Showing posts with label daisy merrick. Show all posts
Showing posts with label daisy merrick. Show all posts

Wednesday, January 15, 2014

Blog Repost 1639: Blog Entry 1,249

Roughly a year ago, I wrote this post commemorating my 1,249th post.  Today, I can claim 1,639 of the insipid things, minus, of course, this one, and other reposts -- unless in the prologue to the reposting, I manage to produce something substantive.

It was written about a month before Daisy Love Merrick died. Not sufficient that the world should lose such a planetary citizen and surfer evangelist, I lost my writing groove and the whole-hearted embrace of my pseudo-sponsorship of pediatric cancer patients became something of a bad grappling take-down technique when I wrote my best poem ever, and then ruined it, in her name.  [Daisy Love Merrick:  An Abandoned Villanelle]

The problem? Me.  Me:  Reductio ad absurdum.  A year later, and the problem hasn't changed, budged, morphed, evolved.  There's just me and this lump of a blog, and a palpable, chewy, nasty fog of self-pity.

On the up side?  Robert Frost's Mending Wall.

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Why do I follow and try to support individual pediatric cancer patients?  I try to keep it to four at a time, as time, itself, has somehow shown that to be manageable on an emotional and time-management level.

If you've decided, after carefully reading the 1, 248 blog entries comprising elle est belle la seine la seine elle est belle that I am one of the besotted Altruistic and Prayerful Loving People of the Interwebs, then -- Whoa, Nelly! -- do you ever need reading comprehension lessons!

There are times when keeping the number at four is very hard to do.  Sometimes, these children are dropping and dying with a swiftness bordering on rude.  Sometimes, they (or usually, their parental chroniclers on CaringBridge or CarePages) sneak new names to you, requesting that you stumble and mumble more prayerful stumblemumbles on behalf of the child they just met next door to them at their hospital, or the nifty eight year old who is in crisis down the hall.

These chronicling parents become daredevils at asking for what they think they want and need.  They can get downright bossy, pushy, and presumptuous.  Most are simply marvelous and in the midst of radical reformation, and the thought of what I might be going through (a cat scratch, having to wait for my first cup of coffee in bed, dropping more carrots on the kitchen floor than actually make it into my stock pot) escapes their attention.

We begin as strangers, and that, to me, is the exceedingly weird part -- how quickly that normally carefully cultivated societal divide is obliterated.  Sometimes on "first contact," like a failed Star Trek Prime Directive; Sometimes over weeks and months, as their initial politeness and crying hosanna is worn down by the frustrations of children with raw bottoms and the inability to swallow due to mouth sores and white plaque sneaking down painful esophagi.  Oh, and the scariness of a child no longer behaving like him or her self, but succumbing to the metamorphoses demanded by tumors and weird neurotransmitters of that most mysterious organ, the brain.

There is nothing much sadder, or terrifying, than to read:  "This is not him.  This is not her." Then, they love on, but the mission changes and becomes one of regaining the personality and impishness, politeness, innate loveliness, and spontaneity that were the hallmarks of these little hard beset beings -- a mission sometimes more important, ultimately, than saving their physical lives.

Steroids are often blamed, and I just roll my eyes, as I'm going on my 15th year of corticosteroids. The eye roll is not one of exasperation on my part, but of imagining all the unsaid weirdnesses going on in their home, their hospital room.  Thrown food, pouts, rages, moving from ecstatic utterances to gloom-and-doom within 60 seconds.  Moon faces and huge guts in children barely eating  or the same in children single-handedly destroying the household food budget.

Sometimes all of the official four scheme to die within weeks of one another.  Occasionally, remissions and cures and a gradual withdrawal from reportage (they don't need "us" any longer, thank goodness), leave holes in my desired level of involvement.  So I will begin to follow some new child they've mentioned as in need... only to have remission turn into relapse.  They are all the time screwing with my desired and well thought out number of only four kids at once (plus there is the growing number of alumni of the cured who remain active fighters in the battle to get more funding and attention paid to pediatric cancers).

There is little doubt that precious, precocious Daisy Love Merrick is dying.  It's been clear for quite some time.  The Merrick's have insulated themselves brilliantly as her circumstances have changed, as she entered the active phase of dying.  These are dynamic people, surrounded by friends and family, neighbors and the fruits of living lovingly, wisely, and with generous hearts.  They don't need the support of internet pediatric cancer groupies, ready to pray at the drop of a hat, or a wink from their cute kid.

And man, has that had me pissed off.

I actually reentered the world of real prayer for Miss Daisy, for her Mom Kate, for her Dad Britt, and for her sweet brother Isaiah.  None of that formulaic nonsense for Daisy, no siree.

A note on "siree," from that favorite former fad, the Urban Dictionary:

it is a word that a gay but popular man used to say a lot, then everyone else said it because they thought it was cool. and now everyone uses the word even though it has absolutely no meaning.
No, I'd not fold my hands together -- as if I still could -- and become one of these famous yet scary -- in an icky sort of scary way -- "prayer warriors" whose goal it is, apparently, to "storm" heaven.
I tended to look at her picture, imagine her pain, and wish for it to end -- but end well, for everyone's sake.

Back when I was intimately entwined with a Presbyterian Church, as intimate as one can get with Presbyterians, I'd actually schedule an entire very early morning hour for intercessory prayer.  Please note that it never occurred to me to pray for myself and my lacks and needs -- much easier to zoom past one's own sad self to save the day for these poor, god-energy-sucking prayer entitlement hogs.  In so doing, I was establishing my Goodness, my Humility, and my everlovin' Love for my fellow man.

It helped me when I decided to quit smoking, because it got me through the day's first coffee hour. I'd sit and sip and pray, no breaks for cigarettes.

