Sunday, September 2, 2012
Well the adventure continues. Last monday Pam had some labs drawn that by Wensday had the Oncologist concerned that we needed to get some chemo started. Initially we were going to try to get this done at home. It was however going to be difficult so we decided to get things started at the hospital. Sort of glad we did. Friday was a miserable day for Pam; very nauseated and it took a lot of drugs to keep her comfortable. This only succeeded in making us miserable since she was stoned. Well the doctors decided that despite the fact that CT scan seemed unchanged the GI doctor rescoped her and found that her stomach was not emptying. They could not decide if the emptying problem was mechanical versus functional. Mechanical would be bad and complicated to deal with. Functional would be something to work with. So another day in radiology for Pam and an NG tube. Despite another day of testing a mechanical obstruction was not absolutely ruled out. They started her on some meds to stimulate her gut. Over the next few days she made some real progress. Her mobility increased. Her nausea was minimal. Need for pain meds was decreasing. Eating better but it will take some time to catch up from the last 6 weeks. Your prayers and support have been life saving for all of us. We also had a wonderful visit from Pam's family. The infusion of family and humor was timed perfectly. Kendal and Scott are and will also be home this week. Mama D is coming next week.
Livin' Large... and Headed Back Home!
With summer drawing to an end in a few weeks, I didn’t want
to miss the opportunity to share some fun photos from a great summer weekend I
got to spend with the Ds. As you probably know, the Dedinskys have a home away
from home and that is their fabulous houseboat on Dale Hollow known as the
“Pirates of the Meridian”—a play on their Meridian Street home address!
Attached are some fun photos from that weekend, which was just prior to Pam’s
first stay at the hospital just over a month ago. It was so relaxing and truly
a wonderful and special getaway weekend. I totally understand why they try and get down
there as often as they can.
Pam and Greg have some colorful and fun houseboat neighbors
and the one who particularly stands out to me is “Kurt.” A ‘good ole boy’ from
Kentucky, Kurt enjoys life especially when there is some “moonshine” around. When I asked Kurt how he was doing one day, he
replied, “I’m livin’ large!” Wow,
what a great answer and more importantly, what a great attitude towards living
your life!
Since that weekend, Pam has definitely hit some bumps in the
road on her journey to healing, which was shared in an earlier blog. As I write this she is on the last day of
her second stretch in the hospital. She headed home today!—YEAH! Even during her hospital stays, she continued
to smile despite the pain and hasn’t lost that unique Pam sense of humor and has
been heard to still say, “Are you kidding me???”, one of
her classics.
Pam and I have discussed faith and what a gift it is. Last
week we shared an extra special time. I was organizing some magazines for her
and came across several prayers that were special to her, including some that
she had only recently received from family and friends. I read each one of them
to her and her face absolutely lit up and she told me how much reading those
prayers help her. Please continue to pray for Pam and her family…and send her a
special prayer. Those prayers are working as she had a positive CT scan today and will,
in fact, be going home tomorrow.
My dear friend does have a strong faith and is surrounded by
an incredible family who loves her so much. I’ve had the gift of seeing Greg,
her beautiful daughters, Pam’s mother and sisters help care for her the past
week at the hospital as her pain lessened, she gained strength and her appetite
came back allowing her to return home. Yes, Pam is “livin’ large” based on the
love of God, the love of her family and friends, and the special way she has
touched each one of our lives.
Thank you, Pam, and can’t wait to see you livin’ large back on
Meridian Street and back down at the Pirates of the Meridian. Please say hello
to Kurt for me. J
Love ‘ya-
Kim Graham Lee
(aka., Dr. Mama Lee)
Friday, August 10, 2012
Empty-Nesters (As told by Ellie)
Friends and family,
As I am off to school on Wednesday, I thought that
I would write a blog entry before my family ships me off!
As you can tell from the previous post, mom hit a
bit of a rough patch last week. Many calls came in with concerns;
however, I think that the pictures maybe made mom look a little worse than how
she felt. The beginning of the week in the hospital was a tough battle.
But, I think that mom handled it as gracefully as Ryan Lochte losing the
gold to Michael Phelps; head high, looking good. In leu of the olympics,
this process has been more of a marathon, as last week was a 100-meter huddle
sprint! Man, I really love the olympics. And as the olympics kept
us entertained in the hospital, so did the countless phone calls and visits.
Everyone's prayers have kept mom fighting as hard as she can since day
one.
