We have four wonderful children in our family, three of whom happen to be incredible adult men. We have spoken honestly and candidly with the boys (ok, we still call them "the boys") since the time of diagnosis.
Now that we have gathered all of the information and settled on our surgical plan, it is time to tell our daughter, who is four, that Mommy has FBC (though we will leave out the F-bomb in our discussion).
As much as I wish this experience were only happening to me and that I could shield my husband and children from the pain, the reality is that cancer happens within the ecosystem of family, friends and community.
Children are incredibly intuitive and smart. We adults do not give them enough credit. From the time of a diagnosis, children are keenly aware that something major has happened and try immediately (either on their own, or hopefully, with adult assistance) to make sense of the situation and develop coping mechanisms. In my professional experience as a pediatric hospice nurse and social worker, I have seen first-hand that children know something serious is going on even when no one says anything to them.
At every age, children deserve to know what is happening. Silence is not golden. They deserve open lines of truthful communication. Truthfulness is the best (and only!) way to establish and maintain a bond of trust, with everyone, but especially with children. Discussing illness honestly and openly will teach children that parents are trustworthy and that honesty is a core family value.
Many loving, intelligent and responsible parents find themselves trying to hide the truth from children because they think children can't understand what is happening. That is pure and utter malarkey. Children as young as a year know when things are haywire in a household, whether it is divorce or FBC. They know.
Another common excuse adults use to avoid telling children is they shouldn't be exposed to something so awful. Well, that's 100 percent true. Exposing children to FBC is brutal. Heart wrenching. For me, it is the worst part of this whole FBC. However, life has its way of throwing us some hefty challenges. In this situation, denial only makes things worse.
With these assumptions -- about lack of knowledge and a limited capacity for pain -- parents unintentionally (or intentionally!) throw a blanket over the elephant in the room and spend enormous amounts of energy either avoiding or distracting the children from that elephant. I happen to adore elephants and when they are in the room, I prefer to welcome them and offer them some tea. Or a martini.
For those people who have a challenging time talking with children about difficult things, like FBC, the motivating factor to address that elephant head-on is that no matter how hard adults try to hide information, whatever is being discussed in the house (even behind closed doors) will be heard, either all, or partially, by the children. When children overhear information, the likelihood of misunderstanding is high.
Avoiding communication with children also sends the message that either they are too unimportant to share the information, or that it is so awful that it cannot be discussed. Either way, a child is left alone with the distressing information. How awful is that? Further, this alone-ness forces them to draw inaccurate conclusions or find maladaptive ways of dealing with FBC. While it may seem hard to believe, we all need to know that a child's imagination has the capacity to create things far worse than the reality. Really.
Furthermore, if children catch you in a lie of omission or deception (even though lovingly intended), then from that point forward, they will always wonder: "Are Mommy and Daddy not telling me something?" Avoidance feels better to parents now, but has the potential to do long-term damage.
Therefore, including children (of all ages!) in the disease process and in treatments, though emotionally burdensome and painful, will ultimately be the greatest gift parents can give them. Inclusion enables children to have an accurate, healthy and hopeful understanding of the situation and learn adaptive coping mechanisms. Words, actions and love will determine the positive impact of illness. Yes, I said positive. Remember: there are Silver Linings (SL) everywhere!
So, we are obviously going to discuss this situation with our four-year-old daughter. Now, I'll tell you exactly how we are going to tell her that Mommy has FBC.
When discussing a diagnosis and treatment with children, always start from where they are in their developmental process. In other words, you talk with a child who is four differently than you would with a 10 year-old. Children absorb different levels of information and complexity at different ages. Parents are always the best judges of what their children can cognitively understand.
Keep in mind that being honest does not necessarily mean telling everything, especially when a child isn't ready to understand. It does, however, mean always, always, always tell the truth!
Our four-year-old daughter happens to be an inquisitive, precocious and sensitive preschooler (who adores her Ariel high-heels). Typical features of this preschool stage of child development include:
Egocentricity. In other words -- it's all about me. All events happen in relationship to them. (Don't you miss the good old days?)
Associative Logic. This means that any two unrelated things can be connected as if one causes or explains the other.
Magical Thinking. Young children believe in their own omnipotence, which means that what happens around them happens because of them.
Play is a vehicle for exploring reality. Play is the work of children. This is how they acquire information and grow: socially, intellectually and emotionally.
So, where do we begin? We are going to tell our daughter three things:
Mommy is sick.
Mommy's sickness is called breast cancer. (We use accurate names for anatomy in our family.) Euphemisms are confusing and lead to mixed messages and anxiety. It is imperative to use the exact name of the disease.
Mommy is going to be treated by nurses and doctors in a hospital for four sleeps. Then, I will be home. Daddy and I truly believe that I will get better.
Telling your child that you have FBC (or anything of that magnitude) is definitely an emotional experience. As if having FBC isn't hard enough. Phew. While it is important for children to have other adults with whom they can share fears and worries, we cannot shield children from our feelings completely.
