Sunday, August 27, 2017

Electronic Mail (as opposed to the snail kind)

I'd like to share a correspondence. It's actually much more open and frank than the stuff I've posted in this blog so far. And because I hadn't considered posting such personal information before, I think it's more authentic-- nearly dying hasn't necessarily cured me of not wanting to reveal some aspects of my life.

I will, however, edit certain parts of the email and omit identifying names other than my own, to respect some level of privacy, and since I also didn't ask for his/her permission to post this-- though I don't think s/he'd mind. Maybe?

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Jani:
I have been wanting to write you since I saw your FB post about your blog and absence from the [Hume-Fogg H.S.] reunion. First, I want to extend my ... something to you. I don't know what, but my heart goes out to you; not as an expression of pity but of empathy.
I lost my husband, truly my soulmate, last year to prostate cancer. He was diagnosed with stage IV. He endured surgery, radiation, and chemo, all in the first year to reap the rewards of 8 completely blissful years. We were married 13 years.
I say that to let you know that I understand what you're going through, at least as intimately as one can without being personally diagnosed. Also, I wanted to tell you that many of the treatments my husband underwent weren't available when he was diagnosed. In fact, we became friends with the urologist who diagnosed him and gave him 5-10 years. It was years later that he told us he didn't expect to know us for a year. 
I was actually prompted to write after reading your first blog post and "Days You Wonder Why." Of course I had no idea of your situation, but I'm glad you're sharing it. I don't think you realize the impact your story has on folks in a variety of situations. 
For example, I was actually happy to read what can only be described as a rather pessimistic sentence: "I'm not actually starting over. If anything, I might be re-starting from behind." I was happy to read it because it meant someone else feels like I do. I don't have cancer, but I became a primary caregiver to my mother who passed on. I quit my job to become a primary caregiver to my father. He passed in [...]; my husband passed 6 months later. 
For the first time in life, I realized I was completely alone. If I was able, I could start over, completely from scratch. Not many people get that "opportunity" (a word I hate to use in that context). Nevertheless, I also realized I'm [... now] single, still grieving, and I haven't worked in years. Um, can someone give me a hand? Maybe some direction? What the hell am I supposed to do now?

[From a previous blog post:] "I wonder why I'm going through this miserable existence, half awake and conscious to 'where the hell am I?' Real to surreal and back again. It's a bad trip. How do I keep track of priorities when it's hard to tell what they are?"
I imagine that paragraph has a totally different meaning for you than it does me, but every word of it hits home for me, so again, thanks.
I'm going to stop rambling. I just wanted to reach out and share my story and tell you to keep doing what you're doing. It makes a difference.
Feel free to reach out anytime...

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Dear B,

Your words brought tears to my eyes. I feel and know that pain, the enduring pain of loss and, then, pointlessly questioning a God who must be indifferent. Goes beyond "Life sucks!" But childish fits don't help.

What you took the time to write me was important enough for me to sit at my desk and write you back on my computer. Smartphone keyboards make me feel like those writers who never learned to type properly. Better to keep up with the thoughts that form in my head, by typing the way I was taught. Still pretty darn fast on a keyboard... Btw, you didn't ramble; rambling is when you digress so much (e.g. Trump), you go off on that tangent of, say, typing, and you talk about how you miss old typewriters and the tak, tak, ding sound they make. See? Now, that's rambling ;-) Believe you me, I know how to ramble.

Well, I've always been a smart-ass. A coping technique, a form of avoidance, but sometimes the best way to address the harsh realities of life. Because what are you gonna do? Beat up every kid who picks on you? Get back at everybody who's ever slighted you? Just does more harm to you in the long run.

Being a smart-ass (still) helps me see the humor in life and lets me laugh at myself, which is very comforting. That this insignificant grain of sand would dare stick his chin out and mock the Creator. If I can do that, ain't nobody got a chance of touching me or hurting me.

Hope you found peace along the way. Hope you realized you were never really alone. Even when you felt so all alone (I've been there and so have many others I know), you were not truly alone. You could've reached out to friends you didn't even know you had, whose hearts are filled with love and kindness and understanding.

