Thursday, December 25, 2008
MERRY CHRISTMAS!!
Friday, December 19, 2008
Freaky Friday
I took some pictures so you can see how big the dressing is and how beautiful she is a mere 4 days after a major operation.
Isabella was actually excited about going to school - it was pajama day. Bedtime this evening went super smooth.
We finished the day with a movie - I say 'we' but it was really just me. Samantha was doing something on the computer and Jeremy fell asleep on the couch.
Samantha needs to get her antibiotic 4 times a day - her evening dose is at 10:30 pm and I need to stay up until it finishes - so say at least another hour. Then I will need to get up at 4:30am for the next one. I am regressing back to the baby schedule days. :)
Good thing tomorrow is Saturday and I can just work on the house and Christmas stuff a bit at a time.
Another side effect of waiting for the antibiotic is that I was finally able to upload Isabella's Winter Program performances to You Tube. Here are the links:
http://www.youtube.com/watch?v=OQRtQI1XKRE - This is Isabella singing 'A Partridge in a Pear Tree'
http://www.youtube.com/watch?v=FBbLeHcTXcQ - This is her Country Christmas Dance
A couple tips for You tube - when you click on the link it will bring up a screen, on the bottom right - just under the volume control, is an option to 'watch in high quality'. It helps. I wasn't the best photographer - I was trying to watch with my own eyes instead of thru the camera and we were back a bit. Also on the left is 'More from Layergal' - you can click on this and see all the videos I have posted without having to come back to this page for the other link.
Thanks to everyone who has posted encouraging words for Sam and the family. It was a tough week but we got thru it just fine and we will handle the next challenge just as well I am sure with the help of every one's thoughts and prayers.
Night and Love to everyone!
Thursday, December 18, 2008
Home Sweet Home
Samantha chose to come home today. She is feeling good and managing her pain great.
The doctors have arranged for a nurse to come to the house and show us how to care for her broviac and administer the antibiotics. We are waiting for the nurse now.
Samantha is taking a quick shower, Isabella is sleeping after we giggled a bit and read a couple of books. I missed putting her to bed!
Daniel is at his dad's tonight, relieved that finals are over and looking forward to a nice break.
Jeremy and I are both looking forward to some quiet times at work (knock on wood!)
It was so familiar leaving the hospital today, but I realized on the way home that we don't have to go back for another 4 weeks - just enough time to start to feel normal again. I felt at home at the hospital but there were so many new faces - a lot of younger kids this time - but the parents all look the same.
It is time to get back into the Christmas spirit, I plan on listening to some of my favorite music and start wrapping packages. I think I am pretty much done - but some will get their gifts late (some things never change). :)
Tomorrow I will probably have to do some grocery shopping and a quick one two on the house.
I will take some pictures tomorrow and post them tomorrow evening - Samantha is looking fantastic, just a big splint on her lower left leg.
Take care!
Love to everyone!
Wednesday, December 17, 2008
My Daughter Super Sam
PT came bright and early and Samantha decided to try and move. She wasn't really happy about it but she did it. She got up and sat in the chair with her leg lowered a bit for quite a while. She tried to use the crutches - but she her right breast area is still tender from the broviac placement. Her leg is also pretty heavily bandaged and awkward. With her weak hip it wasn't realistic that she would be able to crutch down the hall. So the bottom line is that PT agreed that she is doing well enough to go home when she is ready. Dr Heare agreed - if she decides she wants to - we will go home tomorrow.
In the meantime, we continue to watch Gilmore Girls during every waking minute and try to find something that Sam will eat. Good Times... :)
I hope everyone is happy and healthy!
Love to everyone!
Tuesday, December 16, 2008
Day 2 - Quick update
Dr. Heare wanted the epidural out today so she was transitioned to oral pain meds. This afternoon they removed it for good and she seems to be managing the pain ok. Even though the Dr and physical therapist really wanted her to stand or at least sit on the side of the bed, she would not do it.
