Archive for the ‘loss’ Category

Death and Children

October 30, 2007

There’s a quote I don’t particularly like, but it does concisely relate how I feel about the vulnerability of children: “To become a mother is to forever have your heart walking around outside your body.”

I know several people online who have lost their children to death. Somehow, they got up the next morning, continued to feed themselves, continued to breathe. Some had other children before the death; some went on to conceive the siblings after the fact. In any case I am always humbled by the strength of their humanity, supremely grateful for them that they still have children to love in the here and now.

Every new parent who actually bonds with their child knows a fear of loss. Entrusted with this new life, this entirely helpless, squirming bundle for whom you’ve been overwhelmed with love, most of us have elaborate fantasies about how we will protect them from all comers. Modern consumer society is happy to oblige this instinct, selling parents everything from car seats to outlet covers to crawling-baby kneepads. Some are useful and reasonable, most are just an elixir one can purchase to buy off that feeling of NEED. If we buy enough protective gear, then maybe that pit of fear will go away. We can protect them! We can keep them safe and with us!

Most parents get over this in time. Every woman has a benchmark: “she’s past the age of SIDS now,” or “he’s three, he can eat popcorn safely now.” They grow beyond the need to take the baby to the bathroom with them, and the parent-child bond reaches a more manageable level. I make great fun of “first time Moms” because I was a classic example of the hyper protective, freaked out Mommy. I would use a stroller in the mall for my first daughter, when I wore a sling everywhere else, because I could put her carseat in it and make this hermetically sealed baby bubble, shielding her from strangers’ eyes and germs. By the time we had our third child, he never even got to use the travel system; who had time to navigate all that equipment?

The truth is, however, there is a big part of my heart still trapped in first-Mommy mode. We all know how horrible it must be to lose a child. We all know that our days are not promised to us. We all say we can not even imagine the heartache…. but frankly, I think I can. My daughter was 13 months old when she had her first anaphylactic reaction to peanuts. She was 18 months old when her allergist told me her IgE count was unusually elevated, even for his office. “This is one very allergic little girl,” he said to us. But I was already well on my way to trusting the child, trusting life to take care of itself. He knew I wasn’t understanding him. When someone looks you in the eye and tells you deliberately, “Listen to me. She will die if you don’t keep these substances away from her,” life pauses. Time stops. He got our attention. He changed my life.

Since then, her general health has improved to the point where she’s probably healthier than most of her peers. While she still reacts to things, she hasn’t had an anaphylactic reaction since she was three. It’s easy to become complacent when her allergies only manifest anymore as the stuffy nose that so many of us walk around sporting. To look at her, to see her life and how easily she navigates our world, most people have no clue. She looks like a flourishing little girl with a nose-picking habit. I am both grateful and proud (for the flourishing part, anyway.) But sometime, at some point during nearly every day of my life, I feel that chill. This is something I do pray for: please let my children outlive me. please.

In my home community, the general attitude regarding food allergies isn’t very accomodating. “Just don’t eat it!” or “YOU need to keep her HOME if she’s that sensitive,” were the prevailing sentiments. They either didn’t get it, or more likely, they truly didn’t care. For us, with our awareness of a new layer of cruelty in the world, it wasn’t until she was six that we started to relax out of that first-parent fear a bit: “She’s old enough to say she’s allergic. She’s old enough to ask about it, to say no.” Even now, I know she’s not old enough to discern whether people are wrong, though, and it dismays me every time I have to correct an adult who has told my child to eat something that would harm her. Every time, I think about what would have happened had I not been there. Every time, I get nauseous and realize that my experience as a mother, our experience as parents, is different from most others’. They can’t understand and they never will.

Nathan was seven this year when he died. Quinn would have turned seven this October. Their mothers know what it is to lose that greatest privilege and joy. Yet they’re still breathing. They’re still mothering. I wonder whether they resent their courage and the admiration they receive; because to them, those qualities are not a result of anything they have chosen for their families. They are coping with something they hate. I care for these women, I grieve with them. But just the fact they exist proves these things happen. The idea that our children were born the same time just pierces me. Death does come for children, and the obnoxious reality is that for some of us the odds are higher than others. All I can do is outwardly ignore the possibility and take comfort that we’re doing the best we can. So is G.

My focus has shifted from protecto-mode to life mode. The allergy doesn’t manage us anymore, we manage it. It’s taken me years to get here, and I remind myself to take each moment into my heart. It’s her life, and I gave it to her to live it.

How can it be over there?

August 19, 2007
How can it be “over there” when it’s in our own living rooms?

I was reading the paper today when I was jarred out of my complacency by this juxtaposition:
(click for clearer image)

Nathan has passed

July 30, 2007

Little Nathan has passed.

Please join us in praying for his parents and his siblings. There is a family tonight beginning a new leg of a journey they never invited or imagined.

