Kimlin Tam Ashing, PhD
City of Hope
Dr. Kimlin Tam Ashing is professor, and Founding Director of the Center of Community Alliance for Research and Education (CCARE) at City of Hope Medical Center. She received her doctorate in Clinical Psychology from the University of Colorado, Boulder. As an advocate-scientist, her work is advancing population health. She is a Population, Behavioral Scientist working to develop and implement evidenced based, culturally, clinically and community responsive health improvement interventions. Her mission is to engage advocates and civil society in science to speed-up and ensure the public benefit of biomedical research and advancements.
Dr Ashing holds several national leadership roles within the African-Caribbean Cancer Consortium; National Advisory Council for the Asian Pacific Islander Native Hawaiian Cancer Survivors Network and the Young Survival Coalition; and on the Executive Council of American Cancer Society, Los Angeles. She is a Life member of the Association of Black Psychologists and a licensed Clinical Psychologist. She served as Board Member and continues on the Scientific Committee of the American Psychosocial Oncology Society. She serves as Scientific Advisor to Latinas Contra Cancer, Caribbean Medical Providers Practicing Abroad and the Love Research Army. She is scientific partner with the Association of Black Women Physicians, Los Angeles Chapter, and The Take Action of Health Initiative--a community benefits partnership among National Urban League, Anthem and Pfizer. She was awarded the prestigious Fox Award for advancing the field of Psychooncology by the International Psychooncology Society, and is a member of the Human Rights Taskforce. She sits on the Minority in Cancer Research Council of the American Association of Cancer Researchers - the largest body of cancer researchers in the world.
Dr. Ashing is the notable leader in examining health disparities, and cancer inequities, survivorship and quality of life. She has published over 80 articles and book chapters. Her scholarship is to understand how culture, ethnicity, socio-ecological, structural and systemic contexts influence health and patient centered outcomes including mortality, morbidity, distress, symptoms and quality of life. She applies this knowledge to implement interventions to improve well-being and reduce health inequities
She partners with community advocates and multi-sectoral stakeholders to develop and implement community participatory programs and interventions to reduce the risk and burden of chronic illnesses, including cancer, obesity and diabetes. She is a community-minded researcher who is guided by the intersectionality of society, biology, culture and person. Her studies are multicultural with diverse ethnic groups, including African Americans, Afro-Caribbean Americans, Latino Americans, Chinese Americans, Japanese Americans, Filipino Americans, Korean Americans and European Americans.
As a woman of color raised in a multicultural (Chinese and Afro-Caribbean) and multilingual home, and the youngest of eight siblings, she recognized the salience of culture and context very early in her life. As the daughter of two former cancer survivors, and as a psychologist, she is compassionate and passionate about her work to reduce cancer disparities and inequities, and enhance health outcomes for underserved communities. Dr. Ashing is the mother of three children: Joshua - enjoying a career in Market Research; Kemi - a poised, math, science and technology enthusiast High School Senior; and Ajorin - a sport enthusiast 6th grader. She lives in beautiful Altadena, California. She thrives on faith, family, work and organic gardening.
Karen Basen-Engquist, PhD, MPH
MD Anderson Cancer Center
Karen Basen-Engquist, Ph.D., M.P.H., is a Professor of Behavioral Science and the Director of the Center for Energy Balance in Cancer Prevention and Survivorship at The University of Texas M. D. Anderson Cancer Center. Dr. Basen-Engquist's research focuses on cancer survivors and the role of health behavior interventions in decreasing the severity of late effects, improving physical functioning, optimizing quality of life and reducing risk of chronic diseases. In addition, she studies intervention methods for behavior change and innovative real-time methods for assessing symptoms and behavior in cancer patients and survivors.
Dr. Basen-Engquist recently completed an R01 study funded by the National Cancer Institute (NCI) to investigate the mechanisms of exercise adoption and maintenance in endometrial cancer survivors, using a social cognitive theory model that tests the social, physiological and behavioral predictors of exercise adherence. Additionally, 2 NCI-funded pilot studies evaluated the benefits of exercise for advanced colon cancer patients and cancer survivors with chemotherapy induced heart failure. She currently directs a prevention program funded by the Cancer Prevention & Research Institute of Texas (CPRIT) to increase physical activity among medically underserved breast cancer survivors.
Through activities at the Center, Dr. Basen-Engquist endeavors to expand energy balance research by facilitating collaboration among investigators and expanding research in 4 broad areas - the effect of exercise, nutrition, and weight control on outcomes in cancer survivors and people at increased risk of cancer; biological mechanisms underlying relationships between energy balance and cancer; dissemination and implementation research related to energy balance interventions; and basic biobehavioral mechanisms underlying exercise, eating behavior and weight loss.
Donald Berry, PhD
MD Anderson Cancer Center
Don Berry is a professor in the Department of Biostatistics of the University of Texas M.D. Anderson Cancer Center. He was founding Chair of this department in 1999. Dr. Berry received his Ph.D. in statistics from Yale University, and previously served on the faculty at the University of Minnesota and at Duke University. He has held endowed faculty positions at Duke University and M.D. Anderson. Since 1990 he has served as a faculty statistician on the Breast Cancer Committee of the Cancer and Leukemia Group B (CALGB), a national oncology group. In this role he has designed and supervised the conduct of many large U.S. intergroup trials in breast cancer. Through Berry Consultants, LLC he has designed many innovative designs of clinical trials for pharmaceutical and medical device companies and for federally funded collaborations in many different diseases. He is well known as a developer of Bayesian adaptive designs that efficiently use information that accrues over the course of the trial. These trials minimize sample size while increasing the likelihood of detecting drug activity.
Under his direction the Department of Biostatistics at M.D. Anderson designed over 300 clinical trials that take a Bayesian approach. He is co-developer (with Giovanni Parmigiani) of BRCAPRO, a widely used program that provides individuals' probabilities of carrying mutations of breast/ovarian cancer susceptibility genes BRCA1 and BRCA2.
Dr. Berry is the author of several books on biostatistics and over 300 published articles, including first-authored articles in the New England Journal of Medicine, the Journal of the American Medical Association, and Nature. Dr. Berry has been the principal investigator for numerous research grants from the National Institutes of Health and the National Science Foundation. He is a Fellow of the American Statistical Association and of the Institute of Mathematical Statistics.
