Robin's Breast Cancer Blog

This collection of messages was written as we've been dealing with Robin's breast cancer for several reasons: (1) To keep our friends ("extended family") up-to-date. (2) To educate folks about "the cancer trip". (3) To help us absorb what was happening, and purge any negativity that might affect Robin. Robin must maintain a positive, hopeful attitude, but with realistic understanding. We follow the mantra, "One day at a time", and trust that God will make good come from difficulty.

Monday, April 25, 2005

Robin's Sixth Chemo - 4/28/05

 
At my last writing, Robin had just completed tests for blood clots, and her chemo was rescheduled for April 5th. Dr. McClure also ordered additional tests: Echo Cardiogram, Bone Scan, and CT Scan. They were all completed on Monday, April 4th, and (amazingly) Dr. McClure had the results the next morning.

On April 5th, we started the normal course. Robin's blood counts were good and the doctor could not detect the lumps by touch. Dr. McClure reviewed all the test results from the day before, and said everything looked very good. All the tumors had shrunk more. The lymph node between the heart and trachea was not visible on the CT-Scan. There was some fluid buildup in the chest, but it was considered coincidental and unimportant. We discussed the surgeries and we were told to start scheduling them.

I stayed for the chemo this time. It was a sort of celebration for us since it was the last (for now, anyway). I had arranged for flowers to be delivered, and they arrived just as we were moving back to the chemo room. I was the hit of the chemo room. All the "little old ladies" ooo'ed and aaahh'ed over the flowers. The chemo was uneventful otherwise. I had purchased a hat for Robin that says, "Cancer Sucks" and a bunch of buttons with pithy sayings on them. One of the other oncologists saw my "Cancer Sucks" button and asked where we got them. I told him (www.choosehope.com, in case you are considering great gifts for a person with cancer), and I gave him my button, which he said he would wear (but not at work). We kept a couple of each button, and gave the rest to the nurses in the chemo room. We figured they could cheer some folks up with these.

While Robin slept, I explored the cancer education room and I found some materials about Inflammatory Breast Cancer (a.k.a., IBC). The materials stated that the normal course of treatment for IBC is to follow surgery with four more chemo treatments and six to eight weeks of radiation (five days a week). Needless to say, this was not pleasant news, and we were disappointed that Dr. McClure had not discussed this with us. On reflection, though, we guessed that maybe this is not cast in concrete, so Robin's therapy may differ. (Keep praying).

The after-effects of the chemo were more pronounced and longer than before, lasting eleven days. On Saturday evening, April 16th, she finally started to get better, and she seemed normal (except for her digestive system) on Sunday. Her digestive system has been in an uproar, with problems at both ends. Dr. McClure had tests done to make sure she didn't have an infection, then prescribed some stronger medications. They have helped, but Robin doesn't take them until she has a problem (too late), and that isn't pretty. Just in the last week or so, the leg swelling has come back, but other than these two problems and her total lack of strength, she seems to feel pretty good.

On April 12th, we met the thoracic surgeon, Dr. K (nobody can pronounce his Greek last name, so everyone calls him Dr. K or Dr. Katz). He reviewed the pictures from Robin's scans and discussed the procedure. He will make a one-inch incision just above the collarbone and run the probe down along the trachea. He will snip a piece from the lymph node and they will do a "frozen section" (cancer test) immediately. If it comes back negative, he will try again a couple more times. If all are negative, they will declare it non-malignant (good). If it is positive for cancer, he's done. They will not remove the lymph node. Instead, it will probably be treated with radiation and more chemo.

This week, he scheduled the biopsy for May 5th, and once that date was known, Dr. Mason scheduled Robin's mastectomies for May 12th. Since I am getting laid off on April 29th, I will have plenty of time to take care of her for the pre-op festivities, through the surgeries, and into the post-op. Wasn't it thoughtful of the company to give me all this free time? ;-)

May is clearly going to be an exciting month. Besides the medical stuff, my first day of unemployment is May 2nd, John will be in the State Track Meet on May 5th for Pole Vaulting, Robin's parents, Hal and Johnnie, will arrive on the 12th, we celebrate our 29th wedding anniversary ("Twenty-nine years of living HELL," as we call it) on May 16th, John goes on his "Senior Trip", and he graduates May 27th. Whew!!!

I think that's all I have for now. I will write again after the results of the biopsy are known on May 5th and again after the mastectomies on the 12th.

Keep us in your prayers for the month, especially during the first two weeks or so. We really need it!!!

With love and thanksgiving for all the prayers and support,

Larry and Robin

P.S.: By the way, one of our favorite people at St. Luke's sent us a website that is dedicated to Inflammatory Breast Cancer.

If you are interested, the website is:

http://www.ibcresearch.org/

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