Monday, December 14, 2009

Kris, Dave and the Lumps: Round 3, Chemo #7, Last of the Ixempra

2009-Dec-11, Friday
Went in for Chemo, sleepy. I actually dozed off reading to Kris in the Drs
office while waiting for him to arrive. Apparently I was tired enough that
Kris observed if she hadn't known better, she'd think I was drunk for
slurring my words. :) I then proceeded to really doze off while talking
with Kris and Dr Moran! The issues were her Migraine on Thanksgiving, the
tingling in her fingers and the twitching of her left eye. Dr. Moran is
convinced that the finger sensitivity and eye twitching are all in keeping
with the Ixempra and today is the last dose of that drug. He stated that
the Migraine is more likely an effect of the anti-nausea medication they
give when giving the infusion each time. He switched to a different
medication for at least this round. Her spirits were up for the infusion
and she even managed to drop a few cards and dice, though we didn't have to
shock the nurses by scuttling about for them. Because of my being so
tired, she insisted that I occupy a chair and distress the other patience
by snoring loudly at them... then she insisted on driving home! Yeah,
she's tougher than I am. :)

2009-Dec-13, Sunday
When I got home from work (in the ball park of 9 am for those that don't
know my schedule) Kris was up and about and generally functioning well but,
she rapidly slowed down. By noon she was achy and complaining and I talked
her into taking a Darvocet. Then I went out and got Pizza since we didn't
feel like cooking. By the time we were done eating, and watching an
episode of CSI she was feeling better (about 2:30 pm, half an hour after my
bedtime). When I got up tonight she was watching America Speaks and doing
ok but she was quite run down. Here's hoping tomorrow things are going
well.

Monday, November 30, 2009

Kris, Dave and the Lumps: Round #3, Chemo #6, followup

2009-Nov-26, Thursday, Thanksgiving
Slept in, pretty much on purpose. When we got up Kris started to work on
the Apple pie. In the process she realized that she hadn't gotten enough
apples and sent me off to get 2 more Braeburns for the stuffing. When I
got back, she was laying on the couch with a look of abject misery on her
face. I asked after what was wrong and she said that she had a migraine.
Now, for the record, Kris doesn't get migraines save when they are
chemically induced. She would get them with Citoxin, and she got one with
the initial dose (double) of the anti-viral medication she was prescribed
for shingles. She took Tylenol (she's not allowed aspirin due to the blood
thinners) and that did nothing. That meant she had to wait until the
Tylenol was out of her system before she could take one of her Darvocet
since Darvocet also has Tylenol in it (and for those that don't know,
Tylenol is quite hard on the liver, so, doubling up is not a good thing).
She finally went up to bed and lay down in the dark for quite some time. I
managed to cook the bird and get dinner done. About the time she was able
to take the Darvocet, dinner was ready and she was feeling better though
certainly not 100%. Due to the nausea associated with the migraines pain,
she was barely able to eat dinner. She did tolerate the pie better than
the rest of the food.

2009-Nov-27, Friday
Much better today. No migraine and plenty of energy, so, things seem to
have sorted themselves out.

Tuesday, November 24, 2009

Kris, Dave and the Lumps: Round 3, Chemo #5

2009-Nov-20 Friday
Infusion day. Kris' I&R suggested another adjustment of her blood
thinners. Her other blood work looks good. She's still got some
sensitivity in her finger tips but the Dr thinks everything is in keeping
with the Chemo, and we tend to agree. For the record, this is MUCH better
than Xeloda (for Kris)!

2009-Nov-21 Saturday
Kris is feeling a bit run down already. Not yet achy or in pain but just
not enough energy for everything, though she managed to keep plugging along
through everything we wanted to do.

2009-Nov-22 Sunday
More run down though up in spirits and up and about.

2009-Nov-23 Monday
Kris stayed in bed late today to wait for the pain killers to kick in
before she would brave the day. Other than the pain, she's doing well and
her spirits are up.

I need to insert a note to Carl. You will be missed and our thoughts are
with Grace and the rest of the Sato crew.

Thursday, November 12, 2009

Kris, Dave and the Lumps: Round 3, Chemo #4

2009-Nov-6, Friday
The infusion went without incident... which includes no giggling and
rolling around on the floor looking for cards, much to the nurses relief.

2009-Nov-7, Saturday
Kris is already feeling the effects of the Chemotherapy. Mostly just a
little run down, nothing major.

2009-Nov-8, Sunday
Kris is more run down and achy. She took a pain killer this night to go to
sleep. Things are definitely occurring earlier in the cycle.

2009-Nov-10, Tuesday
Kris is pretty much back to normal. Tastes are back to normal and the
achiness is pretty much gone.

Only one more round to go then we cut back from 2 drugs to one. I'll nail
down which drug we are finished with in the next update.

