Tuesday, November 23, 2010

My Trip to the Oncologist's Office

I had my first appointment with my medical oncologist, Dr. Nancy Peacock, today. She was great. Granted, I was highly annoyed because I had to wait nearly 45 minutes past my appointment time to see her, but once she entered my room, you would never have known that she had other patients to see -- ever. I almost had to rush HER out of the room at the end of our 45-minute meeting. Seriously, this woman was NOT in a hurry with me, which was so nice, since I had a ton of questions for her. The upshot of the meeting? No chemotherapy for me!! Whew!! We will proceed with radiation treatments, beginning in December, after which I'll start a five-year course of a drug called Tamoxifen. Tamoxifen, which studies have shown can cut recurrence risk in half, somehow binds to estrogen before it can move around in the body and cause things like breast cancer.

Dr. Peacock and I talked quite a bit about recurrence risk and the things that do and do not contribute to that risk. Unfortunately, studies have shown a connection between alcohol consumption and breast cancer, so I'll be cutting back a bit on my wine drinking (the studies show that seven or fewer drinks or glasses of wine per week is fine; more than that can increase your risk). I don't think that I drink much more than seven glasses of wine per week, but it depends on the week, I suppose. Personally, I find this whole alcohol/breast cancer thing highly annoying and incredibly unfair. If any group of folks deserve to drink wine to their hearts' content, it's all the ladies out there who have had and beat breast cancer, but we have to deal with reality and if the docs are telling me to limit my alcohol consumption then you can bet I'm going to do it!

So, on this Tuesday before Thanksgiving, I'm feeling beyond blessed to have received such good news from the oncologist. You can imagine that Thanksgiving will be particularly special for me and for our family this year. I hope that it is for each of you, as well.

Have a wonderful, safe and blessed Thanksgiving with your families.

Erin

Tuesday, November 16, 2010

Dr. B

Had a great appointment with Dr. B yesterday. She said I'm healing up fine, and that I can start running again. Yeah!! She has the nicest office staff. Those people have been incredibly kind, polite, caring and respectful to me through all of this. If anyone lives in Nashville or close by, and is ever in need of a surgeon (Dr. B is a general surgeon, although she does a lot of breast surgery, and is widely regarded as one of the best breast surgeons in town), I really and truly cannot say enough about Jeanne Ballinger and her staff. Highly, highly recommended.

Next up: meeting with the medical oncologist next Tuesday. Not sure whether I'll post between now and then, or not, but if not, I'll try to post something about the appointment before we leave for our Thanksgiving in Evanston, Illinois with Eli's family. Really looking forward to getting out of town and enjoying some time with family.

My best to everyone.

Erin

Sunday, November 14, 2010

One Month Later....

What a difference a month makes.

On October 15th, I was seven days out from having received my biopsy results, and went to my first appointment with a breast surgeon. It was an absolutely awful appointment. Eli and I showed up, pretty happy-go-lucky about the whole thing, and I left there, more than two hours later, a nervous wreck.

I've alluded to this appointment in past posts, but didn't say much about what happened there, so here's a short synopsis. Most of the appointment was spent with the doctor's nurse practitioner who, while well-meaning, said a few things to me during the course of the appointment that completely freaked me out. Her worst transgression, in my view, was the completely unwarranted comment she made about my lymph nodes. During her exam, she decided to do a breast ultrasound, during which she took a quick look at a few lymph nodes, and then proclaimed "well, those look pretty good and normal, but the doctor may want to do a needle biopsy just to make sure everything is okay." Huh? My lymph nodes had not factored into my worries at that point, and honestly, I just looked at her and said "Well, I'm sorry, but I can't deal with that." The doctor came in a few minutes later, looked at the ultrasound picture, tried to assure me that the nodes looked fine, particularly given that I'd just had a biopsy eight days earlier, and told me that no biopsy was necessary. His efforts to calm me were effective, but rather short-lived; I spent the rest of the day and much of weekend (which our family spent at a cabin on Center Hill Lake, by the way) obsessively worrying about whether the cancer in my breast had already spread to my lymph nodes. An unfortunate turn of events, to say the least.

The following Tuesday, I visited a second surgeon, Dr. Jeanne Ballinger, and decided to have her do the surgery. Tomorrow, one month after the upsetting visit with the first surgeon, I will have my 2-week post-surgical visit with Dr. Ballinger. It's hard to believe how much has transpired in such a short period of time. I am so happy and relieved to be on this side of the surgery, and to have received such good news about the state of my disease. I am guessing that Dr. Ballinger will be pleased with my healing process. I've had almost no pain, and only a little discomfort under my arm where she removed two lymph nodes.

