When the Psychotherapist Meets Cancer

I always thought that I’ve done very well in building up resilience, taking care of my physical and mental health, since that is basically what I do for a living. I am a Psychotherapist and am specialized in Cognitive Behavioral Therapy (CBT). I love the CBT approach in working with clients since it is a here-and-now approach, is time-limited, and is structured. I offer individualized treatment plans for each client that outline clear behavioral goals, as well as take an active role in coaching my clients by directing their therapy and assigning homework.

After undergoing a biopsy, my OB/GYN told me on my daughter’s 2nd birthday, “Unfortunately, it’s cancer”. I just sat there, repeatedly saying, “No, that can’t be true!”. I completely went into freeze response. It was like an out-of-body experience, while I was standing on the Edge of the Abyss, all around me was complete darkness. As I was shaking and crying, all I could continuously say was, “No, that can’t be true!”.

(The definition of Fight, Flight, Freeze or Fawn is the body’s natural physiological reaction to stressful events. It is activated by the perception of threat, quickly igniting the sympathetic nervous system and releasing hormones to reach the underlying goal of springing into fight, flight, freeze or fawn to decrease, end, or evade danger and to return to a state of calm and control.)

My OB/GYN’s office scheduled my first CT scan for three hours later and as my husband, who was thankfully with me at the appointment, brought me outside the office, I started throwing up while I talked to my sister on the phone telling her, “I have cervical cancer”.

At this point, I knew nothing about “my cancer”. Had it spread? Am I going to die? What stage am I? Will I see my girls graduate high school? Is it treatable? What is the chance that my cancer can be cured? What other tests and procedures do I need? How can I deal with that? I’m not the type of person that will be able to handle something like this.

The day after my diagnosis, there I was, sitting with all those thoughts, feelings, and emotions, not knowing what to do. I knew nothing anymore; I wasn’t even able to think. On this beautiful summer day, everything seemed to disappear into this deep fog surrounding me.

I, the psychotherapist, who always comes up with great treatment plans for all kinds of mental health problems my clients are dealing with, but who is now unable to even stop my own thoughts and worries. Wow, great job. I was disappointed in myself. I was disappointed in what my body had done to me by developing this cancer. And on top of that, I wasn’t even able to drag myself into a more positive state of mind. Hell, I could not even think one, clear thought.

So, when I wanted to cry, I cried. When I wanted to scream, I screamed. When I wanted to sleep, I slept.  When I wanted to talk, I talked. And I went on walks, a lot of quiet, long walks. At one point, I went on Google and gathered information about cervical cancer. I reminded myself about one of the things I tell my clients, “Information is on the other side of fear”. 

Then I realized that what is happening is grief. I’m grieving my cervical cancer diagnosis. I’m right in the middle of it and my psyche is doing what it’s supposed to do all on its own. 

We usually reserve the word, grief, for loss, secondary to death. Well, that’s just one form of grief. Grief is an adjustment to loss. When we get our cancer diagnosis, that is loss. Loss of potential quality of life, loss of certain physical functionality. It may even be the loss of time. At some point, everyone WILL go into grief. However, not everyone will go through the stages in a prescribed order, there is no linear and predictable pattern, and we often switch back and forth between the stages.

The classical, six stages of grief are simply tools to help us frame and identify what we may feel during our cervical cancer journey:

Denial: Feelings of avoidance, shock, fear, confusion. Believe that the diagnosis is somehow wrong and holding on to a different reality.

“I feel fine.” – “No, this can’t be happening to me.”

Anger: Feelings of frustration, anger, anxiety. Faced with the new reality, looking for someone/something else to fault, to leash out.

“Why me?” – “It’s not fair.” – “How can this happen to me.”

Bargaining: Struggling to find meaning. Seeking to get out of facing the new reality by promising something to change or to do differently or seeking for help through a higher power.

“I’ll do/give anything for a good outcome/a few more years.”

Depression / Sadness: Feelings of being overwhelmed, helpless, hopeless. Settling into sadness and unable to move forward.

“Live will never be the same…” – “What’s the point of going on?”

Acceptance: Feeling of exploring different options, a new plan in place, moving on. Embracing the new reality and finality of what has happened.

“I’m going to be ok.” – “I can fight it.” – “I may as well prepare for it.”

The more we give grief space to run its course, the more likely we are to have a better outcome. Sometimes we feel guilty for taking too long to grieve. NO, WE DON’T TAKE TOO LONG! Emotions work their way through us, don’t fight them, don’t rush them.

Years ago, I went to a lecture about grief and the professor added “Finding meaning/Purpose” as the last stage of grief in the circle and that stuck with me. Now, I always add that stage for my clients because I have experienced it myself.

