Meet the Family Advisory Council members
Together, the volunteer members of the Boston Children's Hospital Family Advisory Council (FAC) have decades of experience navigating pediatric health care. These individuals joined the council to share the experiences, knowledge, and insights they've gathered along the way. In collaboration with FAC leadership, physicians, nurses, hospital administrators, and support staff, members of the Family Advisory Council work hard to improve aspects of patient and family experiences for all who seek care here at Boston Children’s.
Interested in joining the council? Fill out our Family Advisory Council Interest Survey and one of our team members will reach out to connect with you.
Member since: 2016
Experience/Areas of Interest: pediatric hematology/oncology, Dravet syndrome/neurology/epilepsy/rare disease, research, clinical trials, Emergency Department, Child Life
Natasha Aljalian is mom to Gabriel (born 2008) and Mary (born 2013). Gabriel was diagnosed with B-Cell acute lymphoblastic leukemia in 2013. He was cared for by the Boston Children’s Pediatric Hematology/Oncology and Blood Disorders Center, in conjunction with Dana Farber’s Jimmy Fund Clinic, for three years while he underwent cancer treatment and care for after-effects of treatment. Mary was diagnosed in 2015 with Dravet Syndrome, a rare form of epilepsy, and is cared for by the Department of Epilepsy and Neurophysiology at Boston Children’s.
Natasha and her family are grateful for the care that Gabriel and Mary have received from almost every department at Boston Children’s. She feels fortunate to have formed partnerships (and friendships) with her children’s care providers, and she has appreciated being a valued member of the team for her children’s treatment plans.
Natasha joined the Family Advisory Council to share her insights as a patient parent and to partner with Boston Children’s in working to improve aspects of the care experience for all patients and families. She is also a member of the Boston Children’s E-Advisors Program.
Brenda Allair (emeritus member)
Member since: 2012
Experience/Areas of Interest: pediatric solid organ transplant, rare diseases, palliative care, visual impairment/blindness and complex health needs, transition to adulthood
Brenda is the parent of three young adult children, including her youngest, Jill, who was born with a rare genetic condition, WDR-19 related disorder. Jill was initially seen at Boston Children’s Hospital when she was just 8 weeks old, and she has continued to be supported by the physicians, nurses and other staff in multiple outpatient clinics over the years. Jill had a kidney transplant when she was 15 months old, and in 2020 she received a liver transplant. Jill is followed closely by Pediatric Transplant Center, and over the years Brenda and her family have developed friendships with other Boston Children’s Hospital transplant families. Having experienced over two decades of care with Jill at Boston Children’s, Brenda is grateful to the many clinicians, staff, and other providers who bring compassion, humor, dedication, and excellence in care to their work every day.
Brenda joined the Family Advisory Council in 2012 to support the hospital’s many initiatives to increase parent and family engagement and leadership. Brenda is passionate about creating and sustaining programs and initiatives that support the needs of diverse families and highlighting the needs of families and caregivers of children with complex medical needs.
Member since: 2019
Experience/Areas of Interest: tracheobronchomalacia, airway stents, endocrinology, common variable immune deficiency, CAT/CR, IVIG, neurology, neuro-opthamology, neuroimmunology, hemicrania continua, intracranial hypertension, feeding/swallowing disorders, hematology, genetics, allergy, G-Tube
Katie lives in Boston with her husband, Rick, and son Jack. Following his birth in 2015, Jack was admitted frequently to another Boston hospital for respiratory illness. In 2017, without answers as to why Jack’s health was so poor, Katie and Rick brought Jack to Boston Children’s, where they found out that Jack had been born with several airway abnormalities. Since then, Jack has had many surgeries to fix parts of his airway and his lung. Jack also receives care for neurology challenges and has an immune deficiency that brings him to Boston Children’s for monthly treatment.