Another thing the Merrick's did that pissed me off -- they established a successful, well-run organization on Daisy's behalf and they did it before she died.  It has a director and everything.   Set up to raise money to pay for her experimental treatment in Israel, it achieved that goal, but is now primed and set to move forward as whatever they would like it to become.

I shouldn't have thought of "foundations" because "pissed off" doesn't really begin to cover what then happens in my evil heart.  Every family that loses a beloved child wants to bring about change in the world in honor of that child.  Often, the kid herself will have stumbled upon some nice way to cheer up fellow cancer-sufferers while still alive -- collecting and distributing toys or gift baskets, usually.  Some, like Kate McRae and her family, concentrate on one or two events, in her case, Kate's Crazy Cool Christmas, where they gather and distribute not just stuffed animals, but gas cards and restaurant gift meals.  They remember not just those currently in the fight, but those who have lost, and are in danger of being forgotten during that horrible period when they are too tired, too beat down to care.

But most of the foundations are misguided, most slowly fade away.  There is a natural resistance to want to join established, already successful projects because that takes away the uniqueness that was their child -- his name, his image, him.  I wish that would change.

And don't get me started on the "christianity" aspect of all this.  Lord, lord.

And since when does God need to be asked or beseeched, or even praised, twice?  Is this all too much for him? (Fear not, we won't be going *there*.)

I love the Mothers and Fathers who go nuts and vent their anger.  Again, almost all devout Christians, they do so with a certainty that their God can take it.  They also crack the best jokes.

Every single damn post that I've ever written has been written because I wanted to explain why and how a certain thought, decision, or reaction came into my head.  That's not a normal reason for writing, I don't think.  But it is mine, and as I try to point out at least quarterly around here, whose blog is it, anyway?

So just what the hell inspired me to write about this 4-kids-with-cancer monkey on my back this morning...  Okay, well, afternoon?

Dreams.  Angry dreams about my own dying, how it will likely be alone, how I might have been more comfortable these past years if I had sued the pants off of St. Joseph's Hospital, Eric Carson, Steven Sween, Leslie Kelman, and that idiot nurse in the ICU -- you know the one.  The Lying Liars, I call this group.  I'd add, of course, the then VP of Nursing and every lawyer in the Risk Management Department.  Dreams of Fred, tossed out of Marlinspike Hall, forced to become a Cistercian Postulant, under the quivering thumb of the alcoholic Abbot Truffatore.

Which reminds me, I have a draft, a very ongoing draft (other pseudo-writers may know what I mean!), in the works about the Abbot.  It begins:

Abbot Truffatore arrived unannounced last night.  No, "Abbot Truffatore" is not some exceedingly weird euphemism for "Aunt Flo." He is, in fact, an abbot, more specifically, the local head of the Cistercian monastery whose territory abuts our apple and cherry orchard, divided by Robert Frost's wall -- we meet to mend it, faithfully.*
And yes, of course, I slammed that asterisk down so that I could paste Frost's marvelous "Mending Wall" at the very bottom of the unfinished thing.  Several times a year, I force its reading. But what am I doing talking of poetry, when I was awash in being pissed off?

I woke angry also at Walmart.  Their pharmacy, in particular, which tried to run a scam, the same scam they tried about a year ago, robbing me of $16 and the acknowledgment of a payment toward my considerable deductible.  Yes, God bless Barack Obama and the Affordable Care Act, and the creation of PCIP.  Now, if someone would just give me the money to afford the affordable.

In my just-under-the-surface-of-sleep dreaming, I also wanted to blow the whistle on the ambulance company that got paid $2000 to transport me from a doctor's office across an alley to the hospital emergency room.  And the anesthesiologist who administered the paralytic before being ready to intubate, before sedation, and after being politely asked to tell me what he was going to do before he did it.  His epistolary obsession with me has been all about the joy of Double Dipping -- balanced billing, in other words.

And I wonder why I ended up in the hospital with my stomach weeping blood?

I couldn't even start the day correctly.  No face-washing, no teeth-brushing, no precisely dripped coffee, no insulin, no morning meds. All I could do was the absolutely necessary Feeding of the Manor Felines -- because Buddy decided to sit on my snoring face.

There was also the still fresh memory of yesterday's phone call to the Mother-Unit.  Or day before yesterday.  I cannot remember.  Such fun to hear yourself and your most beloved siblings trashed by an amazingly astute woman who croons, "Did your Father leave you lots of money when he died?"  My body begins to do the shimmy again at the mere thought of that conversation, in which children aged anywhere from newborn to ten were blamed for her maternal inabilities.  I think she might be a sociopath.

Anyway, blessings forever and ever, amen, upon Buddy and his feline behind.  I had a fever of 101 when he so sweetly woke me, but something made me check emails before hoisting and leveraging myself back into this bleeping bed.

Daisy had already crossed my mind several times, even such a mind as the one I've described, vengeful, hateful.  I still see her face at will, at "not will," I still see her face, and wonder.

There was an update.  I thought, "She has died." But no, she still lives, though it is hard living.  She, good as she is, is trying hard to have a good death.  Anyway, her mom Kate wrote the update piece, and part of it went like this:


Daisy is as courageous as ever, full of grace and maturity as she voices her needs without ever whining or being rude. She once again is saving her downy hair for the birds by our house, hoping as they have spring babies they can enjoy her softness.  
One last thought, as a parent and as a human being; opportunities to love surround us. When we take those opportunities time seems to stop, and in that timelessness is where memories are made and beauty is beheld.  We will never regret rising to the occasion.  I believe it has something to do with the fact that God is love and we are made in His image. Suffering isn’t what we are made for, but it can be fruitful in ways we could never imagine. 

And so now I don't know what to do with my damn day.  I am still stuck in bed, in horrible pain, high fever, and with the mounting frustration of no coffee and bedhead.  My feet are ice, my face fire.

But Fred just fed the birds (an ice storm cometh) and made me some excellent coffee.  If I wash the remnants of Buddy from my brow, and sterilize my mouth, I'll feel better.  A hair band will have to tame the frizzy curls.