Monday, October 12, 2009

Kris, Dave and the Lumps: Round 3, Chemo #3, followup

2009-Oct-11 Sunday
Kris is... tired. She's also in enough pain that she decided to take a Darvocet before going to bed. That said, she was resting peacefully when I trundled off to work.

Saturday, October 10, 2009

Kris, Dave and the Lumps: Round 3, Chemo #3

2009-Oct-9 Friday
Went down to Boulder, by way of the Original Pancake House, for chemotherapy. We also stopped by the book store to pick up some Sudoku books. Ours were getting old and we've made friends with a gal, I think her name is Edina, who was interested in Sudoku but we didn't have anything but my iTouch to demonstrate/teach it on and she does not like the iTouch interface.
When we got there I asked if it was ok if I stuck around. I caught some weird sort of cold about the time of the last Chemotherapy session. Just a tickle in the back of my nose, then a bonafide sore throat but, it wasn't very sore at all. Finally it moved back into my sinuses as 'pressure' but not true blockage. Now it's migrated into my chest for vacation and apparently it's enjoying the place 'cause I can't seem to shake it. No fever, no chills, no aches, nothing but this 'pressure' and a cough for trying to clear my lungs. I've been very concerned about passing this to Kris and thus have gone well above and beyond the call of duty trying to NOT spread it. Kris did complain about a mildly sore throat but she must've beaten it back since she got no other symptoms
So, we headed back to the infusion room where they gave her the anti-nausea medicine in a drip to avoid giving her nausea like it did last time. Yes, that is the definition of Irony. We settled in and played Cribbage throughout the day. Unlike normal, we managed to spill the cards twice and the cribbage board three times... this is a record for us! The most spectacular of which happened when Kris dropped a card down in her chart... now these are comfortable chairs but, they are on the cheap so the space between the arm and cushion goes straight through. We've dropped cards down that way several times and the cards have always appeared on the floor below that side of the chair. Imagine our surprise when she dropped and ace and nothing showed up! I got down on the floor to look as close as I could... no card. While I wasn't watching, Kris, IV tube and all, got down on the floor to look with me. I stood up, saw her craning her neck laying on the ground with an IV tube reaching up to the IV pump and said 'something is wrong with the picture of you laying on the ground searching for cards while getting Chemotherapy.' Just at that point, one of the nurses walked up with a panicked look at which point Kris broke out into peels of laughter at the situation! So, we all had a good laugh (including the other patients).
The short of it is that the infusion was uneventful. Now we have to weather the next 4 days of achiness and pain as the drugs work their magic.

Tuesday, September 22, 2009

Kris, Dave and the Lumps: Round three, Chemo #2

2009-Sep-17, Thursday
Kris' scalp/hair has been more and more irritated as time goes on. We discussed cutting her hair off in the near future, sometime fairly soon after Chemo Friday.

2009-Sep-18, Friday
Chemo. Appointment is 1045 and will take about 6 hours, so we got breakfast at the Original Pancake House then headed out to the clinic. Kris' I & R is 2.4 which is perfect so we're leaving her Warfarin dosage alone. Met an interesting soul at the clinic during infusion who likes Irish folk, as well as other more eclectic music, as much as we do. One point of note is that the nurse 'pushed' one of the anti-nausea drugs rather than administering it by drip. Ironically this has the effect of making Kris quite nauseous as it was too rapid a delivery. Other than this, things went quite a bit better this time than last time.

2009-Sep-19, Saturday
Kris decided that we'd do the buzz today. This time we handled it ourselves. Took us a bit to get our clippers to work the way we wanted, and we decided to go so far as to shave but, in the end everything looks great! Yes, that's right, I have no problems at all with bald women. :)

2009-Sep-20, Sunday
Towards the afternoon, Kris began feeling a bit run down. This is early but in keeping with normal Chemo reactions.

2009-Sep-21, Monday
Kris is still run down and starting to feel achy. Enough that she waited long enough to take the Darvocet she has for pain. Other than this her spirit is up and she even worked a bit today. Note: I am very appreciative of her work support structure for helping her through times like these. I can't go into detail but her manager, among others, have done a lot to help Kris work through this with minimal stress and I wanted to say thank you to those co-workers for doing so.

