We are all doing fine.... Grier has just finished his 14 day stint with accutane... and now we are trying to regain some control over his chapped lips... and peeling skin.  We have a few new things in the arsenal of lotions to try.  I think I could fill a whole cabinet with all the stuff we have for skin. During the 2nd week, he experienced the "tin man" effect... I just call it that because he walks/runs stiff... and that is not how he normally is while playing.  He was a little more frustrated this time so I made the call to the Dr. to ask the question "do you think this is accutane?" -- we think it is and were advised to go get Epsom Salts for bath time... so that has been added and the walk has gotten better...  Everything else is good.. the glasses and the eye patch are still a challenge but honestly in the scheme of things this is the small stuff... and I am not that worried about it...

Many of you know I turned the BIG 40 yesterday... and had a great birthday.... even if I did have to gather the crazy posters that were hung all over town with a picture from middle school-- think Sue from THE MIDDLE!!! Thanks Mom and Ross... :) Grier is still chanting Lordy, Lordy Amy is forty-- he helped make some of the signs!! I had the best treat and that was a night OFF with my friend, Anne.... we went to the Ritz and took a nice break from reality... I am kind of thinking it should have been 40 nights off-- one night for every year!  Anne has spent time with us at the Ronald and this was like night and day compared to the Ronald.... :)

what else??? That is it-- we are busy as ever... and starting to think about what kind of Cookies For Kids Cancer event we will do in May... Glad has announced they will match up to $225,000 for money raised in May. So, you know that was the icing on the cake to get our wheels spinning again.  Why May?? Well, Liam would have turned 7 and what better way to celebrate than to have a bake sale... not really one bake sale but the goal is 700 across the country JUST in May!  We are thinking BIG again... need new places and NEW faces... maybe the golf tournament or Speed Street... hmmm.. maybe NOT speed street... I still remember last May at the Speedway when we had a bake sale and I had beer spilled on me and smoke exhaled in my face as I said "all money donated goes to help children fighting cancer"-  Might need a little more time to pass before I do that again... :)

MORE DETAILS TO FOLLOW... was the last email I got about the possibility of doing 3F8 ( a week long antibody infusion that is quite painful)  I went about my day thinking there could be a possibility to start shots today and fly to NYC on Sunday for the week.  I did not know for sure but that was the mode I was in.  I had to get to the DMV to renew my license because it was going to expire on Monday... and TSA had already warned me I only had a few more days with my ID being valid when we went through security in LaGuardia.  That was top on the list today... and after waiting and waiting I am renewed but the card will not be in my hands for 8-10--- I even asked if I could pay more to express ship it--- He said - NO-- oh well!


Later this afternoon the details came in.... He wants to put him on the schedule in 4-5 weeks... His scans need to be done before.  Grier is already scheduled for scans in a month.  We will continue the accutane until then.  Another option was to give him high dose chemo after accutane... but I am sticking to the need vs quality of life.  I can not make him feel like he does when he is on high dose for nothing.... if there was even a question or a statistic to help me change my mind I would but there is nothing.... 4 weeks.... we will know more.




Good thing I did not express ship the license.... because plans changed a few times today.... 

all over the place on this blog!

oh wow-- I just did an entire blog... and checked my email and it looks like plans are changing a little for Grier's treatment.  We just got the OK to do HIGH DOSE 3F8 ... now I am waiting for the time line.... what a crazy ride we are on~




Another 10 days have passed in between BLOG entries.... it seems like a year when I think what we have done.  Don't worry I am not going into detail... I will just hit the highlights of the past 10 days... assuming I even can remember them!

Grier started accutane last Monday after a visit with Dr. M in Charlotte.  He had some intial blood work done before treatment and then took his two huge pills that night.  Grier is up to 43# so his dosage increased since the last time he was taking accutane last April.  He is going to take 60mg twice a day for 14 days and then have 14 days OFF... The lotion has been bought and the aquaphor has been restocked at our house.... the skin issues started on day 3... as did a few emotional spells that normally would not have happened over something so little.  He also has been wearing his eye patch twice a day... and one day it was "accutane mood swing" vs. eye patch-- and I declared accutane the winner.. and the eye patch came off and there was peace. His lips are the worst right now.. and I have ordered the special lip balm one of the WDS teachers gave us last year... I am hoping I can get permission to use it since he is not on 3F8 right now. It really is the only thing that works!  His appetite has decreased... and his legs ache... just the symptoms that make me crazy.. but he has had them each time with accutane. Today we had to go back to the clinic to run a blood test to make sure his blood levels were ok-- b/c of the medicine --He said as we were riding the elevator... Maybe we should ask them to "take a Picture" of my leg?? WHAAAT??? WHY?? He said.. because they are sore...and continued to share how fast he ran on the playground...I explained no picturs were needed right now... maybe he could just slow down a bit!

Grier got his glasses this weekend and it has been more of a challenge than I thought... the eye patch is much easier.  He has been slowly wearing them but swears he can not see with them on... He was shooting baskets outside with his new rec specs and came running in to put them up-- MOM, these make me miss!  He was reading  a book and kept peeking over the top of the lenses to "see" -- he just couldn't see the words when he looked through them!  I thought he was going to put these glasses on and tell me all the things he has been missing since his sight is so bad... not the case yet~!

Yesterday I flew to NYC for the day with Lesa and Ashley.  We were going to celebrate Liam.  We left Charlotte at 10.. got to NYC... ate lunch at Lenny's...walked down 3rd Ave for a little and then headed to the most amazing service I have ever attended.  As soon as we got out of the cab we heard the bagpipes ... we entered the church and all you could see was a "sea of orange" and pictures of Liam with his grin.  The NYFD processed in and the service began with the cast of the LION KING singing a Circle of Life... a few more songs were sung. Bob Woodruff, Dr. LaQuaglia, and Linda talked about Liam... The Liam I knew was the same Liam they knew... the stories were very accurate and a perfect picture was painted of a little boy with a love of life. There was not a dry eye in the church and then Gretchen spoke.  I still don't know how she did it... but she did and delivered the best of the best for Liam. The song He Lives in Me from the Lion King was sung as well as a Season of Love.  The NYFD talked about Liam's visits he made to the firehouse and his locker.  They talked about cancer, neuroblastoma and the amount of harsh treatments he had in 4 short years.. but the message was clear.. Liam lived each day even the days called "hospital days" and by lived I mean... scootered all over Manhattan, went to the museums, loved to go to school, you name it he did it... he was not stopped by cancer... The hardest thing to explain is the amount of treatment these kids get compared to Adults... if an Adult were to get the same they would be complaining and missing work and doing nothing... but these kids keep living. They do not know any different.  I had moments in the church where I was so thankful that my child was treated at the same hospital as Liam.  It is an awesome place.. even with all that waiting we have to do!  I am so glad I went ... it was a very short trip... but an experience that will impact me forever.

