My Legacy, My Cervivor Footprint…In my Community

Cervivor is committed to closing the disparity gaps that have plagued communities of color for decades. In an effort to close those gaps, Cervivor invited cervical cancer patients and survivors from around the United States to participate in the Cervical Cancer Patient Advocacy Retreat for Communities of Color in our nation’s capitol, Washington D.C.

Why is this so important to our mission?
Research shows that while the rate of cervical cancer has been declining for decades in the U.S., health disparities persist. Hispanic women have the highest incidence rate of cervical cancer, followed by non-Hispanic Black women. Additionally, Black women are more likely to die from the disease than women of any other race or ethnicity. 

So, what is the consistent theme with these health disparities?
The consistent theme for these health disparities are health literacy and trust within the communities of color. As we navigated these themes, Cervivor ensured that each attendee:

  • Had a safe place to share their struggles, hurdles, and concerns in reference to their community and cervical cancer.
  • Was provided with information concerning cervical cancer, treatments, and screening. 
  • Understood their role as a trustworthy change agent in their community.
  • Embraced the opportunity to learn from various speakers and their fellow survivors about how they could utilize their voices to end cervical cancer in their community.
  • Developed a strategic plan to impact their communities specifically.
  • Made a commitment to assist in closing the cervical cancer disparity gap in their community.

It’s imperative that those impacted by cervical cancer have the knowledge and empowerment to lead the charge in changing the narrative for communities of color. Read the personal testimonies from a few of the attendees and the progress they have made since the retreat below.

Gwendolyn shares her thoughts on what this retreat meant to her:

The Community of Color Retreat had great impact on my life and I have not been the same since. The moment I arrived at the retreat, I noticed everything was planned with so much love and hope, and personalized for us as a collective but also individually as well. We cried, we laughed, we learned, we inspired each other, we listened, and we gained confidence and much knowledge to not only advocate for ourselves but for others as well – within our families, jobs, and communities.

Since the retreat, Gwendolyn has been instrumental in planning the National Patient Advocacy Awareness Day event with other Houston Cervivors and in co-leading an upcoming health fair for cervical cancer awareness.

Rosalinda shares her insights:

For many of us, conversations easily continued into dinner, late evening, and early morning coffee meet-ups! We were clearly vibing and opening up to be vulnerable, witnessing and holding space for each other. Native American, African American, Asian, and Latina cervical cancer survivor’s coming together to listen, share, teach, and support each other was a powerful experience! My heart is filled with gratitude for how effortlessly this all unfolded. My most precious take away? Tamika’s loving challenge that following the retreat we step up and use our talents, abilities, gifts, unique perspectives to Do Something small or big, to end cervical cancer.

After her retreat experience, Rosalinda has jumped in on National Patient Advocacy Day planning, joined as a Cervivor Español Outreach Committee Member, and continues to set goals for reaching low-income populations to ensure they have access to education, screening, and cancer prevention resources.

Janice gave us her thoughts too:

Hope – grounds for believing that something good will happen. This retreat provided a breadth of information about studies on cervical cancer, as well as how to raise awareness in our communities. Discussing the health disparities across the nation opened my eyes that more needs to be done and that we need to be able to have open, sometimes uncomfortable dialogue to inform others so that they do not have to go through the same things that we did.”

Following the retreat, Janice has been spreading awareness about HPV and cervical cancer through various tabling events at her local college campus and by helping Cervivor raise funds during an early 2023 Kendra Scott Gives Back event.

Although the retreat has ended, the work does not stop. Each attendee made the commitment as a Cervivor Patient Advocate to assist in closing the cervical cancer disparity gap; by creating a culture of diversity, equity, and inclusion which includes supporting, educating, and motivating their communities that have been affected by cervical cancer.

It’s a great reminder that each day we all have an opportunity to provoke change by elevating our voices. We hold the power to save lives for generations to come. Help us continue to shine a light on these disparities by sharing our content with your networks.

Cervivor, as an organization, authentically embraces diversity, equity, and inclusion across all aspects, ensuring that individuals from various backgrounds feel valued, respected, and represented. The organization recognizes that diversity encompasses a wide range of identities and experiences, including persons with disabilities, religious or ethnic minorities, people of color, native/Indigenous peoples, women, gender identity, and sexual orientation.

Interested in learning more about future Cervical Cancer Patient Advocacy Retreats for Communities of Color? Connect with us at [email protected]!

How We Went from Pudding to Acceptance

Two years ago, my husband and I received the devastating news that I had been diagnosed with cervical cancer. At the time, the mere mention of the word “cancer” was enough to send us into a state of panic. To cope with the fear and uncertainty, we came up with a unique way of talking about my diagnosis: we referred to it as “a pudding.”

This simple act of renaming the disease allowed us to talk about it more openly, without being overwhelmed by fear. We could discuss my treatments, prognosis, and how we were feeling without feeling like the weight of the world was on our shoulders. I used this little cute pudding emoji when I texted someone about it, and encouraged some of my close friends to do the same. 

As the months went by, we faced numerous challenges and struggles, from painful treatments to emotional turmoil. But with the support of family, friends, and a dedicated medical team, we slowly but surely found the strength to keep fighting. Over time, our outlook on life changed as we learned to embrace each day and live in the moment.

Fast-forward two years, one of my friends texted me saying “how is your pudding?”, and this was when I realized that the word “pudding” is no longer a part of our vocabulary; we can now say “cancer” without fear or hesitation. My husband didn’t even remember the fact that we used to call it a pudding. This represents a major shift in our mindset and how we perceive the disease. We have learned to accept the reality of my diagnosis and move forward with it. We have come to understand that cancer is just a word, and it does not define who we are or what our future holds, although I also feel like cancer is now a big part of my life in both good and bad ways.

This journey has been incredibly difficult, but it has also taught us so much about ourselves and life. We have learned that it’s okay to be afraid, and it’s also important to face our fears and embrace the journey. By being open and honest about our experiences, we hope to inspire others who may be going through a similar situation and help them overcome their fears and pains.

In conclusion, our journey from “pudding” to acceptance has been a powerful reminder that we are strong, bonded and we get through difficulties together. By embracing the reality of my diagnosis and focusing on one thing at a time, we have found the strength and resilience to overcome the difficult situation and move forward with hope. I am currently facing issues with my body due to side effects from cancer treatments, and those sometimes make me feel like I am mentally not well, but one thing we know is I will feel better again. We will get through this. I am now much more confident and have more faith in myself.

Survivor & Caregiver

Looking back over the past two years, time and patience were the most important things in this process of moving forward. In my darkest moments, I turned to a support group of fellow cancer survivors, Cervivor, who provided me with comfort, encouragement, and a sense of community. I am amazed by the resilience of these individuals, who have gone through similar experiences and come out on the other side. Their stories gave us the courage to keep moving forward, even on our toughest days. This is why I am writing this blog post, hoping to give a ray of hope for anyone who is currently suffering. I will continue to tell my story as a way to inspire others and to remind you that you are not alone. 

Anna was born and raised in Japan and came to the U.S. in 2015. After she survived cervical cancer in 2021, she became a Cervivor School graduate in 2022. She is a business development professional working for a Japanese corporation. She currently lives in Washington state with her husband and their fur babies. In her spare time, she enjoys gardening, cooking and watching shows & movies. She is passionate about fostering dogs to give them a second chance.