It’s 2:30am on my
third night home from the hospital. Adjusting to survival is turning out to be a challenge. The struggle of my life has always been struggling with my life or, perhaps my more generous friends would say, getting out of my own way or maybe they’d just say that I’ve been nuts. I don’t know what I’m being shy about. The hardest part of my life up until now has been depression. I spent more than thirty years in therapy with the same psychiatrist [BTW, if any reader is familiar with what’s doing with Dr. Lawrence Bloom in Montclair, NJ, I’m very curious about how he and his family are doing]. Depression feels like a funny name for the emotional cocoon I was wrapped in for all those years, out of date, like referring to Klaatu’s ship as the cutting edge of space travel. A lot that has changed over time would have changed without my doing. I had a very disapproving father who passed a few years ago, taking much of his disapproval with him and leaving a very generous estate in its place. It was a lucky exchange. The antidepressant medications available now make the tricyclates I started off with years ago feel like a boilermaker with a pickled egg on the side. I’m in a very happy marriage and my mother is alive and my daughter is doing well. What could be depressing? Yet Sunday, following a visit from the Grubmans and from Birdie, I exploded into hysterical tears like I can not remember occurring after boyhood. [I of course was undyingly sad after Dorit’s death but I was too much the manager, too much in the center of things to give in to bawling – the one time I remember I gave up to sobbing uncontrollably was when I received a malpractice award concerning her medical miscare and the injustice of me being the surviving one was too overwhelming too move on]. And there on the 17th floor of NYU, I couldn’t stop weeping. I had come so close. It was so frightening. I looked down and saw the scars, the trail of my disease made flesh. So that’s how it started Sunday. Monday, around midday at the hospital, I was waiting for my turn to go back into the endoscopy lab when one of the GI residents came in and told me they had decided I didn’t need anything else before being discharged, that I could get ready to leave. I thought about the many nights many years ago I had kept my father company at the hospital, bringing in Chinese food to share as he slid from aphasia to full dementia, my uncle Bill, who was on NYU’s architectural review board, managing his care and I thought of Bill’s own final visits to the hospital, events I was protected from knowledge of as I was recovering from my lymphoma at the time and I thought “I’m the only one who gets to walk out. In the only one who healed.” And again, I could not control my tears. And as I waited to leave, I read a FB post by Marc Nathan lamenting his distance, in Nashville, from friends who needed him and I had the hubris to think I was one of them and that, yes, it would have been better if he was around. You can see, I’m very tender at this point but I’m also completely alive. I’m letting my yea be yea. It’s all coming through to me in a way that’s inconsistent with being depressed and though I was celebrating, you couldn’t call it happy. So Jolean and I get a cab home. We make camp in the bedroom and I start posting favorite songs on FB, each a tearjerker, or at least designed to jerk my tears. And as I’m doing this, I discover something – just about every Bruce Springsteen concert I attended from 1974 until 1980 is available for streaming online. I think about this. 42 years of me and Bruce, sharing our eyes, our thoughts, our changes and favorite covers. And I think about Jeff Peters, Shelley Abramowitz’s friend when Shelley, Ken, Larry and I were roommates on Cummings Road in Boston. Jeff pulled us to that first show Springsteen show at the Academy, he begged us to go, we had to see this guy. Of course I still remember the show, the still unreleased “Jungleland”with the violin, the cover of “Cupid”. Of course, I remember Jeff who Shelley told me, when I saw him two years ago, is also gone. I’m not sure I can quite describe the insight I’m going for here. Yes, it’s a wonderful world. Yes, there’s beauty and sweetness and tragedy to be sifted from the ether, to be netted like a butterfly and then released to fly again. That’s not what I mean. I mean the miasma these all float in, the stuff of perception itself, is a kind of madness. Or maybe I mean there’s all kinds of madness and sometimes it blinds you and sometimes it’s as essential as clarity in mediating the world. Our maybe it’s just thrilling to survive. I don’t think I can continue to live on this edge I’m on right now too much longer but there’s nothing you can do that’ll make me willingly step back.
This weekend was my first at home after two weeks in the hospital and I feel like crying with gratitude for having had it and I feel very afraid about needing to go back since, after 14 days, the blood leak that caused my anemia wasn’t found, never mind treated. The only thing I came home with that I didn’t have when I left was a surgical wound on my belly. It’s grotesque. I’m also afraid of the anemia returning. The last time I had it, the incident that provoked the hospital visit, I didn’t have the strength necessary to get off the bed. I went to the emergency clinic by ambulance. The worse things about being in the hospital are the loss of autonomy, the pain of the many, many needles you must endure, nurses and doctors are free to come and go at any moment and the ugliness of your surroundings. When I arrived home, the bed was covered by a duvet we had just bought, kind of a deep Mandarin red with gold paisley, and it looked so comforting and inviting and big, big enough to lie down next to my wife, which reminds me of something of another effect of the hospital – the loneliness, because even if you are, like me, lucky enough to have your best friends and closest relatives visiting you at all hours, they’re leaving and you cannot leave with them and just that fact reminds you of your isolation. All you seem to talk about is your illness, which is really all you’re thinking about because, what else is there, and that makes the visit bittersweet. So does the knowledge that they’re there for you, to help take care of you and you hate to do that to them. Or you’re thinking about food, where will the next meal come from or even whether you’ll be allowed a next meal, since, for the bulk of my time there I was limited to clear liquids. I would eat the hospital’s jello and Jolean would go down to The Pastrami Queen and bring back quarts of chicken soup. Missing your wife at night and knowing that, when she arrives, you will have a list of foraging for her (which she will cheerfully take care of) as opposed to home, where you can hold her and love her and for a while forget that you’re the one being taken care of. All your stuff is home and the anchoring quality of being among your stuff is not to be undervalued. There’s my guitar. There is a pile of books. There is the footboard of the big brass bed.

Donald says stupid things. He is stupid. Not like Paul. And yet, Paul wants Donald to be president because maybe, just maybe, if Donald is president, he’ll call up Paul and say, “Now. Now’s the time. I don’t know how to govern and I need you to open your envelope.” Paul knows he will never ever get that that call if Hillary is president. So he sits and watches Donald on TV and waits and waits. He hates him so much.