Here is a link if you want to see a brief video of the day.
http://www.nydailynews.com/ny_local/2011/02/15/2011-02-15_bravest_hearts_cry_for_lil_liam.html

On the flight home yesterday, I remembered a conversation I had with another cancer mom, from Charlotte last April. Her son did not have NB.  She asked me if I was excited that Levine's is started a coalition for cancer?  I said, yes. And she said, you wont have to travel anymore for treatments. I told her that would not change.  I take Grier to specialists for a reason... they see NB all day.  Our docs don't treat other pediatric cancers... they specialize in NB.  I also shared I didn't have time to wait for the coalition.. maybe I should have been more excited... NO.. she really has no idea the complexity of this cancer. After listening to the surgeon and the Nurse Practitioner talk I knew that was a good choice we made when we chose MSKCC.  That feeling was reaffirmed today when we went to clinic for a blood test... and I was asked by the nurse what type of test did Grier need?  hmm.. well, it should be in his chart... I told her we were told to come in a week after accutane to make sure his liver levels are ok.. and she said, we don't deal with accutane a lot so I was just checking... well, that was my icing today... accutane is actually part of the COG protocol... and Levine is a COG hospital. I am pretty sure most of you reading this will be saying WHAT in the H is she talking about???? :) I am just talking about the disconnect I feel when I have to explain things to some people that should be explaining things to me!


On a final note... THANK YOU to those that went to Ben & Jerry's yesterday to support Cookies For Kids Cancer.  We raised around $1000.  The exciting news is that there were many fundraisers going on yesterday in Liam's honor.  There was a restaurant called Poole's in Durham? that donated 100% of their profits yesterday.  Yep, 100%... and they did not pick a random day.. they decided to do it on one of their busiest days.... Valentine's Day.  It is my wish that people will do more of this... have a bake sale ( it does not have to be a bake sale on STEROIDS!), ask a business to do a CFKC day or night.... plan a 5K for CFKC... I just want to see people do it... It is not hard... Lesa and I are trying to get different people to help and participate... we love our "regulars" that always come to anything "Cookies" but it is time to make it bigger and better... so, I know you are all busy.. me too :)--- but think about what YOU can do to raise some awareness... Do you think Charlotte has a restruant that would donate a days sales to CFKC??? I bet we do... 

‘Hope, Love and Ice Cream’ to honor child’s life

‘Hope, Love and Ice Cream’ to honor child’s life

Oh my... this week was CRAZY...  The eye appointment turned out to be needed... Grier basically can't see... seriously!  I have been feeling very guilty especially after being told how bad his eye sight is-- one eye is worse than the other so the "better" one helped... but it still does not make me feel any better!  He has picked two pairs of glasses out.. they are on order- and they are THICK! He also has to wear an eye patch 2 hours a day to try to strengthen the other eye.. this has been a little hard because we are covering the "better" eye-- and he is frustrated because he can't see to do what he wants to do in the 2 hours... I know it will get easier... but WOW... I didn't expect any of this... Our week with one appointment turned into a week with 3 eye appointments... 2 of which we spent shopping for eye glasses!  Anyone who has shopped with Grier knows he looks at everything and when he decides there is nothing that can change his mind.  He found NIKE glasses at the first place we looked.. We compromised on the color... the sample was BLUE.. and I said OK, if he would get WALNUT-- He agreed but later that night this was our conversation..


Grier~ Mom, Do I have to wear my glasses on the playground?
Me~ Yes
Grier~ Well, you know I might lose them ...
Me~ no... you will be fine.. don't worry about it
Grier~ Mom, when I run they might fall off and they are the same color as the MULCH!




I also heard from our doctor in NYC this week...and the verdict is to do accutane again... UGH!!! I hate that stuff but studies show it fights off NB... so at this point I feel like I can't argue about it-- because I would rather do this than NOTHING~ even though the side effects are awful.. DRY skin, bloody noses, headaches, muscle aches, and crazy MOOD swings- But I am not done pressing the issue of why we can't do 3F8-- and looking into what CHOP has... I really did not want to have to fly to Philly with Grier just to talk.. but I may at this point-- I am still trying to get more info.  Actually not sure when to squeeze all this in because NYC has actually changed our scan schedule.. instead of 12 weeks -- he wants Grier scanned again in 8 weeks.. so we are already on the schedule for March 17th-- not much time in between scanxiety this time!  I was really worried that they are watching something but after talking to our CLT clinic... all scans looked fine.. urine and LDH was normal... so I think he is just keeping a closer eye on him.... 


Yesterday we ended the week at the Urgent Care for Grace.... she hurt her wrist playing goalie on Thursday night... and on Friday she still was complaining a little.. so for peace of mind I took her for an x-ray.  She has a bad sprain... it is not broken and it is in a splint.  She said... MOM, this has been a busy week at the doctor's office.... yep... she was very right...! 


I finally got my car serviced...  and now I just need to make it to the DMV... 
Not sure when I am going to make it there but it is on the list.  


Grier has an appointment with Dr. McMahon on Monday afternoon.... he needs some blood work done before he starts accutane. 


If anyone needs an idea for Valentine's Day... On 2-14-11 Ben & Jerry's in Charlotte (Woodlawn, Fairview, and Myers Park), Gastonia and Davidson will be donating a 25% of their sales to Cookies For Kids Cancer.  If you order an ice cream cake they will donate 50% of the sale... They have really cute conversation heart cakes.. we got one last year when they did this and it was the perfect Valentine's Day treat.  Check out www.cowolina.com for more information and locations.  Lesa and I are flying to NYC for the day so we will not be there so we will need every one's help to make this successful.  Please add this to your calendar and share with your friends.... 

Hurry up and wait....

All tests are back and no signs of the nasty NB beast was found... I wish I could say I took I deep breath and exhaled but this time has been very different. Last week when I found out he might have to do high dose chemotherapy again really threw me... It was as bad as the day I heard he had to do ICE last May. Now, we are once again waiting for them to decide what to do... Heard that before... Crap, I think I have heard that for the last 6 months--while we have been chasing out own tail stalling with lose dose chemotherapy! So.. We wait.. I should be good at it but I am not...

