Tuesday, June 30, 2009
Life is Good - God is Great - but I'm pooped!
I have come up with a Title. I think that is supposed to be the hard part.....
Life is Good - God is Great - but I'm pooped!
June 30, 2009
Life has been going on - guess that is always good. Tim went in for a CAT scan yesterday and we will see the doctor on Thursday to get the results.
Tim is planning a quick trip to Florida with his family. They will leave Thursday night and drive all night to fort Walton Beach. This will have to be a wild trip. Stan, Tim's brother, bought a 30 foot motor home. He wants to transport as many as possible to Florida. I think he has about 12 going so far. I think he should attempt to head through Texas and take as many as he can to Mexico. This can be an opposite type drop. They can scatter through Mexico and we can see how quick they are sent back to the US as rejects!
Actually, they are going to a surprise birthday party. The motor home should hold 9 somewhat comfortable. Three more will wedge in somewhere. Now, remember that 12 people mean at minimum 12 suitcases! And they are planning on "partying" all the way down and back so that means at least 6 coolers of drinks! And surely they need some munchies. Not only will they look like sardines - they may begin to smell like sardines after 12 to 16 hours......oh, watch for the update on this trip!!
Today, is Scott's 25th birthday! Happy Birthday - Scott!
Tuesday, May 12, 2009
April - May 2009
He broke out all over in a red rash - and it is nicknamed "red man". He broke out about April 10, 2009. It is now the middle of May - and he is still trying to "kick" the rash. He is always cold - and wears several layers of clothes to stay warm. I tease him that the rash is a Heat Rash.......
We returned to cleveland for a check-up on April 21. All was going fine other than his rash. He had a pacemaker check - good; and an Echo done - fine!
We return to Cleveland on May 18/19 for another check up and to have the clot filter removed.
He has lost lots of weight and stays rather thin. I hope to get him eating more....
More appointments and follow-ups in June.......
Wednesday, March 25, 2009
Wed. 3/25
Tim is re-cooping and doing pretty good. I'm sure he will be ready to go fishing in a few months!
The dogs are glad to have their fearless leader home and snuggle up to Tim every opportunity they get!
I went back to work on Monday. Somebody has to keep the insurance rolling!
I'm afraid to say we are back to normal. I don't really know what that is......and I'm afraid to say all is fine.....before a doctor gets to charge their final fee and tell us. But I will whisper that we are getting there! It is good to be home - and hopefully on the mend. I'm afraid there are still many hoops to jump through - and every time we think we are done.....another hurdle seems to rise in front of us! This time I'm hoping the hurdles are done - and Tim can re-coop and start to enjoy his retirement!
Saturday, March 21, 2009
Today is THE DAY!!
Thank you to everyone that has been praying, reading this trivia everyday - and overall just letting us know that we have such great friends and following! We appreciate every one of you and everything all have done for us. We cannot thank you enough!
Tim still has lots of mending to do. He has 6 weeks of IV antibiotics to get. In 6 weeks we will make a return trip to Cleveland to hopefully have the antibiotics "turned off"; to have his clot screen removed; to have his pacemaker checked (that will be monitored in Lafayette for ever); and whatever else they decide he must do!
Tim is still fairly hoarse - so won't be ready to talk on the phone - but we will look forward to seeing everyone soon.
Friday, March 20, 2009
3/20
We are just hanging out! I think our insurance must be too good - why let us go?? Several of the doctor's fees have been posted to insurance....wow!! The surgeon's fee is about 4x what it is in Lafayette....but worth it!! Some of the other charges make you wonder. They barely stick their head in the door.....
Tim's count - i'm not even sure what they are counting anymore - isn't up or down or sideways or backwards - or however it's supposed to be yet. We are starting to hear some talk in the hallway that we may be able to get out tomorrow. Other jab is we're staying on into next week!
I took the car and got out a little this afternoon. Overall, there isn't anything I want - so it's hard to pick a place to go! I told Tim my mission was to go buy a new car.....but couldn't find a dealership where I wanted to stop. Tim's car has decided to act up - and it's a little unsettling. It will kind of jump forward (when you are sitting at a stop). Then it will shake and rattle and shut off. I'm hoping it will head for home with no problems. I think there must be some transmission problem. I think it's time to trade it off. Tim likes his car...so we'll see. I'm tempted to park it on the street tonight and see if there is anything left in the morning!
Tim is currently sleeping through some of the March madness games.
