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Sherita Rischer, a TWU student and breast cancer survivor, shares how she found strength and resolve during her recent battle with the disease.

Sherita at a Pioneer Breast Health activity only weeks after her initial diagnosis.

Sherita at a Pioneer Breast Health activity only weeks after her initial diagnosis.

     On May 13, 2008, I received the following diagnosis at the age of 36:  stage 1, ductal breast cancer.  My tumor was 2cm, HER2, triple negative, with no lymph node involvement. As you can imagine, this diagnosis was a huge shocker! There is no history of breast cancer in my family, and I never imagined facing breast cancer at my age!

     I had never done regular breast exams, but after taking a developmental sexuality class  at TWU, and also covering a unit on this in a women’s health course, I decided to give myself an exam. I was terrified when I felt the lump. I immediately went in to see my doctor and was sent for a mammogram (my first one) and then a biopsy. The day I received my results was like a nightmare. I heard the nurse, but I kept asking her to repeat herself.

     After meeting with my doctor and the surgeon, I was even more terrified. All I remember thinking about is “Am I going to die? Am I going to lose my breast? What will happen to my son?” I felt like my world was crumbling around me. 

     On July 14, 2008, I had a lumpectomy of my left breast and 6 lymph nodes removed. On September 5, 2009, I had my first of eight rounds of chemotherapy. During this time, I really felt like giving up, the side effects were horrible and there were days I couldn’t even get out of bed. Losing my hair was terrifying and took a huge toll on my emotional state. Four months later, I began my radiation treatments (1 of 36). During this time, I also received several treatments for severe skin burns.       

     During my entire ordeal, my family was right there. My mother (my best friend), my younger sister (my rock), and my son (a real trouper) were there every step of the way. Their smiling faces kept me smiling and their courageous spirits kept me strong. My family is very spiritual, and we prayed for healing and trusted in a higher power for deliverance. I focused on maintaining a healthy attitude and staying positive. I also joined a support group and maintained contact with a “survivor mentor” from TWU’s Pioneer Breast Health & Community Outreach. I needed to communicate with women that were going through what I was going through.    

     Once I had my follow-up and was told that the cancer was gone, I was overjoyed and relieved. Although I have several more appointments that will consist of mammograms, sonograms, etc., I am very optimistic about my future.     

     I want all women to know how important it is to be aware of what is normal for your body so that you can detect when something is wrong. Also, I want you to know that all women are at risk—even women under 40! Early detection is the key. Make it a part of your normal routine to perform monthly exams. Don’t take for granted that it won’t/can’t happen to you. Be proactive about your health!

Francine Ciulla (left), granddaughter Allie (center), and daughter, Diana (right) walking in Susan G. Komen's Race for the Cure
Francine Ciulla (left), granddaughter, Allie (center), and daughter, Diana (right) walking in Susan G. Komen’s Race for the Cure

      Mrs. Francine Ciulla, wife of  TWU Health Studies adjunct professor, Don Ciulla, writes about her journey with breast cancer and the special bond she shares with her granddaughter, Allie, who is a leukemia survivor.

      My life has been touched by cancer in many ways.  In June of 1991, when I discovered the lump on my chest, I was in disbelief. I asked my husband, Don, to feel it, looking for a second opinion. He was insistent that I go to a physician and have it checked out right away.

    Then next day, I called the place where I had received my mammogram, five months earlier, and the person on the phone told me it was a “fluid like cyst” and not to worry about it. Well, I did. I then called my doctor who told me to come and see him right away. He felt what I had been feeling. The next day, I was scheduled for another mammogram and a biopsy.

     On June 21, 1991, I was officially diagnosed with breast cancer (insitu). My doctor never formally used the word “cancer.” He just came into the room, looked at me with concern in his eyes, and said, “Francine, it’s not good.” He didn’t have to say anything else. I just burst out in tears, and he left Don and I alone for awhile. It was a fast growing tumor, and within 5 months it went from one centimeter to two. I had a mastectomy and several reconstructive surgeries, but thanks to a wonderful physician, breast self exam, and my unwillingness to take ”no” for an answer, I am an 18-year survivor!

    There was a period of time, however, when I was going through the treatment, that I hated everyone– even God. Before this had happened to me, someone had given me a card that read, “What happens to thee is God’s will.” I had kept it on my nightstand. When I was diagnosed, I suddenly hated that card, and I hated God for allowing this to happen to me. It took the love and courage of my granddaughter to change my thinking.

    In 1994, a few years after my mastectomy, our first grandchild, Allie Elizabeth Ciulla was born. She was beautiful, and she was just what I needed to divert me from the cancer in my life. Cancer struck again, however. Allie was diagnosed with leukemia before she was one-year old. I was shocked and angered once more. I remember praying to God to give me back my cancer and to take it from my precious granddaughter so she could grow up to live a full life. Allie went through months of treatment, and Don and I stood by her side and watched this brave little girl get poked and prodded for hours day after day. What a trouper she was! Seeing her go through this and maintain a sweet, positive countenance, changed my life. I felt so bad about the way I had faced my own crisis. Allie helped me to face my own cancer fears; I was not afraid anymore, and I had learned to accept life and all of its unpredictability.

