Tuesday, March 29, 2011

Ending of a long day.

I am happy to report that the hole in William's lung appears to healing AND the air that leaked into the cavity has been absorbed and is therefore no longer a large concern...

As with everything else related to William's treatment, I have learned so much during the past 36 hours ( I am seriously considering becoming an oncology nurse)

For those of you that are interested, here is a quick rundown of  everything that has happened..

William's first central line:
William's Second Central Line:

William's Pneumothorax:

















Anyway, William is spending another night at Sutter. His blood pressure has been running unusually low so we will be keeping an eye on it. If everything continues to improve then tomorrow we will be starting chemo, thus spending an additional three days at Sutter Resort and Spa.

William had his bone scan and pelvic CT scan this morning. I am a little nervous about the bone scan as halfway through the procedure the nuclear medical tech left the room to "ask the Dr. a question". When the tech returned a few minutes later he had a strange confused look on his face and stated that additional scans were needed of the spine.... I don't know what that means, nor do I want to read too much into it (but I am!) Hopefully the reports will be ready for me to "analyze" first thing in the morning.

William is doing really good. He is back to being an extremely energetic, loud, funny and messy little 8 year old boy.  Besides a little discomfort and sore chest, there is is absolutely no sign of Sir. William being sick, and this is a blessing!

We appreciate every one's prayers, phone calls, text messages, emails and visits...

Keep on keepin on.
Live Strong in God's miracle of healing.



Update

X Ray results throughout the night - No change -
William's blood pressure, blood oxygen level, heart beat and breathing are all within normal range SO even though the hole is not closing on its own or as fast at they would like, he is in no immediate danger.

Waiting for the surgeon to arrive so I can find out what our next course of action is going to be. I have no idea how this stupid little whole is going to get fixed....

I will keep you posted.

Keep on Keeping on.
Live Strong in God's miracle of healing.

Monday, March 28, 2011

It must be Monday

Today is March 28th, my 30th birthday and William's surgery day.

Let's start with some positive news - I received William's PET scan report, it reads as follows:
"Whole body PET scan showing multiple hypodensities throughout the liver associated with low-grade FDG activity. When his PET scan is compared to the prior dated 12/28/10, these hepatic lesions have remained stable in size, number and in low-grade FDG activity. All nodal sites that were previously identified have normalized to background with the development of no new sites of abnormal FDG activity to suggest metastatic disease in new anatomical locations. Findings suggest stable to improved PET scan when compared to prior scan. "

As many of you know, William had surgery today to place his new central line. In my previous blog post I commented on the small chance that there could be some complications from the surgery.... Long story short, William's lung has a small  hole in it and now there is the concern that his lung is leaking air into his chest cavity which could cause his lung to collapse.

So, here we are in Sutter Hospital trying to make the best of the situation...

William will have lung X rays done through out the night, I will keep this blog updated on the results.....


On Friday night GiftToCure had it's first annual Masquerade Gala. We did not sell as many tickets as initially hoped for but, I am happy to report that those that did attend had a great time and got some great silent auction items at amazing prices;)  I want to thank those of you that did attend, your support is greatly appreciated!


We would certainly appreciate every one's prayers!
Keep on Keeping on. Live Strong in God's miracles of healing!

Wednesday, March 23, 2011

Surgery, swimming and scans.

William's surgery for a new central line placement is scheduled for Monday morning.  
My mom and I met with the surgeon (Dr. Joy Graf) today and after an extensive Q & A most of our concerns have been addressed and dealt with.
Due to the fact that a vein may only be used once for a central line placement, William's new line will be located on the opposite side of his chest and instead of the line running  through the vein in his neck, the new line will be placed under the collar bone into a vein that runs on top of the lungs(YIKES!!!) The biggest risk with this surgery is that the lung may collapse and/or get punctured( YIKES!!!)  Dr. Graf has been doing line placement surgery for 20 years (@ 2x week) and she has only come across lung complications twice. I feel better knowing that the surgeon has experience, but I am still nervous!

As mentioned in a previous post, William's lack of central line comes with some perks aka swimming ;) For the last couple of days we have enjoyed the pleasures of our local sports club's heated pool ;) William has also been able to take showers, something that has not been done in months as baths are the only option for patients with central lines.  Entry points for the central line into the body has to be kept sterile and dry at all times, therefore William's baths (with the central line) always involved a long tedious prepping process that included saran wrap or aqua guards.  I do enjoy the luxury of temporarily not having to worry about sterile dressings or all the prep work involved with William taking a bath.

