Turning 70 and Trying Not to Worry

I turn 70 years old this summer. I have a rocking chair on my patio, and just as I imagined years ago, I spend a good deal of time in that chair reflecting. And I think a lot about my daughter and her husband in Virginia and my son and his wife and our grandson on Long Island, New York.

I try to practice my spirituality in terms of accepting the fact that I cannot control events in the world, but it is very difficult not to worry about my family, and their families, and my daughter-in-law’s sister who is an emergency room nurse on Long Island in a hospital that saw Covid19 patients quintuple over the weekend.

Meanwhile, on the East Coast, our kids and their families worry about us. One could probably call it reverse parenting. They keep reminding us to wash our hands, not touch our faces, not do our own shopping, not go out unless we absolutely have to. You know the drill.

So here we all are, unable to be in the presence of the most important people in our lives, trying not to worry, trying not to give in to our fears in this environment we have not experienced before with leaders struggling to agree on what the next steps should (or should not) be.

I heard a psychologist this week say that there are three factors that can lead to our fears spiraling out of control. First, the experience is unpredictable. Secondly, it is uncontrollable. Thirdly, it is sustained and chronic with no clarity about how long it will last.

Well, there you have it! No wonder that at night the vultures come out and sit on our bedposts and we lay awake worried about so many things.

In December I wrote about “The Thing I Can’t Write About.” Well, I am still having trouble writing about it as evidenced by the fact that I haven’t posted the next 3 blogs I said I would write. I am still stuck on what I wrote in December, especially now that my daughter, Jessi, is quarantined with what her doctors think could be Covid19, but are not sure because she does not yet qualify for a test.

Here is that post again, slightly revised. As I state at the end, it is so very hard for us to talk about the fears we have for our children (and they for us) but finding the courage to share those worries and fears creates community and helps each other face and take on the pain and uncertainty of the present days:

I have written about all kinds of things in my blog and in my book, but there is one thing I cannot write about. One would assume that this is because it is not important. To the contrary, sometimes the thing we can’t write about (and have trouble talking about) is one of the most important things in our lives. For me, this has been my daughter Jessi’s mental and physical health.

However, she has had the unbelievable courage to write about it herself, and today I decided I have to find the courage to write about it also. I begin with the words (and picture above) from her Facebook post three days ago, on December 17, 2019: 

    --8 years old: Diagnosed with Diabetes

    --10 with Anxiety

    --15 with Depression

    --16 with Suicidal Tendencies

    --29 (Today) with Bipolar II

I’m trying to process the latest diagnosis. It wasn’t a surprise, but it still comes as a shock to the system. It's knowledge and questions answered, but I’m heartbroken. With this knowledge comes ugly statistics and painful stigma. I’ve spent so many years afraid of the dark that I didn’t speak honestly about the light; the ignition that arises and becomes the outgoing, fast-talking, overly productive mania. It was a relief most of the time swinging up. I never thought to mention the swing in the first place. So, this is bipolar, eh? I guess it’s time to become a spokesperson for it.

It all began in November 1998. Jessi was losing weight and had little energy. We went to our cabin for Thanksgiving, and Jessi had difficulty walking through the snow. At home she wanted me to carry her up the stairs to bed. We made fun of her for being lazy. I still feel guilty about that. 

On Monday of the following week we took her to her pediatrician. It did not take long for him to render a diagnosis of Type I Diabetes. He sent us immediately to an endocrinologist, who gave her an injection of insulin, and then we all returned home to begin the process of trying to come to terms with this disturbing diagnosis. 

[Picture of a very thin Jessi at Halloween before her Diabetes diagnosis]

That night we had company coming from out of town. We didn’t know what to do, but visited the best we could, not telling them what was going on for us. However, as soon as they left, and Jessi had gone to bed, I looked at my wife, Mary, and blurted out: “I hope I die before I see anything bad happen to her.”

There are those times in life when our words are not meant to be taken literally: they are just pure emotion. And yet such words often reflect the great ambiguity of life as we face the suffering of those we love most. What parent would not be willing to take on their children’s diseases and suffering if it would keep their child from that suffering? What parent would not willingly die before seeing their child die?

But once our emotions begin to subside and our minds clear, we realize our calling as parents is to live for and with our children doing everything we can possibly do to mitigate their pain and to support them as they struggle through life.

Well, I haven’t died, but I have seen so many bad things happen to Jessi. I have had trouble talking about it outside of therapy, and I haven’t been able to write about it. I’m not sure why, but I have decided that now is the time.

Six days ago Jessi, who lives in Virginia with her husband Rob, called Mary and me at our home in Phoenix and told us she was not “safe” (our code word for when she is having suicidal ideations) and asked us to call Rob at work because when she is not safe she cannot be left alone. Mary called Rob on her phone and I kept Jessi on my phone. I talked with her until Rob got home and then we put together a plan so she would not be alone, including seeing both her therapist and psychiatrist. Mary flew out immediately to Virginia to be with her this week and Rob took off work until Mary could get there. And it was through those doctor visits that Jessi was diagnosed this week with Bipolar II.

Two months ago Mary and I walked Jessi down the aisle at her wedding, and I officiated the service. Jessi wanted to do the “first look” for me, and then Rob. That picture is now my FB Profile picture. As powerful as a picture can be, it still can’t capture the depths of the pain, joy and hope we feel when we look into the eyes and hearts of our children. 

All of us parents carry that experience every day of our lives. It is so very difficult to speak and write about it, but there comes a time when, for our own sake and the sake of those we love, we must. We also write and speak about it as a way to help each other face our parental fears and hopes as a step in supporting each other.