Showing posts with label traditions. Show all posts
Showing posts with label traditions. Show all posts

Saturday, April 16, 2011

Let The Sunshine In State of Being

Flying Over Tennessee:

"I don't want to go to the beach," said Miguel. "There's too much sand."

So we spent three full sun-splashed days an hour north of Miami, with temperatures in the mid-upper 80s and two golf courses and one CVS on every corner, and never reached the shore. Miguel and Maya frolicked in the pool at my brother's hotel one day and at my aunt's pool the next.

The Florida we visited was a combination of traditional Friedman family values meets 21st century ethnic enclaves. We were there first and foremost to spend time with my father and stepmother, who each turn 80 towards the end of this month.

We were also there to help support my father and stepmother as they deal with severe physical and mental limitations. My father has a very bad back and is bent over all the time, and not in the way of Apollo Ohno gliding across the ice. He said this morning, "The pain is there everyday."

My stepmother needs a cane to walk and is experiencing some cognitive decline, so it is impossible for my father to care for both of them. My step-siblings are there now to initiate conversations with them about seeking support from Jewish Family Services.

All I did was remind my father that it was OK to utilize help. "Dad, you can't go it alone. Please listen to Michael and Andrea."

Florida was also seeing different cultures, Haitians, West Indians, African-Americans, that Miguel and Maya have almost no contact with in a California county that is 85% Caucasian.

On Thursday we drove to the Gulf side of the state, to Ft. Myers and Lehigh Acres, to spend time with my aunt (father's sister) and uncle, two of their children (my first cousins), several of the cousins' children, and a few of my aunt's great-grandchildren (and my aunt is only 74 at the most). Outside of my aunt, whose been in California in the past ten years and was at Verna's funeral last September, I haven't seen my Florida family, who grew up 1/2 mile from us, since late 2001.

Soon after we arrived at my cousin Sharon's house, she pulled me aside and shared what was going on in the family. One sister, Elaine, who lives nearby, has been in and out of the hospital for the past few years. She was in there again.

"Steven, it's been so frustrating," Sharon said. "We are all so worried about Elaine."

Sharon and I have a special relationship. We are the same age and always went to the same school. We always sat together on the school bus and reserved a seat for each other. Even after we drifted apart in middle and high school, I never forgot sleeping over at her house, having a wicked crush on her, or all the times we talked on the phone, sent each other postcards over the summer, and spent holidays together at the shore.

Sharon's third child, Brooke, who is almost 16, and Sharon's sister Arlene's youngest son, Alex, who is almost 17, are as close. Sharon said to me, "Brooke asked me, Steven, if Alex is going to move away from me like you did."

"Sharon, you moved to Florida before I left Connecticut," I responded. But I got her point. Sharon's and my lives are not that intertwined, though we talked a lot during Verna's illness, and Brooke fears a future separated from Alex.

Frankly, Alex is pretty special. I don't think Brooke should worry right now. After Verna died last August, Alex decided to organize a relay team for the American Cancer Society's 24-Hour Relay for Life. He named his team Verna's Heroes and he pledged to raise $2500. So far this lithe high school student with size 14 sneakers and sandy blond hair has raised more than $800.

"I told him it's OK if doesn't meet his goal," said Arlene, his proud mother.

Alex had plans Thursday night. He was supposed to hang with some buddies from school, but stayed home to meet me. Once I heard about Verna's Heroes, though, I wanted to meet and hug him.

"Have we ever met before?" he asked me.

"I was there when you were eight days old," I said.

I happened to be in Connecticut for his brit milah (Jewish circumcision ceremony) and the rabbi and mohel (the one who does the circumcision) had recently had throat cancer, so he asked me to chant the prayers while he performed the ritual mutilation. The rabbi's wife chimed in whenever I slowed down to pronounce a word I hadn't seen in a while.

So this amazing kid was also what Florida was about for us: A generosity of spirit in honoring Verna's memory and raising money for cancer research. I made sure to remind Miguel a few times that Alex opted not to spend the evening with friends because he wanted to chill with us.

So we missed the beach and consumed very few citrus fruits, but we did experience what was really important about the Sunshine State.

Tuesday, December 14, 2010

So This Is Christmas

Warning: this blog contains stories about me celebrating Christmas. If you find it offensive for a Jewish person to do so, please discontinue reading. Some people were extremely bothered when I wrote about kneeling in Church with Verna on Easter in 2006, three months after she was first diagnosed with and treated for breast cancer.

Maya and I kicked off the Christmas holiday season this past Saturday afternoon. While Miguel was long-boarding with his buddy Chris, Maya and I were spooning homemade ice cream into our mouths at Silberman's in San Rafael. She ordered creamy peppermint, I went for egg nog.

"I love it, daddy," she said. "This is our playdate." Flecks of bright pink peppermint ringed her lips.