Wednesday, September 9, 2009

Kris, Dave and the Lumps: Round 3, Followup with Dr. Moran for Chemo #1

2009-Sep-8, Tuesday
Met with Dr. Moran. We catalogued the issues we saw with the first round of Chemo: Headache and tiredness the day of, Achy (pain) and run down 3-5 days later, buzzing in fingertips, white tongue 2 days later (Kris noticed this because she had an odd taste in her mouth, when she looked in the mirror, her tongue was sort of 'white' and she was able to brush off what was apparently dead skin), and most recently some minor sores on her tongue. For the sores he gave us a prescription for a mouth wash that helps with them. He said that for the achiness 3-5 days after the infusion, it was ok for her to take the Darvocet she was prescribed for pain after surgery. The rest is pretty much expected or understood (the problems the day of we think were just heat from sitting directly in the sunlight from the window during the 6 hour infusion). Kris' I&R was 3.0 today after they adjusted the dose to 3.5 mg of Warfarin each day. He wants her to go back to 3 mg each day to try and titrate it back to 2-ish (it was 1.4 the last time). Long and short is that things are proceeding nicely, or at least 'as expected' and we will just keep on keeping on.

Thursday, September 3, 2009

Kris, Dave and the Lumps: Round 3, post Chemo 1


2009-Aug-31, Monday
Kris was back at work and things were ok over the weekend.  However, towards the end of the day she started feeling achy, rundown and had a headache.  Her chemotherapy drugs do advertise that you may get flu like symptoms about 3 days after the infusion so, this was expected, though not this late.

2009-Sep-1, Tuesday
Achy and rundown feelings are worse and she can barely wait long enough to take her Tylenol for her headaches.  She's only allowed the Tylenol as the other medicines thin blood and she's on blood thinners for her port.  When she went to bed, she decided to take a Darvocet left over from her surgery to help with the pain and allow her to sleep.

2009-Sep-2, Wednesday
Pain is still there but much reduced.  She was not nearly as... closed is the best description I can give.  That look folks get when they are in pain and trying to function, brow furrowed, etc.  She was in brighter spirits and able to go longer without the Tylenol.  Looks like we are on the mend.

Dave Hart
BCRS support for pSeries and iSeries
Dept. HJ3A
Nextel Mobile: 303-472-8826
Anything might be accomplished with the will to do so  . . .
. . . nothing will be accomplished without it.

A conclusion is the place where you got tired of thinking - Anon
...or where you ran out of options - K. Carson 1999

"...the blank sheets are IBM property, but they do serve the purpose of keeping execs busy trying to understand them."  - Kilroy

Saturday, August 29, 2009

Kris, Dave and the Lumps: Round 3, Chemo #1

2009-Aug-28, Friday
Went in for Chemo, 10 am Appointment. Saw Dr. Moran and he upped our dosage of blood thinners as Kris was at a 1.4 where they want her at a about a 2 for I and R (clotting factor).

When we got to an infusion station, the nurse asked us if we know about the ins and outs of the drugs we were to receive: Avastin and Ixempra. Kris explained that one worked in a similar fashion as Herceptin and the other worked similar to Taxotere. The nurse indicated that was all wrong and went off to get paperwork and a consent form. She came back with paperwork saying that Avastin attacks blood cells that 'feed' a tumor. This causes the tumor to, essentially, starve and die. It's a targeted therapy and thus the nurse had a better understanding of why Dr. Moran described it as being 'like' Herceptin since Herceptin is a targeted therapy. Ixempra is not a targeted therapy and has the side effects we don't want: hair loss, sensitivity in hands and feet, sores can show up in the mouth, headaches, etc. It is also in the same family of drugs as Taxotere and the side effects put it in a similar enough category that the nurse again understood why Dr. Moran described it as similar to Taxotere (score two for Kris!).

The one big surprise was that the infusion took something less than 6 hours. We didn't leave until 4 pm. Now, we did expect the first infusion to be slow since they like to monitor for allergic reactions but, this seemed a long time to us.

While there Kris talked with a gentleman who has reoccurring Lymphoma. The treatment is a protein which feeds the Lymphoma. The twist is that they give him a protein from mice, twice a year. The cancer jumps on, and eats, this protein like a cat jumping on a saucer of fresh cream. However, once the cancer eats this protein the body rejects the cancer as it's now got appearances of being from a mouse!

We also saw a young man, about 17 give or take a year, who was being treated with Gemzar which we recognized as a cancer drug Kris had used in Round 1. Not sure what he has but it was sad to see someone so young with cancer. That said, he looked to be quite fit and was well supported by what looked like a father and girl friend (sisters just aren't that affectionate... or at least, I hope they are normally not that affectionate). Because of this, I don't doubt he will recovery quickly and do well in the long run!

After the treatment we were suitably hungry. Oh, I should note that early in the treatment Kris was cold (even before the infusion started). So, I grabbed a couple of blankets for her. She cast them off as the sun Westered since the center is a room with one wall of glass facing the mountains and the room got to be quite warm. When we left, it was 90 degrees outside. As we were heading to the restaurant we'd chosen, she complained of being achy (one of the side effects) but, it seemed to her to be far too early for side effects. She decided that maybe it was the heat. So, we headed home instead. Oddly, she felt better as we were driving home and other than being a bit tired, she seems fine.