If parents get upset while talking with children, that's okay. Simply acknowledge to the children that parents sometimes feel scared, sad, angry or worried, but that it won't last forever. Let children know that it is okay for them to sometimes feel those things too. In fact, sharing a few tears together can reassure children that feelings do not need to be completely overwhelming, and that parents will be there to support them and to try to understand how they feel. This sounds so much more difficult than it actually is. Pinky-finger promise.
At some point or another, there will be three questions that our daughter will ask, either internally or externally:
Did I cause the cancer? This question arises directly from Magical Thinking. A preschooler could easily surmise that she caused the cancer. So sad, I know. But true. This is the reason that adults have to address this issue head-on and assuage any misconceptions.
Is it contagious? Our daughter has just learned the word contagious and uses it every chance she gets. She understands that colds are contagious, for example. She could quickly and easily use associative logic to connect cancer and cold. After all, they both begin with the letter "C". We need to dispel this notion immediately.
Who will take care of me while Mommy is sick? Thanks to their egocentricity, preschoolers are afraid of being left alone. They need to be assured that someone (whom they know) will be there to take care of them while the treatment period takes place. Along those lines, consistency is of utmost importance because it equates to security.
We will bring up these questions whether she articulates them verbally or not, because inevitably they will enter her mind. Fundamentally, we will provide enough information to dispel our daughter's immediate fears. We will reassure her that we will keep her informed and prepare her for what's coming next.
Along the trajectory of this illness, we will encourage our daughter to process facts and feelings. We will encourage her to share with us what she hears about my illness, or about cancer in general, from other adults and children. This encouragement sends the loving message that she shouldn't worry alone. Worries based on misconceptions can be easily dispelled. Just knowing that they are shared can lessen other worries. Additionally, it is incredibly important to encourage children to ask questions, anytime.
Inevitably, the subject of death will come up. People do die from FBC. I happen to believe that I'm not going to be one of those people. The pre-school age is the period in which children develop a developmentally appropriate fascination -- bordering on obsession --with death. When this topic arises, as difficult as it may be, parents need to be completely open to answer questions honestly, without evasion or embarrassment.
What else are we going to do? Maintain a consistent schedule with normal discipline (e.g., the use of good manners) and limit setting just as before the diagnosis. Often, adults make errors of kindness. For example, they may allow children to stay up late to watch a movie or eat whatever they want because Mommy is sick.
Most people know my feelings about sleep and diet: they are absolutely, positively the most important fundamentals of childhood. Without a good night of sleep, everything else goes haywire. As if things aren't already haywire enough. No matter what: keep bedtime and eating routines normal -- normal-normal.
We are also going to teach her about Silver Linings: finding the good in something bad. Now that's an SL in an SL!
While we cannot protect all of the world's children from the big and little "lumps" of life, our approach to handling this FBC will lay the foundation for how our daughter handles the inevitable future "lumps" in the road.
Children are wonderfully resilient. We have two choices in how we are going to handle this FBC: from a position of fear or love. We are choosing love. Our daughter will mirror our words, actions and emotions.
Next week, I will discuss the FBC surgery.
To read more about Hollye's holistic and humorous journey over, around, above and below breast cancer, please visit her blog, Brookside Buzz (www.brooksidebuzz.com). You may e-mail her at hollye@brooksidebuzz.com.
Follow Hollye Harrington Jacobs on Twitter: www.twitter.com/hollyejacobs
Darryle Pollack: The Power of a Punchline
I now work for an organization that raises funds for breast cancer research and supporting services through the sport of volleyball (www.side-out.org), and I will be sure to share your article. It is the perfect resource.
Sending you wishes for good health and a wonderful spring,
Julie
PS I checked out your blog and your dog is adoooorable!! My two pups were the best caregivers I could ask for. The first night I went in to the hospital, I requested pet therapy and the hospital program made sure I had a dog visit every day the entire month I was there! :) The power of animals is so incredible.
On Brooksidebuzz.com (under "Bambino" on the right hand side of the column), there are resources to help you in your conversation with your daughter. Please let me know if I can be of assistance.
Sending all my very best wishes to you and your family!
As a sister in cancer, Hollye, I'm with you in spirit and again, admire your strength and beauty as you battle the FBC. I too believe you will be alive in 5+ years! "our" target to really feel "cured".
So glad that you are 2 years out and that your last MRI was clean.
All my very best wishes for continued good health!
When I went looking for books to help explain my BC to my young son, what I found portrayed the mom as an emotional mess and kinda freaky looking, were really super technical for young kids, or just too sad for my liking.
That's why I wrote Nowhere Hair (www.NowhereHair.com), and hired a Dutch fashion illustrator to create a hip mama who happens to be bald. It tells the story of a youngster who tries unsuccessfully to find her mother's missing hair, only to learn that medicine has made it fall out. She learns that she didn't cause the cancer, can't catch it, and that Mommy still is very much up for the job of mothering. It explains hats, scarves, wigs, going bald in public, and the idea of being nice to people who may look a little different than you. It ends with the idea that what is inside of us is far more important than how we look on the outside.
Thank you for your note. I couldn't agree more with the books that are on the market. They frightened ME when I read them....thinking "am I REALLY going to look like THAT"? Not a chance, I quickly decided.
Thank you for writing your book. I look so forward to reading it. What a great moral to end with, for both children and adults alike.
All my very best to you!