Little Nathan

July 8, 2007

We are praying for this boy: my dh and I, my fellow Tenters, and the many people whose lives Nathan has touched personally. Unlike many of our Junebugs, who we’ve visited or have visited us, Nathan probably has no idea who I am. He’s been sick most of his life with neuroblastoma. The doctors caught it late as far as the disease goes, when he was a toddler, and the resulting prognosis was 7 years. I remember vividly digging through the internet like a madwoman, trying to find anything to the contrary. I remember passionate conversations with Angie, Leti, Dawn and Kim about how certainly by the time 6 years was up, the researchers would have found something. He’d make it! Surely that was such a long time that the medicine would catch up!

As parents, we now know how fast that time goes past.

Most of us under the tent have children born within days and weeks of Nathan. He turned 7 years old in June. Every birthday he had, we’d celebrate silently as if it was our own child given that extra year. In a way, I suppose, it was. Every lost tooth of Nathan’s held a different meaning than our children’s. He didn’t find it exciting when chemo ruined his smile. Every picture, with new hearing aids, or fresh surgical tape pointed out to us how different his life path would become. It somehow started to seem unfair that we had healthy children. We celebrated life itself when Nathan achieved NED status, and cried in devastation when his disease returned after almost 2 years. Most of us refused to turn away, despite the pain. We kept following their lives, their story, feeling as if we could provide some invisible army, some huge community that would make Nathan’s life even bigger than it ever would be on its own.

None of us who know Susan take our children’s lives for granted. I have never written about him before because I have always felt it was not my place, not my story. But now, his family has been given the news that “Nathan has days to weeks left, rather than weeks.” They have called in hospice and the boy takes more morphine than an adult could normally handle. So I am posting because I believe in the power of positive intention, prayer, pulsing, whatever you personally call the communication your soul has with other energies. I don’t ask for him to be saved, because it is too late for that. But I am praying for his parents and their ravaged hearts. I am praying for his two little sisters, who will know a loss they can’t understand. I am praying for little Nathan, who is soon to leave the only life he has ever known. Nathan, who lies about needing pain meds so he can be awake longer with his family. Nathan, who said just yesterday that he’d rather do yard work his mom than sleep on the couch– and did it.

I am praying for Grace, for everyone involved. I hope you will send some of your energy as well.

We need to pass the stupid immigration bill already

June 18, 2007

One way or another. This inanity has to end.

http://www.king5.com/video/news-index.html?nvid=152238&shu=1

My friend writes:

My son speaks (on the radio)
Listen to it please.
Ok, so the day that I interviewed with the news channel, we also interviewed with an alternative radio station in Portland Oregon. They gave my children the opportunity to speak.

The spot is about 4 minutes, myself and my son are in the second two minutes.

My son is about 2 weeks short of 7 years old here.

If you support undocumented immigrants being deported without question. If you can still support such violation of families after hearing ~D~, I worry for your sense of justice.

http://www.kboo.fm/node/3319

Uncle Bill

April 10, 2007

I am stinging from this loss. I am not one of those people who moved across country and had my relationships persist as if I had never left. So, I haven’t talked to Uncle Bill in two years, since we moved out of the neighborhood adjacent to him. Bill and Deanie were cornerstones of my childhood. Very simple, salt-of-the-earth people, they were family icons. They didn’t do much outside love their family and their church but they were just really, really good at it.

Bill, at 19, married Deanie when she was 13. They stayed together for the rest of his life and had three strong sons who all smile the same–just like their Daddy. Bill was the family fix-it guy who would come to work on your toilet or car, whether you asked him to or not.

They didn’t really understand me when I grew up, or why I couldn’t stay around my toxic mother (whose behaviour they blame on her divorce and my slacker sister) but they never treated me poorly. I feel bad for Deanie. Beyond bad. I can’t imagine losing a partner of 56 years. I just can’t.

William William Reese Harvill, 75 of Charleston, SC, entered into eternal rest April 1, 2007.

Bill was the son of the late John and Elsie Harvill. Mr. Harvill proudly served 26 years in the United States Air Force, retiring at the rank of Master Sergeant. He was a devoted member of the First Church of the Nazarene on Yeamans Hall Road in Hanahan, SC. He is survived by his beloved wife of 56 years, Elizabeth “Deanie” Donnally Harvill, three sons, David and his wife Kathy of North Charleston, Ronald and his wife Christine of East Hartford, Conn., Daren and his wife Anna of Warner Robins, GA; seven grandchildren and six great-grandchildren, one brother Phillip “P.O.” Harvill of Biloxi, MS. A funeral service will be held on Thursday, April 5, 2007, 1:00 PM at CAROLINA MEMORIAL FUNERAL HOME CHAPEL. Burial to follow in Carolina Memorial Park. The family will receive friends from 6:00 to 8:00 PM Wednesday, April 4, 2007, at CAROLINA MEMORIAL FUNERAL HOME, 7113 Rivers Avenue, North Charleston, SC. In lieu of flowers, donations may be made to the First Church of the Nazarene Memorial Roll in honor of his name. Visit our guestbook at www.charleston.net/deaths.