    After many months, treatments and prayers, our precious Allie Elizabeth went into remission in December of 1994. Her doctor could not believe it. No one had expected her to live past Christmas, and she had proven them all wrong! Allie is now a 15-year cancer survivor, and she, my daughter, and I will be running in the White Rock Lake marathon in December to benefit the Leukemia Society. Allie will be doing the last leg of the run, and we will all be waiting at the finish line for her.

     The thing I want to share with people is that they are stronger than they think they are, and cancer does not always win. Allie has taught me this. Each day is a gift. I take nothing for granted. I am no longer afraid. I keep going, and so does Allie. She walks for me in the Race for the Cure, and I participate in the American Cancer Society’s Relay for Life and support the Leukemia Society in honor of her.

     As an 18-year cancer survivor, I have become quite the health advocate! I spend a lot of my time now raising money for organizations like American Cancer Society, Susan G. Komen for the Cure, or the Leukemia Society. I firmly believe a cure is within reach. You, too, can help make this happen by supporting organizations that sponsor cancer research. October is a great month for all of us to remember that cancer touches all of our lives, and it is within our power to make it a thing of the past.

By Dr. Venita Lovelace-Chandler

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      I knew I wanted to be a physical therapist when I was 8 years old.  Very quickly, I also knew that I wanted to work with children.  I got the opportunity to go to college and then to physical therapy school, and I began to work with children with special needs.  I specialized in pediatrics and practiced for several years before I earned a PhD and became a professor of pediatric physical therapy.  While I limited my practice to pediatrics, I certainly learned about other diagnoses while in school and during many years of practice.  I had listened to presentations on breast cancer by students and colleagues.  I had learned breast self examination (BSE) while in my physical therapy coursework, and I did BSE every month for 26 years until I found my breast lump in March of 1996.  A colleague of mine once stated “Nothing I could have learned in a classroom would have taught me more about the complexity of treating cancer patients than my own experience living as one.”  I could not agree more.

  I had no history of breast cancer in my family, and I was not really worried about breast cancer when I performed BSE as a student.  However, I found a mass which later proved to be cystic, not a cancer, but I realized in 1970 that I could understand my breast tissue through BSE.  Luckily for me, I continued to do the monthly exam.  I started mammograms when I was 40 years old, and I had a mammogram in August of 1995 before I found my lump in 1996.  The mammogram showed that the old cyst had changed a little, and so I had a more definitive mammogram which revealed nothing more suspicious.  As it turns out, the cancer was growing then and had grown into the old cyst, but I had a type of breast cancer which did not show on mammogram.  In March of 1996, the tumor was large enough for me to feel it, but it was still too small for my physicians to find.  I would find the mass, have my physician place his fingers over my fingers, then slip my fingers away.  Then my physician could feel the mass.  So having done BSE for all those years and knowing my breast tissue better than anyone else could know, probably saved my life.  I would recommend that all women learn and perform BSE as a part of Breast Health just as they have regular clinical breast examinations and mammograms (as appropriate). 

     I knew almost immediately that the mass was a cancer because I could actually detect the lobular edges of the tumor.  The official diagnosis did not come until May, after several other diagnostic tests and a lumpectomy.  I was worried, but I used my ability as a professor and physical therapist to begin to study breast cancer.  I read hundreds of articles and went to conferences while I waited for the official diagnosis and treatment plan.  Many other women assisted me by sharing their stories and even allowing me to see their reconstruction so that I could make an informed choice.

    The type of cancer I had, invasive lobular, was not considered to have a good prognosis at the time I was diagnosed.  One oncology in May of 1996 said that I would probably not live until August and that I should get my affairs in order.  Instead, I found a more aggressive oncologist who was willing to do more.  I had a bilateral mastectomy and a TRAM reconstruction.  I had chemotherapy for the remainder of 1996 and finished my reconstruction in early 1997.  My hair grew back, my strength returned, and I went on with life.  But, I continued to do BSE because I knew that the mastectomy might not possibly have removed all cancer cells.  In March, yes March (I always need to get past March each year), of 2000 while conducting BSE, I found a new tumor.  I had lumpectomy, chemotherapy, radiation, and a year of herceptin treatment, finishing just before the holidays in late 2001. 

     My hair grew back, my strength returned, and I went on with life.  I continued to do BSE.  In March (can you believe it) of 2005, I found a level three lymph node mass.  At that time, I had extensive chemotherapy first to shrink the tumors (two had formed but looked like one), and I had surgery in October of 2005. 