Julia Brody, PhD
Silent Springs Institute
Dr. Julia Brody, executive director of Silent Spring Institute, is a leader in research on breast cancer and the environment and in community-based research and public engagement in science. Brody's current research focuses on methods for reporting to people on their own exposures to hormone disruptors and other emerging contaminants when the health effects are uncertain. She also recently led a project connecting breast cancer advocacy and environmental justice in a study of household exposures to endocrine disruptors and air pollutants through a collaboration of Silent Spring Institute, Communities for a Better Environment (a California-based environmental justice organization), and researchers at Brown University and the University of California, Berkeley. Since 1996, Brody has been the principal investigator of the Cape Cod Breast Cancer and Environment Study, a case-control study of 2,100 women that includes testing for 89 endocrine disruptors in homes and historical exposure mapping. The study was the first to measure estrogenic activity in groundwater and drinking water. Results have been published in Environmental Health Perspectives and elsewhere. Dr. Brody led a two-year review of scientific review of evidence on animal mammary gland carcinogens and epidemiologic studies of breast cancer and environmental pollutants, diet, body size, and physical activity, which was published in a special supplement to the American Cancer Society peer-reviewed journal, Cancer.
Brody's research is supported by the National Science Foundation, the National Institutes of Health, the New York Community Trust, and the Avon Foundation, among others. Her research collaborators include investigators at Harvard and Brown universities, the University of California, Berkeley, and elsewhere. The U.S. Environmental Protection Agency recognized her research with an Environmental Merit Award in 2000, and she has been honored by the Heroes Tribute of the Breast Cancer Fund. She presented one of the Distinguished Lectures at the National Cancer Institute in 2002 and the Keystone Science Lecture at the National Institute of Environmental Health Sciences in 2009. She serves on the National Advisory Environmental Health Sciences Council, appointed by the Secretary of Health and Human Services, and she is as an advisor to the California Breast Cancer Research Program and breast cancer activist organizations.
Dr. Brody is an adjunct assistant professor at the Brown University School of Medicine. She earned her PhD at the University of Texas at Austin and her AB at Harvard University.
Jessica Clague DeHart, PhD, MPH
Clarmont Graduate University
Dr. Jessica Clague DeHart is a molecular epidemiologist, an Assistant Professor at Claremont Graduate University, School of Community and Global Health and a Visiting Professor at City of Hope. Dr. Clague DeHart graduated from the University of Southern California with a bachelors in health promotion and disease prevention. She completed a masters of public health in chronic disease epidemiology from Yale University and a PhD in molecular cancer epidemiology from UT Houston and MD Anderson Cancer Center. Dr. Clague DeHart completed her postdoctoral fellowship at the City of Hope in the Division of Clinical Cancer Genetics where she investigated hereditary breast and ovarian in Hispanic populations. As an assistant professor at the City of Hope she developed a research program that uses data from large observational studies to design wellness intervention trials for cancer survivors. Dr. Clague DeHart is currently the principal investigator on several community-based intervention trials that investigate the impact of nutrition and physical activity on molecular markers of cancer prevention, progression, and symptom management. A major focus of her research is the identifying and preventing collateral damage of treatment in cancer patients and survivors.
Mia Gaudet, PhD
American Cancer Society
Mia M. Gaudet, PhD is a Scientific Director of Epidemiology Research at the American Cancer Society. Her research focuses primarily on the clarification and identification of genetic and non-genetic risk factors for subtypes of breast cancer with an emphasis on more fatal subtypes in the Cancer Prevention Study cohorts and other collaborative efforts. In the Cancer Prevention Studies, she initiated and oversees the collection and characterization of breast and ovarian tissue from women diagnosed with these cancers. She also participates in research projects related to associations of risk factors with risk of endometrial and ovarian cancers. Prior to moving to ACS in 2010, she held academic appointments at Memorial Sloan-Kettering and Albert Einstein College of Medicine. She obtained her doctoral degree in Epidemiology at the University of North Carolina at Chapel Hill and her post-doctoral fellowship training at the Division of Cancer Epidemiology and Genetics, National Cancer Institute.
Lisa Kay Jacobs, MD
Johns Hopkins University
Dr. Jacobs specializes in melanoma and breast cancer. Her initial practice was at the University of Missouri at the Ellis Fischel State Cancer Center, which is the designated cancer center for the state. Since joining Johns Hopkins in 2004, she has taken a leadership role regarding clinical research trials for the surgical division of the Johns Hopkins Breast Center. In 2012, Dr. Jacobs established a new breast center at Howard County General Hospital. As director of that program, she treats patients with all types of breast disease and melanoma.
Dr. Jacobs has a clinical interest in treatment of early stage melanoma. She has worked closely with dermatologists and medical oncologist at Johns Hopkins University and Howard County General Hospital to improve awareness and care of melanoma patients by participating in educational programs and clinical research trials.
Breast cancer care has been a focus of Dr. Jacobs clinical practice since finishing her surgical oncology fellowship. Her primary clinical interest is in improving overall quality of life for breast cancer patients. To achieve that goal, she has initiated research programs in lymphedema and oncoplastic surgery, which attempts to increase the number of women eligible for breast preservation by combining lumpectomy with plastic surgery techniques to reshape the breast. In addition, she has a research funding to investigate a new device that may reduce the number of surgeries required to achieve breast preservation
Corrine Leach, PhD, MPH, MS
American Cancer Society
Dr. Leach is a Senior Principal Scientist in the American Cancer Society's Behavioral and Epidemiology Research Group. She conducts original behavioral research in the areas of cancer survivorship, aging, and chronic-disease self-management. She has a passion for understanding the factors that contribute to healthy aging and learning ways to help people live healthier lives, including after a cancer diagnosis. In addition, she is Adjunct Assistant Professor in the Rollins School of Public Health at Emory University.
Corinne currently serves as the ACS-lead of the ACS-NCI online self-management platform, Springboard Beyond Cancer, for cancer survivors which launched October 2016. This eHealth tool empowers cancer survivors to better manage their symptoms (both in treatment and post-treatment), live healthier after cancer, improve their communication skills about their cancer/other conditions with their healthcare professionals, family and friends, and will leverage the Cancer Survivors' Network to provide peer-to-peer support. She recently led the user testing, qualitative evaluation, and the pilot randomized evaluation trial of the online platform.
She also serves as the PI of the ACS Cancer Survivor Transition Study, a longitudinal, mixed-method (qualitative and quantitative) national project to identify and prioritize gaps in information and resources for cancer survivors as they transition from active treatment back to the community care setting.
