I developed secondary lymphedema in the fall of 2024 and quickly realized how limited local resources were. Although I was referred to an Occupational Therapist, the earliest appointment was two months out. In the meantime, my arm and hand became increasingly swollen and painful, and I began to experience nerve impingement. It was a frightening time—I was concerned not only for my health, but also for how this would affect my ability to work and care for my family.

As someone with a background in biology, I was alarmed by how little attention the lymphatic system received from my providers, many of whom referred to my condition as “just swelling.” What I needed wasn’t just advice—I needed support, education, and connection. When I discovered that our local OT was seeing 4–5 new lymphedema patients a week, I realized I wasn’t alone—and that others might not have the tools or internet access to find the information I was desperately seeking.

That’s why I stepped up to help build a support network for those affected by lymphedema, lipedema, and vascular insufficiencies in Western Arkansas and Eastern Oklahoma. My hope is that no one else feels as lost and overwhelmed as I did early in my diagnosis. Through LE&RN’s Arklahoma Chapter, I’m committed to offering education, community, and—most importantly—hope.