Next appointment is Monday with the Surgeon in follow up of the Port installation. Then it's Dr. Moran a week from this coming Tuesday. And three weeks from now for the next Chemo treatment.

Wednesday, August 19, 2009

Kris, Dave and the Lumps: Port installation #3

Friday, 14-August-2009
On Tuesday Kris pointed out that she had a very minor infection on one of her fingers. Dr. Moran hemmed and hawed over it and decided to write out a prescription for antibiotics. If the infection didn't go away Thursday, fill it and start it. So, Friday... we filled it and started the course of Anti-B's. In no small part because we had surgery coming up and figured it'd be a good idea to be on them prior to the surgery.

Monday, 17-August-2009
We took Kris in at 10 AM for the surgery to install her newest port for the Chemo Therapy and everything was quite boring, which in surgery speak means things went incredibly well!

Tuesday, 18-August-2009
Kris is doing well. Well enough to do some work which made her a wee bit tired so she knocked off a little bit early... it's not like she'd had surgery recently or anything. Things seem peachy though. Now it's time to heal up from the surgery and wait until Chemo on the 28th.

Wednesday, August 12, 2009

Kris, Dave and the Lumps: The Good, the Bad and the Ugly

Prequel:
Kris saw Dr. Jones last Thursday as a follow up to her biopsy surgery... he was 'ho hum' about things as her recovery from the surgery is going fine.

The Good:
Saw Dr. Moran (Oncologist) yesterday afternoon. Once again he was... guarded but, in my opinion, not as much as last time. The thing I was most worried about was the brain scan as it had implications I didn't even want to consider. Dr. Moran talked about everything throughout the conversation except the Brain scan... finally, at the end, I asked him if his lack of talk about the Brain scan meant that it was clear and he confirmed that there was nothing on the Brain scan... well, there was evidence of the usual stuff, just nothing tumor like.

The Bad:
He's decided on two drugs. One was Avastin and he described this drug as being about as difficult to tolerate as the Herceptin, which Kris took totally in stride. The other is in the Taxol/Taxotere family of drugs and it will mean that she will lose her hair, again. She's decided she's only allowed to have hair about 2" in length! :) The down side is that this means she'll have to have another port installed. This will happen in the next two weeks followed fairly immediately by her first treatment.

The Ugly:
To be honest, the Ugly we already know about. It's what we don't know. Basically the cancer is being more tenacious than we'd all like and we are, to a certain extent, shooting in the dark. They don't have a tumor to aim at, and thus they don't have a lot of material to experiment with to come up with a good solid plan of attack. The current plan is to basically hit the system with the options we have left in hopes that it will kill the cancer. The only other option is to just sit back and wait for it to express itself in another tumor. Which runs the very real risk of waiting for it to metastasize, which it has not done. I asked and he agreed that it's entirely possible that the Herceptin was keeping the cancer at bay but, it's obviously not killing it so he doesn't seem to be enthused about using that drug again.

Wednesday, July 29, 2009

Kris, Dave and the Lumps: Brain Scan

Just a note that Kris had her Brain Scan yesterday (the 28th) and
everything went smoothly.

She's still upbeat but we are concerned that her energy is low. This, and
the nagging cough, are two symptoms we associate with cancer, at least for
Kris. However, her energy usually comes back after the cancer has been
taken care of. My sense is that though we've had the surgery, the cancer
hasn't been dealt with... that's what the Chemo is for.

Dave Hart
BCRS support for pSeries and iSeries
Dept. HJ3A
Nextel Mobile: 303-472-8826
Anything might be accomplished with the will to do so . . .
. . . nothing will be accomplished without it.

A conclusion is the place where you got tired of thinking - Anon
...or where you ran out of options - K. Carson 1999

"...the blank sheets are IBM property, but they do serve the purpose of
keeping execs busy trying to understand them." - Kilroy

Kris, Dave and the Lumps: Brain Scan

Just a note that Kris had her Brain Scan yesterday (the 28th) and everything went smoothly.

She's still upbeat but we are concerned that her energy is low. This, and the nagging cough, are two symptoms we associate with cancer, at least for Kris. However, her energy usually comes back after the cancer has been taken care of. My sense is that though we've had the surgery, the cancer hasn't been dealt with... that's what the Chemo is for.