Susan McCann, PhD, RD
Roswell Park Cancer Center
Dr. McCann is a registered dietitian and has completed training in nutrition, epidemiology, and methods of analyzing complex dietary and epidemiologic data. Her research interests include the relationships between diet and cancer, especially cancers of the breast, endometrium, and ovary. More specifically, she is interested in phytochemicals as dietary compounds affecting cancer risk and prognosis, and is further interested in the effect of genetic variation on these relationships. She has conducted several dietary intervention studies to investigate the role of dietary components in cancer or cancer related risk factors. She has also been involved in research that utilizes data reduction analytic methods such as principal components analysis. Finally, she is interested in the application of metabolomics and genomics to problems of diet in the etiology and prognosis of cancer and the role of the gut microbiome in cancer etiology.
She has conducted several clinical trials funded by the National Center for Complementary and Alternative Medicine and National Cancer Institute (NIH) studying the effects of flaxseed on breast cancer etiology and survival. Dr. McCann has recently investigated the role of modification of dietary glycemic load in expression of miRNAs related to cancer and energy metabolism and reported that a low glycemic diet may affect expression of several miRNAs related to energy metabolism and cancer processes. She is currently conducting a flaxseed intervention study in healthy African American and Caucasian postmenopausal women to investigate the interaction between the gut microbiome and genetic variation on changes in steroid hormone metabolism in response to the flaxseed intervention.
McCann has authored or co-authored more than 80 journal articles, abstracts, and book chapters, is a First Editor of Nutrition Research Reviews, and serves as an ad hoc reviewer for the American Journal of Clinical Nutrition, American Journal of Epidemiology, Cancer Causes and Control, and Cancer Epidemiology, Biomarkers and Prevention.
Dr. McCann is actively involved in the education of scientists at Roswell Park Cancer Institute. She has mentored numerous graduate students in the Interdisciplinary Sciences Masters degree program, and several masters and doctoral candidates in Epidemiology. She designed, and teaches annually, PTR 502 Analysis of Health Related Data.
Sofia Merajver, PhD
University of Michigan
Dr. Merajver is Scientific Director of the Breast Cancer Program and Director of the Breast and Ovarian Cancer Risk Evaluation Program at the UM Comprehensive Cancer Center. She is also Professor of Internal Medicine and Epidemiology.
Dr. Merajver's research laboratory is devoted to understanding the molecular and metabolic regulators of very aggressive breast cancer types. The primary areas of focus are systems biology, mathematical oncology, biophysics, cell biology, genetics, and drug development. She works in concert both in the lab and in the clinic, making the lab advances immediately available, through novel interventions and clinical trials, to her patients.
Lisa Newman, MPH, FACS
Johns Hopkins University
Dr. Newman is Professor of Surgery and Director of the Breast Care Center for the University of Michigan in Ann Arbor, Michigan, where she also serves as Program Director for the Breast Fellowship. Dr. Newman obtained her undergraduate education and Masters Degree in Public Health from Harvard University. She attended medical school and completed her general surgery residency training at the State University of New York Health Science Center at Brooklyn. She completed her fellowship in surgical oncology at the M.D. Anderson Cancer Center in Houston, Texas.
Her extensive research related to disparities in breast cancer risk and outcome has been published in numerous peer-reviewed medical journals and was recently featured on CNN's documentary 'Black in America 2'. She holds leadership positions with the Society of Surgical Oncology (Executive Council; Disparities Committee Chair), the American Society of Clinical Oncology (former Chair, Health Services Committee; current Chair, Disparities Advisory Board) and serves as editorial section editor for the journals Cancer (Disparities Section Editor) and Annals of Surgical Oncology (Breast Section Editor). She also serves on the editorial boards for CA- A Cancer Journal for Clinicians; Journal of Clinical Oncology; and Breast Cancer Research and Treatment. She also serves on the Breast Prevention Section of the National Comprehensive Cancer Network. She maintains a very active community service record, and currently serves as Chief National Medical Advisor for the Sisters Network, Inc., a national African American breast cancer survivors support organization. Her current disparities-related research program involves a partnership between the University of Michigan and the Komfo Anoyke Teaching Hospital in Kumasi, Ghana.
Julie Palmer, SC.D
Dr. Julie Palmer is Professor of Epidemiology at BUSPH, Associate Director of the Slone Epidemiology Center at Boston University, and Associate Director for Population Sciences for the Boston University Cancer Center. She received her BA from Brown University, MPH from Boston University, and doctorate from Harvard University. Dr. Palmer's major research interest is the etiology of breast cancer, with a particular focus on African American women. She was instrumental in designing and implementing the Black Women's Health Study, a cohort study of 59,000 women, and has served as co-investigator of the study since its inception in 1995.
A major goal of Dr. Palmer's research program is reduction of breast cancer mortality in young African American women by identification of modifiable factors that influence development of hormone receptor negative breast cancer. To that end, Dr. Palmer is one of three multiple PIs who organized a collaborative NCI Program Project (AMBER), which combines data, germline DNA, and tumor tissue samples from four epidemiologic studies of breast cancer in African American women for identification of factors related to specific breast cancer subtypes. Dr. Palmer's research has provided convincing evidence that breastfeeding reduces risk of hormone receptor negative breast cancer and that, in the absence of breastfeeding, higher parity is associated with an increased risk of receptor negative disease. She is now assessing the possible interaction of those factors with genetic variants in pathways related to hormone metabolism and inflammation. Dr. Palmer has also led work to develop an effective risk prediction tool for breast cancer in African American women that can be used by primary care providers to refer high-risk women for additional screening (e.g., testing for high-penetrance genetic variants, breast MRI, etc.). She is currently working on methods for subtype-specific risk models, while leading analyses to identify appropriate candidate factors for possible inclusion in the models.
Dr. Palmer is Chair of the NIH Cancer, Cardiovascular, and Sleep Epidemiology Study Section (CHSA panel). She serves on the Scientific Advisory Boards of the NIEHS Sister Study and the University of Pittsburgh Shanghai and Singapore Cohort Studies and the Editorial Board of Breast Cancer Research.
