Wednesday, March 30, 2011

Before we get started with today's update, I ask that everyone please take a moment to enter your e-mail address into the "follow by email " box  --------------------------------------------------------->>
Entering your email address will allow for you to receive automatic updates, vs. me sending them.


Moving on...

William started chemo and for some reason, he is taking this round a lot harder than he  has in previous 5 rounds.... All day William has been struggling with extreme nausea, headaches, diarrhea, hiccups, and cramping tummy. What can I say, today is not a good day.

I received the much anticipated Bone Scan report and I am at a loss of words..... The report is below so feel free to read it. Even though it sounds like there is new cancer, some of the existing cancer is apparently dying and therefore, William is considered to be "Stable" I am not taking the news of "new" cancer very well, in fact I am having a little mini melt down.  DSRCT in the maxillary sinus is extremely rare, so not only does William have an extremely rare cancer, he now also has it in an extremely rare location.

I still have a lot of unanswered questions regarding the report but, I am scared to ask those questions as the answers may lead to even more negative findings.


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