As my PleurX catheter worked beautifully after being plugged and not working.
Today, Tuesday, January 14th, my PleurX catheter was taken out, removed...no more!!
It's been quite a crazy last few days...
The PleurX worked beautifully Monday through Thursday of last week
Then Friday it showed signs of slowing down again
And on Saturday quit working completely after drawing only 300ml of fluid
Question:
Do we go in Saturday night?
Or wait until Sunday morning?
When of course I'd prefer to ignore that there was a problem and not go in at all:)
Except I REALLY felt REALLY bad!
My whole body for weeks had been feeling worse little by little
And over the past few day had felt as bad as I ever remembered feeling:(
This along with a regular fever
Tipped the scales into going to the ER Saturday night
Boy...are we ever glad that we did!
As I write this blog on Tuesday night, January 14th...
I am still in the hospital!
Yep:)
This is a summary of what has happened leading to MAJOR changes in moving forward!
Saturday night the ER doctors decided quickly
After looking at my frequent flyer history at the ER
And my extreme body pain and fever
That something had to be figured out
Rather than just draining my lung and sending me home.
What a novel idea:)
Thus began the drawing of much blood, and the doing of many tests
e.g. urine, lung fluid, etc.
To try and figure out what was causing the increase in body pain and fever
And the steady increase in lung fluid,
Not to mention that the PleurX catheter was not working!
I was admitted into the hospital around midnight
And finally a bed became available around 10am Sunday morning!
Harrison Hospital is a busy place
And the care we have received there has been incredible:)
After the many tests and many conversations with doctors
The realization was come to that the pain and fever
Were not from any infection
Or the flu
(although anyone coming into my room did need to wear a mask as a precaution even though the tests cam back negative for the flu!)
BUT...from the cancer growing:(
It was the cancer causing my misery....pain and fever and fluid
Wow!
This after the hair sample in December indicated a slight decrease in the cancer?
What was to be believed?
The facts were becoming pretty clear that my body was saying
That the cancer was progressing...
That we needed to do something different quickly
"If we could"
Or God's timing for calling me home may be very soon!
This marked the turning point...
"If we could"
Because when Seattle Cancer Care Alliance and University of Washington
Had deemed me incurable
And only eligible for palliative care
The current treatment plan that I've been doing
At least brought hope
That there might be hope
And it has been successful for some
But seemingly not for me
As the reality that I was getting worse daily
Was becoming starkly clear
So "if we could"
Happened this morning, Tuesday, January 14th
A PA friend working in oncology
Came to the hospital yesterday to meet with Cindy and I
She again pointed out the "handwriting on the wall"
Was that the cancer was getting worse
And highly recommended us meeting with
An oncologist of whom she thought highly
We agreed
She walked over to his office
Chatted with him
And he agreed and did, in fact, come in to meet with Cindy and I this morning at the hospital
Thus the turning point!
SCCA and UW let me go
After a scope and biopsy were done,
And it was evident my lungs were filled with mesothelioma
And I would not qualify for an immunotherapy clinical trial.
The turning point?
The local oncologist offered me the very immunotherapy
I was unable to get through a clinical trial at SCCA and UW
Even though my insurance company
Would not pay for it!
Hope was again being offered
Out of the blue!
This is a MAJOR change
Switching from the pancreatic enzyme treatment protocol
To immunotherapy supplemented by chemotherapy
But we believe it is the right decision for me at this point.
Again, thank you so much for your prayer and support and encouragement
The past few days have been really rough
And we know there are still some rough days ahead
Remember that I mentioned that my PleurX was removed today?
It wasn't working.
My lung will be observed for the next several days/weeks
To decide if...
Another should be installed
Or
Periodic thoracentesis procedures should be done
Or???
That about wraps it up...
If you made it through this whole blog
Congratulations!!!
Dave
We are continuing to hope with you and pray for you Dave! All our love to you & Cindy.
ReplyDeleteGod has your cradled in His hands, the very hands on which your name is inscribed. As to what that exactly means for the next 5 minutes, 5 days or 5 decades--He alone knows. But the rest of us are on the sidelines watching and praying. Because our turn will come. Maybe not with mesothelioma, but with lessons from the Inscribed Hands.
ReplyDeleteYou are a special gentleman, Dave, and my heart goes out to you. I am sending Prayers. God be with you.
ReplyDeletePraying that this turn will produce some much desired results.
ReplyDeleteHolding you and Cindy and all the family so very close to our hearts and in our thoughts and our prayers...constantly. We love you Dave. J & J
ReplyDeletePraying and thinking about all of you.
ReplyDeleteDave, My family and I pray for your comfort that only our Father in heaven can bring. I want to tell you what a great article you wrote for the Sun; so much love, faith and courage in it that you didn't even mention your illness. You and your staff and family have so greatly impacted the Kitsap community fo the saving of young people and the glory of God.Thank you.
ReplyDeleteWe are praying for you Dave. - Joshua, Lauren, Grayson, Ari, and B
ReplyDeleteWhat a hard road God has called you both to walk. Praying you feel His presence through the trials, and His blessings in the triumphs no matter large or small. Dale and Nora
ReplyDeleteChanges can be good even if they come from some of the hardest experiences. Praying these changes lead to better outcomes!
ReplyDelete