Although I didn't have cystic fibrosis-related diabetes, I avoided dealing with my blood sugars. Now that I do, I feel stronger physically and emotionally.
Diagnosed with cystic fibrosis at four months, Megan received a Master of Public Policy degree with a certificate in health policy from Duke University after earning a BA and MA from Stanford University. Megan has spent her career working in health policy, focusing on Medicaid. In 2019, she joined the governance board of the Cystic Fibrosis Reproductive and Sexual Health Collaborative, a nationwide online collaborative committed to responding to the needs of the CF community through partnerships that pave the way for improved sexual and reproductive health resources, healthcare, and knowledge for people with CF. Megan enjoys dance, barre fitness, and yoga. She lives in Silver Spring, Maryland, with her husband, Bobby, and son, Henry.
Blog Posts
Pulmonary function tests (PFTs) are a standard component of quarterly cystic fibrosis clinic visits, but they can often cause a great deal of stress for people with CF. Here are a few strategies that I've found helpful for reducing my own PFT anxiety.
When it comes to my cystic fibrosis care, some might say that my situation is a bit unique. Although having not one -- but two -- CF care teams can be challenging, I strongly believe that has made me a better, smarter, and more engaged patient.