I think it is a bit harder for her because she has been here before and knows that it is going to hurt when she finally does move that leg. She is resisting. Tomorrow she won't have a choice and I have a feeling it will be a hard day. Then I am thinking we will be able to go home on Thursday.
Isabella is doing ok - a bit of a rough start this morning but she had a blast playing in the hospital playroom this evening. She remembers this routine as well. She just wanted to make sure Samantha and I would be home before Christmas.
Daniel was actually nice to his sister today - played some x-box video game with her for a while. He had part of his Calculus midterm today and he finishes up the rest of his tests on Thursday.
The weather is still cold but at least the sun came out today so the roads are improving.
I think that is it for now - sorry for the short report tonight - but I am beat.
Until tomorrow - Love to everyone!
Monday, December 15, 2008
It's About Time
I am so sorry about not updating for so long. Life has been busy and long story short, Samantha's infection in her ankle was getting bad and so we decided to move up the surgery. It was today.
During the time between Thanksgiving and now we have been meeting with doctors and preparing for this day. Thanksgiving was nice and relaxing - my very favorite holiday! Food, good wine and most important - friends and family.
Samantha has been working at keeping caught up at school and even took a couple of her midterm tests early. She has been doing wonderful at school!
After careful consideration she decided to try and save her ankle. If you remember - she had to chose between a below the knee amputation or 3 to 5 surgeries and another year of healing. No one should have had to make this decision - but my bright beautiful daughter took on the challenge and did what she felt was right. She woke up this morning happy she made the decision and now that she is resting comfortably this evening - I am happy.
We packed our hospital bags this morning and listened to Sam's favorite music (super loud) on the drive to the hospital. We checked into the hospital and fell right back into the old routine. It is kind of scary how easy it was - even though it has been 9 months since we have been back for an overnight visit, it is very familiar.
As I waited for Samantha's surgery to finish, I was thinking that last time this year we were here for one of Samantha's hardest times. I remember being upset because I wasn't able to do Christmas shopping, I remember the small Christmas tree set up in the corner. I remember Samantha's swollen lips and all the pumps pushing food and medicine. That stay was 10 days - and we can be glad that this visit should only last 4 days.
At least this time I was prepared. I am almost done with Christmas shopping - we visited Santa yesterday (as you can see by the picture) and the kids baked 'grandma's cookies' yesterday. Perfect timing, since they help settle Sam's stomach after being under this afternoon.
Samantha received an epidural to help manage pain - I am grateful for that. We have to watch - move her around a bit and monitor her blood pressure, but she is comfortable so for that I am happy.
Today's surgery was to remove all the hardware and the cadaver bone, put in an antibiotic coated rod as a place holder and a broviac for her antibiotic treatment over the next 4 to 6 weeks.
The next surgery will be in 2 to 4 weeks. Dr. Heare and a plastic surgeon will try to repair the muscle and tissue around her left ankle. To do that, they move a muscle from her back to her ankle. They hook up the veins and arteries - this will help get good blood supply down to her toes and allow Dr. Heare to close the wound better once the new cadaver/rod is placed in her leg. She will also have to have a skin graph. It seems like a long hard process and it is - but Samantha knows and is ready for the challenge. At any time during the next few months, if she decides that it is too much - she can opt for the amputation or if it looks like the infection won't go away... But for now, we are all just hoping for the best. So far it is good and Dr. Heare says we have a 60 to 70 percent chance of success. As always - we will take it a day at a time.
Daniel is doing well. His favorite class is graphic arts - he is really good at it - his teacher is pushing him since she sees his talent. He is preparing for his midterm tests and will take them this week. I think he is pretty excited for Christmas and the break.
Isabella has been on a Santa 'high' the past couple of weeks. She loved decorating for Christmas and was super excited to see Santa. She had a upsetting dream the other night - she woke up and was pretty upset because in her dream, she wasn't on Santa's 'good' list and only got a rock in her stocking. I forgot how nice it was when the kids are this age and they work extra hard at being nice... But I think her favorite is the advent calendar and she hasn't forgot to get her candy once all month! :)
She also had her winter program at school last week. I took some video and will try and get it uploaded to You-Tube soon.
