Sunday, September 27, 2009

Buddy Walk Pictures 09


Having a little fun getting ready for the walk!


Beautiful blue eyes against the beautiful blue sky. It was a PERFECT day.

Chloe's friend Teighan. Teighan is also the proud owner of an extra chromosome! :)

Our good friends the Letterios.

Teighan and Sandi.

Lou and Sonia Baghdady, News Channel 8.

Tori, Sadie and Lou.


Terry and Timmy.

The Mini's

Vvvvrrrrmmmm. Babies, start your engines.
Ready to walk!

BFFs

The kids take a beach detour.

Chloe's Crew

Casey, Van and Finn

The walk was AMAZING! Chloe's Crew has raised $770 so far. Donations are still trickling in as they are welcome up through the end of the year. There were over $13000 people and over $88,000 raised by the start of the walk. More donations were expected. It was such a glorious day with absolute perfect weather. A special thanks to ALL our supportors! Donators and walkers. Dillon's mommy Melissa and Jax were never far from our thoughts as they're both needing prayers right now. Hope you'll send some their way too (you can read about them by clicking on their names above.)

Friday, September 25, 2009

Buddy Walk 09

So tomorrow is our first Buddy Walk. We're sooooo excited. Chloe's Crew is all ready to go. We have a team of 25 walking and we've collected over $600 in donations! :) Wooo hooo. And since donations can continue to come in until the end of the year, we're hoping they'll continue to trickle in. We also received our team t-shirts FOR FREE from the t-shirt company. I'll post their name and website, if they have one, once I have it. It's very amazing when people reach out to help others.

I'll let you know how it goes!!!

Thursday, September 24, 2009

Prayers for Jaxson

Our little friend Jax is in the hospital and off to a risky surgery tomorrow. He is a VERY complicated case and his mom is very worried. Please say some extra prayers, send them some positive thoughts and mojo, or do whatever it is you do to help him get better and back home soon. You can visit his blog by clicking here. We're hoping and praying for you here Jax!!!

Wednesday, September 16, 2009

Sweet Ella Grace

Thoughts and prayers for our dear blogging friend Sweet Ella Grace! She has a bone marrow biopsy today to look for leukemia cells. Click on the link to see her blog and beautiful pictures of her (and hopefully good news about a clean biopsy). Spread the word. She NEEDS positive thoughts and prayers her way!

Monday, September 14, 2009

Back From Iraq

Obviously I haven’t just returned home from Iraq, but I feel, on some level, as if I have. Now I realize this comparison may seem extreme to some (especially my brother who has actually served over in Iraq), and I don’t mean to imply that the hardship we have faced is even CLOSE to the degree to which our nation’s heroes suffer during deployment, but what I am experiencing is like the psychological text book acclimation back into “the real world”. ‘What the hell is she talking about?’ you might be asking yourself. Well let me explain, for this blog is not only about my need to write and vent and do whatever cathartic expression I can to feel better, it is also a little bit of a window into my soul – a soul that is taking a journey of a lifetime.

The past few months have been intense for me. As most of you know Chloe’s health has had a nice gradual improvement for months now. While she has thrived, I have not had things so easy. I have racked my brain with how I could possibly be having a hard time NOW when we’re finally out of crisis. I started to realize I felt sort of “post traumatic”. But that didn’t completely describe how I was feeling. It got me thinking, though, more about war time and the transition from war back to home.

At times, watching your sick baby suffer or struggle wondering what will come next is in its own way, a constant war ground. Just trying to go through each day as if everything is fine just waiting to hear that not so distant enemy fire. But it hasn’t been the kind of war that leaves you in a constant state of physical threat. Rather it has been the kind of war that terrorizes your psyche on a daily basis. I think all humans have an ethical dilemma with attacking even the enemy’s children. Yet here I was on a daily basis, watching my child struggle to breath. Struggle to LIVE. I was living in my own war zone.