While in the hospital last week, William and a couple of our favorite nurses engaged in a much anticipated and planned (on William's part) Nerf War... The video below is just one of the many battles that I captured ;)

Our nurses are more than just medical care providers, they are angels that always find a way to put a smile on my son's face!!! Thank you!!

On Friday morning William will have a PET scan, it will be the first scan that we have done in 4 months and since the start of our new chemo protocol.  Scanxiety (scan- anxiety) is a terrible emotion to have! I ask that everyone please keep William in your prayers! Please pray that the chemo is working and that William's body is in the process of becoming cancer free

Remember our hospital buddy William M? His parents have received the best news ever, William M is in remission. This is such amazing news and I am so happy for them, a little jealous, but extremely happy! Thank you God for healing!  Another one of our hospital buddies, Spencer, finished his last round of chemotherapy last week ;) You go Spencer! We are so incredibly proud of you!

Don't forget that on Friday March 25th, GiftToCure will be hosting a Masquerade Gala at the Arden Hills Resort Club and Spa.  For more information please visit http://www.gifttocure.org/eventforcancer.
 
William and My Mom (Grandpa, we wish you were here)

Thank you for all of your continued love, support, friendship and prayers!
Keep on Keepin' on. Live Strong in God's promise of healing!

Monday, March 21, 2011

It's just not fair!

This weekend the DSRCT community lost another of its family members. Taylor was a 19 girl who had been fighting DSRCT for a little more than 3 years. Last year on her 18th birthday she finished her last round of treatment and was NED (No evidence of disease) for a few a months when the disease suddenly returned again.

For the last three weeks Taylor endured a collapsed lung, breathing and draining tubes, kidney failure, immense pain and constant vomiting; not once did she ever give up! Taylor fought a brave battle until the very end.

I ask that everyone please keep Taylor's mom, Kendra, in your prayers!

Since November the DSRCT community has lost about 10% of its family members (Less than 100 known surviving patients world wide and less than 500 ever diagnosed) I can't help but feel an immense sadness and hopelessness. I despise this horrible cancer and I despise what it has done to so many people. My heart is broken today and I can't seem to find the energy to force a smile.  I try to hide my crying for William because he is not really aware of how serious this disease is, nor am I about to tell him. The last thing I want him to know is that a person with is same disease had earned her angel wings.

I am so frustrated!!!I am angry and I am so terribly sad...It's not fair that there is a mom in Texas that is planning her daughters funeral! It is not fair that so many other people that go through live unaffected by all the horrid events that us DSRCT moms experience on a daily basis. It's not fair that this disease only allows for a 15% chance of 5 year survival. It's not fair that my son is sick and I cannot do a darn thing to heal him. It's not fair that William has cancer!


Taylor does have a caringbridge page, for those of you that would like to leave some encouraging words
http://www.caringbridge.org/visist/taylorhargrove


On Friday night (March 25th) GiftToCure will be hosting it's first annual Masquerade!
The event will be"unmasking" DSRCT. We need every one's support to make this event a success! Event will include a live Jazz band, silent auction, food, drinks, and local celebrities!
Please attend and support GiftToCure in it's quest to fund DSRCT research!
Tickets must be purchased online at
http://gifttocure.givezooks.com/events/black-tie-masquerade-unmasking-dsrct-an-elegant-fundrai

I would appreciate it if you would please tell all of your friends and family members about the event!



Keep on Keepin' on.
Live Strong in God's promise of healing!

Tuesday, March 15, 2011

Procedure Update

William's broviac has been removed and surgery was a success....
Thank you for all your prayers!













The new broviac will not be inserted for about two weeks ;) This means that for two weeks William will be able to go swimming and participate in some other activities that he has been restricted from during the last year ;)

If everything continues to go well we will be able to go home on Friday. We ask that every one please remember that William's immune systems is still a little compromised and therefore we ask that you please not visit at this time. I will let everyone know once his ANC goes up a little more

Thank you....

Monday, March 14, 2011

Plan of action

William's blood cultures have come back positive for Kokorea Rosea (please feel free to research on internet)

Tomorrow William will have suergery to have his broviac (central line) removed. After surgery a peripheral IV line will be placed and hopefully after three days of antibiotics, his blood will be clean and clear of all bacteria and infection. Next week William will once again have surgery, this time it will be to insert a new central line.

