Juggling Gratitude and Luck

I was diagnosed with Stage II cerivcal adenocarcinoma just before Christmas in 2015, caused by HPV 16. Lots of people remember the date they heard those words. I don’t. I remember the fear, the disbelief, the questions, the pounding feeling in my head, and the instinct to run, far, far away. Just keep running away so this would never catch me.

October 5 will mark my five year anniversary of NED (no evidence of disease) diagnosis. I have been waiting for this day, this special marker in the cancer world, since I heard those three words, “You have cancer.” I imagined this day multiple times throughout the years. In my imagination it would be a day of huge celebrations, with a big party with my friends and family to commenorate this huge milestone. It would be a day where I would finally feel relief from the constant worry of recurrence. It would be the day my life went back to “normal” and I could magically turn back into the “pre-cancer-me .”

I was wrong.  

This day comes with many mixed emotions for me. When I was diagnosed, I thought I would go through treatment, recover, move on and never look back. Nothing could be farther from the truth.

I went through the treatments, the chemo, the external radiation, the internal radiation. Treatments that made me so sick I couldn’t work, couldn’t take care of my children, couldn’t do simple tasks like walk up the stairs or eat a small meal. Treatments that took away my fertility and put me into menopause at age 36. I went through countless side effects, including an allergic reaction to chemo, stents being placed in both ureters, a radical hysterectomy, reconstructive bladder surgery, not to mention the daily side effects I still currently deal with. These treatments almost broke me. There were many times I wanted to give up, throw in the towel and declare cancer as the winner.  It is only because of my children that I didn’t do that.

Once I had finally gotten through the treatments for cervical cancer, and hit the one year mark, I was excited. I was on the right track, moving forward. I began to get more involved with Cervivor and advocacy. I began embracing my story and sharing it with anyone who would listen. Then I got the news that I never, ever expected to hear.

I was diagnosed with pre-cancerous lesions on my vaginal wall. A new and different type of cancer, still caused by HPV.  Never, not once, did I imagine I would be dealing with a second, even more rare type of pre-cancerous lesions.  It hit me like a ton of bricks. And yet, with my new found support system through Cervivor, I felt I could handle it. I would do chemo again. I would change my diet and eat zero carbs and zero sugar to help curb the growth of these lesions. I was a woman on a mission and no one could stop me.

Two months later, after treatments, the lesions were gone but the relief still didn’t come. I went to each six month appointment expecting the worst. I became a basket case every six months, for the week leading up to my appointments and for the following week waiting for the results. I was basically incapacitated.  

I was lucky. For the next four years I had clear exams. At my four year appointment, my oncologist told me she didn’t need to see me in six months and that I could wait a full year until my next exam. I felt like this was a huge milestone.  She wasn’t worried, so I could let my guard, just a little bit.

I was wrong, again.

My five year exam revealed that once again I have lesions on my vaginal wall. This time it has wrecked me. The chemo has been very difficult, painful and exhausting. I feel like I have the flu all the time. My anxiety is through the roof, and my physical and emotional stability are precarious, at best. 

And I am still coming up on five years free from cervical cancer. I have so much to be grateful for and to celebrate.  I have not had a recurrence of cervical cancer, which means I most likely won’t. I have two beautiful children and a supportive, adoring husband. My family is amazing and continues to lift me up when I fall. My mom, in particular, is there whenever I need her, day or night, near or far, she is always there for me.  

I am grateful for the way that cancer changed me. It gave me a new purpose in my life, I have been able to lobby with ACSCAN in both California and Washington D.C. I have met the bravest, kindest, most caring women in the world, through Cervivor. Women I never would have met, had it not been for the “exclusive club,” that we were all forced to join. I have learned that I am stronger than I ever thought possible and that my voice and my story matter.  These are all things to celebrate.  

And yet here I sit. Tears streaming down my face.  

I am crying for what I have had to go through. For what my family, my husband and my children have had to go through. And for what we all continue to go through with this round of lesions and chemo. I am crying for the fear that I still have, and will always have, about my future. I am crying for the women I know who weren’t as lucky as I am, and didn’t get to see their five year mark. Because that’s what it boils down to. Luck. Women with the same diagnosis and treatment, and some of us survive and others do not. No one isn’t fighting as hard as they can. None of us leave anything on the table when it comes to this fight against cancer and HPV. Some of us are just lucky, and luck is a very hard thing to celebrate.  