I am on the road to recovery. I know that radiation will be long and tiring, but I'm ready to move forward with that, too, so that I can get all of this behind me.

I'll be in touch soon. Thanks again for reading and following my journey.

Erin

Tuesday, November 9, 2010

What's Next?

If you're wondering what the next steps are for me, you're not alone. I'm a little unclear, too, but based on the wonderful pathology report from last week, it seems virtually certain that I will not have to do chemo. I do, however, have an appointment with a medical oncologist on November 23rd, presumably to discuss whether or not I should start taking Tamoxifen, a drug that has proven effective in reducing recurrence of breast cancers that are estrogen receptor positive (which mine was). I suppose we'll also talk about chemo, although my surgeon seemed to think that it was not in the cards for me, given the fact that the pathology report showed that the cancer was completely contained in the milk ducts.

This journey and my treatment are not quite over, though. I will have to do radiation, and although I know that this will be a nuisance and tiring, etc., radiation is a completely different beast than chemo, and much more tolerable, from what I've heard and read. I will begin the treatments in December, and the bonus is that my radiation oncologist is Dr. Rosenblatt whom I like very much (I wrote about him a few posts ago). I will receive 33 treatments over the course of about 6 weeks. When combined with a lumpectomy, radiation dramatically reduces the chance of recurrence, so I'm all for this being a part of my treatment plan, even if it is inconvenient and not exactly the way I'd like to spend the holidays.

As I process through things this week, it is hard for me to believe that the really hard part of this journey is behind me. Needless to say, the month of October was difficult. It was scary and stressful and even gut-wrenching at times. I clearly, however, am one of the really fortunate women who had their breast cancer detected at an amazingly early stage (I haven't received my official "stage" of breast cancer, but I'm guessing it will be a Stage 0 based on the pathology report). My hope is that my story might motivate other women to take charge of their health and be vigilant about getting their annual mammograms. Doing so might just save their lives, as it did mine.

As I was checking out at Kroger yesterday, I saw, sitting next to a trash can, some of the cardboard breast cancer awareness advertisements that had been up in the store during October. They were folded up, crinkled, and clearly bound for the dumptster. It made me kind of sad. I had just seen a friend in the store who has been battling breast cancer for more than a year -- chemo, mastectomy and all. The two of us are living proof that this disease doesn't go away at the end of October. If only we could fold up our diseases like those pieces of cardboard and toss them in the trashcan. Wouldn't that be wonderful. But, the fact is that this disease is very real, and affects the lives of millions of women and their families all year long, not just in October (or as one disgruntled breast cancer blogger calls it "Pinktober").

I'll be in touch soon. Thanks again for your love, support and encouragement.

Erin

Saturday, November 6, 2010

Forty Four

Today marks my forty fourth year of life. It's hard for me to believe that I'm in my mid-forties. It seems like just yesterday I was graduating from high school, going to college, starting law school, getting married, and having babies. But it wasn't yesterday. Those things happened many years ago and a lot of "life" has happened since.

One thing I can say about my most recent experience with a potentially life-threatening illness is that it has drastically changed my outlook on birthdays and getting older. It wasn't but a few months ago that I was really starting to fret about the lines around my eyes and about my impending "mid-forties" birthday. Not now, though. Quite to the contrary, in fact: I can hardly think of anything better than turning 44, expect, perhaps, for turning 45, 55, 65, 75, and if I'm really blessed, maybe even 85 and 95. Getting older is now something I view as a pure gift, and I am beyond grateful for this changed perspective.

It's a busy day at the Richardson household. Eli and Wes have gone to the Vandy/FL game and then Wes will go to a recording session this afternoon. Virginia has two performances of Les Mis today, and I will go to both of them. There will be no party for me today, no hoop-la, no fanfare. Just another day in our little family's life. If you had asked me what I wanted for my birthday last weekend though, before this past Monday's surgery, this is exactly what I would have asked for: just a normal day with my family. After so many days filled with fear and uncertainty, normal is beyond wonderful, and something for which I am extremely grateful.

Have a wonderful weekend.

Erin

Thursday, November 4, 2010

The Surgery

If you've been following my blog, or are a close friend or family member, you know that I had surgery on Monday to remove a cancerous lesion from my breast. One of the things I really like about blogging is that it is, for me, a form of journaling, which is something I've regrettably never had the discipline to do. This blog will serve as a record of my experience with breast cancer, and so, I wanted to write about my experience on Monday, mainly as a way of preserving my memory of the day. If you are squeamish or just grossed out by things involving needles and doctors in white coats (or, in this case, scrubs), do not read on. If you are interested in hearing about what is involved in a lumpectomy and sentinel node biopsy, feel free to proceed. But, by all means, please do not feel compelled to read this post.

