Showing posts with label pediatric cancer. Show all posts
Showing posts with label pediatric cancer. Show all posts

Tuesday, September 2, 2014

thinking of kate...

a quick note to ask for good thoughts, vibes, prayers, and meditations for kate mcrae, her mom holly, dad aaron, brother and sister, will and olivia.  kate began having seizures a few weeks ago, and instead of things improving, the seizures have become more frequent.  they may be a result of the intensive radiation she received and that sent her into a remarkably long period of remission, or... cure.  they may also be signs of a recurrence of her cancer.  until now she's been doing remarkably well, balancing physical therapy and a triumphant return to school.  she is again walking a tightrope...


Kate Mcrae on CaringBridge

holly's entry on caringbridge just a little while ago:

Untitled

It's been unfortunately eventful. In short after an ambulance ride we are in the ER awaiting a transfer to CHLA for admission. They are hoping to repeat her EEG tomorrow while inpatient and hopefully do her brain MRI. There is much going on. Much to ask and pray for. Join us. Not least of all that cancer will not be present. And that they can stop these seizures for good. 



© 2013 L. Ryan

Tuesday, July 29, 2014

Update on Brayden, Hugger Extraordinaire...

For those of you who have followed some of the CaringBridge kids that have been featured in this blog, here's an update on the irrepressible Brayden Martin, his Mom Maranda, wild brother Mason, and super grandmother Robin -- and more friends and family than a person could count.

Maranda took him to the ER due to behavior changes and a mother's instinct.  There's been a determination of disease progression in Brayden's brain, with the inevitable side effect of swelling.  In a heap of bad timing, his port has stopped working, and he won't get another until tomorrow.  If an MRI confirms the CT findings from the ER, Maranda has made the difficult decision to take Brayden home on hospice care.

He's been on corticosteroids and so is obsessed with food, and despite the dire situation, this has brought some levity to their days.  Hopefully, he'll be off the stuff soon, and his mind can shift to other things than constant hunger.







The goal is to raise money to help Brayden's Family with his hospice care. Right now, we want him pain free and to alleviate as much stress on the family as possible during this time as they look at options. Anything you can donate will help in doing so. If you have any questions, please contact me at ashley.klanac@gmail.com
Nolan Blake and Brayden Martin

Tuesday, May 6, 2014

Nolan laughing...






Nolan's mother Brittany wrote:

A few years ago Nolan was laughing hysterically on the couch and I couldn't help but think I better catch this on video. What if he looses his ability to laugh one day? I found it today. With tears streaming down I just listened to it over and over… I miss the sweet sound of his voice.
Brain tumors can take away your ability to walk, talk, eat, show emotions, smile, laugh and the list goes on…

Nolan is not doing well, so laugh for him today, send a good thought, send a prayer.  He and Brayden Martin are good buddies.

Nolan Blake, April 27, 2014

Brayden Martin and Nolan Blake
April 2014

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.

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

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."

Wednesday, July 24, 2013

Brayden Martin: Always on My Mind

Hi, Dear Readers --

It is good to be back after my hiatus dealing with spamming and reprobate relatives.  How did those problems work out?  Well, amazingly enough, the universe conspired to remind me what matters, and what does not.

If you're smiling, it's likely that you rank quite high on my "He/She Matters List."  It's akin to a gratitude journal in shorthand.

Relatives that I don't really know who are acting like hoodlums are hoodlums and, insofar as they do not cause my Mother-Unit stress or steal her worldly goods and happy outlook, they may merrily launch themselves off their local choice of cliffs.

Pornographic spam was generated due to my vocal refusal to allow truly suffering people to be taken advantage of by CALMARE / CTTC and the shady practitioners who are having a last ditch moment of money-grubbing as the whole affair circles the drain.  I think flooding my blog with porn spam is a bit ridiculous but these are not ethical people.

So let's concentrate on someone who matters.

Brayden Martin comes to mind.  He's had another rough spell, and, finally, his mom Maranda and his primary oncologist decided an early MRI to assess the efficacy of this new chemo protocol was warranted.
That happened yesterday and today Maranda and Brayden found out that, unfortunately, his tumors have doubled -- which was, I think, what Maranda already sensed.

She (and he, of course) is a tough cookie.  But no one is tough or ever prepared for this journey, be it the journey of a child or an aged beloved grandparent.  There is no preparation.

Brayden is charting new territory for relapsed pediatric medulloblastoma.  There are NO protocols to which they can refer for guidance.  And so Maranda and her guiding physicians, and her faith, are groping in the dark.

