2015 Light The Night

Team Whitney will be participating in this years Light The Night walk in Lawrence 

on 

September 12th, 2015

Whitney worked very hard raising money for the Leukemia & Lymphoma Society in 2014 to help Team Whitney win the 2014 Top Friends and Family Team.

Let's keep the streak going in 2015!

Register today to come out and walk with us and honor Whitney's memory.

Donations can be made through this link.

Whitney's Legacy

Miss Whitney lost her fight with Leukemia on September 22nd, 2014.

We knew when the cancer came back so quickly after the transplant that we were in trouble. The treatment path we chose was what we thought gave her the best chance to beat it, but her poor battered body couldn't handle the treatment and her liver failed. It has been 2 months since she left us and I still cry as I try to write this. Things turned so quickly and our world was so chaotic that I didn't write any blog entries since her relapse.

I turn back to this blog as our plans for her legacy come together. We knew right away that we needed to honor her love for the University of Kansas Women's Basketball program, so we sat down with them and decided that the best way to honor Whitney and help the team was to endow a Women's Basketball scholarship in Whitney's name.

When scholarships like these are endowed, the "seed" money for the scholarship is raised at a level that allows for the annual interest to pay for the scholarship. This will allow Whitney's story to be re-visited every year when it is awarded to one of the basketball players.

Whitney won't be able to out live us herself, but with your help, her memory will.

We are doing good job of raising money for this, but we still have a ways to go. I am asking for your help to keep Whitney's story alive. Donations are tax deductible and even the smallest amount helps.

Send donations in honor of the Whitney Van Dyke Live Life To The Fullest And Fight Harder Scholarship benefiting Kansas Women's Basketball to KU Endowment, P.O. Box 928, Lawrence, KS 66044 or give online at www.kuendowment.org/givenow. Be sure to put Whitney Van Dyke Live Life To The Fullest And Fight Harder Scholarship in the benefit box of the form.

Donations are eligible for Williams Fund credit if requested.

Whitney Relapsed

Whitney started feeling a little "weird" last Monday, August the18th. She told Lisa that it felt like the cancer was back. She showed signs of CDF and the doctors started treating that. By Thursday her blood counts were a little off and the doctors ordered a bone marrow biopsy. The biopsy came back full of cancer cells that were just starting to make it to her blood stream.

We met with the doctor on Monday the 25th to figure out what to do. He said that given how strong and fast this cancer is coming back, we were in trouble here. We decided to try a drug newly approved for chemotherapy that shows some promise on FLT3 positive patients. We are looking at a 20% chance that we can get her back into remission. Our only other real option was to go back in patient with the same type of heavy chemotherapy that we started off with. We are looking at about a 20% chance she would make it through the chemotherapy, much less get into remission.

Given the overwhelming bad odds we are dealing with here we really want to be sure that Whitney could try to do some of what she wanted to through this process. We discussed time frames and windows of opportunities. We decided that we were not going to put her back into the hospital and try this newly approved treatment. Current plans are for two 28 day cycles and re-evaluate. No promises and no guarantee of a cure. We are going to try and get her home often and get her to the basketball games as we can.

Live each day to it's fullest, tomorrow is not a given.

Transplant Time

Whitney will be starting the transplant process this Saturday morning with an outpatient chemotherapy treatment.  Prior to receiving the donor's blood stem cells, the doctors must destroy Whitney's immune system so that it doesn't attack the new stem cells. This will be accomplished by another round of chemotherapy along with whole body radiation treatment called Total Body Irradiation (TBI). The TBI treatment must be within 24 hours of the actual transplant, so timing is critical. The actual day of transplant is Wednesday the 18th and the TBI is scheduled for the morning of the 18th with the transplant expected to take place on the evening of the 18th.

We had been under the impression that this was going to be an inpatient process for the first 30 days and then transition to an outpatient process for the next 70 days. After some discussion, the treatment team decided that the best option would be to try a less aggressive process to destroy her immune system due to her secondary issues. This puts us in a completely outpatient process for all 100 days. We weren't ready to get a place to stay in the city yet and this last minute decision has left us scrambling for accommodations. We have options and will deal with this just fine, we just weren't ready for it and that irritated me.

We will have to be very selective about Whitney's exposures during this process and this is the primary reason why we want to get a private apartment. We will also be limiting visitors during the initial phases of the process to help avoid as many exposures as possible while she is in a compromised state.

I am also working on a recap of Whitney's "vacation" and I might get it done tomorrow night if everything works out.

~Doug

Taking a break

Whitney will get to come home later today for a welcomed break in her treatment process. We know at this point that she will get to spend the memorial day weekend at home with us. She is schedule to go back Tuesday, as an out-patient, to get her next bone marrow biopsy and the sinus polyp removed.

Where we are in the big picture of things is we are just finishing up what they call the induction therapy part of the treatment path. The goal of induction therapy is a complete remission of the cancer. We don't expect to get the results of the biopsy until Wednesday to know if the cancer is in remission or not. Either way she should get a couple week break before her next options are initiated.

If the cancer is still present in Whitney after these two rounds of chemotherapy, the disease is then classified as what they call refractory AML. At this point we will probably have to do much more consultation and seek a second opinion from another hospital. Not a path we want to venture down.