Ana & Jeff

My five year cervical cancer NED anniversary is a conundrum of mixed emotions. I am both optimistic and fearful about my future. I am sad and in a constant state of sorrow for what I have had to endure, and for what others have had to endure, and for the luck of the draw. And yet, I am grateful. So, so, grateful. The amazing thing about being human is that we can hold all of these things at one time. 

So, here’s to five years. In honor of my journey I ask that today you live your best life. Do something that brings you joy, hug those you are close to, and reach out to those who are far away. I ask that you please make your appointments for your Pap and HPV tests, and most of all that you vaccinate your sons and daughters against HPV.

Ana is mother of two, wife, educator and Cervivor Ambassador. She was diagnosed with cervical adenocarcinoma at age 35 and has been diagnosed twice with vaginal lesions, caused by HPV. Ana is currently finishing chemotherapy treatment for these lesions. Her goal is that no woman feels alone when they receive a cervical cancer diagnosis and that her generation be the last to to deal with HPV related cancers.

Mother’s Day When You are Struggling to Become a Mother

While Mothers Day is a beautiful day to celebrate motherhood, it can also be a difficult day; especially if you are missing your Mama or struggling to become a mother yourself. The journey to motherhood isn’t always smooth or what you may expect.

I spent six Mother’s Days wishing, more than almost anything in the world, that I was a mother. While I was thankful to celebrate my Mom, who is and always has been great Mom!, part of me was also sad; very, very sad. I mean truthfully I was sad every day for a long time, but Mother’s Day always brought it home.

You see, I have three younger sisters, spent years babysitting, and spent several years working with mothers and babies as a nurse. I’d had lots of practice. I knew without a doubt that I wanted children; being a mother was just something I always wanted to be. But at 25, I was diagnosed with cancer that immediately robbed me of my fertility.

The specialist took one look and said, “It looks like you have cervical cancer. We’ll do what we can to save your fertility.” Cancer? My fertility? I hadn’t even attempted to conceive. I thought I had time, a lot more time. But, my tumor turned out to be too large for the procedure I hoped to have. So instead, in January of 2009, I had a complicated surgery that included a hysterectomy followed by chemotherapy and radiation.  I knew I would become a mother, but I knew my journey to motherhood would no longer be a traditional one. 

After that, my journey to motherhood was a rollercoaster. It involved more heartache than I could have imagined. But, I did eventually become a mother.  We had our son, Carter, in 2014. 

After that, we thought we were done. We thought our family was complete and, to be honest, we weren’t completely sure we could survive going through it all again. But, Carter had more faith. He started doing things like pointing to an empty chair when we were at a table for 4 and saying, “someone is missing there.” We finally decided that maybe he was right. Maybe he was seeing something that we were too scared to see. Maybe we were supposed to try again. Amazingly for us our same angel of a surrogate was willing to try again. And guess what, it worked – the first time! We had our Caroline in 2019!

I am now the proud mother of two beautiful children, my Carter and my Caroline, who I wouldn’t trade for anything in the entire universe. I’m more than a little bit obsessed with them! I tend to take a lot of pictures and videos of and with my kids. And now, you know why… Although I’ve been N.E.D. (No Evidence of Disease in the cancer world) since 2009, I like my family to have the ability to look back on our love and adventures together. And, I like to share the happiness we’ve found with others.

Struggling to grow your family is difficult, no matter the circumstances. My biggest piece of advice is to remember that there is no right or wrong way to add members to your family. What is a “traditional” family today anyway? Sometimes you have to open your mind and/or get creative. For now, remember that you can be a Mother in many ways. 

If you ever want to talk to me about my journey to motherhood, please reach out. I have personal experience with fertility preservation, adoption, and surrogacy (gestational & traditional) and would love to help support you during your journey in some small way. You can find me @cervicalcancersurvivor, @infertilitysurvivor, and follow my family @crystalcoastfamily.

Sending love to all of you Mothers out there – past, present, and future. Happy Mother’s Day to you all.

Love,

Kristin

Kristin Ferree was diagnosed with cervical cancer December of 2008, at the age of 25. After treatment left her infertile, she vowed not to let cancer keep her from her dream of becoming a mother. Now a 10-year Cervivor, she lives in Morehead City, NC with her loving husband, David, two miracle babies, Carter and Caroline, a sweet rag-doll kitty, Lilley, and a snuggly puppy, Toby. She is currently taking time off from being a Family Nurse Practitioner to spend more time with her children and loving every minute of it.