This is what she wrote today and it details the next treatment to be tried:

To just be blunt, the chemotherapy did not work at all. Instead of having two spots lighting up he now has 4. We have one option left and it was a road we were trying to avoid. Photon Radiation. It is dangerous with many side effects. Even the chance we could lose Braydens personality. I believe with prayer with everyone praying, we can keep those negative things from happening. With prayer we will keep those good cells from being damaged. With prayers we will hopefully get all of this cancer dealt with. I am going to pray that this treatment works and that he will come out the other side, the ornery, funny, little rockstar, we all know and love. Right now he is on a triple dose of steroid, that is always a ton of fun :o). Three weeks after the radiation is done he will start in patient chemotherapy. We were hoping this chemo would work, but I never had a great feeling about the treatment he was on, and this one I feel has a better chance of destroying this cancer. We have to stay positive. We are stronger than cancer will ever be. We love each other all the way to the moon and stars. We are going home this afternoon, there is no point and staying and doing in patient rehab, we need to start radiation as soon as possible. We will get back to doing therapy as well. Brayden went all over the hospital today in a little car, using his legs like a pro. He is tough as nails. I asked him if there was anything he wanted me to tell you all. He said that he likes to play a lot, with cars, and he likes to play guitar, and be a rockstar, and play on the Wii. We cannot wait to get home, this is an even more difficult place to be when you are sad. Every time he has progression it gets harder. I will continue to try and stay positive. We need some prayers to get through this meeting we will have this afternoon with Dr Aguilera. My Mom is here with me, and we are trying to find someone to come and sit with the boys while I go to this meeting at 3 o clock. We love you all. I will update once we are home and after my meeting with Dr Aguilera. 
                                           Love Always,                        Maranda, Brayden, and Mason 



We love you, Brayden!



© 2013 L. Ryan

Wednesday, February 20, 2013

Daisy Love Merrick's Memorial Information





ALL INFORMATION FROM THE PRAY FOR DAISY BLOG:

Daisy’s Memorial Info

Date: Saturday, February 23
Place: Reality Santa Barbara (At the Santa Barbara City College Sports Pavilion)
Time: 3 pm
Attire: See words below from Kate
Webcast: Daisy had many friends and supporters around the world for which we are so thankful. In order to honor these relationships we will be streaming her memorial live. Tune in at Pray For Daisy to watch it.


A few words from Kate:

Dear Friends…

Early Saturday morning we had the privilege of witnessing Daisy’s departure from earth to a place outside of time and space where her joy is complete: heaven.

Our darling girl gave us kisses at midnight, with lips dry from thirst and hot with fever.  Tiny and sweet, the words “that’s awesome” came from her tired body after letting us know she was having good dreams. She is safely home… Finally well.

I have refrained from giving details of her suffering over the last few weeks, as it was immense.  Out of respect for her dignity and loveliness we have been keeping these painful moments sacred.

Thank you for your partnership in loving our girl. Please know we are broken hearted for ourselves but so happy for Daisy, who is with Jesus in paradise able to run and eat and play with abandon. We believe that wholeheartedly, and as they say in Narnia, she is going further up! And further in!  She left the Shadowlands for a place more real in every sense.

Please join us as we celebrate the strong, kind, brave, goofy, thoughtful, amazing girl we call Daisy Love. Please wear what you feel best in; sandy feet and boardshorts, tutu and snorkel mask, or the prettiest dress in your closet. Wear black only if you must, but I’m wearing what Daisy would like most.  On her last night on earth, she requested we watch “The Hobbit” (70’s version) and dress like hobbits.  If ever there was a girl confident in her own skin, it was her.  Among her favorite ensembles are animal ears of all kinds, astronaut, flightsuit, monster, pirate, dinosaur, Indian, mermaid, bear, cowgirl, fireman and explorer.

Feel free to laugh and cry and hug. There is no single way to grieve. And while we miss her on earth, we will pick up where we left off when I have the privilege of going to where she is, in the presence of God where there is fullness of joy.

My final request to all who read this blog: love. Love your babies, your husbands, mothers, sisters. Love each day like it’s your last. All you mamas out there, you have been entrusted with the precious gift of a human life who depends on you. Enjoy your gift. Breathe in the scent of your child’s hair, breath. Let them cook with you and make a mess of the kitchen. Play hide and seek with them, build sand castles with them, take them on picnics, read to them!  Listen to them, value and respect them, never shame them.  Your words they will carry with them their whole life and you have the power to give them wings or stunt their growth. Motherhood can be tough but it’s worth it. It can be exhausting, boring, tedious, but never for long. You blink and they’re grown. It has been my honor and privilege to love Daisy these last 8 years. I’m thankful for every minute; the joyful and the terrible alike.

