Wednesday, December 30, 2009

Last IV Chemo of 2009, bring on 2010, we've been waiting for you.

Yesterday was Emily's monthly IV chemo and exam. She gets them every 4 weeks, so technically this is the second one we have had in December, it's just the way the calendar worked out.

Emily's exam went well. Nothing really notable, except she has had this persistent rash for a while and what Dr. Link called "Chemo skin". He gave her a referral to Dermatology and said the order would be expedited so Emily can start treating the rash in the correct way. Since she is on her Prednisone this week, when she woke up this morning the rash was gone, so maybe we won't need the referral? I know at the end of treatment she will temporarily have a lot of skin issues, it's just what happens when you come off her type of Chemo.

Emily has grown, both taller and because of her medication also gained some weight. As a result we have to again increase her dosage. Both her 6MP and Prednisone doses were increased. Unfortunately the Prednisone increase is just enough to bring back the depression she experienced during earlier higher dose phases of chemo. You can really tell this week that she is having a hard time. Last night after chemo she was supposed to have a sleep over at Grandma's house, which is usually a huge reward. She called us at about 7:30 crying and wanting us to come pick her up and bring her home. We did. she even slept in our bed with us, she just wants to be with her parents. I am also worried that with the increased dose of 6MP she may start to experience the nasuea symptoms that you hear about with people on chemo. We have been told she doesn't throw up all the time because her dose is relatively small, but increasing it could change things. I hope I am just worrying too much. And at least we only have 71 days to go.

Hapy New Year ! 2009, was MUCH better than 2008, but we've been looking to March 12th 2010 for about 2 years now, and have high hopes for this coming decade.

Thank you to my blog readers and facebook readers, your support is much larger than you will ever know.

Thursday, December 24, 2009

Labs were great, and we are set for Christmas.

I can't believe it is already Christmas Eve, 2009. It was a year ago that Emily started growing her hair back and we had settled into maintenance chemo. This past year has somewhat cruised by with its share of challenges along the way.

Emily's labs yesterday were great, her ANC was around 2900 which is pretty high but still in the acceptable band. I'm a little surprised because Haley and I have a cold, and I would think Emily will be getting it soon. Though next week is Prednisone and IV treatment, so her ANC will be high again no matter what due to the drugs. Emily will remain on %100 chemo for the week. Next week her IV treatment will be a day earlier than normal because of the holidays, the scheduling at the clinic is a bit off.

We are pretty much set for Christmas. This year not much decorating happened, we were so busy and time flew. We do have a nice tree and have the stockings up, and the girls don't seem to mind that some of the other decorations never made it out of the box this year. Both Emily and Haley are getting some nice presents, and tomorrow we are also going to tell them about the Disney Cruise we are going to go on in the Bahamas at the end of treatment. Including next week's IV treatment, there are 4 left, which means just 17 weeks to go, or around 75 days!

Wednesday, December 16, 2009

Back to full power

Emily's ANC was up in the 2000's for today's lab session, that means she is finally back on %100 chemotherapy dosage ! This is what we expected and its always wonderful to hear positive news. With winter break coming up maybe we can keep her virus free for a few weeks? Though she is going to the Sharks game with me tomorrow night and there is sure to be some exposure there.

Tonight Emily, Tracy and Haley went on a horse drawn carriage ride through our neighborhood to see the holiday lights. Our neighborhood has been doing this for the past couple of years. They had a really good time and Santa was there handing out cookies so of course that was a hit. Both Emily and Haley are excited about Christmas. Next week they will be going to the Nutcracker up in the San Francisco, and then I am joining them and we will go out to dinner and Christmas shop, and stay over night in Union Square. We will be spending Christmas Eve at my Mom's. Then on Christmas Day we are are having my Mom and brother over here to our house. Tracy has to work Christmas day starting at 3pm. On the day after Christmas we are all driving up to Auburn to spend a day at Tracy's parents home. It's going to be a big party up in Auburn, Carol and Steve have 7 grand children and they will all be there! I'm sure the other kids are excited about it, because both Emily and Haley are really looking forward to seeing and playing with their cousins.

Wednesday, December 9, 2009

Going strong

Emily is back to herself, the flu is gone, and she is getting excited about Christmas. Today her class walked to a retirement home nearby the school and did a few songs from her performance. Emily seemed to really enjoy doing the show and really liked being with the older folks. I am sure the seniors enjoyed it too. Today was also Emily's lab day. It was the first time in quite a while we didn't have to be isolated because of H1N1, and Emily was allowed to wait in the normal waiting room and have her blood drawn by the Oncology team, who know how to draw Em's blood really well. We got the results in a couple hours and her ANC was around 2200, which was great. Per her protocol she will remain at %75 dosage. If she maintains that ANC level she will return to %100 chemo next week. It's so hard to stay clear of viruses at this time of year for kids, but she's trying.

Thursday, December 3, 2009

Holiday Performance



I will add a higher quality one tomorrow. This was the final song in the performance. The rest of the performance was filled with holiday songs. Also, one of Emily's third grade classmates and our neighbor Alex Zhau played the violin for us, last month he had performed at Carnegie Hall, he was amazing.

Wednesday, December 2, 2009

Monthly Chemo and H1N1 update

Today was Emily's monthly IV treatment in the day hospital and an exam in the oncology clinic. Since she is known to have H1N1 when we get to the hospital we have to check in and then wait outside for a nurse to come clear her for entry and then escort her to an isolation room. The same protocol is followed for weekly lab draws. We had to wait about an hour and a half for some reason in the exam room. We pass the time with Iphones, laptops, and a lot of good humor and sometimes not so good humor. Sometimes when we wait Emily becomes "Dr. Emily" and pretends to give us exams. It's fun to play, but you also learn a lot of how Emily views her care and her disease. We almost never complain to the staff about having to wait, we know that they are probably busy with kids who are much more sick than Emily, and we remember those days all too well.

Dr Link, or NP Karolina, and a student NP all gave Emily an exam. Dr. Link has to really exam her lymph nodes in her throat area and it hurts Emily, he does it so hard that today he left red marks that remained for an hour or so. Her exam itself went great, there were no concerns and we again we assured her CT looked great. Then it was time to discuss H1N1. They told Emily that they were going to swab her to see if she still has the virus. Then they told us something that we were not expecting. Apparently Emily has a mutated form of H1N1, that Stanford Infectious Disease (ID) has only seen in Emily and one other patient. Since there are laws to protect that other patients privacy I don't know anything else other than just Emily and patient X have had this. They jokingly said that Emily was "famous in the ID dept." Dr. Link then ordered a chest x-ray. He said he wasn't too worried because Emily is not symptomatic but also wants to get her virus free. So to sum it up, the last time she was tested she tested positive, which we all knew about, but we didn't realize that it was a mutated form. The other patient that had this was ultimately cured with a higher dose of Tamiflu, so we expect that if Emily is still virus positive she will be put on an increased dose of Tamiflu, and we just hope she remains symptom free. She is NOT especially contagious, so don't worry. She does not have a fever, a cough, or really any symptoms of the virus and she is clear to be at school. They treat her with extra care in the Oncology area because there are kids there with absolutely zero ability to fight anything, the kids waiting for bone marrow transplants for example. Overall we aren't terribly concerned about this, but at the same time it's a bit unsettling to think she has a form of the virus they have only seen once before. We should get the results of the swab in the morning.

After the exam we had the x-ray in radiology. She moved during one of them so we had a re-do. Then from radiology she was escorted to the day hospital on one north for her IV treatment. She turned on "Sponge Bob the Movie" and tuned out. I don't think she even realized the IV needle went in. She was watching the movie, and because we were so delayed the Sinera patch had her hand completely numb. The IV insertion and lab draws went very great, and then she got her IV medication and were done. All in all we were at the hospital for 5 hours today.

This evening Karolina called us with her cbc results. The important part was her anc was 3200 so she can increase her chemo done up to %75. Her chest x-ray was clear too.

Wednesday, November 25, 2009

Labs and CT results

Today was Emily's lab day. I was able to take her this week and give Tracy a break. Since Emily is still H1N1 positive she has to be isolated from the other 1 North patients. There are kids in the waiting room who are waiting for bone marrow transplants, with resperators on that really can't risk Emily being near them. We had her labs drawn and she did a great job. Then they told me that Dr. Link wanted to see Emily. At first I was a bit alarmed because Dr. Link doesn't usually see people on their lab days and even more rare to see him without an appointment. Then I remembered that we had a CT scan Monday and he must have the results. Again this was the first time we've had CT scan where I was much less worried than I have ever been about the results. I remember the first few CT scans were so hard on me because we had to wait days for the results, and the results are so important, they are THE true diagnostic that the treatment is working or that it isn't. But this time I think I actually worried hard for about the 2 minutes I was sitting there waiting for Dr. Link to come in the room. He walked in all masked up and said to Emily, "Your CT looked GREAT! What's for dinner tomorrow night?" And they started to talk about Thanksgiving.

They told me they need to swab her next week for H1N1 again to see if it's gone, but until then she remains on Tamiflu. One of the side effects of Tamiflu are bad dreams, and or hallucinations, Emily's has been reporting some bad dreams lately. We don't know what she is dreaming about because she tells us it's too scary to talk about. Sometimes the dreams are about her and sometimes about Haley. We are keeping an eye on her well being but she really seems great otherwise.

Tomorrow we will be having a very early Thanksgiving Lunch at my Mom's house, Tracy has to work the evening shift so we are getting the meal in early so she gets to be there.

Happy Thanksgiving to Everyone. Have a wonderful day with your families and loved ones.

Monday, November 23, 2009

Emily still has H1N1

We got call on Saturday from the ER doctor at Stanford to inform us that Emily's swab for H1N1 was positive. We were surprised that was the reason for Friday's fever. Actually we aren't sure it is the reason for her fever, she could still be fighting H1N1 and have a second virus. Since she is on active therapy the protocol calls for her to go back on Tamiflu while she is positive for H1N1.