But now things are quiet. We’re back “home” to normal, or our new normal, that doesn’t involve weekly doctor visits and frequent trips to the ER. The suction machine is even beginning to accumulate dust. For us, the war is all but over. Chloe has been stable for almost 2 months now. A record amount of time without a single breathing episode. So what could possibly be my problem???? It’s like I said. I feel like I just returned home from war, back to normal, but things don’t FEEL normal. I’m not the same person. Things don’t feel the same anymore. And I’m left with that constant sense of guilt and confusion. There are people we have grown to love that remain in the trenches. . . over enemy lines. Even though I can’t help them when I’m there myself, there is some sense of togetherness that I can provide. Ridiculous, I know. But the truth. And I’ve learned to function in crisis. I’m having to relearn how to NOT be in crisis. And then when you finally start getting used to feeling good with your new normal you can’t help fight that feeling that you might have to go back after all. WHAT IF. . . What if you get called back to war. Back to that horrible place that although it has a sense of familiarity and you have glimpses of wanting to return, you REALLY REALLY can’t even imagine going back to that horrible place. In fact, really thinking about it can take your breath right out of your lungs. You watch the news waiting to hear of the latest battle. . . “swine flu”. . . “pandemic”. . . “children are particularly susceptible”. . . “children with underlying health conditions”. . .”death”. . . This is real world shit that I can’t escape, yet I have to. I have to take a deep breath and remind myself that we are home and we are safe and that no matter what the news says we’re not going back to that horrible place. But if we do. . . if we HAVE TO, ready or not, we will do our best and find the strength in our hearts and souls and the love that surrounds us, and forge on.

And to my little warriors out there that are still fighting the battle every single day my heart aches for you. I join your fight in my positive thoughts and prayers that I send your way. Hang tough my little heroes. You have AMAZING AMAZING strength.

A Test

Chloe's got the beginnings of a cold. I suctioned out some mucus this morning and there was NO gagging or breathing episodes! whooo hooo! So far so good. But this will be the test as to how she handles colds now. Wish us luck!

Saturday, September 12, 2009

Number 2, Comin' In

Well, Chloe's 2nd tooth is starting to poke it's way through. It is in the same place as the other one, just other side. I'm actually starting to think they're eye-teeth and not molars. Those are supposed to be pointy and the one that's sticking out is REALLY pointy.

She did GREAT standing today. Really enjoyed it. Puts a big smile on her face. And therefore our faces as well! She sat on a stool for a long time too. I'm just so proud of her. I'll post pictures of her hard work soon.

Chloe started in my program on Tuesday. It's been a little bit of a weird transition for me. The other kids are so much bigger and "better-abled" and so now she's suddenly seeming very small to me. She just looks like such a baby. But the program (which is a toddler transition and preschool prep program) is so good for her. It is so great for her to be around other kids. And it's great for me to be working again! :)

As for 9-11 and all the posts, I too will NEVER EVER EVER forget. I chose not to post about it because I find thinking about it is one thing, but reliving it enough to put my thoughts down in words was not some place I wanted to go. Maybe next year. But for this year I chose to remember privately. I thoughts and prayers are for everyone who was affected.

Wednesday, September 9, 2009

NO MORE CPAP


Well, after all the frustrations we've been having with Chloe's CPAP machine, her doctor reviewed her previous sleep studies and determined that she can go without it because he believes she is just improving at this point and it isn't worth the struggle and frustration. Wooooooo hoooooooo! She slept in her crib last night with no CPAP stress. :)

Wednesday, September 2, 2009

Chloe does Bang Bang

She has a tooth!!!!

Okay, so maybe just the point of a tooth, but she's got one poking through!!! And true to Ds uniqueness it is one of her BACK teeth! Silly little monkey! It's a sharp little sucker too. Poor little thing. She's been crabby with hard poops, now a tooth and this is about when she should have a reaction to her last vaccines if she's going to.

More commando crawling! She is READY TO GO! Watch out!

Monday, August 31, 2009

New Legs

Check out the brand new legs (otherwise known as "orthotics", "AFO's" or"leg braces". They may or may not help her walk any sooner, but they provide her with the support she needs to stand which is what she should be doing developmentally. You can see the pride and excitement in her eyes when she stands with them on!
She LOVES standing! :)

Saturday, August 29, 2009

Lots of Progress

Wow! Chloe has had a BUSY week with LOTS of good progress made! Monday she showed her OT how she has started to move forward on her belly in a commando type crawl. Soooo exciting. Then she showed her Speech and feeding therapist how far she's come in feeding. :) That afternoon at her 1 year old appt the doc told us she has grown a good bit in length! Wooo hooo. Tuesday she got her new AFO (AKA "orthotics" or leg braces). The are plastic and support her feet and the back of her lower leg. They go up to just below her knees. I'll post a picture soon. Wednesday she enjoyed some fresh air at the beach. When we got home she took a WHOLE ounce and 1/2 from a bottle! That's more thin liquids then she's EVER HAD in her whole life!!!! Thursday during PT she pulled herself to stand for the first time ALL BY HERSELF with her braces on!!! She is standing beautifully with them on. (pictures of that to come too). Just warms my heart! After that we joined my mom for lunch and sweet Chloe ate her first ALL SOLIDS meal - I mean NO purees!!!! She had carrots from my soup, banana, and kiwi. She did GREAT! And another ounce and 1/2 from the bottle when we got home. Then Friday she was back to impressing her other PT (physical therapist) with her commando crawling skills and her new standing skills! It's been a busy, exciting week.