Friday, July 24, 2009

Kris, Dave and the Lumps: Cautious Optimism

Saw Dr. Moran today. His demeanor was... guarded. He told us that the Lymphnodes and tissue that Dr. Jones removed were all positive for malignancy and were the same cancer as the breast cancer she'd most recently had. The tissue was, and he thought this odd, basically fatty tissue.That's the bad news. The good news is that he considers this an extension of the breast cancer and thus Kris is not, I repeat NOT, stage 4. She's got a rather difficult case of stage 3. He said that there is no immediate danger as they are confident that Dr. Jones was able to pull out all of the tissue. However, there is concern in that the disease is obviously still running around in her system. I'll take each consideration one at a time:

Radiation: The Boulder panel was discussing our case and they still feel they can not use radiation as a treatment plan due to the radiation she received with her first bout of breast cancer. Even though the lymphnodes in question were in her neck, she was radiated from about mid neck to, effectively, just above her heart and generally on the left side of her body. There have been recent commercials about a radiation technology used called 'cyber knife' which is supposed to be able to irradiate very discreet and precise areas of the body. Dr. Moran said that the concern about preexisting tissue damage due to the previous radiation treatment is still a concern with this kind of technology and the fact is that because of the surgery, they simply don't have a tumor to aim at. This problem is... I'll use the word systemic but, I feel I need to explain that so no one panics over it. Which I will do in explaining the next thing the Dr. said.

Chemo: Ok, a short lesson in cancer. However it is begun in a person, cancer is essentially a set of cells gone rogue, however, they are still cells of the body. Thus, liver cancer is essentially a liver cell that mutates into something that is like liver tissue but not and has a voracious appetite for copying itself and it grows... by normal growth patterns it grows very fast. The body isn't sure how to respond to this since it thinks that it's one of it's very own liver cells, just one that's more productive than most and it reacts in a way that is not truly helpful. Note that though my example starts in the liver, the cells of the body do not all stay in place, they can break off and wander the system. So, much like a virus or bacteria, some of these rogue cells go roaming and can cause problem with cells in other locations. One of the ways for these cells to move about is through the lymphatic system, which is why it can get infected first and why a localized infection of the lymphatic system does not, in and of itself, raise your stage from 3 to 4. Remember: Stage one is cancer of a localized organ and a tumor of a small size (I don't have the size numbers at hand). State 2 is a larger tumor. Stage 3 is multiple tumors in the same organ and local lymphnode infection. Stage 4 is infection of multiple organs or of the lymphatic system outside of the region of the infected organ. So, in the liver example, one tumor with traces of the livers cancer in the breast lymphatic system would be stage 4.

So, where does that leave us? Kris apparently beat her breast cancer into submission but it looks like it was still in her lymphatic system floating around. It's possible that the Herceptin treatments were suppressing the cancers ability to express itself but not eradicating it. Thus, when her Herceptin treatments stopped last May, the cancer was free to latch on and do it's thing. One of the possible ways to address this is to just sit back wait and watch and see where the cancer builds a new tumor giving us a target to attack. Dr. Moran thinks that this is unwise (and I very much agree) and that we need to treat this at the cellular level through drugs. The reason I say this is 'systemic' is that when you take drugs they don't know where to go, rather they go to the whole system and the fact is that we want to kill, or at the very worst suppress, the cancer from getting away and getting anywhere and we simply to not know where it is.

Thus, Dr. Moran has asked us to return in two weeks. During that time he will be researching ways to attack this new threat and Kris will be getting a brain scan. That raised a bit of concern for us. One of the places that breast cancer will tend to roam to when it leaves the breast is the brain. He has every confidence nothing is there but he wants to rule that possibility out... and we agree with that. He actually said he wants a brain scan to make sure nothing is going on up there... which caused Kris to laugh and point out what he'd said. He laughingly replied, "that didn't come out the way I wanted it to." I've also asked him to take a look at the question of 'what is causing this to happen.' I am concerned that there may be something in our environment causing this to occur and if we don't find a way to remove that, we'll just be back in this boat again in too short of a time and it should be obvious that we don't want that. I want a happy and healthy Kris.

Note: Kris's demeanor is strong and happy, as evidenced by the joke in Dr. Morans office... if anything, I've been the bleary eyed wimp this time around.

So, now you know why I titled this entry: Cautious Optimism. There is a new threat on the horizon but, I have to stress this as it's important: not stage 4 and we don't have any tumors to attack. Right now I take this as a positive and I'll take any positives I can get... and yes, we'll do research with places like the Cancer Centers of America though we have full confidence in Dr. Moran and the Boulder area team (panel) that is involved.

I'm getting wordy but I feel I need a bit more on that. Apparently there is a team of Drs that meet in the Boulder area every Tuesday to discuss interesting or problematic cancer (and I'm sure other) situations. I noted that whenever we see a Dr. for Kris' cancer, we hear 'yeah, I remember discussing your case at panel', even with Dr.s we've never previously seen before. It lends a sense of community and support amongst the Dr.s that gives us more confidence than I think we'd otherwise have... and, I like it.