Let's see - I probably am missing a whole bunch of info from the last few weeks - but it has been a long day. I promise to update more often and let everyone know how we are doing.
Until tomorrow - take care - stay warm - and lots of love to everyone!
Sunday, November 16, 2008
PINK is everywhere!
Last Saturday we went out to celebrate Samantha's birthday with the uncles and Donna - Sam's friend. It was a wonderful dinner - but we probably won't be going back soon - it was gourmet so that meant really good food but really tiny portions and big prices. :)
Night and Love to everyone!
Friday, November 7, 2008
We left the house and arrived around 11 am. She had her left leg and pelvis basic x-rays. The old bone scans that she usually gets consisted of in injection of some kind of radio-active fluid, then a 2 hour wait and the 1 hour bone scan. This time she got a PET scan, it is more detailed and she only has a 30 minute wait until the actual scan.
The result comes out in a 3 dimensional image of her body - we looked at it beginning at the top of her head all the way down to her toes - kind of like her body as a tube that we look into. All areas of high metabolic activity show up colors from blue (cool) to red (hot). Of course her brain is mostly red - lots going on there as it should be - then down to her lungs which were nice and blue with no hot spots. Further down there were a couple of expected hot spots in her left leg where she is healing and then a bit lower where she has her infection.
The good news is that she is still cancer free - took me long enough long enough - huh? :)
After hearing that great news from the docs we then turned to the talk of her ankle and the options. Not much has changed, however, Samantha had an opportunity to actually look at a prosthetic and she again asked extremely insightful questions. Dr. Heare was proud of her.
I believe after all is said and done - she is leaning back toward the amputation. The infection in her ankle has gotten a bit worse so we will definitely be taking care of things in December. Samantha wants to be able to enjoy Christmas so I am thinking it will happen on the 31st... of course this all depends on Dr. Heare.
Samantha wants some time to talk with her friends about it and then she will give me the final ok to let Dr. Heare know.
I know the next few months will be hard but we will just do it.
In the meantime - I am going to try to start sleeping again hopefully without dreaming. I have had a couple funky ones this week - from flying in an airplane when the door is opened mid flight to getting lost in an extra large parking lot where I wander around looking for my car. You don't really have to be Freud to figure those out, huh?
Isabella is finally back to normal, Daniel is trying to figure out Calculus and Jeremy is trying to find a way to deal with the stress of his job on top of all the family stress.
I think we have good game plans in place and we are looking forward to the holiday season.
Samantha has detailed the plan of her room to me and we will be working on that tomorrow. Hoping to have dinner with the uncles on Sunday to celebrate her birthday and then she is planning a party next weekend at her dad's house with her friends from school.
Back to normal! :)
Love to everyone!
Tuesday, November 4, 2008
Ups and downs
The big kids were with their dad over the weekend, but Samantha stopped by to trick or treat at the house and said hi. Isabella was excited to go out - but even more excited to stay in and hand out candy. She sat on the mat in front of the door and every time someone came toward the house she would call out 'MOM'... totally cute.
The weather here in Denver has been fantastic - just about perfect, so we decided to head to the zoo on Saturday.
Here is Isabella and Jeremy posing on the Hippo sculpture.
The carousel is an Isabella favorite. She also enjoyed seeing the giraffes - they had 2 babies (who are much taller that Jeremy and I).
Thursday, October 30, 2008
Life is Good
Monday, October 20, 2008
Glad to be Home
Well we left Denver on the 8 am flight on Wednesday. Isabella was full of energy but well behaved on the airplane. When we left it was 28 degrees and we arrived to a sunny warm day in San Fran.
We took the train downtown and hung out around the Embarcadaro and Pier 39. We tried to find a spot to store the luggage while we did some sight seeing - but there was nothing available. Unfortunately we had to haul the luggage around with us. As you can see from the picture - Isabella hitched a ride.