Today we are at the hospital again, for a scheduled CT scan. This is to check to make sure she is still in remission.

Friday, November 20, 2009

Another trip to the ER

Today Emily spiked a fever of 101.6. We were surprised since it seemed like the other night she had beaten the current virus. Since she was Neutropenic on Wednesday with an ANC of 630, we had to take her to the ER right away. They were ready for her when she arrived, they did urine cultures, started an IV and drew blood. Her urine was really cloudy so we were worried it could be an infection. They also swabbed her for H1N1, but since she just had it, they were swabbing to prove it was gone, they don't think she has it again. In the hospital her fever was 101.2. I've noticed our thermometer is always a little higher than the reads at the hosptial, I think %100 of the times we've gone, maybe it's time for a more accurate one? Anyway it was still high enough to justify being in the ER, anything above 100.3 for Emily is a serious fever.

It took a while to get results, but the results were good. Her ANC has bounced back to 1800. Also her urine was clean. The Dr. told us she was surprised about the urine too, she was also worried when we gave her the sample....though she didn't tell us that at the time. So, Emily was given discharge papers and will be home in time for dinner.

I don't know if this is a good thing or not. This time I wasnt worried about Emily, I knew she was going to be OK, I was just mad that my Friday afternoon was gone. I feel like I am getting too used to this.

Thursday, November 19, 2009

We averted a hospital trip last night

Yesterday I updated everyone that Emily's ANC had fallen to Neutropenic levels and that she probably had a new virus. At 11pm when Tracy went in to give Emily her Chemo she noticed she was warm. We took her temp and she was 99.5. That is technically not a fever, you have to hit 100.3 to be considered to have an official fever. But we know Emily very well and we know that her temp usually runs around 97.7, so to us when we have seen fevers in the 99 range it has meant she was on her way up to above 100.3 levels. So we were pretty sure that within an hour or two we would be heading to the ER for blood and urine cultures, and since she was neutropenic it would also mean she would be hospitalized.

To my amazement an hour later, she was cool again. I think she fought off a virus and avoided the hospital for the first time in treatment. This means she is strong. This one isn't H1N1 since it was resistant to the Tamiflu she was on up to yesterday, it's most likely Rhinovirus aka the common cold.

I called the Oncology Fellow last night at 11 to warn him we would probably be seeing him later in the night. In that call he told me there was a study done recently that kids age 1-5 have a active virus in them 150 days out of the year. This really explains why all parents get sick when their children go to preschool. But I was surprised that is was 150 days a year .....Wow.

Wednesday, November 18, 2009

Emily's blood counts greatly reduced, so we reduce chemo

I was surprised last week when her ANC was in the 2000's and she had H1N1. Well this week it caught up to her, and her ANC was only 630, meaning she is neutropenic. To remind my readers what Neutropenic means, at a high level. All of us healthy people have White blood cells that fight virus and infection. Emily's chemotherapy suppresses her immune system. Each week she needs to have labs and what they are looking at among other things is her Neutrofil count. Our Neutrophil count describes how many of these T-cells we have to fight virus and disease. If you have a number lower than 1000, you dont' have enough neutrophils to fight an infection or virus, and thus you are classified as Neutropenic. If you aren't on immunosuppresion and you showed up with a number lower than 1000, it would be a very bad sign. I believe HIV patients battle neutropenia as well.

So Emily is neutropenic this week,and most likely with a reduction in 6MP and Methotrexate her levels will return to "normal" or normal for Chemo. however if she gets a fever and is neutropenic it means she has to be hospitalized in an isolation room. We will probably keep her home since it's flu season.

Friday, November 13, 2009

Update about the blog

Hi Blog readers. Over the past couple of days we have had some activity on the blog that I need to shut down. Somehow ad for Cialis and Viagra are being put into comment fields on the blog.

As a result I am going to start to moderate comments. What this means is if you enter a comment on Emily's blog, Tracy and I will get an email asking if we approve the comment. If we do it will be posted, if not it will be obfuscated.

While these comments are being put in really old posts and probably only Tracy and I are aware of them, I want to keep Emily's blog as "pure" as possible, because one of the reasons I am writing it, is so I can give it to her so when she wants to as an older person, she can go back and read about all she went through.

Thanks for understanding. Onward and upwards !

BTW All 4 of us have H1N1 now. Emily with her Tamiflu and vaccination was definitely the least effected so far, so if you can get one, I would really recommend getting yourself protected.

116 days of treatment left.

Wednesday, November 11, 2009

H1N1 and lab update

Despite having H1N1, Emily's counts are totally where they should be this week, so she will remain on %100 Chemo. I am surprised to be honest, but the clinic said that with H1N1 they aren't seeing counts reduce. I read that H1N1 kills because it produces a wild response in your immune system called a Cytokine Storm, which backs what the clinic told us. At any rate despite this flu, Emily continues to do really well.

She isn't all the better from the flu but she is up, dressed and walking around doing normal "Emily stuff". It seems she is going to get over this with little trouble. The clinic does want her on Tamiflu for 10 days, which is twice the normal duration for the drug.

We plan to send her back to school tomorrow.

Tuesday, November 10, 2009

Celebrating 1 year on Maintenance

We just realized that this week marks one year that Emily has been on maintenance chemotherapy. We can't believe it's been a year since we ended intensive chemo, and that we have been in this maintenance mode for a whole year. Maintenance mode means giving Emily a pill at 11pm every single night, waking her up, getting her to wake enough to swallow pills, and then putting her back to bed. We just keep doing this until March 10th 2010, and then we stop. There is no taper, no change, you just stop taking pills one day.

I remember Dr. Davis telling us on the day they told us Emily's official diagnosis....."Here is your protocol, you can see that every single day from now (March 2008) until March 2010 is planned out. One thing is for sure, there will be challenges along the way, we don't know what they will be, but there will be challenges, but it will work, hang in there. You may not believe this but we want to save Emily just as bad as you do."

Emily will have labs this week and next week as usual. On 11/23 she is going to be having a scheduled CT scan to take a look and make sure everything is OK. Those are hard because there is a lot of anxiety on the results. Hopefully we will have the results on wednesday the 25th before Thanksgiving.

Monday, November 9, 2009

Update on Emily's H1N1

Early this afternoon we got a call from the ED at Stanford saying they had just heard back from the County virology unit that Emily's test for Influenza A came back positive. H1N1 is Influenza A and the county says that %99.9 of influenza A is H1N1 virus, so Emily is a positive for it. They had already started Tamiflu treatment in the ER, so all we were supposed to do was to continue with the treatment.

I went to Target to get Tamiflu to find that they didn't have any of it. Not only did they not have it, but Emily requires the liquid version. She can swallow pills fine, it's a dosage issue I expect that she needs the liquid. I asked Target to call Walgreen's which they did, and luckily the county had just dropped off doses of liquid Tamiflu there. Since they were from the county Walgreens could not charge me for the medication, so thanks to Santa Clara county not only did we get the medication, it was also on the tax payer.

Emily is doing REALLY well. Her only fever was the original one that brought us into the hospital. That fever broke around 6am this morning. She is conjested but not too much worse than a bad cold. I would say her energy level is a little low. But really this is very mild and at this point I am not too worried about it. Since her ANC was 2400 she is continueing on %100 chemo, even though she has H1N1.

I will have an update tomorrow.

H1N1

Last night Emily started to get a fever around 11pm. Earlier in the day we could hear a new virus starting. It's really discouraging when you fight to keep her away from virus, and then she still gets one. Her fever went from 100.9, then up to 101.5. Anything over 101.2 and we need to go right to the ER to have her ANC checked. Emily spent the night in the ER while they ran tests, blood, urine, nose swab for H1N1. She has all the signs of H1N1 flu and the doctors said we will need to wait for conclusive results, but more than likely she has H1N1. The GREAT news is her ANC is 2400 so she was not neutropenic so she gets to fight this flu at home, rather than having to be in an isolation room at the hospital. She was also given Tamiflu because they are that certain this is probably H1N1 virus. She threw up her first dose so we need to give her another one later this morning.

It was amazing how calm and or numb Tracy and I are to all this. Last night when Tracy first discovered the fever she came and woke me to tell me. I was concerned of course, but I actuallly dosed back off to sleep, knowing we needed to wait for the fever to be there an hour. A year ago, I would have been freaking out, jumping to 100's of conclusions about what was going to happen to Emily, and this time, I thought to myself, let's just wait and see, she's doing so great, she's going to be fine. Now that she most likely has H1N1, I am still not too worried. Tracy and I are both a little nervous but confident Emily will fight through this like a champ. Emily was also very calm and matter of fact about having to go in to the ER. We all know the drill by now.

When we were in the ER we ran into Dr. DeSouza, who was the attending physician WAY back on March 9th 2008, and was the person who diagnosed Emily originally. He still remembers us and the day as well. He said, "next time we run into each other, let's hope it's Stanford Shopping Center".

More updates as this virus progresses.

Wednesday, November 4, 2009

very long scheduled day at the hospital

Today was Emily's scheduled monthly IV chemo and physical exam. Our N.P. Karolina ordered a stomach x-ray again today to make sure Emily's blocked GI had resolved. We suspected it had and sure enough she is cleaned out, which is really great news. That meant that we could go ahead and continue with all the scheduled chemo.