Patricia Parker, PhD
Memorial Sloan Kettering Cancer Center
Patricia A. Parker, Ph.D. is an associate member and associate attending psychologist in the Department of Psychiatry & Behavioral Sciences at Memorial Sloan Kettering Cancer Center. She is also the Director of the Communication Skills Training and Research Program. In this role, she leads a behavioral science team to provide training to clinicians to enhance their interaction with their patients and research that evaluates novel communication skills interventions and outcomes. Her research primarily focuses on healthcare provider-patient communication and decision making and quality of life among different cancer patient populations. She has conducted several studies examining aspects of physician-patient communication including how patients are told news of their diagnosis and the impact of the physician-patient encounter on patients' psychosocial adjustment. She has received peer reviewed funding from NIH and other sources including a Patient-Centered Outcomes Research Institute (PCORI) project to examine clinical and psychosocial outcomes of contralateral prophylactic mastectomy, a NIH-funded R21 to examine decision making about contralateral prophylactic mastectomy in women with unilateral sporadic breast cancer and an NCI-funded career development award (K07) and R03 that examined physician-patient communication and psychosocial adjustment of individuals with metastatic cancer of unknown primary site (CUP). She has 59 peer-reviewed publications that focus on aspects of communication and quality of life in cancer patients and survivors. Dr. Parker received her Ph.D. from the San Diego State University/University of California, San Diego Joint Doctoral Program in Clinical Psychology and completed her postdoctoral fellowship at The University of Texas MD Anderson Cancer Center.
Alpa Patel, PhD
American Cancer Society
Dr. Patel earned her B.A. in Zoology from the University of Florida in 1996, followed by a master's degree in Epidemiology from the Rollins School of Public Health at Emory University in 1997, and a doctoral degree in Epidemiology from the Keck School of Medicine at the University of Southern California in 2002. Dr. Patel first joined the Epidemiology Research Program at the American Cancer Society as a research analyst in 1997, and then rejoined the group following her doctoral work. She is currently the Strategic Director of the Cancer Prevention Study-3, a large nationwide prospective study aimed at better understanding the lifestyle, genetic, and environmental causes of cancer.
Dr. Patel is a cancer epidemiologist whose research has focused on the role of the physical activity in cancer prevention and obesity as a risk factor for cancer. She is particularly interested in the public health benefits of being physically active and limiting time spent sitting.
Peggy Reynolds, PhD, MPH
Stanford University and Cancer Prevention Institutes
Peggy Reynolds, Ph.D., is a Senior Research Scientist at the Cancer Prevention Institute of California (CPIC), Consulting Professor at Stanford University, Department of Health Research and Policy and a member of the Stanford Cancer Institute. She received her Ph.D. in Epidemiology from the University of California at Berkeley, and spent several years in the California Department of Health Services, directing the statistical research unit for the California Cancer Registry and San Francisco Bay Area SEER (Surveillance, Epidemiology and End Results) program, and as the Chief of the Environmental Epidemiology and Geographic Information Section. She currently directs CPIC's Environmental Research Group. Dr. Reynolds has conducted a number of cancer epidemiology studies, with a particular focus on environmental risk factors, including several geographic information system based studies of patterns of cancer incidence in areas of high agricultural pesticide use and high levels of air pollution in California, as well as a number of studies of cancer in occupational cohorts. She is a founding member and co-investigator for a large ongoing prospective cohort study of women initiated in 1995: the California Teachers Study. Much of her research has focused on risk factors for breast cancer.
Annette Stanton, PhD
Annette L. Stanton, Ph.D., is Professor of Psychology and Psychiatry/Biobehavioral Sciences at the University of California, Los Angeles, senior research scientist at the UCLA Cousins Center for Psychoneuroimmunology, and a member of the Division of Cancer Prevention and Control Research in the Jonsson Comprehensive Cancer Center. Her research centers on specifying factors that promote psychological and physical health in individuals who confront health-related adversity. In the area of psychosocial oncology, she conducts longitudinal research to understand the influences of personality and contextual resources, cognitive appraisals, and coping processes on the quality of life and health in individuals diagnosed with or at risk for a range of cancers, including cancer of the breast, eye, lung, and prostate. She then works to translate her findings into effective interventions for individuals living with cancer through conducting randomized, controlled intervention trials of psychosocial and behavioral interventions. Dr. Stanton has received the Senior Investigator Award from Division 38 (Health Psychology) of the American Psychological Association in recognition of her research contributions to health psychology. Current funding for her research is provided by the National Cancer Institute, the Breast Cancer Research Foundation, the Lance Armstrong Foundation, and the Susan G. Komen for the Cure Foundation. She has received a number of awards for undergraduate teaching and graduate mentoring. In 2006, Professor Stanton was honored with both the J. Arthur Woodward Graduate Mentoring Award and the Distinguished Teaching Award in the UCLA Department of Psychology.
Saraswati Sukumar, PhD
Johns Hopkins University
Saraswati Sukumar, PhD, is the Barbara B. Rubenstein Professor of Oncology and Professor of Pathology, and a preceptor in the Human Genetics and Pathobiology graduate programs. She is the Assistant Director of Faculty Affairs. She has served as the Principal Investigator of the DOD's Center of Excellence, NCI's Specialized Program of Research Excellence (SPORE) and of the AVON Breast Cancer Foundation. Dr. Sukumar has worked in the breast cancer field since her postdoctoral training at National Cancer Institute at Bethesda MD. There she established that ras oncogenes were present in carcinogen induced mammary tumor models in rats and mice, and showed that the nature of the mutations in the oncogene reflected the chemical specificity of the carcinogen action on DNA. She joined her first faculty position at the Salk Institute in La Jolla, CA in 1988, and then moved to Johns Hopkins Oncology Center in 1994 as Associate Professor to assume the position of Director of Basic Research at the newly formed breast cancer research program. She was promoted to Professor in 2001. She has authored more than 150 publications. Her laboratory's work spans the entire spectrum of basic research to preclinical studies, and all the way to translation to the clinic.
Dr. Sukumar is very active both in the Johns Hopkins and outside community. She has participated and chaired many grant review committees in the NIH, DOD, and Susan G Komen Foundation. She is currently a scientific advisory board member of the SGKF for the Cure. She is a senior editor for Cancer Research and several other journals. Beating this drum and demanding equal representation for women faculty in the center as well as in the school of medicine as a whole has resulted in closer attention to this question. She has mentored over 40 postdoctoral fellows and researchers in her career, many of whom are in academic research positions. She is committed to their success not only as fellows but also as independent researchers, helping them get established in their careers.
Kala Visvanthan, MD, FRACP, MHA
Johns Hopkins University
Dr Visvanathan is a cancer epidemiologist and a medical oncologist who conducts epidemiological research focused on reducing breast and ovarian cancer incidence and mortality. Specifically she is interested in understanding the underlying etiology of these diseases, genetic and environmental risk factors and implementing early detection and preventive strategies to women in the general and high-risk population.
