Elizabeth Lee
B.Sc., R.N., BCPA Candidate
Empowered Choice

Elizabeth Lee
B.Sc., R.N., BCPA Candidate
Empowered Choice
Advocate Location
Gilbert , AZ 85234
Specialty
Medical Guidance
Other Services
Survivor Support
TeleAdvocacy Available
Offers FREE Initial Consultation
*Greater National Advocates Terms of Use Apply
How I Can Help
Elizabeth Lee provides comprehensive patient advocacy services, specializing in reproductive healthcare, infertility, high-risk pregnancy, perinatal bereavement, and complex medical conditions, including rare diseases. With a deep understanding of both the medical and emotional aspects of these journeys, she helps patients and their loved ones navigate the healthcare system, ensuring they receive the information, support, and care they deserve.
In reproductive medicine, Elizabeth assists individuals and couples facing infertility, guiding them through treatment options, insurance challenges, and the overwhelming decision-making process. She advocates for patients pursuing IVF, donor conception, surrogacy, and fertility preservation, ensuring they have access to evidence-based information and ethical care.
She also supports individuals experiencing pregnancy complications, miscarriage, or loss, providing compassionate navigation through a difficult and often isolating process.
Beyond reproductive healthcare, Elizabeth advocates for those facing medical uncertainty, misdiagnosis, and systemic barriers to care. Having personally endured the challenges of navigating an underinformed medical community, she understands the frustration, fear, and exhaustion that come with fighting for proper treatment.
She helps patients secure accurate diagnoses, access specialists, and communicate effectively with providers, empowering them to take control of their healthcare journey.
Elizabeth also supports families and caregivers, ensuring they have the tools to advocate for their loved ones while managing the emotional and logistical burdens of complex care. Whether navigating insurance denials, coordinating multidisciplinary teams, or simply providing a knowledgeable and empathetic voice in overwhelming situations, she is committed to making the healthcare system more accessible and patient-centered.
Her mission is simple: to ensure that every patient has the knowledge, autonomy, and support they need to make informed decisions about their health. Through expert guidance and unwavering advocacy, Elizabeth is a lifeline for those facing some of the most challenging medical journeys.
In reproductive medicine, Elizabeth assists individuals and couples facing infertility, guiding them through treatment options, insurance challenges, and the overwhelming decision-making process. She advocates for patients pursuing IVF, donor conception, surrogacy, and fertility preservation, ensuring they have access to evidence-based information and ethical care.
She also supports individuals experiencing pregnancy complications, miscarriage, or loss, providing compassionate navigation through a difficult and often isolating process.
Beyond reproductive healthcare, Elizabeth advocates for those facing medical uncertainty, misdiagnosis, and systemic barriers to care. Having personally endured the challenges of navigating an underinformed medical community, she understands the frustration, fear, and exhaustion that come with fighting for proper treatment.
She helps patients secure accurate diagnoses, access specialists, and communicate effectively with providers, empowering them to take control of their healthcare journey.
Elizabeth also supports families and caregivers, ensuring they have the tools to advocate for their loved ones while managing the emotional and logistical burdens of complex care. Whether navigating insurance denials, coordinating multidisciplinary teams, or simply providing a knowledgeable and empathetic voice in overwhelming situations, she is committed to making the healthcare system more accessible and patient-centered.
Her mission is simple: to ensure that every patient has the knowledge, autonomy, and support they need to make informed decisions about their health. Through expert guidance and unwavering advocacy, Elizabeth is a lifeline for those facing some of the most challenging medical journeys.
Important Information About Me
- I offer a FREE Initial Consultation
- I offer TeleAdvocacy Service
- My geographical area of practice is Phoenix, Arizona and surrounding
My Survivor Support Advocacy Qualifications
I am a survivor of HEDS, MCAS, HyperPOTA, Stage 4 Endometriosis, Surgical Accidents, Infertility
Elizabeth’s journey to motherhood through both adoption and IVF has given her a profound understanding of the financial and emotional toll of infertility. A passionate advocate, she combines professional expertise with lived experience navigating complex medical challenges, including the lasting impact of a surgical accident that paralyzed her dominant arm and the devastating consequences of an inadequately disclosed black box medication warning. Diagnosed with Stage 4 Endometriosis, Ehlers-Danlos Syndrome, Hyperadrenergic POTS, and other rare conditions, Elizabeth intimately understands the frustration of medical uncertainty and systemic barriers to care. Her mission is to empower patients with knowledge, autonomy, and the support they need to navigate their own healthcare journeys.