Katie serves on the FAC because she wants to leverage her experiences at Boston Children’s Hospital and elsewhere to help improve aspects of the patient and family experience for others. Katie sees this as her opportunity to give back to a hospital that has been life changing for her family. Since joining the FAC in 2019, Katie has taken part in many projects that have had direct impacts on the care that Jack and other patients receive at Boston Children’s. This is something that Katie finds incredibly rewarding. She also serves on the Emergency Department FAC and E-Advisors Program.
Member since: 2019
Experience/Areas of Interest: hematology, emergency medicine, infusion therapy
Kate is the mother of two children. In 2017, her 16-month-old son was diagnosed with severe hemophilia A, a genetic bleeding disorder for which there is no cure. Due to the outstanding care that her son has received from Boston Children's Hospital, he is thriving today. Kate joined the Family Advisory Council in 2019 with the hope of using her family's experience to improve the care and experiences of other Boston Children's families.
Member since: 2021
Experience/Areas of Interest: pediatric nephrology, endocrinology, genetics, nephrotic syndrome, chronic kidney disease, autism, neurodiversity, non-speaking patient advocacy, CAT/CR, creating a sensory friendly environment
Jackey is mom to Keith (born 2016), who has two rare diseases: nephrotic syndrome, a protein-spilling kidney disease, and Chromosome 15q11.2-13.1 duplication syndrome (Dup15q), a genetic abnormality causing autism and intellectual disability. Keith is followed by the Boston Children’s renal team and spent much of 2019 and 2020 either inpatient or visiting the hospital for frequent infusions. Keith is also followed by Genetics as more is learned about his 15th chromosome duplication.
The Bennetts are grateful for the wonderful care Keith receives at Boston Children’s. Keith has been able to have some fun experiences at the hospital, including making gingerbread houses with Rob Gronkowski, visiting Santa, and a fourth birthday party from the CAT/CR nurses.
Jackey joined the Family Advisory Council because she has a passion for advocacy and an immense appreciation for the staff at Boston Children’s and their efforts to create a positive healing environment. She aims to give back by serving as a voice for families of children with unique sensory and communication needs in conversations about improvement efforts across the hospital. Jackey also wishes to empower parents to access the services their children need, through partnership with Boston Children’s staff who provide care and comfort to patients and families, in order to create a positive and trauma-free experience for their kids.
Jackey; her husband, Tony; and son Keith live in Windham, New Hampshire.
Member since: 2020
Experience/Areas of Interest: GI, feeding disorders, swallowing disorders
Chava is a wife and mom to three children, two boys and a girl. Shortly after her middle child was born, both of her boys started seeing the Aerodigestive Center for feeding challenges. Right from the first appointment, Chava was impressed at how collaborative the doctors were, and how they incorporated her questions and concerns in the treatment plan. She knew right away that Boston Children's would be a place of healing and hope for her boys. The youngest of her three children, a daughter, also receives care at the Boston Children’s Aerodigestive Center.
Chava wants to use her own experiences at Boston Children’s to help make patient and family experiences even better. She joined the FAC to help ensure families feel supported and heard.
Chava lives with her husband and kids in south Florida, where she is involved in the Jewish community and is raising her children.
Lisa Burgess (emeritus member)
Member since: 1989
Experience/Areas of Interest: multi-complex care, palliative care, home care nursing, research, clinician/family communication, government relations, SIM Lab teaching and technology, transition, anticipatory grief/bereavement
Lisa has been married for 30 years to her husband, Mark, and is the mother of three sons who have all received care at Boston Children’s. Lisa’s eldest son, Benjamin, was a patient in Primary Care and Ophthalmology. Her middle son, Jamie, has been a multi-complex patient since 1985, and her youngest son, Dakota, was diagnosed with autism.
Lisa’s passion for true family-centered care for medically complex patients began in the mid-1980s, shortly after the birth of Jamie. His journey includes 24 diagnoses (primarily cardiac, pulmonary, renal, neurological, and immunological) and many years later, a diagnosis of an extensive chromosome deletion. Jamie has had more than 500 admissions and continues to have multiple appointments at Boston Children’s, although some of his care was transitioned to an adult hospital in Boston.