If everything goes as planned and there are no complications with surgery (I am told that it is not a big deal and is often done in outpatient) we will be able to go home on Friday! WOOO HOOO!

Please keep William in our prayers!

Wednesday, March 9, 2011

Stupid Infection!

On Monday night William spiked an extremely high fever of 103. Needless to say, no one got any sleep that night! On Tuesday when we arrived for our outpatient chemotherapy the nurses took a blood culture (figure out th cause of high fever). This morning we received the call - William received a positive on his cultures.
So, here we are at Sutter Resort and Spa........
Shortly after arriving, William was given a dose of Vancomycin (broad antibiotic) and shortly after receiving the Vancomycin, William broke out in hives and had an anxiety attack. So, long story short..... Chemo Suck, Antibiotics Suck, Germs suck, Pain sucks, Watching our little boy going through all this crap SUCKS..

Monday, March 7, 2011

No News is Good News

WOW, I cannot believe that is has been more than two weeks since my last update! I am sorry for not writing sooner and keeping everyone updated...actually, there's not much to update you on.

William is doing really well; after his last cycle of VP16 and Carboplatin his blood counts took a huge dip in numbers but, that was to be expected.  So, besides the dozen or so transfusions that William has received during the last two weeks, we really have not been doing a whole lot.

Today is day 1 of William's 10 day outpatient chemotherapy.  William was originally scheduled to start this more than 10 days ago but, due to his blood counts being so low the entire process was postponed.

So, here we are in the month of March, a month that in my opinion most American families would correlate with March Madness, Mardi Gras,  St Patrick's Day, Ash Wednesday and Lent.  In our house, March will no longer be the happy and fun month  in which we celebrate Grandpa's or Mommy's birthday, nor will it be the month in which we would normally celebrate our anniversary, instead it is the month that we look back on remembering the horrible words spoken by William's pediatrician "There is no easy way to say this, your little boy has cancer"

I guess it is to be expected that for the last week I constantly find myself looking back and remembering all the events that happened exactly 1 year ago.  William's diagnoses was not an easy one...It took us almost 4 months filled with emergency room visits, several different pediatrician consults, and countless urgent care appointments before the tumors were found and his cancer had already progressed to stage 4.

Today there has been a lot of should-offs, could-offs and what-ifs running through my mind  and heart.....We have so much to be grateful for so I will not allow myself to dwell on the negative, but still I'm sad and terribly scared.

I wrote this a few months ago in the old blog, and I feel it is appropriate to say it again.....


You know that feeling you get in the bottom of your stomach when you suddenly realize that you forgot to do something important? You know, the feeling of nausea, anxiety, stress, fear, anger, and disbelieve. It’s a sensation that turns your feelings into an emotional storm, a Hurricane Katrina in the center of your heart and mind. Well, that is the feeling that you have all time when you are an oncology mom.

Don’t get me wrong it’s not all bad, there are good days too, no, there are great days! But, even during the best of times and the most memorable days, your eyes are always on the approaching storm. It is that awareness and constant knot in your stomach that is a relentless reminder of the horrid reality you now call life...

 Being an oncology mom comes with a lot of emotions, pressures, education, and physical strains!

Emotions- No, I am not talking about the everyday happiness, anger, fear and stress. I am talking about anxiety that without any warning will send you spiraling into a tornado of confusion, frustration and an emotional disconnection. I am talking about anger, hurt and a sense of helplessness that causes me to be an unstoppable blubbering mess. I am talking about the inconceivable emotions that William is attempting to deal.

Pressure- Pressures to stay on top of medication and broviac maintenance schedules. Pressure that we place on ourselves to stay on top of the treatment road maps, protocols, and all other possible test trails. Pressure to maintain a balance in our relationships and not neglect those we need as our emotional anchors. Pressure from financial strains and fears. Pressure to always be prepared for the unexpected. Pressure to be your child’s advocate because you know that no one else will be. Pressure to try harder at being the person, daughter, sister, cousin, wife, and mom that others want you to be, think you should be, or expect you to be.  Suddenly, the pressure of keeping everyone informed, educated, happy and content, all falls on your shoulder, whether you want it to or not!

