Friday, September 14, 2012

Shop My Closet

I HATE having yard sales... well, I do now that I have 3 small kids. 

The last one that I had my 5 year old was negotiating with anyone that was trying to by his old toys and to make matters worse, he was taking all the things that I had on the tables and slowly smuggling them back into the house.

Needless to say that sale was a literal revolving door, he would bring it in and I would take it out.... repeat about a million times. 

I hate having to deal with all the hagglers that come wanting something for nothing as well. I promise, one year before we moved to Indiana I was trying to sale as much as I could before the move. I had a SWING SET for sale and some fella tried to talk me off of the already amazingly low price. He literally argued with me at MY sale, he wanted an entire swing set for $20.... 20!!!! REALLY.

Anyway, I thought that I would post it all on here as well and have a virtual yard sale.... a BLOG sale.... If you see something that you are interested in just comment here or message me. I will send you a PayPal invoice. Simple as that... 
And because I have no clue how to make it all fancy, this is as good as it gets.
Items are always changing as well. When it's sold I will take it off.
Happy Shopping

Monday, September 10, 2012

Humbled

I LOVE Brac's hospital. When we decided to move it was hard only because I LOVED our NC hospital as well. He had such wonderful docs there and I was afraid of what he would walk into in Cincinnati. I did lots of research and was pleased that Cincinnati Children's was among the nations best. I mean, this was my child's health in their hands. I was sure they were perfectly competent but it takes a lot to gain a mother's trust. 

Cincinnati Children's has proven to be fabulous. Brac has one on one attention from his amazing doctor, Dr. O'Brien. I just love her. As does Brac. She gets down on the floor with him. She makes him feel amazingly special when she talks to him. 
Children's has an annual Survivors Picnic at the Zoo, hosted by Cincinnati Zoo.... oh what a fabulous event. An event to celebrate life and in SEPTEMBER at that... perfect time since this is Childhood Cancer Awareness month. We had the privilege of going this weekend. The weather was AMAZING. It was so humbling to see all these amazing kids... SURVIVORS... some still in treatment, but surviving. Some have grown up and some were obviously still in treatment. It was so nice to mingle with other moms... just like me. It was also important for Braxton to see that there were other kids just like him. Kids who fought and WON .... or kids that were "almost" winning. I was so glad for him to see that he was not alone. 



Eron's parents aka Papaw and Nana... came to enjoy in his special day as well. Boy, you should see these kids faces light up as soon as they spot them. They made the day so much more special. To have that one on one time with them. Not mention how much help they were for me. Thanks so much. 



We were given free admission to the Zoo, given a fabulous lunch and the kids received lots of goodies. One thing that is awesome about these events is the way they include the siblings. Zoe has never been left out. I also got some fabulous info on things for Braxton.


There is this fabulous organization called Monkey in my Chair. They place a monkey in the child's seat if they are ever out of class so that even though they are not there, they kind of are. It's a fabulous way to make him feel included even when he can't be. I have requested his. Excited to get it. 
Find out more here > Monkey in my Chair

I have also decided that since Braxton is ALMOST FINISHED (4 more clinic visits after today and one more spinal tap) that I want to start giving back to the organizations that have helped us so much. I am going to start volunteering with the Leukemia and Lymphoma society as well as a fabulous organization call The Dragon Fly Foundation. They bring special things to the kids while they are in the hospital. Things that make there extended stay more bearable. As a mom who's "been there" I am really excited to help out those moms (and dads) just like us. 

We are praying that Brac will get through these next 4 months without being inpatient. As I type this I got a call from Eron telling me that his port is not drawing back, so we are also praying that this will resolve itself and not be anything at all. Brac's been so tough, so strong and amazingly brave through every month of his treatment. Through every stick and through every hospital stay. We are so blessed to have him. 

And I couldn't let a post go by without a little Zoe/Caleb action... 
I'm not sure if you can tell but that's her big brother under there. I definitely think she has "middle child syndrome"
He's crawling, climbing and now making messes all by himself... at 8 months!

                                   
TTFN

~ The Sassy Southern Belle ~

Thursday, September 6, 2012

The Light's getting warmer...

3 years ago we started on a journey with Braxton. 

We have learned to cope, we have adjusted to a different "normal". We are so close to the light at the end of the tunnel that we can feel it on our face.

Today he asked me if this was the last one. Sadly I had to say no.

I look forward to telling him "yes" in January. Talking about it now chokes me up so I can only imagine how I'm going to be on that actual day... January 15th 2013. 
I think the doctors even get excited. Their faces light up when they talk about it too.

