
Presented by: Twin Tiers Young Professionals -
Life Stories:
| Breast cancer: After family deaths, I'm prepared
Everyone told me when I was growing up that I had my grandmother's nose, the same mischievous eyes, a love for the outdoors and flowers.
I wouldn't know. I never met her.
As I got older, everyone told me that I looked so much like my mother. We carried ourselves the same way, they said, and the smile - the smiles are virtually identical.
Brooke Sherman is shown above with her mother, Judy Sherman, in 1996 on the day of Brooke's homecoming dance during her junior year of high school. Judy Sherman died of breast cancer a week after Brooke graduated from college.
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Brooke Sherman sits on her mother's lap on her first day of first grade in 1986.
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I miss her smile.
I carry with me so much from these two women, lessons from my mother, and an appreciation for life somehow similar to my grandmother's. Yet, I carry something frightening from them too. I carry the fateful thought that, like them both, I too may one day face the horrifying thought of breast cancer.
I lost them both to that destructive, two-word disease that stands alone in my mind as something unfathomable: breast cancer.
My grandmother's battle was long. She was young, only 52 when she was diagnosed. She did things by doctor's orders - a mastectomy, chemotherapy, radiation. She went into remission. She reveled in my brother's infancy. The cancer came back. She grew angry. It was too late.
She was 56.
My mother watched it all. She rarely talked about it. She only told me when I was 21 that it was breast cancer that stole my grandmother from our lives. I asked her immediately if she had a mammogram and did self-exams. Of course, she told me then. I'll never know how much my grandmother's battle with breast cancer scarred my mother.
My mom lost her own battle with cancer in less than one week. She was diagnosed with cancer - the doctors were unsure of what kind - on a Tuesday. She died that Sunday, one week after Mother's Day and my college graduation.
She was 50.
A month after her death, her doctors called me and my father in to see them. They had something they wanted me to know. My mother had breast cancer that had filled her body, traveling to her liver, her lungs, her lymph nodes. By the time they found it, it was too late.
My mother didn't have mammograms, come to find out. I don't know if she did self-exams. I didn't get a chance to ask her. I know that she was scared. I saw it in her eyes the day I took her to the hospital. She was so very sick. She paused as we left the house to look at her home for the last time. We both knew it.
It's been nearly four years. I keep waiting for it to get easier. It doesn't. I can talk about it, but I rarely write about it. It's just too painful, still.
I talk about breast cancer to other women I love, though. I tell them how hard it was to lose my mother, to never know my grandmother. I tell them how important it is to take care of themselves, to get mammograms and do self-exams.
I do and I will.
I promise myself one thing should someday I have this other unfailing similarity to these important women - my beautiful mother and grandmother.
I promise it won't be too late.
Brooke J. Sherman is a staff writer for the Star-Gazette. She can be reached by e-mail at bsherman@ stargazette.com. First Person offers immediate reaction from readers affected by stories of interest.

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Beating breast cancer: If something doesn't feel right, persist in finding out the reason.
First Person column by Cindy Burdick
My name is Cindy Burdick. I am 54 years old and I am a two-year survivor.
I was diagnosed on April 7, 2004, with inflammatory breast cancer. Only 1 percent of women who develop breast cancer have this type. I didn't have a lump. I didn't have pain and I had just had my mammogram a month earlier. But, one of my breasts felt firmer.
I called the doctor and got in to see the physician's assistant. She felt that it was fluid built up in my breast, but sent me for an ultrasound. The technician didn't see anything and the radiologist came in and asked what he was supposed to be looking for because he didn't see anything in the ultrasound. I explained and he said he agreed it was fluid because nothing showed. After a couple of months, my breast was still getting firmer, so I called and said that I had to see the doctor.
After an exam, I was sent immediately for a needle biopsy. There was something there. They called my doctor and it was decided that I should go to Rochester for a digital mammogram and core biopsy. (By this time, four months had passed.) Two days later, Dr. Joseph Navone called and wanted my husband and me to come to his office to discuss the results (This was not a good feeling.). He informed us of the findings and said I was to start chemotherapy the following week. At that point I was in the third stage of breast cancer and it was only five months since my yearly mammogram.
I went through five months of chemo at Dr Navone's office with wonderful people there to see me through (Thanks, Ken and Maryanne), a mastectomy in Rochester and radiation five days a week for seven weeks at the Falck Center (Thanks, Karen you are still my favorite Zapper!). I owe “big kudos” to Dr. Navone (my life saver), Dr. Nancy King, Dr. Rose Byland and Dr. Andrus.
My family was a “rock” through this ordeal, especially my two granddaughters. Brianna was always there to lend me a hand. She especially liked to shave my head. (When my hair started falling out after my first chemotherapy, I decided to go bald my way!). My other granddaughter, Emma, was born seven weeks early, two months before I was diagnosed. She was sent for a reason. I would sit and rock her or she would lay with me if I was too ill to get up. They are my angels!
