Hello all :) Coleen here :)
So I found a few minutes today. This will be short..more to come tho :). Ella is about to start her 4th round of chemo this Thursday. She was supposed to have started last Thursday but her numbers were not quite where they needed to be yet. No cause for alarm..they just delayed by a week to make sure her body was up to the next round. I'm going to summarize a bit here because I have to take Ella to the hospital for labs/clinic soon.
Good news...
-Ella is alive :)
-Ella has made it thru 3 of the 4 mixtures of chemo that she will be receiving and still doesn't have an NG tube (a tube inserted into her nose that remains there permanently for feeding/hydration/medication administration). We were told that she'd likely have one early on (after the first round).
-Ella is still VERY vivacious (when she recovers from her chemo sessions) and excited about her treatment being over and being able to "go to school, gymnastics, karate..anywhere I want!"
-We are halfway thru her six rounds of chemo prior to her bone marrow transplant.
Exciting news....
-While Ella was in patient initially, the hospital had a film crew come in for their most recent ad campaign and film for 2 days all over the hospital. They filmed Ella riding a tricycle while "connected" to her "pole". (her dad is off to the side running with her :)). If you google Seattle Children's Hospital tv ads you will find their most recent commercials which seem to be running constantly out here. Ella is in the 30 second and 15 second spots :).
Bad news...
-Chemo sucks....soooo much. Poor Ella was down to 18 kgs, which (for us Americans) is barely 40 pounds, after her last round of chemo. Cisplatin can die in a fire as far as I'm concerned. We had her on anti nausea meds every 1-2 hours round the clock from her first day of chemo (yes, even at night) and she was still having alot of breakthru nausea the whole time she was in for her chemo and for 5 days after we left the hospital (for those of you that are counting, that's round the clock meds for 10 days straight). We had to end up staying one extra day (torture) because her nausea was so bad.
-The time between Ella's second round finishing and her third round starting almost killed all of us. They had told us it would be brutal, and it was. She had to get a shot every day, EVERY DAY, of a substance that was boosting her white blood cell count in preparation for her apheresis (removal of stem cells from her blood to be used later to give back to her for her bone marrow xplant). She was still nauseous the whole time and had to be on regular doses of Zofran (we love Zofran by the way../hug Zofran). We took Ella to Children's every day ..she rode in the car the whole way knowing she was going to get "poked" and her face showed it...but she rarely cried..she just looked incredibly sad. Looking at her in the rear view mirror threatened to shatter my soul more times than I can tell you all.... She had labs and clinic visits every 3 days during that time and we were all watching her numbers carefully for the moment to harvest her stem cells to come. She ended up having to have 2 transfusions 2 days before her harvest, platelets and red cells. But her numbers, the day she DID get the harvest done, were higher than any the apheresis nurses had ever seen :). They needed to collect 5 million stem cells from her to have enough for her later bone marrow transplant but they don't keep little ones on that machine for more than 5 hours. So, of course, we worried. BUT, they ended up having her on there for 3.5 hours and called us 3 hours after she was done and said not only did she not have to have a second collection, but they had collected 116, yes one hundred sixteen, millions cells :) Those were separated into 4 bags and stored. One bag will be used for her transplant in about 3 months, the rest will be stored forever should she need them. Of course her dressing on her hickman line had to be changed every week still and yeah..it was absolutely exhausting....but, it's done. Once Ella's nausea subsided from that (two Saturdays ago) we really have just tried to rest and recuperate.
Ok so I will go into more detail soon :)
BUT, very important to say some thank yous...I will let Dave do his own special ones. I'd like to thank my brother Chip, my mom and my brother Matthew for getting here on the spot. And especially to Chip for dealing with all the horrible crap he's dealt with with his own health for the past year and for still making Ella and I his priority and being here when I(we) needed him more than he'll ever know.
I'd like to thank Small World Montessori and the families there for their undying support. Christina Greene, Noel Stockman and Miss Lissa are the special stars in this thank you. Christina, thank you for not going away...thank you for not letting me put you off by never answering the dam phone....thank you :). Special thank you to Ella's class, she loves you all sooo much. Thank you ALL so much for the love you've shown our baby. Mr. Brian, Ella goes to sleep most nights playing the CD of the songs you recorded for her. Music is her passion....thank you for sharing that with her :). I understand one of you also donated blood in Ella's name and that a blood drive at the school in honor of Ella is in the works. You are all my heros :)
I'd like to say a special thank you that some of you may not understand. I play an online video game called World of Warcraft. I'm in a sizeable "guild" in this game. Altho I have not met these people face to face, they have been there for me in so many ways as this insanity has unfolded and quietly shored me up and given me strength thru their ability to make me laugh and get me out of my own head for awhile each day :). Cindee (Tiny), thank you for cutting your hair and donating it to Locks for Love in honor of Ella (and never saying a word publicly about it, so I am, right now :P). Rage, thanks for getting angry that the world can do this to a little angel. Micky (Elo), thank you for being so amazing and doing something that is SOO what we need for Ella right now and coming up with it, running with it and handling it. You get it, thank you :) /hug. Imma, thank you for always, ALWAYS being there to let me talk to you without me having to worry about the "ulterior motives" /wink. /hug. Shald, thank you for my "chopper" and for being there thru so much of this for me. Shunahe...your spirit lifts me up..every time I see you...thank you..and NOICE singing voice there buddy ;). To the chix, you know who you are :). My girls have my back. Verah, Siryn, Shadow, Kaleri.../love to you all :). Thorge, Gal and Mite, thank you for having the sharpest of wits, caustic, hilarious jokes and for seeing the humor in the dark side. Special shouts to Wramphist and Darvenn for always coming back ;). And a big shout to Sleepless Knights...you've all been there for me in ways you'll probably never know. Thank you :).
Thank you to all the ladies at Other Mother's (my old job) and especially Shirley and Laurieanne....that book is helping me Shirl..thank you, and Ella loves her tutu :). Thank you to Roxanne Meehan and the members of her church for the amazing care package you sent Ella. Thank you to Steve, Dave's friend from work, who took our cats and whose family is giving them love while we focus on protecting Ella and helping her get well. Thank you to Dave's sister Val for coordinating dinners with her coworkers to be frozen and brought them to us for that first 32 day hospital stay (and for being El's loving auntie Val :)).
Last but MOST certainly not least AT all! Thank you to the doctor's, nurses and staff at Seattle Children's Hospital. You saved our baby's life....how do you thank people for something like that. /sigh. You're amazing folks and thank you for tolerating my headstrong manner so often, I'm a fighter, especially when it comes to those I love..and most of all, for my one and only baby. Thank you for caring for her :).
So many people to thank...and yet we're so caught in the maelstrom still.....please forgive me if I have neglected anyone. My brain is pretty well fried right now :)
Tuesday, April 14, 2009
Thursday, February 19, 2009
Been awhile....
Hey all,
Coleen here this time. Ok, trying to catch everyone up from where we left off. I think I will summarize where we are now, what we know for sure and what we're told will come soon in the future.
Ella was given her first round of chemo from Sat., Jan 31-Wed, Feb. 4th. Ameding our earlier description of the cycles, Ella will be chemo'd for 5 days, the first of which starts the timer on a 21 day cycle til the start of the next chemotization (yes I made that up). During that 16 days between, she will, theoretically, be home. If she so much as gets a slight, lasting (full day or overnight) fever, she will be admitted. Many other health issues, almost ANY other health issues, can be cause for immediate readmission to the hospital as well. While she's home, she will be going back to the hospital 2x per week for "clinic" visits. Blood is taken at these visits and immediately tested for ANC levels to see where she stands. 0 means she has no ability to fight any infection/virus, 500 or so means she can have someone over to the house but no public (malls, grocery stores, school, library, museums, any where with more than one other person...) contact. Then the levels go up from there for when she can actually go to a store or a park and play freely. She will have a whopping 2 days, potentially, since we've gotten home, that her counts will be high enough to safely have visitors over /sigh.
