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Wednesday, January 25, 2012

Erie High School Girl's Basketball Team Plays With Heart'

DESTINY BURTON....YOURE OUR INSPIRATION TO PLAY WITH HEART.


"Tammy, our whole team wrote this on our wrists tonight, in honor of you and your family :]"
Was the message from Nicole, my friend, assistant and sitter.

I woke to Benny's asthma attack at 1:15 this morning to find this. Words cannot express our gratitude for Nicole, and for the members of her basketball team at Erie High for thinking of us


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Wednesday, January 18, 2012

Girls Just Wanna Have FUN!


This video was taken on our last day in the hospital! I think the spaghetti-mouth just adds to the song!

Ms. Destiny Ann improves each day!

On Monday, she practiced writing the alphabet...now this is not an easy feat for this little girl, but she did it happily!


Notice her new highchair - known to her as her table rocket chair. Notice her "Princess Crown Helmet" and her sippy cup! This child loves them all!! - She truly has the best attitude and i am so lucky! (Her mama is still adjusting to the changes...fortunately these things mean something entirely different to Desty than they do to me.)

Things change, we evolve and Life Goes On.

On Tuesday, we woke Desty up @ 9:45AM, and had her try Patchwork from 11-12:30...This was the first day after Patchwork that she hasn't fallen asleep in my arms @ pick-up!!!! And I kept saying, "she looks so good!"


She then went with Jamie, our Super-Sitter/LPN and continued to have a good afternoon and evening, and only taking brief cat-naps.

I, on the other hand, napped deeply for 4 hours!!! I finally woke up @ 6PM screaming, "Where's Desty?". PTSD! I thought it was AM and Desty was gone...I forgot I took a nap!

Today was a great Desty Day!


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Saturday, January 14, 2012

Destiny's Emergency Admit

"You've Been Holding Out On Us"

My jaw dropped and I wracked my brain for some piece of significant medical information that I had forgotten to tell all the dozens of medical people I had spoken with. Our attending, Dr Nell, said this our second or third morning here at Children's Hospital in Denvrer. Was she gonna put me to shame in front of all of her resident mob?

Then she told everyone about this site and my efforts to pay for Stripentol, and of my love for and determination to help Destiny. She had spoken to our Pediatrician that morning, whom she referred to as "quite the character". I love Dr. Doody beyond words...He is the picture perfect pede!

This meant a lot to me...I was able to express my love for this child openly and appeal to the senses of these future doctors, and beg them even harder to figure it out and save my Destiny. It gave me a chance to breathe, trust and to see our residents compassionate faces, when not in the midst of crisis.

Destiny was admitted through the ER on late Tuesday night. She was unresponsive. I'm not going to get into many details here...just share some reflections and pictures. The short of it is that is toxic on Depakote, thus on ammonia also, and it basically shut her brain down from last Saturday on. Much more complicated than I care to discuss ever again for the rest of my life!

There's been a few frightening moments, I.e., when it took 25-minutes of sternal rub to awake my Princess...usually it only took 10-minutes! Or the few days she was awake for 30-minutes total. Or when her blood pressure dropped very very low. Or when the doctors/future doctors kept saying, "We don't know yet...we have no answers..."

There is one thing that really brought me back, made me glad to be me, in those excruciatingly dull days. The choppers. Oh, I despise the sound of them! We're on the 9th floor; they are very close. I dunno...is it bad of me to not really think about the child in the chopper, but to feel heartbreak for whoever was left as the chopper flew away? I pray for the mother, father, siblings of the child landing on the roof. I realize that my child and I arrived here in our van, and we will leave the same way.

Finally, I think about our Dravet brothers and sisters who are frequent flyers, and I gain further acceptance that the possibility of me being the one left on the ground to chase the chopper in my van is increasing. This is good though; I really do better when I'm prepared. It's 45-minutes from my house to the hospital.

Okay! That was intense!

Now for a couple of funny stories!...All of you Facebookers know this story, but some of my blog followers are not on Facebook....On Friday, I was weakening emotionally, my tears were release! Very little progress had been made, I was beginning to doubt the expertise of the staff, I was so exhausted, etc. That afternoon, my son, my dog and my friend arrived. I went down to get them and GET THIS! Tank came in, no questions EVER! I hid my son in a wagon, covered him with blankets and bags to hide him & sneak him in!!! That was sooo FUN!




And we almost got CAUGHT by a rather stern nurse as B was climbing out of his wagon.
Desty was awake, eating and looking good at the time. Silly girl says, "Where's Benny?" (hello! Like the first time she's coherent!!) then she looked past me and said, "Oh, there he is". Oh man! Her speech is so sluggish, I don't think the lady fully got it but she did try to look around, Buck jumping in front of the Sneak! Benny's grin priceless!!

The hospital has a 'no visitors under 14 rule' for good reason (I guess!) but this is his sister!...and you know I'm a non-conformist! ;-) This will be a fond memory!

