Valiant Voice – a Column by Lara Govendo

Note: This column describes the author’s experiences with tacrolimus and prednisone. Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy. I’ve been dealing with a different and unexpected symptom these past eight months, one that’s challenged my pain threshold on a…

I’ve been in pain so long that I can’t remember a time when I didn’t feel pain in one part of my body or another. Through surgeries, procedures, medication side effects, and the injuries of everyday life, pain has been a constant companion for me and continues to affect my…

I took part in physical therapy (PT) on a weekly basis to build my strength during the lead-up to my double-lung transplant nine years ago. PT was mandatory to complete the prerequisite requirements to be listed for a transplant, but I learned so much about myself in ways that…

I celebrated nine whole years with my new lungs on Aug. 18. My husband took me to my favorite lake, where we logged some hours at the beach, jumped into the cold water, and ate at our favorite local spots. The day gave me some much-needed time to reflect on…

There’s nothing I love more than alliteration. It might be a bit dramatic, but I think Advocacy August, one of my favorite months, warrants the drama. I’m passionate about advocacy, both from personal experience and as a therapist. Living with cystic fibrosis (CF) and navigating the healthcare system…

Living with cystic fibrosis (CF) made me very aware of breathing. Before my double-lung transplant eight years ago, I’d check the weather before committing to any plans, because protecting my lung health from allergens, weather triggers, and anything that could cause inflammation was essential to my well-being. Since…

There are three F-words that describe a few of the changes I’ve experienced since having a double-lung transplant eight years ago. After living with cystic fibrosis (CF) lungs for 30 years, having new lungs has been a miracle. It hasn’t come without adjustments, though. The three areas most affected…

Germs. I imagine them floating through the air, gravitating toward me because they know somehow that I’m immune-compromised. I picture them swirling around my face, getting sucked into my nostrils and pulled into my transplanted lungs, threatening my very existence. I’m pretty sure that’s also how it went when I…

Sometimes, memories are triggered by my senses — things I hear, see, smell, or touch — and before I know it, I’m spiraling down a rabbit hole of past trauma from my life with cystic fibrosis (CF). It’s fascinating how my five senses remember everything and often transport me…