For some reason our N.P. was really behind on her schedule today. She likely had a sick child, or a new patient, or something but she was going to be so far behind that they gave us a pager and told us to go grab lunch. Emily is on her monthly Prednisone this week and she doesn't like the cafeteria so unfortunately that led to her not eating much, yet still being hungry for the rest of the day. Her x-ray was at 11, and we finally got to have her exam at 2:30. Then after that and being cleared for chemo, we didn't hit the day hospital until 3:30 or so. I went home to make dinner for the girls when they got home from picking up Haley and having a quick play date with Olivia and Stella the girls good friends. Emily's good friend Olivia lives near my Mom who takes care of Haley on Wednesdays when we go in for labs or treatment. So one of the big things to look forward to after chemo is getting to play with Olivia for 30 minutes or so at the Haley pickup. Haley is hard enough to "control" at the hospital, but with the swine flu no one under 16 is allowed in the hospital unless they are a patient. So no Haley in the hospital I think probably until Emily is done with treatment.

We still don't have today's lab results. Karolina warned us that she was so far behind today that she might not get back to us until the morning, and for tonight just to continue on her %100 dosage. I think since she is on her prednisone it may mask the effects of her cold on her ANC, so she may skate by and be able to continue at %100 dosage this coming week. We shall see.

125 days of treatment to go.

Monday, November 2, 2009

Long unscheduled day at the clinic

Emily has been having issues with constipation for a long time. I don't write about it much because I don't want to embarrass her. Today things got a little worse so we had to go into the clinic. Tracy gave Emily her morning Em all of a sudden didn't feel well and both threw up and had diarrhea, really watery suggesting there was something obstructing her GI tract. Since we've been going through GI issues they wanted to see her. After an exam and a lot of questions they decided to give her an x-ray and see if she was truly blocked. It turns out she is blocked in two spots in her intestine and the N.P. was surprised she wasn't complaining of more discomfort. We are treating her with magnesium citrate tonight. It's really important that she is un-clogged before IV chemo on Wednesday, or they may not give it to her. The Vinchristine, her IV medication, is known to cause really bad constipation and is the original cause of this complication. All the exposure to her vinchristine is catching up to her side effect wise. Luckily it's fairly easy to treat.

On the upside she was able to get a dose of swine flu vaccine. The clinic had just got 200 doses today. They didn't actually tell us, I just asked if they had some, and the N.p. seeing us today ordered us a dose. She needs to get a second one 4 weeks from now. Hopefully by then it will be a little easier to get.

Wednesday, October 28, 2009

Emily is back to %100 chemo dose.

After about a 6 week lag Emily has been cleared to go back to %100 chemo dose, since her ANC was over 1000, at 1039. You can see that it was barely over so it's really important that she attempts to avoid sick people and to wash her hands like crazy. Both Tracy and I have really been pushing the hand washing, sometimes having the girls do it for no reason. We also mix sanitizer in there from time to time.

We were hoping that Packard would have the H1N1 vaccine today, but they are still waiting. I hope they get it soon, I really want Emily to get it. I've been following it on the news and they expect it to peak next week. Luckily her school hasn't had any out breaks of it yet.

This weekend is a big one. Friday is Emily's actual birthday ! She is really excited about her birthday this year, and she is so much healthier than last year so we are trying to make it as special for her as we can. Her class is already having a Halloween party that day but Em still wants to bring donuts, so she's going to. On Saturday some good friends of ours are having a Halloween Party which we are going to go to during the afternoon, and then come home to our neighborhood for trick or treating. Emily and Haley are super excited about trick or treating. Emily is going to be a Ferry and Haley is going to be a Witch. On Sunday is Emily's birthday party which is going to be a ice skating party in the afternoon. It's going to be a long and fun weekend, and of course full of sugar.

(Wahoo fish Taco will give your kids a free meal if they give them all of their Halloween candy. Not a bad idea.)

Wednesday, October 21, 2009

remain at %75

Emily had another week of good lab results. Her ANC was around 2600 so that means she will stay on %75 dosage again this week. Her protocol says she can only step up every two weeks after a reduction, so this is exactly the news we wanted to hear. When Emily changes her dosage of ANC she gets a rash on her face, we've noticed it three times. She had it again this recent reduction in chemo, it isn't anything to worry about. There really isn't anything remarkable going on in Emily's treatment. We just are trying to avoid crowds where there could be sick people.

Emily is getting ready for her birthday party. She is going to have an ice skating party and she is really excited about it. She has only ice skated once at a Brownie event but she really wants to do this and she is really excited about it.

Wednesday, October 14, 2009

great labs again

Emily had her weekly labs and her ANC has bounced back up to 3200. That's good considering her %50 dosage. Now she will go up to %75 dosage for this week, and hopefully the following week. After that, and if she can stay virus free, she will be back at full dosage on her chemo. I feel a lot better having her on %75. The whole family has had the flu shot as of today. I was the last one to get it, I waited until they had it at work, so I could get it free. In a week or so Emily should be given swine flu vaccination when the clinic gets their allotment of it.

Thursday, October 8, 2009

Another monthly IV chemo complete

Emily had her monthly IV treatment and physical exam yesterday. The exam and IV treatment went very well, she looks good and there were no issues accessing her vein for IV and lab draws. The vein in her left hand is getting harder to access, she has to hold her hand in a specific position for it to work. It is getting scared and hard the nurse said. Good thing we only have 5 of these remaining in her treatment.

Emily has gained some weight again so we are once again increasing her prednisone dose from 13mg x3 per day to 14mgx3 per day, for her 5 day Prednisone flash. The side effects of Prednisone are troubling from minor ones to some possible yucky severe ones. I think of all her medications we see the effects of Prednisone the most.

Her ANC was really low considering she is on Prednisone. Usually on her Prednisone week we see ANC's of 4000 - 6000, this week just 1840. What you can read into that is she is still really battling her virus, or that she is fighting a new one. Her school is a virtual virus incubator right now, and we have been holding her out of school more often, through she is there today. With an 1840 she remains on a %50 dose of her chemo. I think it's going to be a while until she's back on %100 dosage. I'd like to remind everyone to please get your flu shot, wash your hands more often, and stay away from people when you have a cold. Yes I am talking to you.

without going into the details Emily had a really challenging day yesterday. I went to pick her up from Gymnastics and she told me she had spent most of the hour in the bathroom crying. I told her that I thought it was incredible that she was even at Gymnastics hours after being in the hospital for treatment. After Gymnastics she choose to do her homework over watching TV with me, again I was proud of my little girl.

Wednesday, September 30, 2009

As expected, a week off chemo and Emily's levels increased !

Emily was on hold from her medication this past week. While it's a worry therapy wise for me, it's also just part of therapy. You are on this treatment for 2 solid years and you are going to get a cold or two. Emily enjoyed the break for a few reasons. Firstly we have to give her the Mercaptopurine (6MP) at 11 P.M, which means every night, we have to wake Emily up at 11, enough woken up that she can swallow two pills, or on Thursday nights 10 pills. So, she really enjoyed some solid nights of sleep, she commented on it several times during the week. On therapy she also can't eat any food after dinner, so her stomach is empty at 11, it's very important. This week she got a kick out of having an after dinner snack. This points out simple pleasures we all take for granted. I asked her if she felt more energy or "better" when she was off her medication. She told me that her energy seemed the same, but she wasn't nauseous all the time. To this point I hadn't thought she was feeling nausea but apparently she has been. The Mercaptopurine is the medication that in larger adult doses makes you throw up and not be able to eat, the symptoms we all associate with chemotherapy.

Today was lab day and her ANC had increased from around 340 to 1100. That's still low, but high enough to resume chemo at %50. Starting tonight at 11pm she'll be back on therapy. When her N.P. reviewed the lab results she could see leading indicators in her neutrophils that she is on her way out of this virus. With an ANC of just 1100 and resuming chemo, we need to be on high alert that she could slip back into being neutropenic over the week. But in usual Pepper fashion we're just going to live our lives as normal as possible, minus trips to malls or movie theaters. We could pull Emily out of school but we try to limit how often we do that.

Right now Emily's two top priorities are, planning her 8th birthday party, and what to be for Halloween.

Thursday, September 24, 2009

Update on Em

We kept Emily out of school today with her ANC so low. She didn't mind too much, but it's funny or maybe typical that on days she has to go to school she wants to stay home, and then on days when she has to stay home, she's sulking because she didn't get to go to school. Her teacher, Mrs. Nishimoto dropped by some work after school, so Em didn't miss out on the days lesson plan. It's great living two blocks from school and we are blessed with a truly awesome school, great teachers and administration.

During the day we found out that one child in Emily's class has strep throat and another has a confirmed case of Scarlet fever. (Honestly I somehow thought that didn't exist anymore, but it does). So that data added a bit of stress to an already stressful situation.

Putting all the worry aside, Emily is doing fine, no fever and I think her scratchy throat sounds a little better. And even if she were to start to get something now, she has a day off chemo and I am sure her white blood cell count is increasing, and getting close to levels where we wouldn't need to be as worried. I think I want to keep her out of school tomorrow just to be sure and keep exposure all the germs that just naturally exist in a school.

I think I wrote a few weeks back that she would probably get sick when school started, and sure enough it happened. After a day to absorb the news, I can start to see that it's going to be all right.

This roller coaster ride only has 167 days left.

Wednesday, September 23, 2009

Emily's cold caught up to her, ANC at 340, chemo discontinued.

The cold Emily has been fighting here caught up to her, and today her ANC plummeted to 340, which is pretty neutropenic. We need to stop all chemo and watch for fever and be ready to go to the hospital if she start to get one. Obviously given the flu season starting early this is a pretty big concern. She has not had her swine flu vaccination yet either. I haven't discussed this with Tracy yet, but I am planning to hold her out of school tomorrow so her counts can regain. Next week they will retest her and hopefully we can start chemo again. Taking complete breaks like this makes me very nervous and stressed out.

Thursday, September 17, 2009

300th Blog Post

the Blog has reached another milestone, the 300th post. It's amazing every time I think about how much Emily and our family has been over the past 18 months. I can't believe it has been that long. To me it seems like Emily just got sick a couple months ago. I am so glad to have the blog as a record of what has gone on, and for Emily to have for when she wants to know more about what happened to her.