Grier finally seems to be feeling better... He missed school last Friday because he woke up with one of his headaches... He had not had much to drink or eat the day before and the coughing was non-stop at times. He took a cough medicine with codeine and I thought the good nights sleep he had on Thursday would have been the best medicine. The Friday morning headache was bad.. The worst part was he knew his class was going to the circus and you could see him tying to get ready and go to school...about the time it was time to head out of the door he got sick... His head was really hurting so no school... He fell asleep after he got sick and about an hour later he woke up and said.. Are all my field trips to the circus? I had to break it to him and say no... And he said I always miss the fun things. About 10 minutes later he asked to eat.. Looked 100% better and said do you think I can go to school now? I told him the kids were already on the bus. He said, can you take me and we can find my friends? So.. The crazy mom that am said sure.. And we headed to the circus... I was actually suppose to chaperone and I had to find someone to do it for me... Thanks susan! Grier and I got into the circus with no ticket and found their class :) He enjoyed it... Took a nap after we got home and I am glad he did not miss it-

So the waiting continues... This week has no clinic appointments that I know of.. But we are finally going to see the eye doctor..the message from the office said to be prepared for a 2 hour appt.-- hmmm.. I hope NOT..! Wish us luck and hope that the school eye test he failed was a fluke :) I have got to get to DMV sometime soon... And get the maintenance required light taken care of in my car....I was wishing for normal and you can't get anymore normal than that!

close to home

***I haven't said this in a long time... and basically have written a censored version of GGG for awhile. Facebook has more "real" posts.  This blog is not to be read to children. A lot of the things I may write are things my kids may or may not know-- and I don't want them to be told by other kids-  I tell them things in an age appropriate way ... and when the time is right.  Sorry for the disclaimer but some need a reminder.  Please use your filter... don't ask me questions about Grier in front of Grier or the other kids.  ****


After the last blog update I had full intentions to write about the fish bowl feel at the RMDH house last week during the BIG meeting of execs ... the TSA craziness at LGA, the 101 things that people say to me that make me nuts, the lack of attention pediatric cancer gets in the local newspaper, or the story of the rude woman that threw a pen at Lesa and I when we picked up a check... but it all seems a little stupid now.

Grier's test are trickling back in... so far he has clean scans.  The only test that is not back is his urine test. He ended up missing school on Tuesday because he had a fever just under the "magic number" for a hospital admission Monday night.  I took him to see Dr. McMahon on Tuesday to check on him.. he ended up getting a chest xray to make sure the cough was "just a cough" and that the antibiotics he was on for his ear infection wasn't masking anything else.  His ears were better.. chest xray was fine- so we went home... 
The next step is the BIG ? these days... Today I got an email that our Dr. wanted Grier to do a HIGH DOSE round of chemo next week- I freaked... seriously??? I was so confused... and did not know how I would tell Grier that he was going to feel like shit again, lose his hair, and miss a lot of school.  Turns out that is NOT the plan now.  I told a friend I felt like I won the lottery when I got that email.  But we don't have a plan... the vaccine that we have been waiting for has no more slots open.  So, we wait... 

On Monday, the NB world received some devastating news.  Liam Witt, son of Gretchen and Larry Witt and Big Brother to Ella lost his 4 year battle with Neuroblastoma at the age of 6 1/2- This news of a child losing their battle is not new... honestly there is not a week that goes by that I don't read about someone.  But Liam's news hit close to home.  He just had scans last week. His scans were not good.. or as his mom posted on FB “I can’t talk. The scans were awful. His disease is now at the point where it’s laughing at chemo. This is not good. I’m laying in bed with Liam who just wants to be “snuggle bunnies” together…and that’s all I want to do…snuggle with him and keep him comfortable. To say my heart is breaking, no shattering, would be a gross understatement. It is imploding in sorrow. It feels like I’m being gored alive. I need more time with him to love him and be loved by him. He is pure love and life and joy and kindness and strength. Why? And how can that be taken away from me?”  Liam had beat this many times before so that is why it was so shocking.  Liam was the inspiration for Cookies For Kids Cancer that his parents worked tirelessly on at the same time providing him with the best care possible.  He had had cancer for more 3/4 of his life but when you met him that is not what you noticed first.  He had a great smile, a love of learning, and was very caring. He loved Jack Johnson, the color orange, his orange scooter and his ipod and ipad.  He knew everyone at MSKCC and I am sure they are missing him right now. Last May when we saw them.. we hung out with him in a different building and he made a "poster"-- he pulled out his markers and asked me to write "cookies for kids cancer bake sale"-- he drew the cookies.... when he was done he walked desk to desk in this hospital office building and asked for tape.  I had no idea what he was going to do-- but as soon as he talked someone into giving him tape he proceeded to tape his bake sale sign on the door!  All the security guards just watched him but never said a word!  This was not an easy task because he was pushing his "shopping cart" that held the HUGE backpack full of fluids that he was getting because he had just had chemo that day. That was the same day he taught me how to get a cab... long story but he gave me some advice and tricks.. and I can now say I know how to hail a cab and it does not take me FOREVER!  That was also the same NYC trip that Grier relapsed for the 2nd time.  His mom was so helpful to me as I waved the post-it note in Liam's room with the chemo regimen that Grier was going to have to have...I could not even get the word out of my mouth.  It had three letters on it... I C E- She came out and told me it would be OK-- She reassured me -- Liam's kindness was something he learned from his mom. She and everyone that knew him is heartbroken. She is encouraging everyone to continue the fight ... she does not want Liam's fight to be in vain.  She wants people to be a good cookie.. stop ignoring pediatric cancer, and have a bake sale or donate money to cookies for kids cancer.  She said if they had 10 million dollars that could have granted all the grants that applied for this year alone. That is the goal --10 million this year. He would have turned 7 in May and the goal is to have 700 bake sales around the country take place.  There really is nothing easier than throwing a bake sale-- you could even have a virtual bake sale and make you own online fundraising page. I think Liam will make this happen. 


Liam's celebration of life will be on Valentine's Day.  We were planning on doing the HOPE, LOVE, & ICE CREAM fundraiser again on Valentine's Day at Ben & Jerry's.  This year it will be in Liam's honor.  The Woodlawn, Myers Park, and Fairview Ben & Jerry's will donate a portion of their sales on Valentine's Day from 12-9p to CFKC . They will have the cute conversation heart cakes like they had last year.  Share with your friends--- make it a fun family treat.
The one piece of good news this week was an email about our Dec.4th Bake Sale from Bank of America... here is part of it...I know the original goal was for Bank of America to provide a grant in the amount raised, but we would like to provide $50,000 to support the organization’s work and celebrate the accomplishments of the local group. So, instead of the $35,000 they are giving Cookies For Kids Cancer $50,000-- WOW- is all I can say. Imagine if it was that easy to get everyone to care- This brings our Dec. 4th bake Sale total to almost $90,000---thanks again to everyone that helped with the Charlotte, NC bake sale- 

My favorite picture of Liam-

In lieu of flowers, we request you honor Liam’s love and life by making a donation to the organization he inspired us to create, Cookies for Kids’ Cancer, through a special online giving page we have set up in his honor -http://cookiesforkidscancer.kintera.org/iloveprinceliam. 

