Posts tagged ‘billy collins’

June 21, 2011

S

When I asked S to write a guest post, he readily agreed. He told me he wanted to write a public love letter to me.  Boring, I told him. If you want to break up with me in public, now that would make for interesting reading, but a piece on “how do I love you, let me count the ways”? Yawn. I asked him to write about life as someone who is married to a person with CF. Boring, he told me: it is what it is and there’s not much to say.  While I admire and appreciate his certainty that CF has little impact on our relationship and the evolution of our love, I think it’s a worthy topic that may be of interest to people who have CF, to parents of children with CF, or to people who are currently in a relationship with someone who has CF. Perhaps S will be willing to venture into the murky depths of CF and his feelings about it for a future blog post. For now, the winning topic is… poetry. Poetry always wins; do you remember a time without someone writing it and someone else complaining about it? Along with cockroaches, poetry will survive the end of the world.

Please welcome my tall, dark, and handsome S who after writing this guest post is now tall, dark, handsome, and poetically inclined.

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When Lizi invited me to write a guest blog, I was honored and excited. But also, if I’m honest,  nervous. What could I, a neophyte to poetry, add to the dialogue?

I considered commenting on the Slate article that found poetry in the official descriptions of dog breeds.

I considered song lyrics such as The Police’s “Message in a Bottle” (Walked out this morning, don’t believe what I saw/Hundred billion bottles washed up on the shore/Seems I’m not alone in being alone/Hundred billion castaways, looking for a home) or the lyrics at the end of “Eclipse,” a song in what is often considered the greatest rock album of all time, Pink Floyd’s Dark Side of the Moon: And everything under the sun is in tune/But the sun is eclipsed by the moon.

I also recalled my teachers who told us of the debate between those who think poetry can and should be read without any knowledge of the poet or time in which she wrote, and those who think poetry can only be fully understood with the proper historical, cultural and political context. Which reminded me of another scholarly debate about whether text is alive, a breathing animal, or a petrified relic of times past. All heady topics ripe for dialogue.

But it was a discussion at work of all places that answered my question. A colleague of mine ended several emails in an email chain with one or two line aphorisms, whose authors he considered “poets,” and not just any poets, but “famous” ones. He took umbrage when I questioned whether the quotations met the test for poetry. I may have offended him when I said the lines he chose belonged inside  fortune cookies.  I told him that what I considered poetry, by contrast, was a piece recited by Billy Collins at the recent poetry reading Lizi and I attended.

I thought back to something Billy Collins mentioned: kids invited to hear poetry as part of his “Poetry 180” program often scoffed and squirmed at the concept of poetry until they heard a poem that resonated with them. Then they felt conflicted by their visceral reaction to the word “poetry” (with its connotation of sonnets and stanzas and Emily Dickinson and Keats) and their enjoyment of the powerful words they just heard. And it occurred to me: the reason I didn’t like poetry before, or thought I didn’t, was that I didn’t understand what poetry actually was.

It would be presumptuous for me try to define poetry, and anyway I wouldn’t know where to start. For me, poetry has an emotional content that transcends the fonts on the page or the pixels on the computer screen. Sometimes it’s humorous and maybe serious and serene and mournful and bittersweet, or all of those. And sometimes, it is set to music. But the commonality is that hearing a poem, in whatever form, always challenges me. Sometimes the challenge is to unwrap its lyrical knot. On other occasions, it’s about holding still, not resisting, and letting the torrid currents wash through me.

I have Lizi to thank for patiently leading me into its shallow water and helping me to gradually immerse myself in the pool of poetry. I now see that poetry is not an exotic forest but more like the air we breathe and the water we drink, the collections of words and feelings that come spilling out from people every day, whether they have PhDs or MFAs and conduct poetry readings, or write inspirational cards, dog breed guidelines, or stuff fortune cookies. The truest test of a great poem has nothing to do with who wrote it, or its length, or the sophistication of its vocabulary. It’s about whether, upon reading or hearing it, one’s view of the world will never be quite the same.

Have you encountered any poetry lately in unconventional forms?