My battle with cancer made me more dependent than I cared to admit or acknowledge. But the good thing was that my stubborn pride was squashed by my feeling so vulnerable. No place for pride amidst relentless and agonizing personal suffering. I can see that you discovered, yes, very intimately that you don't have to have cancer to know what it feels like. You live the battle, too. In the same way, you don't need to be the cared for, the patient, to know what he or she is going through. A loving caregiver feels the loved one's pain and confusion and suffering, and even the drifting off into death. A piece of you really does die as well. 

B, you and I are kindred spirits in many ways. I can tell you that cancer isn't the worst thing that's ever happened to me. The worst is the loss of my little boy Noah who I held in my arms as he left me, as his body became lifeless in my embrace, and I couldn't let go. I wouldn't. I pleaded for him to come back. It took me a while to accept that that's also a part of life: "to love what death can touch." (It was his time. Born with multiple disabilities, Noah required round-the-clock attention and a private duty nurse during the day. I was his caretaker on weekends and evenings. Quit working full-time to care for him full-time. Sure, the grief doesn't ever go away completely. But it consoles me to know that he's no longer in pain.) Then, as if the flood-gates had opened wide, one of my dear and closest friends died in a car accident only months afterwards; my wife and I separated for over a year (we're now back together); and I was diagnosed with cancer-- not to mention the succession of friends whose fathers died all in one month. 2015 ('16 to half of '17) sucked! Never been to so many goddamn funerals in so short a time. And yet, life goes on...

I'm glad my words are relatable to you and others. Yup, I don't realize the impact they have on people. But it's nice to share and, if some folks find comfort or connection in my stories, I feel very flattered and honored.

Mrs. C suggested I publish some of it. My reaction? I was aghast! Frankly, I don't like all the bitching I do in the blog. Let me rephrase that. It's not about liking or disliking the bitching since it's rather a good form of therapy. I can't imagine not cursing and venting out loud in my writing, serious or not. I guess I can't really find a place for it in my overall body of work. I know, sounds kinda snobbish of me. Guilty as charged. Sometimes, I feel that being an academic actually gets in the way of good writing. Yeah, I have to learn to get out of my own damn way, and just let the words flow. D was good at getting us to do that. Sure do miss those old HFA days, the good parts anyway. (See? More rambling. I make it an art ;-)

Hey, I don't have your number. If you ever want to talk, feel free to reach out: 00-0. Text me or leave a voicemail. Like most folks these days, I don't usually answer if I don't recognize the number. (I absolutely abhor unsolicited sales calls.)

Please know that you're surrounded by people who can relate, who love you for the strong person you are.

Kindest Regards, Best of Wishes (my two best sign-off's),

Jani

Friday, August 18, 2017

Recovery


Lots of back-and-forth thinking this past month. That's about how long it's been since my last chemo treatment. I keep wondering what's ahead now. That's what causes anxiety, I suppose. It also makes for a certain level of healthy excitement. Not knowing what the future brings can be exhilarating, if not fearful.

I tend to embrace the unknown. Makes it easier to accept mortality and the pains and suffering of so long a life-- "slings and arrows of outrageous fortune," as Hamlet would have it. Joys are much more fleeting. Taking comfort in enduring pain is more lasting. Yes, comfort in pain. You grow intimate with it more so than with happiness and joy.

The starkness and indifference life has to offer is a strange realization. You deal with it with no sense of bitterness or anger. You just deal with it. How do we justify getting angry over what we can't control? Life throws all kinds of obstacles in the way of personal progress. Again, you just deal with it.

Fighting, surviving, trial and tribulation, suffering, pain, agony, despair, disorientation, fatigue, strife, blood, sweat, tears-- all sound so aggressive and almost meaningless. After a while you can only laugh at the worst that life puts before you, and finally have to ignore or side-step all the muck. Maybe recovery is something like that-- knowing how to get passed and leave behind so much that's bad, and move on.

Sure, there are always reminders. Physical pain is hard to ignore. It takes a whole lot of courage, a whole lot of knowing how to muster that courage, to move forward. Fearless, I'm not. Likewise, fearful, I'm not. I just go with the flow, tumble and stumble around the rocks, and make a way for myself. No small amount of courage.