I have decided that since I am going to have a little more time on my hands in the coming year, that I am going to dedicate more of my time to the cause. I have learned in this journey that cancer research, especially pediatric cancer research, is horribly under funded. I am going to stand up and become an advocate. I am going to volunteer more. I have also decided to sign on with the Make-a-Wish foundation. They did a wonderful think for my son, and I want to give back. 

On October 13th we are going to be participating in our very first Light the Night walk in downtown Indy. 
I am super excited about this. I am excited that Braxton will be carrying that white survivors balloon and I will be carrying a gold balloon for my grandpa that passed. 

I have learned that despite the circumstances we are blessed abundantly to still have Braxton here. We are blessed because he got "the good cancer". I know that there are so many wonderful, amazing children out there fighting so hard to win the "bad" cancers. 
Braxton is for sure a fighter and I am going to celebrate this ever moment I get because he is my hero everyday.

You can join our team here:   Braxton's Team  You can be a virtual walker and help raise money for his team, all proceeds will go directly to the Leukemia and Lymphoma society. Please feel free to share to the link.



He has clinic on Monday. A spinal tap and chemo. He already feels crumby so I am sure that he is not going to feel wonderful when it's all said and done. Please remember him in your prayers as Monday draws nearer. 4 more!!! And he's DONE!!!!! 

Saturday, September 1, 2012

Childhood Cancer Awareness Month



In my younger, pre-mommy-hood years and then even into my early new mommy years, I can remember hearing the St Jude commercials and seeing the pictures of the sweet little ones battling all sorts of cancers and illnesses. I can also, so clearly, remember me saying "I'm so thankful that's not my child..."

And then in a split second all that changes. It becomes YOUR child....

You can remember playing as a child. Staying out for hours. Getting dirty, drinking from the water hose, baking in the sun because you were having too much fun to come inside. NOW, imagine all that being taken from you, because you are confined to a bed for 8 hours receiving a poison that is killing good and bad cells. Later leaving you sick and motionless. The toys lying idol on the floor because you are too tired to play... at 5 years old. 

Not a pretty picture huh?!?

I've said this before, but when you have your first sweet blessing from God, you never, ever imagine them so sick. Yes, a sniffle, a cough. But never the ugly "C" word. It just doesn't happen to people like me. It's a one in a million chance. Then, that ONE becomes YOUR baby. What now?!?!

Braxton has taught us so much, our eyes have been opened to an entirely different world. A world that is so often over looked, possibly because a person can't stomach the site of such a little person fighting for their life. 

We have met so many people along this road with Braxton. Some have finished the fight victorious and some are still fighting, with everything in their tired little bodies for one more day. Fighting to win this awful thing that takes so many way too young. 
Children have more fight in them than we realize. They don't complain, they aren't grumpy. They are just kids, trying to be normal in a world of chemo, tummy aches, body aches, blood transfusions and hospital stays. They want to play and run around just like their friends. They are hero's, warriors in the fight to survive. 



Sitting here I can name so many besides Braxton: Vinny, Maci, Benjamin, Lily, Westley, Austin, Ashton, Hunter and the list goes on and on. A couple of these names have sadly earned there wings, too early. 

The very first night that we were in the hospital with Brac, I can remember the diagnoses being presumptuous,  they were sure it was Leukemia but not 100%. Dr. Wofford, told us that the research being done has shown the leukemia cell, in as early as the heel stick the newborn receives in the hospital. Meaning they can see it premature, years before the child is ever diagnosed. To me that is AMAZING!! A CURE!!! Oh it is so close but in order to have it, we must be AWARE that there is a shortage in research funding. Research can not continue without the proper resources. So this month I ask you... when you go into an Old Navy look to see if there is an Alex's Lemonade Stand, all proceeds go to pediatric cancer research. When you see a sign asking you to donate a dollar, think about hard.... think could that be my child or someone close to me one day. There is a cure somewhere. A cure so that children of the future will not have to fight as hard as these amazing children have. 

Visit this foundation, set up by a dear friend to help raise awareness and funding for a cure. Money donated here, helps the families fighting with these warriors as well. 
Also, keep these children that are fighting these different cancers in your prayers, remember their families, remember their doctors. Your prayers are felt. They are desired and very much appreciated. 

You can also donate here: Alex's Lemonade Stand , Leukemia & Lymphoma Society ,              St Jude Children's Research Hospital