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S loved the experience of hearing Billy Collins read his poetry. That experience, more than anything else I’ve ever discussed or shared with S, warmed him up to poetry. Today’s poem is in honor of S and anyone who is willing to give poetry a try. (click link to read entire poem)

Introduction to Poetry by Billy Collins

I ask them to take a poem

and hold it up to the light…

May 23, 2011

10 ways to a woo a word lover.

10. Do not give her diamonds; give her books.

9. Date night? Scrabble. Bananagrams if you want to shake things up a bit.

8. Court via letters. Your hand-writing on paper does something that no email, no matter how romantic and well-written, can ever achieve.

7. When she cries about feeling lonely and misunderstood, tell her she is avant-garde. What a word! She’ll perk up. Immediately.

6. Do crossword puzzles together. Gives new meaning to the phrase you complete me.

5. Tell her that her glasses make her look like a sexy librarian.

4. When she mentions that she’s never read Philip Roth’s Portnoy’s Complaint, give her the copy you read in college so that she can devour the book with the sprinkling of your adolescent marginalia adding to the flavor.

3. Understand that she might never pay attention to you with the same intensity that she lavishes on the book she’s reading.

2. Use the word “covenant” as a verb in a poem you’ve written. Yes, this means you must write her a poem.

Almost 1. Edit her work and point out typos. Especially glaring mistakes in the title.

1. Take her to hear Billy Collins read his poetry.

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I love people that make me laugh. I love poets. Billy Collins is a poet that makes me laugh. Here is just a little taste.

Today’s Poem: (click link to read entirely) by Billy Collins

I Chop Some Parsley While Listening to Art Blakey’s Version of ‘Three Blind Mice

And I start wondering how they came to be blind.

If it was congenital, they could be brothers and sisters…

May 7, 2011

Mama mia.

My mother and I are extremely close. We’re also extremely different. My mom is loud, spicy, Mexican, talkative, overflowing with joy and enthusiasm, and has more energy than the Middle East. She loves to dance, sing and eat chocolate and ice cream. Me? Not so much. None of the above. As a child I’d often ask my mother to turn down the volume of the record player (yes, record player) so that I could concentrate on my book. Despite the differences, it somehow works for us.

This blog has occasionally been difficult for my parents to read. I’ve considered censoring myself but for the sake of getting ever closer to truth (my version of it, at least), I’ve written what I’ve needed to write and forced myself to ignore their potential discomfort. I don’t think either of my parents knew what a sailor mouth their daughter has…

Today I’ve caused my mother even greater discomfort by asking her to answer some of my questions about her experience raising two kids with CF born over 30 years ago. She did it side by side with my father (who I adore and who I am painfully similar to) but because it’s Mother’s Day, I will be focusing on my mom.  She is phenomenal. She wrote much of her doctoral dissertation cramped in the tiny bathroom of my brother’s hospital room.

My intention, other than publicly declaring my love and admiration for my mom,  is to hopefully provide some insight and support for mothers whose children have recently been diagnosed with CF. At the very least, I want you to feel a little less alone in your aloneness. I want to acknowledge you; mothers struggling to do your best with the challenges that have fallen into your warm, frightened, loving laps.  I want to hug all the moms who make this world a better, kinder, softer place.

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How did you feel when you received the diagnosis of CF for your first child?

With the first diagnosis I felt numb. Rationally, I knew it was a sickness, but because I had never even heard the name of the illness, I imagined that my baby would somehow be cured very soon. I couldn’t rush home to google CF. There was very little information and even doctors didn’t know about CF! Your brother’s first pediatrician told us he wouldn’t make it to age 10.

How did you feel when your second child was born and received the same diagnosis?

We had consulted a geneticist before getting pregnant and he (incorrectly) informed us that the chances were slim to none of it happening again. So we decided that with low statistical probability on our side, so much love for the first child and more love to give to a second baby, we’d have another one. When the doctor told us that you had CF, we never looked back. We never regretted having you, CF or not.

Do you feel that a period of “grieving” is a natural and necessary part of the journey with CF?

