Tuesday, February 17, 2009

A couple of transfusions

Yesterday James took Grace to the cancer clinic to get her counts checked. They were:

HGB = 7.1
Platelets - 12
ANC - 1500?

I'm not sure how the ANC can be as high as it was, but that's what they were. Last time they went up they said it was the tail end of the neulasta injection giving its last hurrah.  We'll see what they are on Friday. So needless to say Gracie got a transfusion of packed red cells as well as platelets. Much to my surprise they were on their way home at 5:15. She seemed to do well with the transfusions. Although when she got home and was so wired that she wouldn't go to bed I was wondering why low hemoglobin is such a bad thing. I kind of like lethargy, especially at bedtime.  Eventually she did fall asleep though. She's scheduled for another platelets transfusion on Friday. Hopefully this will be her last! 

Sunday, February 15, 2009

Update on Gracie's treatment

Gracie has an appointment at the cancer clinic in Austin, TX tomorrow scheduled. We are planning to have a platelet transfusion done at that time. They will check her blood levels and see if anything else is needed. The last couple of days we have noticed increased bruising and Gracie has been a bit more tired than usual. We continue to hope and pray that all goes well with this last round of chemotherapy. She is actually going to miss all of her friends at the blood clinic and cancer clinic each month. She talks about them often and asks when she can go back to see them.

I just thought I would take a little space here and clarify where we are in Gracie's treatments. 10 days ago we spoke with Dr. P in Houston following Gracie's most recent EUA.

THE LEFT EYE
We were thrilled to find that Dr. P saw significant improvement in Gracie's left eye. There have always been two tumors in the left eye, one small and one medium sized. Dr. P reported that the small tumor was "flat." This means that the cancerous cells are likely all dead and the tumor will not grow again. The area where the tumor was is scarred but it has not affected her vision. The medium-sized tumor showed significant improvement, in that Dr. P noted the coloration of the tumor changing and some reduction in size. Dr. P feels that the laser treatments are finally working and should continue to work to flatten and kill this tumor. Should the laser treatments not work or the tumor start to increase in size we will have to consider other options. Laser treatments for these types of tumors are really the least invasive and have the fewest potential negative effects for Gracie. So, up to this point, we have only used laser treatments (shining laser directly at the tumor to kill cells) and the global chemotherapy (IV chemotherapy drugs each month that attack replicating cells throughout the body- which would include cancerous tumors) on the left eye. We will continue to monitor that eye on a monthly basis and use laser treatments until the medium-sized tumor is gone. We hope and pray that these treatments will be all that are needed.
While I can not give you an exhaustive list of treatments available, should the laser treatments not work, some of our options include:
Cyrotherapy- the use of extreme cold temperatures on the tumor to kill the cells. This would typically be done by getting access to the back of the eye and putting some sort of freezing agent on the back of the eye adjacent to tumor location.
Radiation plaques- a radioactive plaque would be placed on the back of the eye adjacent to the tumor location. This releases radiation to the concentrated area where it is placed and thus kills the cancerous cells.
Proton beam radiation- This is similar to laser treatments only using radiation instead of light and heat. Radiation is concentrated onto the tumors. Typical radiation effects a relatively large area around the target cells and has been shown to sometimes cause other cancers later in life for young retinoblastoma patients. Proton beam radiation results in less "fall out" for cells around the tumors and have shown great promise recently in treating patients. This technology is relatively new and not available everyone in the USA, however, Houston does do proton beam radiation.

Each of these treatments come with risks and benefits so will be considered carefully- if they are ever needed for Gracie. Dr. P does not do these three other treatments but has sent her patients to Dr. G in the past. We are fortunate that Dr. G will begin taking a leading role in Gracie's care sometime in the next couple of months. They are starting a new retinoblastoma center at the Texas Children's Hospital and Dr. G will be the head pediatric ocular oncologist. The timing seems perfect from our stand point and we have heard nothing but good things about Dr. G.