Fell asleep during the first 1/2 of the MIBG

MOM, look outside... another BLIZZARD!~Grier

The Lifesaver when we have a lot of waiting!

Trying out wii JUST DANCE in between football games

We made it home late Friday night...Friday was good.. Grier did well staying still for the MIBG scan-- he actually fell asleep as he listened to his iPod and was covered up in the warm blanket! There is nothing better than a warm hospital blanket! Grier always asks me if we can get one of those warmers for our house. He was sleeping soundly and the tech went and asked the radiologist is they wanted a spec CT.. A more detailed look.. And she pulls up the scan and says yes.. We have gotten these before and I was actually planning on it this time... I had even asked to have Grier's scan in room 1--t is the only room with a spec CT scanner...anyway we weren't in room 1 so I had to wake Grier up and we switched rooms with another child and started the second part of the MIBG--40more mins and this time he did not fall asleep. At the end of the forty mins.. Grier was asking how many more minutes and i was doing everything to stall-- and I look over to the glass room where the techs are and see 3 people in white coats.. Pointing at the screen and I felt the color rush out of my face.. I sat down -- after a minute I asked the tech who they were and she said oh, just scientists! Don't worry-- right.. Easy for her to say... We were done and got our standard good luck from everyone as we walked out of nuclear medicine and headed up to the 9th floor. Grier was chatty and I was still recovering from the moment..we had to wait for his bone marrow aspirations in the procedure room. During our wait we chatted we the Kings from Indiana, Ursula came out and we saw her.. And the first question I asked was about the 3 folks in the MIBG room.. Then we saw Rachel, a nurse who has taken care of Grier since we started coming to MSKCC in 2007-- she used to be in the room when Grier had anesthesia so I asked her if she has seen the scientists before and she said yes...I was feeling a little better..
Grier finally got called back to the procedure room.. I picked him up and put him on the table and he was ready to push his white medicine! He shut his eyes quickly and I left the room and waited. The doctor came over to me as I waited and said he did fine.. And said the MIBG looks fine and nothing jumps out at him but it was not the final report --his CT still was not ready yet.. He said depending on the tests we will have to do something.. Most likely an escalated dose of 3f8-- the vaccine has enough participants in the trial and it is closed at this time.
I continued to wait in the tiny waiting area.. Talked to a Dad that I met. He was from South Africa-- he and his son were here for scans too-- they had been making the trip to MSKCC since 2006-- wow! And I complain about my travel time.... Grier is famous for napping after anesthesia.. They usually let him sleep.. I was waiting a while.. At one time Rachel came out and asked what time our flight was! He finally woke up and we headed out of the hospital. We did not even make it to the elevator before his groggy voice asked if he could take his hospital bracelet off!
We had a quick lunch.. Cleaned the room, packed our rent a box-- and even had time for a quick ping pong game in the playroom... Our car picked us up @ 5-- we headed to LGA and started the process of going home. We landed in Charlotte at 10-- a little delay due to weather... But we slept in our bed and not at LGA!
The rest of the weekend was like normal.. Hard to believe we were in NYC for three days.. Reentry is always hard for me.. Grier is good at it..
Hopefully we will know this week how everything looks on his pictures... The waiting is the longest part...
Our friend, Adam got good news.. as well as Brice, Kate, and Kieran- I am still in shock and numb with Liam's latest news... His family has been such an inspiration to many and brought awareness to this awful disease and it is so unfair that they are dealing with this-- the scary part is we are all one scan away from it.. So much more needs to be done.. More companies need to be involved like GLAD..money needs to go to research and families fighting for their children need to concentrate on them.. It is too much to have to raise money for a cure and fight for your child -- more people need to decide kids are a priority ... It is time to change...just like the world changed when it was cool to be "pink"-

Another L O N G day.... lots of waiting for 2 procedures that took all of 20 minutes!!! Our day started later... we did not have to be at the hospital until 11:30-- Grier woke up at 7 and started asking when he could eat something!  I knew these four hours were going to be FUN.  We slowly got ready... did some scratch off lottery cards... and got all our items ready for the day.  As soon as we got to clinic he was allowed to start drinking his CT contrast... not a problem.. before I knew it he had finished the entire cup! He did an amazing job getting accessed -- he has a difficult port... it is tilted a little and they had to adjust it after the needle was in... he stayed still and handle that like a champ.... We waited in the playroom for them to call us back... it was a long time... but it passed quickly because I was chatting with other moms I had not seen for a few months... and playing "horse" with Grier.  They finally called us around 1 to get his check up by the team... "he looks great" is the first thing I was told by one of our docs... :) I told him I wanted him to say that to me tomorrow when I see him in the procedure room to do Grier's bone marrow test!  During his exam they told me that he has an ear infection in both ears... Grier says his ears don't hurt... but he is on antibiotics because he has a port and fever and rick of infection!  He has had several ear infections.... always after we fly and MSKCC always finds it! We finished the exam... Grier co-signed the consent for his bone marrows and we left for CT -- there we waited and waited... we both were starving at the point... and by 2 they called him back.. He did great... I was suited up in my lead vest... They called from the office to ask my first name after the first 2 pictures.... and I must have looked stunned!  I told them and then asked WHY they needed to know-- He said.. Don't worry just need it for this book about the exposure levels???? Then the nurse came in and needed to put the contrast in his line... I tell her the wrong side of where his port is... and Grier says... Wow, MOM you forgot where my port was! The nurse starts to laugh because that was in his 20 year old voice... and she said oh Grier, you mom has a lot on her mind right now-- and he smiled his halfway smile.. 
2:20-- we were out of there headed to lunch and then had to go back again for his MIBG injection- Waited forever in the HOT waiting room and finally got the quick injection and went back to the RMDH--- played in the room a little... a few quick games of ping-pong and then we had to go get his antibiotic for his ear.
He talked me into a quick trip to Lester's ... looked at every pair of shoes they had and didn't like anything!  We ended up at Southern Hospitality for dinner... then a brisk walk back to the RMDH!  He fell asleep around 8:30-- tomorrow we have the MIBG scan at 9:30 and bone marrows after-- around 11:30?? nothing to eat or drink until after he wakes up from bone marrows... 
we have not heard anything yet.... not sure if we will by the time we leave... 
can't wait to wake up and see what the weather will be like.. Grier is packed and ready to go.... not quite sure where those dog are going to fit!! I might have to put them in the pink bucket.... but you know USAirways will count that as a carry-on!!!!

more tomorrow- and we did not win the lottery this morning :(

Our day started at 5:30 this morning..... Grier hops right up.... I was trying to decide if I should hit snooze and then telling myself I should have gone to bed a lot earlier than I did~ We got to the hanger around 6ish... and flew out on our flight around 7... landed in Teterboro and the car took us to the Ronald.  Our flight was awesome, easy, and relaxing. Grier played on his ipad and chatted... We have flown with BofA enough to know the pilot and some flight attendants... They are always going out of their way to make this easy.  Grier wanted to wait to eat... he said it was a little too early.. The driver of the car was extremely nice... I think Grier entertained him a bit because there is nothing like riding in a car with a NEW reader... he spelled everything and sounded things out for the entire ride... the driver started answering him by the time we made it to the Ronald!  He also told us he knew we were from NC so he turned the heat up in the car.... sounds like a perfect trip... but reality is we aren't on vacation!


