have to mean being cancer
free and done with it... Survive is what we do at stage IV.
What if, just what if,
because of all of the pink... if this awareness leads to action? Some stats say
there are 155,000 women in the US
living with Stage IV breast cancer. Y'all what if I could be the end of it?
What if what I am going through, what others are going through, what research
is being done, what awareness and early detection and treatment that is going
on could lead to NO MORE STAGE IV? I am ok with that!!! The early stages are
treatable - even curable! So let's be stuck there!
Pink is for National Breast
Cancer Awareness this month. Yes, we have been seeing pink in October since
Marilyn Quayle's work during the Bush-Quayle Administration. Folks that's a lot
of awareness! But at some point, there must be more than just awareness.
Somewhere along the way there has to be a change of heart for action too! Just
like as I walk in faith, I often become "aware" of sinful words and
actions on my part. But once God has changed my heart on the matter, then I can
take action. Sometimes I get hit time and time again with the awareness piece
before the action starts! Well, even with the pink representing awareness, know
that there is action out there! I get so excited during October when I am
reminded of the various organizations out there that are in action against
breast cancer. Not just detection but treatment for me too! Remember I am in my
second clinical research trial for treatment. So friends be aware and if you
are led then follow through with action - whatever that action might be (for
yourself or for others). I want to be the end of Stage IV Breast Cancer!
Thanks again for your
continued prayers and encouragement for my family. times are tough, but God is
good to us!
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