One Word: Victory!

A friend took these pictures for us for our upcoming benefit. Kelle Hampton, you are magical!! I told her that I wanted pictures of Chase's scars but I wanted it to be more of a celebration of his victory rather than a photo to show all the pain and fighting he's been through. I think she did so beautifully!!!

Calling all short gut parents and families!

The Omegaven Benefit is official. February 21, 2010 here in southwest Florida. I am sending out a request to other short gut families for as much "stuff" as possible that could be used at the benefit: stories, pics (especially before and after pics), or even items that can be auctioned off during the raffle/silent auction/live auction. Reaching high for this one! $25,000 to be exact. Please send this to other SBS families you know. The more personal involvement the better!!!!! Thanks to all!

For more info. you can contact me at my e-mail: sherbearsis7@earthlink.net

Heather Cleckler

Extra, Extra!! Read All About It!

So I've finally gotten the courage to spread the news that I will be running in the Disney Princess Half Marathon on March 7th to raise funds and awareness for Omegaven. So for the next 5 months I will be relentlessly training for the race and, more importantly, raising money for Omegaven Research so more babies can get the treatment they need for short gut syndrome and so families can rest in knowing that their child is on their way to recovery!

My goal is $25,000! But passing this goal would be a true blessing. You see, families receiving Omegaven do not pay for the treatment. Because it is a research project the lipid is provided to the family at no cost. The only difficulty is getting the families to a hospital that uses Omegaven, which is a small handful throughout the United States. (Will provide that list soon!) So funds donated specifically to the Omegaven research may enable the research team to treat more patients and encourage more hospitals to use Omegaven at their facilities. If more hospitals use Omegaven, more children and their families will have access to the lipid, and more lives will be saved. I am sure of this!

So to jumpstart this fundraising I will be sending out newsletters monthly to provide facts and tidbits about Omegaven, where we are in our fundraising, and names of those who have donated. If you would like to receive this newsletter please just e-mail me with your mailing address or e-mail address at sherbearsis7@earthlink.net. Please type "newsletter" in the subject line so I don't delete the e-mail as junk mail!

I do plan on having different fundraising events and activities in the near future as well!! If you would like to help in anyway please e-mail me at the address above with "fundraising help" in the subject line.

It is about time the world hear about this lipid that can save the lives of kids struggling with short gut syndrome. It saved my son's life. It has saved over 100 kids who have received the treatment at Children's Hospital Boston. There is no reason this number shouldn't be in the thousands. Let's put pressure on other hospitals to provide this treatment. The last thing a family needs to worry about for their child with short gut syndrome is if their liver will survive. Omegaven can do that!!!!! No more excuses!!!!

It's out!

So the mic-key button came out with no problem yesterday. And we even haven't had any leaks!!!

What was really cute was when Chase said "I did it!" while we were walking out of the doc's office yesterday. We're so proud of our little fighter and apparently so is he!!!

Good Bye Mic-Key Button!

Mic-key button comes out tomorrow!!! Once again, doing my happy dance.

Not looking forward to all the messy that comes with it, but hey, I'll take it!!! My son will officially be "medical parts" free!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

(The button is that little plastic thing on his tummy. It's a feeding tube, but we haven't used it in over 2 months!)

Good News!

The Mic-Key button comes out this week!!!!!!!!!!!!

Also, I totally should have asked for prayer for the poopies sooner because, literally, the day after I posted the request his poopies went down to 4-5 poopie diapers a day and better yet, PASTY POOPS!!!!! What was I thinking?!?!?!?!?! Once again, we give all thanks and glory to the MAN above......HE ROCKS!!!!!!!!!!!!!!!!!!!

Picture update...........FINALLY!!!!

Okay. So I really don't have an excuse for being such a slacker. It's just been really busy around here. Chase is now up and running so you can imagine I'm just kind of chasing him around all day :) Lots has happened in the past month. All of us, except Randall, were sick (first time I've been sick since Chase was born, thank you Lord!), Randall has gone back to work, we've been working on our new house, LOTS of diapers to change, we got to share our testimony with a fellow church who were big time prayer warriors for us, a trip to Disney for my birthday (thank you Randall!), and GATOR FOOTBALL HAS BEGUN!!!!! Go Gators!!! More importantly, Chase is doing great. We weighed him last night and he is a whopping 22 pounds!!!! He has had really wet and frequent poopies since the line was removed but it doesn't seem to affect his growth or hydration. We'd still like some prayer for it, just to be sure. We are praying for less frequent poopies and poopies that aren't so wet. We miss our pasty poops!!!

We'd also like to ask for some serious prayer for some of our friends we have met during this journey. Preston was recently diagnosed with a form of cerebral palsy. Of course the docs have given a list of things Preston may not be able to do, but we know better. With God, all things are possible!! Hang in there Chris and Julie. Eli, a little boy with heart problems, is going through a rough patch right now. And Ellie, the one who led us to Omegaven in Boston, has been going through a really rough patch and is NPO (no food by mouth). A drastic step back for this family. But you wouldn't know it with this family's courage, hope, and strength. Not to mention Ellie's intelligence, strength, and just plain "cuteness." She is a force to be reckoned with!!!! You can visit her site at www.eleanorbrogan.blogspot.com

So here are some pics. Pics from before and after the line was removed. And of course, Chase's first real "dunk" in water. Again, I am sorry. Enjoy the slideshow......there are a lot of pictures!!!
(this is for you Uncle Joe and Aunt Dawn!):

Chase's bathtime before the line was removed. Daddy is holding up the central line so it doesn't get wet. This is the line that the IV fluids (TPN) went through and were dumped into his bloodstream right at his heart. Scary.
Chase's medical storage shelves. I had a blast getting rid of all of this "stuff."

Chase at Ronald McDonald House just hours before the surgery. (check out that hair!)

A groggy Chase after the surgery

Check out the frog wallpaper in our room after Chase's surgery! "Coincidence is just God's presence not being acknowledged!"

SWIM DAY!!!!!!!!!!!!!!

Colton had a blast, too! Before, Colton would play in the pool alone and Chase would watch from his stroller. Not anymore!!!!!

SPLASH!!

Mmmmm, popsicles!

Pappaw actually got in that tiny pool with the boys but I figured I wouldn't embarass him by putting the pics up! He did promise Chase he'd be right there with him when he took his first swim. He kept his promise!! Thanks Pappaw!

Chase's first REAL bath! With bubbles and all!

Colton doesn't look anything like his cousin, Jayce, does he??? :)

Riding the tractor with Pappaw

Colton fishing. He can cast and everything!! His daddy is SOOOO proud!

Colton definitely has the "mean" face down!

A day in the cowpens. Who do you think is Colton's favorite person?!

This is Chase's first time in the cowpens. Hey, who's that hot guy in the middle?

Chase taking care of the calf. He wasn't scared a bit.

Chase's first ride!

Chase before his first haircut. (Don't worry. The curls just got curlier!)

Old-timers day at church. There's that hot guy again!!!

Chase loved Disney. Colton on the other hand........