Saturday, January 28, 2012

January 28th

I love living in the Bay area especially when the weather is like this in January!

To take advantage of the super nice weather, and the time off from Chemo, we headed out to the beach today.  As usual, I didn't get a single photo with me in it, but here's what the others were doing. 

Soaking up a healthy dose of sunshine!




Tuesday, January 24, 2012

Still waiting

We are still waiting for Sadie's ANC to go up before we can continue with her treatments.  We were told it was normal to be delayed a week, even two.  But it's been three weeks now.  Her doctor left a message saying on Wednesday we would discuss what to do.  Hmmmmm.  I'm not sure what to think or expect.  I'm having flashbacks to the hospital.  Maybe it just takes Sadie's ANC a long time to recover, and then one day, poof! it will be there! 

On a positive side, it's been super nice to have Sadie feeling well.  And her WBC, hemoglobin and platelets have been slowly going up.

Wednesday, January 18, 2012

A typical clinic visit

It starts with Lidocaine cream on her port site.  Cover it up with press and seal, and we're good to go!  Sadie has a back pack with everything we need for her visits.  Snacks, paper, pencils, water, binkies, mask, our "family handbook", etc.  When we arrive, we're supposed to valet park, so we pull up to the front and head on in.  The hospital is under construction right now because their expanding, so Sadie is supposed to wear a mask while outside and near the doors.  Sometimes she does great, and other times I just can't keep it on her.  It's really annoying and I need to reconfigure the mask so it will fit better.

Then on to the clinic.  We check in and she's given her ankle bracelets and allergy band.  Then we wait.  Sometimes we wait for around an hour, other times we're in in 20 minutes.  Labs are first.  We're taken into the lab draw area where they access her port.  This is the worst part for Sadie, but we're told it will get better.  I don't think it hurts her much, but it really makes her nervous.  She's so tough though and she gets a lollipop at the end that magically makes it all better.  They draw what they need, then heplock her and we're back into the waiting room for the doctors' visit.

While we wait, there's usually a movie playing (but it doesn't interest Sadie), and books (she's not really interested), there's some computer games (that are usually occupied), and sometimes she'll sit and color.  But most of the waiting involves Sadie wandering around the room and climbing on the chairs. Today she fell backwards off the chair she was sitting in and hit her head.  Oh boy!  The room completely came alive!  Sadie was screaming.  One receptionist rushed over.  The other receptionist grabbed the phone and asked if I wanted a nurse.  Then two nurses rushed into the room to look her over.  They asked what her platelets were, but I didn't know.  They asked questions and in the end, it was much ado about nothing.  But I learned what they watch for and what's important.  Because she had cried right away, she didn't lose consciousness, and her platelets were fine (they checked for me), there was so concern.  She was fine, but I was kind of embarrassed about all the attention.  Another mother in the room told me the same thing happened to her once. 

Next we're taken into the clinic where someone will weigh her, measure her, take her temperature and blood pressure.  Then we're given a room to wait in for the doctor.  The oncologist will look her over, listen to her heart and lungs, look in her mouth and ask questions.  We discuss her lab results and the plan for the upcoming week.  And they answer my questions.  Today I felt so grateful for the specific doctors Sadie's been assigned to.  They're a perfect fit for me, and Sadie adores them.  Today I was given a much needed pep talk about how to keep Sadie safe, but still have a life.  They made me feel better and it gave me more courage to get out and go places.  It was just what I needed to hear. Lately I've been struggling with whether I'm making the right decisions and really wanting to get out, go places, and see people.  They explained in more detail why a fever is so scarey and why we would be sent to the ER.  They explained that it's not the viruses that are scarey, but the bacteria.  But viruses can cause fevers and will land us in the ER as a safeguard.  I am really thankful for two wonderful doctors that I can lean on and who can give us support and advice.  (I say "doctors" because there's the attending oncologist and then there's the fellow.  The fellow has been with us since our very first visit to the ER after Sadie was diagnosed.  She's great!)

Next we schedule our upcoming visits and we're on our way home!  We usually stop and see the trains on the way out and Sadie usually falls asleep in the car on the way home.  Today she slept four hours after we got home!  I think clinic visits wear her out.

Here's a photo that has nothing to do with the post:
Sadie and Andrew play so well together despite their age difference.  I don't know what we're going to do when Andrew starts Kindergarten this fall!

Still no chemo

We went back to the clinic today.  Still waiting for Sadie's ANC to go up.  Today she was around 400.  No chemo again this week.   We'll keep going back Mondays and Wednesdays until her ANC is at least 750, then we'll start on Chemo again.  But while we are waiting, we are enjoying the fact that Sadie feels great!  She's about as normal as we've seen her in a long while.

On a fun note:  Have you seen this video?  It's Sadie's absolute favorite!  She loves dancing to it and I've tried to catch her on film, but she's becoming camera shy.  You'll just have to picture her mimicking Fiest's every move down to the bow at the end.  It's priceless!