Thanks to all who are still reading.....hoping this story ends soon!!
Thursday, March 19, 2009
Thursday, 3/19
Over all we are just here - but now that March madness has begun.....Tim's in 7th heaven! I don't know how long the NCAA games last - but I can see our stay extended - again!! He must be feeling better - he's looking for ways to get pizza, wings and beer delivered to the room. I can see the nursing staff hanging out in our room! Guess we'll call that "personalized care - pass the wings!"
Of course I'm looking for anything to giggle about - the nurses start in about 4am - drawing blood; then bringing in meds and something to drink; then it's breakfast - and coffee, etc.; then he must get all hooked up with his IV's for antibiotics - and then....a shot of lasik! Up to this point, Tim has been in bed - enjoying all the attention. The shot of lasik goes to work quite quickly - and he is working madly to scramble out of bed and into the bathroom. This happens regularly every morning like clock-work!
Tim doesn't have a lot of hair - but needs a haircut. I've thought about looking for some surgical scissors to trim him up. I'm a little hesitant as I'm not real good with cutting hair! Probably by the time I'm done - the doctor is liable to walk in and wonder what is wrong with him - and make us stay another 2 weeks - while the hair has a chance to grow back out!
I had plans to get out today - and am leery about going in the afternoon - when traffic is more busy with school getting out and everyone getting off work. I'm also getting into a lazy pattern - but hope I can get out in the morning - and tour around Cleveland a little and be back by mid-afternoon - for a nap!!
Purdue is playing - so will stop and watch the game!
Wednesday, March 18, 2009
Wednesday
We both need hair cuts. I may attempt to drive somewhere later and see if I can find a place. I may see if I can get some sissors and do Tim's. He could probably fit in the blues group upstairs with his shaggy do! (He and his hair are the wrong color.....but with his raspy voice - they might not notice! haha).
Not much to do now - except "hang out". This seems like a "bad" place to hang out - there are sick people here.....and I surely don't want to catch something "new".
Tuesday, March 17, 2009
Tuesday Night
He's been doing fine - and I have been counting the hours till we could get out of here.
The hemo/blood doctors came in this evening and dropped their bomb shell. They want to get Tim started on blood thinner therapy.....and once they can get it started, they will want him here for at least 5 days. I'm already going nuts - as I'm sure Tim is - and this is overwhelming to me at the moment. I'll cross my fingers that this place where time stands stiller than a mannequin - will move a bit faster. (I think of better things to write in the middle of the night.....guess I should get up and write then....it doesn't seem to matter whether its day or night here).
Megan's parents came by this evening to visit! It was really wonderful having someone here. I'm sure my return company wasn't great - I'm in a bummed mood about going home - but someone NOT dressed in hospital garb was a fantastic site! Thanks for the company and dinner! It was really appreciated! (For those reading - Megan is Scott's girlfriend!)
Signing off for another night!
All about me!
I'm living and vacationing in the CCH hotel. It is a nice place - but not very high on my recommendations! I can get clean towels and sheets and blankets - but otherwise for the most part ignored! (And that is expected!) I don't think there is any sound proofing - you can hear everything in the halls, doors opening/closing, anyone walking by, etc. Starting about 3:30 am the night staff comes alive and there is always someone in the room. At least I do have the luxury to turn over, cover my head and attempt to go back to sleep. I'm not the one being poked for blood or vitals taken to see if I'm still alive. The TV works ok - but not lots on! Overall, it's boring and tiring sitting here all day. Probably why the blog entries get longer and more boring the longer that we are here.
I would love to get out and walk around the area - but I don't want to miss a doctor coming by. I have lots of questions for them - and if they come in when I'm not here - and I ask Tim what was said - I get the teenager answer....."I don't know". So, I stay to catch them.
Last night, I did get out and went to Wal-Mart. It was nice to get out and wander around the store and just be away! It was also an ethnic trip! I was looking for some hair gel - and found shelves of items I'm not used to seeing. I was looking for something that would help me put some curl into my hair - and all I could find were products that would help relax the curl in my hair! I need a hair cut - and could probably get one and come back with some kinky waves and beads. Definitely a culture shock here! We are starting to hear talk of being dismissed.....I'm not holding my breath yet......but I am getting excited about the prospect of breaking out of here!!