Lisa has more than three decades of experiential knowledge helping families navigate the system, from scheduling appointments to finding a range of supports. Lisa believes that empathy and communication are key tenets of patient- and family centered care, as evidenced with her children and countless others. She has worked on many projects during her time on the council, including Family Centered Rounds, the Children’s Hospital Advocacy Network Legislative Breakfast in Washington, D.C., and Aligning Family-Clinician Expectations During Pediatric Surgical Informed Consent.
Serving as member of the Family Advisory Council and E-Advisors program, Lisa has found ways to help make meaningful change for the patients and families that come to Boston Children’s for answers every day.
Member since: 2021
Experience/Areas of Interest: pediatric oncology/neuroblastoma, bone lesions, hematopoietic bone marrow transplants, endocrinology, allergy, dermatology, MIBG/CT/MRI/z-ray, neurology/developmental delays, urology, ophthalmology, orthopedic, cardiology/EKG/Lipid clinic, audiology/otolaryngology, in/outpatient surgery, home care, central line care, long-term inpatient stays
Lisa Cleary lives in Franklin with her husband, Greg, and her two boys, Jack and Nicholas. In April 2015, 22-month-old Nicholas was diagnosed with stage 4 high-risk neuroblastoma. He immediately started his treatment on the oncology unit at Boston Children’s Hospital, in conjunction with the Jimmy Fund Clinic. Nick has been in remission since 2016 and is thriving. He is followed by multiple specialists at Children’s to manage side effects and other medical issues. In 2017, Jack, then 7, was diagnosed with a bone cyst after breaking his wrist. He is doing great after several procedures, under the care of the Orthopedic Specialists. Lisa felt humbled by the overwhelming support from the staff since day one, and found comfort in how much the care providers valued parental opinions and feedback.
Since 2015, Lisa has connected with and advocated for many families whose children are battling cancer. She has also been involved with several fundraisers and awareness projects for Boston Children’s Hospital, her favorite being Moms on a Mission, co-founded by Lisa and other “momcologists” whom she met during their children’s treatment. Lisa joined the Family Advisory Council as a way to give back to the organization that not only saved her son, but helped her family cope during their darkest days.
Prisnel Dominique (emeritus member)
Member since: 2018
Experience/Areas of Interest: Neurology, Neurosurgery, ENT, Infectious Disease
Mr. Dominique is a father of three living in Sharon, Massachusetts. Father to Jayden, Jasmine, and Arrivee, the Dominique family went through a severely traumatic experience when Jasmine was diagnosed at 7 with a condition called Pott's Puffy Tumor. Prior to coming to Boston Children’s, several different types of antibiotics were given to Jasmine to treat symptoms associated with a sinus infection. Prisnel’s wife, a nurse, noticed that her daughter's forehead was beginning to protrude and that she was not improving with antibiotics. A decision was made to take Jasmine to the Emergency Department at Boston Children’s. Within minutes of seeing a physician, they mentioned what they thought it might be and ran tests to validate that Jasmine had a Pott's Puffy Tumor. Because of the time that had elapsed during initial efforts to treat Jasmine the tumor had progress to a point where Jasmine required emergency surgery. Prisnel was impressed by how the nurse educator explained to Jasmine, in a way she could understand, what her surgery would entail. The conversation ended with the nurse educator explaining to Jasmine that she would sort of be like a unicorn with no horn. That seemed to make perfect sense to Jasmine! Jasmine’s procedure was successful, and the care that she received enabled her to return to her normal activities following a recovery period. It’s this and 100 little positive stories nested within that have put Boston Children’s in a special place in Prisnel’s heart. Saving his daughter’s life wasn’t enough. Along the way staff made her happy, safe, and even helped her have a little fun along the way.