Tuesday, January 10, 2012

Quick update

No Chemo Tomorrow.
Sadie is doing well.  She's eating well, she's drinking well, she's feeling well.  She went in on Monday for labs, and she should be going in tomorrow for chemo, but her numbers are too low.  They want her ANC to be at least 750 before they'll give her this next dose of chemo.  This means she gets a week off!  On Monday her ANC was 300 and we expect it will be back up by next week.  Her Chemo days switched from Thursdays to Wednesdays.  This works a little better with our schedule because on Mondays, Wednesdays, and Fridays, Andrew is in preschool.  Tomorrow we'll be in for a clinic visit only.

Thursday, January 5, 2012

Happy New Year!

Here's four reasons why I'm the luckiest woman alive :

Evan

He is loyal and brave with almost superhero instincts.  If he sees someone who needs help...he doesn't hesitate.  In a lot of ways, I wish I could be more like him.  Last year in school, Evan was sent to the principals office because he was in a fight.  I wish you could read the letter from the principal.  Honestly, it seemed like a formality.  I'm not ashamed of his actions.  Some other boys were picking on one of his friends, so Evan stepped in to his rescue.  Evan knows not to fight, but he won't hesitate to help a friend.  As punishment, he had to write a letter explaining what he would do differently next time. 

He rolls with the punches and can laugh at his mistakes.  He's honest.  One time while I was showing a vacant apartment, Evan and Andrew were outside playing.  Evan came up to me in tears trying to tell me something.  He had peed on the garbage bins!  (I hope my boss doesn't read this blog!)  He knew after he'd done it that it was a bad choice, and he knew he needed to tell me even though I'd be mad.  I wasn't mad.  I could see his predicament.  He needed to go, there wasn't a bathroom and he didn't want to disturb me while working.  I was disgusted, but I was proud he told me the truth, I just wish it wasn't in front of potential tenants!  We talked later about what might have been a better choice than peeing on the garbage cans.  I know if I ask Evan a question, he'll give me the truth.

Andrew:

He's determined.  He's perceptive.  He's sensitive and sweet.  He prefers his family over friends.  As much of a challenge as it can be right now, when I need to leave him with someone or drop him off at preschool, I try to picture him as a teenager and remind myself that someday he might not want me around anymore, and that will break my heart. 

He's strong willed. He likes to work hard.  His memory is incredible!  And he's incredibly giving!  For his birthday this year he was flipping through a toy magazine and actually picking out things that Evan and Sadie would like!  He told me he was going to ask for these for his birthday and then give them to Evan and Sadie.

Sadie:

She is a joy.  She's the happiest little human I have ever met.  She's polite.  The other day she was watching a Barney episode.  Evan was playing his guitar...loudly.  Sadie very sweetly walked over to him and tapped him on the shoulder.  She put her face right in his and very sweetly in her own way with hand motions and pointing, asked him to be quiet because she was watching Barney.  We all got a kick out of it. 

She's patient.  She submits to her pokes and medicines without understanding, but with trust in us.  She is brave.  She loves people, and people adore her.  On Thursday when we went in to receive a blood transfusion, I realized what a fan base she has!  The minute we walked in it was all "Hi Sadie!" and smiles and waves from doctors, nurses, cleaning staff.  And Sadie loved it.  Her nurse said they were all fighting over who got to be Sadie's nurse today.  And on the way out she was giving hugs, and waves and "byes" to them all.  She is so easy to love! 

Dave:


I don't want to embarass Dave too much, but I will say that I love this guy!  So much of what I adore in our kids personalities come from him.  He's a rock.  (And I'm not just talking about his body!)   He's brave and tough, yet sweet and caring.  He's brilliant, yet funny.  It's hard to find a man like him and I'm lucky he's mine!  We've had a crazy 9 years, and this year will be no exception!  But I'm so glad I get to go thru it with Dave by my side.

Sunday, January 1, 2012

Ardenwood

If I could raise my family anywhere, no limitations, it would be here.  I know.  Keep dreaming!  But I love this place! 


Yesterday, we took a trip to Ardenwood Farm.  Everytime I come here, I feel life slow down.  Dave points out how much work it would be to own something like this.  He's totally right.  But work doesn't scare me, and it's good for the boys.  Plus, I'm only dreaming.   I do think it would be really fun to raise kids on a farm, especially in this area where the weather's great and there's still lots of other places to go.  It's only a dream.


Sadie's favorite animal was the sheep.  The first time we went here, she was terrified of them.  "All done, all done!"  She kept saying everytime they baaaa'd.   This time she wanted to pet them and feed them.  "Here sheepey!" as she carried around straw.  It was great to be outdoors, away from the crowds and hustle and bustle and together.

Mom, Dad, I can explain.....

Just look at their faces!  All three of them.