On another note, Xander started school and loves his new teacher. He's very happy to be back and starting the 3rd grade. Sadie is still home for another 1/2 week returing to the same school, but new classroom next Thursday. Then the following Tuesday we start our program. To say we're busy is a little understating things. But at least it's all good stuff.

Sunday, August 23, 2009

Chloe's First Birthday Bash Extravaganza!


Her pretty but GINORMOUS birthday cake!

The beautiful birthday girl. Happy Birthday angel.

The birthday girl with her friends! :)

Chloe's good friend Chelsea came to celebrate with her!

Chloe's really thinking "get this stupid thing off my head".

Happy First Birthday Baby! (Chloe with her dairy free, chocolate frosted cupcake that was in fact quite delicious!)

Chloe's not too happy after making a huge mess with her cupcake and getting it all over her face. She didn't get the idea of eating it. She just made a big mess.

Penny and Mo doing some art together. They really got "into" their project - literally - they decorated themselves! :)

The Ridge Hill gang.

Playing with her new Pound-a-Ball that she LOVES! She was demonstrating her new "bang bang" skill. Mommy and daddy were soooo pleased. Thanks Mo, Scott, Penny and Nathaniel. What a perfect gift!

Ha ha, I love that title. Just makes it sound so important! It WAS important. We had a great time and I wanted to post some pics. Hope you enjoyed them. We had about 30 adults and 30 kids! My husband kept saying "30 KIDS?!?!" The weather held out for us and we all had a great time. Especially the birthday girl! :)

Friday, August 21, 2009

A Nice Surprise!

I left the room with Chloe moving around on her belly and returned a bit later to find her SITTING UP! It's the first time she went from her belly to sitting up all by herself!!!! I was soooo excited. I don't know HOW THE HECK she did it, but she did. I can't wait to tell her therapists. I was totally surprised!

Tomorrow's Chloe's big birthday bash. Don't ask me why I decided to take on the stress of a large party. And to make matters worse the weather is very questionable. Argh. Let's hope for a nice day so we can honor our special girl and all the people who have supported her over this past year. I can't believe she's one. She's still like such a baby. Birthdays with a medically complicated child who also has special needs are paradoxical. There's the feelings of elation and celebration regarding her success and, well, her LIFE. At the same time, there are feelings of loss (loss of her infancy) and frustration at how hard she has to work to do things younger babies are doing. . . there's also some period of re-living this year, which at times has been heartbreaking. But fortunately the feelings of joy and celebration dominate and I'm left with great pride in how far this amazing angel has come.

If you happen to be local and want to join us for a very casual BBQ in her honor please contact me through email for more information. :)

Monday, August 17, 2009

Update

Well, we're thoroughly enjoying our new pup Miles! He's such a delight! He comes from a family with children so he is very comfortable with our kids. We're still watching him like a hawk of course, until we get to know him, but all in all, things are going quite well.

Chloe's doing great. Enjoying being one. :) She likes watching Miles and getting kisses. She has started eating fresh banana and peaches in little chunks. I'm so excited! So she's still eating purees and now mushy food chunks. She's so cute when she's chewing it up. She gets this look on her face - a mix of bewilderment, concentration and pride. It's very cute and very funny.

An update on Zoey - thanks for the thoughts and prayers for our sweet friend who's test came back negative. :) We're still sending thoughts and prayers for her as she finds out what is going on and to sweet Jax who is always fighting a new battle of some sort. They are amazing kids!

Saturday, August 15, 2009

Our Newest Addition!


Welcome Home Miles!!!!

We're still settling in and getting to know each other, but he is one sweet boy! We can't thank everyone at The Chi Society and Rescue Road Trips enough for making his adoption possible! What amazing people! Peggy, Lee, Lorry and Greg are all amazing people. If anyone in the Northeast is looking to adopt I hope you will give these guys a chance. Lee and Lorry were so patient with me and never made me feel like the pain in the a** I KNOW I was! I wanted so much information and pictures and even a video (which they figured out how to do and after several attempts and lots of patience posted on you tube). Click on the highlighted group names to link to their pages and "you tube" above to see his video.

Wish us luck! :)



Fun with a New Friend


Teighan and Chloe posing for the camera!

Hello there baby.

Checking each other out!