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Showing posts with label Irinotecan. Show all posts
Showing posts with label Irinotecan. Show all posts

Thursday, May 05, 2016

Three Treatments Down


Yesterday we left for the clinic at 8:45 AM and arrived back home at 3PM.  Five of those six hours were spent in the infusion chair. It was a LONG time! I watched other people come and go, get hooked up and unhooked.  Only my fellow infusee in the next chair was in there almost as long as I was and we chit-chatted a little when both of us were awake- although we both drifted off a few times.  He has pancreatic cancer and has been  on chemo for almost a year, too. He said he'd lost about 70 pounds  since his diagnosis and lost all his hair at one point, although most of it has grown back now. He couldn't believe I had lost neither weight nor hair. He is a fairly upbeat person, although most of the people I've talked to who come in for treatment the same time I do are philosophical about the whole thing and are pretty upbeat.  My chairmate told me there was no family history of cancer, but that he had already lost a son to cancer several years ago, before he himself was diagnosed. His son left behind a four year old and a five year old child. We commented how hard it is to watch a young person with  his or her whole life ahead of them be struck with this devastating disease, and it does seem that an increasing number of younger people are being diagnosed. I sometimes wonder whether it’s because diagnostic tools are much more precise and are able to detect disease earlier, or whether there really is an increase caused by environmental factors.

Yesterday was my third treatment with the Irinotecan and  Cetuximab. I did have one mishap.  On one of my trips to the restroom, (and after all that liquid is pumped into one there are many trips, believe me) I managed somehow to  pull the needle out of the port.  That was  quite a shock and I didn’t have the presence of mind to close the clamps on the tubing so I leaked a little of the chemo, but I’ll know to do that if it happens again. Fortunately, the nurse was close by and got me rehooked straight away. Except for the fatigue and the skin rash I’m tolerating the treatments  well so far.  I did go to sleep when we got home yesterday and slept most all of the evening and into the night, with frequent wake up calls by my bladder. I still feel tired this morning, and the rash and flushing are spreading down my neck and onto my chest. Most of the acne-like pustules that formed during the first and second treatments have pretty much cleared up, thanks in part to the clindomycin gel the doctor prescribed- at almost $100 a tube. I also had some eye problems that developed after the first treatment- my eyes were crusted shut when I’d wake up and then start running and itching.  That cleared up after a few drops of the prescription eye drops. Now I am  left with very red, very rough, very dry and flaky patches of skin.  I feel as though  tightly stretched alligator hide has replaced my skin! I have switched from coconut oil to emu oil- I figured a bird might be a better adversary for an alligator than a coconut would be and so far, so good.

I have been able to remain active, for the most part,  attending events and   working in the garden. On the Friday of the off week between the first and second treatments I attended a wonderful performance of Beethoven’s Fifth Symphony performed  by the Birmingham Symphony Orchestra  at one of their coffee concerts. These concerts, held in the morning, are less formal, less expensive than the evening concerts and are not as crowded.  I have  been lucky in being able to get my favorite seats in the Dress Circle very close to the exit and   almost in touching distance of the bass  section. I also get a wonderful side view of  our marvelously dynamic conductor, much better than looking at his back for the whole concert!

Our forty third anniversary fell two days after my second treatment, on Friday, April 22.  I slathered on some SPF 30  sun block,  donned my hat and a long sleeved shirt and we celebrated by attending the Magic City Art Connection, a wonderful  three day  show of arts and crafts held in  Linn Park in downtown Birmingham.  The weather forecast hadn’t been too promising but  the rain, except for a few sprinkles, held off for the duration of the show. It was great to   visit  some of my artist friends  who had work for sale, to enjoy the live jazz music, and to run into two of my favorite street photographers and a few other friends while we were there.