Education – When you enter the unwanted society of oncology parenthood you unknowingly enroll in “Oncology School”. The first week is a blur; all you will vaguely remember is the small pieces of information written on the documentation, explanation brochures, and reports provided by the medical team. The second week is spent doing research and finding associations that could provide you with support. Somehow you also try to figure out the medical language because you know that if you don’t, you will be left with more confusion than what you started with. Knowing the lingo of ANC, WBC, HGB, RBC, Neutropenia, PET, CT, MRI, Bone Scan, Nuclear Medicine, BP, and NPO will lead to a conversation with doctors that feels almost alien. Weeks 3 and beyond you will transition from student to professor. You will turn into an encyclopedia of facts and a diary of events. You will turn into a mathemagition and start gathering facts, odds, statistics and probabilities. All of the information that you now have will somehow be used to come up with an equation that will result in patterns, behaviors, results and expectations.

Physical Strains- We all deal with the pressures and stress of seeing our children suffer in different ways. Some of us gain weight and some of us loose it (yeah, I am not one of those lucky ones). Some of us struggle to regain any form of control in our stormy emotional lives, so we do something drastic to our appearance (Yep, that’s me). The point that I am trying to make here is that the only physical resemblance Oncology Parents share is the look of constant exhaustion and immense fear. We might as well be wearing a scarlet letter on our shirts; Spotting us is as easy as looking at the dark circles under our eyes, dried tears on our cheeks, smell of chemo pee and vomit on our clothes, and a constant frown line that will forever be tattooed on our foreheads. The only way we can blend in with the “normal” parents is to somehow find a balance between sleeping, being a care provider, and finding a way to cope with our new realities.

It is devastating how this storm has left areas of disaster in practically all the regions of our old life!! Randell and I are blessed because not only do we have each other, but we have the support and companionship from a lot of you! So much has changed in the last year that it is hard to determine the next year ahead of us. The only constant is that God is in control and our faith and believe in Him is what will calm our hearts and fears.

If you are an Oncology Mom or Dad,  I want to let you know that YOU ARE AMAZING! We are a sister/brotherhood of relentless fighters that will defend our children’s rights for proper medical care, emotional support and the best medical staff available. We are a sorority/fraternity of parents that will unfortunately forever be bonded together by the shared pain, fears, guilt, anger, sadness and happiness. We are not alone, we have each other and the love and support of those around us.

We would appreciate every one's continued prayers for complete healing!

Loiss and Randell
The proud parent's of Sir. William

Monday, February 21, 2011

Reminders

For all of our friends and supporters in the greater Sacramento area, please remember that William's fundraiser at Chicago Fire Restaurant is today!

Remember, if you would like to attend, please print out the flyer (click on the picture for a larger view) and present it to your waiter/waitress. 15% of your order will be donated to William.


William and I are currently at Sutter Hospital where he is receiving some much needed transfusions.  The blood report from this morning was the lowest I have ever seen it and it is really how quickly his numbers drop! Remember he received a transfusion on Friday,3 days ago, and today he his little body was basically empty! 


This is a copy of William's CBC (Complete Blood Count) today. The first column is a description of each item measured. (FYI ,WBC = White blood Cells
RBC = Red blood Cells) The second column is William's counts from today and the third column is the normal range ...


















Keep on Keepin' on.

Friday, February 18, 2011

The good, the bad, the kind, the love, and the unknown.

Day 10 of Chemotherapy round 12.

Yesterday William was scheduled to receive platelets; however, when we arrived on the 5th floor
(pediatric outpatient) we discovered that all of the rooms were full and the waiting room was filled with 6 additional families waiting for beds to open up. We decided to not wait around and chance William being exposed to hospital germs, instead we decided that it would be best to return in the morning.  So, here we are on the 5th floor waiting for William's platelets to arrive.  The transfusion of platelets is normally a 30minute to 1 hour process but, we usually wait an additional 2-3 hours for the the paperwork to get completed, platelets to arrive, benadryl to get administered etc. etc. It is normally during this waiting period that William and I do homework and catch up on his cub scout activities.

This morning's activities in the room is different, William is sleeping off a strong dosage of Dilaudid and I am desperately trying to catch up on some much needed insurance paperwork. UGH! When we arrived at the hospital this morning William had a slight low grade fever (99.0) If his temperature rises above 100.5 
 a 0.6 degree difference, it would be an indication that his little neutropenic body is trying to fight off an infection, and that means that we would get admitted for observation and antibiotics. We recognize that a low grade fever admittance is a safety precaution, but we really don't want to stay here for the weekend.