Where we are now. Ella has been home since the Friday after her chemo finished (Feb 6th) and has not had to be readmitted. She's given us a few scares with mild fevers, mouth sores and a sore in her ear but so far so good. We are scheduled for a final pre-chemo clinic visit on Friday (Feb 20th) and the second round of chemo to start for El on Monday, Feb 23rd. We were warned, when we first took her home, to be prepared for her to "pop" a fever (the "in" term for onc patients :P) and we'd be right back in. Also, we were told she'd most likely be exhausted, possibly have no appetite etc and maybe need an NG tube again. She came home and was full of energy this whole time except for about the last 3 days (not today but the 3 previous days) when she was fighting something off we think. I think the biggest loop Dave and I were thrown for was when we went to her first clinic visit the Tuesday after we came home and her counts were at zero already. We'd have had no way of knowing from Ella! She's had a pretty voracious appetite, especially when we first got home. Her counts have stayed at 0 until this last visit we had on Tuesday, 2/17, when it went up to 88. Yes..only 88..a healthy persons is somewhere around 1000 I believe, if I'm recalling that correctly. So imagine...and still, she shines :).
What we know. Ella has high risk neuroblastoma. There is a 40% survival rate from this type of cancer even with the very best known treatment being given. And from what Dr. Park has said, it's the cancer that kills those that don't make it..not the chemo. We have had two very serious, very intense "heart to heart" conversations with Ella's care "team" to talk about why the recommendation is for our daughter to go through the same treatment as a child that showed up fully metacisized with tumors. Ella's bone marrow ended up showing clear, her isotope tracer (MIBG) was clear and her bone scan (scans the exterior of all the bones in her body) was clear. So to us, as lay people, she had a tumor, it was completely removed, two lymph nodes were removed, one of which was right on the tumor so that makes sense that it was affected and the other was far enough away to cause concern when the cancer cells were discovered in it. But it was removed, and no further evidence of disease has shown up anywhere in her body. We were not comfortable with the answers from the first meeting, mostly because, as I figured out later, our questions were not formulated properly. So our most recent meeting, on Friday of last week, was to get to the hardcore and it was just that. As hardcore as it gets. Dr. Park basically told us that Ella shows 5 different "markers" which lead them to the recommendation of blasting her with the hardest stuff they have. They are 1. The fact that she's 5 (most neuroblastoma's show up in 18 mo. to 2.5 year olds or younger and older children, according to Dr. Park's research of 8000 children worldwide over the last 20 years with neuroblastoma, older children's tumor cells do NOT revert to a benign state on their own, as they very often do in children under 3). 2. Her tumor bled, leaking blood with cancer in it into her abdominal cavity. 3. She has that N-MYC gene in abundance in her tumor cells (Dave discussed this in one of his earlier posts). 4. Cancer cells were found in the abdominal lymph node that was removed (Dave talked about this earlier as well) and 5. She had heightened, sustained LDH levels. The blood leaking into her abdomen and the heightened LDH levels were both things Dave and I JUST heard about at this meeting on Friday and we were pretty unhappy that no one had mentioned those things to us earlier. I'll let Dave talk about how apparently rare we are as parents in the way were handling/responding to this situation :).
At one point during the conversation, Dr. Park became clearly uncomfortable as we were being very smart and firm with our questions and our need to understand before we would be willing to allow the recommended treatment to continue on Ella. I was elated. She looked at me and said "Look, I would NEVER recommend that Ella be put through this if I thought there was any other way to treat her and still give her the best shot at the best outcome". That was what I needed to see, that discomfort. I needed to know my daughter was not a lab rat or someone's ticket to a fellowship at Oxford, or better yet, the key to some funding source opening up. Cynical you say? You better believe it :). I needed to know that she had gone through great angst and read and re-read Ella's information and her own research and that she had been up a few nights at least, fighting with herself internally before she came to this recommendation. Because, as she said, Ella (as seems to be the case with my whole damn family's health issues lately) keeps getting put in the rarer and rarer category as you look deeper into her case. And when I say rare, the numbers of cases she has from a pool of 8000 kids over the 20 years that are "similar" to Ella's is a whopping 3-5 kids...ever...yes, 3-5 other children. So she is not cookie cutter by ANY means. Ergo, everyone involved needs to understand this is EXTREMELY complex and decisions are being made based on the data that does exist on Neuroblastoma risk markers in general and alot of instinct. The art of medicine is being applied heavily here.
I will go into some other things about learning "flush lines" and administer meds and all that crap on a later post. Suffice it to say, you become real savvy, real fast about how to do many things medical that you sooooooo could have gone your whole life knowing nothing about :P.
What the future holds....Well the first answer is who knows. The second answer is that this will be an especially insane month for our family with what will be happening. El is scheduled for 5 days of chemo starting Monday, home on Saturday most likely and then will be back in possibly 7 -10 days later for her "stem cell collection". They will basically be hooking her up to a machine developed at the Fred Hutchinson Cancer Center that will pump her blood out of her body, put it thru this machine which will collect her stem cells from the blood and pump it right back in again. And if that sounds scary to you..I'm with you. In order to do this, we are told she "may" (which usually means will, we've found) need a femural line put in her leg as one of her current tubes in her Hickman line is probably not big enough to handle the volume of incoming/outgoing blood for this procedure. So, in essence, Ella would need to be put under for inserting the line, removing the line and on one other day this round, be put under again to do her next round of MIBG, CT scan/possibly bone marrow sampling. She will start receiving daily shots (no, no other way to do it) starting on Mar. 1st and going for 14 days. This shot will be to stimulate production of her stem cells and there is a special team that comes over from "the Hutch", El's own nurse even, to do this procedure, which is obviously inpatient. She will NOT be put under during the collection process were told but will instead, need to be very still for like 3-4 hours as I recall. This, will be, interesting....
So, our calculations, since the femeral line insertion would be an inpatient surgery which she'd need a day to recover from (inpatient) before they could start the collection (which may take 2 "collection" processes to complete over 2 days), are that Ella will spend possibly 7 days this month (10 is optimistic) out of the hospital. 21 days total - 6 days of chemo(5 plus one recovery day)-2 days of line insertion/removal-2 days of stem cell collection - 1-2 days of ct scan/MIBG/bone marrow sample leaves you with 10 days at the most. Basically, once she finishes her testing and stem cell collection, it will pretty much be time to start her next round of chemo. By the way, it's easy to type all of this but ALL of it is dependent on Ella's "counts" (markers in her blood tests). Certain things can't happen til certain markers are met so this is all nuts because we have to take it pretty much day by day to see when we will be doing what this month.
So..there we are..and there we will be. I will go into more of the day to day things going on and send out our thanks to the literally hundreds of people that are now making up Ella's group of angels in her life. I am too tired to go into all this now but I wanted people to have an update to where she is now. I will share this...
Today, Ella and I took a walk outside around our apartment complex which sits on a beautiful, small lake that is protected as a bird sanctuary. She ran across our huge lawns laughing in the sunshine and quacking at the ducks in the lake and running head on into this old grey goose and her mate that are ALWAYS in our back yard area and ALWAYS ornery! She found a small, bent, slim branch on the ground that curved ever so slightly and told me she wanted to go sit by the lake and "go fishing" (her version of this is dipping the end of the stick in the water repeatedly while complaining that there are no fish showing up ;). She delighted in the purple flowers that decorate the lawns in a few places around our complex, even finding a BEE! of all things, pollenating the flowers in the middle of February...go figure. She's magic ( or mackage, as she used to say til she was about 3 and a half ;).