Finding meaning/Purpose:

  • Help other people with the same diagnosis by sharing your story
  • Write a book
  • Pull back from work/toxic people
  • Join an organization
  • Smell/water flowers
  • Take a walk every day
  • See the beauty of life

For me personally, finding meaning/purpose just started in November 2021 (yup, not too long ago), when I decided to participate in one of Cervivor’s Creating Connections virtual meetups. I’ve always been pretty private about my cancer diagnosis. I was terrified about this cancer, I just wanted it to go away, I did not want to share anything with anyone other than my closest family. 

At this first meetup, I literally just listened to the other participants and there was so much hope, so much encouragement, and so many awesome ideas being shared for the upcoming Cervical Cancer Awareness Month (CCAM) in January, that I decided to participate in a second meetup. There, I started to introduce myself, shared a little bit of my story, and thought about ways to integrate some mental health ideas into CCAM.

Since then, I participated in Cervivor’s CCAM virtual activities and even spoke about self-care and mental health at the Cervivor Summit 2022. And today, here I am, continuing to find my meaning/ purpose. 

“Cancer cannot cripple love, it cannot shatter hope, it cannot conquer the spirt.” ~Author Unknown

Jessica Martin was born in Germany and holds a M.Sc. in Psychology. She moved to the USA in 2018 and was diagnosed with cervical adenocarcinoma 1B2 shortly after her move. Jessica is passionate about the mental health aspect for healing.

21 Years of Cervivorship

Today, we’re celebrating a special edition of #TealandWhiteTuesday. Our Founder and Chief Visionary, Tamika Felder is celebrating 21 years of Cervivorship!

Tamika was just 25 years old when she was diagnosed with cervical cancer on April 12, 2001. She endured a hysterectomy stripping her of her fertility, followed by chemotherapy, and radiation. Cervical cancer changed her life forever. 

In 2005, she started Tamika & Friends, Inc. a nonprofit dedicated to cervical cancer survivors and their friends and family. At the time there truly wasn’t any support for cancer survivors and the Internet was just getting off the ground. Tamika needed support. She found the more she told her story, the more it reached other women. Tamika wanted to help empower others to share their stories and that’s how Cervivor was born!

But Tamika didn’t stop there. She understood her calling of living her life beyond a cervical cancer diagnosis. Over the years, she has continued to transform the lives of each person impacted by a cervical cancer diagnosis. Tamika not only empowers them to use their voice, but she teaches them that their pain can have purpose, and they have the power to create change.  

Here are a few things she’s learned as she looks back on her experience with cancer:

  • I was a survivor from the onset of my diagnosis. Each day is survivorship. Sure, there are huge milestones. The first year, the magical number 5. But what matters is each day is another day from the one before. 
  • No matter your faith (or lack thereof) cancer is scary. And it’s okay to be scared. 
  • We all get by with a little help (or really a lot) when it comes to cancer from our friends/family. 
  • You won’t ever be the same. As with any traumatic experience you are forever changed.
  • Accepting that cancer has changed you and living in the “new normal” means that you can move forward. Even if it’s at a slower pace. 
  • Life is meant to be lived. And it doesn’t matter how much time. Sure, I’ve never be told that there is nothing left but what I’ve learned from others who have is that you have to live while you have life within you. 
  • Surviving cancer doesn’t mean you have to live in a bubble. It also doesn’t mean you have to become a daredevil. 
  • Surviving means living. 

Tamika has dedicated her life to cancer advocacy from eliminating the stigma of the human papillomavirus (HPV) (and being deemed a “Cancer Rebel” by Newsweek), to training patient advocates to share their stories, and to eliminating the healthcare disparities within communities of color.

“My greatest lesson is that life comes with an expiration date — from cancer or otherwise. It matters what we do with our time here. Life continues to surprise me. I was diagnosed with cancer when I was 25. I’ll be 47 this year and life is still surprising me in the best way possible. I don’t know how many years I have left, but what I can tell you is that I am going to live in a way that says I survived cancer.”

– Tamika Felder, Founder and Chief Visionary, Cervivor


This is only a small fraction of what Tamika has accomplished since she began her journey with cervical cancer and we couldn’t be more grateful for her resilience and leadership to create the community we now know as Cervivor. Thank you, Tamika!

Join us in celebrating Tamika’s 21 years of Cervivorship by:
1. Start living life for YOU. Don’t wait until something traumatic happens to start living life.
2. Vote for Becky’s video. People die of cancer. I’m blessed to still be here. 
3. Donate $21 to Cervivor.
4. Schedule your cervical cancer screening.
5. Vaccinate your children and protect them from HPV-related cancers.