Surprise!

We received quite a surprise last night.  The nurse walked in our room around dinner time....  She said "You're going home!!!"..."Right Now!"!!!!!!!!!!!!!!!!!  We were SO excited!  Piper was well enough to be released.  We packed our things and headed home right away!

We are home, and things are well.  Piper is so happy to be down on the floor playing with her sister!

I will post again later to let you know more information.  Right now we know that she will not have surgery on Friday.  We have our next clinic appt. on Tuesday.  We will find out in the next week if we are going to proceed with surgery soon or continue with another 6 weeks of chemo first.

...  and I have to add that I have an amazing husband.  When we left for the hospital on Saturday, I had just made chicken parmesan for dinner.  The kitchen was a mess!  I was soooo far behind on the laundry, and the house needed some serious attention!  I came home last night, and the laundry was all done.  The kitchen was clean, and the house looked great!  I Love my Husband!

Big Day Tomorrow!

Tomorrow at 11 am, Piper has her CT. We are praying for great results. Ultimately, it is the surgeon's decision if we proceed with surgery or go to another 6 weeks of chemo.

We were told today that we can't go home until her ANC is 250+ for 2 straight days. ...so, we are here until at least Thursday.   We are also going to have to start giving her shots every day to help boost and maintain her WBC count. I am not looking forward to that.

Overall, it was a good day. Piper has an amazing little spirit. She is still very happy and playful. She has even started to blow real "smoochy" kisses!  She did it for the first time this morning. ...the lucky recipient? .... A nurse!

So, we settle in for another night...

Its quiet time and all is (kind of) well...

The 5th floor at Duke observes quiet time each day from 1-3pm. Try to tell that to a 13 month old, though.   The lights are all out. It's quiet and peaceful, and she is sitting in her bed clapping her hands and throwing toys and pacifiers at me.

Unfortunately her counts came back lower today than they were yesterday, so we are still here. We don't really know when we will get to go home. We just have to sit here, entertain ourselves, and wait. We pray a lot. We play all sorts of variations of peek-a-boo, and we go for walks around the hospital when we are really bored.

Today we are waiting for a visit from Emma and Papa Bell!  Piper gets really excited when Emma comes to visit. Tomorrow we are scheduled for a CT to see how much progress Piper has made since she started chemo. We are praying for some good news to come our way.

Thanks to everyone for the continued prayers.

Monday

We are still here at Duke. Piper had a good day. Her energy was up, but she is still not eating well. She didn't drink much today either. We were told that we can't go home until they see that her counts are definitely recovering. I think they want her ANC to be 500 or more. When we were admitted Saturday night, it was just over 100. Today it was just over 200. They are supposed to draw labs around 3 or 4 am again, so we are praying that we see improvement. We would REALLY like to go home tomorrow!

I have learned some interesting things about "life on the 5th floor" ...  there is a Ronald McDonald House room that offers free snacks and beverages to all parents. You have to sit in their room to enjoy these snacks, though, and they can't allow patients in the room for safety reasons. I have also learned that I am able to take Piper anywhere (within reason) in the building. We just have to sign her out and back in. We also have to pull her IV machine with us. So, today we visited the cafeteria to get me some dinner!  Maybe tomorrow we'll visit Starbucks!  I think it did us both a lot of good to get out of the room for a while!!!

Papa and Nana Bell have been super helpful, and they have been spending some time with big sister, Emma. I am so grateful that we have them in our lives!  We love and appreciate them so much! .... and Daddy and Emma came to the hospital today for a visit!!! As you can see in the pictures, Piper and Emma enjoyed seeing each other. They miss each other a lot!  I can't wait until we are all home and together again!!! 

Another day at Duke

Piper had a good day today. Her counts were very low so they had to do a transfusion. As soon as they did that she perked right up!  She has been singing and bouncing all afternoon. Big sister, Emma got to visit today. She seems to really like the hospital.   I think she really enjoyed the time spent with "Daddy"!!

Hopefully, if all goes well, we will be heading home tomorrow. They did say 48 hours, though, so we don't know if we get to go tomorrow or Tuesday morning.   Piper has just gone to bed for the night. I am trying to stick to her normal bedtime and sleep routines.

Thanks for all of the prayers. We will try to post another update tomorrow.

Things had been going quite well...

Piper just completed her 6th week of chemo on Friday. We are scheduled to have her CT on Wednesday to see how much progress we've made. Her blood counts were down on Friday but not enough to require a transfusion. Today she has been very sluggish. She is typically a very spirited and playful little girl, but all she wanted to do all day was lay on Daddy's lap. She also had a temp of 100.4 so the Dr.s wanted us to come into the ER. We came, they did another CBC, and her counts are still quite low. She has been admitted and we are here until at least Monday. We are praying that there will be no sign of infection and that she will start to feel better soon!  We will try to keep everyone posted on her progress.

Update on Piper

Piper has been handling treatment very well!  She hasn't had many 'bad' days.  She has shown some signs of nausea, so we have been giving her the nausea medicine as needed.  It's really hard to determine if she isn't feeling well because she is such a happy and playful little girl!  Her platelets were low on Friday, so we have to have another CBC done on Tuesday. 

She is doing a little better with eating.  We are trying to increase her calorie consumption as much as possible.  She rejects just about anything with lumps or texture.  We met with a nutritionist, and she has recommended that Piper drink at least 16 oz. of Pediasure each day.  That will make sure she's getting the nutrients that she needs.  She also recommended adding heavy cream to mashed fruits or canola oil to vegetables or other foods, when possible.  So, we will keep trying to introduce different solids.  We have determined that she likes pudding and brownies!  .....  high in calories, but not so nutritious!

Piper is also going to start participating in the Governor Morehead Preschool program.  An instructor from the school will come to our house every other week and spend time with Piper.  We are excited to see how this might help her progress.

We are scheduled to go back to Duke next Friday, April 8th for another chemo session.  The following Wednesday, she is scheduled to have a CT done.  The doctors and surgeons will review the CT and determine if the tumors have shrunk enough to do surgery or if we need to continue with another round of chemo.  If they decide it is time to have the surgery, it will probably happen the next week.  We are praying that we will have good news soon!

We are so grateful for all of the continued prayers and support.  I will try to keep everyone posted as much as possible.