Yesterday she had her weekly labs, and she was doing great. Her ANC was around 2600 which is right where we would to see it for this week of her monthly cycle. She even has a little cold she is fighting. She seems to be really strong right now !

Wednesday, September 9, 2009

18 Months down, 6 to go.

Today Emily had her monthly IV chemo treatment and physical exam. This month went a lot more smooth than last month. Last time it took them 4 pokes to get a good IV, and today they got her on the first try. The infusion of chemo was uneventful and was over fairly quick. Her exam also went well, again nothing extraordinary to report. This marked the 18th month of treatment, we are %75 of the way through Chemotherapy.

This week Emily is on Prednisone and quite moody because of it. With her recent dosage increase we have noticed more side effects all the way around from her chemo. She's puffier, moodier, and a little less coordinated, all normal side effects for the medication she in on. Haley also has a cold and Emily is starting to get the symptoms we think, so we'll see how that goes as the week goes on.

Today at the appointment I had questions for Karolina, our NP. What about the swine flu? They feel that for Emily the risk of swine flu is no greater than any flu, she doesn't need to get either. If she did get any type of influenza they would give her Tamiflu, which has been quite effective with the hand full of cases they had last spring and already this fall. Once the vaccine is ready, Emily and all the high risk patients in the country will be the first to get the shots. I think the whole family will be getting both swine and the regular flu shot at that time. Karolina cautioned us that it's likely with flu season coming on that at some point Emily will most likely get neutropenic and may have in patient hospitalizations again. It doesn't mean that her treatment isn't going well, even as we get up close to the end, it's just an effect of being on immuno-suppresive drugs.

I also asked her about what happens at the end of chemotherapy. I have avoided asking about it, but I feel like it's time to start thinking about this part being over. For the first year Emily will only have to go to the clinic once a month for an exam and a CBC blood draw. Then every other month the second year, then every three months the third year and so on. At 5 years if she is able to avoid a relapse she would be considered "cured" of this episode. At that point she would be just as likely to get cancer as any of us are at any time. Then she will go into an after care program, and she can access that for the rest of her life if she chooses to do so. The after care program collects data from kids who have gone through chemotherapy, for example they will measure her learning abilities, growth, and other vital stats. They learn valuable things about the long term effects of treatment, and are there to both help the kids who have gone through chemo, and also help the medical community make changes and advances in treatment for people who will be diagnosed in the future. Karolina said, "at some point Emily will have questions about having children", and she will be able to consult with the after care program to learn the latest about what they know about the risks she may have due to her treatment.

Today we also ran into Dr. Kara Davis, who was the Dr. who was on call the first weekend Emily was hospitalized 18 months ago when we started this battle. She hadn't seen Emily in a very long time, and right out of her memory she said "Hey it's the Peppers, how are you Emily?" I am always impressed with the staff and how well they get to know the kids. To much of the staff I am "Emily's Dad" but everyone knows who Emily is, from the pharmacists, to the woman who hands out our parking passes, it's quite common to be walking around the hospital with her and someone in a lab coat passing by says, "Hey Emily". Since she has to be there it's kind of nice for her to feel like she's a big shot, and it's also nice she feels so comfortable there.

Sunday, September 6, 2009

Quick update...

This is Tracy this time, since Chris has been at Burning Man since Wednesday. He asked me to update the blog while he was gone and I kept putting it off/forgetting until now. The main thing we wanted to say is that Em's ANC from Wednesday 9/2 was 1600, which is up from 900 the week before, and that's without decreasing her chemo dose. We were super-thrilled, because we (or at least I) thought that another week's worth of school germs would drop her counts further. But they didn't! Yay! So she got to power through another week of full-dose chemo. Chris was more than thrilled that she was not neutropenic while he was at Burning Man, where he would have no access to the "outside world." If she had been, let's just say it would have put a significant damper on things while he was there.

So while Chris was out of town, my parents drove down from Auburn to help watch the girls while I was at work some of the days. I'm so thankful that they were able to help us out like that. Chris will be home later tonight or tomorrow, depending on how tired he is! Then you will be back to your regularly scheduled blogger.

Thursday, August 27, 2009

Blood counts dip

Yesterday was lab day and for the first time in a really long time Em's ANC was under 1000, it was 900. She is mildly neutropenic but they are going to keep her on %100 dosage this week. I am worried that all the exposure to germs at school is paying its toll and I hope she can regain her counts and stay on %100 dosage. She hasn't made it through a 3 month cycle at %100 and she is so close I'd like to see that happen.

Emily is really enjoying school and yesterday started a gymnastics class.

Wednesday, August 19, 2009

Third grade here she comes

Today Emily had her labs. I wasn't certain how her levels were going to be, since just yesterday she spent the entire morning throwing up. She either had a virus, food poisoning, or maybe side effects of chemo, we aren't sure but she woke up sick and was better by 2pm. Apparently whatever it was had little effect on her ANC, because it was at 2800 today when we got get results from today's draw. That means she remains on %100 dosage and continues to march to the end of treatment and being cured from her disease.

Today was also the LAST day of summer vacation. I personally am sad to see her go back to school, the vacation seemed much too short. At 4pm today the classes were posted and Emily got the teacher she really wanted and was happy about it. On the sad side her best buddies, many kids she has been with since first grade are not in her class. I think it will be a good experience for her and I am highly confident she will make new friends and keep her old ones close too.

I am often asked, "Chris, how is Emily doing academically in school?" I always and correctly say she is doing well and even though she has missed a lot of school, so far she has kept up. To back that claim I have her STAR test results, and Emily tested at "Advanced Level" in both Language Arts and Math. I also want to point out that she had to take these tests the day after returning from a hospitalization for pneumonia and was really sick. This goes to show just how smart of a person Emily is, she has missed a good part of both first and second grades and has been through so much that most can't even relate to, and she still manages to score high in school. I am just totally amazed and want to brag about her.

I can't believe this cancer treatment has spanned 1st, 2nd, and now 3rd grade. Talk about a marathon. Tracy and I want to thank everyone for your support so far, we are almost there, just 6 months to go.

Saturday, August 15, 2009

Thursday, August 13, 2009

Emily's counts were perfect.

We got Emily's lab results this morning since the lab draw was so late yesterday, her results were "perfect" as they have been for weeks now !

WBC 7.1
Hgb 13.3
Plt 389K
ANC 6000

Her ANC is higher this week you might notice, that's to be expected as this week is Prednisone week, and that's what it does.

Wednesday, August 12, 2009

Monthly IV Chemo, exam, and quarterly chest x-ray

Today was a big day at the clinic, Emily was in for her monthly treatments. We started her Prednisone this week and she is just finishing up day 2 of 5. This month she had a chest x-ray along with her physical exam. She looked great and her xray was clear. Dr. Link also noted her blood counts have been looking really good.

After her exam, it was time for her IV Vinchristine and blood draw. This was probably the roughest IV we have had in treatment, it just didn't go Emily's way. They had to poke her 4 times to get a vein and they never really got a good draw at all. In the end they were able to give her the medication. Both Emily's hands were used and she will probably have some bruises.

Besides treatment Emily is still enjoying her summer. Swimming as much as she can, riding her bike anytime she can get me to take her for a ride. She is so tan and healthy looking and gets compliments on her "hair cut". She starts third grade one week from today, I can't believe how quickly the summer has passed.

Wednesday, August 5, 2009

Back home

Our vacation ended last night, we flew from Denver back to San Francisco and then drove back down to San Jose. The second half of the trip was not quite as fun as the first half because Tracy got really sick with a bad head cold that put her in bed for 2 days. We all made the best of it and still managed to have a really fun trip.

After Breckenridge we went to Boulder CO. In Boulder we met up with some really good friends, a couple who I had gone to college with. They used to live in Colorado and were also back in town for a visit before they move to Germany later this month. They have a son 6 months younger than Emily and a daughter a year younger than Haley, so we had a good pack of kids to explore the town. We had ice cream up on "the Hill" and then walked to Pearl Street where the kids played and we eventually had dinner.

Towards the end of that day Tracy started to feel sick, and by the next morning she was officially down for the count. We had been invited to a all afternoon get together in Littleton. I left Tracy with some cold medication and she got some rest in the hotel, and I headed down to the Denver area with the kids. We had the best time. Our friends, the Rasmussen's, were there and a lot of their friends from the Denver area, and everyone had kids, most of whom were 8 or younger, and most of them girls. Tracy was able to sleep all day, and the girls and I had fun into the early evening. We got back to Boulder around 9pm and went to bed. The next day we slept in late. We moved from Boulder down to Denver for a change of scene. Tracy was still really sick and wanted to be in bed. We checked into a really nice hotel with really comfortable beds and Tracy got some more rest. I spent the afternoon shopping with the kids and kept them as entertained as I could in Denver. Tracy started to feel better that evening, with one last day on the trip.

Tracy and I wanted to do something really fun for the kids. We researched and found a place called "Water World" which boasts to be one of the nations largest water parks, it was 64 acres. So on the last day of the trip, which was a nice hot summer day we headed out with the kids to Water World. It was a really fun day and Emily has been talking about it ever since, so it was worth it. Tracy stayed with Haley and did mellow water fun, and Emily was up for pushing her limits on some CRAZY water slides, and I had a blast going with her. At the end of the day we changed from our swim wear into clothes for the plane and headed to DIA to fly home. We grabbed a bite to eat and all sat together on the plane and flew back home.

Today, our first day back I was worried about Emily's lab tests. We had played so hard, and she had been sharing a hotel room with Tracy who was really sick, 2 plane trips with potentially sick people etc. We had been in the altitude and she was just plain worn out. Well, I think a week in Colorado must be good for you, because her ANC today was up to 1600, 600 higher than the day before we left.

Friday, July 31, 2009

Big fun vacation day.




