No Pain!

Carol is resting comfortably . . . really comfortably . . . on the Eastern Shore tonight. This afternoon she had a procedure called a celiac plexus block - a deadening of the nerves in the area of her worst pain. As far as she can tell, it was a great success. She'll know for sure in two weeks when the local anesthesia has worn off and the true impact of the block will be realized. But, so far so good!! And if it truly works she will be able to give up the morphine and all its nasty side effects. What a blessing that would be!

Thanks to each and every one of you for your many, many prayers. Carol felt prayed for, loved and finally pain-free. Actually . . . she was so happy in the recovery room she was inviting the nurse to come to their house in Georgetown for drinks when she and her husband come to town next. AND she insisted that Frank write down their address and telephone number!!

Carol promised to write tomorrow. But for now, know that your prayers were heard!!
Sally

Call for Prayer!

Good morning everyone! This is Sally writing with a brief update and specific prayer requests for Carol.
Carol's pain continues. And management with drugs has proven difficult and uncomfortable. So the wonderful doctors at Johns Hopkins have suggested a procedure called a celiac plexus nerve block to relieve much (if not all!) of Carol's pain and hopefully allow her to use less painkillers. The procedure will take place tomorrow (Friday) at 1:00pm. Please pray fervently that the block is successful and brings relief!
In the meantime, today brings a new round of chemo. Carol seems to be responding well to the new "cocktail" JH has devised at a slightly lower dose. Less fatigue and nausea! An answered prayer, for sure!!
More updates from Carol are coming. Just wanted to let you know what's happening. And ask you to keep Carol in your prayers these two important days!
Sally

Blog update – April 29

Piling on of Good News; then life after that.

After the great news of Thursday of how the PET showed, compared to the baseline, that the cancer “hot spots” were Dimmer – which means the cells are not as active and possibly diminishing. (I hope I got that last part right), we continued celebrating along with all of you this miraculous news! Well, the next day, I received an email from Dr. Dan Laheru (as you will recall from the beginning of all this, we learned that every person who has cancer has an elevated blood marker, called CA 19) . Here is the email from Dr. Dan:

Hi Carol:
This tumor marker CA19-9 is down from 2755 to 2261. That's pretty good and goes along with the PET scan results. Have a good weekend Dan

So that was wonderful news that I should have posted right away…but unfortunately the weekend/week did turn out as I expected. The celebrating was short lived b/c after a really active workday on Friday of client meetings by phone; at about 4:30 pm I just hit the wall. I didn’t expect it at all b/c the week before, remember, was my full week “off chemo” and I was busy as bee, working, out in the garden, walking, etc and I was all ready to get back into chemo-fight-mode. Besides this was a big weekend ahead…☺

On Friday, friends of Christine came from all over the country for a Bachelorette Party at a West Virginia Winery Saturday afternoon, and dinner at her house Saturday evening. On Saturday morning all of the bridesmaids were coming to the house for a fitting and I had planned a little brunch with fruit and pastries and mimosas and lots of giggling. I was on low energy chemo mode (more than I expected) and thankfully Frank and my good friend Mary Anne (who came from California for the weekend with her daughter Brittany – a bridesmaid!) got everything looking beautiful and special for the bridesmaids! It was such fun. I sort of parked myself in a corner and enjoyed all the action. Erik’s mom, Ruthanne, was there too, along with my friends June and Patty, who were hosting a bridal shower for Christine and Erik the next day. Our only missing bridesmaid was Kelly, ☹ Erik’s darling sister who lives in Vermont. But his other sister Heather was there, so that was great to have almost full “Maginnis girl” participation in the fun. (Ruthanne took a photo in our Georgetown garden of the bridesmaids for Christine’s scrapbook, I’ll try to get it on the blog) By 11:00 the girls were off to gather the rest of the friends and head on the limo-bus to the Winery for their luncheon. I was off to bed.

Whew, I was surprised how wiped out I was….but I was committed to resting up for the bridal shower that June and Patty had so graciously planned. Sunday came and I felt worse…and (here’s where I started asking “why, why?”) on this day that was so “about Christine” I had some rough spots…like all the symptoms hitting me in the car on the way to the shower. Fortunately we were a block away from a friends house, Frank called on the cell phone, they had the front door open and I dashed in and scooted in to the bathroom. (tell me that someday we will laugh about this.) I settled down a bit there at Dick and Pam’s house, but was anxious to get on to the shower b/c I knew Christine would be worried. So, attempt #2 to get to the shower. Good timing, arrived and directly to the Ladies Rest Room.

