Jim had his testing done last Thursday (6/19). While he was supposed to do a chemical stress test, he ended up walking on a treadmill due to the fact they could not get a good vein for the IV solution for the chemical test. It was tough on him but he walked the treadmill (uphill) for 8 minutes.
Because one of the numbers was low, they want him to have a cardiologist just sign off that his heart is ok to undergo the surgery. Just can’t catch a break. While we know this is routine for such a major surgery, we feel quite certain Jim’s heart is just fine and just sets us back another week or so. His cardiologist appointment is next Tuesday (7/1).
Dialysis is really starting to take a toll on him. While he has good days and bad days, it seems it takes him longer to feel ok after each dialysis. Gout continues to be a problem in his knees and feet. It seems like a constant ending circle. He walks to build up his strength, but then that seems to activate the gout in his legs, he takes medicine for the gout and it upsets his stomach, he takes medicine for his upset stomach that gives him diarrhea, he takes medicine for diarrhea and it makes him nauseated, he takes medicine for nausea and that upsets his stomach, he takes pain meds for the pain in his knees and that constipates him. It never seems to end.....
Hopefully “Joe”, his new kidney, will help make all of this go away.
Friday, June 27, 2014
Tuesday, May 27, 2014
Just can't catch a break.....
Jim’s detour in his journey for a new kidney had yet another detour last week. After eating dinner last Saturday night (no more eating at Sybergs), Jim started experience food poisoning like symptoms and severe pain in his belly. About 10:30 that night we went to the ER at Memorial. They agreed it looked to be something he may have eaten, but wanted keep him to make sure he wasn’t dehydrated from the nausea. Assured us it was clearly for observation and would most likely go home the next day.
He started feeling better Sunday but then found out his INR (blood levels) was too low which meant his blood was too thick and could start clotting. He has been on Coumadin for the past several months ever since they found a blood clot in his lung in March. Neither his primary doctor nor his nephrologist had been monitoring it. He was started on a heparin drip immediately. After 2 days in the hospital, the level was pretty close to where it should be and he could go home. His nephrologist will continue to monitor it at dialysis while he is there.
While this is just another detour in his journey, it was probably for the best we postponed his 6-minute walk until the next week. He started with gout in his knee as soon as he came home from the hospital. This poor guy just can’t catch a break....
He has been feeling pretty good being home and we are once again gearing up for the walk this Thursday. I’m confident he will do well. After all.....what else could happen????
He started feeling better Sunday but then found out his INR (blood levels) was too low which meant his blood was too thick and could start clotting. He has been on Coumadin for the past several months ever since they found a blood clot in his lung in March. Neither his primary doctor nor his nephrologist had been monitoring it. He was started on a heparin drip immediately. After 2 days in the hospital, the level was pretty close to where it should be and he could go home. His nephrologist will continue to monitor it at dialysis while he is there.
While this is just another detour in his journey, it was probably for the best we postponed his 6-minute walk until the next week. He started with gout in his knee as soon as he came home from the hospital. This poor guy just can’t catch a break....
He has been feeling pretty good being home and we are once again gearing up for the walk this Thursday. I’m confident he will do well. After all.....what else could happen????
Friday, May 2, 2014
What a Great Day for a Walk
Saturday was the annual National Kidney Foundation walk at SLU campus. Last year Jim, Joyce and I walked in the cold and rain. This year was 75 degrees, bright sunshine and 35 of our best friends and family.
We were also lucky enough to have raised over $3,500. Jim was quite overwhelmed by the amount of generousity from everyone.
Thanks to all who participated and donated!!
We love you!
Monday, April 7, 2014
Getting His Head in the Game
Last Wednesday after dialysis, Jim had an episode that has proven to be unexplainable. His speech was garbly and all symptoms pointed to a stroke. I immediately took him to Barnes ER and after a grueling 21 hours there, MRI's taken, CT scans taken, blood work taken, there seems to be no explanation. They say it may have been a "mini stroke" that would not appear on the MRI, or perhaps it was delirium. He was hospitalized for 2 days with no further test. His speech has improved and his cognitive senses seem ok now.
While this was terribly disturbing and scary, I think it has taught Jim he has to have his head in the game. He worries a lot and tends to keep things inside. Perhaps it was an overload of worrying and depression from all that he has gone through these past several months. Needless to say he has been very apprehensive about dialysis since this all seemed to occur right afterwards, but the doctor tried to assure him it was merely a coincidence. Having just dropped him off, I took am anxious to see how he is reacting.....ok I hope.
Once again Jim seems to be on track. He had the drain bag removed last Wednesday prior to this episode and things we thought were looking up. His appetite has improved the last few days. He is eating (and enjoying) it much better. His nutrition has been so poor with all he has gone through. Once weighing as much as 260 lbs., he is now down to 211.
After my talk with him and the doctors telling him so much of his recovery is psychological, I think his head is finally starting to get into the game.and he is starting to realize he must be in a better frame of mind. He has a lot to be thankful for whether he realizes it or not. I remind him that everyone has problems and some are a lot bigger than his. Let's hope things improve. Like I said before...enough is enough.
While this was terribly disturbing and scary, I think it has taught Jim he has to have his head in the game. He worries a lot and tends to keep things inside. Perhaps it was an overload of worrying and depression from all that he has gone through these past several months. Needless to say he has been very apprehensive about dialysis since this all seemed to occur right afterwards, but the doctor tried to assure him it was merely a coincidence. Having just dropped him off, I took am anxious to see how he is reacting.....ok I hope.
Once again Jim seems to be on track. He had the drain bag removed last Wednesday prior to this episode and things we thought were looking up. His appetite has improved the last few days. He is eating (and enjoying) it much better. His nutrition has been so poor with all he has gone through. Once weighing as much as 260 lbs., he is now down to 211.