Her research areas of interest include: the evaluation of non-toxic inexpensive agents for breast and ovarian cancer prevention, evaluating the short and long term effects of oophorectomy, an established preventive strategy, identifying novel breast cancer risk factors to improve breast cancer risk stratification, molecular characterization of precursor lesions of breast and ovarian cancer as a target for prevention, and the conduct of early detection and prevention clinical studies.
Doug Yee, MD
University of Minnesota
Dr. Yee holds the John H. Kersey Chair in Cancer Research. He was previously co-leader of the Women's Cancer Program. He was named Director of the Masonic Cancer Center, University of Minnesota in 2007. Dr. Yee received his MD in 1981 from the University of Chicago. He received his internal medicine training and was Chief Medical Resident at the University of North Carolina. His medical oncology training was done at the National Cancer Institute in Bethesda, Maryland. Prior to coming to Minnesota, he held faculty positions at Georgetown University Medical Center and the University of Texas Health Science Center at San Antonio.
Breast Cancer Care & Research Fund
Michele Atlan is a 7-year breast cancer survivor and a patient research advocate. After her diagnosis, Michele became certified as an Emergency Medical Technician. In 2015, she graduated from Project LEAD, the National Breast Cancer Coalition’s (NBCC) scientific training program, and subsequently took part in the Advanced Project LEAD pilot program. Michele now participates as a frequent Project LEAD mentor to help her fellow patient advocates understand the science of breast cancer.
Currently serving as president of the Breast Cancer Care & Research Fund (BCCRF) in Los Angeles, Michele has participated as a consumer reviewer for the Department of Defense’s Breast Cancer Research Program and is a member of the California Breast Cancer Research Program’s (CBCRP) Advisory Council. Recently, Michele was a finalist and the Audience Award winner for the CBCRP’s “Global Challenge to Prevent Breast Cancer” competition. She co-authored an article expanding on this contest submission that was subsequently published in the International Journal of Environmental Research and Public Health in 2019. Since 2018, she has been an alternate board member of the NBCC and participated in their 2020 Artemis Project research think tank.
Virginia Breast Cancer Foundation
Vernal Branch is a breast cancer advocate who has worked with national organizations like the Department of Defense's Breast Cancer Research Program as well as the National Cancer Institute and the Komen Foundation. She has served on the Board of Directors of the Virginia Breast Cancer Foundation and today she is able to directly pursue her desire to help women access resources for breast cancer through serving on the board of Reach Out for Life and contributing to its effort to provide free breast imaging to low income women. Her travels have taken her to the White House to speak about health care with Michelle Obama and Jill Biden. She also spoken before a congressional committee about how the Affordable Care Act affects cancer patients.
Women of Color Breast Cancer Survivor's Support Project
Shirley H. Brown, MS, JD, is a 22-year Stage III breast cancer survivor. She is a retired educator of the Los Angeles Unified School District, with experiences as an elementary teacher, school psychologist, central office administrator, and adjunct professor at California Lutheran Univeersity. Ms. Brown has worked with numberous public agencies including the California Departmmment Of Education, Los Angeles County Regional Centers, Departments of Mental Health, Children and Family Services, California Children Services and is an active member of community and professional organizations. She is a former member of the Board of Directors of National Breast Cancer Colition Foundation representing Women of Color Breast Cancer Survivor's Support Project, and is a 2001 graduate of NBCC's Project LEAD, Quality Care LEAD, and Clinical Trials.
Ms. Brown is a Scientific Advisor Committee Member to the Dr. Susan Love Research Foundation and has been a consumer peer reviewer since 2006 for the Department of Defense [DOD BCRP], and Susan G. Komen for the Cure for breast cancer research grants, reviewing hundreds of research proposals providing and submitting written critiques and summaries for pertinent areas of the proposals. Ms. Brown has participated as a consumer advocate/navigator on City of Hope Center of Community Alliance for Research & Education Division of Population Science/ breast cancer research grant projects. Ms. Brown is a former member of the Board of Directors for the Women of Color Breast Cancer Survivor's Project, and the City of Hope Community Advusory Member for Breast Cancer Research Projects.
Ms. Brown has attended the San Antonio Breast Cancer Symposium, California Breast Cancer Research Programs and Johns Hopkins University/Cochrane & Campbell Collaborations Summit - Keystone, Colorado as a participant. She has also attended annual NBCC conferences and summits, as a participant, speaker, presenter, panel member, Team Leader and has participated as a NBCC Task Force member - Quality Care, Health Care Reform, Breast Cancer Deadline 2020; Era of Hope as a presenter.
Ms. Brown was recognized by Lifetime Television - Breast Cancer Hero Award - 2005, Sisters Helping Sisters - 2009 and a recipient of the Entertainment Industry Foundation's - Revlon Run/Walk Rise & Honor Volunteers Award - 2013; and by the National Breast Cancer Coalition - Grassroots Advocate of the Year Award - 2016.
Ms. Brown is the mother of two daughters and two sons, and grandmother to four lovely grandchildren.
Metastatic Breast Cancer Alliance
Passion, motivation, and personal experience of living with metastatic breast cancer for the past 8 years, drives Lesley’s desire to partner with communities, researchers and organiza-tions, in aiding the funding of research for a cure, bringing awareness to this over-looked stage of breast cancer and support to those who live daily with Metastatic Breast Cancer. She has been actively involved in metastatic breast cancer advocacy since 2015, training with the inaugural Hear My Voice Volunteer class presented by Living Beyond Breast Cancer. She was invited back as a mentor in 2018 for new advocates and was awarded the Living Beyond Breast Cancer Leadership Volunteer Award in the Fall of the same year. She is the Co-Founder of the Annual Make Good Moves, Climb for a Cure (www.climb-foracure.net) that is held annually in Southern California, and Southern Oregon which funds research for a cure. She enjoys working with researchers and other stakeholders in the metastatic breast cancer field. She is a member of the Metastatic Breast Cancer Alliance, and is asked to speak on her experiences of living with metastatic disease in various capacities. She has always been an advocate, having previously run her own non profit, Dandelion Wishes, Inc, prior to her metastatic diagnosis in 2013. She brought therapeutic art to the marginalized, international and incarcerated communities.
Lesley has transferred that advocacy to her personal life experience with cancer, and desires to extend her advocacy roles to include the underserved and rural communities. She is currently working on a new endeavor entitled Project Life, A Metastatic Breast Cancer Survivorship Initiative, which will address the discontinuity in survivorship programming that leaves out the metastatic patient.
