My husband, John, has been in the hospital a lot recently. I've lost track of the number of times, but I think he's had six hospitalizations in the past few months.
His immune system never came back after his bone marrow transplant. He's just one of the few who had that complication. So he just keeps catching things this year, even with his IVIG treatments. I guess his IVIG treatments -- 9 hours at a time in the chemo room -- just aren't enough to keep sickness at bay. His cancers are definitely NOT back -- he just hasn't quit catching things this year.
Three of John's hospitalizations were for graham negative and graham positive infections.
During the last hospital stay John actually got sepsis. He had a graham positive infection in his blood.
The doctor took me aside and told me there was a chance John wouldn't make it. She went over to his bedside and explained to him that he must fight very hard. She sort of explained the situation to him.
Her telling John the truth of his situation really surprised me, as I am not used to John's local doctors, as a whole, dealing with us in such a straight forward way. I was most grateful, however, for her straightforwardness, as was John. It allowed John the information he needed to have to fight, and the ability to do so if that's what he chose to do.
I explained to him a little more of what the doctor had said to me while he had been sleeping. "Krissy, I'm going to do it. I'm going to fight," John said to me, looking at me weakly, but in his determined way.
"OK," I said. "I'm going to be quiet then, and let you go into your survival mode, and do whatever you do when you do this, then."
"OK," John said quietly.
"I love you, Honey," I said, and gave him a quick kiss. Then I leaned over and drew a little cross on his forehead. "Good night."
"I love you too," he said. "Good night."
Then he quickly shut his eyes, and with a very determined look on his face, John slipped off into that "survival zone" he goes to when he fights to stay alive. I've seen him do it many times before. He's working hard to stay alive there in that place. Nobody can distract him from that task. Nobody can reach him there until he's ready to come back. Not even his wife. I can't distract him there. He can't hear me. But somehow I think he knows I'm at his bedside.
I have no desire to distract him when he's fighting to survive. He needs all his energy. When he's fought himself safely through he'll be back to talk to me. I can wait. I always wait. Because it's always worth it. Do what you need to do, John, until you're done. Whether you're awake or asleep -- stay in "the zone". I can wait. I always wait.
So I wait for him to come back. To let me know he's going to live. And like each time before this one, he does a stellar job again. Just because he wants to live. Which is more than reason enough.
But I think I made it all sound too easy!
It was scary when he was first sick. In my heart I knew he'd make it, but sometimes I was a little scared.
The first night John's temperature shot up so high that they put him under a "cooling blanket". It was basically a sheet with ice packs sewn into it. He was under that thing for about a day.
At first John didn't respond to any antibiotics they gave him -- I guess the graham positive infection, which had since become sepsis (blood poisoning), was now antibiotic-resistent. But then after a day or two the doctor found an IV antibiotic that worked. Dactomycin.
So after several days of Dactomycin, some time under an ice blanket, and lots of old-fashioned just fighting to survive -- John was good as new.
Except you're never as good as new after these things. It always takes a toll on you. And you need some time to recover. From something or the other. John's latest something or the other is something called "encephalopathy". He got it as the result of the sepsis. It effects his cognition. But that's a subject for another post. That post will come soon enough. I think I've already given you more than enough to read about for today!
I just wanted to let you all know what's going on. I'll keep you updated.
I hope everyone is doing ok. Thanks for continuing to read and comment. God bless you all! :)
Showing posts with label John Knox. Show all posts
Showing posts with label John Knox. Show all posts
Sunday, December 15, 2013
John was In the hospital a lot recently
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Wednesday, September 19, 2012
Maybe John has Cancer Again
It's going to be another trip to Hershey, PA today -- tomorrow my husband John will be seen in the Hershey Medical Center, Cancer Clinic.
A few things are going on with John physically. And it is hard for him in other ways too. He's undergone a lot of stress. And to say I haven't gone through a lot of stress also, would definitely be an understatement...
because John just keeps keeps getting unusual and far more rare complications than most other BMTers. It keeps happening, inevitably, year after year. Maybe the complications are finally slowing down. I do hope so! Especially for John's sake.
John and I are leaving for Hershey, PA, in a few minutes. We want to leave early enough so that we'll be at the American Cancer Society Hope Lodge soon. We want go to bed early, and be fresh in the morning, as John's first appointment is very early.
At 8 am, John and I are expected in the Infusion Room, directly above the Cancer Clinic. John will get labs done in the Infusion Room.
Many things go on in The Infusion Room beside getting labs done. Some cancer patients get chemo while in the Infusion Room (John has had over 90 rounds of chemo), while other cancer patients get cells (cells from white cells in plasma), that will strengthen their immune system. This process is called getting IVIG. IVIG stands for Intravenous Immunoglobulon. IVIG is given to cancer patients to strengthen their immune system, because as I stated, they don't have one. That's because after a bone marrow transplant, some BMT patients immune systems go away, and some never even ever return. It doesn't happen often, but it does happen. So having low antibodies, and not getting his immune system back, did happen to John, of course, LOL.
I said "of course"
Because I want him to be more confident that he can relax some, that he can embrace life to it's fullest, to be more secure, and to just love life! I want him to really step out and live his life now.
Being confident and secure is somebody John has always was, but has had a little bit of trouble being this way, during this last cancer he's had. I mean this third blood cancer John's had. Actually, I'm not sure if he is on his second or third blood cancer right now. I've heard two doctors say he had three cancers. The cancers were Non Hodgkin's Lymphoma, MDS (preleukemia), and AML (leukemia). Some of the other hem/onc doctors said he had the first two cancers but not the leukemia. Dr Claxton, His blood cancer doctor says he had NHL (lymphoma), MDS (bone marrow cancer and preleukemia), and Leukemia. I am going with what Dr Claxton says, as that is his Dr, and he has known him the longest and the best... He told us this just a few months ago, that he had all three of these cancers, and that at that time about four months ago -- that all four cancers were in complete remission! Like he thought, 99% John wouldn't be coming out of remission anyway!... So why didn't I tell you all yet? I don't know, I just wanted to be sure or something... Make sure I heard him correctly or something... I know I heard him correctly, Dr Claxton I mean, but I just wanted to ask him a few questions first, before I announced it to you, my friends, and to the world!!