And Walmart, St. Joseph's, Carson, Sween, Kelman, and that ICU nurse will all have to fend for themselves today.  The anesthesiologist?  Pshaw.  The ambulance company, as will all of this crowd, as will I, will continue to accumulate karma.

Prayer isn't going to happen either.  Yearnings, yes. Some reading. I am reading possibly the worst bit of historical fiction, ever.  Ever! So in between chapters, I foresee Mahjongg.  Bianca and I need to discuss the terms for her repayment of our upteenth contribution to bailing her out of her umpteenth trip to jail (a lovely apartment over Tante Louise's freestanding garage).

Pray For Daisy

MENDING WALL by Robert Frost

Something there is that doesn't love a wall, 
That sends the frozen-ground-swell under it, 
And spills the upper boulders in the sun, 
And makes gaps even two can pass abreast. 
The work of hunters is another thing: 
I have come after them and made repair 
Where they have left not one stone on a stone, 
But they would have the rabbit out of hiding, 
To please the yelping dogs. The gaps I mean, 
No one has seen them made or heard them made, 
But at spring mending-time we find them there. 
I let my neighbor know beyond the hill; 
And on a day we meet to walk the line 
And set the wall between us once again. 
We keep the wall between us as we go. 
To each the boulders that have fallen to each. 
And some are loaves and some so nearly balls 
We have to use a spell to make them balance: 
'Stay where you are until our backs are turned!' 
We wear our fingers rough with handling them. 
Oh, just another kind of out-door game, 
One on a side. It comes to little more: 
There where it is we do not need the wall: 
He is all pine and I am apple orchard. 
My apple trees will never get across 
And eat the cones under his pines, I tell him. 
He only says, 'Good fences make good neighbors'. 
Spring is the mischief in me, and I wonder 
If I could put a notion in his head: 
'Why do they make good neighbors? Isn't it 
Where there are cows? 
But here there are no cows. 
Before I built a wall I'd ask to know 
What I was walling in or walling out, 
And to whom I was like to give offence. 
Something there is that doesn't love a wall, 
That wants it down.' I could say 'Elves' to him, 
But it's not elves exactly, and I'd rather 
He said it for himself. I see him there 
Bringing a stone grasped firmly by the top 
In each hand, like an old-stone savage armed. 
He moves in darkness as it seems to me~ 
Not of woods only and the shade of trees. 
He will not go behind his father's saying, 
And he likes having thought of it so well 
He says again, "Good fences make good neighbors."

Sunday, June 23, 2013

UPDATED POST: do what you do...

UPDATE 6/23/2013

hello, you gorgeous loving readers, you!  i don't have it in me to write a whole new post about "my" caringbridge kids and families, but there are some updates some of you may appreciate.

sadly, ashley riemer died yesterday afternoon, but on her own terms -- at home, with her family.  her decline was rapid, such that some may call it a blessing.  she was up and about, even out shopping earlier in the week, and then on the 20th was brought low by pain.  hospice was ready, and her pain was managed.

she was elven; she was on the cusp of womanhood;  she was brave, ardent, angry, faithful.  she knew long before the blood tests and the bone marrow biopsies that this was the last fight.  i'd love to have known her at 90 -- i imagine blond and pink pig tails, cherry red lipstick and those cutting, pixie eyes.

her mom wrote, at the end of her post notifying everyone of her passing:  "Ashley donated her body to Georgetown Medical University as she was a lifelong learner."  damn straight.  good on you, ms. ashley.

brayden is on his make-a-wish trip, and enjoying it thoroughly.  like so many of my heroes, he is keeping those he loves and who love him, in laughter, no matter what.  his mom, maranda, writes:
I hope you all have had a nice week. I am sorry I have not updated, we have been so busy. The boys go, go ,go and then they drop. Brayden is totally in love with Blue Skies. He now is asking me to buy him, a jacuzzi bath tub- which he does not think would be too expensive. He also wants a golf cart- which he said should probably only cost about 5 dollars. 
brayden and his buddy nolan (nolan had to be admitted yesterday
for pneumonia, so good thoughts for brayden's best bud)


that's the end of this update.  i've discovered that crying clears up my vision much longer than eye drops.  keep brayden close to your heart, and ms. hannah, too, as she is in the midst of the planned destruction of her immune system prior to receiving what the whole darned world hopes is a life-saving bone marrow transplant, the gift of an anonymous lovely, adorable man in europe.  her mom updated this morning:

One week down in the BMT. Hannah's doing better thanks to Reglan/Benadryl & Zofran. She will get Cytoxan and ATG today. Please continue to pray she tolerates with no/minimal side effects. 

END OF UPDATE... thanks for tolerating my lazy blogging.

********************************************************************************



To begin with, and this is especially important for those of you visiting the blog for the first time, I found the doggone ankle brace.  Rather, Fred found it.  There are certain loads of laundry too heavy for me to transfer to the dryer, so he's frequently in receipt of the cryptic request, "Please transfer." Well, as he transferred one bedspread, guess what fell out, now not only a boon to a cracked ankle but also sweet smelling and spotless?  Yes, the thing that mashes all those plates, pins, and screws back into non-jostling positions.

The other thing a new visitor to the blog should know is that I (Retired Educator, aka profderien, alter ego of one Bianca Castafiore, the famed Milanese Nightingale -- oh just read "About this Blog" over in the right hand margin...).  Hellfire. Choo?  Train of thought?  Ah, yes.  I follow, at any given time, four pediatric cancer patients, patients that are in the beginnings, middlings, and endings of their journey's trek.  My means of following them is respectful and done primarily through a wonderful creation and organization called CaringBridge.org.  Support them if you can, and definitely check them out.  Remember that CaringBridge is there should your family ever suffer a medical crisis or catastrophe and need a means to communicate news to family and friends -- as well as to blog and vent, and cry and beg for prayers, and send complete strangers into whirling dervishes of ecstasy the day you are declared NED -- No Evidence of Disease.