The vacation is going really well, everyone is in a great mood and making the best of our time. Yesterday we didn't get much done, it was in fact the coldest July 30th in recorded history in Denver, and up here in Breckenridge. There was fresh snow on Mt. Baldy and the Continental Divide that the 10 Mile Range. It also rained mixed with thunder and lightning. Despite that picture we still had a great time poking around downtown Breckenridge. The girls found sweatshirts and T-Shirts they wanted to get, and Tracy and I did some window shopping. The sun was actually out when we were downtown. We had to reschedule our horseback ride to today. We just had a good family time together all day. In the evening Emily and I went in the hot tub, and after dinner the whole family did a mile long walk to a park and the girls played on the playground. Despite it being 25 degrees lower than the average for this time of year everyone was happy with the day.

This morning we woke up to sun, mixed with clouds. We wanted to make the best of the weather, so we made breakfast and headed up to the Breckenridge ski resort area. During the summer they have all sorts of outdoor activities. They have a maze, trampoline, mini golf, etc...but what we were there to do is something called "Alpine Slides" It is basically like a Tobogin (sp?) on wheels on a track. You ride the chair lift up and ride down on a slide. You have a break in case you want to slow down. Emily and I each rode our own slides , and Haley and Tracy rode together. This also marked Haley's first chair lift ride. We all had a lot of fun, it's really exciting to do. Then almost out of no where a rain storm rolled in and we were worried that we may have to cancel our horseback ride. We decided to just "go for it" and it was a really great call. No one else was as daring as us, and when we showed up to the stables, we were the only people who showed up for the ride, and I have to admit I was worried it was going to pour, it was lightly drizzling. Well the opposite happened, about 50 yards up the trail the sun popped out, and we were off on a 1.5 hour trail ride up into the Rocky Mountains. Emily led the way on her horse named "Biscuit", I was on "Captain" and Haley and Tracy took up the rear on "Rudy". I was nervous at first, Emily was really on her own on the horse, but she did REALLY well. These were trail horses who were trained not to run, and to follow the trail. There are usually 15 maybe 20 people on one of these rides, and it was just our family and the guide, on a perfectly sunny afternoon ride. If you have ever skied at Breckenridge we essentially rode up Peak 9. We didn't ride up the ski slopes themselves but off on trails in the trees, it was exceptionally beautiful with green grass, quakeing Aspen trees, and tons of wild flowers along rushing mountain creeks. The ride lasted about an hour and a half as promised and we headed into town for another round of shopping and an early dinner so we could get Haley to bed early. I don't feel sore yet, but Emily and I are going into the hot tub again a little later on.

Tomorrow we pack up and head down to Boulder. We have decided that we want to come back to Breckenridge next summer, but that time we want to do a full week up here.

I was interested in what was going on a year ago, so I looked at some posts I did in the blog one year back. Last year today, Emily had a 100 degree fever and was too sick to be admitted for high dose methotrexate treatments, and then on August 4th was hospitalized for treatment. It's a point I keep making in the blog, but I am blown away by the stuff we are doing this these days when last year we were just struggling to get through each day. I think it was harder to go through than I could ever have really explained in the blog. I also wanted to keep the blog positive so I could stay positive back in those days. Today just seeing the smiles on Emily and Haley's faces during the horseback ride was enough to keep me going for a while.

Wednesday, July 29, 2009

We got here, 9600 ft!

Today was a big travel day, for our Colorado trip. Last night I flew by myself from SFO to Denver. Tracy, Haley and Emily were using miles and left at 6am this morning. It would have cost me more to fly with them than the flight I took, that's why we traveled out here on different planes. Tracy, Emily and Haley caught a 6am flight out of SFO, made a stop over in Las Vegas, and then onto Denver. I was at Denver Airport with the car already rented. Once they arrived we grabbed our bags and headed up I-70 to Summit County. We are staying in the town on Breckenridge which is around 9600 ft above sea level. You can really feel the altitude.

We are staying in a great house, that I have actually rented before on a ski trip. It is also owned by some family friends of ours. Once we got here we explored the house. Emily and Haley were excited about the bunk room with bunk beds. Em, Haley, and I played a few rounds of hide n seek, this house is pretty large and new to us, so it was actually a lot of fun. The rest of the day we unpacked, shopped for food and made dinner. Tracy and Haley crashed early and Emily and I are up watching a little TV.

Tomorrow we have reservations to go on a 1.5 hour horseback trail ride. Emily also wants to rent bikes, so we will probably do that on Friday.

We are all having a really good and fun time.

Tuesday, July 28, 2009

Emily is cleared for the plane

Today Emily had her labs a day early so we could leave for our vacation to Colorado. she isn't going to need a lab draw for 8 days which we think is the longest she has gone without a needle since we started treatment. We will be in Colorado for the week, half the time up in Summit County in Breckenridge, and then had the time in Boulder, where I went to college.

Emily's lab results were good, her ANC was only 1080 but high enough to get on a plane. We hope she doesn't get sick while we are on our trip, but that is just a risk we live with daily.

Hopefully I'll post some pictures from the trip this week on the blog.

Thursday, July 23, 2009

Emily's lab results were great !

WBC 4.3
Hgb 11.4
Plt 408
ANC 3090

This all means she continues at %100 dosage.

Wednesday, July 22, 2009

What didn't Emily do this past week?

Emily had her labs late this afternoon. It was so late we don't have the results back. I think she's going to be OK based on the way she is acting, but she thinks she is feeling a cold start to come on. Once I know the results I will make a quick post about it.

This week Emily was up to a lot. Just last week she was feeling sad about not being able to do some of the things other 7 and 8 year old's are doing, specifically swimming and riding a bike. She wasn't very accepting of the excuse we offered her....that she has been in the hospital and in therapy every week and there hasn't been time. She just wants to be "normal". This week she made tremendous progress at "catching up". Over the weekend Tracy, Haley and Emily went up to Auburn to visit Tracy's parents. They have a really nice home in the rural part of Auburn and one of the more exciting parts is the swimming pool on the property. The pool actually belongs to Tracy's Aunt, who lives next door to Tracy's Mom. Emily and Haley swam a lot over the weekend and Granpa Steve taught her how to dive, and also jumped off the diving board. She also treading water in the deep end of a pretty deep pool. As if that wasn't enough to convince everyone she could swim, the other day she passed "the deep end test" at her friend Julia's swim club. The life guard makes sure kids can swim across the pool.

Then tonight she learned how to ride her bike with no training wheels. It took her about 30 minutes (not exaggerating) to learn how to ride. Now she's really excited to do it more. Luckily we are going to Colorado next week and can rent and ride bikes in both Breckenridge and Boulder.

I am really happy she's doing these things. She look so healthy, she is more tan than I have ever been in my life, has curly bleach blond hair. It is hard to forget she is still on chemotherapy.

Wednesday, July 15, 2009

Another monthly chemo.....DONE

It seems like time is flying because today was Emily's monthly IV chemo. She is also on her 5 day course of Prednisone. So far she is reacting reasonably to the Prednisone. She seems a little more irritable than normal. Things went well at the hospital today. Her exam was unremarkable, in fact we talked to the NP more about what is going on in our lives, than talked about Emily's specific issue. She's doing well, still is the main point to take away.

Her IV stick was a little rough at first, the nurse didn't hit the area that the patch had numbed. It was ok though and they were able to get the IV in to take blood out, and to put Chemo in. Emily stared at the TV most of the time through the procedure and didn't even realize she was done when it was time to go home.

I get exhausted on Chemo day but not Emily, she's off to the pool AGAIN.

8 more IV chemo sessions and she will be complete with Chemo. I almost don't want to say this because I seem to jinx myself from time to time, but I can see the end finally, wow.

Thursday, July 9, 2009

4th of July fun and wonderful lab results

Our camping trip over the forth went really well. The kids had a blast and Tracy and I had a great time too, though the kids exhausted us. We were at Big Basin up in the Santa Cruz Mountains. If you like to camp and haven't been there I highly recommend it. The camp sites were nice and the bathrooms were clean and had showers. We were out for two nights which was nice because it takes a long time to setup and take down a camp site. We were there with our friends the Scotts and Emily, Olivia, Haley, and Stella had so much fun together. We went on a fairly long (4mile) hike on the 4th and for the most part didn't need to carry anyone, though Haley and Stella needed some help the last 1/2 mile or so. It was a great way to celebrate the 4th, though there was not one firework to be seen, which was totally fine with us, nice and peaceful and quiet.

Yesterday Emily had her weekly labs. I left work early to take her, to give Tracy a break since she goes nearly every week. I was nervous because last week was our first week back on %100 dosage and I worried that her ANC may have dropped. The great news is that she completely handled going to full dosage and her ANC was at 2400, which is PERFECT for being on her level of 6MP. This means we stay on %100 dosage. She also cleared the tests so she can get IV chemo next week. I can't believe how fast time seems to be flying in between monthly IV treatments.

This week besides labs Emily is getting in some swimming, so much that she is totally tan, which in our family is a rarity as Tracy and I burn. she and I also went to Ice Age 3D last night after the labs. Today Emily, Tracy and my Mom were given tickets to see the King Tut exhibit up in San Francisco at the De Young Museum. This weekend I am going to attempt to teach her to ride a bike without training wheels. That was supposed to be last summers project, but she was so sick it had to be delayed.

Wednesday, July 1, 2009

She's back to %100 dosage

Today Emily's ANC was around 2600 which means she can go back to %100 dosage. It's been a good 6 or 8 weeks since she has been able to be at this level. We will all be extra good about washing hands at home, and really consider where we take Emily and the risks of being exposed to sick people. This week we will see how it goes and if she can keep her levels up it will be good for her treatment.

Today I was thinking about Independence Day coming up this weekend. It got me thinking about what was going on a year ago. I remember we were going to be in the hospital for an in-patient high dose methotrexate treatment. Those were tough days, I have a picture of Emily on the roof top garden at the hospital, her hair was really thin and she looked much more sick than she does now. She's gone through so much this past year, but also come through so much and thankfully she is responding well to treatments and her body is holding up.