Eva May, MBA
National Cancer Institute, National Breast Cancer Coalition, FORCE
Eva May is an entrepreneurial leader with a passion for meaningful participation in the paradigm shift to patient-powered research and personalized healthcare for all. Prior to her immersion in cancer research and patient community advocacy, Eva was the founder of a national advertising agency, developing successful consumer-centered marketing programs across multiple cultures. In 2008, Eva was diagnosed with Stage 1 breast cancer and subsequently learned that she carries a BRCA2 gene mutation. Her personal breast cancer journey opened her eyes to the world of translational research, and her interest was strong enough that she closed her successful advertising agency and moved to South Dakota to join the leadership team of a startup breast cancer research organization seeded with a $100M gift. She thoroughly embraced the opportunity to regularly interact with scientists and clinicians involved in breast cancer research and treatment, and to personally witness the promise of personalized treatment and care. Since 2014, Eva has dedicated herself to becoming a patient-powered health and research advocate, applying herself in many areas of cancer research and patient community engagement.
Eva is an active member of several national clinical trial steering committees and work groups, including the Breast Immuno-Oncology (BIO) Task Force of the NCI Breast Cancer Steering Committee (BCSC), the NCI’s NCTN Core Correlative Sciences Committee (effective 7/2021) and the Alliance for Clinical Trials in Oncology. She participates as a patient research advocate on several grant-funded research study teams. Eva is also a member of UNC Lineberger Comprehensive Cancer Center’s Community Advisory Board, as well as an Advocacy Core member for the UNC Breast Cancer SPORE. Eva serves as a Patient-Centered Outcomes Research Institute (PCORI) Merit Reviewer and Health Care Horizon Scanning Patient Commenter, as an advocate reviewer of academic research project applications submitted to the Cancer Prevention & Research Institute of Texas (CPRIT), and as a consumer reviewer of research applications submitted to the Breast Cancer Research Program (BCRP) sponsored by the Department of Defense. Eva is a graduate of the National Breast Cancer Coalition's Project LEAD® Institute and has participated in the AACR Scientist ↔ Survivor Program. She is also a volunteer research advocate and a peer navigator for FORCE (Facing our Risk of Cancer Empowered) and an Advocate In Science and grant reviewer for Susan G. Komen.
Eva believes that as cancer researchers and healthcare providers adopt some of the engagement and loyalty-building strategies and tactics that successful marketing companies have used to drive their success, we will see significant improvements in reducing health disparities and improving health outcomes for all. As a research advocate, Eva strives to help develop bi-directional researcher ↔ patient community partnerships, to ensure that study participants reflect the entire patient population, to improve the success of clinical research and to accelerate the discoveries and uptake of treatments that significantly improve patient outcomes. As a member of the Love Research Army Scientific Advisory Committee, Eva seeks to help build member awareness of and interest in participation in inclusive and diverse research studies, in order to speed study recruitment and meaningful discoveries.
Eva received her MBA in Marketing and Finance from Columbia University and her BA in English from the University of North Carolina at Chapel Hill.
Anne Marie Mercurio
Memorial Sloan-Kettering Cancer Center
Anne Marie Mercurio, a SAC member since 2014, has been a volunteer with the Love Research Army for over five years. She serves as a consumer reviewer on the Department of Defense CDMRP and was appointed Scientific Review Office for METAvivor Research and Support commencing with their 2015 grant cycle. Anne Marie reviews manuscripts for The BMJ. A three-time participant in the AACR Scientist - Survivor program, she now serves as an advocate mentor. She has presented posters at annual AACR annual meetings focusing on the role social media plays in facilitating the work of patient advocates and highlighting the importance of patient partners throughout the entire research continuum. She was an invited speaker at a several high profile meetings including AACR and SWOG and is currently serving as a patient advocate on a number of ongoing grants. Sandwiched between her mom, who was diagnosed with metastatic disease decades after her initial primary diagnosis, and her daughter who already had her first scare and is now being followed very closely, Anne Marie is uniquely poised to appreciate the need for research across the entire spectrum: primary prevention, prevention of distant recurrence in early stage patients and prevention of mortality associated with metastatic disease.
South Dakota Breast Cancer Coalition
Patricia (Pat) Haugen, is a 14-year inflammatory breast cancer survivor, and is the National Breast Cancer Coalition (NBCC) Field Coordinator for South Dakota and a graduate of all of the NBCC Project LEAD science training courses. She participated in the NBCC Measuring What Matters Project. She has consumer experience in cancer research peer and programmatic review and currently serves as the Chair of the Department of Defense Breast Cancer Research Program Integration Panel. She has also served as a consumer reviewer for the California Breast Cancer Research Program, and as a member of the National Quality Forum Clinician-Level Cancer Care Steering Committee and the Patient Outcomes Steering Committee. Pat serves as a community representative board member on the Sanford Health Institutional Review Board (IRB) for community cooperative group cancer clinical trials, and is a board member of the National Cancer Institute Adult Central IRB. She recently completed service as the consumer representative to the Advisory Board of the Consumer Operated and Oriented Plan (CO-OP) Program. Pat has served on the South Dakota State Advisory Council for the American Cancer Society is a member of the South Dakota Women's Cancer Network. She also has experience as a public policy advocate and as a SPORE advocate. Pat spent over 30 years in the information technology industry and serves as a board member in higher education and long-term care. She has an undergraduate degree in mathematics and a certificate in public health.
Metastatic Breast Cancer Alliance
Andrea Hutton is a critically acclaimed writer, speaker, and patient advocate. She is the author of Bald is Better with Earrings - A Survivor's Guide to Getting Through Breast Cancer which was published by HarperCollins in 2015. Her work on breast cancer and women's wellness has been featured in such varied outlets as: The Washington Post, Women's Health and Psychology Today. As a breast cancer survivor diagnosed in 2009 with metastatic disease, who has 'been there, had that' Andrea Hutton is on a mission to empower and educate women on how to take charge of their own health. She is also a State Leader for the Young Survival Coalition, a graduate of the National Breast Cancer Coalition's Project Lead advocacy training program, an Alamo Scholar with the San Antonio Breast Cancer Symposium, and a Komen Advocate in Science. Andrea has served as a consumer reviewer for the Department of Defense Breast Cancer Research Program and a peer reviewer for Komen Research grants. She is a member of the Metastatic Breast Cancer Alliance and serves as a co-chair of the Alliance's Information Task Force.