But give it some thought.  For parents with kids given tough diagnoses, it's generally not a good sign for there to be extensive or regular blogging and journaling on CaringBridge.  Who'd have time, what with time proved so precious, and the days being near perfect now that the little ones are getting better?

All of which means that bad news is coming in, thus far, in twos.  I'm bewitched into the "it comes in threes" belief, and am waiting for the third bit of sadness.

In the middle of it all, great joy!  For Kate McRae, another completely clean MRI of both brain and spine.  "Miracle" is not much in my vocabulary -- you'll note it's even set aside here with the embracing arms of quotation marks.  This may be one, though.  There's no way this child should be alive, and as untouched by the ravages of the chemo and radiation as she is.  Oh, she was touched -- there are struggles, daily, and sadness at what she cannot do that she once could, but she's ALL there, is Miss Kate McRae.  She is every bit herself, and we're better as a species for it.

Kate McRae
Why don't the doctors listen to the mothers?  Or are there so many mothers tugging at the pediatric oncologist's hearts, telling them they "know" something is wrong, the cancer is back.  They "know" it but the protocol for the chemo, or the radiation, or the study, or the only schedule that insurance will pay for... is every 3 months, or sometimes even six.

Maranda has been struggling for so long now, her son Brayden cruelly afflicted with Metastatic Anaplastic Medulloblastoma.  He has relapsed several times.  And now has again.  I am trying to arrange a meeting with her, as we both live southwest of the Lone Alp, but perhaps this is not the best time to pop in for a coffee.  She has a toddler, is a single, unemployed mom.

Anyway, for you to stare at, enjoy, and contemplate as you meditate and pray for Brayden, here is a recent photo of the little guy.  I love his face.  It's grown up but it's tricky.  I bet he's a trickster... Peace on you, Brother Brayden, and on your mom Maranda, and on his favorite little person, his brother Mason.



Now, I do have a thing or two to say about Brayden and Maranda.  They treat Maranda, it sounds like to moi, somewhat badly as she struggles to get to the clinic as scheduled, without daycare for Mason, and having been pegged an overanxious mother.  She asked them repeatedly to move up the MRI and was pretty rudely brushed off, with suggestions for therapy for anxiety or some psycho-crapo get-her-off-my-back shit.  The day of the MRI, same day as Kate's, his oncologist was out of town.  After they got home, Brayden, who has trouble controlling his bowels, needed changing and Maranda set about doing that... and in the process, his leg bent the wrong way, and broke, badly.  So back they went to the hospital... and she exhausted, and he in pain, and she could not stop worrying about the MRI results, even with the drama of the broken leg.

So a nurse finally prints out the MRI report and hands it to her.

That's how she discovers Brayden has indeed relapsed, and that's how that nurse got herself a few precious minutes of not being stressed out by Brayden's Mom and her worry-wart ways.

Maranda is smart as a whip but waited for the oncologist's return, and her phone call.  Today.  Monday.


Brayden's cancer is back.Dr A called me this afternoon. I will be going over options with her tomorrow, she is even calling St Jude's and MD Anderson, please keep praying for God to heal Brayden. I don't want just a little longer here with Brayden. I want a lot longer and I know that's not promised to anyone but if you could all please pray for that I would really appreciate that.

Jeez life is painful sometimes. It is worth it though, I feel like my heart is broken. I will update tomorrow with whatever treatment is decided.

The other person who is in decline is no longer a child.  She had leukemia as a kid, and relapsed once.  Then, last year, first year of college, it came back.  She only qualified for a certain highly experimental protocol, and I think she knew from the beginning of this latest round in the fight, this last trek as a pilgrim, that this was going to be her death.  But it is coming now so fast and furious that my heart breaks at the thought that she might not be ready.  Which is pretty freaking presumptuous of me.

All I can do is show you the picture that made me fall in love with her, and tell you that Ashley is now suddenly on hospice care and in severe pain.  She is from a very religious and faith-driven family and community, and I hope that is a source of immense and unending comfort.  Throughout the past months, she's pitched a fit to be able to attend her Japanese classes, and has kept the state of her coiffure right where it should be -- at the forefront of everything.  She's a beautiful nymph. You'll see.  You'll fall in love, too.





Ashley Riemer, September 2012I write tonight with the news of the biopsy results from last week. Ashley's cancer in her bone marrow is showing 70%. This is very high and alarming. Ashley is now receiving Hospice care for pain. 





Ashley Riemer, May 2013



Prayer of Pan Cogito – Traveller

Lord
Thank you for creating the world beautiful and of such variety
And also for allowing me in your inexhaustible goodness
To visit places which were not the scene of my daily torments

- for lying at night near a well in a square in Tarquinia while the swaying
bronze declared from the tower your wrath and forgiveness

and a little donkey on the island of Corcyra sang to mi from
its incredible bellowing lungs the landscape’s melancholy

and in the very ugly city of Manchester I came across
very good and sensible people

nature reiterated her wise tautologies the forest was
forest the sea was sea and rock was rock

stars orbited and things were as they should be – Jovis omnia plena

- forgive me thinking only of myself when the life of
others cruel and irreversible turned round me like the huge
astrological clock in the church at Beauvais

for being too cowardly and stupid because I did not understand
so many things

and also forgive me for not fighting for the happiness of
poor and vanquished nations and for seeing only moonrise and museums
- thank you for the works created to glorify you which
have shared with me part of there mystery so that in gross conceit

I concluded that Duccio Van Eyck Bellini painted for me too

and likewise the Acropolis which I had never fully understood
patiently revealed to me its mutilated flesh

