Thursday, February 23, 2012

Mixed Day


Today's results came very late in the day and were mixed.  Her hemoglobin (part of the red cells above) went down again, this time from 7.4 to 7.1 (normal ranges are listed in the last post).  This keeps her on the border for needing a transfusion however she tires easily and will need the boost with school staring again next week.  Thus we'll be spending another Friday at Children's getting transfused.  On the up side she was able to make some platelets this past week and those numbers went from 6,000 to 11,000 (there are high error margins with these numbers as they just count a random sample of cells, like those above, from a sample of her blood).  Nonetheless we're always happy to see any evidence that her body hasn't just stopped producing blood cells all together.  Additionally, her ANC (absolute neutrophil count, the infection fighting part of her white cells) also went up, this time from 590 to 700.  That is always good as she needs that to be out in the germy world.  We have one more blood test before our meeting with her doctor on March 2nd.  I'm guessing that will be a significant meeting discussing a treatment plan but everything else has taken longer than I think so who knows.  As always much thanks for the support!

Thursday, February 16, 2012

CBC


We've settled into a bit of a routine with having blood draws Thursday mornings and appointments for transfusions on Fridays.  If the blood counts aren't low enough for a transfusion then we get to skip the Friday appointment.  Today's blood counts made a solid drop but not quite enough to need a transfusion tomorrow.  A CBC or complete blood count is reported on a sheet like the one above.  I WISH this was a CBC for Annie, but her major values are way below the reference ranges above.  One group of cells that are still in the normal range are the neutrophils.  These are the part of the white blood cells that fight infection.  If these get too low she has to stay home so as to not be around sick people.  So, as long as we can keep her safe, we'll be out and about until next week's CBC.  Thanks for the well wishes and prayers!

Thursday, February 9, 2012

Salsa dancing polka dots


Today's blood test showed Annie's platelets did not drop and her hemoglobin went up from 8.1-8.2 (normal for children is 11-13).  This is promising as we'd expect it to drop as the transfusion wears off.  Hopefully this indicates that by increasing her cyclosporine (immunosuppressive medicine) back up again we can keep her from needing transfusions while a treatment plan is being explored.

Thus Annie gets a green light for another week at school.  One of her teachers recommended practicing visualization techniques and Annie had her first success with it this morning.  Last week the phlebotomist had trouble tapping into a vein for Annie and it was a weepy experience for both of them.  This week, Annie visualized her blood moving to the draw site and things went perfectly.  Then she spent the car ride to school brainstorming visualizations for the proliferation of her blood cells and their happily sticking around.  Her final choice was of polka dots popping up all over and then doing a kind of vibrating salsa dance ... I'm pretty sure it's just a matter of time before this procedure gets published in the New England Journal of Medicine.

Wednesday, February 8, 2012

What's going on in there?



The results of Annie's biopsy came in and, fortunately, she still only has one serious condition ... instead of three.  Things can always be worse and we are grateful there was no evidence of MDS or leukemia in her bone marrow.  Since we're on the topic of bone marrow here is a short primer on what aplastic anemia looks like on the inside.  First, the name.  "aplastic" means empty and "anemia" refers to blood cells.  Thus Annie's bone marrow is "empty of blood cells."  When they look at a slide of her bone marrow under a microscope it looks like the bottom picture above.  Mostly a lot of empty, white space.  Someone with normal blood counts would have bone marrow that looks like the top picture.  Bone marrow filled with cells.  Now if a cure were only so simple :)

Friday, February 3, 2012

Platform 9 3/4


Annie is home and happily recuperating from today's biopsy.  This was her fifth bone marrow biopsy but her first at Children's.  She was off food since dinner and liquid since 6 a.m.  Although she was scheduled to arrive at 8 a.m. the procedure was delayed and didn't begin until 10:30 a.m.  Nonetheless she did fine with just a little anxiety about being in a new setting and having gas anesthesia versus through an IV line.  She was also happy to have a special friend along - a former student and babysitter who recently graduated from nursing school.  Nothing like having your own nurse on the team!

It was interesting to note the differences from her last hospital.  First, being a children's facility, they explained and showed pictures of the procedure and rooms so she knew what to expect.  Second, they had a team of six nurses and one doctor versus one nurse and two doctors.  Third, it was in an operating room and parents weren't allowed to stay for the procedure (but she was asleep so it didn't seem too bad).  But a really interesting difference was that while you wait during the surgery you watch a large board like at a train station.  Each child has a number and you see which room they are in and how many minutes they have been "in pre-op," then how many "in op," then when they move to "post-op" and "recovery."  While it's no eurorail, it does ease some of the tension.

Now we wait and transfuse until the results from the biopsy and marrow search come in.  The next meeting with her doctor is March 2nd so it will be a bit of a wait.  One thing that helps in the meantime is that she was prescribed aminocapoic acid for any "bleeding events."  Since they don't want to transfuse platelets and they continue to drop (9,000 vs normal at 150,000-400,000) this will hopefully help in an emergency or when she gets a bloody nose.  Her last one required pinching her nose for 1 1/2 hours in the middle of the night so that is a welcome help.

We'll report after next Thursday's hospital visit and hope we have no "events" before then!