This weekend we are going camping at Big Basin State Park, which is just over the hill from us in the Santa Cruz Mountains off of Hwy 9. We are going camping with our friends the Scotts who we camped with last October. Emily is excited that her "best friend" Oliva will be camping with us. I will be thinking about our independence from the hospital this year as I enjoy the redwood forest.

Thursday, June 25, 2009

Lab results were good

Em had her labs yesterday and her ANC was in the 3000's on %75 dosage. This is a really good result, though they are going to keep her at %75 for at least one more week to be sure. All her other numbers were good too. I don't have much else to report at this time.

Monday, June 22, 2009

Great Father's day weekend

Emily finished up her 5 day blast of Prednisone this past Saturday. She did pretty well on it this month. Her behavior was pretty controlled and so was her appetite. She definitely ate more, but wasn't bugging us for junk food the entire time. She seems to be doing well on her %75 dosage and we will know more about that on Wednesday when she gets her labs results. My best guess is that even if her ANC is a little high they will keep her on %75 dosage another week. We had a really nice Father's day. We went out for breakfast, later in the day Haley and Emily each gave me a framed photo of us together. I also BBQ'ed some really yummy chicken for dinner, my Dad's "Super Chicken" recipe in his honor on Father's day.

This week the big news will be lab results Wednesday. I'll update the blog when I have some news.

Wednesday, June 17, 2009

Great results from the CT and Labs

Today we got the results of Emily's CT she took last week. The great news is she is still in remission. We were obviously happy to hear this. Both Tracy and I had a great deal of anxiety about the results but weren't really telling each other. So it lifts a lot of stress to have that out of the way. We only get CT's every 6 months so it's not something we get used to in treatment.

Emily's lab results were really good too. She is on her monthly Prednisone and her ANC was over 6000. Prednisone makes your ANC increase. Her other levels that we track looked really good too. We are going to increase her chemo to %75.

Dr. Link had a longer exam with Emily than normal, probably connected with the CT scan. About once a quarter we start a new cycle of chemo and this is one of those times. He explained that most likely we are going to stay on %75 dosage for a while because she has had trouble in each proceeding cycle. But if she is looking strong they will look at increasing again.

After her exam Emily got her monthly IV chemo.

This week Emily will finish out her Prednisone and take her daily chemo. We don't have anything else planned medically. She is out of school for the summer and is looking for play dates. We also have a community pool that is really popular with Emily this summer.

Wednesday, June 10, 2009

CT Exam and labs



Emily had her CT Scan this morning, along with her weekly labs. We have learned through experience now, how to coordinate the lab draw with the IV placement, so Emily only gets stuck once with a needle. Today her Synera patch didn't work on making her numb so the needle stick hurt, but she still did great and they got her blood for labs and prepped her for CT.

For a CT Scan you have to go through Admitting at the hospital, once that was done, you go to radiology where they take you to another waiting room, where Emily could drink her Contrast for the CT. They mix it with Gatorade and Emily doesn't seem to mind. We waited in the waiting room a good half hour, maybe a little longer, until they came in and brought us to the CT Scanner. They must just have one CT scanner at Packard because we have had the same once through treatment. Emily gets hooked up to her IV next. Then I leave, but Tracy opts to stay in the room and wears protection. I did once but don't anymore, there is no need for both for all of us to be in there. The scan itself it pretty quick, and we were done. I don't expect to get results until maybe next week at her physical exam, but we may hear something sooner, you never know.

We got the results of the labs and her blood is looking better. She isn't neutropenic anymore. Her ANC is 1962 as you can see below. We would expect a rise in ANC on %50 dosage and we have it. They are going to keep her on %50 dosage this week.
WBC 3.0
Hgb 12.9
Plts 307
ANC 1,962

Next week is her monthly IV treatment and Prednisone along with an exam from the doctor.

Saturday, June 6, 2009

Weekend away

Tracy and I did get away for our "mini getaway" in Las Vegas. It was a good time, we saw a good show, ate some amazing meals, relaxed, slept in, swam a little in the pool. I am really glad we were able to get away and don't regret it, but also being away allowed me to focus on all we have going on, and it was somewhat depressing. I don't think I was able to stop worrying about Emily the entire time, both short and long term about what will happen to her. I am happy we have one more weekend day to all hang out as a family.

This coming week Emily will be having her CT Scan. It's an anxious time for Tracy and I when we have these scans. Hers will be on Wednesday. She will also have a blood draw to check her levels. I hope her ANC starts to rebound on this lower dose and we can start to talk about increasing it in a few weeks.

Wednesday, June 3, 2009

Emily's levels are still too low, they are going to lower her dose

Emily was neutropenic again this week with her ANC at 490. She has been low for so long now that her NP talked to Dr. Link and he wants to lower her dosage this week back down to %50. Let's hope that she is able to over come whatever virus she has had here so she can get back on track with her chemotherapy at %100 dosage where it really needs to be. Next week she is going to have a CT Scan which I am also really anxious about.

Tracy and I are going away tomorrow for two nights in Las Vegas which we are really looking forward to, but it's mixed feelings for me at this point because Emily is neutropenic, since it increases her chances of being hospitalized. My Mom is going to watch them and for a night, and then Tracy's parents for the next night. They are all capable of caring for her, and want the best, but they also don't know as much about Emily's care as Tracy and I do, so I fret about going.

Wednesday, May 27, 2009

Emily's Wednesday, still moderately neutropenic

Emily had her labs today and her ANC is still pretty low, around 580 which is moderately neutropenic. That means we have to keep our eyes open for fever ever more than normal. Haley has been sick with a cold, so there is that risk that Emily will get it and then have issues. So far things have been going fine though. She still has some sniffles and a little cough. Overall her attitude has been up-beat and she has been going to school. Today she went on a field trip to the Tech Museum in San Jose. Her class took the light rail to get there, she was really excited about it.

They are going to continue Emily at %75 dosage this week. They are talking about changing her over all dosage if she can't get back to %100 here. They explained to us that Emily has not gone 1 full cycle (roughly a 3 month period) without having to have at least some reduced dosage, so a total reduction might be needed. We are going to hear more about it next week.

We don't have anything else planned medically this week, and will probably take it easy over this coming weekend.

Wednesday, May 20, 2009

Emily's I.V. chemo went well. 275th post in the blog.


This is the 275th update to Emily's blog. Wow it's been a real journey hasn't it? I went back and re-read the the first two months, and there were some things in there that I almost don't want to remember. Actually I am really happy with the blog, it's given me a chance to express how I feel and to also feel all the support of the people who are following Emily's courageous battle with cancer.

The picture above was taken tonight at Open House at Country Lane School.

Today went well. We had I.V. chemo, labs, and a physical exam. The Exam came first, and Emily checked out on all the things they check her for. A typical exam starts with any question or concerns we have. Then they ask Emily a ton of questions, ranging from how she is feeling to what she is learning in school. Then they get her up on the exam table and they check the sites in the body where we all have a lot of lymph nodes. The neck, stomach area, pelvic area. They listen to her lungs and heart. Then she has to take at least 4 steps on her heals and 4 steps on her toes. The heal and toes exam is to asses neuropathy which the Vinchristine can cause. Early on in treatment you'll remember Emily couldn't walk and needed a wheel chair, neuropathy was the reason for that. It's a side effect of her chemotherapy. Today she checked out fine, like she has for the past several months.

After the exam we get moved into the Day Hospital, which is a part of the ! North Unit. Here is where they take Emily's blood sample and give her I.V. chemo. She has a really good vein on her left hand that we save each month for the I.V. needle. Our nurse did a great job getting her vein on the first try. I think these 1 North nurses are amazing they have to stick kids with needles all day, and they do it so well. The hardest part if accessing the vein and once that is over the blood sample and Chemo go really quick. Today we hung around about 10 minutes after the I.V. because Emily got a visit from a dog that was in the clinic today to help brighten up the kids day. When the pet therapy animals are on site, you can sign up for a visit, which we had done.

Stanford/Packard are really quick with the lab results, the Cancer ward has their own lab which really expedites things. By the time we drove home we had a voice mail with the results. Emily's blood levels were good and they moved her from %50 dosage up to %75 dosage which makes us really happy! let's hope she can stay away from colds, she really needs to stay on higher doses, that even got brought up at her exam today.

Saturday, May 16, 2009

Day in SF

We went up to San Francisco today and it turned out to be a really good day up there. We drove up after breakfast and a slow morning at home. It was around 90 degrees with no wind in San Francisco which is very unusual, it was almost too hot. We took the girls out on a ferry ride to Saucalito in the afternoon, which is just across the golden gate bridge. It was a really nice day to be out on the bay, maybe the only slightly cooler place today, it was so hot. We spent a little time in Saucalito, and then caught the Ferry back to the Ferry building in S.F. We had dinner in the ferry building and made our way back home. The girls had a great time, and so did Tracy and I.


Emily is feeling great and her cough is all but gone. She has a ton of energy, and she's always having fun with her little sister. This coming Tuesday she will start her 5 days of Prednisone. On Wednesday she will have her I.V. chemo and her exam from her doctors.

Thursday, May 14, 2009

Emily's lab results and an ask for donations for research.

Emily had her labs drawn yesterday. It was a tough lab draw for her as her favorite phleubotomist wasn't on call. They were able to get their sample of course, it was just hard emotionally for Emily. Stanford does a great job at continuity of staff for their patients so you really notice when someone is missing.