I would call it grieving if you’re referring to anger together with sadness and limitless fear. If this is your definition of grief, for me it started when your brother got very ill when he was 10 months old and needed to be taken to the hospital where I lost his beloved stuffed animal (Laika) and I lost my belief in the fairness of life. Somehow I could handle the emergency hospitalization but losing that dog broke my heart a million times. It still hurts.

Did CF influence your approach to parenting?

I can’t tell you if I would have been a different type of mom to a child without CF because I never had that opportunity. Looking back, I wish we would have been more open or comfortable with CF  so it wouldn’t have been such a heavy burden on all of us, trying always to appear as if everything was ok. Because of the almost secrecy, I allowed CF to take too much energy, prominence and space in our lives. By trying to pretend it wasn’t there, we allowed it to define who we were. I also think I was too lenient.

How did you manage your fears and worries? (You always made me feel that everything would be okay, that everything was okay. Now that I’m a mother, I know what a hard thing this is to do when you’re falling apart inside).

I have never managed my fears completely but I have NEVER lost hope either (except once for a short period, before your brother’s transplant). I’ve done everything to deal with my fears: cried till my eyes hurt, prayed a lot, bargained with God a lot, banged walls and hollered, talked non-end about it, kept silent about it. In order to deal with it I have kept busy with work, dance, art, too much bad food,  and I have been helped by a husband that will listen and doesn’t cry when I need to cry, having a mother who shares the tears with me; having one sister and a few friends who try to understand.

What is the worst thing about CF for you?

There is not a single worst thing about CF for a mom. There are various: my guilty feelings because it is a genetic disease, my impotence of not being able to make it “all better”, no matter how much I try; coming to terms with the randomness of life’s “justice”; and of course witnessing how you and your brother suffer when you don’t feel well, when you get bad news, when you’re frightened.

Is there any good that you think has come from us being a family with CF?

Yes, believe it or not, there are good things about being a family with CF. We don’t take time, health, laughter and life for granted. Every day counts, and every good thing that happens is worth celebrating. Not many families live like that. Most people live as if they are owed a good life. We have been VERY lucky to be aware of the miracles that have been given to us, such as the success of your brother’s transplant, you getting pregnant and giving birth to your angel, being witnesses to how courageous a human being can be (as we have watched you and your brother); witnessing the love that S has for you. Lots of sadness, but how many families laugh and love the way we do? Both somehow come from the same place of deep love for each other and for life.

How has CF affected your life personally (not just as a parent)?

For a long time CF defined my life. When I used to wonder “Who am I?” my first definition was always a CF mom. That definition always made me feel different from other moms and I hated every mom that had a healthy child. That has changed with time. Now I am a wife, mom, grandma, daughter, dancer, sculptor, etc. And, oh that’s right, my kids have CF.

If you could, what would you tell mothers and fathers of children who have recently received the diagnosis?

Today’s parents have a lot to look forward to in terms of research and many new treatments in the pipeline. Even though CF is a genetic disease, it’s NOT YOUR FAULT! Nobody chooses to give an illness to a kid. It is simply life happening. So if you need to, get psychological help ASAP and get over the guilt. If your child needs to be hospitalized, do whatever you can to have a family member there 24/7. You can (and we did) prevent errors from happening if you’re there and you’re watchful. A support system is very important. Even though everyone else seems to have healthy kids, don’t lose your friends; you’ll need them. Do not despair, there is ALWAYS hope. Doctors know a lot, but they don’t know everything. Nobody knows what the future holds. Take time to take care of yourselves (mom and dad) and find activities that take your mind, body and spirit away from CF (yes, fundraising and outreach are important but don’t let CF become your entire life). Do not forget that you and your child are alive right now- don’t lose the now because you’re worried about the future.

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Thank you for answering my questions Mom. Thank you for being my Mom. I love you and today’s poem–my little offering– is for you.

Happy Mother’s Day to anyone who is a mother and anyone who has a mother.

(click link to read entire poem)

The Lanyard by Billy Collins

The other day I was ricocheting slowly

off the blue walls of this room…

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