I will leave you all with that thought..and one wish from me: hug your babies and your family. Love them like your life depends on it. You will be rich beyond your dreams with something no one can take from you if you do :). Thank you all for your good wishes, meditations, prayers, thoughts and of course, deeds done in caring for our angel with us. We love you all...
Col <3
Coleen here this time. Ok, trying to catch everyone up from where we left off. I think I will summarize where we are now, what we know for sure and what we're told will come soon in the future.
Ella was given her first round of chemo from Sat., Jan 31-Wed, Feb. 4th. Ameding our earlier description of the cycles, Ella will be chemo'd for 5 days, the first of which starts the timer on a 21 day cycle til the start of the next chemotization (yes I made that up). During that 16 days between, she will, theoretically, be home. If she so much as gets a slight, lasting (full day or overnight) fever, she will be admitted. Many other health issues, almost ANY other health issues, can be cause for immediate readmission to the hospital as well. While she's home, she will be going back to the hospital 2x per week for "clinic" visits. Blood is taken at these visits and immediately tested for ANC levels to see where she stands. 0 means she has no ability to fight any infection/virus, 500 or so means she can have someone over to the house but no public (malls, grocery stores, school, library, museums, any where with more than one other person...) contact. Then the levels go up from there for when she can actually go to a store or a park and play freely. She will have a whopping 2 days, potentially, since we've gotten home, that her counts will be high enough to safely have visitors over /sigh.
Where we are now. Ella has been home since the Friday after her chemo finished (Feb 6th) and has not had to be readmitted. She's given us a few scares with mild fevers, mouth sores and a sore in her ear but so far so good. We are scheduled for a final pre-chemo clinic visit on Friday (Feb 20th) and the second round of chemo to start for El on Monday, Feb 23rd. We were warned, when we first took her home, to be prepared for her to "pop" a fever (the "in" term for onc patients :P) and we'd be right back in. Also, we were told she'd most likely be exhausted, possibly have no appetite etc and maybe need an NG tube again. She came home and was full of energy this whole time except for about the last 3 days (not today but the 3 previous days) when she was fighting something off we think. I think the biggest loop Dave and I were thrown for was when we went to her first clinic visit the Tuesday after we came home and her counts were at zero already. We'd have had no way of knowing from Ella! She's had a pretty voracious appetite, especially when we first got home. Her counts have stayed at 0 until this last visit we had on Tuesday, 2/17, when it went up to 88. Yes..only 88..a healthy persons is somewhere around 1000 I believe, if I'm recalling that correctly. So imagine...and still, she shines :).
What we know. Ella has high risk neuroblastoma. There is a 40% survival rate from this type of cancer even with the very best known treatment being given. And from what Dr. Park has said, it's the cancer that kills those that don't make it..not the chemo. We have had two very serious, very intense "heart to heart" conversations with Ella's care "team" to talk about why the recommendation is for our daughter to go through the same treatment as a child that showed up fully metacisized with tumors. Ella's bone marrow ended up showing clear, her isotope tracer (MIBG) was clear and her bone scan (scans the exterior of all the bones in her body) was clear. So to us, as lay people, she had a tumor, it was completely removed, two lymph nodes were removed, one of which was right on the tumor so that makes sense that it was affected and the other was far enough away to cause concern when the cancer cells were discovered in it. But it was removed, and no further evidence of disease has shown up anywhere in her body. We were not comfortable with the answers from the first meeting, mostly because, as I figured out later, our questions were not formulated properly. So our most recent meeting, on Friday of last week, was to get to the hardcore and it was just that. As hardcore as it gets. Dr. Park basically told us that Ella shows 5 different "markers" which lead them to the recommendation of blasting her with the hardest stuff they have. They are 1. The fact that she's 5 (most neuroblastoma's show up in 18 mo. to 2.5 year olds or younger and older children, according to Dr. Park's research of 8000 children worldwide over the last 20 years with neuroblastoma, older children's tumor cells do NOT revert to a benign state on their own, as they very often do in children under 3). 2. Her tumor bled, leaking blood with cancer in it into her abdominal cavity. 3. She has that N-MYC gene in abundance in her tumor cells (Dave discussed this in one of his earlier posts). 4. Cancer cells were found in the abdominal lymph node that was removed (Dave talked about this earlier as well) and 5. She had heightened, sustained LDH levels. The blood leaking into her abdomen and the heightened LDH levels were both things Dave and I JUST heard about at this meeting on Friday and we were pretty unhappy that no one had mentioned those things to us earlier. I'll let Dave talk about how apparently rare we are as parents in the way were handling/responding to this situation :).
At one point during the conversation, Dr. Park became clearly uncomfortable as we were being very smart and firm with our questions and our need to understand before we would be willing to allow the recommended treatment to continue on Ella. I was elated. She looked at me and said "Look, I would NEVER recommend that Ella be put through this if I thought there was any other way to treat her and still give her the best shot at the best outcome". That was what I needed to see, that discomfort. I needed to know my daughter was not a lab rat or someone's ticket to a fellowship at Oxford, or better yet, the key to some funding source opening up. Cynical you say? You better believe it :). I needed to know that she had gone through great angst and read and re-read Ella's information and her own research and that she had been up a few nights at least, fighting with herself internally before she came to this recommendation. Because, as she said, Ella (as seems to be the case with my whole damn family's health issues lately) keeps getting put in the rarer and rarer category as you look deeper into her case. And when I say rare, the numbers of cases she has from a pool of 8000 kids over the 20 years that are "similar" to Ella's is a whopping 3-5 kids...ever...yes, 3-5 other children. So she is not cookie cutter by ANY means. Ergo, everyone involved needs to understand this is EXTREMELY complex and decisions are being made based on the data that does exist on Neuroblastoma risk markers in general and alot of instinct. The art of medicine is being applied heavily here.
I will go into some other things about learning "flush lines" and administer meds and all that crap on a later post. Suffice it to say, you become real savvy, real fast about how to do many things medical that you sooooooo could have gone your whole life knowing nothing about :P.
What the future holds....Well the first answer is who knows. The second answer is that this will be an especially insane month for our family with what will be happening. El is scheduled for 5 days of chemo starting Monday, home on Saturday most likely and then will be back in possibly 7 -10 days later for her "stem cell collection". They will basically be hooking her up to a machine developed at the Fred Hutchinson Cancer Center that will pump her blood out of her body, put it thru this machine which will collect her stem cells from the blood and pump it right back in again. And if that sounds scary to you..I'm with you. In order to do this, we are told she "may" (which usually means will, we've found) need a femural line put in her leg as one of her current tubes in her Hickman line is probably not big enough to handle the volume of incoming/outgoing blood for this procedure. So, in essence, Ella would need to be put under for inserting the line, removing the line and on one other day this round, be put under again to do her next round of MIBG, CT scan/possibly bone marrow sampling. She will start receiving daily shots (no, no other way to do it) starting on Mar. 1st and going for 14 days. This shot will be to stimulate production of her stem cells and there is a special team that comes over from "the Hutch", El's own nurse even, to do this procedure, which is obviously inpatient. She will NOT be put under during the collection process were told but will instead, need to be very still for like 3-4 hours as I recall. This, will be, interesting....
So, our calculations, since the femeral line insertion would be an inpatient surgery which she'd need a day to recover from (inpatient) before they could start the collection (which may take 2 "collection" processes to complete over 2 days), are that Ella will spend possibly 7 days this month (10 is optimistic) out of the hospital. 21 days total - 6 days of chemo(5 plus one recovery day)-2 days of line insertion/removal-2 days of stem cell collection - 1-2 days of ct scan/MIBG/bone marrow sample leaves you with 10 days at the most. Basically, once she finishes her testing and stem cell collection, it will pretty much be time to start her next round of chemo. By the way, it's easy to type all of this but ALL of it is dependent on Ella's "counts" (markers in her blood tests). Certain things can't happen til certain markers are met so this is all nuts because we have to take it pretty much day by day to see when we will be doing what this month.