THE RIGHT EYE
Dr. P informed us that the right eye still has showed little to no improvement since the first time Dr. P looked at it. There remains large tumors on the retina and many vitreous seeds. While some of the seeds may have calcified (basically been killed) to some extent the tumors have neither grown or shrunk noticeably in the last 6 months. This is a bit of a quandary for everyone involved. There is a small chance that the tumors have stopped growing and will never grow again, given that no growth has been seen. If this is the case then the right eye can be monitored and left alone as it does not impact Gracie's vision. The seeds are not a huge problem in the short term but can cause problems and spread in the future (or they too could die and not ever be a problem). No one wants to remove her eye if the tumors are not growing and her vision is unimpaired but everyone wants to prevent the tumors from growing and leaving the eyes to cause bigger problems elsewhere. This brings many questions that we cannot answer until we see Dr. G and know what options we have. Dr. G is going to look at the right eye and let us know if there are any radiation treatments that are available that may help in her case. He will provide a his recommendations and then we will know what options are available. It is also important to see how the tumors progress over the next couple of months without monthly chemotherapy sessions. Whether the chemotherapy was stopping the tumors from growing or whether the tumors, in the right eye, had already stopped growing is unknown.
So basically we would love to see no future growth in the right eye and have to do no further treatments on that eye but to leave the tumors right where they are. This means regular (likely monthly) EUAs to check for growth. If no growth is seen then we would leave everything alone. If the tumors in the right eye ever start to grow then we will have to quickly decide how to proceed- radiation treatment, enucleation or some other option as yet undetermined. Because the tumors are so large and one is so near the optic nerve then it would be imperative to stop any further growth immediately. So our best option is that the tumors are dead in the right eye and we live month to month monitoring them to make sure they stay dead.

Gracie is doing remarkably well and we are blessed with the best family and friends that anyone would ever ask for. We have seen many little and big miracles throughout everything that has gone on and continue to hope and pray that Gracie will keep both her eyes. Thank you all for your continued love and support!

Thursday, February 12, 2009

Today's Counts

HgB - 9,2

Platelets - 68
TWC - 2.7
ANC - 702

Her bone marrow is definitely getting tired. To give you an idea of what the cumulative effects of chemo are on bone marrow I'm going to post what Gracie's counts were on this day after her Jan and Dec Rounds. Her ANC is taking the biggest hit from month to month, but the platelets aren't liking this any either. But the good news is that this is her last nadir coming up!!!!

January
HgB 10.5
Platelets -65
TWC - 4.4
ANC - 1800

December
HgB - 9.9
Platelets - 133
TWC - 4.6
ANC - 2700

Monday, February 9, 2009

Gracie's Take On Her Hair

After about a week and a half of going back and forth between, should we shave it, should we not we bit the bullet. I was literally shaking when I went to do it and couldn't. James just went and got a chair and said "Come on Gracie, we're going to give you a hair cut." And that was all there was to it. She didn't fight, she thought it was pretty cool. She did mention once to James "Are you going to cut my hair like yours?" But she wasn't upset when she said it, she was just inquisitive. I think she thinks it's pretty great, no more having to brush her hair. Really what 3 year old girl wouldn't enjoy that? She's still absolutely beautiful and we were pleasantly surprised at how nice her head is shaped, we were kind of worried about that. She's been losing more and more hair everyday and because it was so thin any loss made a difference. That's why today we finally just did it. And we can rejoice in the fact that the chemo did the job and that Gracie is so incredibly happy no matter what happens. There's no keeping our Gracie down!!

Hair Cut for Gracie


What do y'all think of my first job as a hairdresser?
Stephanie gets to cut hair all the time but this was my first go at it.
Isn't she gorgeous! (Even with the not-so-subtle reminder of retinoblastoma in the right eye.)

Sunday, February 8, 2009

Home Again

So how does it feel to be done chemo? Actually I have pretty mixed emotions. As I've mentioned before in the week preceeding the EUA I'm always nervous, usually starting Sunday night (she always has her EUA on Thursday). So I was nervous as usual, but it started a little early this time - maybe around Friday. But then after we spoke to Dr. P. about the EUA results the best descriptions for my feelings is giddy. I was so excited about everything being the last time. On Friday night James and I gave a cheer when they hung the last bag of chemo (I had fallen asleep by the time they took it down). I just thought that we only have to go through one more nadir, one more Neulasta injection, 3 more weeks of staying home from church and play group and all the other fun things we'd like to do, hopefully only 2 more platelets transfusions.

 As we were walking out of the hospital Saturday morning tears started to form in my eyes in the hallway. By the time we got in the elevators they were running down my cheeks and by the time we got to our car I was full out crying. Here we are done chemo. 6 rounds ago I thought we'd be completely through with this cancer by the time we were done the chemo. And we're not. I know cancer will always be a part of our lives now, but THIS cancer was supposed to be gone by now. And we're really not planning on dealing with another one, but we know we'll always have to screen. But right now the tumors are still there. We still don't know what treatments we're going to do next. Are we going to do radiation? Dr. M. assured me that because the vision is still so good no one is in a hurry to do an enucleation for the time being, but it's still on the table. These are why the feelings are mixed. I felt a mixture of pure happiness and stress. I wish this was over, but it's not, so I'm trying to focus on the positive.