Her lab results were good, putting her ANC near 2500, which is in the range we want it. However remember that's in the range, but only on a %50 dose of chemo. That means Emily is still working on getting over her virus. Per the protocol she needs to stay on %50 dosage for one more week, and then we will step up to %75 dosage for 2 weeks and then finally back to %100 dosage in about a month. It's understandable why they need to keep the dose reduced, but it's also really frustrating that we need to. If you read the literature on being cured and reduced risk of relapse, it's important to be on %100 dosage as much as possible, and the past 2 months she has rarely been able to take that much. As much as anyone tells me things will be OK, I know too much at this point to not worry a bit about this. Next week is Emily's prednisone and IV chemo treatment on Wednesday.

Many of you may have received an email from me this week, for those of you who did please excuse the repeat ask here. A friend of mine is riding the Leukemia and Lymphoma Society Team in Training ride around Lake Tahoe in early June. He is doing it in honor of Emily and I am trying to help him with fund raising. The money raised goes to fund important medical research for Leukemia and Lymphoma. It's important, maybe people in the future won't have to go through what Emily has gone through. I can say as a parent, a %70 cure rate is OK but certainly not high enough for Tracy and I not to constantly worry. Please donate to Mike's cause if you can. We'd love to see some donations made in honor of Emily. Here is the link to donate, any amount you can.

http://pages.teamintraining.org/sj/ambbr09/mgolliday

Monday, May 11, 2009

Emily just deals with it

I forgot to include this story when I posted last night.

Yesterday afternoon I took Emily and Haley to the park to play. They were playing together in the sand pit, and after a few minutes two other girls came up and started playing next to Emily. About 5 minutes later I heard one of them say to Emily with a very mean face, "Your hair looks like a boy's haircut." Emily responded very directly to her by saying, "That's because I have cancer." The girl responded back, "What's that?" and Emily replied "It's a disease I have that could kill me, and the medicine I have to take made my hair fall out, but it's growing back now." The girl didn't really know what to say, and Emily looked over at me, trying to make a smile and shrugged her shoulders and continued to play. A few minutes later Emily was playing with the girls who had been making fun of her.

I am so proud of her for sticking up for herself, and ultimately not backing down and running away, but instead befriended them. I asked her on the way home how she felt about it and she said that the girls had apologized while they were playing and she thought they were nice. I don't think I'd have the guts to do anything close to that when I was a kid, I remember crying because someone made fun of a shirt I wore once, and to think of Emily dealing with being bald and now with short hair is just a testament to how strong of a person she is. I constantly learn from her.

Sunday, May 10, 2009

Emily seems to be getting better

It looks like the reduction of chemo, taking it easy, and finishing the course of anti-biotics is paying off, Emily's cough is much, much better. it's not completely gone, but she's not coughing herself to sleep anymore. She finished her medication for pneumonia last night and now is just on her reduced chemo dose. She will be having her blood checked this Wednesday and we will find out if they will increase her dose. Emily is looking forward to getting back to school tomorrow.

This weekend was Mother's day and Emily was really excited about it. She and I went shopping for Tracy on Saturday and Emily wanted to get her a bottle of perfume. This morning we gave it to Tracy and Emily and Haley "helped" make her breakfast. The original plan was to serve it to Tracy in bed, but she got up before Emily so we just had it at the table as usual. Tracy had to work this afternoon and evening so we only had Tracy home for part of Mother's day.

Wednesday, May 6, 2009

Cough returned vigorously last night, chemo reduced, chest X-Ray

The past two nights Emily hadn't been able to go to sleep because her persistent cough had returned, and it was/is getting worse. This really made Tracy and I concerned that the pneumonia either wasn't getting better, or even worse that something else was going on. Today was her lab day and we insisted that Emily be seen by her NP and or Doctor after her lab draws.

First result from the blood test is Emily is borderline neutropenic with an ANC level of 540, which is about as low as you can get without having to cut chemo dosage all together. Starting tonight she will be a on %50 dosage. That's discouraging because she's been on so many reduced doses in the past 8 week, and ideally patients need to be at %100 dosage. There isnt anything we can do about this, but hope she starts to get better so we can just be on full dosage for the summer. From here we will probably be on %50 dosage for 2 weeks, then %75 for two weeks and then finally and hopefully back to %100 dosage. It worries me that this keeps happening.

After her labs she saw both Dr. Link and Karolina or NP. She sounded clear but they wanted to do a chest Xray to see if the pneumonia was clearing up. What they told us was if the pneumonia had gotten worse, or was the same as it was in the ER the other week, they would probably switch her to another antibiotic. However, the great news was her pneumonia was much smaller than it was a week and a half ago when we were in the ER, so the antibiotic is working. Her cough is just something we need to live with, and try not to worry about. Given the extra exam and chest Xray, Tracy and I can both rest assured that she's OK.

My opinion is the cough is related to the pneumonia but since she dropped to near neutropenia her defenses are too weak to fight the cough, so reducing her chemo SHOULD help with the cough and allow her immune system to kick the pneumonia and cough to the corner. Let's hope that happens. So while it's hard to reduce the chemo from a cancer point of view, it's probably a good thing holistically. It's all related. Blood cancer is so tough to manage, isn't it? I haven't talk with Tracy about it, but I think we may want her to stay home from school at least for tomorrow to get her levels back up.

Monday, May 4, 2009

Emily is back in school, getting better every day

We thought Emily's cough is to the point where we could send her back to school today. She is only coughing at night, and even then it's getting less and less frequent. She had some apprehension about going back today after a full week off, but once she got there, I am sure she is doing fine.

Her energy level is pretty good, however she and I went for a walk to the shopping center on Saturday for some coffee and hot chocolate. On the way home she had to stop and sit several times. I do this walk with her a lot and it was unusual for her to take so many breaks. Then about 20 minutes after we got home she came to me and said "daddy remember you asked me to be honest with you if I am ever not feeling well?" to which I said "yes, sweetie what's wrong" and she said, "I am having a hard time catching my breath." I was worried but since I knew she had pneumonia, it was probably the reason. She also complained about cramps on her left side, which I also nervously passed off as the pneumonia. Her cramps come from time to time, and really scare me every time she reports them. The reason they scare me is before she was diagnosed she complained of really bad cramps, which looking back were the formation of her tumors. Cramps can be normal, so it's one of those things that I try not to worry about, but knowing what I know, it's hard not to.

This week she will have a lab draw on Wednesday and right now that's the only thing that is scheduled medically. She remains on %100 dosage of her Chemo.

Friday, May 1, 2009

Emily is still doing great

Emily has been home from the hospital for 2 nights now and she is still doing great. In fact she has bounced back to her normal self almost completely. Her cough still remains from time to time in the night, and last night she coughed so hard she woke us up, but after some water and a little talking she was able to go back to sleep. Tracy was a little concerned about the cough so we called the clinic today to report it, but they assured us that Emily was on the right dose and this would just take a little while to clear up. When the cough is all gone she can go back to school, hopefully on Monday but we'll just have to wait and see one day at a time. During the day the cough is pretty much non existent though, which is a large improvement over the past several weeks. Looking back, she had had the cough for a while leading up to the pneumonia diagnosis. She is really bored having to stay at home and wait this out. Even though the swine flu is very over blown in the media, any flu is bad for Emily so we are keeping her away from crowded places for that reason too. So on this rainy day it would have been fun to go to a movie, but a movie theater full of people is one of the last places you want to be if you want to avoid a virus.

Last night Tracy and I went out on a "date" while Grannie and Grandpa Steve stayed home with the girls. We had a really fun night out together, having some drinks and then a nice slow dinner up in Mt View. Tonight will be the first night in many that we aren't going anywhere and all the family is home, which is really nice too. It's the first time in a long time on a Friday night I am looking forward to doing absolutely nothing.

Wednesday, April 29, 2009

The amazing Emily beats the odds again

Emily was discharged from the hospital early this afternoon ! She is feeling, looking, and sounding much better than she has in a while. Her pulse has normalized, her fever is gone, and her cough is much better. The cough is still there but it's so much better than it was leading up to the pneumonia diagnosis. Emily is going to be on antibiotics for 10 more days (I think) and will restart chemo tonight at %100 dosage. Today her anc was down to 2000 from 7000 yesterday so her white blood cell count is back in the range we like to see on therapy. The orders are for her to take it easy until next Monday and then she can likely go back to school. Given this swine flu scare/epidemic we are going to watch her exposure to sick people the best we can. Swine flu gives symptoms like viral pneumonia and having that on top of bacterial pneumonia wouldn't be good, to say the least. She ate dinner last night, really the first food she had had since Sunday, so that's a great sign too.

Tracy and I are so grateful for all the support you all have given us these past few days. We were really scared when this first happened and she ended up being hospitalized, every time we go through something new, the stress level is extra high and knowing people are thinking of us really helps.

I am working today so that part is back to normal. Both Tracy and I are really sad we are missing our trip to New Orleans, we would be in the air right now, but we know we made the right call staying home.

I am sure Haley will be happy we are all home too, she's been all over with different people watching her the past few days and while she can't express how hard it is on her, we know it is, and having big sister home will make her extra happy.

I will keep you all updated more regularly over the next few days as this pneumonia chapter resolves itself and we are back to our boring every day lives.

thanks again

Tuesday, April 28, 2009

Things are looking up, really likely a discharge tomorrow

They are preparing Emily's discharge papers, and baring a turn for the worse she'll be out tomorrow and even resuming her chemo. The main reason for keeping her was the high fever and low O2 saturation levels in her blood. The O2 saturation is already back at an acceptable level, %97 (she is usually %99 or %100 but yesterday was at %90), and her fever is going away, the last temp read was 99.7 degrees, so a tiny bit elevated but lower than the threshold for keeping her, as long as it doesn't spike again, it's very likely she'll be sleeping in her bed by tomorrow night ! At this point I plan to sleep over in the hospital with her tonight and head right into work from there, and meeting the family when I get home.

I am home for a nap before heading back in for tonight.

I am feeling much better that she's going to be back on track very soon. Emily is SO tough, I know she knows she's going to be fine, it's Tracy and I who worry most.