The visit from Trudy and Pam was definitely an interesting and special treat. Those two always keep us laughing.
Another special shout-out to "Dr." Mamma Kim Lee, who truly has
been a blessing for my family since my mom's diagnosis. She is one
amazing person and we owe her a million thank-you notes.
Onto better news!
This week, mom is back home almost in full force.
She continues to go to physical and occupational therapy on Mondays and
Wednesdays to get motion and use back into her left arm. She got a new,
fancy arm brace that makes her hand look like Wolverine's. AWESOME.
Honestly, I am a little bit jealous. Past the cool new look, it
allows mom better use of her hand by assisting her in gripping and holding
objects. Although she hasn't quite gotten back to her nimble
guitar-playing hands, I assure you she will be back to strumming ASAP. I
know I can't wait.
Mom is going to be taking a break from treatment at
the lake this week. Hopefully she will get some needed R&R, since
last week took a lot out of her, as well as the family. We are headed
down to Dale Hollow for a family vacation before we all part ways. Dad
will be needing extra prayers as he makes trips back and forth to pick up and
drop off suburban-loads of people throughout the week.
I move in on Wednesday! As excited as I am to
start this new chapter in my life, I wish that I could stay home while my mom
continues to heal. She assures me that we can have Skype dates - I will
be seeing her bald through my new macbook rather than in person - because chemo
is the next plan for her fight! She has dealt with it well in the past, as
you all know - so we are very hopeful. She will hopefully regain her strength
back with the upcoming break in her treatment. I have complete faith that
your prayers have kept us going during this marathon. I can't thank all of you enough.
Please Keep up the prayers!
God Bless,
Ellie (The last, but CERTAINLY not least)
p.s. because I am leaving this year, my parents
will be empty-nesters... for those of you who live close, PLEASE, do not let my
parents stay home. I will send out cash donations to those of you who
would like to help :) JUST KIDDING!
p.p.s. Also...I'd like to add one more thought from Lauren's
close-friend (and future NBA star), Errick Peck. What a guy!
From Errick:
I took a visit to the Dedinsky household yesterday and as
always, they took good care of me. I just wanted to leave a small quote on this
blog to hopefully motivate you, show my concern for you, and let you know, Mama
Dedinsky, that you are in my prayers.
"The trials and pressures of life--and
how we face them--often define us. Confronted by adversity, many people give up
while others rise up. How do those who succeed do it? They persevere. They find
the benefit to them personally that comes from any trial. And they recognize
that the best thing about adversity is coming out on the other side of it.
There is a sweetness to overcoming your troubles and finding something good in
the process, however small it may be. Giving up when adversity threatens can
make a person bitter. Persevering through adversity makes one better."
JOHN C.
MAXWELL
Thursday, August 2, 2012
Bumpy Road
Well we have had an adventure this week. Not a real planned
one either sooo….how about a little background.
Since starting radiation Pam’s only real symptom had been fatigue and a worsening local sunburn. About 2 weeks ago she started having increased belly pain. We were initially able to control this pain with oral narcotics . Actually we were able to go down to the boat. While there, Pam managed to explode a gel pack and get second degree burns on both forearms. You got to be careful in the meth lab. The following weekend we had a repeat performance of pain. Monday of this week after radiation we got a celiac nerve block and had very good results for 7 hours. The next day while at radiation we all noted the Pam had a definite yellow hue: Jaundiced. This was confirmed by lab results. The concern was that the cancer was progressing. She was admitted to the hospital for hydration and testing. The tests showed that biliary tree was enlarged suggesting there was an obstruction. Again the concern that the tumor was progressing. Today Pam underwent an endoscopic exam that was to accomplish 3 things. 1)get a stent across the obstruction (2) reblock the celiac nerves (3) evaluate if there was obvious tumor. One and two were accomplished. Number 3 was a bit more ill defined. There was no obvious mass but there was some fullness in the area of the bile ducts. And what does all this mean? The good news is that radiation is over. PAM “RANG THE BELL”. The plan moving forward is let her Jaundice resolve and then restart some systemic chemotherapy. What and how long is yet to be determined. We are all doing better since Pam is better. If you have any questions let us know. We appreciate all of your love and prayers.
God Bless,
Greg
P.S. Special thanks to ("Dr.") Kim Graham Lee for being with Pam every day as well as being our photographer! We love you.
Below are some of her pictures...Enjoy!