So..there we are..and there we will be. I will go into more of the day to day things going on and send out our thanks to the literally hundreds of people that are now making up Ella's group of angels in her life. I am too tired to go into all this now but I wanted people to have an update to where she is now. I will share this...
Today, Ella and I took a walk outside around our apartment complex which sits on a beautiful, small lake that is protected as a bird sanctuary. She ran across our huge lawns laughing in the sunshine and quacking at the ducks in the lake and running head on into this old grey goose and her mate that are ALWAYS in our back yard area and ALWAYS ornery! She found a small, bent, slim branch on the ground that curved ever so slightly and told me she wanted to go sit by the lake and "go fishing" (her version of this is dipping the end of the stick in the water repeatedly while complaining that there are no fish showing up ;). She delighted in the purple flowers that decorate the lawns in a few places around our complex, even finding a BEE! of all things, pollenating the flowers in the middle of February...go figure. She's magic ( or mackage, as she used to say til she was about 3 and a half ;).
I will leave you all with that thought..and one wish from me: hug your babies and your family. Love them like your life depends on it. You will be rich beyond your dreams with something no one can take from you if you do :). Thank you all for your good wishes, meditations, prayers, thoughts and of course, deeds done in caring for our angel with us. We love you all...
Col <3
Wednesday, January 28, 2009
Cautious Hope
Today Ella had what is called an MIBG Scan. The way it works is they inject her with a radioactive form of iodine ("less radiation in her body than you would get on a cross-country flight" we are told, though) as a tracer, and then they give her a CAT scan to see where things are glowing, basically. The tracer is drawn to any areas where there is rapid cell growth (like cancer cells), and helps to show where else it might be in her body. It also gives some false positives as certain spots in the body naturally have rapid cell growth (the brain and heart, for example).
Anyway, she had that test today, and we got the results. First, a caveat: in 10-15% of cases, the cancer for whatever reason just doesn't bond with the tracer, and since the tumor is no longer in Ella's body for them to know for sure "we know there's cancer there and it is/isn't glowing, so we know whether or not it bonds", they can't be completely sure, but the scan was completely clear. There's nothing in Ella's body.
This won't change anything about the treatment regimen, as they want to be absolutely sure they kill any cancer cells that might be hiding somewhere, so we will still be doing the chemo, transplant and radiation, but it starts us from a much stronger place. A lot of kids that go through this have the cancer spread all throughout their bodies.
Some other stuff I forgot to mention about the treatment options earlier - Ella qualifies for a clinical trial - a test of alternative methods of treating the cancer, in hopes of finding better treatments for future patients. In some hospitals, the first phase of the clinical trial adds in another chemo medication. However, since Seattle Children's was part of a pilot program for this clinical trial, and they came to the conclusion that it worked better than the existing methods, the first phase actually is identical to their standard "BAT" (Best Available Treatment), so there is no change there. In the second phase, however, there is the option to have two bone marrow transplants (and the two intensive chemo treatments that go with it). We're still not sure whether or not we want to participate in the second phase and put Ella through all that, however we are participating in the first phase, since it is exactly the same treatment Ella would ordinarily be getting, and the data will help their research for kids in the future. The lead doctor on this particular study is actually Ella's oncologist, Dr. Julie Park, so that's pretty awesome. As a few people have said to us, fighting Neuroblastoma is her life's work. I think Ella's in good hands. We've also decided to let them take part of her tumor for research as well (a "biology study").
Anyway, she had that test today, and we got the results. First, a caveat: in 10-15% of cases, the cancer for whatever reason just doesn't bond with the tracer, and since the tumor is no longer in Ella's body for them to know for sure "we know there's cancer there and it is/isn't glowing, so we know whether or not it bonds", they can't be completely sure, but the scan was completely clear. There's nothing in Ella's body.
This won't change anything about the treatment regimen, as they want to be absolutely sure they kill any cancer cells that might be hiding somewhere, so we will still be doing the chemo, transplant and radiation, but it starts us from a much stronger place. A lot of kids that go through this have the cancer spread all throughout their bodies.
Some other stuff I forgot to mention about the treatment options earlier - Ella qualifies for a clinical trial - a test of alternative methods of treating the cancer, in hopes of finding better treatments for future patients. In some hospitals, the first phase of the clinical trial adds in another chemo medication. However, since Seattle Children's was part of a pilot program for this clinical trial, and they came to the conclusion that it worked better than the existing methods, the first phase actually is identical to their standard "BAT" (Best Available Treatment), so there is no change there. In the second phase, however, there is the option to have two bone marrow transplants (and the two intensive chemo treatments that go with it). We're still not sure whether or not we want to participate in the second phase and put Ella through all that, however we are participating in the first phase, since it is exactly the same treatment Ella would ordinarily be getting, and the data will help their research for kids in the future. The lead doctor on this particular study is actually Ella's oncologist, Dr. Julie Park, so that's pretty awesome. As a few people have said to us, fighting Neuroblastoma is her life's work. I think Ella's in good hands. We've also decided to let them take part of her tumor for research as well (a "biology study").
Hey everyone
Ella is fully recovered from surgery, and we just wanted to share how excited we are about that -- we are back in the SCCA department now, and she recovered amazingly well. Almost twice as fast as was expected of her. One indicator of her speedy recovery was that she was hungry right away, and the other was that she had almost no pain, aside from some wincing when she tried to sit up the first few days. She has been walking on her own for 4 or 5 days (the initial walking was at her own request, even). We don't want to hang our hats on it, but we see this as a good sign that her body is overall healthy enough to recover from extremely intensive surgery that fast.
Coleen wanted me to say:
We know that many of you have told us that you feel very helpless (as we do) and would like to figure out a way to do something for our family. Coleen came up with the idea of all different kinds of cool hats, since it's very cold still in Seattle, and we will most likely all be hairless as a family soon, hats or other head coverings would be very appreciated. The crazier and more colorful the better. Matching sets, stuff just for Ella, whatever works :)
Another quick side note:
Thanks everyone for the notes, comments, calls, e-mails, etc, sorry we haven't responded all that well, but I'm sure you understand.
Coleen wanted me to say:
We know that many of you have told us that you feel very helpless (as we do) and would like to figure out a way to do something for our family. Coleen came up with the idea of all different kinds of cool hats, since it's very cold still in Seattle, and we will most likely all be hairless as a family soon, hats or other head coverings would be very appreciated. The crazier and more colorful the better. Matching sets, stuff just for Ella, whatever works :)
Another quick side note:
Thanks everyone for the notes, comments, calls, e-mails, etc, sorry we haven't responded all that well, but I'm sure you understand.
Treatment
Okay, here's the deal with the treatment:
This Friday, Ella will begin chemotherapy treatments. She will go through a course of chemotherapy that is 5 days of chemo, then 3 weeks off, 5 days of chemo, then 3 weeks off, etc. This will go for 6 "cycles". During the 3 weeks off, she will come into the hospital for "clinic" visits, 2 days a week. At some point during the chemotherapy, they will remove blood stem cells from her system and freeze them. After the initial chemotherapy phase, there will be a very intensive chemotherapy treatment. So intensive, in fact, that it will kill the bone marrow in her system (thus the stem cells). Following that treatment, she will have a bone marrow transplant, putting the frozen stem cells back into her system to regrow bone marrow and blood cells. After that, we see where everything stands, if everything is good, she will go into a maintenance phase.
During this time, her system will be very susceptible to infections and such. So much so, that if Coleen or I (and obviously anyone else) get sick at all, we won't be able to be around her.
