The January Lymphedema Patient Roundtable kicked off the new year with an honest, patient-centered conversation about living with lymphedema and easing into 2026 with support and shared experience.
The discussion focused heavily on compression in real life, building on insights from the January Research Roundtable and the STRIDE framework for compression selection. Panelists shared candid experiences about what makes compression workable on a day-to-day basis, how comfort and routines affect adherence, and how needs and preferences can change over time.
We also explored navigating care fatigue and burnout, including how to recognize when self-management becomes overwhelming and what helps make care more sustainable long term. In recognition of Cervical Cancer Awareness Month, the Roundtable highlighted the connection between cervical cancer treatment and lymphedema, underscoring the importance of awareness and early support.
Thank you to everyone who joined us live and contributed to such a meaningful discussion! And a special thanks to our trio on the panel:
- Karen Ashforth, MS, OTR/L, CLT-LANA
- Alexa Ercolano, Lymphedema Patient and Lympha Press Marketing and Communications Specialist (@lymphielife)
- Catherine Rosenberg, Lymphedema Patient (@crosenberg1982)
Links and Resources mentioned during the program:
- Tips for the Traveler with Lymphedema and Lipedema (Webinar)
- Innovations in Lymphedema Management: STRIDE 2.0 and the Paradigm Shift in Compression Therapy (Webinar)
- STRIDE Professional Guide to Compression Garment Selection for the Lower Extremity (PDF)
- STRIDE Professional Guide to Compression Garment Selection for the Trunk and Upper Limb (PDF)
- STRIDE Quick Reference Guide to Tissue Texture (PDF)
- Academy of Lymphatic Studies Therapist Database
- Lymphatic Education & Research Network Find a Therapist Resources
- Lymphology Association of North America Therapist Database
This Roundtable was originally recorded live on January 13, 2026, and has been edited for time. The views and opinions expressed in this Patient Roundtable are those of the individual participants and do not necessarily reflect the official position of Lympha Press.
This video is intended for informational and educational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult your healthcare provider with any questions about your condition or treatment.
Lympha Press is proud to offer these monthly Lymphedema Patient Roundtables and support the lymphedema community. The Roundtables are held on the second Tuesday of each month at 8:00 PM EST. Sign up to attend any of our live webinars at https://linktr.ee/LymphaPress.