And so will my memory of Harry, our neuro med student. From the very beginning I was annoyed by his presence! I felt it a huge waste of time that they would send in a med student that was completely ignorant about Dravet, if not everything, to give me updates from neurology and answer questions that he had to take back to the real doctors. I challenged the poor guy...and he ended up rising to the challenge, though I think it was a painful process! His second day I corrected him on the difference between Clonazepam and Clobazam, then I mentioned to his boss that maybe he needed to know that. (YIKES! Ok! I was so stressed! I didn't want him to be in ANY trouble, but I wanted him to know the difference ;-)
Instead of hating me, Harry came back so genuinely eager to help us, and to listen to me, my concerns and my pleadings. He learned about Dravet, the drugs, and took a sincere interest. He is eager to learn details that he may never need to know again, and listen to crazy parents with information. By Friday, he sat in a chair beside me, telling me what he learned about Dravet Syndrome, taking final notes about contraindicated medications for Dravet. He does a rotation in the outpatient neurology department beginning on Monday...I hope to see him and show him that he was right: my little girl just needed time.

Desty has come a long way,
and I thank my Dravet family who told me to rush her in, Buck for sticking with us, Harry and the residents, the nurses and doctors who really did their best to help my baby, the many friends who took care of Benny, Tank and Fishy, got us clothes, food, Patchwork for supporting Benny, and all of the prayers and thoughts from everyone via Facebook!

Tonight Princess Destiny is fully back to previous cognition, speech and energy, and her ataxia has made significant gains today! The detox worked!!!!!!!!! Outta here tomorrow, guys! Homeward Bound!

I hear a chopper...

All I can ask now is that people keep donating when you can to Destiny's Stripentol Fund!!!





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Thursday, December 29, 2011

Night of Princess Magic

I'm going to regret this tomorrow! HA! -Quite the first-liner, right?! It's approaching 3AM, and aside from some sporadic Myoclonics, Destiny has been "seizure-free" tonight. It's always like this...she will have a bad, even atrocious few nights...nights when my lack of sleep almost feels excruciating, and then when the cycle ends, and she begins to have "good nights", mom can't sleep...Total creature of habit!...Also, I tend to be overcome with anticipation and gratitude for the upward turn...I think it must be hard to understand unless you've been there/here, as a parent or loved one of someone who fights for their life.

We have been on vacation, living in our Salt Lake City "apartment" since 12/18? Though, my eternal friend Lori managed to swipe us a free night in a suite one night earlier. So many things to write about, but I feel an urgent need to record some highlights from last night. Not even real highlights, but my personal reflections.

Now, wait! - first things first! - the drugs from Europe ARE still working. Stripentol and Clobazam = a treatment method, which far from a cure! Destiny has bad days and "atrocious" nights, but in perspective, compared to September and October, they are very decent ;-) but weird.

A bad night now looks like this: she'll sleep for 5-10minutes, have a 40-120second Tonic Clonic or Partial Complex seizure, followed my some myos, wake slightly, fall back asleep for 5-10minutes, have a 40-120second Tonic Clonic or Partial Complex seizure, followed my some myos. Rescue meds no longer touch these clusters. I may wake her up, try a mid-night Popsicle, but as soon as we get in bed to try again, we are right back where we began. Just gotta ride the night out. In my delirium, I fear Desty may never ever sleep again without seizing!

Okay, this post hasn't been about any Princess Magic at all yet!!!

So, to make an incredibly amazing and magical story short, these heroic, angelic, coolacious people threw a Grand Princess Ball for Destiny, in part to raise funds for her medication, but mostly to make her wish of being and meeting a princess come true!

Many thank you notes to come for this! It's a good thing we homeschool ;-)

The evening was filled with magic for Destiny, and magic for me - separately! The child was princess crazy, full of life and unrestrained energy as she would meet a princess, then quickly say with urgency, "I need to go find more princesses!!" To my astonishment, what began as 5-6 traditional Disney princesses, grew into gobs of mainly teen/young adult women in gorgeous gowns, who'd be introduced as "Princess _______". I swear they must've called their friends in to keep Destiny entertained!

Destiny LOVED the Queen dearly! My favorite quote: "Mama! The Queen has FIVE daughters! That's a LOT of surgeries!"

Pure Princess Destiny magic!

For me, the magic was the non-character guests...there are just a few that I will reflect on.

Ariell (that's really her name!) who I have known for 21 or 22 years. We met as twelve-year-olds and now our girls (and boys!) are growing up as cousins! This picture of Kysaija at 4 and Destiny at 6 so reminds me of the relationship that Ariell and I had at age 12! Kysaija is Ariell's mini-me - totally....


Ariell and K are literally one of about four "sides of our family". How lucky my kids are!! LOLOL! And how confused they will be! What grade do you do your family tree? Remind me to homeschool those years!!!