That's enough for now. I'll keep the mail list going as we move forward to keep you all posted.

Thursday, July 23, 2009

Kris, Dave and the Lumps: Neck Biopsy

2009-July-22
Went to the hospital for the biopsies today. Turns out they found 2 areas of question near the mastectomy/reconstruction site and we had two in the neck. Dr. Jones said that he may not pull the lower spot in the neck out as it's behind the clavicle (collar bone).

Surgery went quicker than I thought it would though we still got there at 11am and weren't out until after 5pm. Dr. Jones came to me in the surgery waiting area and he looked upset. He said 'it doesn't look good' in relation to the tissue he pulled out which, naturally, upset me quite a bit. He also noted that he found a pocket of fluid in the area of the tram flap and Kris now has a drain in place for that fluid.

When Kris came out of surgery, it was obvious Dr. Jones had not talked to her and I felt I had to be straight with her. If we are going to beat this thing, again, it has to be done up front, I feel. I broke down and she broke down and I was very surprised at how rapidly she bounced back and was smiling and joking with the nurse staff very soon after I gave her the news. When I was able to talk again, I told her that we really don't know what the issue is, we just know that 'it doesn't look good.' Fact is, it could be a number of things but, unfortunately, the odds are it's cancer again. I need to point out that both of us noticed that she's starting to cough. Each time she's had cancer, she's had this minor nagging cough that has a distinctive... sense... to it. That is how she's coughing now.

So, it's wait and see. We see the Oncologist Friday and we hope he will have answers from the biopsy then... and I hope that it will not be cancer... and I know that whatever it is, we'll beat it.

Wednesday, July 22, 2009

Kris Dave and the Lumps: Scans

I got home yesterday and Kris said that she'd gotten a call asking her to go in for a sonagram. I'd had a very bad day at work so I opted to go along with her though the appointment was pushing it for my schedule.

We got to the surgeons office and they told us to go to Radiology. Went there and waited for a room to open up. When all was settled, I watched as the technician found... nothing. She revealed that the recent pet scan had found... something... near the site of the left breast reconstruction. Since she couldn't find anything, she asked one of the imaging Doctors to come in and give it a try. He too could find nothing. So, they sent us down for a CT scan. Their they attached a 'target' to the area they knew they would find the problem in and zoomed in for a closeup. What is different is that they found the aberration each time with her left arm down, and the CT scan was done likewise. They marked a target on her with permanent marker and we were back to the surgeons office.

Dr. Jones (the surgeon) stated that it was something that was right on the edge of, and sort of hidden by, the tram flap. It could just be some sort of aberration introduced by the tram flap such as necrotic tissue. Based on that I asked if it could actually be a diminishing spot, ie: a bit of necrotic tissue that the body was in the process of absorbing. He agreed but his demeaner was such that I felt he didn't want to give us false hope. When he does the biopsy, later today, they will remove the original lump we found in Kris' neck, a new one they found pretty much straight down from that and just below her collar bone and the one by the tram flap.

Tuesday, July 21, 2009

Kris, Dave and the Lumps: Lymphnodes in the neck

So, about 4 weeks ago, Kris turns to me and says something about a lump in her neck. Her attitude was such that I spoke up about the lump in my knee (which has since been surgically removed and biopsied, nothing but a bone spur). We bot laughed and passed it off as nothing.

About 3 weeks ago Kris has me feel the lump in her neck. It felt like a grain of rice under the skin and was positioned to the left side and a bit low on the neck, an inch or two above the collar bone and left of the carotid artery. To me I thought it felt like a cyst but told her to make an appointment with the oncologist just to be sure. She wasn't sure we needed to see the oncologist especially since she had an appointment in the not too distant future anyway.

About a week later I was talking with Linda on the phone and between us we convinced Kris to get an appointment to get it checked out. So, the following week she kept trying to get to talk with someone at the oncologists office and kept getting delayed. Finally she got an appointment for the 13th of July in the afternoon. Dr. Moran said that the lump was in line with the Lymphatic system and, given her history, it needed to be checked out. He set up an appointment for a pet scan and asked her to see the surgeon to have a biopsy.

She had a pet scan Wednesday the 15th and set up an appointment with the Dr. Jones (surgeon) for the 20th.

Dr. Jones said that the pet scan showed two spots. The one we knew about in her neck and another just below the collar bone and in line with the first. There is a third spot in the area of the breast reconstruction but he's not worried about that. He said that we could do a needle biopsy but, that would be inconclusive. We opted for the biopsy to be done on Wednesday the 22nd and we have another appointment with Dr. Moran for Friday the 24th.