We got to the RMDH around 10:40--- it took along time in NYC traffic... Our room was not ready so Grier wanted a HOT Chocolate... he thinks the dunkin doughnuts in NYC makes the best---- I totally forgot the no chocolate rule... but he ended up taking a sip and not liking it... whew..I don't think a sip will mess up the urine test! Can't wait to get that urine test out of the way so he can eat without me worrying about the "list"-
We walked backed to see if our room was ready and it was.... made beds... unpacked our "BOX" from storage... and met up with Julie and Adam.  We got some lunch and met up with Julie and Adam again after their last appointment.  The boys were being treated to a VIP tour of FAO schwarz so we walked to FAO and met our toy soldier, Rich.  Barbara from Candlelighters of NYC planned this amazing tour --- Adam said it was his best day ever in NYC... :) Grier was a little shy but has talked about it non-stop tonight! It was alot of fun... they toured the whole store and danced on the piano and ended with a shopping trip using their gift card that candlelighters gave them.  Grier SHOPPED  and looked at everything... changed his mind 4 times... but is the proud owner of 2 new stuffed dogs... yes, bigger than a matchbox car for those that are wondering! The 4 of us took a cab home... and went to dinner at the RMDH.... it ended up getting delayed so we played BINGO for an hour first and then ate dinner... I think I said to Julie... I feel like I have been here for 3 days already!!! 
It was a good day in NYC for us... I wish I could say that was the case for everyone here.  The reality is we wouldn't be here at the RMDH if it weren't for pediatric cancer... and that is the case for the rest of the people here... we would be at home with our families in all parts of the world.  


Tomorrow our scans start... we don't have to be anywhere early.... whew... it will be a different kind of day... reality will hit hard as they access Grier's port and I make a game out of sucking down contrast for his CT.  He informed me tonight he liked the CT because it makes him "warm"--- that is a new one... He is describing when they inject the contrast!  He also is looking forward to the white medicine.. aka anesthesia... all things that are our reality right now... 


pray if you pray or do whatever you do for clean scans for us and all our friends here scanning this week... also for options for those that did not get good news... 

Ready to FLY

The countdown to our NYC trip has been on for a week or so.... Grier gives me the countdown at least daily... you would think we are going on a vacation or something! He has a plan.... and I have a plan... mine is all medical hence my nickname Grier has given me... "medicine momma!"-- everyone else has another nickname.. Grier is more worried about "his NYC routine"- that is how it should be.. I guess! I will worry about the medicine part of these trips.  He told me the other day that he thought we should bring an extra suitcase with us... when I asked WHY, he said because he wants to go shopping at "FAO Shorts"~ funny.. since everytime we go I always tell him to pick something small like a matchbox car that will fit in our suitcase home!! He was ahead of me this time.  
Our schedule is very packed with appointments.... Thursday he will have his CT-- he can not eat or drink anything before except for the HUGE amount of contrast.  After CT.. he will need to take his SSKi drops ~2 hours before his MIBG injection  Friday will be the MIBG scan-- the long slow scan looking head to toe for NB cells... This wil be the 5th one I have actually gotten to sit beside him in and entertain him and keep him relaxed so he stays still as a statue. I have yet to watch the screen as it scans his body... I honestly think I would throw up if I saw the screen!  I have been dreaming about this crazy schedule since last week.... there are so many things to remember and I forgot something in my dream.. and missed our flight home.. clearly scanxiety has taken over my sleep! 


The surprise for us this week was a flight showed up on Corporate Angels.... We are flying with one of the banks and someone we know so it will be fun- crazy that I am not allowed to say the bank name.. but this bank is on my favorite list! This earlier flight  will give us all Wednesday to get ready for the two days at the hospital and maybe squeeze in something fun. I am hoping there will be something fun at the RMDH Wednesday Night...or maybe we will try to venture out and see a Rangers game... who knows... Grier might have me shopping for a Jets jersey after last nights win! 


After the MIBG scan on Friday, he will have his bone marrow tests... we will go back to the RMDH and clean the room and pack our crate and then we will try to get out of NYC.... and head home on USAirways! Hopefully he will not be in too much pain... I also just checked the weather and it will add to our excitement on Friday... storm possibly coming to NYC?? This is a quick trip packed full of questions about what is going on in his body right now... and what trials we should try to keep NB away.  I just recently started a process at CHOP... I wanted to know about a vaccine trial I heard they had that was opening up soon.. so it looks like scans and reports may be sent to philly as well-- just to see what all are options are at the time.  Really... I am most concerned about NYC this week -- one day and city at a time :) 


Nothing else really to report.. the kids had some photos taken by an awesome photographer that happens to be in the family.  She captured their personalities and even made them look like they enjoy each other.  I am not sure when all the growing up took place... but they look older and wiser.  If you need a some pictures taken.... check out Jennifer.... she did a really nice job! check out her site..www.jlhphotography.com


Next update from NYC on Wednesday the 19th... if we have internet at the RMDH :) 


www.gogriergo.com for pictures that I am talking about.... caringbridge has a size limit

Maintenance required....

I have been anxiously waiting for an email with our plan from NYC... the clinic here did not hear anything so we were in limbo this week-- The maintenance required light came on in my car... and I have been staring at it--- because I know "maintenance IS required"- I am not talking about the car but Grier!! That light is just another reminder... It is scan time... and time to switch gears and head to NYC.