Next week William is scheduled to start phase two of the new chemo regimen. Phase two is the outpatient combination that we get to do at home and on the 5th floor. Fortunately this combination allows us to spend nights at home with Randell. Unfortunately, we are not sure how William's his body will react to receiving the two two different combinations(Carboplatin and VP 16, and Irinotecan and Temador), so close to one another. Last month William had no side effects with the Irinotecan and Temador, but then again his body also had 30 days of rest and recovery in between the previous Carboplatin and VP 16 chemo treatment, this time there is only a 12 day break. I can't help but to get anxious and scared. I like to be prepared for all of William's medical needs, unfortunately it is hard to be prepared for the unknown.

My mom will be coming to California in March- WOO HOOO - During her stay here Randell and I will be able to take a much needed break. Together we have done an amazing job in coping with reality but, we are both tired and in desperate need of RandR. On March 25th GiftToCure will be hosting a Masquerade Gala at the Arden Hills Spa and Resort. The event will be strictly black tie (and mask) and will focus on the awareness of DSRCT and much needed research funding.  A silent auction, live music, and local celebrities are a few of the evenings attractions ;) Arranging an event of this magnitude is exhausting. Stacie Hubbard, one of the wonderful volunteer's with GiftToCure has taken on this project and sacrificed a lot of her time and energy...Thank you Stacie for being so kind and gracious -  You are truly and angel!

Emails and blog posts about the event and ticket sales will be sent out in the near future.  In the meantime, please keep an eye out for an email from GiftToCure regarding silent auction items.

William and I want to send out a special thank you to all of our friends at Chevron in Houston - This group of strangers has in the last few months become a big part of our lives. Their unconditional love, support, prayers, positive words of encouragement and kindness has made a big difference in our lives. They say everything is bigger in Texas, well this is true because this group of strangers have the biggest hearts. To all of our faithful  prayer warriors, supporters and friends in Houston, Thank you! Thank your for William's gracious gifts,kind cards, and Thank you for the love!

We appreciate every one's continued prayers and love! It is the kind words that get us through the toughest times!

Keep on keepin on! Live Strong in God's unconditional love and the miracle of healing!

Wednesday, February 16, 2011

Gloomy winter days

William is on day 8 of his protocol and I am sorry to say that the side effects are creeping in on us.
William is on a 24/7 feeding regimen of Zofran and Reglan (+benedryl) both of these drugs are used to prevent and/or stop nausea, unfortunately their side effects are headaches UGH!  Dilaudid, William's pain medicine,  is usually the drug of choice for his headaches and other pain; however, Dilaudid causes nausea so we are staying clear of that. Tylenol would be great for stopping the headache but unfortunately it could also mask any fevers. So, the next best option is Motrin but, Motrin does have the side effect of causing serious bleeding in chemo kids.... So, the big question for the day is WHAT DO I GIVE WILLIAM THAT WILL MAKE ALL THE PAIN GO AWAY AND HAVE MINIMUM SIDE EFFECT?  I have called the doctor and I am waiting on him to call me back with some hopeful answers, in the meantime all I can do is rub his head and give him hugs.

This morning I noticed that William's knees and ankles all have small bruises from them rubbing together while he sleeps. So, when you add it all up:
bruising+tears+tired+nausea+headache+constipation = BAD CHEMO SIDE EFFECT

Tomorrow afternoon William and I will be returning to the hospital for transfusions, hopefully he feels better after that. It is the worst feeling in the world when you, a mom, can  do nothing to make the pain and chemo monsters go away. 

That's all for today.

Keep on Keepin on. Live Strong in God's promise of miracles and healing.

Monday, February 14, 2011

Happy Valentine's Day

To all of our friends, supporters, aunts, uncles, grandpas, grandmas, cousins, sisters and extended family members...................

Chicago Fire Restuarant - February 21st.

If you are attending the Fundraiser - Please click on the below image, a new screen will open up and you will be able to print the flyer from that screen.

Saturday, February 12, 2011

The best day ever!

Today one of our hospital buddies, Kaleb Phillips, had a fundraiser at Airsoft Battlegrounds. Some of the activities and attractions at the event included face painting, jumping castles, airsoft battles,  various karate demonstrations, photo booths and food vendors.

From all of the conversations leading up to today I knew that William was excited; however, I did not expect the amount of energy that came exploding out of his little body! From the time we arrived at 11am until the time we left at 3pm, William was constantly running around, participating in all the events and having an absolute blast.