- I pray that you do not forget to reward the white-haired old
man who brought me fruit from his garden in the bay of the island of Ithaca

and also the teacher Miss Hellen on the isle of Mull whose
hospitality was Greek or Christian and who ordered light
to be placed in the window facing Holy Iona so that human
lights might greet one another

and furthermore all those who had shown me the way and said
kato kyrie kato

and that you should have in your care the Mother from Spoleto
Spiridion from Paxos and the good student from Berlin who
got me out of a tight spot and later, when I unexpectedly
ran into him in Arizona, drove me to Grand Canyon which
is like a hundred thousand cathedrals standing on their heads

- grant O Lord that I may forget my foolish and very weary
persecutors when the sun sets into the vast uncharted
Ionian sea

that I may comprehend other men other tongues other suffering
and that I be not stubborn because my limitations are
without limits

and above all that I be humble, that is, one who sees
one who drinks at the spring

thank you O Lord for creating a world very beautiful and varied

and if this is Your temptation I am tempted for ever
and without forgiveness 






Daisy Merrick


Thursday, April 4, 2013

A Note From Joey's Dad

3-D mold of Joey's thumbprint

It cannot have been just last November that Joey Keller died.  It was such a prolonged agony, in the most basic of the etymologies of agony, that my mind had hid it away.

When I don't get a CaringBridge update notification for the children I follow there, I tend toward hope and don't think much about them.  When we drive by the local huge Children's Hospital here in Tête de Hergé -- where there are only tonsillectomies performed and broken bones fixed with psychedelic splints and casts -- I do remember them, back in that other world where kids get cancer and sometimes die in the middle of their youth.

I confess to looking at pictures of Daisy Merrick rather frequently, but for the smile she brings. None of us are naive enough to avoid our private picture book of what she must have looked like at her end, and no reassurances by preacher men and preacher women, even when they are that child's parent, can fool me. I've seen Death.  So have you.  But those are the pictures we've been given as fodder for the dark.  Daisy was, when vibrantly alive, nothing but light.

Anyway, Joey's Dad just about drove me insane in Joey's last months.  How dare he?  A man with scientific gleanings and leanings, he was, and will be again, a believer in miracles.  L.I.T.E.R.A.L.L.Y.  To such an extent that I prayed for Joey to please die.  I did that once, because as you know, that's the extent of my praying -- if, in the great crap shoot, he's aware of such needs; if, indeed, such needs even matter, then praying once to omniscience and omnipotence ought to square things.

I don't believe Joey's Dad ever slept.  He kept on working, too, for many reasons, I imagine, insurance coverage likely topping the list.  But his devotion almost bordered on abuse, to me. To me, I say.  He was pure love to his son and his son reflected pure love back, but you could also see in his wizened yellow face that he had had it.  But they clung, so... Well, isn't this an old tired story?

Anyway (the best of segues), he posted something tonight on CaringBridge and I want to pass it on, for those of you who may have followed Joey's story at the reserved distance of an odd blog.  Note that you don't hyperventilate while reading him.  Note that he's in a place I cannot imagine -- but then I cannot imagine any of the places he has had to traverse in the last five, six years.

I wrote him a comment, something I rarely do on CaringBridge, particularly when the parent or person blogging there is very religious, as my propensity to say something perceived as uncaring becomes an insulting danger that I just don't want to risk.  "You write well," I said.  I told him that I hoped he would keep at it.

Of course, this was also a ploy to not have to go to Facebook to follow the foundation doings that are getting underway in Joey's honor (Legos, what else!?).  I hate Facebook like I hate telephones and their bad news and their insinuations, like I hate the noise of the mall.  I prefer CaringBridge and the illusion of intimacy.

Nick, the dad in question, has shortened Joey's "Story" on CaringBridge to this:

 Joey lost his battle to medulloblastoma November of 2012. I wish I could list the stories and testmonies of all of us that were inspired to live better because of watching Joey's short life. His positive attitude was contagious and he wanted to encourage everybody he came into contact with. He inspired Elizabeth and me, more than words could ever say. Joey's attitude, faith, and generous spirit lead to the creation of TEAM JOEY, a not for profit (501c3) organization dedicated to getting Legos into the hands of every child battling cancer, and funding research to END pediatric cancer, once and for all. See link below:
http://www.HeroesFoundation.org/Programs

And of the many fantastic photographs they captured of their son, Nick and Elizabeth chose this one to head the new page:


This is what Nick blogged about today, and, again, if anyone wishes to hook up with CaringBridge, it's an easy site with which to register --