Last May when I got the news there was a new spot on Grier's hip, a wise friend told me to think of the relapse as a "pit stop"... so we did... and this has been a LONG pit stop... I thought we would have a new direction after we got the NED status in October~ but instead we did more low-dose chemo for 3 weeks.. every 21 days. Other than going to the clinic for 15 days for a few hours each time it was not that bad in terms of other treatment Grier has had to have.  He still was able to go to school, play sports, and be a semi-normal 6 year old.  I was able to juggle all those appointments, raise some $$ for better treatments options for children ... carpool, pay bills, manage a house of 5, manage the holidays and be a semi-normal mom~well--not really!!  We will soon find out if the low-dose chemo kept the NB cells away -- scans have been scheduled in NYC.  It is THAT time again... You would think after almost fours years of dealing with THAT time I would be a pro at it-- and in some regards I am -- so is Grier!  The last two days I have been cleaning and organizing... probably nervous energy... or maybe a "nesting" instinct-- but I tend to make changes and throw out stuff right before and after scans... funny.. I know-- I guess there could be worse things to do--! Grier and I will fly up to NYC on the 19th... and come home on the 21st-- Hoping corporate angel  has a flight for us-- just to have an easier time traveling~ you know we don't want to be exposed to radiation from airport scanners!!! ~sorry.. I could not resist!!! We are scheduled to be up there the same time as another friend of ours that has NB--- Adam and Grier have been 3F8 roomies... always nice to see a familiar face in hospital!  Julie and I can have scanxiety together while the boys play in the playroom!! What a twisted world I live in NOW!!!  I really wanted to go next week but the hospital is FULL-- hmm.. who knew pediatric cancer was such a booming business!!! Actually I have not ever seen the clinic NOT full!  14 days at home will be plenty of time for me to mentally prepare for the trip... I swear Grier must have an internal clock that tells him it is time for NYC again... he started asking a few days ago when it was time to go to NYC again? 


some normal stuff--
Grier was very excited to go back to school... he asked over and over if he was going to be in the same class again... a pretty good question considering he has taken LONG breaks before and ended up in different classes. There was a possibility of another round of low-dose chemo this week--- turns out we got the week off-- He can get back to a routine of school....golf... and today he had his first swim lesson! I have been trying to fit swim lessons in our schedule for a LONG time... and today just seemed like the perfect day... :) 


2010 ended nicely for the 5 of us... I would include Tucker, our golden in the total but his "counter surfing" gave him a tummy ache after he ate a stick of butter...  we need to teach him to use a "pink bucket!!" There is never a dull moment around here!

Do you dream BIG?

I am pretty sure I would classify my self as a dream big kind of person.... I don't want to do something little when the need is HUGE.  I tend to have people around me that share the same idea and drive because there are some days I just can't give 100% to anything.... and other days I get so much done it is unbelievable-  Lesa and worked well together on the last fundraiser in September.... 30 straight days of fundraising..... it was a lot of fun and a lot of work but well worth it in the end when we sent a check to cookies for kids cancer for over $15,000--- We can call September our warm up to the Dec. 4th Bake Sale @ Blackhawk & Birkdale ( Julie Sparks and her team did an awesome job with the Birkdale location... weather was so much worse for them)-- Lesa and I like to do this event with minimal to no expenses... because every dollar spent on fluff does not go into the hands of a researcher that is working on a promising clinical trial for children.  We are so pleased to announce that the hard work by all of you that volunteered in some way to help us have a successful bake sale has paid off. Our bake sale total is over $35,000-this TOTAL does NOT include the two matches-- We are thrilled and excited that we have raised this kind of dough with "some cookies"!!  All of this money will go to pediatric cancer research in hopes of finding better treatments and a cure... We could not have had this record breaking sale without each of you helping us -- THANK YOU!  We broke the record that Richmond, VA held from the bake sale they had on Sept. 11, 2010-- we love friendly competition like this especially since the real winner are the scientist that are working hard on ideas for children and they are just waiting for funding to get their ideas to the bedside.  Charlotte has had several bake sales for Cookies for Kids Cancer... this bake sale also beat the one at Taylor's Finish Line Festival as well as more than doubling the last year's bake sale at Reid's and Blackhawk.  WAY TO GO Charlotte and Birkdale--- This is quite a feat since we did this with no help from the media -- we actually got more money today from a mini bake sale & and live nativity scene in the Foxcroft Neighborhood. who would believe that we raised $35,000 from offering cookies for a donation??.... we also had a great group of raffle items and silent auction items BUT $35K??? Sometimes I just can't believe it.... but when I allow myself to dream big - I never doubted it would be huge-- We are already thinking about next year... WHY?? Because the need for funding is HUGE... and until we all make the commitment to children fighting cancer the need will remain HUGE.

ok-- enough of that soap box... good thing I wrote that days ago because after the recent events with friends I would not be so upbeat-- Neuroblastoma just sucks!!!  Grier has been doing really well-- we managed the BIG D side effect of chemo with lots of Imodium..and his counts have stayed in the good range... He had another finger prick today and the news was the same... good counts!  The other exciting... hmm, not sure exciting is the right word... but the NEWS from NYC is that Grier's blood test came back and he is HAMA negative again.  That is all we know... Since he is "due" for his scans in January this may add other options for the NB team... meaning besides this low-dose chemo that he has been on for the last six months and waiting for his immune system to kick in so he could qualify for the phase 1 vaccine trial... he could now do 3F8 (again)! Grier heard me ask Dr. McMahon if the vaccine would be better to try or should I push for 3F8?  He answers... I AM NOT DOING 3F8 again!!! He caught us both off -guard... and Dr. M just shook his head and said it is not right he evens knows what 3F8 is!  I said... oh, being 6 1/2 is going to be fun... and then I asked Grier, what is 3F8?  He said it was when he had to go in a room by himself and they lined up lights on him and SHUT the door and left him in there by himself ( can you tell he does not like to be by himself?)... whew!!.. he was not talking about 3F8.. but radiation!!! Not that it is any better he knows what that is but 3F8 is a lot worse! I asked more questions about what to pursue next... I even asked if we should look into CHOP ( children's hospital of Philly) to see if they have anything we should try... and the answer is good and bad... the good is Grier has had a positive response to chemo every time he has relapsed.  The bad is.. keeping him clean is the needle in the haystack we are looking for and the rest of the Neuroblastoma world.  He suggested we could do a bone marrow transplant now... but there is nothing proven that this would keep him clean.. and we would be burning lots of bridges doing that! So... we are still in a good/bad spot.... I know it could be worse..  We are going to enjoy the holidays and then get scans done and I am sure we will have a treatment plan.  January will be spent in NYC for scans... and who knows what else...I am going to email tomorrow and start the scheduling process.. I think I am close enough to Christmas that there is NO chance to have to leave town in December!!