The year 2004 was the most traumatic year of my entire life and with the help and prayers of my loving family, dear friends and caring medical staff, I made it through with flying colors!! (Pink, of course!) The biggest, most important part of this or any disease is your attitude and outlook. No, it wasn't easy. Yes, I had pain. Yes, I was sick. Yes, I was bald. And yes, I was petrified, but I had a positive, upbeat attitude and I was not going to let it get me down. My advice to every woman of all ages is you know your body and if you feel something isn't right, keep insisting on finding out what it is.
If I hadn't, I would not be here to enjoy life.
Cindy Burdick lives in Erin and works for Chemung Canal Trust Co. in Elmira. First Person offers immediate reaction from readers affected by stories of interest.

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From a teenager who’s mom was diagnosed with breast cancer
As I hear the talk again, I glance off in to the field. I see the green and white scoreboard. It say’s visitors zero, with one light blown out in the corner of the zero, it’s the top of the first. I know what I have to do; I know what I am capable of. My eyes begin to water and the allergies kick in with the smell of fresh cut grass and all the spring pollen in the air. As everyone begins to run to their position, I head towards first base. I jump the white chalky line as I always do for good luck. With the baseball in my right hand and my leather chance for opportunity in my left hand, in the infield, the shortstop and second baseman are ready for me to throw one their way to warm up.
As I roll the first grounder I begin to think back to April 16, I was 14 years old, it was the bottom of the 7th inning. The score was 7 to 6. We were winning. They had a guy on second and third there were two outs. I look back at my friend in right field and I yell to him “lay out for anything; this is the game”. I could see by the stone cold look in his face that he was ready. And as the ball came off the bat it was coming right at me, as it skipped up off the ground, I dropped to my knees to take it in the chest to knock the ball down and take the out at first to end the game. But as it hit the ground it hit that one stone in the infield of dirt and the ball kicked off to the side into the outfield. I had let my team and coaches down. As I sat in the cold plain white dugout for an hour after the game, I was so alone I felt that nothing could be worse.
When I arrived home I didn’t talk to anyone. As I walked up the stairs they cracked every step as if to laugh at me, I grabbed my blanket and pillow, turned the music on and lay on the floor. I never wanted to leave that room and I didn’t understand how I could have misjudged that ball, the same play I had made 10,000 times before that. As drifted off to sleep so many things were going through my head. When I woke up the next morning and looked at the clock, it was 9:17. I lay there for 5 minutes before my mom came into my room and sat next to me.
As she sat down she started to cry and I had no idea what was going on and she told me that she was sick, had been to the doctor and was told that there was a spot. She had breast cancer. It put everything into perspective. It made me realize that sports are not life. There are things a lot more important than what happened on the field. As I looked at my mom seeing her looking so scared I knew that I could not start to cry. I had to be strong for her, I tried to hold it back but a few tears crept out and flowed down my face like two giant boulders. I have never felt a pain such as that in my entire life. Who would have ever thought a spot the size of that pebble in the infield the night before would change my entire life.
As I scoop the ball in warm ups I know I will make that play in the seventh inning. Because if I am strong enough to help my mom get through all the pain and fear she had to go through, I am strong enough to get through anything that life throws my way, and I know I can't take advantage life. That experience changed my whole life, after that I knew I had to start trying harder in school and get a good education so I can be as proud of myself, as I am of my mom for making it through the most difficult situation she has ever had to face.
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Deborah Dickerson
Burdett, NY
50 years young
It was March 2002; I was fast approaching my 48th birthday. It had been 3 years since I had a physical and a mammogram, something we’ve all put off at one time or another. Some little voice told me to call and start scheduling appointments. That little voice probably helped save my life.
I left work early for my appointment at the hospital. Mammograms are never pleasant but it’s what I call a “necessary evil”. The technicians at Cayuga Medical Center in Ithaca know what they’re doing and a good tech can make all the difference.
She took pictures from all angles and, as routine; I waited for the doctor to check the films. She came back in and this time didn’t tell me I could go. There’s a small area we want to get a closer look at and the ultra sound room is open - do you have time?
A week later a biopsy was performed and yes I heard the dreaded “C” word. The tears began to flow. The worst part was telling my 3 sons, the youngest was still living at home and a freshman in high school. I sat on the edge of his bed the following afternoon, tears falling; I told him I had to have surgery to remove a cancerous mass in my breast. He was so brave - put his arm around me and told me things would be all right. My two other sons were living in an apartment in Syracuse. My husband and I thought it best to tell them in person so the weekend before surgery we drove to Syracuse to take them to dinner. The son in medical school seemed to take it in stride but his brother had a harder time dealing with it.