I am haning in there ok. Megan brought me a care pack - and I have lots of yogurt, fresh fruit, crackers, muffins, G2 fruit drink, magazines and puzzles to keep me entertained! It's definitely a luxury. I'm starving for a steak - and can't wait till we are out! Everyone is welcome to come eat a steak dinner with us!! See you there!!
Tuesday Morning
Tim rested really good last night. He had been kept from food and drink all day to be ready for the pacemaker procedure. This morning the night nurse came in and wanted to know why he didn't have to "go" and said he should have been drinking all night.....he had better start drinking some water (they never bring you any) so he could/would have output. She finally brought him a couple of little bottles of water - which Tim drank - and "went" without any problems. Then transport came in and took him to have his Hohn catheter put in. About an hour later his nurse came looking for him - and said he was to have no food or water today for his procedure. I said they had already gone.......about 10 minutes later they brought him back.....he had gone for a pacemaker follow-up. (He has to wait all day for the other procedure - no food or water all day again). Something was not correct with his pacer - and they will have to decide if they can fix it externally or decide if they will have to re-open his pacer area and fix the lead wires internally. Tim says that surgery and placement hurts worse than the open heart. He is very sore and tender in the shoulder area and is dreading if they decide to open it back up.
Monday, March 16, 2009
Monday Night
He is sleeping..... and after a few more TV shows....I'll try to sleep some, too!
Good Night!
Monday afternoon
It's like pre-surgery you see someone every 15 or so minutes. After surgery you are lucky to see a doctor every 15 days (or so it feels).
Tim has not eaten today - in hopes of getting the pacemaker this afternoon. Of course they do not bring in his meal trays...... but the ones that pick up the trays still come looking for them and think you are hiding this food for later under your mattress. Then the nurse's aid comes in and wants to know how much you were able to eat and drink. Tim has been cautioned that he needs to drink as much as possible so he can flush his system and hydrate his veins for "pokes". Hmmmm, he's on a NO eat or drink order since midnight. Maybe it's good we don't see many as this is frustrating! Tim made about 3 laps around the ward this morning - and has now been napping all afternoon. He didn't get much sleep last night, so it's good to see him catch a few zzzzz's. The last we heard he is on track to have the pacemaker put in about 5 this evening.
Will catch up again then! Keep your fingers crossed!
Monday morning
Tim is waiting to hear if he is on the pacemaker list for today. He is not allowed to eat - unless they can't get him scheduled in. It is about 11am and we should hear by noon if he gets lunch or not. If they bring him food, it means we do this again tomorrow. I don't know why I say"we" I ate a delicious grapefruit and yogurt this morning!
Tim is up and around pretty good today. He has made a couple of laps around the block and then rehab came by and took him for another lap. He is attached to a pole - so that always has to go rolling with him. As soon as they do the pacemaker he can walk more freely and, I hope, get in line for being discharged a few days later.
He is always a challenge. Since he has this clot on the left arm - they will put the pacemaker on the right side. (Last time it was in his left shoulder area). They also want to put in a PIC line and it can't go on the left and supposedly it can't go on the same side as the pacemaker. I think they will mutate a new arm so they have somewhere else to poke and put things. His right arm has been poked so many times they couldn't even hit a simple place for blood this morning.
They are starting to look at my arms as surrogates. YIKES!!
We don't see doctors on the weekends as they have the weekend off - and now that surgery is done, they don't come around as much. We (I) have lots of questions - and not sure where they are.
Hope to update a little after lunch!
Sunday, March 15, 2009
Sunday afternoon
They have slowly removed all his hook ups. He is off oxygen. I had him take a walk down the hall and the nurse came in to check him when we got back. His oxygen level was 80! That's much too low! While she was in a panic and getting out his oxygen hook-up - you could hear Tim inhale - and his level immediately went to 99. We all started laughing - not sure if he was holding his breath on purpose or what. Once he started breathing - he was fine! Gotta always remind these baritones to do something. We told Tim he has to remember to breathe!!
The only wires Tim has left are the pacer wires. He's still pacing to his own beat......and not needing any prodding.....so while I kind of hope they don't do a pacemaker - I think it is still on the list. The pace maker is always a good back up incase it's needed - but on the other hand, he doesn't need any more foreign things in his body to attract infection.
The infectious disease doctor is still stumped what caused this whole mess. Tim does not have any infection in his body - nor could they find anything positive when we got here a week ago. They can not simulate anything in the lab - so all is much a mystery. Could be an episode for "House". I have some ideas and will ask ID. I wonder if this "cavity" they found for infection is from the last time and all the antibiotics - and whatever invaded this time was just some kind of flu/fluke. I suppose my idea is as good as anything they can come up with.