Member since: 2022
Experience/Areas of Interest: Autism, Ehlers-Danlos syndrome, Opthalmology, Blue Cone Monochromacy, Metabolism Program, Psychiatry, Rheumatology and Neuro Immunology, homeschooling
Alisha is mom to four amazing boys, all of who have received care at Boston Children’s. Alisha’s eldest son often needed care for illnesses as a young child. Her three younger boys have Ehlers-Danlos syndrome, a condition that effects their connective tissues, and autism. Alisha’s youngest two sons have retinal disease, and one of the boys has bipolar disorder, OCD, and additional challenges. Homeschooling plays a big part in this family’s life and how Alisha navigates the boys’ medical needs.
Alisha has years of experience coordinating the complicated care her sons need at multiple hospitals and medical practices. As the list of medical specialties supporting her sons continued to grow and their needs became more complex, she decided to bring her sons’ care under the umbrella of Boston Children’s.
Alisha joined the Family Advisory Council to represent her family and others in conversations that will impact Boston Children’s efforts to improve care experiences across the hospital.
Member since: 2019
Experience/Areas of Interest: congenital hypothyroidism, managing chronic conditions, Milagros Para Ninos, transition of patients returning to school after extended absence
Steve is the proud father of four wonderful children. He and his wife. Lauren, consider themselves incredibly fortunate to have had the opportunity to bring their oldest son to Boston Children’s Hospital when he was diagnosed with congenital hypothyroidism at just 5 days old. As new parents, they were anxious and unaware of what this would mean for their baby boy and their family, but knew that the best place to support him moving forward was Boston Children’s Hospital. At their first meeting in the Endocrine Clinic, Steve and Lauren were overwhelmed with the compassion and support of their son’s care team. The time spent educating Steve and Lauren, reassuring them as new parents, and simply listening to their questions and thoughts is something that they haven’t forgotten.
Steve’s position on the FAC is one that represents his family’s appreciation for Boston Children’s and all that the hospital provides to families. At the same time, it is a way for his and Lauren’s passion for Boston Children’s to be shared with others.
Valerie Fleishman (emeritus member)
Member since: 2012
Experience/Areas of Interest: liver disease, GI clinic, radiology, endocrine, emergency department, digital health, care coordination, patient and family experience, patient safety and quality
Valerie is the mother of two children. In 2004, at just 8 weeks old, her son was diagnosed with biliary atresia, a rare, chronic liver disease. He underwent immediate surgery at Boston Children’s and later, in 2017, received a new liver. He continues to be cared for by the Gastroenterology and Transplant teams and serves on the hospital's Teen Advisory Council.
Valerie served as past parent co-chair and serves on the Patient Care Assessment Committee. Her deep connection to Boston Children’s comes from her family’s experiences with the doctors, nurses, and other staff and the extraordinary care they have provided her son. She is passionate about advancing patient-centered care and working in partnership with Boston Children’s to improve the patient and family experience.
She lives in Newton, Massachusetts, with her husband and two children.
Serena Hadsell (emeritus member)
Member since: 2014
Experience/Areas of Interest: ICU, ECMO, outpatient cardiology, high reliability
Serena is the mother of two children, Julia and Sebastian. In late 2013, her daughter, then nearly 4 years old, was transferred to the Boston Children’s Medical/Surgical Intensive Care Unit (MSICU), where her breathing difficulties from RSV required advanced intervention. She spent six days on ECMO; the Extracorporeal Membrane Oxygenator takes over the function of the heart and lungs while the body heals. Since her recovery, Julia has been cared for by cardiology and the Cardiac Neurodevelopmental Program.
Serena feels immense gratitude for the expertise and care that Boston Children's offers. She joined the Family Advisory Council in 2014 and, for many years, represented family voices on the hospital’s largest cultural initiative, the High Reliability Initiative, which aims to eliminate preventable harm to patients and employees. Serena seeks to bring to light the emotional needs of patients and families. On the weekends, Serena can be found walking in the woods with her husband and children, listening to the woodpeckers and enjoying the stream near her house.