Since starting radiation Pam’s only real symptom had been fatigue and a worsening local sunburn. About 2 weeks ago she started having increased belly pain. We were initially able to control this pain with oral narcotics . Actually we were able to go down to the boat. While there, Pam managed to explode a gel pack and get second degree burns on both forearms. You got to be careful in the meth lab. The following weekend we had a repeat performance of pain. Monday of this week after radiation we got a celiac nerve block and had very good results for 7 hours. The next day while at radiation we all noted the Pam had a definite yellow hue: Jaundiced. This was confirmed by lab results. The concern was that the cancer was progressing. She was admitted to the hospital for hydration and testing. The tests showed that biliary tree was enlarged suggesting there was an obstruction. Again the concern that the tumor was progressing. Today Pam underwent an endoscopic exam that was to accomplish 3 things. 1)get a stent across the obstruction (2) reblock the celiac nerves (3) evaluate if there was obvious tumor. One and two were accomplished. Number 3 was a bit more ill defined. There was no obvious mass but there was some fullness in the area of the bile ducts. And what does all this mean? The good news is that radiation is over. PAM “RANG THE BELL”. The plan moving forward is let her Jaundice resolve and then restart some systemic chemotherapy. What and how long is yet to be determined. We are all doing better since Pam is better. If you have any questions let us know. We appreciate all of your love and prayers.
God Bless,
Greg
P.S. Special thanks to ("Dr.") Kim Graham Lee for being with Pam every day as well as being our photographer! We love you.
Below are some of her pictures...Enjoy!
Keep up the prayers!
Sunday, July 8, 2012
"Grandma Pam"
Pam continues to amaze me! As she mentioned in her last
blog, her journey has taken a new turn with radiation treatment the next 5
weeks to help her gain more functionality in her left arm. (In case you didn’t
know, she is a leftie!) She started radiation therapy Thursday.
It was a longer session than will be
typical as they wanted to position her just right in the “linear accelerator”
(pictured here—no, that isn’t Pam in it!) and all the necessary markings were
on her body to ensure that the radiation was hitting the exact targets. If she ever wanted a tattoo, she now knows
what it feels like with the different black marker-like lines and circles on
her upper body. We were laughing because one of the markings looked like a
continuation of the pattern on the shirt she was wearing!
Your love, thoughts and prayers continue to give her
strength. Keep ‘em coming. Thought I would close with something I heard earlier
this week. The opposite of fear is faith
and Pam is indeed walking by her faith! You inspire me, dear friend. Love ‘ya!

Pam was a real trooper laying flat on her back for almost 90
minutes, left arm extended, head tilted to the side, knees propped up and body
completely still. Her back has been bothering her and I know she was really
ready to be done though she never complained. Fortunately, treatment sessions
will last only 15-20 minutes each day. She really likes Dr. Patel who is overseeing
her radiation treatment.
I also wanted to quickly follow-up on the news in her last
blog about the latest Dedinsky addition. Pam is a “Grandma.” No, while Kendal and Scott are high
achievers, they didn’t work that fast! However, their gift to Kaylin for
helping plan their incredibly beautiful and fun wedding was a miniature Golden
Doodle, Louis. Kaylin informed me that his official name is St. Louis Ludwig
II. Pam is crazy about “Lou” as you can see from the photo of the two of them
below.

-Kim Graham Lee
Monday, June 25, 2012
Something New
Our last blog was SO long ago. In that time, we cerebrated a
marriage, two graduations, and the continued success of chemotherapy to keep
this cancer at bay! As many of you know, the weeks following Kendal’s wedding
have been a bit harder for me. My abdominal pain has been more consistent but
continues to respond to pain medicine. The bigger problem has been my left
arm. The pain is the worst two days
after chemotherapy, and I have had significant functional loss. For example, it
is very difficult to write so my girls have been having to help me pay bills. J
As a result, we have decided to hold chemo for a few weeks
to do radiation to the tumors above my clavicle and under my arm. The thought
is that those lymph nodes that contain cancer are pushing on the nerves that
run in that area and control strength in the hand and arm. The goal of
radiation is to shrink those lymph nodes. Meanwhile, I am also having a biopsy
of one of the lymph nodes. We will send that tissue to a lab in Boston that
tests tissue to find out what kind of chemotherapy the cancer is potentially sensitive
to. With that information, we will resume chemotherapy after radiation.