To be perfectly honest, I really, really wanted to skip the holidays and be magically transported to January, lying on a secluded beach and buried in an engrossing book. Thanksgiving was essentially hell. I missed Verna so much and I was so overwhelmingly sad that I moped around the house her family had rented in Lake Tahoe. I actually felt as if I was in the throes of the Jewish mourning rituals, where one removes him or herself from joyous living and concentrates on grief and coping.

I did not party in Tahoe. I did not go out gambling (which I hate) or drink to excess (I had one beer in five days and no hard liquor). I avoided singing Karaoke, a Wefald Family tradition that, even though we sound more like the Manson family than the Andrews Sisters, is always filled with fun and laughter. One of my sisters-in-law called me a party pooper.

But I did force myself then to live in the moment. I went running every day, even in an all-day snowstorm with limited visibility and icy roads. I took Miguel and Maya sledding twice, made snow angels, raced Miguel in two-foot deep snow, and threw several snowballs at my children and family. All that helped me to cope.

However, I was fearful that Christmas and all the build up to the world's major holiday would overload my emotional circuitry. Christmas had always been huge for Verna. She loved the lights, the smells, the trees, the giving. Christmas music blared in our home pretty regularly from the end of November until December 26.

How would I deal with my pain and longing and prepare for the holiday and give the kids at least a chunk of something to celebrate?

Hospice by the Bay came to the rescue. They offered me free tickets to the Marin Ballet's late afternoon performance of the Nutcracker last Saturday.

"Miguel, do you want to see the Nutcracker with Maya and me?" I asked son #1 early last week.

"No way," he said. "Count me out."

"But you saw the Nutcracker in San Francisco three times."

"Yeah, dad, that was when I was a little kid. A long time ago," he said.

Ouch.

So Maya and I had ice cream and bought a birthday gift for a neighborhood friend and ate an early dinner at home so we could get to the Nutcracker by 5 PM. One friend insisted I dress both Maya and myself up. I just wanted to warble, though, "But I gotta be me."

Maya wore a floral print dress over a long sleeve shirt and pants. Her usual array of necklaces and bracelets dangled, making her appear, to me at least, very stylish and festive. I had on blue jeans, a t-shirt and zippered sweatshirt, and a Giants World Series cap.

Maya had never been to any kind of show in an indoor venue before. She hasn't even yet seen a movie in the theater. So I was slightly concerned how she might fare during the performance. Would she talk and talk and talk, as she often does, when the lights dimmed, forcing me to rush her into the lobby?

As it turned out, she knew a fair amount about the Nutcracker because her ballet teacher was working behind the stage and had shared with her students just that morning details of Tchaikovsky, Petipa, and E.T.A Hoffman's creation. Her ballet school had sponsored and put on the performance. Maya told me about Clara and other characters. She seemed mesmerized. At one point she asked me if the characters lived onstage. It was very real for her.

On the way back to the car, Maya twirled and pranced with a mile-wide grin on her face as if she were a ballerina. I couldn't help but smile even though I wished Verna had been there to share the precious moments with us.

Hospice by the Bay came through in a way the following day as well. Hospice counselors and literature advised that creating new holiday rituals is one way to cope with the onslaught of grief and emotions during the festive times of the year. A few weeks ago, one of my friends and co-workers suggested we chop down our own Christmas trees this year, breaking with the tradition of purchasing one from a tree lot.

"I'll find the place for us," he said.

So we drove 20 miles north to Petaluma this past Sunday to a family Christmas tree farm, where you pay one price no matter how high the tree, $49.99. Miguel and Maya scouted out the Douglas firs as our friends Erik and Megan and their two-year old son, Brady, shopped for their ideal tree.

Miguel held the red saw as Maya and I pulled the specially designed tree cart. He set his sights on one tree, slightly lopsided and rising at least 15 feet in the air.

"No, Miguel, that's too big." I said.

"Yeah, Miguel, look how it's tilting," Erik said.

Miguel exclaimed that he wanted at least a 10-12 footer. I said six to seven feet max. Erik then chimed in yet again.

"Miguel," he said, looking at me, "Two words: honor roll," which Miguel had made a few days earlier.

"Erik," I said, "Two words: F.U."

Miguel and Erik chuckled. With my prodding, er, encouragement, Miguel and Maya finally settled on a tree that, with its star branch pointing upward, was about seven feet tall. Miguel knelt down and made an initial cut before he started sawing. It was slow going because there were several underbranches blocking him from leveraging his body against the saw and tree.

"Miguel, do you want some help? We could be here until tomorrow," I said.

"No," he said. He was a young man on a mission.

While Miguel and I postioned ourselves next to the tree and Erik and Megan contemplated which tree to slice into, as if they were deciding when to launch the Allied invasion of Europe, Maya and Brady strolled through the rows of trees.

"Let's hold hands, Maya," Brady said. "Let's hold hands."