My gardening efforts are ongoing, but there is still a lot of work to be done. We’ve had a few rainy days, which seemed to give a lot of slow starters the impetus to get going. I t also   gave the weeds a  growth spurt, so there’s always some  good and some bad effects  when it rains.  The beans are coming along nicely and  will need to be thinned out, I think since the seeds seem to have drifted and  they look quite  crowded in spots. I  planted out some of the calendula I’d started from seed, some strawberries in the tub planter and  Mr G dug up and moved a clump of Echinacea, some Tagetes lucida, a couple of thyme plants and  I re-potted some of the plants that go on the deck, so it does look as though something has been accomplished.  Today it’s quite windy, sunny and a little chilly, so in between the weather and my fatigue I won’t even try to get out and work in the garden today.  Maybe tomorrow, because, after all, to plan a garden or to plant a seed is to believe in tomorrow.


Thursday, April 07, 2016

Progress Report- Good News and Bad News


 Spent another long day in the oncology clinic yesterday; we got there at 8:30 AM and left just after 2 PM.  One of the oncology nurses had phoned on Monday to ask if I could get there an hour early because the doctor was changing my chemo drugs and the new combination would need to infuse at least four hours.  I figured the CT scan results from last week’s scan must not be what we had hoped for. As it turns out there was some good news and some bad news on the CT scan. The bad news is that the liver tumor has increased in size by 18%. The good news is that all the other hypodensities in the liver and pancreas have remained stable and that the stomach, small bowel, appendix and colon appear normal and the rectal mass is still unseen. Based on the growth of the liver tumor, my oncologist started me on a new chemo regimen today.  I thought at first that I would be getting FOLFIRI plus Erbitux, but I’m actually just getting the Erbitux and Camptosar (Irinotecan), both of which have some fairly nasty side effects, but have shown a lot of promise in clinical trials, especially in patients with wild type KRAS gene, which I have.  So I guess that makes me a wild child. I’m hoping I can tolerate the side effects without having to stop the treatment early. One of the side effects of the Erbitux is an acne-like rash which I hear is quite unpleasant.  The doctor said if I did get the rash to call and they would phone in a prescription for a gel to use on the rash.  I hope it doesn’t come to that.  One should not have to deal with acne in one’s seventies; I am sure there are better ways to fake a youthful appearance!

Once in the infusion room I saw that someone had already taken my favorite chair so I wasn’t as close to a plug for my Kindle. It didn’t really matter as it turns out because I kept drifting off to sleep anyway and didn’t use the Kindle much.  I took the Tylenol the nurse brought, and then she hooked me up with some benadryl and  anti-nausea drugs. After that, we got the heavy stuff.  A short while after the Erbitux began flowing I began to itch.  Furiously. On my arms, legs, abdomen, buttocks. Then welts started popping up.  I looked and felt like I had been closed up in a roomful of angry, hungry, biting mosquitoes!  The nurse stopped the Erbitux and hooked up something to stop the itching.  It worked, thank goodness!  She told me my mouth would get very dry, like it had cotton stuffed in it. Sure enough it did, but she had brought me a cup of water and a peppermint candy- they helped a lot. We were able to continue the infusion of the Erbitux, then they hooked up the Camptosar and after another hour and a half, I was unhooked  and on my way.  The best part is that I’m not on the pump any more! The doctor took me off 5-FU. Hallelujah!

Much as I dislike this whole set of circumstances, I am constantly reminded that some people are a lot worse off.  One poor elderly woman who came in for her first treatment didn’t yet have a port.  It took three nurses to try to get a vein that would work.  She kept hollering in pain telling them to take it out, she’d just come back tomorrow.  They finally gave up and   took her down to radiology, so she might be getting a combination of chemo plus radiation. I hope she gets her problem sorted out, but she has a rough road ahead, for sure.
  
When I went back to the waiting room to find Mr.G he said I looked pale as a ghost, and after looking in the mirror I have to agree with him.  I could probably try out for a part on the Walking Dead and not even need make-up! Once we were in the car, I kept dozing off and went straight to sleep once we got home.  I slept most of the afternoon, off and on and felt completely wiped out.  This morning I still look like death warmed over, but am feeling much perkier, although my face feels hot (no fever) and has a strange mottled appearance with some red blotches, grey skin  areas. To make things worse the bags under my eyes look like I’ve been packing them for a trip. This too shall pass.  At least I hope so!