«

»

Jun 08

This might be the longest, roughest weekend ever!

This is day 16 of my baby, Serenity, being diagnosed with and treated for Leukemia.  Day 13 is here. 

This weekend has totally and completely sucked.  I’m sure a big part of it is the compounding effects of the events of the last two weeks, never being able to catch up on sleep, bumpy stuff with work, etc.  But the weekend that just won’t end started early Friday afternoon on a bit of a good note – I headed home earlier than planned. 

Turns out I wouldn’t have been there much longer anyway since on the way home Adria called me and said that Serenity had been completely not herself, pale, ornery, in pain.

Pain is expected – Leukemia hurts.

Ornery is expected – being on steroids just does that to a person.

But, rule 2,483,123 of having a child with Leukemia states: “If the child is not being herself and her color isn’t right, take her to the E.R. and get her blood checked.” It might be rule 2,483,122 – I’m not positive – actually, I think that one talks about never expecting your life to be normal again.

So, I cancelled my fantasy of maybe being able to actually go do something with Adria Friday night and got on the phone and started making arrangements for the other kids while I drove home, Adria packed our bags.  I got home and we loaded up Serenity and headed to the E.R..  She really didn’t look good.  By the time we got to the ER at Utah Valley, the oncologist had already been on the phone with Triage and they knew we were coming.  As we pulled up, I had my little speech prepared to keep us out of the waiting room (neutropenic means her neutrophil (a type of white blood cells) counts are extremely low and she has little to no immunity):

“This is Serenity Burns, she was recently diagnosed with Acute Lymphocytic Leukemia, she is neutropenic and is symptomatic of requiring an immediate blood transfusion.”

I spouted that a few times, feeling a bit like Jane from Firefly in the episode where they break into the hospital.  Anyway, they sent us into a room to check us in and the first question out of the RN’s mouth after hearing my little speech is:

“Has she recently been on any medications”

I was stunned for a minute, couldn’t think of anything to respond with that wasn’t just rude.  After a second I said without further hesitation, “well, with recently being diagnosed with Leukemia, she is now on chemo, zofran, dexamethazine, prevacid, oxycodin, PEG injections, sephra on mon and tues, and has recently had about a dozen blood transfusions and as many platelet transfusions – but that really hasn’t changed in the last few days.”

Then it was her turn to be stunned and ask me to repeat the list slowly.  hehe. 

Anyway, we spent the next four hours in the emergency room.  They had to call a nurse down from the pediatric ward because they didn’t know how to access her port.  Then when the labs started coming back, we asked them for specific results.  They told us her ANC was 1.7 – it has never been above .01 since this started and we were startled.  They were ready to discharge us when I told the doctor how surprised we were about her ANC count.  As I explained the history, he nodded and then left.  A few minutes later the nurse came in and said, “umm, her total WBC (white blood count) is 1.7 – her ANC is zero and the doctor is on the phone with the oncologist”.  It would appear that we were a little more versed in blood chemistry than the ER doc, which isn’t really surprising since he’s not an oncologist. 

The good thing was that her platelets were 51 – which was pretty good for being 5 days since her last transfusion, and her red blood counts were good.  So we checked out of the ER and went home.

Now, those of you who know me well know that we are normally very tolerant, almost too tolerant, when it comes to medical situations with our kids.  After raising 8 kids you tend to get that way.  We haven’t taken one of our kids to the hospital in years and barely ever take them to the doctor.  We’ve had half of them at home, the twins have only been to the doctor once after they were first born.  The point is – we have been very clearly told that when it comes to Serenity we have to now be extremely paranoid.  Even though she was fine, we did the right thing taking her to the ER, the oncologist is the one that said we should.  We’ll probably do it dozens more times and be wrong, but on that one time we’re right it’ll be worth it.

So, that was a late night in semi-crisis mode.  She was up all night not feeling good at all.  Then Saturday everyone was really tired, Adria started getting a migraine and I had this bizarre allergic reaction to something – Adria thinks the new dryer sheets she switched to are the culprit.  So I took 50 mg of benadryll to combat the hives I was covered with and crashed around 2 pm – and woke up about 12 hours later feeling much better.

Adria woke up this morning with a killer migraine and I felt like crap.  At about 5:30, Sarek (13 year old son) walked into the kitchen and threw-up all over the place.  That was fun.  We pretty much just lazed through church – we didn’t really ever say “we’re not going”, just nobody had the energy to get up and get ready.  Serenity is incredibly needy.  I’ve thought about twittering every time she needs one of us to get up and get something for her, I swear it’s at least once every 5 minutes.  That’s fine, I truly don’t mind meeting all her needs – it’s just VERY tiring. 

