Tuesday, June 30, 2009

CaringBridge Journal Update Notification for Ginny Blaney

Dear Bill,

A new Journal entry for Ginny's CaringBridge website was posted at 4:48:00 PM on Jun 30, 2009.

Read the latest update: http://www.caringbridge.org/visit/ginnyblaney


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Sunday, June 21, 2009

Good morning, and Happy Father's Day to the dads out there! It's a good morning here in spite of another day of rain. I was disconnected from the infusion pump on Friday afternoon, and each day since then I've felt better. Before they removed the pump, the nurse gave me some stronger anti-nausea drugs through the IV, and also some more pills to take, so the nausea has gone for now. This was the most unpleasant side effect. Tingling in the fingers also reminds me to wear gloves when I reach into the freezer--weird!

I'm now looking forward to a good week and a half until my next treatment on July 1. Our son Wes and granddaughter Carys arrive on Tuesday for a week--can't wait for that! Thank you all for your continuing messages of love and support. I am truly blessed by your friendship!

Wednesday, June 17, 2009

I have finally started treatment and can now begin to visualize those tumors shrinking instead of growing! Yay!

The "port" was implanted yesterday at the local hospital by the same surgeon who did the original operation. I felt very well cared for by him and by the nursing staff. It's amazing how comforting it is to have a nurse tuck a warm blanket around you! I was in and out of the hospital in about 3 hours and have had no problems other than a sore chest and shoulder, but I have meds to deal with the pain.

Today I went for my first chemo treatment, also at MDI Hospital. The clinician, Melanie, just attached the liquid meds to the tubes of my port, and there was not a single needle stick required. After the first round of the infusion was finished, about 2.5 hours, she attached a portable pump which will continue to infuse chemo drugs for the next 46 hours. Friday afternoon I will return briefly to the treatment room to be disconnected from the pump.

I'll have to wait and see what side effects I experience, if any. I took anti-nausea pills before the IV was started, and I am armed with more to take at home. Other common side effects with these drugs are diarrhea, fatigue, and mouth sores. Hopefully these will not be a big problem, but I am assured that we can deal with them if they occur. Time will tell.

So, this big new challenge has finally been met and the fight has begun. With all y'all's help, I will put up the best fight possible! Thank you all for being there for me, in so many ways!

Saturday, June 13, 2009

As most of you know by now, I was diagnosed in late April with metastatic colon cancer and had surgery to remove the tumor on May 1. Biopsies confirmed that the cancer has spread to the lymph system, liver, and abdominal wall. Treatment at this stage will be with chemotherapy, in hopes of stopping the spread of the disease and reducing the size of the existing tumors. I met with the oncologist last week to learn what happens next.

After much thought I decided not to participate in the clinical trial that was offered. It would have meant more frequent treatments and more follow-up exams and tests, and I would have had to travel weekly to Bangor, more than an hour's drive. Opinion seemed to be that the treatment I would get in the study would not be better than the standard treatment, so I decided I would rather spend more time with family and friends at home and on Ironbound. The treatments will be given at the local hospital in Bar Harbor--much more convenient.

In order to infuse the drugs directly into my vein without putting an IV in my arm every time, a so-called Port-a-cath, or "port" will be implanted in my upper chest. That will be done on Tuesday, June 17. My first chemo treatment will be the next day. As I understand it, I will get several different drugs over the course of about 3 hours, and then I will be attached to a portable pocket-sized pump which will continue to dispense more drugs slowly over the next 48 hours. I'm hoping I will tolerate the treatments well, with manageable side effects, and have a comfortable week to ten days till the next treatment. We are building a house, and there is lots to do!

I still find it hard to believe that this is really happening to me. I have recovered so completely in the six weeks since my surgery that, if it weren't for the scar on my abdomen, I would say it was all a dream. How can I feel so well when there is a serious cancer growing inside me? It feels like it must be happening to someone else!

I am ready now, though, to get started on the fight that is ahead of me. I'm trying to maintain a positive attitude and focus on how those drugs are going to go after those cancer cells and kill them! I am prepared for that first treatment on Wednesday and anxious to get it behind me.

I can't tell you how much it has meant to me, and to Ben, too, to have received cards, email, and phone calls from so many people. It takes a crisis like this to make a person realize how meaningful such expressions of concern and caring are. Thank you all from the bottom of my heart.