Obviously the treatments have various side effects, some of which are nausea/vomiting, hair loss (Coleen and I (and a few family members) have already decided that if it's okay with Ella, we will be shaving our heads as well), high frequency hearing loss, and infertility. There are some other, less common side effects, but those are the "most likely".
This Friday, Ella will begin chemotherapy treatments. She will go through a course of chemotherapy that is 5 days of chemo, then 3 weeks off, 5 days of chemo, then 3 weeks off, etc. This will go for 6 "cycles". During the 3 weeks off, she will come into the hospital for "clinic" visits, 2 days a week. At some point during the chemotherapy, they will remove blood stem cells from her system and freeze them. After the initial chemotherapy phase, there will be a very intensive chemotherapy treatment. So intensive, in fact, that it will kill the bone marrow in her system (thus the stem cells). Following that treatment, she will have a bone marrow transplant, putting the frozen stem cells back into her system to regrow bone marrow and blood cells. After that, we see where everything stands, if everything is good, she will go into a maintenance phase.
During this time, her system will be very susceptible to infections and such. So much so, that if Coleen or I (and obviously anyone else) get sick at all, we won't be able to be around her.
Obviously the treatments have various side effects, some of which are nausea/vomiting, hair loss (Coleen and I (and a few family members) have already decided that if it's okay with Ella, we will be shaving our heads as well), high frequency hearing loss, and infertility. There are some other, less common side effects, but those are the "most likely".
Monday, January 26, 2009
"My special list"
Unlike most people that have an abdominal surgery, Ella has been absolutely starving since, like, the day after her surgery. We sat down with her the other day and had her dictate to us (with me taking studious notes) exactly what she wanted to eat when she was allowed. Here is her list:
1. Cookies, chocolate chip
2. Apples
3. Donuts
4. Red Gumdrops
5. Raisins
McDonalds Chicken Nuggets, sweety sauce, french fries
Chocolate swirl ice cream cone
Pancakes for breakfast
Cupcakes (pink) with pink icing
Cheese and crackers
Tuna and crackers
Carrots
Onion bagel with cream cheese
Peanut butter and jelly
1. Cookies, chocolate chip
2. Apples
3. Donuts
4. Red Gumdrops
5. Raisins
McDonalds Chicken Nuggets, sweety sauce, french fries
Chocolate swirl ice cream cone
Pancakes for breakfast
Cupcakes (pink) with pink icing
Cheese and crackers
Tuna and crackers
Carrots
Onion bagel with cream cheese
Peanut butter and jelly
Good news, bad news
So we've gotten some good news and some bad news over the last few days.
Good news first, Ella is recovering from her surgery fantastically. She is disconnected from everything but her IVs and today was removed from "nothing by mouth" status to being able to eat and drink whatever she can tolerate. Also, the bone marrow sample that was taken during her surgery was clear of cancer.
The bad news... First of all, during the surgery, a couple of Ella's lymph nodes were removed. They tested these lymph nodes for cancer, and one of them had it. Unfortunately, it was far enough away in her body that it was something to be concerned about (basically, Neuroblastoma -- that is definitely the cancer she has -- is categorized in three categories - low risk, intermediate risk, and high risk. The presence in her lymph node was enough to raise her to intermediate risk). On Friday we got some more information, and that was that her tumor had a heightened level of what's called an N-Myc or MYCN gene. This is a gene that everyone has in their bodies, but when it is in a tumor, and in a heightened amount, it means that the tumor is very aggressive, and classifies Ella's cancer as a high risk. I won't post the numbers here as far as survival rates and such, they're easy enough to google, and I don't want anyone who doesn't want to see them to have to.
I guess that's it for now, we've gotten some information as far as how her treatments will go, and I will post about that soon.
Good news first, Ella is recovering from her surgery fantastically. She is disconnected from everything but her IVs and today was removed from "nothing by mouth" status to being able to eat and drink whatever she can tolerate. Also, the bone marrow sample that was taken during her surgery was clear of cancer.
The bad news... First of all, during the surgery, a couple of Ella's lymph nodes were removed. They tested these lymph nodes for cancer, and one of them had it. Unfortunately, it was far enough away in her body that it was something to be concerned about (basically, Neuroblastoma -- that is definitely the cancer she has -- is categorized in three categories - low risk, intermediate risk, and high risk. The presence in her lymph node was enough to raise her to intermediate risk). On Friday we got some more information, and that was that her tumor had a heightened level of what's called an N-Myc or MYCN gene. This is a gene that everyone has in their bodies, but when it is in a tumor, and in a heightened amount, it means that the tumor is very aggressive, and classifies Ella's cancer as a high risk. I won't post the numbers here as far as survival rates and such, they're easy enough to google, and I don't want anyone who doesn't want to see them to have to.
I guess that's it for now, we've gotten some information as far as how her treatments will go, and I will post about that soon.
Wednesday, January 21, 2009
Surgery update
Hey everyone,
So today (well, yesterday at this point) was surgery day. Everything went great. The surgeons were very happy with how well it went (when the head surgeon came out to talk to us, you could see the smile in his eyes). They were able to remove all of the tumor, or as much as they were able to tell. Ella held steady throughout the whole surgery, and barely bled. The only time her blood pressure dipped a little was when they pushed on the vena cava (there's a prefix i'm missing there -- inferior vena cava I think), which kind of makes sense, seeing as it's a major vein to the heart. The tumor had attached itself (but not invaded) to Ella's diaphragm, liver, kidney, and the aforementioned vena cava. They removed her adrenal gland (which was pretty surrounded by the tumor) but the kidney appears to be okay. They will be biopsying (I don't know if that's a word) the tumor over the next couple of days and let us know what type it is and what our next steps for treatment are. They also took a bone marrow sample to test just in case, and installed what's called a central line -- sort of a big-ass IV with a more direct route to her heart (through the jugular, actually) -- that way she doesn't have to have IV pokes in her arms and legs, everything can be done with this main line, and some medicines and stuff are too harsh to go into normal veins, so they can put those through too.
After a late start, and surgery that felt like forever, they gave us the call we had been waiting for -- they were finishing up, the doctor would talk to us, and then she would be out, maybe in an hour or so. We chatted with the doctor for awhile (he's super awesome, they all are) and then we jetted down to our new room in the surgical ward (speaking of which -- we're in the normal surgical ward, no need for ICU for my girlie :D). After a few short minutes chatting with her nurse, we heard a bed rolling in and there was our beautiful baby girl.
She's pretty groggy and stuff, but things are going well. Guess that's it for now. Onto the next step!
Thank you everyone for all your support, love, thoughts, prayers, food, help, and everything else. I don't know what we'd do without you all. Love ya!
So today (well, yesterday at this point) was surgery day. Everything went great. The surgeons were very happy with how well it went (when the head surgeon came out to talk to us, you could see the smile in his eyes). They were able to remove all of the tumor, or as much as they were able to tell. Ella held steady throughout the whole surgery, and barely bled. The only time her blood pressure dipped a little was when they pushed on the vena cava (there's a prefix i'm missing there -- inferior vena cava I think), which kind of makes sense, seeing as it's a major vein to the heart. The tumor had attached itself (but not invaded) to Ella's diaphragm, liver, kidney, and the aforementioned vena cava. They removed her adrenal gland (which was pretty surrounded by the tumor) but the kidney appears to be okay. They will be biopsying (I don't know if that's a word) the tumor over the next couple of days and let us know what type it is and what our next steps for treatment are. They also took a bone marrow sample to test just in case, and installed what's called a central line -- sort of a big-ass IV with a more direct route to her heart (through the jugular, actually) -- that way she doesn't have to have IV pokes in her arms and legs, everything can be done with this main line, and some medicines and stuff are too harsh to go into normal veins, so they can put those through too.