Member since: 2022
Experience/Areas of Interest: intensive care unit, inpatient care, experimental therapeutics unit (clinical trial unit), psychiatry, chronic fatigue, sleep apnea, complex chronic illness, autism spectrum, vascular anomalies, increasing awareness about special needs through education
Jinah is the mother of two boys, Noah (born 2000) and Isaac (born 2004). Isaac, born with his medical condition, was called “an enigma” by his doctors in Australia, who later named his condition PUVA — previously unnamed vascular anomaly.
In 2015, Jinah and her family relocated from Melbourne, Australia, to the Boston area so that Isaac could receive care through the Boston Children’s Vascular Anomalies Center. At age 15, after many tests over a number of years, Isaac was diagnosed by his Boston Children’s team with PROS — Pik3ca overgrowth spectrum, a genetic mutation that is a major part of his healthcare.
Jinah, who spends much of her time managing Isaac’s medical care and education, joined the Family Advisory Council as a way to give back. As a family advisor, Jinah shares her thoughts, feedback, and pieces of her family’s journey so that they can be woven into improvements here at Boston Children’s.
Member since: 2012
Experience/Areas of Interest: Complex chronic illness, chronic lung disease, care coordination, home oxygen, G-tube, home care nursing, durable medical equipment, feeding/swallowing/voice challenges, long-term inpatient stays
Katie Litterer is the mother of identical twins, Sophie and Maddie, born in 2008. After coming to Boston Children’s from an out-of-state hospital when they were 4 months old, both girls have received a great deal of care for complications associated with their prematurity and complex chronic illnesses.
Katie served on the Neonatal Intensive Care Unit (NICU) Family Advisory Council (2009-11) before joining the hospitalwide Family Advisory Council in 2012. Her journey led her to join the staff at Boston Children’s where she has worked to support the Family Partnerships Program, part of the Office of Experience, since 2016.
Katie lives with her husband, Paul, and their daughters outside of Boston. She is incredibly grateful for the care that Maddie and Sophie continue to receive at Boston Children’s. Katie also strongly believes that by welcoming the voices of our patients and families into improvement efforts here at Boston Children’s, we will find better solutions for those that we care for.
Member since: 2017
Experience/Areas of Interest: integration care, kidney disorders, G-tube, feeding/swallowing difficulties, vision impairment, speech/AAC, home care nursing, complex care
Esterlina is a mother of a young son named Ian. At 4 months old, he was diagnosed with Lowe syndrome, a rare genetic condition that affects the eyes, the kidneys, and the brain. Since her son’s first surgery at 5 weeks, Esterlina has spent countless hours navigating Boston Children’s Hospital, including inpatient, ambulatory, and ER, as well as therapy services. She is grateful for the excellent attention and care she and her son have received at Boston Children’s.
As a result of her journey with her son, Esterlina decided to embark on a new career helping families going through similar circumstances. To complement her personal experience, in 2016, she completed the Leadership Education in Neurodevelopmental and other Disabilities (LEND) Program at Boston Children’s. This is a multidisciplinary, family centered fellowship that covers health and cultural issues related to disabilities, public resources, and policy initiatives. In 2017, Esterlina joined Boston Children’s as an employee, taking on the role of Family Partnerships Coordinator, concentrating her work on developing projects to support and empower Latino patient families who receive care here at the hospital.
Esterlina lives with her husband and son in Medford, Massachusetts, where she advocates for her family within the education system, as well as community and social activities. But, especially, she continues coordinating the care of her son’s complex health condition.
Member since: 2019
Experience/Areas of Interest: NICU, prematurity, inpatient stays, home care, necrotizing enterocolitis, surgery, ophthalmology, and neurology
Emily lives in Franklin, Mass., with her husband, daughter, and son. Emily’s daughter became a patient at Boston Children’s Hospital when she was born prematurely and developed necrotizing enterocolitis (NEC) at just 5 days old. In total, Emily’s daughter underwent four surgeries and was inpatient for 10 weeks. She received follow-up care with various Boston Children’s specialties for needs resulting from her prematurity.