Eli and I left the house around 7:40, for an 8:00 arrival at the Breast Center at St. Thomas Hospital. We were actually early, which is unusual for us. This gave me a few extra minutes to sit and fret, although, in actuality, I was surprisingly calm and at peace that morning (more grace from God, I suppose).

The procedure was scheduled to begin at the Breast Center so that the radiologist could insert a wire into my breast to mark "the spot" that the surgeon was to remove. On Oct. 7, I had something called a core biopsy, during which my friend, the radiologist (she really is my friend; I'm not being facetious) removed a portion of the suspicious area. At the conclusion of that procedure, she inserted a small (very small, apparently) metal clip into the area from which the tissue was removed so that they would know where to go if I had to have surgery. Obviously, the biopsy came back showing cancer, so surgery was required.

So, back to the Breast Center. I was called back, and Diane, who has been my radiology tech throughout all of my visits to the Breast Center over the past five weeks, walked me back and joked about how she was hoping to see me outside of the Breast Center one of these days. As it turns out, my friend, the radiologist, was not working that day, and so I had a different doctor, Dr. Earthman. Cool name, huh?

Warning: next part not for the faint of heart.

I put on the lovely smock they give you and was taken into the "torture chamber." (Read on; actually it wasn't that bad, but it did look like a torture chamber). I sat in a nice comfortable chair and was rolled up to the mammo machine, where they proceeded to take some films of my breast to see where the clip was. Then the fun began. I had my eyes closed during most of this, but I believe that it was Dr. Earthman who gave me a lidocaine injection, intended, of course, to numb my breast before the insertion of the needle that would go in and through which the wire would be inserted. They said the lidocaine would feel like a bee sting, and I must say that it was milder than that. At this point, I've got my eyes closed, and am holding Diane's hand (God bless that woman!) and about a minute later I could tell that the activity around me had stopped, and I opened my eyes. I asked when the needle was going in and they said that it was already in there! Whew. That wasn't bad at all.

Then, they had to take another "picture" of my breast to ensure that the needle/wire was in the right spot. At this point, we encountered what Diane referred to as a "minor complication." It seems that my little lesion was pretty far back in the breast (lovely, eh?), and that Dr. Earthman needed to "advance the needle." These are not words that one in my position really wants to hear. Advancing the needle, indeed, sounds pretty awful, especially when it comes to ones' breast. I must say, though, that Dr. Earthman took his time studying the pictures and even asked the tech for my old films to compare to make sure that he got the wire in just the right spot. Based on the overall success of the surgery (i.e. clean margins, etc.), I'd say that the extra time that Dr. Earthman took in getting the wire in just the right spot, and even the advancement of the needle, as scary as that sounded, were well worth it!

Finally, that procedure was over, and they taped a small styrofoam coffee cup (no kidding) over the wire sticking out of my breast, and put me in a wheelchair to take me to the OR. Out in the hallway, I was joined by Eli and his parents, who had come down for the surgery from Chicago. Diane pushed me and they walked with me up to the "holding area" (again, very scary sounding -- perhaps someone could work on some of this medical lingo) for the operating room.

In the "holding area," I had my own little bay (Bay 18) where Eli and his Dad and stepmom hung out with me for what seemed like an eternity. I think that I used the bathroom about 8 times in a little over an hour. A nurse in the prep area said that I had a "nervous bladder." She was right.

Finally, my turn was up, and someone came and got me in another wheelchair and took me to the prep area for surgery. There, I was put in a bed, had an IV line put in, and had warm air pumped into my beautiful blue hospital gown (weird, but a very nice touch, I must say). I had some lovely ladies attending to me there, and one very nice and cute nurse anethetist named Derek. My surgeon stopped by (was glad she could make it!) and met my anesthesiologist, Jane Thomas. Dr. Thomas asked me if I'd found a lump, and I said no. Dr. Ballinger then chimed in, and told Dr. Thomas that my cancer was caught very early on routine mammo and that I was going to be "fine." A vote of confidence that I desperately needed at that moment.

So, the best part of this story, other than the outcome of the surgery, involves the prep for the sentinel node biopsy. In addition to having my lesion (or whatever it should be called, seeing as how it was all in the milk ducts) removed, I had to have what is referred to as a "sentinel node biopsy." This is a procedure that has been developed through modern medicine in order to avoid having to do an axillary lymph node dissection, which involves removing all of the lymph nodes under the arm (and which can have some potentially very serious side effects). Someone came up with the bright idea that if they could determine where the "sentinel" or first node was, they could check that one (and maybe one or two nearby), and if those were cancer-free, then the other nodes didn't have to be removed.

