I was so nervous last night that I couldn’t sleep. I had itchiness all over the past few days and was worried maybe the billirubin had risen.
This morning we had an appointment with the oncologist dr. van den Berg. He is a very empathic, amiable and knowledgeable oncologist with a good reputation. Dr. van den Berg greeted us kindly and invited us into his office. He asked me how I was feeling. I said I was feeling much better now that I had the antibiotic for the infection and no longer have fevers. Of course I have some minor side effects which cause minor discomfort, but on the whole I feel fine, and don’t have problems such as nausea or vomiting, what many patients experience.
Dr. van den Berg told us the billirubin had stabilized at 22, which was good because normal values should be between 17 and 19. He said the liver had stabilized enough, so the chemo had worked and the liver was functioning as it should.
The CT scan showed that the liver has not yet decreased in size. Also the tumors have not decreased in size or number. But the color of the tumors had changed; they are now a dull, vague color, whereas they were very clear before. This means that they have stopped growing and are no longer expanding. The tumor marker he is tracking is CA 15.3 (CA stands for cancer), which is measured in the blood. The tumor marker has decreased, meaning the tumor is no longer growing. Also, there are no new metastases outside the liver.
Dr. van den Berg said he was moderately optimistic. He said this has increased our chances and has bought me time. He explained that he wants to increase the dosage of the Doxorubicine (Adriamycine) which is the chemo that targets the breastcancer. This is the chemo that was given to me in a very low dosage over 3 weeks, because of the possibility that the liver couldn’t manage it. Now that the liver is functioning normally, he feels it is safe to increase the dosage to more than 3 times what I was getting up until now, which will help to reduce the cancer cells in my body, specifically the liver, but also the breast. We will change to a cure of three weeks, which means one week chemo and two weeks recovery time.
I will start with the new cure (both Adriamycin/Doxorubicin and Cyclofosfamide) next Wednesday (19-9), and will come back to see him in four weeks time (15/10). For now, we’ve got the second cure planned on 10th of October, with a visit to dr. van den Berg on Oct 30th. A new CT scan will be planned just before, unless the blood values are enough to see the progress. Once the cancer is diminished in the liver and the liver is back to its normal size, he will see what we can do about the tumors in the breast and lymph node. For now, the focus is on removing the cancers from the liver as much as possible. Dr. van den Berg believes the higher dosage will have the impact that is needed. So, the new round of chemo will have to do the job! I’m am happy that this round of chemo will be much stronger and – I’m assuming – more effective. I’m sure it will impact me much more than the previous round, but I won’t have as many needles stuck into me which will help because my veins need a bit of a rest. I don’t know how many rounds I will receive, but that will depend on the initial results.
On a lighter now, I just wanted to share with you a line from a movie which we borrowed from Marita, our neighbor. The movie is the Best Exotic Marigold Hotel: for the elderly and beautiful which is a wonderful film about several British people who – for very different reasons – decide to relocate to a hotel in India. Of course, the hotel is nothing like the brochure (“It is a vision, ma’am”, explains Sonny, the young hotel manager, “of how it could be.”). But each guest (and Sonny too) copes in his or her own way, and discovers something important to them. What Sonny tells his guests (and himself) is a life lesson in and of itself: he says “It will all be all right in the end. And if it is not all right, it is not the end.” And that’s how I see it too!
So the next weeks I will probably have little news, but I will keep you posted of how I feel. Thanks for all your lovely comments. I cannot reply to each of you individually, but I am moved by your positive thoughts. Take care!
Dearest Sheila,
Throughout your life, you have been a fighter: remember how you achieved your grades, A grades, in Middle School in Kingwood, TX, without barely any knowledge of English. 13 Years old and studying till late at night. Then you chose to have guitar lessons and it provided you with a different outlook on time (wisely?) spent. We returned to Holland. American School, a short period in an Dutch I.B. School. Bad guidance and few lessons there (long busrides and too many free time hours in between lessons). Unhappy Sheila, who wanted to study, did the dishes at home to forget she had no homework for school. In a desperate move we made, you were accepted back at the American High School. You were 18 when you left on your very own, to study in USA. It is a worthwile story to hear how you managed to live your life in Philadelphia, how you reached your goals, how you worked to earn your pocket money……. After so many years you returned to Holland and started a new life here. So in a way, you are in your third life right now. There will be many more coming, since you have been involved in this fight you intend to win! Go on, go on, dear daughter, and ask for the things you need…..Lots of sweet thoughts for you from your mom.
Sheila, fijn dat je alles zo noteert. Voor jezelf een therapie om alles van je af te schrijven en later nog eens na te lezen en voor je lezers goed om zo op de hoogte te blijven, je hoeft niet constant alles te vertellen, wat ook vermoeiend is.
Goed om te lezen dat de lever reageert op de chemo en ze nu verder gaan met behandelen.
Blijf zo positief denken en alles ondergaan, dat is de beste manier om hier mee om te gaan.
Maar evengoed sterkte voor jou en Victor en de rest van de familie. We blijven aan jullie denken en in ons gebed meenemen.
Veel liefs van Bert en Ria
Hallo Sheila
ja, de Marigold Hotel film vond ik ook heel bijzonder! Heel knap gedaan met geweldige dialogen en situaties om over na te denken.
We zien er naar uit je in Oktober weer even aan de borst te kunnen drukken!
Veel liefs van Paul en Isabelle
Hoi sheila, indrukwekkend hoe je je gevoel en behandelingen beschrijft. Ik kan me nu ook beter een voorstelling maken van wat je doormaakt. Je maakt er meteen ook een studie medicijnen en medische termen van :). Kan je straks naast al je architectuurtermen en stanford “terminologie” ook nog eens de medische wetenschap aan snijden. Veel sterkte met je chemo sheila! Liefs en groeten Pascal
Sheila, I have been reading quietly for the past few months, and I am struck with every entry by your outlook. Your insight and attitude towards life and hardship motivates me to stop and take a deep breath every day. Here’s to an easy next round of chemo. Lots of strength from across the Atlantic, Noa’a (Nancy’s friend)
Sheila, heel veel sterkte de komende tijd. Bedankt voor het delen van alle gebeurtenissen en belangrijke momenten, we leven met je mee en volgen je verhalen.
Liefs,
Ingrid
Fijn Sheila dat de lever weer werkt en de tumoren niet meer groeien..zo kun je de volgende fase/attack in!! Met groot geschut begrijp ik. Opsteker!! X Annet
Sheila, Good to hear some positive news! Stay strong with happy thoughts. We are all cheering for you! Many hugs, Laura
Dear Sheila, I hope for more and more good news! Again, I’m so glad we’ve re-entered each other’s lives. Your comments on exercising remind me of our gym escapades in Philly. Your musings about food remind me of our efforts at homemade pizza dough, and your proposal that a picnic consist of the lone red pepper in our fridge. (I’m sure we must have gone grocery shopping after that…) Consider yourself hugged every day from VA! Lots of love,
Jen
Lieve Sheila en Victor, wat een geweldig nieuws dat de kuur zo aanslaat! Hier worden wij blij van. De eerste ronde heb je gewonnen. Op naar de volgende. We blijven voor jullie duimen. Veel liefs van ons alle vier.
Lieve Sheila, Als ik dit schrijf krijg je waarschijnlijk je hogere dosis Adiramycine. Ben benieuwd hoe het gaat. En natuurlijk geweldig dat het zo goed heeft gewerkt allemaal!Ook wij hebben die film Exotic Marigold.. gezien, en het brengt nog een smile op mijn gezicht.
Het beste vandaag, en daarna een wandelingetje? Op de hei?
Big hug, Mariette