Emily and her husband feel eternally grateful for the care their daughter received at Boston Children’s Hospital, and feel confident that their daughter is alive and thriving because of the incredible treatment at Boston Children’s Hospital. Emily is honored to be able to give back by becoming involved with the Family Advisory Council. She is also a member of the Boston Children’s Hospital E-Advisors Program.
Susan McCarthy (emeritus member)
Member since: 2017
Experience/Areas of Interest: complex medical care, pediatric palliative care, home care nursing, epilepsy, home parenteral nutrition program, and bereavement
Sue lives in Walpole with her husband, Joe, and is a mom to three children: Matthew, Daniel, and Caitlin. At the age of 1, Caitlin was diagnosed with mitochondrial disease and at the age of 5, with Rett Syndrome. Caitlin spent a great deal of time at Boston Children’s, both inpatient and outpatient, and received excellent care from the Gastroenterology, Epilepsy, Complex Care, Palliative Care, Neurology, Nephrology, Orthopedics, Endocrine, Home Parenteral Nutrition, and the C.A.P.E team. Sadly, Caitlin passed away in March 2020. Sue and Joe remain deeply grateful to all of the doctors and nurses at Boston Children’s who cared for Caitlin for so many years, and look forward to continuing to support the hospital.
Sue is particularly passionate about projects which aim to help children with complex medical needs both inpatient and at home. In many ways, Sue pioneered a hospital-at-home model for Caitlin, doing the research and advocacy work so that Caitlin’s needs were met and so that Caitlin was able to live as normal a life as possible at home with her family. Sue hopes to use her knowledge and experience to help other families in similar situations.
Connected with her work as an FAC member, Sue currently serves on the Practice, Quality, and Outcomes Council and the Safety Committee for Central Lines and Catheters. In 2019, she presented alongside Boston Children's safety and quality leaders at the 2019 Patient Safety Forum. Sue also lends her voice through the E-Advisors Program.
Member since: 2012
Experience/Areas of Interest: tracheostomy, G-Tubes, home nursing, durable medical equipment navigation, NICU/ICU, coordinated care, parent-to-parent networking, esophageal atresia, infusion therapy, medical coping psychology, laryngeal cleft, posterior tracheopexy, pain clinic, and Children’s Miracle Network
Sarah Morris is the proud mother of twins, Drew and Emma, born prematurely in 2008. Emma has spent more than 400 nights at Boston Children’s Hospital. Emma was born with esophageal atresia, a type 3 laryngeal cleft, and a primary immune deficiency that brings her to Boston Children’s for monthly infusions. Emma has been able to receive multiple lifesaving surgeries that were first performed at Boston Children’s Hospital.
Sarah has had to learn how to care for a child who does not fit under one specific diagnosis and the post-traumatic stress that comes with it. She has become a strong advocate for her children and is able to skillfully navigate the medical world. She has also worked alongside the Boston Children’s government relations team to help support growth within the hospital. She feels that, as a caregiver, she has been given one of the most amazing jobs which brings surprises every day.
Giving back to Boston Children’s Hospital has always been a priority for Sarah and her husband. Both are former members of the NICU Family Advisory Council and both have found individual avenues over the years to bring the parent voice into different areas of the hospital. Emma has learned to share her story over time. She was named the Boston Children’s Miracle Network Champion for 2020 and 2021.
Member since: 2020
Experience/Areas of Interest: allergy, orthopedics, cardiology, Emergency Department, psychiatry
Katie is a mother of three children, two of whom have received extensive medical care at Boston Children’s. Her elder son was born with a rare congenital condition that required surgery to restore his ability to walk without pain. When researching providers, Katie and her family found Boston Children’s was one of a few hospitals nationwide with surgeons experienced in treating her son’s condition. Her younger son has a congenital heart condition and is also managing antibiotic allergies to almost every class of antibiotics. Katie is grateful for the excellent care her boys continue to receive from orthopedics, allergy, and cardiology.
