Tuesday, May 31, 2011

Much better week so far

Today, we had a visit from our Make-A-Wish wish granters.
They came bearing gifts for Anthony.
Check out his grin with the Toy Story movies. :)

Buzz Lightyear

Toy Story snacks



so excited

Anthony couldn't sit still with all the excitement. :)

We're likely going to visit DisneyWorld in Florida!

The land of Buzz and Woody ;)

Anthony's steroid belly yesterday.

His roid rage was showing today, growling and grumping in the store.

Tomorrow, Anthony should be back to his happy self.

Kelly wanted wavy hair for yesterday, so I did a bunch of small braids Sunday night.



Playing outside on the porch, holding his arms out to be picked up.

Josh was spinning his helicopter toy thingie.







Last week when we returned from Seattle, Andy had me look at my garden.

He installed little sprinklers in each box!

Friday, May 27, 2011

Befores and Afters

This was the other morning, while we were waiting for our late train.
Anthony was having fun pushing buttons, and climbing over Andy and his seat.



Last night, Kelly had a choir concert.

Anthony thought the lettuce sang its own concert.

And, he thought the bowl sounded best over his head.

(Anthony saw the bowl on the table and dumped it down)

Today was a big day of haircuts.

All the children except Maggie and Anthony got haircuts.

Maggie's is next week.

None of them have had a haircut in at least 6 months, I think...

Daniel with his mop.

Kelly, Josh, Lilly

Anthony watching Toy Story 3 while waiting.

Daniel~after


Josh~during

Josh~after

More waiting

Kelly~after (with bangs again)



Lilly~after (she'll also get highlights next week)



Wednesday, May 25, 2011

Held

Tonight I’m tired. Cancer has taken my family hostage.
Anthony doesn’t have any new medical problems. But everything possible went wrong today, except (thank heaven!) for severe weather problems like tornadoes.

Today was Anthony’s appointment for chemo in Seattle. He has these every 4 weeks, like clockwork.
After being deprived of regular sleep for several weeks now (due to hospitalizations and round-the-clock IV antibiotics), I opted to take the train to Seattle and back home so I wouldn’t be driving so tired. This way I could also do Anthony’s medications on the train and not have to stop somewhere and do them in the car.

The train to Seattle started out being late. Almost an hour late at only 5:30 in the morning is not calming to my anxieties of getting everything done on time.

We arrived in Seattle in good time though.
The ride I had arranged several days before wasn’t there. I called the service providing the ride, and they had no record of us needing a ride.
So they called us a cab. A cab with a car seat.
Harrowing drive in downtown Seattle and on the freeway. In the rain. Speeding, almost rear-ending many, sharply cutting in front of other vehicles. Harrowing.

Finally, we arrived at the hospital.
We were 5 minutes late, but the ultrasound for Anthony’s neck was still able to be done, and completely.

After the ultrasound, we needed to go get labs done, then we didn’t have another appointment scheduled for an hour and a half. So, there was some leeway time between appointments. I figured Anthony and I could get lunch and/or walk to the Ronald McDonald House for a few minutes.

We went straight to get labs done.
The most important labwork needed an actual drawing of blood from a vein, not his PICC line. So, a couple of A’s favorite nurses tried getting blood from his other arm (without the PICC) and both feet. Several times. The veins were hiding or just weren’t there.

All day yesterday, I had adjusted Anthony’s lovenox injection timing so that we could have a nurse help me hold him down when we arrived off the train. 2 hours late (remember that his body needs this medicine to be given at regular intervals), the nurse helped me inject the lovenox.

Next, we were sent to the BEST lab tech to see if he could get a good blood draw. He couldn’t even try because the time-sensitive labwork needs to be done 4 hours EXACTLY after the lovenox was injected.

So, we wheeled right around and went back to get regular labs drawn (minus the time-sensitive one) from the PICC line. Except the waiting room filled while we were at the lab. So, we got to wait an hour for that part.

While waiting, I got to see a fellow momcologist (moms who can almost qualify as oncologists because of the reality of living with a child with cancer). She was at clinic to participate in a Care Conference because her daughter is not doing well.

After labs were finally done, painlessly through the PICC, we got to wait 2 hours to get in to see dr. Appointments were running late for some reason. Other families were complaining because they’d been waiting 30 minutes. They didn’t have a train to catch, and we’d been waiting double the time they had.

We missed the train. Anthony did get to see the doctor, which is necessary in order to be given the Seattle chemo.