Miguel only let me cut for thirty seconds or so. He insisted on doing the bulk of the work. Determination etched on his face, the tree succumbed and we loaded it onto the carriage. For an extra $3 you can have it shaken and bound in a manner not too dissimilar to what many are advocating for Julian Assange.

I loaded the tree into the back of our 2001 Chrysler Town and Country and we then hugged Erik, Megan, and Brady goodbye. Erik and Megan were also on a mission: get Brady down for a nap so Megan, who is 7 months pregnant, and Erik could relax.

We hauled the ornaments and lights up from the garage after we positioned the tree against the wall near our dining room table. I was completely unsure of how the decorating might go. So many of our ornaments were really mini-memory factories containing stories of shared moments with Verna.

There was the Baby's First Christmas one Verna and I bought before Miguel was born on a weekend outing to Monterey and Pacific Grove. Or the thin gold leafy one we bought at Multnomah Falls, where Miguel, Verna, her mom, and I hiked for 2 1/2 hours in 2002. Or the only remaining ornament from Verna's childhood, a vital generational link now for Maya and Miguel, a tiny bird with a feathered white head and a blue breast.

Miguel and Maya asked if they could go outside and play in the park. I later saw them zooming down toward the house, seated on Miguel's longboard, Maya's hair flowing in the wind, laughing, as her big brother grasped her tightly.

So I decorated the tree alone, and, strangely, I felt at peace. I felt as if I was carrying out Verna's wishes and acting as her earthly Christmas agent. When I finished putting up the bulk of the ornaments (I left some for the kids), I gazed at the tree and felt satisfied. Then I heard the tiny Nativity carousel Verna had inherited from her mother, that no one had touched for several days, twinkle three notes. I sensed Verna's presence, so I said, "Verna, I miss you so much. Thanks, I think I did a good job. For you and us."

Ho, ho, ho.

Friday, May 8, 2009

Happy Mother's Day, Chela

This will be my wife’s first Mother’s Day without her mother, Maria Graciela “Chela” Wefald, who died last October after a brief and sudden illness. She was 84.

She and Verna were very close, so the past several months have been very hard for her; even more so as the holiday approaches. One woman told Verna, “My mother died ten years ago and I am still not over it.”

So Verna started informally planning about a week ago what we might do on this Mother’s Day. Boom! An idea bolted into her head almost instantaneously.

“I know what we’ll do for Mother’s Day,” she said. “We’ll have a picnic…at the cemetery and then play a game of P & M,” which was one of her favorite family card games.

Either Miguel or I joked that we would have to open the grave so we could retrieve the playing cards Maya threw in on the day of Chela’s funeral and burial.

Maria Graciela Wefald, who was born in El Salvador and came to the United States in the 1950s, was one of the most unconditionally devoted parents and grandparents I’ve ever known. Her selfless embrace of her family reminded me of my maternal grandmother (who died in 1999) and my paternal grandfather (who died in 1992).

Shortly after Verna gave birth to Miguel in 1998, Chela took the bus from San Francisco to our home, 30 minutes north, with a pot of chicken soup. She then walked nearly a mile from the bus center, more than ¼-mile of it uphill, to our shaded duplex overlooking San Rafael High.

I have several memories of Chela I’d like to share. Even into her early 80s, she routinely hiked 2-3 miles. She chided her family to eat their “green things,” which were vegetables. She called root beer soda “ruse beer”.

She and my father-in-law trekked to our home everyday, five days a week, when Verna was first diagnosed with cancer. They came for 9 months, and then thanked us for giving them the gift of spending time with their grandchildren.

She had a reverence for the cycles of life. She truly believed in the power of the moon as a healing force. She felt one had to be near the ocean during a New Moon to fully experience lunar intensity. One time, while Verna, Miguel, she, and I drove up the coast to Portland, OR, we stopped just before lunch so Chela could dip her feet into the Pacific.

She doted on all her grandchildren, but I saw her mostly with our two kids, Miguel and Maya. She actually played with them. She was always on the floor with Maya, building something or getting swept up in other imaginative play. And she tossed baseballs outside with Miguel or played board games with him.

She occasionally gambled in Reno or Tahoe, but almost always played the nickel slot machines.

She was very devout in her faith, but it was a quiet devotion. She always felt humbled and awed in church, but never expected any kind of religious reciprocity from her family.

Verna, her two brothers, and her dad had a musical photographic video made a few days after Chela died, and we viewed it at her funeral and at the memorial gathering at our home later that day.

Maya asks to watch “Grandma’s movie” several times a week, and usually Verna complies. She and I still get teary-eyed and we’ve seen it more than a dozen times. Chela’s death left a gaping hole in our lives and hearts. She is terribly missed but her legacy of devotion and nurturing lives on in Verna and, I hope, Miguel and Maya and all her children and grandchildren, as well as the great grandchild she never met, Lola Chela.

Rest in peace, Chela, rest in peace.