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Courtesy Avery's Bucket ListOn Good Friday at around 3:30 p.m., Laura and Mike Canahuati of Houston got a call from a neurologist confirming their worst fear. The tests results showed their 5-month-old daughter Avery has a rare and incurable genetic disorder.

Avery was diagnosed with spinal muscular atrophy, a genetic disorder that attacks spinal neurons and progressively debilitates muscle function. Avery's was Type 1, the most severe kind, and doctors told them their little girl had only 18 months to live.

"We had several days of sitting in shock and crying and then we pulled ourselves out of that," Laura said. "Since we had such a short time, we knew we wanted to make the best of it."

To cherish every moment with Avery, the Canahuatis created " Avery's Bucket List," a blog written from Avery's perspective where they chronicle her world and track their family adventures, checking things off from the bucket list as they go.

The bucket list includes milestones in every child's life - from sitting up, kissing her mom and dad, to having a birthday party, meeting Santa Claus, losing a tooth, visiting college and more.

"We have our days, it's not that we don't," said Mike Canahuati, 31, who writes the blog in his daughter's voice. "The blog made it into … 'Let's go to the Canahuatis and smile at Avery and appreciate life instead of crying."

"I have a lot of living to do in just a little bit of time," Avery "writes" on the blog. "In everything I do, the two most important things are that I'm spending time with my mommy & daddy, while at the same time spreading awareness for SMA."

Avery's story and bucket list has struck a chord online. Since the Canahuatis started the blog earlier this month, it has racked up close to 500,000 page views, Mike said, with people as far as Malaysia, Hong Kong, Germany and New Zealand visiting it.

"When we saw how many people it was reaching in a few days, that's when we realized we could really get the word out on SMA and spread the word as much as we could," said Laura, who worked as a kindergarten teacher before giving birth to Avery, an 11-11-11 baby.

SMA is the No. 1 genetic killer of children under the age of 2 in the U.S., but most people don't know about it, Laura explained. An estimated one in 40 people are carriers of SMA. If both parents are carriers, like Laura and Mike are, there's a 25 percent chance of their child having SMA.

Laura and Mike urge all parents to talk to their OB GYNs and get tested to see if they are a carrier for SMA.

"Our goal for Avery to be the face of SMA. Just like when you say the word cancer, I don't think there's a single person who doesn't know what cancer is, we want it to be the same for SMA," Laura said.

Avery has already lost the ability to move her legs. She can barely move her arms and doctors say eventually she will be unable to move her head or breathe without the help of a respirator. Last week, she had a G-Tube put in so she can be fed through a line in her stomach and her parents constantly monitor her oxygen levels since babies with SMA have difficulty regulating their breath.

Courtesy Laura and Mike Canahuati

While her parents know Avery won't be able to fulfill many of the rites of passage that are on the list, they are finding joy in what their baby can do - tasting solid foods, taking a "big girl bath," flying a kite and blowing bubbles - and are finding a way to share in some of the later milestones with her now.

Fast forward a few years, Mike and Laura took Avery on her first college visit to their alma mater at Texas State University, earlier this month. Avery just got her very own (faux) drive...cense made - one with an ugly pictures and one with a great picture, hitting two items on her list.

Thanks to some mommy matchmaking, she scored her first kiss from a boy named Cooper "McDreamy," who also has SMA.

"His name is Cooper and he's 19 months old (I just love older men, they're so much more mature than 3 & 4 month olds)," Avery gushes on the blog. "My mommy and daddy said this might be the best kiss since Ryan Gosling & Rachel McAdams in The Notebook."

Tonight, Avery will get to throw out the first pitch at a baseball came for a new minor league team in Houston, the Sugarland Skeeters. Another day, another adventure.

The last thing on the bucket list: to overcome her illness. Laura and Mike know that will not happen since the research is too far off to save Avery, but they hope their daughter's story will raise awareness for the disease and help find a cure.

"No one should have to go through this," Laura said.

That poor beautiful little baby girl.

http://gma.yahoo.com/blog...ories.html

I have a lump in my throat...

such a touching story - how those parents found strength to do all this is just so amazing

and it will be great if a cure is found ~ but only 18 months!!! i just get all choked up

I cried while I read this article. How the parents found strength to make something positive out of this tragedy amazes me,they definetly have more strength then I.

If you wish to join Avery's Facebook page you can go here....

https://www.facebook.com/...BucketList

This breaks my heart

It really is beautiful that this little soul came into their lives to share this much love.

oh man! Children should be immune from all forms of sickness!

banks said:

Stricken Texas 'bucket list' baby dies, father says

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updated 5/1/2012 7:39:49 PM ET 2012-05-01T23:39:49

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A Texas baby born with an incurable disease whose parents created an online "bucket list" for their daughter that became an Internet sensation has died, her father said on Tuesday.

1. Michael Canahuati said in a blog posting that five-and-a-half-month-old Avery died on Monday afternoon after going into cardiac arrest. The little girl was born in November with spinal muscular atrophy, a rare genetic disorder that doctors predicted would kill her before she turned 2.

"Avery's passing this quickly came as a complete shock to all of us, as she had just been given a thumbs up at her last doctors appointment only three days ago," Canahuati wrote on Tuesday.

He made the announcement on the website -- http://www.averycan.blogspot.com/ -- where over the past month he and his wife have been posting fanciful light-hearted blogs written as if penned by Avery herself.

Among the postings was a so-called "bucket list" of things Avery hoped to do before she died. The list included a number of goals -- to swim with dolphins, to get a manicure and pedicure and a tattoo -- that expressed an optimism the little girl would prove the doctors wrong and live a long, rich life.

Avery did many of the things mentioned on the list including moving her legs, tasting solid foods and visiting relatives.

The "Baby Avery" blogs have attracted more than 3 million page views since April, when they first began being posted, according to a counter on the website.

http://www.msnbc.msn.com/id/47255074

I saw that yesterday morning,and I bawled.

If you would like,please sign this petition to make SMA carrier screening standard..

http://www.change.org/pet...g-standard

[Edited 5/2/12 22:54pm]