Hopefully the cancer will be declared in remission and we initiate the transplant process.Here is a brief explanation of that process from cancer.net:

During a stem cell transplant, diseased bone marrow (the spongy, fatty tissue found inside larger bones) is destroyed with chemotherapy and/or radiation therapy and then replaced with highly specialized stem cells that develop into healthy bone marrow. Although this procedure used to be referred to as a bone marrow transplant, today it is more commonly called a stem cell transplant because it is stem cells in the blood that are typically being transplanted, not the actual bone marrow tissue.

We are expecting the transplant phase to be around 100 days total with about 30 days of in-patient treatment and 70 days of out-patient treatment.

Changing the subject a little, the neurology team has diagnosed Whitney with an additional disorder called Dystonia. The definition of Dystonia from the National Institute of Health is:

Dystonia is a disorder characterized by involuntary muscle contractions that cause slow repetitive movements or abnormal postures. The movements may be painful, and some individuals with dystonia may have a tremor or other neurologic features. There are several different forms of dystonia that may affect only one muscle, groups of muscles, or muscles throughout the body. Some forms of dystonia are genetic but the cause for the majority of cases is not known. 

This would be what Whitney is referring to as her shakiness. It is the twitching that people have seen when they visited. This disorder would be in addition to her Cerebral Palsy that is causing the posturing or the rigidness. Reading through the material on this, I think this has been an underlying issue that Whitney manages to keep suppressed when she is completely healthy. The biggest concern at this point is if the chemotherapy has made it worse, or if it is just fatigue. The answer to that question will come with time.

I will sign off for now as I must get the castle ready for the arrival of the princess arrival later today. I will provide updates on the facebook page as things progress today.

#TeamWhitney because #NoOneFightsAlone

~Doug

Weeks 6 and 7

The last couple of weeks have been pretty much a blur. I had to create a new Google calender to keep track of Whitney's Journey. I kind of eluded to this in the last post, but I am back at work and Lisa is staying with Whitney most of the time now. Lisa and I are talking on the phone quite a few times during the day, but it is hard for us as a family. We have always tried to do everything together, whether it was firefighting, 4H, or other activities. We are managing and keeping it together, we really don't have many options at this point.

I would be remiss if I didn't give a big shout out to the 911 crew at Jefferson County. They went above and beyond making all kinds of goodies and washing cars when the weather wasn't the best. The Snyder's brought up the money that was raised at the car wash and bake sale. The first thing that Whitney said was that now she could upgrade her KU Women's Basketball seats to courtside. I am not sure that is the best use for the money at this point, but if it gives her the drive to beat the cancer I am all for it. I am humbled and deeply moved by the love shown for Whitney by not only the 911 dispatchers, but the other responders and citizens of Jefferson County too. My hats off to you all!!!

Speaking of money, the bills are slowly starting to trickle in now and all I can say is wow. My best advise to anyone reading this is to make sure you have some type of health insurance for catastrophic illness if nothing else. The bill from March 28 to April 26 for the room is $268,379.21. Mind blowing, but it is pretty legitimate when you look at everything going on and how many people it takes to do it. What I have as of now the first month bills are just under $300,000. We haven't hit the max out of pocket yet, but we are finding that it doesn't include items that the insurance company doesn't cover by policy. Quite a few little gray areas in billing and we are having to look at things pretty close.

Whitney's condition seems to be better now than after the first round of chemotherapy. We can only hope this means that it has gotten most of the cancer cells. Last round, she was never able to get away from a constant IV drip. This time she is able to get off during the day and they are putting it back on during the night to ensure she stays hydrated. I'm not sure if I have posted this before, but she does have a polyp that is showing up around her sinuses. It has been present since she was admitted and we have assumed that it was part of the sinus infection that she was fighting before we came in. It sounds like they are wanting to go ahead and do a biopsy on it tomorrow. Hopefully we will know more then and it is relatively good news.

That's about all I can think of right now. Most days my brain isn't functioning at full speed either. Until next time,
Doug

#TeamWhitney
#TeamWhitbeth
#NOFA

Week Five

I am writing this a little later than I intended to. I think we are starting to truly feel the effects of this as a family. Our lives are centered around the fact that Whitney is battling for her life right now, but that doesn't mean that everything outside of our world stops. The show must go on. Lisa and I are getting pulled in different directions and we are trying to keep it all together. We are all strong and we will pull through this.

Speaking of this, it was actually two of Whitney's friends that came up with the idea of Team Whitney. Beth and Breezy asked if it would be alright to set up a facebook page and get some shirts made. We were all fine with the idea. The more I thought about it the more I liked it. It takes a team to get through something like this. I also saw the slogan somewhere that no one fights alone and I thought to myself that was perfect, it explains it so well. Team Whitney because No One Fights Alone, hence her tagline was born: #TeamWhitney because #NoOneFightsAlone

That brings us to week 5. I gave an earlier update when we found out that Whitney's cancer count was still way too high to do the transplant and that she would need to do another round of intense chemotherapy. To try and explain the treatment that Whitney is on, it is basically one drug on a 24 hour drip for 4 days straight and a second drug once a day for 3 days. Together these drugs target quickly devolving cells such as blood stem cells. Primary side effects are intense vomiting and diarrhea. The treatment completely wiped her out this week, she didn't want to do much at all. The best news is she made it through. Everyday should get just a little better and we should see some improvement by this weekend.

Whitney did have a few visitors this week, but I have been very hesitant to list everyone for the last few weeks for fear of missing someone. I haven't been able to be there most of the time lately as the show must go on and I must keep everything going. Lisa's sister and parents have helped out and and are staying at the hospital with Whitney on occasion so Lisa can get a break every once in a while.

As always, more to come later. Here are a few pictures from this week.