William officially finished chemo on Thursday night and knowing that his platelets have not yet been affected, Randell and I decided that it would be okay for him to participate in the Airsoft games. For those of you that do not know, Airsoft is a team sport similar to paintball where replica firearms shoot plastic BB rounds. The location we were at today was an indoor arena specially designed for the game. William did two rounds and had an amazing time.  Yes, it does hurt. Yes, William was shot. Yes, William has bruises. Yes, William had a lot of fun!

Somehow even after almost a full hour of running around playing airsoft games, William still had enough energy to bounce around on a jumping castle, participate in jousting games and get his face painted.

Here are some of the photos from today............

 

William and Kaleb!
Kaleb is 7 and he is fighting his second battle with Rhabdomyosarcoma.

While we were driving home this afternoon William exclaimed that he had the best day ever!  The comment and the memories we have from today is the reason why we keep fighting. The laughter, giggles, smirks and smiles is the emotional fuel that we all needed to refill our emotional gas tanks!

It is sometimes necessary for me to function with my emotional fuel gage on empty so I am grateful for today's refueling because not only did it fill me up, it provided me with some reserves ;) I read something the other day that stuck with me "You don't know how strong you can be, until being strong is your only option"  The strength I have is not always shown or expressed in ways that are appreciated by everyone and this leads me to something that I need to say ----------

Even though this blog was intended to communicate William's medical treatment and updates, it has become so much more. The blog has been a journal of my thoughts, fears hopes and dreams. It has been a memoir of events, both happy and sad. It has been a medical journal for treatment options, and it has been a dictionary of explanations and terminology. What this blog was never intended for was the use of a weapon or a tool to be used against me or my boys.

Lately, I feel like there may people out there that criticize and judge me. Some criticism has to do with William's medical treatments, some of it has to do with my relationship with Randell, and some of the criticism even surrounds my intentions with this blog. Sometimes the criticism is valid and I will do my best to correct the error. Yes, there are a whole lot of raw emotions and feelings floating around and it is sometimes easy to loose sight of love, compassion and forgiveness. What I am trying to say is that during the last 10 months I have been consumed with William's diagnoses and somehow, without my intention to do so, I have neglected important relationships.  I don't want to make excuses for the lack of contact, the missing connection or the missed opportunities, what I want is my apology to be heard and for all the anger to just go away!  I am exhausted and I struggle for the energy to defend my family, my relationships and my decisions. My apology is sincere and I hope everyone accepts it.

Keep on Keepin on. Live Strong in God's love!

Thursday, February 10, 2011

Laughter is the best medicine!

Day 3 Chemotherapy Round 12
William will be finishing up on his third dose of VP16 tonight and if everything goes smoothly, we'll be headed home around 11pm. YIPEE!!

For the past three nights we have been sharing a room with Kenji, an extremely sweet 8 year old little boy who is also fighting cancer. We've roomed with Kenji once before so fortunately the two boys are familiar with each other and they get along fantastically! It is great to see the two boys sharing jokes, playing Wii, and comparing spelling skills (the hospital teacher gave them a verbal spelling test) During the past couple of nights there has been a of laughter and giggles between the two boys. Having a buddy to share the room with makes all the difference in William's treatment! Thank you Kenji for being a good buddy!

Speaking about hospital buddies, William M. one of my William's hospital buddies, is currently at UCSF where he is going through the long and dangerous process of getting his bone marrow transplant. - We would appreciate it if you would please keep William Murdock and his entire family in your prayers. 

I almost forgot to tell you about William's stardom! In an effort to raise awareness about DSRCT, William was featured on the KOVR3 6pm news on Tuesday night. William has been on the news a couple of times during the past year but, this is the first time that the report was focused solely on him. Due to the attention and feedback received from everyone regarding the interview, William's self-esteem has raised so much that I now call him Justin Bieber Jr :-)  For the past 11 months there has been a lot of stares and comments from peers and strangers that left William embarrassed about his little bald head and diagnoses (BTW, people need to teach their kids to not stare). Walt Gray did such a great job with William's news story that William is now walking around with a big goofy smile and gleaming pride! There is no more shame about his lack of hair!  Nothing beats the amazing feeling of your child's happiness and it is the bright, cheery, happy and memorable moments like these that give us our strength and courage to continue the fight.

Please remember that there are two fundraising events this month for William.