After my talk with him and the doctors telling him so much of his recovery is psychological, I think his head is finally starting to get into the game.and he is starting to realize he must be in a better frame of mind. He has a lot to be thankful for whether he realizes it or not. I remind him that everyone has problems and some are a lot bigger than his. Let's hope things improve. Like I said before...enough is enough.
Monday, March 31, 2014
Enough is Enough
Jim finally came home last Tuesday after spending 27 days in the hospital. With so many ups and downs, it was finally a relief to be able to leave the hospital. While still weak, he continues to improve after almost 7 days being home. His appetite is coming back and he needs pain meds less and less. He seems to be getting stronger each day.
He entered the hospital with a tube in his belly and came home with a tube in his back. He has a drain bag still connected to the one abscess near his kidney. He came home with 2 tubes on the left side of his chest for hemo dialysis. He came home with 2 other tubes on the right side of his chest for IV medications and blood draws. He has lost 40 lbs. He is on IV antibiotics until mid-April. I have put my nursing skills to work once again and give him the infusions nightly.
He has started hemo dialysis at the Belleville Davita center on Monday, Wednesday and Friday afternoons. Dialysis was something Jim never thought he would have to do. Now he has experienced both PD and Hemo. I must say that PD is so much better. It is so sad and depressing seeing all the people at the clinic needing dialysis to sustain life. Sad....
We hope to finally get back on the right track. It will take time for him to build up his strength but hopefully the transplant will be right around the corner. Let's hope because enough is enough already.
He entered the hospital with a tube in his belly and came home with a tube in his back. He has a drain bag still connected to the one abscess near his kidney. He came home with 2 tubes on the left side of his chest for hemo dialysis. He came home with 2 other tubes on the right side of his chest for IV medications and blood draws. He has lost 40 lbs. He is on IV antibiotics until mid-April. I have put my nursing skills to work once again and give him the infusions nightly.
He has started hemo dialysis at the Belleville Davita center on Monday, Wednesday and Friday afternoons. Dialysis was something Jim never thought he would have to do. Now he has experienced both PD and Hemo. I must say that PD is so much better. It is so sad and depressing seeing all the people at the clinic needing dialysis to sustain life. Sad....
We hope to finally get back on the right track. It will take time for him to build up his strength but hopefully the transplant will be right around the corner. Let's hope because enough is enough already.
Tuesday, March 18, 2014
Hope
Jim is still in the hospital. 3 weeks to be exact. While he seemed to be improving, the last 4 days he has been experiencing belly pain again. After having a CT scan done today, it shows 3 abscesses in his belly. One on each of his kidneys and the 3rd in his pelvic area.The plan is to have them drained tomorrow.
We then hope his pain will improve.
We then hope he will be off pain meds.
We then hope he will be back to normal and able to stay awake.
We then hope he will get his appetite back and once again enjoy his food.
We then hope he will be able to come home.
We then hope he will be able to continue hemo dialysis.
We then hope he will get stronger.
We then hope for a transplant.
We will never give up hope....
We then hope his pain will improve.
We then hope he will be off pain meds.
We then hope he will be back to normal and able to stay awake.
We then hope he will get his appetite back and once again enjoy his food.
We then hope he will be able to come home.
We then hope he will be able to continue hemo dialysis.
We then hope he will get stronger.
We then hope for a transplant.
We will never give up hope....
Monday, March 10, 2014
Good Bye PD Cath
Jim has been in the hospital now for 12 days. While his peritonitis originally was clearing up it has now returned. The culprit they think is now his pd catheter. More tests show there is a fungus growing on the catheter which definitely is the source of the current infection. The only option is to remove it. However, before it can be removed he must have an access for the hemo dialysis which he will have to switch to. However, before either the catheter is removed or the access put in, and because he was on a blood thinners he had to be transfused with blood. That is what happened today.
Tomorrow if his blood is ok, they will put in the access port and hopefully remove the cath. This means he will be able to start hemo immediately. Antibiotics are still being given and hopefully will help ease the pain he is in. For now he is ok with the hemo. This means he will have to go to the dialysis clinic 3 days a week for 4 hours of treatment. Hopefully it will be only for a short period of time until he is transplant ready.
While this is certainly not the road we thought we would be on, it's here and we are dealing with it. It's especially hard since his February 13th transplant date was so close....
My thoughts....There is nothing worse than seeing someone you love in pain and hurting. We all try our best to make things easier. Sometimes that's never enough. We take each day one day at a time and hope tomorrow will be brighter. I walked down to Children's Hospital one day last week to see my friend Alicia and her beautiful daughter Mya. Seeing so many sick kids and what it is they go through I realized we are not in this alone. So many people have bigger problems and that's just part of life. A life no one deserves. I pray for each one of them too.
Tomorrow if his blood is ok, they will put in the access port and hopefully remove the cath. This means he will be able to start hemo immediately. Antibiotics are still being given and hopefully will help ease the pain he is in. For now he is ok with the hemo. This means he will have to go to the dialysis clinic 3 days a week for 4 hours of treatment. Hopefully it will be only for a short period of time until he is transplant ready.
While this is certainly not the road we thought we would be on, it's here and we are dealing with it. It's especially hard since his February 13th transplant date was so close....
My thoughts....There is nothing worse than seeing someone you love in pain and hurting. We all try our best to make things easier. Sometimes that's never enough. We take each day one day at a time and hope tomorrow will be brighter. I walked down to Children's Hospital one day last week to see my friend Alicia and her beautiful daughter Mya. Seeing so many sick kids and what it is they go through I realized we are not in this alone. So many people have bigger problems and that's just part of life. A life no one deserves. I pray for each one of them too.
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