They cannot find any places left for an IV - and will send him for a PIC line tomorrow. They should have done that a few days ago. I asked when we came in and the answer was no....don't think they could have it before surgery...... at least if they put in the pic they don't have to come put in an IV every few days - and can quit poking for blood. His arms are swollen and pretty much black and blue from brusing. Each IV poke is taking about 3 times to find a spot. OUCH!!
I have nothing more for today! Our get well wishes go out to Bob. Get well, stay well and no more strokes!!!
Saturday, March 14, 2009
Saturday night
The nurse has just come in to check on him (it's about 10:30 pm) and is going to get him out of bed and see if she can jiggle some liquids out of him. Seems like there should be room for a lot funnies here..... all there is, is a lot of dust! I guess the "picture" is funny. He's standing there with a plastic urinal to catch what comes out - while drinking some juice. If it were just some free standing plumbing - he could pour it in and catch it on the way out. We need a Betsy Wetsy doll to show him the trick! Wonder if we could take up a collection for him!
I will stay in the room tonight. I hope we will both get some sleep and tomorrow will be a better day! Overall, I don't think he will have much doctor traffic till Monday. Then it will be back to "business" and see what equipment and tests he'll have to jump through to get out of here!
Good night to all! Thanks again for your comments and emails. We do read both!
Saturday afternoon
Tim ate a pretty good breakfast and lunch. He is terribly tired - and needs some sleep. We all know that doesn't happen in a hospital! The nurses are currently attempting to find a place on his right arm for an IV. He has nothing in that arm they can find and he as been stuck so many times it is horrible! They don't want to use the left arm due to the clot. That is the only arm with decent veins - and now it is off limits... Tim still has his catheter and chest tube - so he's not very mobile, yet. Hopefully, more later!..................................
Thursday, March 12, 2009
Surgery is over
I'll send out a finished note this evening! Thank you to everyone for your thoughts, prayers, emails, comments! It's wonderful to know we have such a great support group!
Surgery day continues
We were told that the first incision was made about 9:21 am.
We've just been buzzed at 12:10pm that "the major portion of surgery is underway."
Our next contact will be from the surgeon letting us know how everything went. We probably won't hear anything for several hours. At least they have started without any complications!
No news is always good news!
Next update will be this afternoon after I have talked with the surgeon!
Stay tuned...........................
Thursday, 3/12 - SURGERY!!
The bed guy came by at 6:15 to take Tim to surgery so we were glad we had come in early. Tim is in good spirits - and while not eager to have surgery - he's ready to get it going and have it over with. We all know the ICU and time following surgery is part of the hardest!
Now, we are in the lounge (at 6:30)- and the LONG wait begins. We have a beeper to keep us in touch. We probably won't hear anything till about noon or so.
Check back later for updates as we hear anything!
Keep the prayers going!
Wednesday, March 11, 2009
Wednesday afternoon, 3/11
We are definitely on the "hurry up and wait" list at the hospital. We - or really Tim - is on the wait list to get his screen umbrella inserted for clots. One doctor called it a filter,one a screen and another called it an umbrella - without fabric. When I imagine just the ribs of an umbrella, I can't see it catching much.....so I like the thought of a "screen" better! He was on the list for 6am - then 3 pm and we haven't seen anyone come yet....it's 3:30. So, if anyone shows by 8:30 tonight - I will be surprised. In the meantime - it's no food for the process.....then they said he could eat and brought his lunch tray. So, the hungry pup ate! Then one of the nurses commented as long as he kept it to soup, he was fine......(she ordered his lunch). But, they are on the ball here compared to other places, so not complaining!
Surgery is off......they kind of hang their heads when Thursday is asked, and indicate they are much more hopefull for Friday! So, we figure Monday.....but we are told it will definitely be before the weekend! I'm running out of days in this week......perhaps it is on the schedule for the 2nd Tuesday of this week. Actually, I think a lot of work gets processed on that Tuesday! We'll see. Of course the blood clot is a huge factor - and I'd just as soon they get that screen in place!
Mike asked if we weren't here - and didn't know about it - and Tim was just out running and jumping - (like a fairy?? or leaping dancer??) could he break a clot loose without knowing it. I'm not sure we ever got a straight answer on that one! Probably obvious why we didn't!