Wednesday, June 3, 2009

Kris, Dave and the Lumps: Last of the Stitches

2009-Jun-2
Kris went in to see the Dr, or rather the Nurse, and have the last of the
stitches removed which was uneventful. The nurse did give her some 'scar
tape' which helps to heal the scars such that they are not noticeable.
However, this 'tape' is more like hard plastic so either we aren't using it
right or it's poorly designed for this application.

Not sure the date but the final event will be coming up. One more
procedure to 'finish' the left side and we are done. :)

Dave Hart
BCRS support for pSeries and iSeries
Dept. HJ3A
Nextel Mobile: 303-472-8826
Anything might be accomplished with the will to do so . . .
. . . nothing will be accomplished without it.

A conclusion is the place where you got tired of thinking - Anon
...or where you ran out of options - K. Carson 1999

"...the blank sheets are IBM property, but they do serve the purpose of
keeping execs busy trying to understand them." - Kilroy

Wednesday, May 27, 2009

Kris, Dave and the Lumps: Surgery follow-up, stitches removed

2009-May-26
Got home from work and Kris had a nasty headache and generally wasn't
feeling well. When we discussed things it struck me that she'd had too
little to eat and that maybe some electronics device in the house had fried
(ever since the first round of cancer she's been susceptible to that kind
of thing), so, I convinced her to head out for lunch. After which she felt
better, though the headache was still lingering.

When she got back from seeing Dr. Kuisle and having the first set of
stiches removed (turns out there's two sets to remove). One thing she had
to say about removing the stitches was that it was VERY uncomfortable!
Apparently the Dr. had said that he'd given her cortisone before the
surgery to help with this sensitivity. Now that it's worn off... well,
things are less comfortable. He instructed her to keep an ice pack on the
nerve plexus just under her armpit, about where the bra strap goes around
back. That seemed to help a lot and she was doing better when she trundled
off to sleep.

Tuesday, May 26, 2009

Kris, Dave and the Lumps: Tubes out, looking to remove the stitches

2009-May-22
Saw Dr. Kuisle today to have the drain and RR tracks removed. Ok, the RR
tracks are staples they use these days that make a wound look a lot like
Rail Road tracks. Oddly, since this surgery was less invasive than the
others we are used to, removing the drain seemed to be a bit less
comfortable. All in all the procedure was quick and we were on our way
home, and running errands, in nothing flat. Her next appointment is
Tuesday the 26 th (today) to have the stiches removed and the stitches are
causing Kris conniptions of the highest order! Seems they feel like
needles poking her from all angles when they rub against fabric... <sigh>
This too shall pass and the results will be wonderful! :)

WARNING: what follows is NOT for the squeamish! Do NOT read on if you are
one of those types!

You have been warned.

Ok, when we went into surgery the Dr. used one of his disposable pens to
mark up Kris. Presumably as a guide for the cuts he would make for the
surgery. The guide looked an awful lot like an old fashioned keyhole with
a round opening at the top and the sides at the bottom fanning wide like a
dress skirt. This shape went vaguely from above the nipple down to the
bottom of the breast with another line below and following the crease of
the breast. Now, he'd told us before that this surgery was basically a
boob reduction and lift and as such I expected the nipple to fit in the key
hole but wasn't quite sure what was going on with the rest of the lines.
Having the bandages off was an eye opener! The keyhole had indeed closed
around the nipple and the 'skirt' lines had come together to form one
straight line going down to the horizontal 'crease' line.

Ok, why, Dave, are you going in to so much detail? When I saw Kris the
first time it was a bit of a surprise... if I didn't have my background (my
father is a mortician and I've seen more bodies and autopsies than I care
to admit to) I may well have reacted with shock and dismay... I did not and
it dawned on me that if I had it may well have affected Kris peace of mind.
You see, the fact is that it was not only Kris' first time to see herself
without the bandages but a reflection of how she must look through the eyes
of another. I am quite pleased that I was able to look upon the work the
Dr had done and react to the woman... NOT the scars left behind. The scars
will heal... or they won't. Kris will be there either way and frightening
her based on viewing something that is decidedly not yet healed will do no
one any good.

The lesson to anyone who has to go through this is not to be shocked by the
interim process. This is no different than losing your hair to chemo, it's
transitory and the scars will heal (the scars on the left have). So, for
the sake of your loved one, don't run screaming from the room. If you have
to flinch, do so, but, be sure to be supportive and let them know that the
wounds will heal and things will be wonderful when all is healed. :)

On that note, we were watching the Drs and a gal pulled her wig off (she
was losing her hair to chemotherapy) during the show. It seems that the
wig doesn't make her feel like herself but rather like she's hiding
something she feels she shouldn't have to hide. I agree, however, it was
obvious that she'd not shaved her head and had scraggly hair... ladies,
trust me, keeping half a dozen shoulder length hairs is NOT better than
shaving it off so it's evenly trimmed and neat!