     My hair did not grow back quite as well that third time, my strength took about 3 years to fully return, but got better the entire time, and I went on with life.  I continue routine BSE and visits with physicians.  Someone once asked me if I thought I was the unluckiest woman in the world to have had cancer 3 times.  In fact, I am the luckiest woman I know.  I found a physician who would fight hard with me the first time, and I lived long enough to have cancer again.  I found all of my tumors early enough to be able to receive effective treatments.  I have 4 wonderful children who are adults now, but the youngest was 10 years old when I found my first tumor.  She is 23 years old now, and my ability to watch her become a competent, beautiful woman has been wonderful.  I have 5 grandchildren who I would not have known if I had not survived the initial cancer.  I married a physical therapist who was a student in PT school with me and who was my best friend.  He and my children and my grandchildren and my colleagues and my friends have given me support that cannot be adequately described.  I demand a lot of attention when I am sick, and they always came through. 

     Who could be luckier than me?  Well, maybe you – because maybe you will become interested in your own breast health because I am encouraging you to do so.  Maybe you will learn and routinely perform BSE.  Maybe you will obtain clinical breast exams from skilled practitioners and mammograms at the appropriate age.  Maybe you will never have breast cancer, but if you do find a mass, you will find it early and have it examined quickly to receive good treatment, if necessary.  Maybe you will work to raise money to fight breast cancer or to support women who have breast cancer.   Maybe you will encourage your daughters, mothers, friends, including me, to do BSE.  To other survivors, I would tell you to be proud of yourself and to keep taking care of yourself.  As a physical therapist, I would advise us all to keep exercising and keep our weight to an appropriate level, because exercise and the absence of obesity reduce the risk of having breast cancer and increase the ability to survive if you do have cancer. 

Personally, I still do BSE.  I hope I never have to fight cancer again, but I will try to do my part by walking, eating right, and doing BSE.  Finally, I enjoy the great faculty, staff, students, friends and family that I have around me, and I try not to care about small problems, like bad hair days!

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Kalinda, a TWU student and volunteer for Pioneer Breast Health and Community Outreach, (PBH), recently shared her experience with  us about confronting breast cancer at just 18.  Below is a summary of the interview:

PBH: When were you first diagnosed with breast cancer? What stage and type was it?

K: I was 18 years old and a senior in high school. I had a rare tumor called a  ” phyllodes” that was cancerous. This type of tumor is usually benign.

PBH: Is there a history of breast cancer in your family?
K: No one in my family has had breast cancer.

PBH: Did you have a clinical exam or do breast self -exam before discovering the lump?
K: I was at my yearly woman’s exam, and my doctor  noticed a “cyst”. I was told to stop drinking caffeine drinks (I never drank them) and to come back in two weeks. The cyst had doubled in size when I went back.  I had a sonogram, and it confirmed there was a growth. I had to have a biopsy to determine if it was cancerous. It was. 

PBH: How did you react to the news?
K: I was shocked! Sometimes, I still feel like it was a really bad dream. I was scared when I was told about the surgeries and recovery. I was  nervous about going back to school, and I was devastated that I couldn’t play softball anymore. I had dreams of playing college ball and it all came to an end very quickly. It felt like I was on a roller coaster of emotion. 

PBH: What course of treatment did you receive (i.e., lumpectomy, mastectomy)?
K: I had a full right mastectomy. After the first surgery ,the next one was for a skin expander to prepare my body for an implant. My surgeon would fill the expander with saline through a port every few weeks until my skin was large enough for an implant. After the implant surgery, I had follow-up appointments with the plastic surgeon for the reconstruction. These included a number of surgeries. 

PBH: Did you have a particular family member or friend who was especially
supportive during this time?
K: Everyone was so supportive it was unbelievable. I woke up after my initial surgery and the room was filled with balloons, huge cards, flowers, teddy bears, signs, etc. I never would have guessed that so many people were pulling for me! I was a varsity softball player, and when I attended the first game after my surgery as a spectator,  all of the female players had pink ribbons in there hair! Even the baseball players had pink ribbons in their shoes. That was another touching moment that will never be forgotten! My mother was so strong through it, and I think I actually made her a stronger person too. I remember at one doctor’s appointment she was squeezing my hand so hard and just asking for peace to be with us. I would always ask her not to cry because it was a chain reaction for me. My famous words to her through this rough time were, “I’m a soldier.” I told myself if I stayed positive and kept that running through my head I would be as strong as a soldier.

PBH: What was your reaction when your doctor said you were cancer-free?
K: I was relieved but still nervous. I was scheduled to come in every three months for the next year for checkups that included x rays and blood work. I grew to really trust my doctor. He became one of my best friends through it all.

PBH: Your cancer was found through a clinical breast exam. What message do you want to share about early detection?
K:  Do your breast self exams and have a clinical breast exam! No one is invincible, and anything can happen to anyone at anytime! Now that I have been a survivor for five years, I can truly say the experience has changed the way I view life.

PBH: What advice would you give to other women who may be going through the same experience?
K: Stay strong whether you turn to friends, family, support groups, or religion. Find something that keeps you strong and something that helps you keep believing.

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Are you a survivor or a co-survivor with a story you’d like to share? Please email us at healtheducation@twu.edu or Joomen@twu.edu.

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Participant in the 2008 Susan G. Komen Race for the Cure in Plano. Photo by Dr. Jody Early

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