More - after midnight - maybe we'll be screening more by then!!
Tuesday, March 10, 2009
Golly, What next???
The results of the vascular check is in - and Tim failed. He just can't pass a test! He keeps saying he should have paid more attention in High School .... and on top of that he keeps singing, "If I only had a brain!" If you remember - the brain scan came up empty - and the only test he passed. Tim figures it's because there is nothing up there!
He has a blood clot in the right leg - pretty much from the top of the thigh - all the way down. This is from the Chemo...... Any piece or part can break off - and go to the lung....and once there it's all over. SO, they will treat with blood thinners and have a screen put in to catch any pieces that may break off. The vascular team's preference is to wait 3 months for surgery - but that's not a realistic option. They are ok with this tactic and figure odds are good with the "screen". BUT, Tim never lets any option go that easily. He also has a blood clot in the upper left arm - or near the arm pit or somewhere in that area. They cannot screen for that one - and cannot guage if it's "new" or "old". So, that clot poses the most problem. They figure a clot breaking off from the leg is high - but will be caught by the screen. The percentage of something breaking off from the one in the arm is lower - but if it does, it cannot be caught. Surgery will not occur until most likely on Thursday - possibly on Friday......so until then, they will treat Tim with blood thinners and hope however long they can get some in him will be helpful.
They will probably put this screen in sometime tomorrow.
We are doing our best to laugh when we can - to help make some giggles - to lighten the mood where we can in all this dismal stuff. This surgery keeps getting tougher and tougher - but we are still confident in the surgeon and this clinic. We are probably going to have ask everyone double and triple up on their prayers!
This afternoon has already lasted about 17 hours, but it's only 4:30. I'm not sure I can take any more "news" but as always - I'll update when or if something comes up!
I also wanted to add that I do read all your emails - and often read them to Tim. Thanks for your support and well wishes!
Tuesday Morning
Tim went for vascular testing this morning. I thought they said mascular - and knew that would be a bust. He doesn't have any muscles left after all the chemo. He left the room about 9 - and by 11 I was starting to worry. I wondered if they have taken him directly to surgery. I checked with some nurses and he was MIA. Eventually, he was brought back to the room. The vascular check didn't go well, they found a clot in the leg and something in the upper chest or arm or somewhere. The head of the vascular team wants surgery postponed 7 to 10 days or more.....up to 6 months. (That's not going to happen). The surgeon wants to proceed - but he's in surgery - so will have to wait until he's out and all is assessed and re-assessed. What a roller coaster! We surely don't want any clots moving around - and surely don't want to wait a week or more! GADS! He talked about a "filter" in the stomach area - I'm guessing that would catch any clots that might come loose.
At this point we are back to waiting........I'll update when anything is decided.
Monday, March 9, 2009
Monday Night
I don't know what made the last minute change - I imagine the surgeon had an opening.
They have checked every possible place on Tim's body - inside and out! Due to the cancer and chemo, his bone marrow is soft and his platlettes and red blood is low. They will be boosting that during and after surgery. A little while ago, they took Tim for a brain scan. The hospital had found an exta one and they were trying to locate the owner! Since Tim has been so dopey, they figured he had lost his or didn't have one. Actually, they were looking for pockets of infection - and he is fine!
Overall, Tim seems a 100% improved from Friday when we left home. He has energy - he has been up and down the hall, he's talking everyone's head off, he's hungry - and eating everything he can fine. He has raided the patient fridge several times this evening. He has color. Several of the nurses have questioned the need for surgery! He does need it - quickly - but this turn around is amazing. I hope he comes out of surgery feeling this good - obviously within in time!
It's hard to face the upcoming rehab - knowing what he will have to go through! Hopefully, by the first of May he will be ready to fish and all the great things spring lets you do! I'm hoping for a better vacation this "cruise line!"
More tomorrow evening after surgery! It will be a long afternoon!
Monday afternoon 3/9/09
I still don't think they know a lot about what the infection is that has caused the valve to leak. At first it was pneumonia - then it was the flu - and we all had to wear masks. Now, they say he doesn't have any flu - but think it's pneumonia.....and took away the masks. The comment was that they will put him on antibiotics for a week. So, now I'm wondering if we will just be pushed back a week????? I surely hope the surgeon shows up today to unravel some of the mysteries.