“I know The Lord is always with me. I will not be shaken, for He is right beside me. No wonder my heart is glad, and I rejoice. My body rests in safety. For you will not leave my soul among the dead or allow your holy one to rot in the grave. You will show me the way of life, granting me the joy of your presence and the pleasures of living with you forever.” (Psalm 16:8-11 NLT)


Monday, February 18, 2013

Something to consider, Dear Readers

No offense to my "cancer kids," but if you all would puh-leeze stop dying and relapsing, I'd appreciate it.  Just kidding, young ones, there's a whole host of you who've graduated from "The List of Four" and are now in college, back in fourth grade, on the swim team, and just generally kicking cancer's booty.

Miss Hannah, looking like she might wanna chew glass... but lovely and colorful, as usual! 


I want to talk to my Dear Readers about Miss Hannah -- yes, my hero.  If you've been following my logical and well laid out presentation of her story, you know that she recently suffered a relapse of osteosarcoma, with spread to her lung.  The good news is that a (relatively) simple surgery may have caught it early in the form of a nodule with clean edges.  So, that's worth a "yay!" -- just don't scare your co-workers with too loud a scream of joy.

The down side of chemo for osteosarcoma is the "side effect" of leukemia, which Hannah now has, as well.  That's worth a scream of another sort, and you probably should wait until you've some privacy before letting loose.

But you know me!  I'm not one to wallow in self-pity, oh no!  And in this case, since I am not the one battling two cancers at once, why should I?  Sorry, I got confused there for a moment, or a decade...

So here is the deal. Be a bone marrow donor, because that's what Hannah is now working toward.  It's an arduous process, and she is, of course, taking things zen-like, as they come.  But her transplant coordinators and family can't afford the luxury of laying around doing chemotherapy, relaxing in that comfy hospital bed, and chowing down on jello.

This is the latest post from Hannah's mom, shared at her CaringBridge site:


Today starts week 2 of this 4-6 week stay. She has 3 more days of chemo (including today) and then we wait for her counts to come back up before they let us go home for a few days. 
Today I spoke with the head nurse for Dr B...my other kids were tested to see if they are a match for donating bone marrow to Hannah. We got results...NONE of my other kids are a match for Hannah. The nurse said "they didn't even come CLOSE to being a match". *sigh* Soooo...plan B. They've already started the registry search. Because so many of you have offered to be a bone marrow donor for Hannah, we are in the process of putting together a donor drive. I will let you know when I have details. 
Thank you for keeping us uplifted in thoughts and prayers. 

From the National Marrow Donor Program, here are some frequently asked questions, with answers!  


Matching a patient

Deciding to donate

Donating bone marrow

Donating PBSC

Learning about the patient


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)."

Sunday, November 18, 2012

joey ran his race:::joey flew away!

from joey keller's dad, news that i find relieving, news that is bitter to no end for dad nick and mom elizabeth:

Joey finally met in person (face to face) the person he's loved, trusted, admired, talked to, talked about, and worshiped for years, Jesus, tonight, at 9:35p. Buddy, you loved that song, I'll fly away....you beat me there. Which is not the way it's supposed to be. I will be there soon. I never knew I could love someone like I loved you, son. My heart will be broken until I see you again. You are awesome. I told you often how much I loved you and thought of you. I can only hope to run a race as strong, and focused, and effective as you. In spiritual terms, I look up to you. I love you and am a fractured, torn up person without you. I'll never be right. But I will see you soon. One more time, "Dad thinks you are awesome! You make me happy! I am so proud of you." I'm coming buddy. Pray for me.




Some glad morning when this life is o'er, 
I'll fly away; 
To a home on God's celestial shore, 
I'll fly away (I'll fly away). 


I'll fly away, fly away, Oh Glory 
I'll fly away; (in the morning) 
When I die, Hallelujah, by and by, 
I'll fly away (I'll fly away). 

When the shadows of this life have gone, 
I'll fly away; 
Like a bird from prison bars has flown, 
I'll fly away (I'll fly away) 


I'll fly away, Oh Glory 
I'll fly away; (in the morning) 
When I die, Hallelujah, by and by, 
I'll fly away (I'll fly away). 


Oh. How glad and happy when we meet 
I'll fly away 
No more cold iron shackles on my feet 
I'll fly away 


I'll fly away, fly away Oh Glory 
I'll fly away; (in the morning) 
When I die Hallelujah, by and by 
I'll fly away. 

Just a few more weary days and then, 
I'll fly away; 
To a land where joy shall never end, 
I'll fly away (I'll fly away) 


I'll fly away, fly away Oh Glory 
I'll fly away; (in the morning) 
When I die, Hallelujah, by and by, 
I'll fly away (I'll fly away).