Fork in the Road to Apocalypse is a book written by Jeff Gonsalves, one of William's fabulous nurses and a talented author. All the profits from February sales will be donated to directly to William.  The book can be purchased on Amazon.com

On 2/21/11 All 3 of the Chicago Fire Restaurants will be donating 15% of their sales to William. If you would like to participate in this event, you will need to download and print the flyer. The flyer must be presented to your waiter when placing your orders. 

I want to thank everyone for the continued prayers and kind emails! William loves reading your messages, emails and cards!

Keep on Keepin on. Live Strong in God healing all of the cancer in Sir. William's body!

Wednesday, February 9, 2011

Here we go again!

Day 1 Chemotherapy Round 12
William started round 12 of chemotherapy last night and fortunately everything seems to be going really well. The chemotherapy he is receiving has in the past given us problems with neusea, constipation, headaches and fevers, hopefully we can avoid them this time.

I am exhausted and don't feel like writing, I will try to write more tomorrow....

LOOK AT THE WILLIAM'S BEAUTIFUL HAIR!!!

Keep on Keepin on, Live Strong in God's promise of miracles and healing!

Friday, February 4, 2011

The good, the bad, the ugly and some hope.....


It has been brought to my attention that with all the excitement about our LA trip, I completely forgot to update everyone on William's pinewood derby last week.  DRUM ROLLLLLL......William won his first four elimination races; unfortunately he lost his 5th race by .003 seconds..... Such a bummer. Out of all the participants (40+ total), William placed 15th. We all thoroughly enjoyed the day and William was proud of his accomplishements!

Our trip to LA was a memorable and relaxing experience! William had a lot of fun hanging out with his grandpa and exploring the interesting beaches of Santa Monica, Venice and Long Beach.  We also had the oppertunityt to take William to "Hollywood". William was a little dissapointed that Hollywood was not filled with celebrities walking around everywhere but, he had a great time exploring all the stars, visiting the chinese theater, and taking photos with some of his favorite characters, Spongebob, Shrek,Elvis and Elmo.
William and I returned to Sacramento yesterday afternoon. Unfortunately our day yesterday started at
4:30 am yesterday as Grandpa had a 6am flight out of LAX; Fortunately, the drive was back was filled with little traffic, a lot of eye-spy games, and countless jokes courtesey of William's imagination.

Upon our arrival in Sacramento, William had a clinic visit to check his blood counts and ANC levels.  During the appointment I asked the Dr. if he had spoken to either of the doctors in LA? Long story short, the conversation between us ended up in the parent conference room (nothing good ever comes from that room) where I had an emotional melt down. .........................Before I get too side tracked with my emotional jibber jabber, let's review some facts from the consults we had this week.



Consult number 1
Dr. Clarke Anderson at City of Hope.  
The meeting was extremely positive and discussion included stem cell rescue, whole liver radiation, and high dose chemo.
Consult number 2
Dr. Marcio Malagolowkin at Childrens Hospital of LA.
This consult was not as positive but, treatment options included debulking surgery, Chemobilization, and possibly doing a stem cell rescue.  O' and I need to mention that due to some confusion at the hospital, Dr. Marcio did not have the opportunity to view William's scans prior to the meeting; therefore, everything discussed during our consult was based on assumptions and estimations

The meeting yesterday was a detailed and honnest review of the following: 

William's disease is in the following areas
*Lungs -microscopic
*Mediastina
*Liver-Bulk of the disease
*Spleen
*Retroperitoneal Lymph node
*Left Testes
*Multiple bone masses including spinal cord

Yes, this is a lot but keep in mind that this is a drastic positive improvement from the initial diagnoses 10 months ago.

We have two treatment options:
*Balance and maximize quality and quantity of live, knowing the inevitable outcome.
*Pursue cure at all costs knowing that historical statistics on this disease are not good.

If you know me, then you know that I am not going with option 1. We are fighting this!! William is an amazingly strong little boy and he deserves the chance to grow old! I am not naive, I understand the odds, but 1% is still more than 0.

Now, let's go over how the above mentioned facts correlate with the treatment options discussed with both doctors in LA.
*Whole liver radiation
Not an option. Radiation would mean a delay in chemo and a delay would allow the cancer in all the other areas of the body to grow and spread.
*Chemobilizatin
Not an option. Due to the fact that the cancer is in both lobes, 80% in right and 20% in left lobe
*Debulking surgery
Not an option. There are too many disease sites and recovery would delay chemo.
*Stem Cell Resue
Not an option. Progressive disease in bones

The current and realistic treatment plan:
For the next 3 months, William will do a combination of the following:
Temador and Irotecan for 10 days in an outpatient setting.
VP16 and Carboplatin for 5 days inpatient at Sutter

Temador and Irotecan prevent the cancer cells from growing and spreading.
VP 16 and Carboplatin kill the cancer cells.