National Breast Cancer Coalition
Debra Madden is a two-time cancer survivor who was diagnosed with Hodgkin's lymphoma as a young adult and with breast cancer nearly 20 years later, which was thought to be secondary to the radiation she had received for her original cancer treatment. She is an active cancer research advocate who is a member of numerous cancer support and research organizations, including the ECOG/ACRIN (E/A) Cancer Research Group's Cancer Research Advocate Committee, Breast Core, Cancer Care Delivery Research Committee, and the E/A Cardiotoxicity Working Group. In addition, she serves on several national grant review committees and advisory panels as a Patient Representative, including for the FDA, the Department of Defense's Breast Cancer Research Program (BCRP), the Love Research Army Scientific Advisory Committee, and the Patient-Centered Outcomes Research Institute (PCORI)'s inaugural Advisory Panel on the Assessment of Prevention, Diagnosis, and Treatment Options. Ms. Madden blogs at 'Musings of a Cancer Research Advocate,' located at https://draemadden.wordpress.com/, and is also a regular contributor for the American Journal of Managed Care (AJMC)'s Contributors' Page as well as AJMC's Evidence-Based Oncology journal. She is also on Twitter at @AdvocateDebM.
Minnesota Breast Cancer Coalition
Christine Norton was diagnosed with breast cancer in 1990 at age 44. In October 1991, Chris and Cher Johnson co-founded the Minnesota Breast Cancer Coalition, a totally volunteer organization dedicated to education and advocacy.
Norton's health advocacy work was spurred by her breast cancer diagnosis but for years she has advocated more widely for quality healthcare that works to eliminate over-treatment.
In addition to serving as president of the MN Breast Cancer Coalition, Norton is on the Board of the National Breast Cancer Coalition, the Scientific Advisory Board of the Avon Foundation, the Board of MN Community Measurement and was appointed by Governor Dayton in 2015 to a second four-year term as a Public Member of the MN Board of Nursing. Chris has served as a peer-reviewer on scientific grants for the Department of Defense, the National Cancer Institute, the Avon Foundation, the University of Minnesota and the Komen Foundation. She is also a consumer reviewer for HealthNewsReview.org
Chris retired in 2005 after nearly 40 years as a high school English teacher. She and her husband have three children and three grandchildren.
Breast Cancer Care & Research Fund
Lori Petitti, B.S., M.B.A. is a retired television and documentary producer with over 30 years of experience in Project Management. She is on the board for the Breast Cancer Care & Research Fund and a volunteer mentor with ABCD and SHARE cancer support. Lori is a graduate of the National Breast Cancer Coalition's Project Lead® Institute and has served as an advocate reviewer for the Department of Defense Breast Cancer Research Program. Lori has also been an advocate observer for the California Breast Cancer Research Program’s grant review. She attended the first International Lobular Breast Cancer Symposium in 2016 and became one of the first members of the Lobular Breast Cancer Alliance. She is committed to research advocacy and mentoring newly diagnosed patients.
Breast Cancer Care and Research Fund
Michele Rakoff, a patient and research advocate, activist and breast cancer survivor for more than 27 years, is Executive Director of the Breast Cancer Care & Research Fund in Los Angeles, California. Ms. Rakoff worked in the clinic for 20 years developing mentoring programs for patients with primary breast cancer and support programs for women living with metastatic disease. She is Vice President of the California Breast Cancer Organizations (CABCO) and Board member of the National Breast Cancer Coalition (NBCC).
Ms. Rakoff has taken advocacy into action. In an effort to impact breast cancer research, she held an advocate seat on the California Breast Cancer Research Program's Advisory Council. She has participated as a peer-reviewer for the Department of Defense Breast Cancer Research Program and collaborates with scientists on their research grants. Currently, Ms Rakoff holds an advocate seat on the California Teacher's Study Scientific Task Force Steering Committee; is a member of the Love Research Army Scientific Advisory Committee and the External Advisory Board of the City of Hope Comprehensive Cancer Center and the community partner on a NIEHS grant. She is a member of the NBCC Artemis Project.
Because public policy issues and legislation have an impact on patients and health care, Ms Rakoff is a NBCC Field Coordinator. She continues to lobby for federal funding for research, access to quality care for all, and ensuring that advocates have a seat at the table everywhere health care decisions are being made.
Representing NBCC Ms. Rakoff traveled to China to meet with the Cancer Foundation of China, Beijing Tumor Hospital and other community hospitals. Ms Rakoff believes that the advocate voice is vitally important and that well educated, trained advocates must be included in every aspect of research, clinical decision-making and public policy issues. Her focus is on NBCC's Breast Cancer Deadline 2020!
Chicago Health Equities Collaborative
Rosemarie Rogers is a 22-year breast cancer survivor. She has been involved over the years with numerous breast cancer support and advocacy organizations. Current, Rosemarie is a member of the Chicago Health Equity Collaborative, a partnership of the Robert Lurie Cancer Center of N.W. University, Northeastern Illinois University and University of Illinois at Chicago. The mission is to advance cancer health equity through meaningful scientific discovery, education, training and community engagement.
METAvivor, Metastatic Breast Cancer Alliance, ABC Global Alliance
In 2008, Kelly Shanahan had everything going for her: a graduate of Bryn Mawr College and the University of Virginia School of Medicine, she had a busy and successful ob-gyn practice in South Lake Tahoe, CA; a precocious 9 year old daughter; and a well used passport from traveling all over the world with her family to attend conferences, with a liberal dose of vacation on the side. When she was diagnosed with stage IIB breast cancer in April, she considered it a mere bump in the road; she returned to work two weeks after her bilateral mastectomy and continued to work all through the four months of chemo.
And for five years, breast cancer was an aside, something to put in the past medical history section of forms. Even when she developed sudden back pain, Kelly never thought it could be breast cancer rearing its ugly head – a pulled muscle, a herniated disc maybe, but not what it turned out to be: metastatic breast cancer in virtually every bone in her body, with a fractured vertebrae and an about to break left femur. Kelly was diagnosed on her 53rd birthday.