3 more days and Christmas will be here... I am more than ready!!! After a slow start mainly due to the bake sale being my priority-- we are finally a little ready.  I did not decorate as much... I decided it was ok.... I can't do everything and as they say "something has to give"--- I am a master of that phrase now... I did throw together a photo card... mainly because Grace reminded me that I did not do a card last year... I think she missed it the most.  We got our tree last weekend in the rain... and put some of our ornaments on it.... when the kids were tired of hanging them I decided that it was a "perfect tree" and we were done! Grier will be a Shepard in the Children's Christmas Eve service... he has written his letter to Santa... and we will bake some cookies before Christmas Eve for Santa... well, maybe... might just go buy some :)  I can't wait to see them open presents on Christmas morning... I am sure I will get to see a reaction from Grier.... can't wait to share a picture!  ( NO... it is not a LIVE puppy!!-- I am crazy but not THAT crazy...)

My favorite gift this year was the HUGE donation we mailed to Cookies For Kids Cancer... It was a gift of Hope from the Charlotte/Huntersvile community... that needle in the haystack needs to be found... and knowing 100% of this donation is going to fund trials for children gives me hope... Merry Christmas Eve everyone....we wish you all Peace, HOPE and Health in the new year~

Grier finished his week of chemo last Friday.  He had a pretty uneventful week in the infusion room... his best part was decorating a gingerbread house... It was a welcome break from tracing team logos for me... I am so glad he wanted to change up the routine we have been in for the last 6 weeks of chemo!!  Here is a fun fact-- I got a THIS IS NOT A BILL from Blue Cross/Blue Shield today-- last week's 5day chemo aka as 1 1/2 hour infusion each day cost $15K!!!!!    I am sure they LOVE us... we have done this 6 times!!!!  Tuesday he got nauseous as we got ready to leave the clinic but we just hung out for a little bit until the wave passed... and then went home and he never mentioned it again.  He had his kindergarten Holiday program that night and dressed up and sang songs with this class... He was very proud of himself and I was just amazed he just kept going after the week he had with the infusions.  We went to the clinic yesterday to check his counts and so far he has not really been affected by this chemo--- I am sure it is doing something in his body... well, I hope.. because we are infusing him with poison.  Our friend on the same chemo has had low counts and hair loss again... it is just crazy how the same drugs affect everyone differently... I still can not believe that we are up to the 17th week of chemo since this HELL started over 3 years ago--  Yesterday at the clinic was another milestone.... Grier sat in the IV procedure room in a chair by himself and had his finger pricked.... THIS IS HUGE in our world--- I can not tell you how many times I have had to hold him down while he screamed and BIG tears came down his cheeks.... He was very proud to share this news with his brother and sister.... they were not so impressed.  Last week we mailed a vial of blood to NYC to be tested for HAMA-- I think that 3F8 may be an option for him again-- now we just wait to see if he is HAMA negative again.  I am reliving last year a little... it was last December that we lived in NYC -- Grier did 3F8 and radiation so we were there for almost 4 weeks... Christmas in NYC is fun... I was wishing we were at Radio City Music Hall watching Christmas Spectacular again.... and walking the streets smelling the Christmas Trees as we walked around the city... This is actually the first December since we started this journey that we have not been in the city for a little while... I guess I should be thrilled but some of our new traditions are in NYC-

Other than school, chemo, doctor appointments and wrestling with his brother.... Grier has added Golf after school... he seemed to love it today... but also said it was boring because he knows it all-- LOL!!

I have been very busy with Lesa wrapping up the bake sale.  You would not believe the donations that are still coming in daily for Cookie For Kids Cancer.  I have to keep recounting our total..... Today we heard the total from Birkdale ( our satellite location) and they did an awesome job-- almost $10K-- considering the weather was much worse than ours and they were not covered it is more than great!!! I am so glad Julie helped us make that happen with all her friends--  Julie's son, Adam even had a hospital stay for nutepenia days before the sale.... and she still pulled off a great bake sale!!!
We have lots of stories from the bake sale... My favorite is the email I got from friends that told us they had a donation to give to CFKC at the bake sale.  Their kids had been given money from their Grandparents to make a donation to a charity of their choice and the girls chose our bake sale--- I also got an email from friends that moved to PA and wanted to do something to help but since they were not in town they decided to have a HOT CHOCOLATE stand for CFKC-- Needless to say it was very successful and they helped spread lots of awareness and raised a lot of money to go towards our total donation.
T-shirt sales have been picking up too--- We are almost out of Adult T's BUT have tons of kids T's--- nothing would make me happier... than to sell all of these before we send our check to CFKC this week! Want one or ten??? email me .... amychristenbury@att.net

I am looking forward to saying good-bye to 2010!!! I think this year has been one of the toughest since we started this journey.... not just from a personal standpoint but also from watching what our friends from both clinics have gone through.  I hope 2011 brings better luck for us and maybe gives us the courage we need to make some changes --being "stuck" in quicksand is getting old!- and gives us a well-deserved break from the roller coaster ride called NB--- I know... we have to stay in top of it ... but it would be nice to be in control again.

Buy a cookie!

Buy a cookie!

Posted by CW Editor on December 9, 2010 in News | 0 Comment

Bake sale raises money for pediatric cancer research

by Sarah Gilbert and Mike Parks

Shoppers at the Cookies For Kids’ Cancer research fundraiser event in south Charlotte Saturday, Dec. 4, had lots of treats to pick from. Cookies, brownies and cupcakes were crowd favorites.

Hundreds of south Charlotte bakers, volunteers and cookie lovers came together Saturday, Dec. 4, to raise money for pediatric cancer research with the third annual Cookies for Kids’ Cancer bake sale, raffle and silent auction.

Amy Christenbury and Lesa Helbein spearheaded the event, along with Christenbury’s children, Hayes, 13, a seventh-grader at Alexander Graham Middle School, Grace, 11, a fifth-grader at Selwyn Elementary School and Grier, 6, a kindergartner at Selwyn.

Doctors diagnosed Grier with stage 4 Neuroblastoma, a nerve cell cancer, in 2007.  He was 2 years old. Since then, the family has worked to raise awareness for the fight that Grier and so many other children face.

The bake sale, which organizers held from 10 a.m. to 5 p.m. at Blackhawk Hardware in the Park Road Shopping Center, raised thousands of dollars for pediatric cancer research, as hundreds of people milled around, searching through baskets of treats for the perfect choice.

“The event took months to plan and required lots of legwork, phone calls and emails,” Christenbury said.  “We had 23 local bakeries help out, plus about 100 moms who baked items.  It was cold on Saturday, but it was really crowded and it all went really well.”

The event was packed with volunteers, including Grayson Cassels and Sara Kathryn McCormick, who are both students at Charlotte Country Day School.

Cassels and McCormick were in charge of pulling the Cookies for Kids’ Cancer Little Red Wagon around the shopping center, braving the cold and maneuvering between large crowds to peddle their cookies and brownies.

“Everything we raise goes toward research,” McCormick, who goes to church with the Christenbury family, said proudly. “We’re doing it in honor of Grier.”

