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Tuesday, May 8, 2012

Destiny Bracelets Spread Worldwide




What began as a small cooperative - an idea for one friend to use her talents to help raise a little awareness and funds for Destiny's medication - has turned global, and raised more than $3500 in just three months!

Beading circles are popping up everywhere - circles of friends, church groups, high school groups, birthday parties. Friends are taking them to international conferences, selling and sharing our message of community, entrepreneurship for people with disabilities, Sofia the Lovely, Destiny and Dravet Syndrome. People are uniting - language barriers and social barriers cease to exist when talking about these bracelets and their story. It truly is a magnificent international web of community being weaved from one idea nurtured!!

We are beginning to meet people, by pure chance, wearing Destiny Bracelets.



This past Sunday, there was a beading circle that I missed. This is a message that I wrote to the group of girls (while on I-25 with three kids in the back seat, all fighting for my attention!)

They're making Destiny by helping to save her. I've never been so touched and so grateful for anyone or anything in my life...

My visual is Desty is in a hot air butterfly balloon, floating gracefully above the normal perils of life. I'm holding my butterfly from floating away with all my might with my String of Love...but the winds are becoming stronger and stronger...

Everyone making bracelets, supporting and spreading our message, forms a line behind me, each grabbing hold of the string, strengthening it, easing my burden so that I can enjoy watching and interacting with my beautiful child. The string transforms into a bracelet, a bracelet that is spanning nations. Sometimes this line of bracelet makers can hold the string tight enough to let me climb into the balloon and let me enjoy the view, her hugs, her love, without worry.

Thank you!


And thank you for reading!

We are finally nearing the end of our critical fundraising 'era'. It won't be too much longer until Colorado Medicaid is set to pay for this life-saving medication. If you are interested in getting a Destiny Bracelet, please email Sofia at SoBeads mailto:sofia@stewarthome.net with your color/style preference, and she will take good care of you!

Otherwise, I encourage each of you to click the PayPal button on the left-hand side of this page and make a contribution to Destiny's medical fund. As little as $5.00 makes a difference!

Please donate and share this blog with someone TODAY!!!

This is my Destiny!....



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Monday, March 26, 2012

Turn the World Purple TODAY for Epilepsy



HAPPY WORLD EPILEPSY DAY!!!! We are wearing Purple today for Epilepsy!

What are YOU wearing?!?!?

If you are wearing Purple for Epilepsy, please send us a picture to include in an album for our family, showing the many faces of support this Purple Day! Even if you don't have any purple clothes, find a hat, a ribbon or even make a sign to hold up ;-) we want your picture. Please, if you are so inspired - include a message, poem or prayer for Destiny, our family, or about your experience with epilepsy!

I have shed many tears since last May, when my Love received the definitive Dravet Syndrome diagnosis. We had experienced seizures for years prior. It was actually my son, Benny, who had the first febrile seizure. I remember that night like it was 2 minutes ago.

Destiny's first seizure was different...singing and dancing around, preparing to bathe one moment, and on the ground convulsing the next...My baby...This was my baby...no fever or sickness detected but the ER was certain the fever had to be somewhere...And again....And again...Word had it that Destiny had febrile seizures and also that she was having problems staring, chewing, walking straight, and waking in unconsolable and unresponsive 30–40minute screams because she had a "flakey" personality.

It was the picture-perfect evening in late June/early July of 2010 that led us on the path of no return. A fever was obviously not a trigger. Excitement was!! And temparure!We were eating dinner at a kids play water fountain...Destiny was running in and out of the shooting water laughing, thrilled, with one to two dozen other kids...and suddenly, our world stopped..."Save my baby!" I screamed at the cops and EMT's repeatedly as they gave her oxygen and tried to get history. Close friends met us at the ER for support and to care for my frightened boy, almost weekly after that, for awhile.

I remember her first Anti-Epileptic med, and the neurologist's words, "I strongly recommend you put her on this. It's not going to go away for now.". That was the beginning. Destiny was diagnosed with refractory epilepsy months before last World Epilepsy Day 2011, her genetic test for Dravet Syndrome was being processed, but still, in general, every professional gave me the impression she could still "grow out of it" or get it under controlled.

By April, the thought was she had another devastating epilepsy disorder called LGS - the severity and regression were alarming. In May, genetics confirmed Dravet Spectrum Syndrome (since then, 'Spectrum' has been dropped...)

The same neurologist who saw her for the very first time way back, happens to be the 'Dravet doc" and, well, here we are...no longer do we go to the ER until breathing is compromised...I am the 'expert' and make judgement calls all the time about when and how many times to 'rescue' per bad night, when sleep is sleep or non-convulsive status, who to entrust with her care, what risks are worth taking, when to wear the helmet, all the way down to what treatments to try next and how much of the truth my son needs to know when. I no longer scream "CALL 9-1-1 NOW" or even think doctors can help...I'm much more interested in their machines when we do go in ;-) This is Life as a parent of a child with a rare, unknown by most, life-threatening conditions.

I will be affected by epilepsy for the rest of my life, Benny and Destiny, too, as well as our loved ones, in one brutal way or another, for the rest of our lives. This Epilepsy Day, I celebrate my daughter, her resilience, her strength, her innate beauty inside and out: My heart goes out to our friends with uncontrollable seizures, and I weep for the families whose Angels have grown wings way too soon. I ask for compassion as I beg for a cure!!


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Saturday, March 10, 2012

Destiny's Utopia by Lucia

I first met Destiny back in September through a friend of my mom. Since then I have had the pleasure of consistently interacting with her, and what a wonderful experience it is! Being with Destiny is like escaping to a utopian island of bliss... a place where there are no worries, only laughter and joy. A place full of flying colors and magical creatures, a land of opportunity and possibilities with no end. A place where imagination becomes reality, and you become delirious on joy and contentment.

On a play-date with me at my house one day Destiny transformed into a beautiful girl named Crush. She had discovered the makeup supply in my room. After applying about five coats of blush and eye shadow she jumped up and exclaimed, “I’m Crush! Because I’m different with makeup on. And you’ll be Flush!” (hand held high in the air like Superman). Another day when I picked her up from her house she was wearing a very lengthy wig and announced, “I’m not Destiny, I’m Rapunzel!” In the car later Benny made an embarrassing error; he called her Destiny. She adamantly corrected him. Another time she spent hours with a friend cleaning my yard, every bit of it! The rag turned rather black, but wow did they work hard! She is a powerfully determined little girl. And we want to keep it that way.

Wedged under all this amazingness of Desty’s little brain there are some misbehaving neurons that sputter around crashing into each other and giving Destiny seizures. In order to try to stop this Destiny needs medicine. But unfortunately this medicine, while utterly essential to Destiny’s development, is extremely expensive, and it is ridiculous to assume that any somewhat normal family can afford it on their own. One way we have been raising money is through the wonderful craft of beading. My sister, who has disabilities and who is also another incredible young being, has developed a beading business; a result of her LOVE (or, obsession, you might say :p) of jewelry. Members of our community have been gathering on Sundays to create beautiful bracelets which we then sell to raise funds for Destiny’s medicine.
Please support Destiny, her family, her community, and all the dreams, beauty, and joy that comes with her, by buying one of these bracelets! With each bracelet you will be helping Destiny in her battle against the seizures and you will be a part of this incredible community that is supporting, fulfilling, and realizing Destiny’s magical world.

Wednesday, February 1, 2012

She's Bad, She's Bad - She knows It!

In the hospital now for a planned 5-day EEG...


More soon!



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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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