After a late start, and surgery that felt like forever, they gave us the call we had been waiting for -- they were finishing up, the doctor would talk to us, and then she would be out, maybe in an hour or so. We chatted with the doctor for awhile (he's super awesome, they all are) and then we jetted down to our new room in the surgical ward (speaking of which -- we're in the normal surgical ward, no need for ICU for my girlie :D). After a few short minutes chatting with her nurse, we heard a bed rolling in and there was our beautiful baby girl.
She's pretty groggy and stuff, but things are going well. Guess that's it for now. Onto the next step!
Thank you everyone for all your support, love, thoughts, prayers, food, help, and everything else. I don't know what we'd do without you all. Love ya!
Saturday, January 17, 2009
So far
Hi everyone,
I’m not quite sure where to start, so I guess I’ll just start at the beginning. This may be pretty verbose, as I’m going to tell as much as I can. This is also going to kind of be all over the place, so I apologize in advance. Anyway, here goes:
Sunday night, after her bath, Ella told us that it burned when she went potty. We thought maybe she had a bladder infection so we were going to take her to the doctor Tuesday morning before school.
Monday, we got her up and took her to school, she seemed pretty tired but otherwise normal. Monday afternoon, her teacher, Miss Lissa called us and said that something was wrong with Ella – she was very lethargic, listless, didn’t want to do anything, wouldn’t eat, wouldn’t drink, wouldn’t do anything. In fact, as she was on the phone, she said that Ella was sitting at a table, her eyes rolling back in her head as she fell asleep where she sat. Miss Lissa has known Ella for about 3 years, so she knows her quite well, and for her to call us and tell us something like this, we knew it was serious. When Coleen called me to tell me that Lissa had said that, my response was “why are you still on the phone with me? Go get her.” Coleen picked her up, and she could tell from the way she looked that something was definitely not right. Ella kept saying that she felt weak, and couldn’t walk (if you know Ella at all, WAY out of character). Coleen got her in the car and gave her some apple juice, which she immediately threw up. She took her straight to the doctors office, who, luckily, had an appointment immediately. The doctor ordered some blood tests (Ella didn't even flinch when the needle was stuck in her arm to draw blood -- that's how out of it she was), and told Coleen that she didn’t know what was wrong, but something definitely wasn’t right, so to take Ella to the emergency room right away. I was on my way home from work, and Ella seemed to be responding a bit better after drinking some water, so we decided they would wait for me to get home, and then we would all go together. Right before I got home, Ella threw up all the water she had been drinking. We also got the report from the blood test that Ella's white blood cell count was 25,000, apparently indicating some kind of infection.
We went to the emergency room, and they checked her out. We were still thinking bladder infection. During the exam at the emergency room, Ella had some pain in her side, right about the spot where your appendix is. We immediately got concerned – “oh, no, appendicitis, she’s going to have to have surgery to have her appendix out.” They ordered an ultrasound to take a look at her appendix (as far as we know - we still don't know who knew what when), so we went and did that. After awhile, one of the nurses came in and said that the doctor wanted to see us in a conference room (Luckily, my sister, Val, had gotten off work and came straight over, so Ella didn’t have to be alone). I’ve seen enough doctor shows on TV to know that this was not good. “Aw, man”, I thought, “it’s definitely appendix surgery.”
When the doctor brought us in, he told us that the ultrasound had revealed a growth on Ella’s kidney, about 5 centimeters. It was a tumor, and they were telling us that Ella has cancer. They told us that it is most likely one of two types of cancer, either something called a Wilm’s Tumor, or a Neuroblastoma. We asked how sure they were (despite knowing the answer – they don’t break out the C word unless they’re pretty damn sure, and in fact, that is exactly what her doctor said). They called and had an ambulance take Ella to Seattle Children’s Hospital. Appendicitis was looking real good at this point.
I guess I won’t go through all the check in procedures at Children’s. But, after we got there, they set us up in a room in the SCCA department (Seattle Children’s Cancer Alliance). We got a little bit of sleep and then went in to get a CAT scan Tuesday afternoon. The CAT scan revealed a little more information – it looks like the tumor is not attached to her kidney, as originally thought, but they can’t be sure. It definitely looks like her adrenal gland has been affected. The other thing that the CAT scan revealed was that the tumor was bleeding. As to why, no one really knows. Tumors are nasty little fuckers, and their entire purpose is to grow as much as possible as fast as possible. They think that the tumor probably stole a blood vessel or something to feed itself and grow as much as possible, and in the growing, it ruptured. They took several blood tests over several hours and the main measurement they were looking at was a CBC, or her (I’m spacing a little here, so this might be wrong) “hemocrit” number. It’s basically the concentration of the blood in your system. Ella’s was dropping, and dropping fast (the first one we got, she was at 32, the next, 27, the next, 22 – they told us that usually when someone hits 20, they get a blood transfusion, around 15, I think it was, you start losing consciousness and such). Blood was ordered for her, as they were, obviously, worried. They told us that they were going to do the transfusion and see what happened with that, and that if things took another turn for the worse they would be moving her into the ICU, and rapidly into surgery. They also put her on a monitor to watch her respiration, blood pressure, and blood oxygen levels. They took one more sample before they gave her the blood (it turns out it tested around 22 as well, so she had stabilized, but better safe than sorry). During the transfusion, Ella started to get a rash, sort of like hives, but it never got far enough to officially be “hives” (this is a normal side effect from transfusions they had warned us about, so we were watching for it). Both her ears became fire engine red, it went down the side of her neck from there, and around her neck in a “necklace”, it had also started to get on her face a bit. They gave her a dose of Benadryl, and it immediately cleared the rash up.
I forgot to add in there – she was on constant IVs for saline, and some sugar water to keep her hydrated. She hadn’t had much of an appetite (she voluntarily didn’t eat anything all day Monday, and because of the chain of events of the CAT scan, and then the situation she was in, and possibility she might be in surgery at any moment, she wasn’t allowed to eat or drink Tuesday or Wednesday), and had thrown up pretty much all the water she had to drink on Monday.
After the transfusion, her CBC level was at 31. They continued to check her levels every 4 hours over the next couple of days (with us eagerly awaiting the results). It bobbed and weaved a bit, going to 29, 27, 28, 27, etc, but always within acceptable levels (and even within the margin of error for the test). As far as the bleeding, what they THINK happened – the kidney and adrenal gland are in their own little sac, separate from the rest of the organs. They think that the tumor bled, filled up the sac, and then the sac started to push back. The blood started to clot, and tapenade itself, stopping the bleeding by itself.
Everything stabilized very well, and they spaced out the CBC tests. I can’t remember the exact timeline, but we are now down to once a day. Everyone has been very impressed with Ella and her progress. I had a surgeon tell me “she is showing us how it’s done”, and one of the medical residents tell me “she went from being very unstable and scary to incredibly stable.” She’s an amazing little girl, my daughter is.
Anyway, things are still somewhat touchy, what with the area around her kidney still filled with blood, but at least the bleeding has stopped, and, as I said, everyone is very pleased with her progress.
They are still not sure what type of tumor it is, and are not going to find out until they do the surgery. They have passed on doing a biopsy of any kind, as with the situation with the blood, they don’t want to mess with anything and risk starting the bleeding all over again. They have done a few blood tests, but unfortunately the way the blood tests work, if they come back positive, they know for sure what kind of cancer it is, if they come back normal (“negative”), they can’t be sure one way or the other if it is that type of cancer. They’re just sort of “helpers.”