Katie has a professional background in medicine and joined the FAC to bring her perspective of having navigated the medical system as a provider, and as a parent, to the council.
William O’Donnell (emeritus member)
Member since: 2012
Experience/Areas of Interest: pulmonary hypertension, cardiology, high reliability organization
Bill lives in Medford, Massachusetts, with his wife and daughter, Shannon. Shannon was diagnosed with idiopathic pulmonary hypertension in 2001 has been a patient at Boston Children’s ever since.
Bill feels it’s imperative to give back to the hospital that saved his daughter’s life. In addition to being a member of the Family Advisory Council, Bill and his family have been involved in several fundraisers, including Shannon being a patient partner for marathons. Bill is an avid blood donor and encourages everyone who is eligible to donate.
Member since: 2019
Experience/Areas of Interest: rare genetic conditions, autism, assistance with non-verbal communication, epilepsy
Erin Poirier is a wife and mother of two daughters, Lily and Elise. At very young ages, both girls presented with developmental delays, physical delays, and epilepsy, and were also non-verbal. For many years Lily and Elise were considered “mysteries” to their team in the Neurology Department at Boston Children’s. After 6½ years of searching, both girls were diagnosed with a rare genetic condition called SYNGAP1. Currently, Lily and Elise are two out of 250 individuals in the world with this diagnosis and only the second known sibling set. Erin and her husband, Andrew, are grateful for both the expertise and persistence of their Boston Children’s team for finding the answer to their question of “why?”
Erin joined the Family Advisory Council as a way to help other families on their journey at Boston Children’s and to have a voice in a place that matters most to her family.
Member since: 2020
Experience/Areas of Interest: complex care, managing a home “ICU” setting, IEP for cognitively fine physically disabled children, coordination between physicians, specialty drug, insurance, infusion, respiratory, enteral, home care
As a mother to a complex care child with an orphan disease called infantile pompe, Padmaja has been in immersed in complex care and related issues for over a decade. For her, the lobby of Boston Children’s is the "lobby of hope." It is truly humbling to see the depth of skills, dedication, and commitment of the physicians and staff to help children with various disorders. Seeing this "mission"-driven work is what motivates Padmaja to volunteer at Boston Children’s.
Padmaja and her family experienced a steep learning curve as one of the first patients at Boston Children’s dealing with an orphan disease that was administered a life-saving therapy under clinical trials. The drug has since been FDA approved and continues to be administered through infusion.
The outstanding and continuing support of various physicians and staff has helped Padmaja’s family to navigate this unique journey.
Member since: 2022
Experience/Areas of Interest: Stroke, Hemiplegia, Botox, CIMT, Orthopedics/Physiatry, Stroke and Cerebrovascular Center, NICU, Neurology, Physical/Occupational Therapy, Boston O&P (orthotics/bracing), Opthalmology, Early Intervention, transition to public school, and coordination of care
Suzanne lives in Boston's Metrowest with her husband and their two children. Her son is a perinatal stroke survivor who has been followed by his team at Boston Children’s Hospital since he was just a few days old. Suzanne and her family have a very deep appreciation for their son’s care team who have consistently and compassionately worked together, even across medical specialties, to allow him to thrive.
Finding a way to give back to Boston Children’s Hospital is an important piece of the journey for Suzanne. She has spoken at the Stroke and Cerebrovascular Center’s family day to share her son’s experiences with other families of stroke survivors. As a FAC member, Suzanne is excited by the opportunity to work with other family advisors and hospital staff to improve care experiences for patients and families who come to Boston Children’s. Suzanne is also a member of the hospital’s E-advisors Program. On the weekends she enjoys being with her family, outdoor adventures, fixing up the family's old farmhouse, and traveling.
Member since: 2018
Experience/Areas of Interest: cardiology, in- and outpatient visits, transition to adult care, Boston Adult Congenital Heart (BACH) and Pulmonary Hypertension Team
Erin Sullivan has been a patient at Boston Children’s Hospital since the day she was born. Erin had open heart surgery at 3 months old and has been followed by Boston Children’s cardiology ever since, requiring the expertise that cardiologists trained in both pediatrics and adult cardiology can provide.