THEN, miraculously, it was all over. 180 degrees. Zap! I had a wonderful feeling of energy “no symptoms” …I joined in to the photos, ate the delicious lunch, got hugs from all the beautiful girls that we have missed seeing from the days they all hung out at our house during Georgetown breaks!, sat right next to The Bride and enjoyed every bit of the fun. As the festivities waned, so did I. Time was up! I slept in the back seat on the way home and basically slept through that day and off and on the next few days which were about the worse I have had energy-wise. And I kept thinking---“what’s up with this?” Each chemo month is a “Cycle”, with week 4 always an off week—I am in Cycle 2, Week 1; I had a wonderful week off, felt like the ‘real me’ and so I expected C2,W1 to feel just like Cycle 1 Week 1. Wow, no way. It was as though everything was starting over. The pain meds were not coming close, the nausea was back in full force and the other abdominal battles between constipation (from the pain meds)/diarrhea (from the clinical drugs) going with a vengeance. I was having a tough time drinking (and keeping) the 90 oz of water they want in me everyday.

I meant to get a blog out there to ask all of you to pray for me, but I was just completely and totally wiped out. Crazy. I keep hearing that “chemo is cumulative” but I’m not sure exactly how that plays out. I have days were I am fully, 100 % on my A game; then for no apparent reason, no energy the next.

So….yesterday (Thursday/chemo day) at JH the team decided to do an overhaul on the meds – I forgot to mention that last week the JH team talked to us about cutting back the amount of chemo/FTS they are giving me. Apparently they start with the full mode and are then keep readjusting to the sweet spot by pulling back to the to a lesser level depending upon how the patient can tolerate it. I was pretty adamant of no! no! no! I can do it! I want the full deal. They agreed to give it another week. Well, I had that week.

They also said that in light of the extremely positive results from the PET scans, this “lessening” may be better in the long run, b/c if I kept up with the bad side effects, they would have had to give me a break anyway b/c I just wasn’t really functioning fully.

The other thing under consideration.. And I would REALLY appreciate your prayer on this… is the suggestion that instead of narcotics to control the pain, I consider having an “alcohol nerve block” that basically acts like a novocain to deaden the nerves. We have been praying about this and the advantage seems to be that we won’t be “chasing” the pain trying to get on top of it. (and not doing such a hot job of that) It would also do away with potential side effects that may be coming from the morphine: constipation and some fatigue. They go in with a little needle and shoot alcohol on the nerve endings. I am awake through the process – no general anesthetic, another good thing. They did point out though that one of three things could happen, 1. it works great, blocks all pain for up to 6 months, 2. it partially works and they just don’t get all the nerves so there is some pain from the ones that were missed 3. sometimes, depending upon the patient, the block just doesn’t work at all. Worse case, we’d be right back where we are now.

I am hoping to just have a clear peace about whether this is the right thing to do. For me, I am particularly motivated to get this morphine out of my body and just have the chemo/FTS (the clinical drug) in there storming away on the cancer cells.

So…again, if I can ask for your prayers . . .

But before you lay my list on God, please do praise with great thankfulness, along with us----

• His miraculous use of the chemo and clinical drugs to zap those cells,
• The giftedness that He has given to the AMAZING team at Johns Hopkins; each individual, those we see and the many we don’t who have been given great knowledge that I can’t even comprehend!
• The fact that doors just opened, opened, opened in getting me to JH in the first place and getting the LAST Spot on the clinical trial before it closed.
• And even praise for technology that allows me to feel so close to you and know you are praying for me….unceasingly! that is a thankfulness that I can’t even put into words…but God knows. So please Thank Him for that too!
• And thanks to God for Frank….you have no idea what a guy he is.

For me, please pray for:
• The decision on the nerve block
• Relief from the symptoms
• Less “sleepy time” – and being awake to vomit doesn’t count! ☺
• Practical help in just consuming all of the water that is required

Isn’t this a neat quote ~

Looking back may I be filled with gratitude.
Looking forward may I be filled with hope.
Looking upward may I be filled with strength.
Looking inward may I be filled with peace.

Love to you all,

Carol

Amazing news!

Fantastic news!  We just talked to Dr. Laheru, the head doctor of the
pancreatic/clinical trial team. The team just finished looking at the
results from my PET scan yesterday. They had studied and re-studied the
results of yesterday's PET scan. The doctors expected "no change" from the
baseline PET scan that they did just 4 weeks ago. (This was basically just a
"pro-forma test they do after 3 chemo sessions. I will have them
periodically.) Well, instead of 'no change' they were very surprised to see
the cancer hot spots are "dimmer". They are shocked to see such results so
soon. It means the cancer cells are already less active and potentially
shrinking!! It is such wonderful news! Tears, big smiles, high fives and
hugs all around!

Couldn't wait to share the news!!!!!!  Wrote this during chemo yesterday at JH. 
TO GOD IS ALL THE GLORY!!

Keep praying, and praising and thanking!!!

"Blessed are the prayer warriors out there in cyberspace who have learned to acclaim YOU, who walk in the light of your presence, O Lord. They rejoice in your name all day long; they exult in your righteousness." Psalms 89:15, 16 – with a little Carol-paraphrasing!

Love,

Carol

Photo session today!