touch base-
Written 2 hours ago
 
I'm not sure if anybody reads this anymore.  Many have told me they miss us sharing and asked that when we had a moment, to share a few thoughts. The support and prayers we got from this site (all of YOU), when we were going through the darkest and ugliest experience I could have ever imagined, was unbelievable.  We jumped on tonight for several reasons, the main one being to thank you all for your prayers.  Throughout Joey’s battle, when we got good news, you were there, praying and celebrating.  When the doctor said, "It's all over his brain again," you were reading and following…and praying.  And even as Joey suffocated in our arms, you were praying for Elizabeth and me.  Thank you.  Even now, we read messages from those who understand...who get it.  The pain doesn't go away.  It just doesn't.  Elizabeth and I were talking the other night that we don't think we'd ever want it to.  It's the most unbelievable dichotomy.  To remember him (which is at least every 5 minutes) brings incredible joy and memories that are so good…I get caught in public thinking of him...and smiling....and then intense, searing pain through your heart.  He is gone.  How did this happen?  Our son, our life in so many ways is gone.  We were at dinner with some really amazing people the other night, and we were explaining how it really wears us out to hear people give the typical pat answers, albeit maybe true comments, just not necessarily encouraging ones.  Our friend at dinner said the pain and loss you feel is proportional to the love you had for him.  I do feel bad for the people who just don't understand why we can't just move on, suck it up, and “get to work on God's calling for our lives.”  Not sure they'll ever get it.  When you love someone, really love someone, you give them your heart.  Your commitment to always be there for them, to ALWAYS do what's in their best interest, and to never leave them or forsake them. I wanted nothing in life more than to be a dad.  A good dad.  You wouldn't believe the books I had read, before and after Joey was given to us (born)....the small group studies at church on fatherhood I had gone to...the literally stacks of journal notebooks I have in my office, filled with my handwritten notes from books by Eldridge, Morley, and Dobson, on how to be a dad that God will be proud of.  Nobody wanted to be a good dad and took the job more seriously than I did.  I can say from seeing it first-hand, no one wanted to be a great mom than my wonderful wife.  Why did this happen?  How?  Of course, there is some solace in knowing where he is and that he can't suffer any more.  And we know we'll see him again.  Certainly, knowing how happy he must be in heaven makes us smile.  But we are here.  This is now.  And as long as I'm alive, I'll be without my son.  My family tells me that when I was little, I was always laughing and having fun. That every picture in our albums from childhood shows a big smile on my face.  I do love to have fun and always have pushed the envelope when it comes to pursuing it.  My body has the broken bones and neck, a four level spinal fusion, and scars all over to prove it.  I told a buddy of mine the other day, when trying to explain how I felt (he asked), life just isn't fun anymore.  The joy is gone.  Oh, I can put on a happy face with the best of ‘em, but on the inside, we are still very torn up. I am not too proud to ask for your continued prayers. 
I changed Joey's "My Story" on this CaringBridge site.  Elizabeth's been after me to do this for some time.  We are excited about TEAM JOEY and the kids who are and who will be touched because of Joey’s amazing heart and vision.  We did our first "Lego give" at Peyton Manning Children's Hospital a couple of weeks ago, and RileyHospital is next week.  We are excited.  Joey would have LOVED shopping for the kids, handing out the sets, visiting each room, and praying for the kids. He was so much younger in “years lived” than I am but about 50 years older than me in spiritual maturity terms.  What an old soul. 
I also wanted to let everybody know that, as far as updates for TEAM JOEY and Heroes Foundation, you can find us on Facebook.  We don't have to be Facebook friends for you to "like" the TEAM JOEY Facebook page and receive that latest updates.  I know there are some circumstances, HIPPA considerations, professional restrictions, and other good reasons where people can’t be FB friends, you can still plug in to the TEAM JOEY page. We are contemplating a TEAM JOEY website; but frankly, most people communicate and get a large part of their social information and interaction from Facebook.  I think, all Facebook asks for is just an email address.  And they never send you anything.  It's about as safe as could be, YOU control what is shared.  Get an account, and follow TEAM JOEY on Facebook! Look for: “TEAM JOEY, A Heroes Foundation Program”

Many have told me that I should continue to blog on here.  It got me through some really difficult times, and I'm sure would prove therapeutic now.  I gotta be honest, I wasn't gonna say all that tonight; I was just going to sort of point everyone to the new Facebook page.  We'll see how things go moving forward.  Living without Joey is really tough.  Some really thoughtful families and friends invited us over for Easter.  For several reasons, we just wanted to kind of hole up and rest and shut the world out on Sunday.  We started off strong, then there were TV sermons and shows about Easter, and then the memories of past Easters...nine of them…and I found myself sitting alone on the couch, holding an 8x10 of him, just blown away...he is really gone. This is permanent.  I can’t hug him, or rub his bald head, or talk to him, or hear his laugh or him singing the Ninjago song. We used to have some of the most amazing talks. He would ask me questions that were so complex and deep, that I swore I was talking to an 80 year old man.  All that said, I AM grateful for Easter because it is truly the hope that I have that I'll see my buddy again.  I would be lying, however, if I told you it was a good or easy day for us.
 
In a day and age where everybody’s selling the illusion of control, I knew this posting wasn't going to inspire anybody.  But I had to be honest, and I do thank you all for asking about us, for asking us to continue to share our journey, and, most of all, giving us the space and grace to grieve.  We do, still, have MUCH to be thankful for.  At the top of our list is all of you.  Talk soon!


Thursday, March 21, 2013

This fey freckled daughter

i wrote a poem, heck, i'm a poetic fool these days, but there is one poem that i am proud of, with which i have fallen in love.

that's not to say that i have a lot of ego invested in it... but it does want to be seen.

is that enough of a nervous entry, a schizoid introduction?
if you're a dear reader (and, of course, you are!) you know all about darling daisy merrick.-- wild child, scared child, freckle-face, laughing crying girl... how her family and friends must miss her, if i, a stranger, can ache this much.

tw -- aw... never mind. whaddaya want for your b'day, brother-boy?

**************************************************************

Daisy Love Merrick: An Abandoned Villanelle




This fey freckled daughter bore the task
Of gap-toothed water dancing and good death
Which more pallor than sun's freckles did unmask.

Transparent although tensile strong you never had to ask
Is this the oath, this the path, this the aftermath?
This fey freckled daughter bore the task.

Near sand near surf did lolling Daisy bask
The heavy salted dead of seas lightly bore her breath
Which more pallor than sun's freckles did unmask.

I cannot keep you trapped inside a villanelle! You wriggle wry,
laugh aloud, but took to sobbing in deep sleep, as malignancy
came three times, four times, in more syllables than is fair --

Refused meter, every rhyme. But you, you freckled water whirl,
fey dervish of wide oceans, spun your pippi braids right off, 
twirled unbound in sunlit time, blond hairs eddied in the under sea.

You surfing flower urchin weed, the pallor that cold blue
unmasked, brown pools for eyes, you bore the task,
and left us this oath, this path, this dreaded aftermath.