Why I Became A Professional Health Care Advocate
Elizabeth Lee’s path to patient advocacy was not one she chose—it was one she survived. Her journey has been shaped by both the joy and heartbreak of reproductive medicine, the devastation of medical trauma, and the relentless pursuit of answers in a healthcare system that too often fails the patients who need it most. She has lived the frustration of being dismissed, the exhaustion of fighting for care, and the fear of an uncertain future. But she has also experienced the power of knowledge, the strength of resilience, and the profound impact of having someone in your corner when it feels like the system is working against you.
Her passion for advocacy began with her own battle with infertility. Becoming a mother through both adoption and IVF, she saw firsthand the emotional and financial burdens that come with reproductive challenges—the endless waiting, the crushing losses, the impossible decisions made without enough information or support. She realized that too many patients were left to navigate this journey alone, without clear guidance or an advocate to help them understand their options.
But it wasn’t just infertility that shaped her calling. A catastrophic surgical accident left her dominant arm paralyzed, requiring 18 months of rehabilitation to regain even partial function. A prescription medication with a black box warning—one her doctors never told her about—left her body permanently altered. Years of unexplained pain, medical gaslighting, and misdiagnoses eventually led to life-altering diagnoses of Ehlers-Danlos Syndrome, Hyperadrenergic POTS, Stage 4 Endometriosis, and other complex conditions. She knows what it means to be unheard. She knows what it means to be failed by a system that should be saving lives, not forcing patients to fight for their own care.
Elizabeth became a patient advocate because no one should have to go through that fight alone. She understands the desperation of searching for answers, the heartbreak of feeling like no one is listening, and the loneliness of navigating a complicated medical landscape without a guide. She has lived it, and now she dedicates her life to making sure others don’t have to.
Her mission is simple but profound: to give patients and their families the knowledge, support, and advocacy they need to take control of their healthcare journeys. No one should feel powerless in their own care. Elizabeth stands beside every patient, ensuring they are seen, heard, and given the chance to make truly informed choices—because she knows, more than anyone, how much that matters.
Her passion for advocacy began with her own battle with infertility. Becoming a mother through both adoption and IVF, she saw firsthand the emotional and financial burdens that come with reproductive challenges—the endless waiting, the crushing losses, the impossible decisions made without enough information or support. She realized that too many patients were left to navigate this journey alone, without clear guidance or an advocate to help them understand their options.
But it wasn’t just infertility that shaped her calling. A catastrophic surgical accident left her dominant arm paralyzed, requiring 18 months of rehabilitation to regain even partial function. A prescription medication with a black box warning—one her doctors never told her about—left her body permanently altered. Years of unexplained pain, medical gaslighting, and misdiagnoses eventually led to life-altering diagnoses of Ehlers-Danlos Syndrome, Hyperadrenergic POTS, Stage 4 Endometriosis, and other complex conditions. She knows what it means to be unheard. She knows what it means to be failed by a system that should be saving lives, not forcing patients to fight for their own care.
Elizabeth became a patient advocate because no one should have to go through that fight alone. She understands the desperation of searching for answers, the heartbreak of feeling like no one is listening, and the loneliness of navigating a complicated medical landscape without a guide. She has lived it, and now she dedicates her life to making sure others don’t have to.
Her mission is simple but profound: to give patients and their families the knowledge, support, and advocacy they need to take control of their healthcare journeys. No one should feel powerless in their own care. Elizabeth stands beside every patient, ensuring they are seen, heard, and given the chance to make truly informed choices—because she knows, more than anyone, how much that matters.
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