Talked with the doctors

The Oncology team made their rounds later this morning and I had a chance to meet with them and talk about what's going on with Emily. The good news is once she breaks her fever she can go home, and we are all hoping that will be tomorrow. She doesn't need to have a clear Chest X-Ray to be discharged, the Doctor explained that the chest X-ray will lag behind the actual progress of the cure, so in 10 or so days hopefully she will have a clear Xray. She will likely resume chemo tomorrow and be sent home with oral antibiotics. We are all cautiously optimistic it will happen.

Today my Mom came by for a visit with Emily which she liked very much. Since Emily isn't a big fan of hospital food, my Mom is going to make her some Mac and Cheese and a an Artichoke and come back down around dinner time to bring her a home cooked meal. Our good friend Erik brought her some Jamba Juice which Emily really likes and she's enjoying that now.

They haven't taken her temp in a while but she feels much cooler than earlier so maybe this is starting to break and the pneumonia is getting kicked out of her system. She also seems to be coughing a little less, but you can still hear "gunk" when she does.

thanks everyone for the positive thoughts for Emily and our family.

Tuesday's update from Packard


Emily is still in the hospital, and this morning had a fever of 103. They are treating the fever with some Tylenol and she is a little more comfortable with it and the fever lowered to 101 after taking the medication. We got some results from tests yesterday and we are happy that she tested negative for RSV and Swine flu. We were a little worried since we had been in San Diego the US epicenter for this swine flu outbreak that she may have contracted it, but at least we don't need to worry about it, for now. She is still on 2 antibiotics for Pneumonia and I thought she looked a lot better when I arrived this morning, much less red in her face.

She is in a total isolation room, meaning anyone who visits or comes in to treat her has to wear a mask, and the medical staff wears an extra gown. She also is unable to leave her room, so she can't go up to the play room or go on walks. The play room staff knows of this so they sent someone down to bring Emily some art supplies. She is pretty much just sitting around and watching TV with lack of much else to do. She keeps telling me she misses school, especially Math, so we are going to have her teacher drop some school work by our house for her. It makes me so happy she actually misses doing school work, cause when I was a child I would have done anything not to have to do it. She's just a fighter and am amazing girl who is making the best of her situation and wants so much to just live a normal life, I wish she could.

Today I think the plan is to just be medicated and to wait until tomorrow and do another chest XRay to see if she can go home, but I am not certain they may do some tests today, I haven't seen a doctor so far. The nurses are all the same as when we used to spend much more time here, so at least they are all familiar faces and everyone LOVES Emily so they stop in to just say hi, even if they aren't assigned to her directly. If you have to go through this it's nice to have friends on the inside who care about your child. Packard is really a great hospital, even though some people like to slam Stanford, I think if you are ever faced with something serious you'll gain a new level of respect for the people who work here, even if you have to deal with some B.S. from time to time.

Last night when I went home I felt really sad, I don't want to be overly dramatic but I can't help but worry about what's going on here and I am fully aware of the seriousness of the situation. I feel much happier being here with Emily, so I can care for her and be part of what's going on, it gives me less time to think of "bad" outcomes. Today I am staying with Emily while Tracy gets some sleep at home. this afternoon Tracy will come back for a few hours, and then I plan to sleep here with Emily tonight. One GREAT thing about the new Oncology floor is private rooms and a full sized bed for the parents ! No more "sleeping chair" hell. I have two laptops so I leave one here and one at home so I can stay connected. While Emily watches TV I blog, Facebook, or just surf the net.

I will update this afternoon or evening.

Monday, April 27, 2009

Latest Update : They are keeping her for at least 48 hours.


After a roller coaster night and morning they finally decided to keep Emily in patient here at Packard for I.V. antibiotics and observation.

This all started last night around 2:30 in the morning. Emily woke me up and told me her tummy "really hurt". I could tell by the way she looked that she was going to throw up so I helped her into the bathroom. She threw up and we all went back to bed. We had given her chemo around an hour earlier and thought it was just a side effect. Then around 3:30 am she woke us up again because she needed to throw up. This time Tracy observed that she had a fever. We were concerned because we had been in San Diego about a week ago, and that's where the swine flu had spread so we were worried she could have swine flu. We called the Oncologist and she told us that if we were worried we could come into the E.R. for a work up, so Tracy and Emily came in, and I stayed home with Haley. I will be honest that I really didn't think anything was going to be wrong, because our last few trips to the E.R. have been uneventful. Around 6:30am Tracy called me to tell me they had diagnosed Emily with Pneumonia, about the last thing I expected to hear. She had a fairly large area effected on her left lung on the lobe. I kicked things into gear and made arrangements to drop Haley with my Mom so I could join Tracy and Emily at the E.R. Just after I dropped Haley off with my Mom, I got a text message from Tracy saying they were going to give her I.V. antibiotics and send her home, so it was sounding like it wasn't going to be as serious as we thought. I guess it would be around 8:30 am at this time. Then between 8:30 and 10:30 the doctors were going back and forth about whether she would be admitted or was going home. Her sugars in her blood were low, her potassium was high, and her O2 saturation was on the low side. All of these factors plus the pneumonia ultimately made them come to the conclusion that she needed to be admitted for 48 hours. So, here we are in 1 North at Stanford in an isolation room.

As nice as the new Oncology floor is, we really hoped to never have to be in-patient in it. It is nice, all the rooms are private and Emily is feeling pretty well, all things considered. Since she no longer has her port, she has an IV and is having to deal with additional needle sticks, but she is being very brave and it's going well. Right now as i type this she is eating Chex Mix and watching Zach and Cody on the Disney channel.

Later today the Oncology team is going to do a full exam on her to really assess where we are and how long she may need to stay.

I talked with the Dr. in the hall and asked him what the drill was and what was going to happen. I also asked him if he thought this may be a relapse of the lymphoma. Of course he couldn't say much definitively but here is what he said. First of all it's great news that she is not neutropenic, what that means is Emily has some white blood cells to fight this on her own. She is also on two I.V. antibiotics (Vanco and Ceftriaxone) which they can give large doses of since she is here in the hospital, which should really knock this as well as it can be. He characterized her pneumonia as "fairly large". He said he suspects it is not a relapse of Lymphoma but can't be totally certain, but said since she is in maintenance he really doesn't think it's her cancer coming back. He suspects is bacterial and not viral pneumonia so can be treated with antibiotics. He seemed to be pretty calm about this and told me "it's not uncommon to see this" and his voice cued me to not worry too much.

So, that's where we stand, hopefully she will bounce out of here quicker than expected but right now it's wait and see.

Needless to say, Tracy and my vacation is on hold, in fact Tracy is not going for sure, and I am pretty sure I need to cancel as well. We were going with a group for a friends 40th birthday and that's the only reason I am even considering still going, but I know I would worry the whole time, and if Emily weren't getting better I would kick myself forever for not being here.

Last update until we know more

They keep going back and forth about if she needs to stay in the hospital or not. She definitely has pneumonia, a pretty large on on her left lung lobe. She sugars are also really low, and they are not sure why. She also has low O2 saturation, meaning she can't get enough oxegen on her own, it's borderline. So we are letting the doctors in the E.R. work with the Oncology team to determine what we do. Tracy and I would prefer they keep her over night but we'll see what they decide. Since the news keeps changing i am going to wait to blog until we know a lot more.

Emily will not need to be admitted

I am here at the hospital and they have decided that since Emily is not neutropenic they are going to give her I.V. antibiotics and then send her home with antibiotics for home. This may not be AS serious as we were thinking.

Emily was diagnosed with Pneumonia early this morning.

This is still developing so I don't have many details, but Emily woke up throwing up around 3:30 this morning. She also has a fever and a mouth sore. Given all the scare about swine flu and having just been in San Diego we brough her into the hospital.

While I was typing this Tracy called me to tell me the chest xray says she has pneumonia, which is VERY serious. I am heading into the hospital to be with them. She will be admitted until she clears this. I am so scared.

I don't think we are going on vacation this week.

Thursday, April 23, 2009

I have eased my worry

I talked with Emily's NP today and she told me she isn't concerned about the high counts this week. So, I will stop worrying as much about it. you could tell in my post last night that I was obsessing on her WBC count, but with Prednisone I am told they see these high levels now and again.

thanks for the kind messages that you sent with concern.

Moving onto positive thoughts and looking forward to the weekend.

Wednesday, April 22, 2009

strange / troubling results from Emily's labs

Today Emily had her IV Chemo at the hospital. She also had her physical exam, which was pretty normal. Emily may have pink eye so they prescribed her some eye drops to knock it out. She also has a persistent cough, but it seems to be all in her upper respiratory tract. She still has some fluid in her ears too but the infection seems to have gone away. After her physical exam she got her IV chemo and blood draw. It went really well. So the hospital part went well.

The troubling results are the lab results. Emily's white blood cell count was really high, at 9.3 and as a result her ANC is 9000 which is through the roof. Why that is, is unknown and troubling to me. Her NP said it could be because of the eye or the cough. Prednisone also raises white blood cell count and ANC levels too, and she's on her Prednisone this week. It's a bad sign if ANC is really high, so I am worried that something else is going on. It's scary when something new happens, sometimes it means nothing and sometimes it is a real concern, I just don't know which this one is. This is only me worrying and nothing the doctors said this week, I just know what the levels should be and know this is way out of range. We won't really know until labs next week, so I will be concerned all week and just hope that next week the levels come down to a more normal level, which is around 2000. They also increased her 6mp dose to help suppress her levels. I hope I am worrying for nothing but wish I didn't need to at all.

This week we don't have much going on, just resting after last weeks vacation. Next week Emily will have her labs on Tuesday and Tracy and I plan to go on a vacation to New Orleans on Wednesday and the kids will be staying here with their Grandparents. I hope her levels return to normal so we dont have to worry while we are gone.