Anyway, getting back to John, my beloved husband, the physical things my husband has gone through, all the cancers (especially the last two), all his chemo treatments and the bone marrow transplant, all his complications and their treatments -- these physical things that can make a person a little shaky (even if it's subconscious), I think could hold someone back a little in life. He hasn't told me that any illnesses of his are doing that to him. But I do wonder at times if it happens. I do know that he is in CKD3 (that's Chronic Kidney Disease Stage 3), and that comes before needing permanent dialysis and a kidney transplant (if you're able to find a kidney). And then there's the thing of his antibodies not being high enough (I'm wondering if this is in the back of his mind, I don't know if it is or not, he doesn't share his health with me too often as he thinks it will make me scared and upset), and if John believes his antibodies aren't working well, that his immune system won't function well enough, even with the artificial boost that it's often given (the IVIG), which could cause him to catch something and die. He wouldn't have to catch something too serious to die...
Anyway, getting back to John, my beloved husband, the physical things my husband has gone through, all the cancers (especially the last two), all his chemo treatments and the bone marrow transplant, all his complications and their treatments -- these physical things that can make a person a little shaky (even if it's subconscious), I think could hold someone back a little in life. He hasn't told me that any illnesses of his are doing that to him. But I do wonder at times if it happens. I do know that he is in CKD3 (that's Chronic Kidney Disease Stage 3), and that comes before needing permanent dialysis and a kidney transplant (if you're able to find a kidney). And then there's the thing of his antibodies not being high enough (I'm wondering if this is in the back of his mind, I don't know if it is or not, he doesn't share his health with me too often as he thinks it will make me scared and upset), and if John believes his antibodies aren't working well, that his immune system won't function well enough, even with the artificial boost that it's often given (the IVIG), which could cause him to catch something and die. He wouldn't have to catch something too serious to die...
On the other hand, John, while going through all this, and even considering it, at the same time, does have a pretty fantastic attitude. My John has always pulled for life. My john has always pulled for survival.Each and everyone of us reading this know this.
So once again, he will go on, fighting anything that could possibly try to harm his body, anything that could possibly mess with his mind, anything that would momentarily dampen his spirits. My John, our John, is a Survivor, and will always be a Survivor! Long live the Survivor! So after John's 8 am appointment in the Infusion Room, John and I will be headed downstairs to the Cancer Clinic to see Dr Claxton, John's hematologist/oncologist (blood cancer doctor).
One of the reasons we're going is because John has had numerous complications lately. And one of them is fevers. They have gone on for months. And night sweats. Anybody who has had cancer before knows what fevers and night sweats almost always mean. And they know what they mean if they return.
Fevers and night sweats mean Cancer. Fevers and night sweats returning mean the possibility of cancer returning. But then who knows. We'll see. I guess it could go 50 50. Please pray. We have been up to Hershey three times in the past four weeks. I just don't know. Please pray. Yes, I know this is sudden and direct. I never did beat around the bush, did I, LOL. I always thought it was much better to get to the point, then we could pray, etc. Thanks for the prayers. Got to run,
love you from the bottom of my heart, your krissy :)
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5:22 PM
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Sunday, January 2, 2011
John has posted again
I thougth I'd tell you a little about what has been going on with my husband John.
Because of complications from his bone marrow transplant, which he received to put two cancers into remission, my husband John has been unable to post for two years.
This has caused my posting and commenting to also be very infrequent, but that's another story. I'll be posting regularly this year barring some disaster -- you'll just have to wait and see!
Anyway, John has started to feel a lot better, and was finally able to post on December 26, 2010, just a few days ago.
While it's been a little over two years since John has posted, he is going to attempt to post on a regular basis from now on. Or at least as frequently as he can. He is still going through a lot of health issues, but as you all know, he is very stubborn, too stubborn sometimes, LOL, and he isn't going to give up in many areas in his life!
Stubborness (or shall I call it persistence with him) is often a good thing, so perhaps he's not too stubborn! As well as the Lord, stubborness has kept my husband alive. And it will keep him moving forward as he attempts to find his "new normal" in life as a Survivor.
This stubborness will keep him moving forward as he attempts to find what he wants to do in the next few years of his life, and to see what the Lord has in store for him to do in the future.
It will be exciting for him, and for me as well! The future is feeling brighter...
Anyway, if you haven't visited his entry of a few days ago, and would like to, let me give you the link:
Merry Christmas 2010
If youd like to read more of John's blog you'll find it here:
too stubborn to die
Finally, I'd like to say Happy New Year from John and me. May 2011 be your best year yet! God bless you all.
krissy :)
Tuesday, March 2, 2010
For John -- I'll Stand By You
This song is dedicated to my husband, John Knox, a two time cancer survivor. It's I'll Stand By You by Carrie Underwood. A few weeks ago, John had another cancer scare. We were sure this time his cancer was back. The numbers and symptoms indicated it. I'll tell you more about it later, but I just wanted you to know that as of now, it appears he's still cancer-free. We were stunned when we heard the cancer was most likely back, and just as stunned to learn a few weeks later that it wasn't. But let me digress for a moment. During the weeks when we weren't sure if the cancer was back, or rather, were almost positive it was back, I would sing this song, I'll Stand By You, to John. Now it's "our song." Listen to the words, it's beautiful...
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