But, I wasn’t able to reschedule a surgical appt. next week. I don’t want to take an 8-hour trip for a 10 minute appt. The surgeon has to physically see how A’s incision has healed and is healing before a new port can be scheduled to be placed.

The next train home is tomorrow NIGHT. So, the hospital arranged for Anthony and I to stay at a hotel for tonight.

Because we’re still in Seattle, Anthony’s time-sensitive labs will have to be done before we can go home tomorrow. Then, we’ll have a driver take us all the way back home (3 hour drive). After having the taxi ride today, I’m not looking forward to that. But, the hospital drivers are wonderful, so maybe it won’t be so bad.

Arriving at the hotel, the room we were assigned had not been cleaned. So, we had to move to a different room.

And lastly, I read an update on a sweet baby who underwent what was to be a miraculous surgery on his heart. He didn’t make it. I am so sad for his family.

I don’t like to spread negativity, and always try to look at our situation with gratitude because we really do have things good, as far as cure rate for Anthony’s cancer, our circumstances, and support. I haven’t cried in front of our nurses or doctors before today.

Today there was no new diagnosis that we needed to learn to live with. It was just a frustrating day of everything going wrong.

I HATE cancer and how it has taken our family hostage. Even when we play by the rules, we still have no control over how things will go. Even for what is supposed to be a simple day of appointments. My family is separated for the night. Again.

I am looking forward to the miracle of what tomorrow can bring.

Tuesday, May 24, 2011

More pictures

If A gets on his tippy-toes, he can reach whatever's on the table's edge.

He likes to take the chair to the middle of the room, then climb on.

Anthony has finally started loving on his Woody doll at bedtime. :)

Beautiful irises surrounded by too many weeds.

One weed is just as tall as the irises themselves!



Hospital kits are coming along...watch for a post on those coming soon!

Maggie and Lilly had fun putting them together with me.

Kelly is helping with dinner for a couple weeks.

She likes stir-fry, and was having fun stirring it up.

Our friends bought Anthony a white board. He loves it!





Anthony in one of his favorite spots--right in front of the tv with Toy Story on.

Watching a movie with Daddy while the antibiotics are flowing in A's PICC line.

Friday, May 20, 2011

Home!!

Well, kinda....

Anthony and I took the train home. That was a harrowing experience, with not a lot of help from other people. Seriously, the ONE time I understand I can't do it all myself, there's no one interested in helping me carry medical boxes and stuff on the train!

Anyways, we returned home at 9pm, I gave him his evening injection of lovenox, then prepared our first at-home IV antibiotic.

Anthony's PICC line wouldn't flush.

Flushing is the the first step to IV antibiotics, and is when you push a syringe-worth of saline in the line, to clean it out.
We tried different positions, made sure the line was unclamped, tried different syringes, made sure the seal in the syringe was broken...nothing.

So, I made a call to Seattle, and in to our local ER we went.

I'm not crazy, it wasn't working. One of our favorite IV nurses at home couldn't get it to work either. We ended up having to use TPA, which is a clot thinner. That worked, so the antibiotics (which are now 5 hours late) are flowing in!

We should be able to return home as soon as the pump is done with the dose, and I'm going to go to bed...until the next lovenox shot is due at 8am.

Thursday, May 19, 2011

Going home today!!!

Yesterday, we were assigned a student nurse (we had a fully-accredited nurse as well).
The student nurse the day before said her responsibility was to play with Anthony and help me in any way possible. :)
I was amazed when yesterday's student nurse said she had read up on Anthony's history the day before and wrote a case study on him. It took her 7 hours!!

Anthony knows the first thing to do with markers is eat them. :)




Gotta take a quick break to check out what's on Disney Jr. while coloring.



Still yummy

Look at his hands.

Love the colors



Later on, watching tv through the prison-crib bars.




Anthony and I are headed home today.

This was his second longest hospital stay, after diagnosis of leukemia (that was 2-3 weeks).

Longer than open-heart surgery (10 days).

I don't feel like breaking any more records anytime soon.

I'm tired, miss my family, and they miss us too.



Oh, I have to write that when Andy and the children visited last weekend, they went to the Seattle Science Center again.

With the ball that makes your hair stick straight out, someone had brought hairspray to preserve the look. :)

After the science center, they went to the Old Spaghetti Factory (love that place!) and Kelly thought it was fun to see all the pretty dresses on the girls who were headed to prom. :)



Anthony was so excited!