Sunday, February 17, 2013

Good-bye, Sweet Freckle-Faced Daisy Love...



  uploaded to YouTube by ForTheMerricks·February 16, 2013

Britt and Kate Merrick did the best of jobs in trying to prepare all who had fallen in love with
their family, all who admire their lust for life, and their willingness to go to the ends of the earth, both in desperation and in hope.  We loved the wise parents, all the more so when wisdom failed them and they put one foot in front of the other, out of necessity and faith, combined.  We loved Isaiah for hanging on to Daisy on top of camels, in the oceans and seas, and for his watchful eye and gracious heart.

And we loved Daisy, standing in perfect first position at the end of her hospital bed, shoulders back, chin up, left arm on the barre of the bed's footboard, right hand gracefully extended -- with a foley catheter bag looped over the wrist -- a perfect Degas dancer's face imprinted on her own impish one.  We loved her surfing, clinging wet and happy to her father, and hovering around the tan legs of her mom, who took more pictures and videos than she was in.  Kate and Britt took their family on that final, desperate trip to Israel, Britt gave his cells for cancer vaccines, they tried new things, and in their trying made cures for others so much more probable in the future -- immunological advances, ways to shore up the body to fight.  Daisy, Isaiah, Kate, and Britt went where Jesus walked.  Daisy, like every tourist, I imagine, tried to walk on water.

I don't know these people.

Britt is the founder of a church movement, a pastor, born into one of the greatest surfing dynasties in the world.  He still calls himself a surf board shaper. Kate is private, but what has gravitated to her is of such wonder that you know she is wonderful, herself.  Isaiah is a young man, and inasmuch as I have been trained to read pictures as well as words (ut pictura poesis), I know he is a young man of gravitas -- with as much capacity for silliness as the next kid.

I did not know Daisy.

But anyone could see the emergence of her freckles over time, not just with the Israeli and Californian suns, but with the power of the pallor that cancer brought beneath them. She was funny, bright, lucky, blessed, but I think she pitied us all, somehow, too.  Or tired of us, is more like it.  She was practically a Foundation before she'd even died, the organization upholding her family was that organized.  (I was heartened at how the Merricks and their family and friends, though, closed ranks in these final months, at how they cherished and controlled their precious privacy.  I was glad and relieved to be a proper outsider.)

Even not knowing her, even with the warnings I gave myself -- that Daisy just happened to be one of the four children with cancer that I follow and support at any given time;  that Daisy was just my happenstance -- I fell in love with her.  I will always love her.

Thank you, Kate and Britt, for sharing the journey, for the funny pictures, and the wrenching ones. Thanks even for the sermons.  Thanks for knowing science and medicine as gifts and arts from God.  Thanks for giving Daisy the freedom to have her moments of doubt.

This is what they wrote yesterday:

At 2:40am this morning our sweet Daisy went to be with Jesus. She was sleeping and in no pain.
Christ is with us as the God of all comfort. We are thankful.
Jesus said to her, “I am the resurrection and the life; he who believes in Me will live even if he dies, and everyone who lives and believes in Me will never die. Do you believe this?” (John 11:25-26)
Daisy believed this and so do we. More than ever.
Love,
The Merricks
(At this time funeral plans are still forthcoming. Please check back this week for more info and details.)


Thursday, February 7, 2013

Britt Merrick: "When Sparrows Fall": Matthew 10:28-31



To see previous posts about Daisy Love Merrick, click HERE.  For lots of info on Daisy, her family, and background to their story, visit Pray For Daisy.




This is a 55-minute long video of a sermon delivered by Britt Merrick* at one of the network of churches he founded called "Reality." This is, I believe, his home church, in Santa Barbara.  You can learn more about Reality churches and missions HERE.  They see their growth as part of a process called "church birthing," to emphasize their own emphasis on family, as a reality and as an idea.

Reality is a family of churches. Reality Carpinteria was born on September 7, 2003. Since that time we have birthed churches in Los Angeles, Stockton, and San Francisco, CA. We also have a grandchild in London, England, that was birthed from Reality LA. Our next church will be in Boston, MA and is scheduled to start in the fall of 2012. God has called Reality to be a church planting movement.  We never sought to be this, but it has become clear that this is what God is calling us to do and be, and it is something we are passionate about.
Though planting is the common metaphor for starting new churches, we prefer to call what we do church birthing. Birthing is more labor intensive and relational than the planting metaphor suggests.

Britt is on a leave of abscence from his pastoral duties and this is a sermon that he felt called to deliver to update the community about his daughter, Daisy, Daisy Love, Daisy Love Merrick.  A very cool, brave little girl who is actively dying, trying so hard to die with grace, within the love, grace, and faith of her family, whom she knows to be around her here and waiting for her in Heaven.



The Merricks took Daisy to Israel over the summer for some treatments not available in the United States -- immunotherapy, cancer vaccines, much of which involved the transfer of cells from Britt to Daisy.  They road camels.

Daisy and her brother Isaiah
They surfed and swam.  (The Merrick family is, well, a surfing dynasty.)

Daisy surfing in Israel
Matthew 10: 28-31 reads:

28 Don’t be afraid of those who kill the body but can’t kill the soul. Instead, be afraid of the one who can destroy both body and soul in hell. 29 Aren’t two sparrows sold for a small coin? But not one of them will fall to the ground without your Father knowing about it already. 30 Even the hairs of your head are all counted. 31 Don’t be afraid. You are worth more than many sparrows.

I look at this picture -- among others -- every few days, when I wonder what is happening within. and to, Daisy, Daisy Love, Daisy Love Merrick, Daughter of the Surf. Freckled Little Girl of Inspiring Imagination, and I don't pray.  I prayed for Daisy once, and that -- from all I understand
about omnipotence and stuff -- ought to have been enough.  Whenever Britt or Kate call for prayer, I bow my head, think of them and their terrible pain, of Isaiah's probably anger and confusion, and always, in that dumb bowed head, see Daisy's face, which, although I know its beauty must be greatly changed, I forever see this way:




And while no prayer comes out, I try to send them love from my heart, and I imagine holding their hands -- thin, dry, damp, sweaty, clenched in a fist, open in a stroke, seeking -- scuttling hands, worrying thumbs, wavering fingers.