This evening it was time to flush her port (she was re-accessed at the emergency room and we left her accessed since she has a clinic visit tomorrow).  When I lifted up her shirt I was shocked to find that her port dressing was full of blood!  I called the Home Healthcare Nurse and she came over about 15 minutes later.  She discussed the situation with the oncologist on call and after about half an hour they decided it wasn’t a critical situation. While there was quite a bit of blood, it wasn’t still currently bleeding.  The theory is that her platelets are low again and she probably knocked the needle in her port, causing it to bleed a bit and normally to clot quickly.  But they decided it probably just took a while to clot this time.  So I took a sharpie and outlined the blood levels so we could tell if they changed and the Nurse left. 

Tomorow we have a clinic visit in the morning at PCMC.  The weekend will hopefully end after that – but last time we were at the clinic it went unitl 8 pm.  I don’t really like this weekend.

UPDATE: Day 17 is here.

The story of Serenity’s battle with Leukemia begins here.

9 comments

Skip to comment form

  1. Pamela

    I’m with Marina–I got tired reading that as well.

    As a mom with a special needs child (hemiplegic infantile cerebral palsy) I’ve spent my fair share of time in hospitals and ERs. You are your child’s advocate and can’t rely on the ER staff to understand or even really know what is up—though at first we did trust that they would know more than we did. We came to understand that they truly are ‘practicing medicine’.

    You are amazing!

  2. drt

    Why the chip in widget shows different values in FF and IE? I was glad when I saw it reached 49% but when saw the link in twitter, came to this page on FF and saw it was still 44%, I thought I made a mistake. It turned out that I was looking at my page using IE. When I use IE to look at your page, indeed it has already updated to 49%. Can’t do more but we will keep you guys and Serenity in our prayers.

  3. Phil801

    @Pamela – we’re definately learning that! This was our first trip to the ER as a leukemia parent and we were in for a surprise! They didn’t have most of the stuff we needed. We realized that we should have carried in our own heprin and sodium chloride to flush her port once they were done – they had a hard time finding it. They didn’t have or even know about Cavilon – we had to request some from peds. You’re absolutely right, we have to stand up for our special needs kids in the ER. We left with a large list of things to add to our emergency travel kit. Hope things are well with your child :)

  4. Phil801

    @drt the chipin widget is great, but it definately has a LOT of bugs. I don’t know why it is different between browsers, i hadn’t noticed that. Thanks for the prayers!

  5. Karoli

    Oh, wow. My mind is boggled at the thought of having all those kids to begin with, much less one with such serious needs right now. I know you’re putting one foot in front of the other without knowing how it got there right now. I’ll say a prayer that some sort of routine emerges and her condition stabilizes. It must be the instability that is the most exhausting…try to get some rest.

    Do you have any other close family or friends that can come help out? I sure hope so. Hugs to you all.

  6. Phil801

    @karoli life was pretty routine before this, even with 8 kids :) thanks for your prayers that we’ll find a routine again, that would be very nice! I guess I don’t talk about our support system enough. My parents live about 30 minutes away, as do Adria’s. We both have a lot of family in the area and several close friends – they have all been tremendously supportive in taking some of our kids for periods of time, bringing in meals, and just helping out. It’s a huge blessing right now that they’re so available for us. When we were headed to the ER, my parents were on standby to come get the kids if we had to be admitted.
    …. the instability and lack of a routine is definately exhausting, I get several catnaps but never any good solid rest – except last night when I drugged up on benadryll :)

  7. Nancy B

    Will you be going to this ER most of the time? You may want to talk to the hospital’s omsbudsman (or the oncologist) about what format they want for the current list of meds. If the oncologist already talked to them they should at least have been able to keep track of the notes :-(.

    Serenity is lucky to have such caring parents. I hope that the firedrills become more routine (or never happen again :-)!) and that you continue to be such an inspiration for those learning this long difficult path.

  8. james

    Phil and Family, I’ve posted this before, but feel it needs to be said again. Thank you for posting this so openly. I’m sure it will serve to help others going through the same thing.

    Praying for your family and especially your little girl,
    James

  9. Jeff Barr

    Phil, your hands-on, knowledge-based approach is going to make a huge difference in the outcome.

    Going in to every visit knowing the vocabulary, the medications, the treatments, and the history is actually not all that common. Many people are very squeamish and ill-informed about their own bodies and won’t take the time to help themselves.

    You may also want to create your own independent, long-term tracking system for medications, treatments, symptoms, and responses. When her care is spread out over multiple hospitals, doctors, and nurses, having one continuous record will allow you (and the professionals) to see trends, patterns, and relationships. You could also rank her perceived overall well-being on a 1-10 scale each day to make sure that her long-term trend moves in the right direction.

Leave a Reply

Your email address will not be published. Required fields are marked *

You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>