We had an oyster lunch and checked out the sea lions then hung out at a park to rest a bit. One thing I love about San Fran are the colors - there are so many beautiful plants and buildings - everywhere you look is life exploding. Even the people are colorful. I love the diversity.
I may steal the idea of the little vine cottage and create one for Isabella at our home. She loved hanging out in it!
We hopped back on the train and headed for the Oakland/Alameda area. We stayed with Ashish (Jeremy's boss) and his family. It was really nice - Jill - his wife - took such great care of us. We were totally spoiled.
On Thursday, we hung out in Monterey at the aquarium there. I think we spent close to 5 hours. Isabella checked out all the fish and there was a lot of interactive exhibits just for kids.
Here she is at one of the many touching pools. She not only got to feel seaweed and kelp, but also starfish, sea sponges and coral to name just a few.
Here she is hanging out in a big clam. One play area she was able to put on flippers and hold a fluke to see how it may feel to be a whale and move.
We watched the sea otters eat and train as well at learn about how vast and important the ocean is.
When we were getting ready to leave, Jeremy and I took the pail - filled it with water and washed all the sand off of Isabella. We turned around to pick up our stuff and head to the car. As I looked back - there was Isabella - burying her legs in the sand. We eventually gave up - wrapped her in a towel and strapped her in the car seat. Then headed to Sonny's house to hose everything down.
Our flight out of San Fransisco was at 6 am Sunday. Isabella thought is was so cool waking up at 'night'.
Sunday, October 12, 2008
Brrrrr
This past week has been nice and quiet for the most part. Last weekend Daniel decided he wanted to have a party at his dad's house since it was empty. Well he got caught and was grounded this past week. Chris made it home from India yesterday and added a few more restrictions as well. It was nice having him home for a change, although he may disagree.
Samantha is doing much better. She is back in the swing of things with school and has adjusted to the new pain level in her leg. It is still red and tender but she is making it thru school with out too much Advil. She was excited to see her dad and Sharmi.
Jeremy and I will be heading out to San Francisco Wed thru Sunday. It will just be the 3 of us. He found some cheap tickets a while back and to tell you the truth I am looking forward to a relaxing vacation. His boss Ashish lives in the area and we will be staying with him and his family for most of the time. We are planning on hitting some wineries, the beach, the zoo and the aquarium. Doesn't that sound like heaven?
Last week I mentioned that we went to the wedding reception of a friend from work. His wife couldn't make it because her son was sick after a chemo treatment for Leukemia. Well the he developed a pretty serious fungal infection in his lungs and just couldn't fight it. He died yesterday. Even though I didn't know him personally - it still hit me hard. This was Leukemia - one of the highest cure rates of most children's cancers - but it was the side effects that did him in - not even the cancer. There has to be a better way to cure this stuff. Every day I hear of another child diagnosed or lose the battle... I just hope that awareness starts ramping up - I really don't understand why it is not already there.
I feel truly bless that we made it thru the past year and a half. Hug your kids, families and friends - that is all that's really important.
Tomorrow I promised Isabella that we would decorate the house for Halloween. I will try to take a some pictures and post later.
Night and love to everyone.
Monday, October 6, 2008
My Favorite Time of Year
Well we had Isabella's "friend" birthday party this weekend at the Denver Children's Museum. She and 4 other girls played in the many exhibits. There was a full size firetruck with pint size fireman outfits and hats. There was a big tree house with tunnels and nests so that the kids could play as squirrels (Isabella) or rabbits or birds. I think this room was the favorite. There was also a grocery store and restaurant - an art center (See Samantha's work below) and a dress up and dance room. We will definitely have to go back. There was just too much to do in the time allotted.
There was also a workshop where kids could build things out of recycled wood and plastic. Isabella just liked wearing the goggles but Samantha and Bob really got into it and built a helicopter.