*******     *******     *******     *******     *******     *******

*His biography at the Reality Santa Barbara website reads:

I am the founder of Reality and the current Pastor for Preaching and Vision. This means that I do the bulk of the preaching on Sunday mornings for all three campuses, that I guide the church doctrinally, and lead the effort to discern in community (with a plurality of elders) Christ's leading for Reality. The passionate pursuit of my life is to enjoy Jesus. I love my wife Kate, my son Isaiah and my daughter Daisy. I also love surfing, guitars, motocross and books.

Sunday, January 6, 2013

"this love is stronger..."

Dominic Balli - Daisy's Song Live 2012
Published on Mar 30, 2012
by dominicballi




When that storm comes
Like a hurricane
And the sun seems far away

We will not fear the wind
We will not fear the waves
I can feel your calm within

When this life is shaken
By ragin' seas
We are not gon' be afraid







So if ya walk on waves and wind
Then hold my hand and I'll walk again

This love is stronger than the blood that beats my heart
This love is deeper, than the pain of all these scars
This love goes farther than the hope in answer's arms
This love is stronger
It's strong enough for me

You lived our sorrows,
Befriended all our pain
All that we might rise again

You stole my sickness,
Rested in my disease
All that I might rest in thee

And you alone bring healing,
And for you I'll wait
But we are not gon' be afraid


This love is stronger than the blood that beats my heart
This love is deeper, than the pain of all these scars
This love goes farther than the hope in answer's arms
This love is stronger
It's strong enough for me


We may be crushed but we are not ever forsaken
We may be struck down but we are not ever destroyed
Then when that fire comes to shine through me your glory
We are not gonna be afraid



Saturday, January 5, 2013

::rocking::on::the::water::

Back on December 16, 2012, Daisy's Dad tweeted: "Scan results are in & apart from God's supernatural intervention Daisy’s prognosis is bleak."

Three days ago, the Pray For Daisy website blog reported:

Difficult day
Today is a difficult day for Daisy… with large tumors in her abdomen and trying to recover from two weeks of chemotherapy, her body is struggling. She is extremely fragile and weak.
[followed by an invitation to prayer and fast]
Tyler Morgan
Executive Director
The Daisy Merrick Trust


Daisy and her father Britt




Last night I dreamed about surfing, and, trust me, surfing is not in my repertoire, not even in my impressive and intrepid athletic Days of Yore.  Daisy comes from a surfing family, a surfing heritage. Her grandfather, Al Merrick, is a famed "shaper."

Professionals and amateurs alike have "paddled for Daisy" all over the world...  And so my dreams and my heart are telling me to tell you that and to show you Daisy, and other similar souls, rocking on the water.

Maui, HI
Launiupoko, Maui, HI

Honolulu, HI
Diamond head side of the Hilton Hawaiian pier

North Shore, HI
Ehukai Beach Park and paddle to Waimea Bay



Pacifica, CA
Linda Mar Beach (South side of the beach)

Santa Cruz, CA
Location: Cowells Beach
(north side of the pier in front of the Dream Inn)

Carmel Beach, CA
Bottom of 13th St at Carmel Beach

Pismo Beach, CA
South Side of the Pismo Beach Pier

Santa Barbara, CA
Santa Claus Lane Beach (southside)

Oxnard, CA
Oxnard Shores – 5th St.

South Bay, CA
EL Porto (45th St)

Huntington Beach, CA
HB Pier (South Side)

Newport Beach, CA
Newport Beach Pier (South Side)

San Clemente, CA
The San Clemente Pier

Oceanside, CA
Oceanside Pier, South Side (200 The Strand)

Encinitas, CA
Moonlight Beach



Minneapolis, MN
Lake Calhoun North Beach West Lake Street

Rockaway Beach, NY
Rockaway Beach 90th St, NY

Manasquan/ Spring Lake, NJ
Ocean Ave and Pitney Ave (by the Arches)

Virginia Beach, VA
1st street jetty



Avon, NC
Avon Pier

Surf City, NC
Kinston Street Beach Access next to the pier

Emerald Isle, NC
Bogue Inlet Pier

Wrightsville Beach, NC
Oceanic Street (Access #28)

Carolina Beach, NC
Hamlet Ave Access

North Myrtle Beach, SC
Cherry Grove Pier, 3500 North Ocean Boulevard

Myrtle Beach, SC
Myrtle Beach State Park
4401 South Kings Hwy Myrtle Beach, SC

Charleston, SC
The Washout

Jacksonville, FL
Jacksonville Pier

St. Augustine, FL
FA’s at the North side of St. Augustine Pier

Ormond Beach, FL
Granada approach, A1A at Granada Bvd. (SR-40)

New Smyrna Beach, FL
Flagler Ave. Beach ramp(on the beach)

Flagler Beach, FL
South Sixth St.

Melbourne Beach, FL
Ocean Avenue (beach access)

Deerfield Beach, FL
Deerfield Beach Pier

Panama City, FL
Panama City Beach Pier


daisy surfing



Fort Worth, TX

Kuta Bali
Pantai Kuta, Jl. Pantai Kuta, Kuta 80361


All photos are property of Al Merrick, Daisy's grandfather, from his company website, Channel Islands Surfboards by Al Merrick.  I have a feeling there's no finer place to satisfy your surfing needs...



FLOW from Koastal Media on Vimeo.

"The story focuses on Channel Islands Surfboards founder and world-renowned surfboard craftsman Al Merrick and his special relationships with the team of world champion Channel Islands Team riders and arguably the two best and most influential surfers ever: Kelly Slater (6 time world champion) and Tom Curren (3 time world champion)."