South Charlotte girls brave the cold weather Saturday, Dec. 4, to serve as the first line of attack at the Cookies For Kids’ Cancer fundraiser bake sale at the Park Road Shopping Center. The event, like others held by the south Charlotte nonprofit, was aimed at raising money to support pediatric cancer research.

Three girls stood outside the fundraiser, trying to lure in potential customers with signs and baskets. Customers pulled up and bought baked goods from the girls, who were dressed as cupcakes and chocolate chip cookies.

Bakers from Polka Dot Bake Shop, Nova, Tizzerts, Suarez and others turned out on Saturday to sell their confections and help the Charlotte community raise money.

The event offered a wide variety of baked goods, as well as a raffle and silent auction that included NASCAR tickets, gift cards to local restaurants and spas and art from local artists such as Anne Neilson, Pam Anderson, Caroline Simas and Windy O’Connor.

The event organizers will donate 100 percent of the money raised to Cookies for Kids’ Cancer.

While organizers are still working to calculate the total generated by the event, Christenbury said they raised at least $20,000 on Saturday alone.  Earlier contributions and proceeds from a satellite bake sale held at Birkdale Village in Huntersville have yet to be factored in, and Christenbury said that, days later, people are still sending in donations.

“These events are all volunteer-driven and all of the money goes to research,” Christenbury said.  “Our donation will be matched by both Bank of America and Glad, so it’s easy to see how a couple of cookies can turn into a huge donation.”

According to the organization’s website, the goal of Cookies for Kids’ Cancer is, “raising funds to support research for new and improved therapies for pediatric cancer. Through the concept of local bake sales, Cookies for Kids’ Cancer provides the inspiration and support for individuals, communities, and businesses to help fight pediatric cancer.”

For more information, visit www.cookiesforkidscancer.org/.

I wanted to do a little "bake sale update before my crazy week starts tomorrow-- Grier will be doing chemo all week-- so we will again be in our routine of "kindergarten/chemo"  I also got a message from our doctor that NYC wants them to send blood to test for HAMA --- I am hoping he is HAMA negative so we can move to something other than chemo--we are also pretty close to the next set of three month scans...  I know he will have to scan before the next treatment is decided. Looks like they are adding 3F8 to the vaccine option now---

OK-- we are still counting money but we are over $15k at this point.... we have not added the satellite location, Birkdale yet... so stayed tuned.  Saturday was a great day.... the only thing that could have made it better would have been the weather.... Wouldn't it be nice to be able to control that too?? It would be scary to think how well we could do on a sunny day.... last year's bake sale was rainy too--- I will post pictures soon.... I don't have that many so if you were at the bake sale and taking pictures.. please send me some.

THANKS to everyone that helped us pull this BAKE SALE off-- more to come later...

Amy

ps-- We have tons of T's left-- we are selling them and the money goes into our bake sale total--
They are $5 each for ANYONE that baked, volunteered, donated raffle items or DID ANYTHING to help us-- $10-- for EVERYONE else :)  Please email me if you would like a T- let me know what size... and I will leave it for you ... or send it to you- amychristenbury@att.net

If you would like to donate to our online giving page...

To make  a SECURE ONLINE DONATION WITH YOUR CREDIT CARD... COPY AND PASTE THIS LINK--

http://cookiesforkidscancer.kintera.org/faf/donorReg/donorPledge.asp?ievent=442828&lis=1&kntae442828=6F25D816A54A4D5B90C414151A965933&supId=0&team=3988660&cj

ONE MORE DAY UNTIL WE HOPE TO CHANGE SOME LIVES WITH A BAKE SALE!

I am getting ready to tell you all about the Cookies For Kids Cancer Bake sale which is TOMORROW-- but first I wanted to show you this picture of Grier with his new FAUX-HAWK!!! The last time he lost his hair due to chemo I promised him a MO-HAWK so this is what we have tried first to make sure he wanted it-- He LOVES it!!! He went to bed last night SO worried that is was going to get messed up-- Tonya made his night... and he has been grinning ever since... 

Here is a little glimpse of Thanksgiving in Kindergarten.... Grier also help the Ronald McDonald House of Charlotte make their cards this year for Thanksgiving... I forgot to mention that... They turned out really cute.  

ok-- TOMORROW is the....

 3rd ANNUAL COOKIES FOR KIDS CANCER BAKE SALE

@ BLACKHAWK HARDWARE

PARK ROAD SHOPPING CENTER

10-5pm

1000's of HOMEMADE BAKED GOODS

23 local bakeries represented ( Polka Dot Bake Shop, Tizzerts, Dean and Deluca, EarthFare, Great Harvest, NOVA, Sunflower Bakery, Skinny Cakes, Cakes by Allison, Edible Art and MANY MORE)

There is a satellite location at BIRKDALE across from SANTA TOMORROW as well from 

12-6pm

100% of the DONATIONS will go to CFKC and they will fund research for PEDIATRIC CANCER CLINICAL TRIALS- 100%!!!

This is a great place to buy you holiday gifts for friends and neighbors.... YOU make a donation to CFKC and then as a THANK YOU take some bake goods HOME for you or to SHARE!

The BLACKHAWK location will have face painting, tattoos, a firetruck, colored hair extensions by T. Reid, nail painting by snip-its, cookie decorating from Suarez Bakery etc.... 

Both locations have an AWESOME RAFFLE --- ITEMS that you are going to be so excited about-  Don't forget to check out that table when you come.  

T-shirts will be sold at both events.. kids and Adult sizes..... we will have have "caps for a cure"-they will have BOTTLE cap necklaces--- 

WHAT ELSE CAN I DO TO HELP?? We need your help telling everyone that you know to come to BLACKHAWK on Saturday from 10-5 Please email friends, Neighbors, teams, schools, churches and let them know about the BAKE SALE-- POST it on your FB page or Twitter...

 CASH ONLY?????? Checks ARE accepted…. Please make them out to Cookies For Kids Cancer.  Ask your company about matching your gift. 

To make  a SECURE ONLINE DONATION WITH YOUR CREDIT CARD... COPY AND PASTE THIS LINK--

http://cookiesforkidscancer.kintera.org/faf/donorReg/donorPledge.asp?ievent=442828&lis=1&kntae442828=6F25D816A54A4D5B90C414151A965933&supId=0&team=3988660&cj

What are you going to do with the left overs???  Well-- we are hoping we will sell OUT--- but if your place of business would like to make a bid on all the leftovers...let Lesa or Amy know---- They would be great as a holiday treat for your office!

COME HELP US CHANGE THE STATISTICS ABOUT PEDIATRIC CANCERS ONE COOKIE AT A TIME!!!