After the kids had some time to play, we all gathered back in the birthday room for pink cupcakes and presents. It was still quite a bit of work to bake non-artificial cupcakes (the only thing bad in them was a bit of sugar...), put together healthy munchies, goodie bags and decorations - then load everything up and get to the museum in time to set up in the 15 minutes they give you before the party starts. But the great things was at the end of the 2 hours we got to go home to a quiet house. At least for 30 minutes or so... Grand Bob stayed with the kids and Jeremy and I had to run out to a friends wedding reception. It was really nice but a sad in a way. The brides son has been battling Leukemia for a few months. They planned the wedding around it - but her son ending back in the hospital with a pretty serious infection so only the groom was present. Keep them in your thoughts - he isn't doing well at all. It still makes me cry a bit - I remember my frustration when cancer interrupted our life so many times the past year.
Sunday, September 28, 2008
A Dance and a birthday
Thursday, September 25, 2008
80s Day during Spirit Week
He and Samantha talked again about her options - either the below knee amputation or the 2 stage reconstruction surgery. Samantha asked a lot of really good questions. Dr. Heare said he is looking at the surgery to happen in December over school break unless the infection gets much worse then we would have to make the decision sooner. He wants to see Samantha again in a month to evaluate and in the meantime he is going to arrange for her to meet with a prosthetic specialist to see the a real prosthetic - see her options and ask questions.
If she decides for the amputation - the recovery would be much shorter - she would begin walking 6 weeks after the surgery and probably be walking just fine without crutches before summer.
If she decides to fight for the foot - the first surgery would involve removing all plates, screws and the cadaver bone. Then put the place holder in - during this time she would be in a cast - non weight bearing for 6 weeks. Then he would go back in and start over - we would be looking at 1 to 2 more years before being able to walk without crutches.
Samantha has been talking with one of her cancer friends who has an above knee amputation and was prepared for her conversation today. I was so proud of her!
We don't have to make the decision now - but Sam is leaning toward the amputation and getting on with her life.
Either way - nothing will happen for a while yet.
Monday, September 22, 2008
Music, School Spirit and Cauliflower
I made some fresh salsa - just waiting for chips.
It has been a while since I have used tomatillas - I decided to cook them a bit. I will let you know how it turned out. The last picture is my first fall picture - appropriate since today is the first day of fall. The pumpkin is a casualty - I was trying to get to my broccoli and I pulled up what I thought was yellow squash - but it was my one and only pumpkin plant. Oh well - we will have one green jack-o-lantern ...
Only one of my burning bushes is changing - the other 2 are still green. I don't think this pictures does it justice. The red is beautiful and vibrant!
Ellie and Leah were visiting tonight and the girls were singing - here is Isabella doing Demi Lovatos 'This is me' on You Tube. Too cute!!! http://www.youtube.com/watch?v=kRc5MHg6IyU
Remember that you probably won't be able to watch this thru your VPN. But take a look when you get a chance.
Jeremy missed his connecting plane so we just got home and I am ready for bed.
What a day - life is good!
Love to everyone!
Sunday, September 21, 2008
Miracle Party
Just as we were walking into the party - they called Samantha's name. She went up for the introductions along with all the other cancer kids being recognized. There was music and dancing all evening.
All the kids had banners hanging thru out the room!
Here are all the kids looking so beautiful! Donna and Samantha wore masks (Donna took a break), while Isabella was a princess and Daniel was a pirate.
There was a lot of fun things for the younger kids to do... They had jumping castles, a dress up corner (Isabella spent most of her time there) and a pirate chest. They also had face painting. Both Samantha and Isabella took part in that...
I know I talked last blog about the first ever National Childhood Cancer awareness day - but I thought I would post some of the pictures from the day.
Here are all the survivors that made it that day. Kori is giving a speech - she is the one who started Gold Ribbon Families - my mom's cancer support group.
Layer/Gray Family
- mightymom
- Layer/Gray family includes Jeremy, Dawn, Isabella, Daniel and Samantha. We are active, opinionated and fun loving!