We haven’t done any research on the cancers (actually, that’s not completely true – I googled Wilm’s tumors and read the absolute basics off of the Wikipedia page – but that’s it). From what I understand (as sick as this sounds), Wilm’s is the one that we want her to have. I’ve gotten some anecdotal information that with Wilm’s Tumors, once they are removed and all treatments are complete (i.e. Ella is cancer free), there is a 75% chance that the person will be cancer free the rest of their life. Also, if it ever does come back, it will almost always be around the kidney, so it is easily and quickly spotted and dealt with. I don't know how accurate that is. I ask if anyone does decide to go nuts with the google, please don’t share it with us. We came to the conclusion that even if we did google and learn everything there was to learn about these things, the only thing we would still know is that Ella has a tumor, and they are going to cut it out, and deal with it. Knowing statistics and all that other crap doesn’t do us any good.
Where we stand now – surgery is scheduled for Tuesday, we think at 12:30. They scheduled it so far out, as they want to be sure that everything is as stable as possible before they do surgery – surgery to stop internal bleeding is risky enough, surgery to remove a tumor is risky enough, combining the two is something you want to avoid if you can. If they absolutely have to, obviously, they will do so, it’s just something you want to avoid. The tumor is apparently 7cm in length, we're not sure on the width/whatever other measurements. Ella will almost definitely lose her adrenal gland, they're not sure but they THINK the kidney may be okay. Either way, the loss of either of those should not affect Ella in any way. We will be staying at Children’s until the surgery Tuesday. After the surgery, they will move us to another room, either in the ICU or Recovery area. They are testing her blood once a day, in the morning. They have removed all the monitors, instead spot checking her every few hours. She’s also gotten her appetite back a bit, and has been willing to drink enough, that they’re letting her be off the IVs all day. Today she woke up, asked to be disconnected from the IV, and wanted to go on an adventure, so we wandered pretty much the whole hospital. She hasn’t been hooked back up since. I’m not sure if they hooked her back up overnight (it was a possibility that was mentioned) – I am home tonight to try to get some things taken care of and get some uninterrupted sleep (Coleen did the same last night), but the report I got from Coleen is that Ella’s appetite was pretty good, and she had been drinking quite a bit as well, so probably not.
I guess that’s everything, just wanted to give anyone who knew an update, let anyone who was unaware know what was going on, and make sure everyone had the full story (as far as my addled mind can recall).
The doctors and nurses that we have had have all been amazing. I can’t say enough how great they’ve all been. Everyone loves Ella. We are lucky enough to live near Seattle Children’s Hospital, as they are ranked #5 in the country. We are lucky that my sister, Val, moved up here to Seattle just in time to be here in our time of extreme need. She has been ridiculously helpful. We are incredibly lucky that Miss Lissa knew Ella well enough to know she wasn’t right and call us. We are lucky that our doctor, Dr. Hathaway, was astute enough to trust our instincts, and to send us to the emergency room. It’s been one hellish thing, but we’ve had our good spots along the way.
We have told Ella that she has a bump or lump in her tummy, and that the hospital is “our new home”, and that while the “other home” is still around, we are going to be staying at this new home for awhile while the doctors and nurses fix the bump.
We are in Seattle Children’s Hospital, room T3267, bed 1. I don’t expect anyone to send anything, but if you do, please just know that flowers are not allowed in the area we are in. If anyone wants to visit, please talk to us first, and also know that if you are at ALL sick, even if you have the sniffles, you will not be allowed to visit us (not our rule, but one we’re firmly behind).
I’ve e-mailed a lot of people here, some people I’ve not talked to in quite some time (I apologize for that, by the way). I don’t expect you to reply or anything, the only thing I ask is that if prayer is your thing, I’d appreciate you throwing some Ella’s way. If not, sending a few good thoughts her way would be nice. That goes for everyone, actually.
Feel free to e-mail (use this address, as it goes to my blackberry, which is around us pretty much all day), but I can’t guarantee a reply. Feel free to call, but, again, I can’t guarantee we’ll answer or call back, but I promise to try.
I set up a blog for Ella, it is located at http://ellasultan.blogspot.com For now, the only thing on it is this e-mail. I plan on asking Ella if she has any messages she wants to share with everyone, and if she does, I will have her dictate it to me, I’ll write it down, and then let her type it in one letter at a time (assuming she wants to), as she loves typing on the computer. We’ll probably also throw any updates on there.
I’ve emailed everyone I could think of off the top of my head, but I’ve in no way gotten everyone, so feel free to forward this to anyone you think may want to know.
Lastly, please don’t reply-all to this e-mail, I have a lot of people copied on here.
Love ya all, and thanks.
I’m not quite sure where to start, so I guess I’ll just start at the beginning. This may be pretty verbose, as I’m going to tell as much as I can. This is also going to kind of be all over the place, so I apologize in advance. Anyway, here goes:
Sunday night, after her bath, Ella told us that it burned when she went potty. We thought maybe she had a bladder infection so we were going to take her to the doctor Tuesday morning before school.
Monday, we got her up and took her to school, she seemed pretty tired but otherwise normal. Monday afternoon, her teacher, Miss Lissa called us and said that something was wrong with Ella – she was very lethargic, listless, didn’t want to do anything, wouldn’t eat, wouldn’t drink, wouldn’t do anything. In fact, as she was on the phone, she said that Ella was sitting at a table, her eyes rolling back in her head as she fell asleep where she sat. Miss Lissa has known Ella for about 3 years, so she knows her quite well, and for her to call us and tell us something like this, we knew it was serious. When Coleen called me to tell me that Lissa had said that, my response was “why are you still on the phone with me? Go get her.” Coleen picked her up, and she could tell from the way she looked that something was definitely not right. Ella kept saying that she felt weak, and couldn’t walk (if you know Ella at all, WAY out of character). Coleen got her in the car and gave her some apple juice, which she immediately threw up. She took her straight to the doctors office, who, luckily, had an appointment immediately. The doctor ordered some blood tests (Ella didn't even flinch when the needle was stuck in her arm to draw blood -- that's how out of it she was), and told Coleen that she didn’t know what was wrong, but something definitely wasn’t right, so to take Ella to the emergency room right away. I was on my way home from work, and Ella seemed to be responding a bit better after drinking some water, so we decided they would wait for me to get home, and then we would all go together. Right before I got home, Ella threw up all the water she had been drinking. We also got the report from the blood test that Ella's white blood cell count was 25,000, apparently indicating some kind of infection.
We went to the emergency room, and they checked her out. We were still thinking bladder infection. During the exam at the emergency room, Ella had some pain in her side, right about the spot where your appendix is. We immediately got concerned – “oh, no, appendicitis, she’s going to have to have surgery to have her appendix out.” They ordered an ultrasound to take a look at her appendix (as far as we know - we still don't know who knew what when), so we went and did that. After awhile, one of the nurses came in and said that the doctor wanted to see us in a conference room (Luckily, my sister, Val, had gotten off work and came straight over, so Ella didn’t have to be alone). I’ve seen enough doctor shows on TV to know that this was not good. “Aw, man”, I thought, “it’s definitely appendix surgery.”
When the doctor brought us in, he told us that the ultrasound had revealed a growth on Ella’s kidney, about 5 centimeters. It was a tumor, and they were telling us that Ella has cancer. They told us that it is most likely one of two types of cancer, either something called a Wilm’s Tumor, or a Neuroblastoma. We asked how sure they were (despite knowing the answer – they don’t break out the C word unless they’re pretty damn sure, and in fact, that is exactly what her doctor said). They called and had an ambulance take Ella to Seattle Children’s Hospital. Appendicitis was looking real good at this point.
