Caroline's Breast Cancer Blog

     Well...I was very close to being able to do it.  I was almost able to wait a full 6 months between CT scans this time. I initially scheduled this round of scans 6 months from my last ones, but unfortunately in late September, I had a couple weeks of feeling really crappy, (more than the usual fatigue and not just some achiness, but down right pain, especially in the bones of my left hip).  As I have done before, whenever I feel crappy for more than a few days, I convince myself that my cancer has figured its way around my chemotherapy and that I've entered the phase called "disease progression."  Despite trying to be as reasonable and rational as possible, I know that I'm not over reacting...the clinical trial report indicated that the average ROS1 lung cancer patient on Xalkori will have 19.2 months of disease control.  I've been on Xalkori for 55+ months.  (Pretty soon that will be 3-times longer than expected!)     ...

...but now think I may die at the hands of white supremacists whose fire is being fueled by trump's support of their hate, bigotry and racism...or maybe by a nuclear bomb sent to the Chicago area by the North Koreans because of trump's ignorant and antagonistic rhetoric.  It sure seems like trump is going to get us, Americans, killed...one way or another.       I still may die of cancer.  I prefer that.  It may be sooner rather than later, if the Republicans and trump repeal and replace the Affordable Care Act with something that removes the pre-existing conditions clause and adds lifetime caps.  Despite recent failures to pass repeal and replace legislation, the Republicans and trump seem hell-bent on bringing it all up again because how else will they be able to pass tax cuts for the rich unless they take away health care from 30 million Americans and restrict access to care for those of us with existing conditions? [http://www.cnn.com/2017...

     This summer, like most of my summers, has been a busy time for me.  When we're not working, Wynn and I are usually out riding our bikes, meeting friends, working in our garden, hanging out with our kids, and fitting in a long weekend away.  The past few months seemed to fly by, and although we visited friends in NY in early July, when I looked at our calendar, we haven't done all that much in way of recreation.  What is abundant are medical appointments.       Earlier this summer I was experiencing some new symptoms.  They were very subtle and infrequent, and somewhat difficult for me to describe.  In mid-June I had an appointment with one of my many doctors and I did my best to share with her what I was experiencing.  All of my symptoms could be explained away, but they could also all be caused by a single problem...metastatic disease to my leptomeninges.  Here's what I've learned about the leptomening...

     Until today, this man has been my oncologist.  His name is Robinson Ortiz, MD and I credit him with saving my life.  Dr. Ortiz was the guy on-call the day I was admitted into the hospital, through the ER, for a metastatic disease work-up.  That was in December of 2012.  He was kind from the moment Wynn and I first met him.  He gave us terribly bad news, gently, so we could absorb the words he had to tell us.        As soon as it was established that I had non-small cell adenocarcinoma of the lung, Dr. Ortiz ordered genetic tumor testing for mutations in two genes  known to cause the type of cancer I have.  Based on my demographics, the chance that I'd have one of these was estimated to be 80-85%.  I had neither.        Dr. Ortiz then recommended testing for mutations in a newly described gene  called ROS1.  Earlier in 2012, journal articles associating mutations i...

     As enthusiastic as I've been about the CyberKnife procedure I had to treat my metastatic brain tumor at the end of March, the only way to know if it worked is to have another MRI.  So, that happened last week.        I was disappointed when the report stated that the lesion is still there - big enough to be measured.  But, the report also stated that it is smaller than prior to CyberKnife and is "less enhanced".  Overall, the report sounded like it was trying to tell me that it looks like CyberKnife worked.  I realized that among all the questions I asked before and during my CyberKnife procedure, I never asked what to expect of the tumor following radiotherapy.       So...now I know.  A few days after my MRI, Wynn and I met with the radiation oncologist.  She entered the room with a big smile on her face and said, "The lesion is smaller and less enhanced, so I'm very happy....

CT Scans:      My last scans were in January and I was hoping to avoid my next set until at least June. However, while traveling in Israel, I noticed more upper right quadrant pain so I recently had CT scans and blood tumor markers drawn.  I am happy and relieved to report that everything continues to indicate that my disease is stable, below my neck.  I still don't know why I have periodic pain in my abdomen, but I'm glad that when it comes...it eventually goes.  Copyright: <a href='https://www.123rf.com/profile_highwaystarz'>highwaystarz / The Blood/Brain Barrier (BBB):      ...has been something I've referred to in previous blogs.  I didn't know very much about the BBB, or how it works, so I thought I'd read up and blog about it.  As fascinating as it is, it's pretty complicated.  Some aspects of the BBB are still not fully understood by researchers and some aspects could not be fully understood by yours trul...

     In the past, when my husband and children traveled to Israel, I've opted out because I was afraid.  Traveling to the Middle East seemed irresponsible, given the obligations I felt I have here at home, (family, work, pets, etc.).  Over time, things have changed.  Although it was difficult leaving my elderly mother for nearly two weeks, h aving bad cancer allows me to shed some hesitations about traveling for two reasons:  I'm healthy enough now to go to far away places and really...what do I have to lose?       Our son, Nathan, has been in Israel since last September teaching English to underprivileged children, grades 2-6.  He has been living in a small city, north of Nazareth, called Migdal HaEmek where he works with both Jewish and Arab students. He's created opportunities for himself to see most parts of the country and was a great guide for us.        We started in Tel Aviv/Jaff...