The logistics of the radiation are as follows. I will get a
total of 25 treatments over five weeks (Monday thru Friday.) The radiation will
be painless, and the major side effect is fatigue. The fatigue will be
cumulative so that by the end of the five weeks, I will likely be pretty tired.
I hope and pray that I tolerate this new treatment as fluidly as the last six
months of chemotherapy.
So much for the fun stuff. My hair is starting to grow back.
Where the hell did all this gray come from? I’ll just call this chemo color. My
cranial prosthesis (wig) carries the color for now. Ellie has joined the work
force with a vengeance. She is now working as many hours as sleeping. I get the
sense that IU will not come soon enough. For those of you who need an update on
Lewis: he is one cute puppy. (This puppy was a gift to Kaylin for helping to
plan the wedding.) He does have though one very annoying habit. Greg calls him
the “Ninja Shitter.” We are finding pooh in rooms that no one has seen him in.
But he is cute and that is what saves him. The big dogs are tolerating him
better. Tally and Lewis play like puppies until Tally has had enough and then
she just lays a paw across his neck. Game over.
The newlyweds seem to be adjusting well. Kendal was home
this weekend to go to a wedding in St. Louis. She is a remarkable young woman.
Her help and kindness are invaluable. I guess all the dirty diapers were worth
it. Kaylin has remained busy . Lauren is going to have a minor surgery this
week so we will be couch buddies for naps. Thanks you all for the continuing
prayers, visits, phone calls, lunches, parties at chemo (they had to put us in the back room because
we make too much noise!) Love PAM
Friday, April 20, 2012
Life Still Goes On
We have been negligent writing blogs the past few weeks (hence the deluxe edition today.) It is a busy time for the Dedinsky
household! The girls and Scott were in Europe visiting Lauren the last ten days
of March. They returned to wedding plans amid work (or perhaps work amid wedding
plans!) The girls found the time to throw me a birthday party the day before
Easter. The party was small (but loud) and a great opportunity to reconnect
with longtime friends and celebrate with those who have been so supportive
these past few months.
One of the biggest blessings this month so far was a visit
from a friend who I met during Greg’s cardiac fellowship days. Roxy babysat
Kendal and Kaylin when they were small while our husband’s spent nearly all
their hours at the hospital training. We reminisced about those crazy days over
wine recalling the days of “Stitch and Bitch” with other resident wives. (Neither
of us ever managed to complete a knitting project but man could we do the
other!) It was a quick but wonderful twenty-four hours before Roxy had to go
home to Arizona, but we still managed to find time to hit up TJ Maxx fast and furiously - just like
old times.
I completed my fifth cycle of chemo today. Our last scans
about two weeks ago showed a small decrease in the size of the lymph nodes in
and around my arm. The pancreatic tumor is unchanged from our last scan. We have elected to
continue on course with the same chemo regiment for a total of six cycles. This
puts us into May at which point we will need to make more decisions about the
next step.
As for me, I need a nap earlier in the day than I did in
January, but my side effects continue to be irritating but not debilitating. I
have trouble with sensation in my left hand and arm but have no problems with
strength. I guess my right hand is going to have to start doing some work for the first time in my life. The doctor thinks this loss of sensation is due to chemotherapy and decided to decrease the dose of one of my chemo medications by 25%.
One week from today we will have a wedding to celebrate! We
got out our wedding video this past week. Damn we looked good despite the bad
video quality of 1983. I eagerly await the arrival of family next week, and
anticipate the house will need a thorough cleaning this weekend. Those tasks
will be delegated to my wonderful children and husband as mom has cancer and
shouldn’t be doing house chores. J
I need to store my energy for the excitement of the coming week and the weeks
after that when we will celebrate two graduations. I am thankful everyday that
there are so many wonderful distractions in my life as I endure this challenge!
Looking back to January when I was first diagnosed, we had no idea how I would feel this week in April. By the grace of God, I haven’t missed a beat.
I continue to count my blessings and try every day to
embrace this road that the Good Lord walks with us. Thank you for your continued prayers. I will end with a
poem:
Look on the Bright
Side
For every negative
that consumes your happiness,
Affirm two positives
that sustain you.
For every “should’ve”
you wish you’d done,
Acknowledge something
you’re glad you did.
For every loss that
has altered your world,
Count from it
something you have gained.
For every limit that
has ever beset you,
Consider your
possibilities.
You can’t always
change the way things are,
But you can change the
way you wish to see them.
Never stop looking
For the brighter side
and beyond.
Eric T. Moore
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