Kris, Dave and the Lumps: Post 'adjustment' Surgery

18-May-2009
Went to the surgery center at 9 am, registered and Kris went in... I then proceeded to cool my heals, well, Kris insisted I go to breakfast THEN I cooled my heals. Surgery went without a hitch. Doctor came out about 2 hours later and said she was out of surgery but not quite 'awake' yet. About 15 minutes later he called me down. Kris looked pale but recovered nicely. We were home by 4 pm. She's recovering nicely enough that we had Ginger beef for dinner and she kept down her fair share!

19-May-2009
She's up and about and, in fact, maybe a bit too much up and about but she seems to be fine. I'm chiding her to ice things when she's sitting still and otherwise things seem to be proceeding fine. Next appointment is Friday to have the drain attended to.

Thursday, May 14, 2009

Kris, Dave and the Lumps: Final Reconstructive Surgery Update

There is a schedule change: Kris goes in for her final surgery Monday the
18th of May. She will go in early morning and should be home by 2-ish in
the afternoon. Then it's a matter of me pampering her for the following
week for recovery. :)
Kris' final Herceptin treatment was uneventful, even boring. She had a
consult with her Dr. about an issue that we have been suffering from and
found that there is an acceptable treatment for her. I won't go in to
details so as to not embarrass Kris, but, I will say that if someone is

Tuesday, April 7, 2009

Kris, Dave and the Lumps: Follow up Surgery plans

Straight from Kris herself:
Saw my reconstructive surgeon today. My follow up surgery will be the morning of May 15, which is a Friday. I expect to be off work the following week, and return Monday May 25. He did mention that I might be a bit more fatigued than normal for another week when I get back.
I'll also have an afternoon pre-op appt on Monday May 11.
I'll be blocking my calendar, but wanted you all to have the information.

Kris Dave and the Lumps: Quick update

Just a quick update: Herceptin treatments are almost done and uneventful. Kris' appointments have been... uneventful. Today she will meet with the doctors to find out when she will be doing her final surgery. This is an adjustment so that she is... erm... balanced. I will post more information tomorrow when I have the results of todays meeting.

Monday, January 5, 2009

10-Dec to Present:

Ok, I've been remiss. My only excuse is the Holidays and it's a weak one at that!

Kris saw her Physical therapist, Dale, her final three times and other than the edema where her reconstructive surgery was done, she's fine. In fact, she's exceeded Dales expectations... to the point that Dale tried to discharge her. Kris asked about the edema and Dale relented since dealing with edema from surgery is one of the responsibilities of Physical Therapy.

She went in for her Herceptin last week on December 23rd. While their, she asked the Dr. about a rash that had broken out on her belly... the Dr. said it was shingles! She prescribed a medication for Shingles and we got a lesson in what Shingles is. When I was young, I'd hear folks talk about shingles and the way folks spoke about it, I always assumed that the victims of shingles had been doing something naughty... since it was always in hushed tones or 'behind the hand.' Turns out that if you have Chicken Pox and beat it, the disease can recede into your nervous system as a form of herpes virus. This dormant version creates pockets in the nerves near the spinal column and will be dormant for years. When it does finally awaken, it travels along the nerves until it breaks free through the skin. Looks just like your garden variety rash. The only thing I can say is that the rash Kris has is roughly the size of a half dollar. We initially thought it was a break out of ring worm. The bad news is that what breaks out of the skin is contagious and can spread, of all things, Chicken Pox. Note that the contagion is unlikely to spread save to those folks who have suppressed immune systems... oh, like folks going through Chemo Therapy! However, once the rash scabs over, you are no longer contagious. Fact is, the Dr. washed her hands and had Kris was hers as well before going in for her Herceptin infusion... just in case. Other than that, she wasn't worried. I specifically asked if I needed to worry about this and she said 'no.' So, we filled the prescription and the rash is clearing up quickly and nicely.

Note that if you do not catch this in the first 72 hours, living with shingles can be a living hell! This according to a friend of ours who has had it and did not catch it in time! Apparently it can spread widely and the itch and pain is a nerve itch/pain so it's quite bad. We read up on this and found that in rare cases it can break out on the face (cheeks) and that can cause blindness! Long and short: if you have a rash that you can't explain, don't be embarrassed to ask what seems like a 'dumb' question of your Dr. It may well save you some pain and frustration!

Kris is now back at work! Oddly, it's been quite the fight. I'd love to rant about this but, I won't. I'll just say that, according to Kris' observations, it's costing IBM quite a lot of money to put her on LTD. And that there was some question, in fact, about bringing her back... which makes me question whether or not this really is a benefit. Fact is, it would've been more cost efficient, and less nerve wracking, to just take vacation and a short leave of absence... though, it would've been more costly to us personally.