Tim is supposed to see the dentist here - but they said in a day or two. Gads! I'd like to get this surgery done and him on the road to recovery so we can head home. Tim is enjoying all the attention and everyone waiting on him hand and foot.... He said this was our cruise ship vacation....we didn't get a balcony - but we do have a great view of downtown Cleveland. I was contesting this cruise - he was getting all the attention, meals brought to him, etc - I get to wait on him and clean up after him.
I slept in the room last night. My bed consists of a flip down piece of plywood with a 2 inch piece of foam. The only thing worse would be just the ply wood - I think! I went to Walmart today and bought a twin size areo bed...hopefully, tonight will be much better! Especially if this cruise ship isn't going to dock for a week or so!
I'll update later - although, I think we are done for the day!
Sunday, March 8, 2009
On the road to Cleveland!
Results of the tests!
Out appointment at the oncologists was set for 1:30. We had lunch, I quickly stopped at a store - and we were just in time for out appointment - signed in about 1:28. Phew!! While we were in the waiting room waiting to be called back......my phone rang. I figured it was one of the boys asking about how the day was going - but the voice on the other end was in Russian or ??? and I knew it was the cardiologist. My heart skipped a beat and I handed the phone to Tim so they could discuss the echo. I caught bits and pieces of "what?" "the valve has to be replaced?" (I punched Tim and said - WHAT VAVLE?) The mytral valve had some minor backwash a few years ago.....but not enough to be worried about at that time - so I thought it was the mytral. Tim looked at me between the Russian words and said "Aortic". I couldn't believe my ears, I think my heart stopped and I thought I was going to faint. I couldn't see Tim at that point so I'm not sure if he had also fainted or evaporated. I did hear Tim mumble "something about Cleveland". He hung up the phone and said we needed to decide if we were going to go back to the hospital in Lafayette and check in or call the cardiologist to pave the road for Ohio. I cannot describe the numbness, how words and speech start sounding really funny and how nothing makes sense at that point. My head hurt beyond description - and a nurse was standing there saying it was time for our appointment. "What appointment?"
Oh, yeah - we were at the oncologists to find out about the CT Scan. I think everyone within the clinic was now aware of the conversation with the cardiologists..... the nurse took us back to the appointment room. Tim said we needed to get the name of the surgeon in Cleveland - that the cardiologist wanted to call him. I couldn't remember my name at that point - let alone remember who Tim was..... I said we would have to go home and I could look back in our records. The nurse was overly helpful and said she could look in the files there if that would help, but since the surgery wasn't done in Lafayette - she didn't think much would be there. As the oxygen returned to my head - we had carried back the surgeon results and they had been scanned into the computer system. She looked and looked and finally she found the file and the name for us! The oncologist was ready to come in - and quickly caught up on what we were just learning. Due to the leakage of the valve, Tim is a walking time bomb, and it could come loose at any time - and then our (my) decision would only be funeral arrangements. The doctors there preferred for Tim to immediately go to the local hospital - and he kept murmuring Cleveland. The oncologist very calmly asked Tim what and why - and said - well, it's obvious - go get in your car and GO to Cleveland. In the midst of all the confusion - I looked at him and asked what the CT showed. He said nothing! Absolutely nothing! Tim was cancer free - the the top half of his body! At last some good news!
More of the beginning
Friday. Oh boy! Tim was not excited I had set more tests - but what could he do? He was much too weak to get up and hit me! Thank goodness for some small blessings! :) The girl setting up the echo said since it was a Friday - she didn't want us worrying all weekend - that when they did the echo, if it didn't look right the person would get the cardiologist right then; or the cardiologist would look at the results briefly later and call with any concerns; or if the echo was ok - we would hear from the cardiologists office on Monday or Tuesday - so if we heard nothing all was ok and to enjoy the weekend!
We went for the tests on Friday morning. The CT scan went fine - and we were pushed down the hall for the echo. For the first time I was able to sit and watch. Of course I don't know what I'm watching! I watched the girl take lots of pictures and record lots of sounds. She put some in color and you could see the blue and the red - and I knew from 2 years ago the colors in the different places meant something - but couldn't remember what. Since she didn't seem overly concerned, not did she get up screaming down the hall for a doctor I figured all was ok. Tim had the same feeling and he put his shirt on and we went out for lunch! We had a couple of hours to kill before we went back to the oncologist to give us the results of the CT - which would also show cancer. .........