Our goals with the new plan is to accomplish the following:
*Shrink all disease to microscopic levels
=Stem Cell Rescue
*Kill the 20% cancer in left liver lobe
=Right liver lobe can be removed and Chemobilization would be done in left (remaining) lobe to kill any microscopic disease
*Stablize disease in all organs
=Remove spleen, testes and retroperitoneal mass
*Completely kill disease in lungs
=No further treatment needed for lungs or mediastina
*Radiate bone disease
=Bone marrow transplant

Once all the removal, radiation, chemo and bone marrow transplant has gone as planned, William will need to receive a liver transplant. Because of the strict FDA regulations regarding transplants, William will not be allowed to receive a transplant in the US. Basically, our best chance for liver transplant is for us to find a reputable doctor, surgeon and hospital outside of the US that would take 1/3 of my liver and transplant it into William.


As you can imagine, there is a lot to think about and a lot of information to process...
Keep on Keepin' on. Live Strong in God's promise of healing.


























Tuesday, February 1, 2011

Theraputic break from reality...

William and I have been in southern California with Grandpa for 48 hours and already we feel like different people. It is amazing how some sleep, a relaxed schedule and a lot of sunshine can change your entire outlook on life. 

Yesterday we spent the morning hours on the beach where William was fascinated by seagulls, seashells, and sea enenemies. William's laughter and bright smile made me realize that he needed this break from reality as much as we did.  Yesterday afternoon Granpa, William and I spent several hours at City of Hope Hospital where we met with Dr. Clarke Anderson. The meeting with Dr. Anderson was very encouraging and  extremely informative. The following are some of the main items that we discussed:
-1. City of Hope is willing to do whole liver radiation;Whole liver radiation is extremely rare and practically unheard off, but due to the miracle of some new technology that happens to be at City of Hope, Helical Tomotherapy is a valid option for destroying all the cancer is William's liver.
-2. City of Hope believes that a stem cell rescue and bone marrow transplant is William's best resource in beating this monster. Due to the reality that William has undergone 11 rounds of chemo, there is no guarantee that we would be successfull in getting enough stem cells BUT, at least they are willing to try YIPEE!!!!
-3. Ph. Balance diet has done a lot for William's body. Dr. Anderson mentioned that William's bladder recovered as well as it did because of the specialized diet.
-4. Natural supplements that we are using are probably doing more harm than good. The natural remedies that William is taking works by placing the cancerous cells in a "sleeping" or "hibernation" state. Chemotherapy is only effective against active cells and won't do anything to destroy the cells are not.
-5. The current chemo that William is on should be changed immediately. Dr. Anderson recommends VP16 and Ifosphomide as both of these drugs are aggressive in killing cancer cells and the combination is a good recipe for preparing his kidneys and bladder for stem cell harvest.
-6. City of Hope has extensive experience with DSRCT
-7.  I like Dr. Anderson and William seems comfortable with him.
-8. Patients have private rooms with beds for parents and a refrigerator.
-9. Monthly housing is available on campus at a low rate.
-10. City of Hope will be willing to transfer us in as soon as mid February.

 ------Most importantly, Dr. Anderson reminded us how amazing William's progress has been. William's tumor cell death and shrinkage is amazing and I believe that it is due to William having such good response that Dr. Anderson is so eager to help us-------You go William, I am so incredibly proud of you!!!

Tomorrow the tree of us will travel to downtown LA where we will be meeting with Dr. Marcio Malogolowkin, an internationally known oncologist that specialized in rare pediatric liver tumors. We were told by Dr. Anderson that Dr. Malogolowin provided him with 1/2 of this knowledge on Sarcoma cancers and that he is one of the best he has ever met....  I am eager to hear what Dr. Malogolowkin would suggest and recommend...

Today was our only day that was free of appointments. We spent the wonderfully warm and sunny exploring the Santa Monica pier, chasing seagulls on the beach and people watching at Venice Beach (YIKES). Venice Beach is an interesting location, that's all I am going to say about that....

Anyway, thank you for checking in on us!

Keep on keeping on. Live Strong in God's promise of healing!