Robin Tuohy - Vice President, Patient Support 
25-Year Care Partner | Advocate | Support Group Leader  

Robin has been a passionate and dedicated advocate in the myeloma community for 25 years. Her journey began in 2000 when her husband was diagnosed with myeloma at the age of 36. This personal experience motivated her to join the International Myeloma Foundation (IMF) in 2005, where she focused on supporting patients, care partners, and expanding the IMF’s network of myeloma support groups. 

As Vice President, Patient Support, Robin leads the IMF’s Support Group Team, providing educational resources and guidance to over 150 local and special interest support groups across the U.S. She plays a key role in IMF cornerstone programs, such as Patient & Family Seminars, Regional Community Workshops, and Living Well webinars all designed to provide critical information and support to those impacted by myeloma. Internationally, Robin is involved in the IMF’s Global Myeloma Action Network, helping advocate for the global myeloma community. 

My "why" is rooted in a deeply personal understanding of myeloma and a profound compassion for patients and their families—shaped both by my own experience as a care partner and my professional commitment to the cause. Every step of my journey has been guided by a singular mission: to educate, empower, and unite the myeloma community. My purpose is clear: to ensure that no one faces the myeloma journey alone. Working with the International Myeloma Foundation (IMF), I am honored to contribute to the IMF’s vision of "a world where every myeloma patient can live life to the fullest, unburdened by the disease."

Katie has been working as a clinical social worker for the past 15 years, finding a niche in oncology social work 7 years ago. She most recently worked in an outpatient clinic, serving in the primary role of patient & family counselor and support group facilitator. She is dedicated to advocating for the rights and needs of cancer patients and their families.  She values the opportunity to walk alongside patients as they face cancer and the challenges that come with it, educate the community about available resources, and advocate for patients facing barriers to care. Katie is committed to building lasting relationships with the people she works with, and empowering individuals to navigate healthcare systems and access the resources they need to live their best lives.

Katie was born and raised in North Carolina, where she currently lives with her husband, two daughters, and two dogs. Outside of work, she enjoys running, reading, hiking/camping, and cooking (and eating) vegan food!

Becky Bosley, BSN, RN - Director, Support Groups 
Oncology Nurse Since 2006 | Breast & Ovarian Cancer Survivor | Support Group Leader 

Becky has been an oncology nurse since 2006, and for the last eight years, has primarily focused on myeloma.  Since 2018, she has led the MidAtlantic Myeloma Support Group and co-leads the Living with High-Risk Myeloma virtual special interest group, which she founded in 2023. Passionate about empowering patients with education, she leverages her oncology nursing expertise to support myeloma patients and their care partners. As a breast and ovarian cancer survivor, she brings a deeply personal understanding of the challenges faced by those diagnosed with cancer.   

“Having volunteered with the IMF for several years prior to coming on staff allowed me to see a glimpse into the passion of every single person on staff. I felt the same passion while working with the myeloma coMMunity. The longevity and impact of the IMF is so inspiring in itself and I wanted to be a part of continuing that legacy. Patients know that they can count on the IMF for support and I am proud to contribute!”

Cecilia Romero , Program & Technology Manager 
Public Health Advocate | Technology Educator | Project Management Expert  

Cecilia has more than 10 years of experience in project management and is passionate about keeping projects, programs and initiatives running smoothly through effective processes and procedures. Her background has been in been in higher education with a focus on improving the health and wellbeing in the communities we serve. She enjoys working with such a passionate team focused on improving the quality of life of myeloma patients while working toward prevention and a cure.

Jenn Wieworka, DNP, RN, AGCNS-BC, OCN - Director, Support Groups 
Doctorate-Prepared Nurse | Clinical Nurse Specialist | Support Group Leader 

With over a decade of experience in the oncology field, Jenn is passionate about improving patient outcomes and reducing health disparities. Her journey started in inpatient oncology (2012-2017), where she gained hands-on experience in providing compassionate care to patients facing life-changing diagnoses. From 2017 to 2024, she practiced as a Clinical Nurse Specialist (AGCNS-BC) in radiation oncology, where she streamlined processes and improving patient experiences through process improvement and health literacy initiatives. As a proud Oncology Certified Nurse (OCN), her work is centered on education, patient advocacy, and making complex medical concepts more accessible to patients. Jenn's goal is always to meet patients where they are, creating a supportive and empathetic environment where they can feel informed and empowered throughout their treatment journey. Now, with a Doctorate in Nursing Practice, Jenn is dedicated to advancing evidence-based practices and continuing to champion the role of nurses in shaping the future of oncology care. 

“I’m driven by the belief that every patient deserves not only the best medical care but also the emotional support and understanding that allows them to navigate their health journey with confidence. Having witnessed the impact of cancer on my loved ones, I understand the fear, uncertainty, and need for clear communication in ways that empower patients to take control of their care. Being at the forefront of science and constantly learning helps me stay committed to the latest advancements in oncology care. In my work, I strive to make a meaningful impact by improving processes and policies, while creating an environment where patients feel supported at every step. I’m dedicated to helping people through some of the most challenging moments in their lives with the knowledge, empathy, and dedication they deserve.” 

Yara William, DrPH, MHA Associate Director, Support Groups  
Doctor of Public Health | Community Engager | Patient Advocate 

Yara has a background in public health and health administration, with experience in nonprofit, government, and university settings. She is passionate about health equity, community engagement, and patient advocacy. Her work has focused on bridging the gap between the community and health and social services. In her current role, she strives to break down barriers to resources, making sure every patient and care partner feels supported. Through education and connection, she helps empower individuals and strengthen support networks. 

“No one should have to face myeloma alone. Too often, patients and families struggle—not because resources don’t exist, but because they’re hard to find or access.  I believe in the power of community, in listening, and in making sure everyone feels seen and valued.”