Oh NO! Not again
Tim's last chemo treatment was Jan. 26. His chemo treatments went every two weeks for 6 months. He did ok with them - if you can call being sick at the stomach and diarrhea ok. His 11th treatment was rough and he had to wait an extra week to do his 12th treatment. It was done on Jan. 26. He was pretty weak and felt BAD for several weeks. The took out the port that was used for Chemo on Feb. 2. During his treatments he had developed a clot along the port - and they wanted it out as soon as possible.
He was pretty wrung out from the chemo and by mid-February he was not gaining any ground.
He had a GP doctor check up the 23rd of Feb. He noticed that Tim was pretty short of breath and had a tough time getting around in the office. Tim was fairly anemic from the chemo - and that will contribute to shortness of breath and put him on iron pills. As the week went by - Tim got weaker and worse. Lots of coughing; hyperventalation to breathe, overall could not get up to get from the bed to the shower or from the living room to the kitchen. We were told the iron pills would make him feel a little better in a week.....so the following Tuesday I was nagging for Tim to call his doctor. Well, he tried calling the GP on Wednesday and he was gone for the day. They need to outlaw Wednesday golf! I told him to call his oncologist - his health was just not going in the right direction. He attempted to call some number and got a busy signal.....SO, I picked up the phone and called.....and got right through. I started explaining all the symptoms - and we got an appointment for Thursday. They wanted him to have a CAT scan first and then come to the office. Well, he has to be pre-treated for a CAT and cannot eat before. I asked about both - but was told all was ok........ Thursday morning, on the way to the hospital they called and said it would not be a go because of the above. We rescheduled for Friday. On the way home, the doctor's office called and decided to see us anyway. He looked at Tim and said his condition was not chemo related - but he didn't have a clue. He sent us across the street for a chest x-ray. We took back the pictures and they said the lungs were pretty messy - he had pneumonia! He prescribed some antibiotics - and listened to his chest. He said he didn't really hear anything but nonchalantly asked how long he had a heart murmur? I gave Tim a panic look knowing there shouldn't be one. I asked about scheduling an echo of the heart - and he said why not take care of the pneumonia first - and go from there in a few weeks.........
March 8 - Here we go again!
It is Sunday afternoon. Tim's had several more DR's and follow-ups and will probably do nothing for the rest of the day. (Not that he does anything anyway....). Tomorrow they scheduled a catherization - to look for blockage - and a TEE where they go down the throat to look at the heart. After that we will wait to see the surgeon and hear what he has in store and when. The cardiologist said he hopes for Tuesday or Wednesday....but the surgeon will make all the calls from this point on. Tim has the flu - that is the conclusion from infectious disease. They are not real positive on pneumonia. His lungs are clear. We all have to wear masks - don't worry I have incriminating pictures! The infectious disease doctor caught me with mine off - I told him it was too claustrophobic and I was already infected anyway. He didn't like my comments. Oh, well. He didn't kick me out of the room yet.
I have been working on catching the blog up to date - so hope you have snoozed off from reading, yet. I would hate for you to spill a HOT cup of coffee on your lap!
For this being a "nothing" day - someone somewhere is writing the orders for Tim. The poor little nurse is working her legs off. They have ordered lasics to help with the fluid retention in Tim's legs. It's working.....He has to have an IV set up - they have put 2 in him so far that have not lasted. His veins are small and hard to tap. The poor little nurse just tried poking him 2 more times with no luck. She said she would put a call out for the SWAT team - at least that was what it sounded like. I guess if they can't put in an IV they shoot him and hopefully one of the bullet holes will make a spot big enough for the needle! I asked about a PIC line - and he's not a candidate, yet, due to the open heart surgery - they will PIC him all over at that point to set up lines. They have set up a vein mapping and an ultra sound of his arms and legs - looking for clots. In the meantime, Tim looks the best he has in weeks! His color is back, his breathing is normal, and overall he feels and looks pretty good. I keep telling him he is loving all the attention - he sure didn't get that at home! He is in a private room - I think all new hospitals are headed that way. It is very large; it has a 42 inch Flat panel TV, and there is a bench I can flip down to sleep on. I will stay in the room until he is taken for surgery. While he is in ICU - I will have to find other sleeping arrangements. Once he is moved back to a room after surgery - i will be able to move back in. It will be on a different floor - but similar to this one.
The boys (Aaron, Mike and Matt) were all here Saturday afternoon and left Sunday afternoon. It was nice to have them here - not sure if they and Scott will make it back.