Well, we are getting ready to head back up to Johns Hopkins today for my first “follow up” PET scan and CT scan. They did the baseline scans about a month ago as you will recall. Dr Laheru said that they don’t expect to see anything significant this first month – it is generally the second month of chemo before they can really see anything. But let’s pray that God will surprise them with some nifty photos of my insides! The PET scan is a little creepy b/c that’s the one where they lock me in that lead-lined room, and the guy comes in all suited up and takes a tube from a lead canister, pours it into a “milkshake” and says, “Here. Drink this.” hee hee. Then he gets the heck outta there, locks the doors, turns down the lights and I sit in a recliner-like chair without moving. They repeat the process and after about 45 minutes of not moving they put me in a tube thingy and do the scan. Apparently the nuclear stuff goes to the cancer cells anywhere in my body and the cells glow like little fluorescent beacons. Please pray that the beacons are dimmer than last month…or even GONE!

(I think I got that whole PET scan description right….you may have had one and know way more than me!) I also have a CT scan today whey they inject fluid in my vein and take pictures as it flows through my body. That one is pretty cool. I feel like a human anatomy lesson because I can feel it moving through the veins.

I have learned some very, very interesting things about myself and about God on this journey so far. (Doesn’t that just sound so “poetic" to call this a “Journey”! :)) One thing that I have noticed is how when I read the Bible these days, or hear a pastor teaching, I keep finding myself thinking….”wow, God wrote that JUST for Me, where I am today! Have I never read that verse before?” For example, as I get ready for these tests today…check out this verse from the Hebrew Scriptures:

Jeremiah 32:27 Behold, I am the God of all flesh; is anything too hard for me?

The God of ALL FLESH, and all Cells, and all Organs, and ALL of Me – what comfort that is. HE is in charge. Boy, what a relief. I’m glad that I don’t have to be in charge of this one. It’s too big. And then for God to say “Is anything too hard for ME?” It’s very cool. As I read and read in the Old Testament (Hebrew Scriptures) over and over I learn more and more about WHO God is, His power, His glory, what He has done…and I am confident beyond anything that I know the answer to His rhetorical question of “Is anything too hard for Me?” My answer to God is: “NOPE! Let’s go…we’ve got to get in the car and head to Johns Hopkins today Lord. I’m sure glad You’ll be with us.”

I know that God will be with you today too on your Journey…pretty neat the way He does that isn’t it? ..omniscient and omnipresent…I guess that’s why He is God.

Thanks for your prayers for healing, the scans, (a little anxiety over the scans), and just to get rid of those pesky cancer cells! ..and most of all for patience as I wait upon God’s timing. Oh…and thankfulness that He shows Himself to me so graciously through you guys and especially through His Word…the Bible.

Love,

Carol

p.s. Scans today, back to chemo tomorrow. (but no blood draws, I don’t think. I’ll keep you posted. I’ll get the chemo schedule for tomorrow, today.)

Knowing What We Know

I’m back!! Sally was right ~ the JH heads up for “extreme fatigue” was the understatement of last weekend. I had a really busy work day last Friday until mid-day, then just hit the wall like I never imagined. I, seriously, couldn’t even open my eyes or lift my hand! I would ooze out of bed, to the “facilities” then nap on the bathroom floor for a hour or so, then wobble back to the bed or the couch….all weekend. Plus “symptoms” thrown in, so it was another new experience. But that’s behind me now. Whew!

Tomorrow we head up to Johns Hopkins for a “long day” with Robert-the-phlebotomist. Tomorrow blood tests only, off and on, for 11 hours, then back again to JH for more tests Friday morning. But no chemo!! Now here’s something funny. Last weekend I was thinking, “Wow, I can see why they give you a break after 3 weeks of accumulation of the chemicals in your body. The old bod can’t take it.” – but now that my “Break Week” is here I am surprised that I find myself thinking – “No, no…they MUST give me the chemo. I don’t want to go a week without it. I have to keep fighting. What if the cells grow during the ‘off week’? etc etc.”

I know that is silly but I did find myself thinking that. I trust that the doctors know what is best – and as you know, I am not the first through this clinical trial, so the doctors really know the best way to give this treatment. I have confidence I am in good hands. I was reading this wonderful verse from the Psalms and found myself wondering (again) if the author, David, was experiencing the exact same thing that I am b/c once again David certainly hit the mark for my feelings in what he says in his writing --- Isn’t this a great verse from the Psalms?…"I know the Lord is always with me. I will not be shaken, for He is right beside me. No wonder my heart is glad, and I rejoice. My body rests in safety! Ps. 16:8-9”

It’s a lovely week to reflect on resting in Knowing what We Know.

Sleepy girl!

Carol seems to be following the script . . . exactly as written by the wonderful people at Hopkins. They said the "fatigue factor" grows with each chemo treatment, and most patients really feel it after their third treatment. Chemo #3 was Thursday, and Carol was down for the count all weekend. Good thing this coming week is a week off!
So, all you prayer warriors, the prayer is for Carol is to build herself back up with lots of sleep and good nutrition, so as to be ready for the next treatment in a couple of weeks.
Check out Carol "lunching" with her CBS core group at Debbie Tovar's last Monday!
Sally