Then there's Eric and Addy who came, from the Cutler's "side of our family". I've known Eric for ~9 years, I believe. We have been at family dinners/parties etc., but haven't really spoken until tonight. I feel a special and unique bond with him and his wife, Barb. They have a little boy with uncontrolled seizures, and I frequently seek updates on him...so to my kids, our kids are cousins. It is heartbreaking to hear of their struggles, but a shared experience, when it naturally exists, is priceless. As we parted, there was a moment of, "Yes, yes, I do know what it's like..."

K, I don't know if I can convey anything of anything to make sense with this next reflection. To try to understand it, pause and read this dated post of mine: Visiting Diana. Diana passed away almost a year later, when I was laid up from my hip replacements. I guess you never get over losing such a special friend.

This reality that I am faced with concerning my Destiny's prognosis....there are two people I would give anything to look in their eyes and say "Help! Tell me what to do, think, feel. Tell me what my goal should be in mothering this babe." Diana and Laura are both gone. I swear they both would be able to console me, with their magic!

Anyways, Diana's kids, Spencer and Samara, and their new mama (who I truly adore and I'm soooo thankful for!!!) attended the Ball! I love this picture of Kysaija and Samara dancing with Benny!


Of course, the Galloway's side of our family was there - they helped put it on! I greatly missed Granny and Paz though!

I guess, for me it was a big reunion of people we love, plus many little princesses and their parents that we don't know, coming together to
help my little girl (who shoved her cupcake in my face at the start of the Ball, squealing joyfully "Got'Cha!" ya, you better be glad I think you've seen it done at weddings, my Pretty! ;-).



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Location:Salt Lake City, Utah

Saturday, November 26, 2011

Gnome and Deluxe Fairy Door Raffle for Destiny!

Raffle Tickets Sold Here!!!! Only $2.00 EACH!!





Young or old, all gnomes gneed to believe in miracles. It's just in their gnature to do so. Everygnome is destined for greatness, whether that be through great acheivements or small ones. Perhaps a gnome will one day save the entire garden, or perhaps their Destiny is to just remind their loved ones around them that life is good...

A special friend, Jennifer, of Gniffer's Gomes made this colorful gnome just for my Destiny. A friend of hers, (all the way across the world) in the UK, donated the totally radical Fairy Doorway to go with Destiny's Gnome.

Destiny is going to get this gnome for Christmas to watch over her.

Get your own custom gnome of your choosing from Gniffer's Gomes plus a Deluxe Fairy Door from Enchanted Doorways & Fairy Door Friends!!!

Buy Raffle Tickets by clicking the PayPal Button on the left column of this page and note "Raffle" when you donate! Each RAFFLE TICKET is $2.00. If you donate $10.00, your name will be entered into the raffle five times; if you donate $20.00, your name will be entered into the raffle ten times, and so on.

Destiny's Gnome Raffle ends on Saturday, December 3rd at 8PM (MST)!!!

Destiny will pull the winning name from a hat!!


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Saturday, November 12, 2011

Make a Donation and Shop Simultaneously TODAY!

The Wings for Destiny Auction blasted off on October 30th! Two weeks into it, bids are totaling almost $600!!!

These past few weeks have been simply unreal...I lack the words and energy to describe it - that is why I have not blogged lately. I apologize to everyone who hasn't been updated on Destiny's progress lately. The meds are working!!! Whether they are going to work in eight months/a year/five years, I don't know, and I don't care right now...I can't care right now.

I look into my daughter's eyes and I see Destiny! Destiny's expressions...they just make my heart melt! I had to teach Benny and Desty that ”mommas cry when they're happy". (LOLOL!) I take mental pictures now, quite literally. I know what can happen...I feel so blessed in that way. I have the rare opportunity to, for country fans, Live Like I Am Dying. That's exactly what I'm doing, guys...No regrets!

Destiny is not seizure-free; her med cocktail is not a cure for Dravet Syndrome...I can't 'fix it' (DAMMIT, I say! ;-). But we can and are truly changing this child's life for the better! Seizures have decreased from 50-70 alarming seizures each day to only a handful per week. We were 'rescuing her' 3-10 times a day when her seizures were out of control. We have not given any type of rescue medication in over two weeks!!!

Desty is a fighter, and you and I are her sponsors!

Please take a few minute to look at the wonderful items that were generously donated for auction at Wings for Destiny Auction

This is such a cool way to raise the money for Destiny's treatment!

Anyone can bid! Just put your bid in a comment. Shipping is included. The auction ends on November 30th!!!

Please go today and start a Bidding War! ;-)

Challenge your friend's to bid as well!



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Wednesday, October 26, 2011

What Your Money Has Done



Thank you so very much for helping us bring our Destiny's spirit back!

We love you all!!

Please continue to contribute when you are able!


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