Things happened so fast from that point. I arrived at the hospital on the morning of May 9th, dye was inserted into my right breast and that afternoon a lumpectomy was performed. And eventually I found out that it was Stage 1 cancer, I was one of the luckier ones.
Two weeks later I had my first appointment with the oncologist. We had to chart a course of action. After discussions with the doctor, reading articles, visiting the Ithaca Breast Cancer Alliance, and talking with family members; it was decided to do a round of chemo and then radiation.
My first chemo was scheduled for June 5th. I was having 8 chemo treatments 3 weeks apart. The first one seemed relatively painless. Two days later it hit me hard. I was so nauseous and tired. The next treatment I scheduled for a Thursday was able to take Friday off and by Monday I was ready to great the world again. Work was extremely generous with time off and also appreciated me coming in as much as I did. When my treatments were half way through - they brought in half moon cookies to celebrate! After about 5 of the chemo treatments my blood count was getting lower than the doctors liked. I had to delay by a few days the next treatment. This happened 2 or 3 times during the course of my treatments.
My friends, family and coworkers really rallied around. One friend sent me a cheer-up card in the mail that was timed to arrive the day after my treatments, another brought dinners over and some wonderful desserts, my sister sent me a different angel or a pink ribbon motif every month. I had people come clean my house. But most important of all they were all there for my emotional support!
After finishing my 8 chemo treatments, I had 6 weeks off to build up my strength before starting the next round - radiation.
I was to have 30 treatments total. I scheduled my treatments for first thing in the morning. Before going into work I stopped at the radiologist’s office had a treatment and then proceeded into work. Towards the end of my treatments the radiologist office informed me that the balance of my treatments would be in Syracuse. They rented an extended van, provided a driver and drove between 5 and 7 of us up there on a daily basis. I only had 8 treatments in Syracuse but the camaraderie on these trips was tremendous. You would have thought we were headed on a shopping trip. The laughter and jokes were a great morale booster; if we hadn’t been joking we’d all have been in tears. We would arrive back in Ithaca around noon and I would head to the office.
I received my diploma from the radiologist on February 3rd, 2003.
Soon I will be celebrating my 4th anniversary of being cancer free. To this day when I walk the survivors lap in the “Relay for Life” I am amazed at the caring and support involved. I firmly believe that my situation was made much easier for me to bear because of all the support I received from family, friends, coworkers, and even strangers.
On a recent celebratory trip to Alaska, I was wearing my pink baseball cap when another woman came up to me and asked if I was a survivor. She was just starting her treatments.
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Stefano Ringer
Trinchero Family Estates
194 Bennett Road
Pine City, New York 14871
Eleven months into our marriage, my first wife Maureen was diagnosed with breast cancer. I had noticed a small lump in her breast in August and encouraged her to get it looked at. She procrastinated, saying it was more than likely a cyst, since her mother had them frequently and there was no history of breast cancer in her family. I continued to push for her to see her doctor and she finally did in early December. On December 8th she was diagnosed.
At this point it had progressed to her lymph nodes. The treatment was three doses of chemotherapy followed by a radical mastectomy and three more doses of chemotherapy. All of which was followed by a series of radiation treatments. Maureen lost all of her hair and one of her breast that year. This was 1995 and she was thirty two years old. I reminded her frequently that I didn’t marry her for her breast and that her hair would eventually grow back. I also made her a promise that I would not miss any of her chemo treatments.
Maureen did not fair well with the chemo or the radiation treatment. She was ill all the time and on many occasions had to be hospitalized. She persevered though and eventually got through. 1996 was a good year. The treatments were over and she was feeling much better. Her hair was growing back rapidly and that made her even happier. At the end of February 1997 Maureen experienced some pain down her legs. She went to see her doctor and discovered that the cancer was back, now in her bones. We consulted two Oncologists who both concurred that the best approach was hormone therapy. Two weeks later, Maureen died in Arnot Ogden Hospital. I won’t go into the details of that day here. Let’s just say it came as a surprise to me, but I believe that Maureen new it was her time. She was 34 years old.
I am re-married to a wonderful woman, Sid and we now have two children, Zachary and Gracie. Through this experience, I have learned to enjoy what time I have and try not to “sweat the small stuff”.
At first, Maureen did not want to go through the treatment of her cancer. I encouraged her to, because I didn’t want to lose her. As much as I believe a cure will be found, I struggle with the notion that the cure for her was worse than the disease. Should I have had a chance to do all over again, I’m not sure I would have been so persistent in encouraging Maureen to go through the treatments.
I now work for Sutter Home Winery, Inc. and together we strive everyday to raise money for Breast Cancer Research through our Sutter Home for Hope Campaign. We encourage women and men to get tested on a regular basis.
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