In order to find the sentinel node, though, they must inject into ones' nipple a creepy, radioactive blue dye. The mere thought of this nearly sent me over the edge, and it was one of the things about which I was most nervous. I had read on the internet that the pain from the injection can be excruciating. Well, as it turns out, at St. Thomas, they actually knock you out for 2-3 minutes while they do this procedure. Dr. Ballinger came up to the side of the bed with some scary-looking tube, and I began to panic, realizing that this was the moment. The next thing I know, Derek, the nurse anesthesist, is telling me that my hand may sting a bit from the "medicine" going into the IV. My hand started to throb, and I told him so, to which he responded, "you're being a wimp." The next thing I know, I was waking up from what felt like a deep and wonderful slumber, only to learn that I was out for just a few minutes, and that the dye had been injected. Now, that's what I call compassionate medicine! (Note to anyone having this procedure done: some hospitals allow this and others don't; I believe that St. Thomas is the only hospital in Nashville that does the knock out thing for the SNB, so you may want to consider having your surgery at St. Thomas if you have to have this done, which of course, I hope you don't!!).

Since this is most of what I remember from the day, I'm almost done. After the dye injection, I hung out in the prep area for another 10 minutes or so, and then they wheeled me into the OR. The last thing I remember is moving myself from the wheeled bed onto the operating table, and the next thing I remember after that is being wheeled down the hall after surgery and hearing Dr. Ballinger's voice, and asking her about my nodes. She said that they were "clear," and after that, I was simply overjoyed. My Dad says that I was "glowing" when they pushed me back into the holding area, to which I joked and said that of course I was glowing because they had injected radioactive dye into me. But seriously, aside from the birth of my three children, I can hardly remember a time when I have been happier than after that surgery was over and I had been given, at least preliminarily, good news. After having a Coke and having my vital signs monitored for a little while, I left the hospital about an hour and a half later, went home, sent Eli out to get me a Jersey Mike's sub, opened a bag of Fritos and celebrated having completed yet another step (we'll call this a big one) in the process!

Wednesday, November 3, 2010

Am I Dreaming?

I keep pinching myself today to make sure that this is real and that I'm not dreaming. I am just so delighted with the outcome of Monday's surgery, and with the pathology report (about which I wrote last night). It is just such a tremendous relief, for which I am immensely grateful.

I will write more later about Monday's procedure, but for now, please know how much I appreciate each of you reading this blog, supporting me with your prayers and thoughts, and for supporting my family through this stressful time.

God, indeed, is good!

Love,
Erin

Tuesday, November 2, 2010

Doing the Happy Dance

Well, on this election night, we're doing the Happy Dance over here at the Richardson household, not because our favorite political candidate is winning, but because I just got my pathology results, which were better than I could have hoped for!! My lymph nodes were CLEAR, my margins were CLEAR, and all of the cancer was CONTAINED in the milk ducts. Needless to say, this is a tremendous relief after 35 days or so of uncertainty.

I need to work on dinner for the kids, etc., but wanted to share the good news. I will write more tomorrow about what all of this means (at least what I think it means) in terms of my treatment, but please feel free to raise a glass tonight in celebration of my good news.

I am eternally grateful for the many prayers from so many people over the last few weeks. I am blessed, indeed, to have such an amazing network of friends and loved ones.

Blessings,
Erin

Monday, November 1, 2010

Home, Sweet Home

Well, it's 2:12 CST, and I'M HOME! The surgery went well, I bucked up and acted like a big girl, and right at the moment, anyway, I'm not in too much pain. Overall, I'd rate the experience a 6 out of 10 on the "scary" scale, but really the good folks over at St. Thomas took great care of me. And those meds. Can I say how thankful I am for drugs? The part I was most worried about other than the results was the injection they have to put into your, er, nipple, with the dye that shows the surgeon where the sentinel lymph nodes are. For some reason, this freaked me out more than anything, and I gotta tell you that my rocking nurse anesthetist (sp?) Derek gave me some truly wonderful drug that literally knocked me out for about 3 minutes while they did that. Now that's good medicine!

Dr. Ballinger feels good about the surgery, and the preliminary report on the nodes was that they are cancer-free. I should have the final pathology report tomorrow.

Thanks for the prayers, the meals, the cards, the well-wishes, the e-mails, the text messages and all of your support. I am blessed.

Erin

Off We Go

Feeling surprisingly calm and positive this morning. Just wanting this to be over with. Thanks again for all of the prayers and support.

Much love,
Erin