I guess I won’t go through all the check in procedures at Children’s. But, after we got there, they set us up in a room in the SCCA department (Seattle Children’s Cancer Alliance). We got a little bit of sleep and then went in to get a CAT scan Tuesday afternoon. The CAT scan revealed a little more information – it looks like the tumor is not attached to her kidney, as originally thought, but they can’t be sure. It definitely looks like her adrenal gland has been affected. The other thing that the CAT scan revealed was that the tumor was bleeding. As to why, no one really knows. Tumors are nasty little fuckers, and their entire purpose is to grow as much as possible as fast as possible. They think that the tumor probably stole a blood vessel or something to feed itself and grow as much as possible, and in the growing, it ruptured. They took several blood tests over several hours and the main measurement they were looking at was a CBC, or her (I’m spacing a little here, so this might be wrong) “hemocrit” number. It’s basically the concentration of the blood in your system. Ella’s was dropping, and dropping fast (the first one we got, she was at 32, the next, 27, the next, 22 – they told us that usually when someone hits 20, they get a blood transfusion, around 15, I think it was, you start losing consciousness and such). Blood was ordered for her, as they were, obviously, worried. They told us that they were going to do the transfusion and see what happened with that, and that if things took another turn for the worse they would be moving her into the ICU, and rapidly into surgery. They also put her on a monitor to watch her respiration, blood pressure, and blood oxygen levels. They took one more sample before they gave her the blood (it turns out it tested around 22 as well, so she had stabilized, but better safe than sorry). During the transfusion, Ella started to get a rash, sort of like hives, but it never got far enough to officially be “hives” (this is a normal side effect from transfusions they had warned us about, so we were watching for it). Both her ears became fire engine red, it went down the side of her neck from there, and around her neck in a “necklace”, it had also started to get on her face a bit. They gave her a dose of Benadryl, and it immediately cleared the rash up.
I forgot to add in there – she was on constant IVs for saline, and some sugar water to keep her hydrated. She hadn’t had much of an appetite (she voluntarily didn’t eat anything all day Monday, and because of the chain of events of the CAT scan, and then the situation she was in, and possibility she might be in surgery at any moment, she wasn’t allowed to eat or drink Tuesday or Wednesday), and had thrown up pretty much all the water she had to drink on Monday.
After the transfusion, her CBC level was at 31. They continued to check her levels every 4 hours over the next couple of days (with us eagerly awaiting the results). It bobbed and weaved a bit, going to 29, 27, 28, 27, etc, but always within acceptable levels (and even within the margin of error for the test). As far as the bleeding, what they THINK happened – the kidney and adrenal gland are in their own little sac, separate from the rest of the organs. They think that the tumor bled, filled up the sac, and then the sac started to push back. The blood started to clot, and tapenade itself, stopping the bleeding by itself.
Everything stabilized very well, and they spaced out the CBC tests. I can’t remember the exact timeline, but we are now down to once a day. Everyone has been very impressed with Ella and her progress. I had a surgeon tell me “she is showing us how it’s done”, and one of the medical residents tell me “she went from being very unstable and scary to incredibly stable.” She’s an amazing little girl, my daughter is.
Anyway, things are still somewhat touchy, what with the area around her kidney still filled with blood, but at least the bleeding has stopped, and, as I said, everyone is very pleased with her progress.
They are still not sure what type of tumor it is, and are not going to find out until they do the surgery. They have passed on doing a biopsy of any kind, as with the situation with the blood, they don’t want to mess with anything and risk starting the bleeding all over again. They have done a few blood tests, but unfortunately the way the blood tests work, if they come back positive, they know for sure what kind of cancer it is, if they come back normal (“negative”), they can’t be sure one way or the other if it is that type of cancer. They’re just sort of “helpers.”
We haven’t done any research on the cancers (actually, that’s not completely true – I googled Wilm’s tumors and read the absolute basics off of the Wikipedia page – but that’s it). From what I understand (as sick as this sounds), Wilm’s is the one that we want her to have. I’ve gotten some anecdotal information that with Wilm’s Tumors, once they are removed and all treatments are complete (i.e. Ella is cancer free), there is a 75% chance that the person will be cancer free the rest of their life. Also, if it ever does come back, it will almost always be around the kidney, so it is easily and quickly spotted and dealt with. I don't know how accurate that is. I ask if anyone does decide to go nuts with the google, please don’t share it with us. We came to the conclusion that even if we did google and learn everything there was to learn about these things, the only thing we would still know is that Ella has a tumor, and they are going to cut it out, and deal with it. Knowing statistics and all that other crap doesn’t do us any good.
Where we stand now – surgery is scheduled for Tuesday, we think at 12:30. They scheduled it so far out, as they want to be sure that everything is as stable as possible before they do surgery – surgery to stop internal bleeding is risky enough, surgery to remove a tumor is risky enough, combining the two is something you want to avoid if you can. If they absolutely have to, obviously, they will do so, it’s just something you want to avoid. The tumor is apparently 7cm in length, we're not sure on the width/whatever other measurements. Ella will almost definitely lose her adrenal gland, they're not sure but they THINK the kidney may be okay. Either way, the loss of either of those should not affect Ella in any way. We will be staying at Children’s until the surgery Tuesday. After the surgery, they will move us to another room, either in the ICU or Recovery area. They are testing her blood once a day, in the morning. They have removed all the monitors, instead spot checking her every few hours. She’s also gotten her appetite back a bit, and has been willing to drink enough, that they’re letting her be off the IVs all day. Today she woke up, asked to be disconnected from the IV, and wanted to go on an adventure, so we wandered pretty much the whole hospital. She hasn’t been hooked back up since. I’m not sure if they hooked her back up overnight (it was a possibility that was mentioned) – I am home tonight to try to get some things taken care of and get some uninterrupted sleep (Coleen did the same last night), but the report I got from Coleen is that Ella’s appetite was pretty good, and she had been drinking quite a bit as well, so probably not.
I guess that’s everything, just wanted to give anyone who knew an update, let anyone who was unaware know what was going on, and make sure everyone had the full story (as far as my addled mind can recall).
The doctors and nurses that we have had have all been amazing. I can’t say enough how great they’ve all been. Everyone loves Ella. We are lucky enough to live near Seattle Children’s Hospital, as they are ranked #5 in the country. We are lucky that my sister, Val, moved up here to Seattle just in time to be here in our time of extreme need. She has been ridiculously helpful. We are incredibly lucky that Miss Lissa knew Ella well enough to know she wasn’t right and call us. We are lucky that our doctor, Dr. Hathaway, was astute enough to trust our instincts, and to send us to the emergency room. It’s been one hellish thing, but we’ve had our good spots along the way.
We have told Ella that she has a bump or lump in her tummy, and that the hospital is “our new home”, and that while the “other home” is still around, we are going to be staying at this new home for awhile while the doctors and nurses fix the bump.
We are in Seattle Children’s Hospital, room T3267, bed 1. I don’t expect anyone to send anything, but if you do, please just know that flowers are not allowed in the area we are in. If anyone wants to visit, please talk to us first, and also know that if you are at ALL sick, even if you have the sniffles, you will not be allowed to visit us (not our rule, but one we’re firmly behind).
I’ve e-mailed a lot of people here, some people I’ve not talked to in quite some time (I apologize for that, by the way). I don’t expect you to reply or anything, the only thing I ask is that if prayer is your thing, I’d appreciate you throwing some Ella’s way. If not, sending a few good thoughts her way would be nice. That goes for everyone, actually.
Feel free to e-mail (use this address, as it goes to my blackberry, which is around us pretty much all day), but I can’t guarantee a reply. Feel free to call, but, again, I can’t guarantee we’ll answer or call back, but I promise to try.
I set up a blog for Ella, it is located at http://ellasultan.blogspot.com For now, the only thing on it is this e-mail. I plan on asking Ella if she has any messages she wants to share with everyone, and if she does, I will have her dictate it to me, I’ll write it down, and then let her type it in one letter at a time (assuming she wants to), as she loves typing on the computer. We’ll probably also throw any updates on there.
I’ve emailed everyone I could think of off the top of my head, but I’ve in no way gotten everyone, so feel free to forward this to anyone you think may want to know.
Lastly, please don’t reply-all to this e-mail, I have a lot of people copied on here.
Love ya all, and thanks.
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