Thanks to My Transplant, I Can Dream About the Future

Lara Govendo avatar

by Lara Govendo |

Share this article:

Share article via email
banner for Lara Govendo's column

I never really dreamed about my future until after my double-lung transplant in 2017. My friends who are also transplant recipients inspire me to dream bigger as we navigate this new world together.

Although it’s been over four years, dreaming can still feel risky. But the more time that passes, the more daring I become. I’m still adjusting to the new normal of being able to rely on my health.

Prior to my transplant, I often made tentative plans. I tried to be dependable, but my body wouldn’t cooperate. I felt tremendously guilty because I couldn’t consistently work, spend time with friends, or accomplish my goals. When I agreed to something, I prayed I could follow through, but I always dreaded a health interruption.

This translated into me putting my dreams on hold. Before transplant, I could barely breathe or function. I didn’t have the energy to plan beyond the present moment.

Now, as I cautiously trust in the stability of my health, it’s exciting to think bigger and plan for the future.

Recommended Reading
gain weight, exercise, risks, teenager, covid-19, tips, nostalgia, death

The Cure List: Dreams Achieved and Dreams to Come

Working as a mental health counselor again has been a huge step. I’m also able to write my book, serve in my church, and strategize business plans. These possibilities feel surreal.

Transplant recipients can dream about a future that many of us were told wouldn’t exist, because death no longer feels as imminent. This new lease on life results in radical changes and provides us with cautious hope.

Our conversations have changed since our transplants. I get to listen to my friends‘ hopes and dreams. Some are going back to college. Others are starting businesses. A few are writing books. Several are traveling with no inhibition. I’m in awe of their valiance and excited for them to realize the dreams they’ve held in their hearts for so long.

A few friends and I meet on Zoom every week to work on our books together. Writing and sharing our stories with the world is therapeutic. We talk about how we’ve moved beyond survival mode and now have the energy to live. Our individual journeys are different, but we’ve all undergone major transformations.

Walking this journey together reminds us that we’re not alone. It’s an honor to witness each person’s unique talents and watch their dreams come alive.

I’m so proud of my friends for all they’ve overcome. I love the way they light up when they talk about their hopes and plans for the future. Their boldness encourages me to dream big, too.

I’m grateful to be able to look ahead to new opportunities on the horizon. Doing so alongside dear friends is a rare and beautiful gift.

Note: Cystic Fibrosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Cystic Fibrosis News Today, or its parent company, BioNews, and are intended to spark discussion about issues pertaining to cystic fibrosis.


Leave a comment

Fill in the required fields to post. Your email address will not be published.

A Conversation With Rare Disease Advocates

Your CF Community

Visit the Cystic Fibrosis News Today forums to connect with others in the CF community.