Kelly has been extremely lucky, for after an unconventional 14 month course of combination IV chemo and zometa, followed by a more conventional aromatase inhibitor, she has remained NEAD – No Evidence of Active Disease -- since April 2014. Neuropathy from the chemo did cost her her career, but she has found a new purpose in advocacy. Kelly is one the board of directors of METAvivor; a member of the Metastatic Breast Cancer Alliance; a Komen Advocate in Science and a founding member of the Komen Metastatic Breast Cancer Advisory Committee; a mentor for GRASP (Guiding Researchers and Advocates to Scientific Partnerships); and a consumer reviewer for the Department of Defense Breast Cancer Research Program, METAvivor and Komen. She believes disease and stage appropriate people should be involved at every stage of the research process.
Kelly Shanahan is a mother, a wife, a daughter, a doctor, a woman LIVING with metastatic breast cancer.
Department of Defense
Debra Stafford has dedicated her life to advocating for those affected by cancer since her early stage hormone positive breast cancer diagnosis in 2014. She founded, and is the Chief Visionary Officer of the nonprofit, ROAR: Reclaiming Ourselves After Recovery, to support those affected by cancer with four main missions: helping those affected by cancer build a life they love as they navigate their new normal; providing resources and opportunities for metavivors to build the legacy they want to leave behind in this world; providing education and affordable access to complementary therapies; and, a mentorship program for those interested in advocacy, matching their talents and interests with opportunities to serve. Having been a Certified Pilates Instructor for 23 years and working in a physiotherapy setting for 10, Debra has developed a Pilates program for cancer survivors, which addresses both short and long term effects of cancer treatment and prevention of recurrence. Debra has educated herself in the science of cancer through Project LEAD (National Breast Cancer Coalition), Alamo Scholar (Alamo Breast Cancer Foundation at San Antonio Breast Cancer Symposium), and the American Association for Cancer Research Scientist<=>Survivor Program. She has served, since 2017 on the Department of Defense Breast Cancer Research Program grant review, and is moving into both breast and pediatric cancer advocacy at the National Cancer Institute and the US Food and Drug Administration. Debra volunteers as a patient navigator at Hoag Cancer Center and Breastlink, and as half of a pet therapy team with pediatric oncology and neurology patients and their families. Debra is a practitioner of Reiki, Jin Shin Jyutsu, Medical Qigong, and Aroma Acupoint Therapy (AAT), and is a practitioner trainer for both Reiki and AAT. She is employed by Hoag Cancer Center as a Reiki Practitioner and Support Services Provider/Workshop Leader. She has served on panels for the Komen Education Series. Debra sees herself as a warrior against cancer: representing patients' voices to the scientific to community to help find a cure, research grant writing and advocating for funding of breast cancer research, all in an effort to end breast cancer. And, until breast cancer is a disease of the past, she is dedicated to reminding patients that although they may not have control over how and when they die, they do have control over how they live. Through her work, Debra is committed to giving patients the tools, support, and confidence they need to live life on their own terms and build a life they love.
Male Breast Cancer Coalition
Michael Singer, a Bronx native currently living in Throggs Neck, is a six-year male breast cancer survivor. He's a product of the Bronx school system and had a 31-year career with the federal government as a Facility Maintenance Manager. Michael underwent a mastectomy after discovering a cyst under his left nipple in 2010. He's a member of the Male Breast Cancer Coalition, a not-for-profit patient advocacy organization, bringing everyone together to educate the world about male breast cancer. The coalition provides men and their families with resources to navigate through what is usually a woman's only club. As a member of the MBCC, Michael and his wife Patty travel around the country, with special pins and bracelets in hand, sharing his personal story to raise awareness of male breast cancer. He's a graduate of the Project Lead program sponsored by the National Breast Cancer Coalition and has participated in the Department of Defense Congressionally Directed Medical Research Program. Michael was also selected as a 2016-2017 Ford Warrior in Pink Model of Courage for Ford Motor Company. Michael will be featured in the upcoming series 'Men Have Breasts Too.' From short documentaries with men who have been diagnosed with breast cancer, to the latest news and information from medical experts and stories from family members of men lost to the disease, the impactful series will be launching soon. Thanks to Michael, New York State recognizes the 3rd week of October as Male Breast Cancer Awareness Week. Michael meets with scientists, does countless interviews (CBS News, People, Headline News, NY Daily News just to name drop a few), attends conferences and has dedicated his life to helping others. He wants all men to know they should routinely check themselves and be aware that early detection is a key to surviving this deadly disease.
Living Beyond Breast Cancer, National Breast Cancer Coalition
Janice was diagnosed with early stage Ic triple-negative breast cancer in 2011, with a metastatic recurrence of TNBC in mid-2016. A retired nurse, her passion for research and scientific learning led her into patient advocacy less than one year following her MBC diagnosis. A self-proclaimed lifelong learner, she is continually seeking knowledge about her disease by attending multiple scientific-based breast cancer conferences each year. In addition, Janice has participated in several advocacy training programs including Living Beyond Breast Cancer’s Hear My Voice Outreach program, and NBCC’s Project LEAD. In 2019, she attended the San Antonio Breast Cancer Symposium as a scholarship recipient of the Alamo Breast Cancer Foundation. In 2021, she was accepted into the ASCO – Conquer Cancer’s Research Advocacy Network’s Consumer Grant Reviewer Training Program which will add to her knowledge base for cancer research grant funding.
In her spare time, Janice enjoys reading, swimming, traveling, the beach, being outdoors in the beautiful Florida sunshine, time spent with friends and visiting with her two adult children and three precious grandchildren. Because she has had no evidence of disease since 2016, unlike most with MBC, she is on no systemic treatment which allows her to live life to the fullest. Since her MBC diagnosis in 2016, Janice’s mantra is that she remains realistically hopeful about her future while living with MBC. She openly and willingly shares her breast cancer story to spread hope to others within the metastatic breast cancer community
California Breast Cancer Organizations
Sandy was diagnosed with breast cancer in 1984. In 2000 she was a founder of the Y-ME Affiliate in Northern California and currently arranges a monthly educational program for the Breast Cancer Care and Research Fund / Northern California. She is president of California Breast Cancer Organizations (CABCO) and represent them on the National Breast Cancer Coalition's Board of Directors. She is the consumer editor for the Breast Cancer Group of the Cochrane Collaboration. She has reviewed grants for the Department of Defense Breast Cancer Research Program; she serves on the External Advisory Task Force for the California Teachers Study; is on the Love Research Army Scientific Advisory Commitee; has served on the Council for the California Breast Cancer Research Program. Since she has a background in research, she is frequently consulted as a consumer on research proposals. In her previous employment she worked using a mouse model to study the muscles affected by Duchene Muscular Dystrophy.