 I still get giddy when I think about chemo being done. This morning I gave Gracie her very last Neulasta injection which is a huge deal because it burns like a son of a gun. She and I both hate it. We threw a mini party when it was done. Last night we had an end of chemo party and Grandma made us cinnamon buns and buns for desert and sloppy joes (have I mentioned how much I love it when family is here to visit). We plan on having lots of "parties" this month to celebrate the last of something or other. We've promised Gracie and our other girls a REAL end of cancer party when this cancer is truly gone, and we're getting excited for that and hope it won't be too far away. We're doing a "Go Away Cancer! Go AWAY!" cheer in our family, Gracie is getting really good at it. So we're going to continue being happy, continue celebrating that Gracie doesn't have to go through any more of this horrible chemo and the aftermath it causes and continue cheering loudly Go Away Cancer! Go AWAY!! And above all we'll continue to thank God every day for the many, many blessings that we have in our lives.

Stephanie

Saturday, February 7, 2009

Chemo is done!!

The last bit of chemo just finished for Gracie!! It is 1:15AM and Gracie is just going to get fluids for the rest of the night, no more chemo!! We are so excited. It has been hard to sleep knowing that this was Gracie's final round.
Hooray for Gracie! We will celebrate tomorrow by driving home and getting a good night's rest tomorrow night. Maybe on Sunday we will make a special treat to celebrate Gracie being done chemo, our friend Noah finishing radiation this last week and another friend Isaiah who just started chemo in North Carolina. All three events seem to be important milestones in their respective treatment plans!
Many thanks to you all for your support and love!

Friday, February 6, 2009

Day 2- Round 6 (Final Round of Chemo!)

So yesterday we had our EUA scheduled at 11:15AM. They were a little behind but sent Gracie back at about 11:30AM. We spoke with Dr. P just after noon and were heading up to the cancer clinic just after 1PM. Gracie had been given morphine during the EUA to control any pain and so was quite drowsy most of the day. She slept much of the time in the clinic. We moved over the to the cancer unit at about 7PM. Chemotherapy started at about 11PM and continued for a couple of hours. Gracie did really well and was quite sleepy throughout. I woke up a few times to help her but I was quite tired as well. Stephanie seemed to sleep well.
For whatever reason the doctors had orders for Gracie to stop getting IV fluids during the night. This was fine by me because that would allow Gracie to move around without her IV pole the next day. However, after they stopped the fluids they had to hook her up again to get some Zofran (anit-nauseau medication). This seemed strange to me but I was not reasoning really well before 7AM. Gracie woke up at 8:30AM with an enthusiastic, "The sun is up and its good morning time Daddy!"
Gracie has been quite happy and perky ever since. She has eaten well and been happy to see all of her hospital friends. She has also enjoyed making crafts and watching Little Einsteins. Part way through the morning, one of the child life workers brought her a huge banner for the door. It says, "Congratulations Grace! Its your last hospital chemo." Gracie does not really understand it but Stephanie and I are really excited about it!
Things are going really well and we thank you all for your love and support.

Thursday, February 5, 2009

Day 1- Round 6 (Final Round of Chemo!)

This is a quick update- hopefully I will get a chance to update further later tonight.

We spoke with Dr. P today and got great news! The tumors in the left eye have responded well and we are going to continue treating one of the tumors with laser treatments while the second looks to be completely gone!

We have not seen any change in the right eye for the last six months so it remains a bit of a mystery. Thankfully the tumors in that eye have not grown. We will likely be meeting with another doctor, Dr. G, at MD Anderson in Houston, to see of there is anything he suggests and because he will be heading the new retinoblastoma center here at Texas Childrens. Next month Dr. P will still look at Gracie and treat her left eye and make sure things are not growing. Sometime in the next couple months we will at least consult with Dr. G.

We are excited about the progress today and thank you all for your prayers. They are working!

Monday, February 2, 2009

Friday's Counts

Apparently they called and left a message on our voicemail with these results on Friday, but our voicemail isn't always 100% reliable.

HgB - 9.3
Platelets - 154
TWC - 3.6
ANC - 612

I'm kind of worried about the ANC as it's taking longer than usual to go up. They won't do chemo until her ANC is 750, so hopefully she's already there. When it starts to go up it seems to go up fairly quickly so it shouldn't be a problem.