Erin is grateful for the excellent care she has received at Boston Children’s Hospital. Erin volunteered at Boston Children’s Hospital during high school and college, and joined the Family Advisory Council to bring her patient perspective to the group.
Erin has spent most of her career in healthcare research and education. In her free time, she enjoys running, spinning, yoga, and adventures with her partner, Matt, and miniature golden doodle, Sully.
Aimee Williamson (parent co-chair)
Member since: 2014
Experience/Areas of Interest: spina bifida, neurosurgery, orthopedics, urology, plastic surgery, complex care
Aimee Williamson is the mother of two children, Colton and Lena. She and her husband, Rob, lived in Colorado when both children were born, Colton in 1994 and Lena six years later. Lena was born with lipomyelomeningocele, a form of spina bifida. After an initial surgery at 7 weeks old to untether her spinal cord, Lena’s medical challenges were well controlled for most of her early years.
In 2007, Aimee and her family moved to Massachusetts, and Lena has received medical care at Boston Children’s ever since. A growth spurt uncovered a retethering of her spinal cord in 2011, with new losses in function. Lena’s medical needs became more frequent and more impactful to her daily life, often requiring surgeries, hospitalizations, and frequent visits to her Boston Children’s specialists.
Throughout these challenges, Boston Children’s has supported the family clinically and beyond, giving Lena every chance to thrive. Lena previously served as a member of the Boston Children’s Teen Advisory Committee, and is now navigating much of her medical care independently as a young adult.
Aimee is grateful for the dedication, kindness, and responsiveness of physicians, nurses, and other staff across the hospital. She joined the Family Advisory Council as a way to give back to the hospital for all the time and effort providers have given to her family over the years. Currently serving as the parent co-Chair, Aimee has been involved with a variety of Boston Children’s committees and projects over the years, including work related to patient experience, access, research, and safety.
Hospital leadership and staff members
Lisa Rubino, MBA
Lisa Rubino is the Director of Patient Experience at Boston Children's Hospital. Key components of her work include managing the hospital’s patient and family experience surveys and overseeing the Family Partnerships Program. Lisa also plays an active role supporting the Family Advisory Council, both from an administrative and communications standpoint.
Sara Toomey, MD, Mphil, MPH, MSc
Dr. Toomey serves as Chief Experience Officer (CXO) at Boston Children’s Hospital. Together with Marcie Brostoff, she leads the Office of Experience. Dr. Toomey is an Assistant Professor at Harvard Medical School and in the Division of General Pediatrics at Boston Children’s Hospital. She is a general pediatrician and health services researcher. Dr. Toomey is the managing director of the AHRQ/CMS-funded Center of Excellence for Pediatric Quality Measurement at Boston Children’s Hospital. As part of the center’s work, she is also a member of the core team tasked with developing a measure of pediatric inpatient experience of care, the Pediatric Consumer Assessment of Healthcare Providers and Systems (Pediatric HCAHPS) Survey.
Dr. Toomey serves as the physician liaison between the Boston Children’s Hospital Family Advisory Council and the enterprise. She also currently practices inpatient and outpatient pediatrics.
Jonathan Whiting, DNP, RN, CCRN
Jon Whiting is Vice President and Associate Chief Nurse of Clinical and Patient Care Operations at Boston Children’s Hospital. Jon serves as the Leadership Co-Chair of the Boston Children’s Hospital Family Advisory Council. In partnership with the Chief Experience Officer at Boston Children’s Hospital, Jon leads the Office of Experience.
Jon provides system-level leadership to advance nursing and hospital-wide initiatives ranging from safe and effective care delivery for a broad scope of patients and care services to providing organization-wide leadership during emergencies, including COVID-19. Jon is passionate about improving aspects of patient and family care experiences, and he is committed to partnering with patients and families to do so.