Friday, July 27, 2018

Six Months Later

Six Months Later
July 27, 2018

I wanted to update everyone on how we are doing.  This last 6 months have been a journey that we did not choose or want, but then again, neither were any of Katy's struggles chosen or wanted.  But to be honest, I don't know any other way to be, but to power through the challenges that life has thrown at me.   We miss Katy every single day.  Our hearts ache with the absence of her in our lives.  We cry, we laugh, and we remember every day.  Katy is often in our conversations (meaning we talk about her a lot), and sometimes in our dreams.  She will always be a part of us, and our love for her will be forever be in our hearts.  But life continues, and we must continue on the path our futures hold for us.  Katy believed that she would never truly be gone, and that her atoms will exist until the end of the universe.  That belief brings me solace, as I know she is with me in spirit.  I think of her as my guiding star.

Emily is doing well.  We have kept her very busy this summer.  And she is going to be very busy in the new school year.  Her outlook on life has become more positive and I know she wants to live her life in a way that would make Katy proud.  She decided that being angry is not honoring the memory of her sister.  I love her new attitude and see evidence of it on a regular basis.  Both my daughters have gone through tough experiences and both have made me proud.  

I am still in the process of finding a meaning to my days.  Emily keeps me busy, but I want something else to focus on.  But I am giving myself time to grieve and sort all this out.  I have ideas, and if any come to fruition, I will let you know.  Jim is talking about retirement in the next few years and looking forward to that transition in life.

I had the privilege of reading a speech a fellow PH Mom gave at the International PH Conference in Orlando in June 2018.  I was so impressed I wanted to share it on Katy's blog.  This speech can apply to all challenges we have in life.  At the end, she talks of a Mom who, 6 years ago, at her first PH Conference, told her "she could do this".  That mother was me.  I am happy to report that Cheryl and her family are facing the challenges given to them with grace and wisdom.  It is not easy, but we do the best we can do and keep it real.  I am posting it separately as it is long.  You can choose to read it if you like.  I believe it is well worth your time.

We thank every single one of you for the support, flowers, cards and the outpouring of love we continue to receive.  

All our love,
Christina

Cheryl Wegener's Speech

The following speech was given by Cheryl Wegener at the PH (Pulmonary Hypertension) International Conference in Orlando, Florida in June 2018.  The last time I was at a PH Conference, it was in Orlando at the same hotel, six years ago.  It is when I met Cheryl. And I was on a panel of speakers that year as well. She refers to our meeting at the very end.  But that's not why I'm posting it.  I love her analogy to the Velveteen Rabbit.  If you have time, read it.  For those of you who also have a sick child, whether PH, cancer, or some other problem, read it.  

Love you all!....

"My objective in speaking today was to address not only the needs of the PH child, but also the needs of the entire family, as caring for a child with a life-threatening illness is, at times, both draining and difficult for all parties involved: the parents, the child, and any siblings.
When I was first approached about speaking at conference, my initial reaction was, “Are you kidding me? I’m the poster child for how not to handle this disease.” My friends responded with, “That’s exactly why you do need to speak. You keep things real.”
I keep things real. What does that mean? And in contemplating that question, I was reminded of the children’s book The Velveteen Rabbit, and, more specifically, a conversation that takes place between the stuffed toy rabbit and the wise, old skin-horse. You see, the book follows the life of a stuffed rabbit that is made of inexpensive material and filled with sawdust. He is given as a Christmas gift to a young boy, and as the rabbit sits among the more expensive and flashy toys, the rabbit feels shy and insecure. He wants to fit in with his peers, and he hopes to become special to the boy. The rabbit befriends the skin-horse, who has been in the nursery longer than any of the other toys, and one day the rabbit asks the horse what it means to be “real.”
I’m going to read to you a short excerpt from this scene:
“Real isn’t how you are made,” said the Skin Horse. “It’s a thing that happens to you. When a child loves you for a long, long time, not just to play with, but REALLY loves you, then you become Real.”
“Does it hurt?” asked the Rabbit.
“Sometimes,” said the Skin Horse, for he was always truthful. “When you are Real you don’t mind being hurt.”
“Does it happen all at once, like being wound up,” he asked, “or bit by bit?” 
“It doesn’t happen all at once,” said the Skin Horse. “You become. It takes a long time. That’s why it doesn’t happen often to people who break easily, or have sharp edges, or who have to be carefully kept. Generally, by the time you are Real, most of your hair has been loved off, and your eyes drop out and you get loose in the joints and very shabby. But these things don’t matter at all, because once you are Real you can’t be ugly, except to people who don’t understand.”
It’s a story about growing up. The rabbit is trying to find himself and his worth. Growing up is hard—you’re trying to figure out yourself and how and where you fit in; you’re trying to figure out what’s real. 
So how does this connect to the PH world?

Similar to growing up, processing the multitude of thoughts and feelings that accompany a PH diagnosis does not happen all at once, either. Instead, this is a process that can be very taxing, leaving us physically and emotionally changed and worn. And when I use the word “us,” I am not only referring to caregivers, and I think this is very important to recognize: This disease will affect everyone in your family unit. Recognizing this fact and knowing that people often react in different ways and at different times is one key to tackling the tough emotions. 
Emotions of the PHer
My daughter Madison was diagnosed after she inexplicably passed out in her first-grade gym class. We were lucky enough to have the right people at the right time in the initial steps of our journey, but emotionally, as a parent or, I’m sure, as the patient, this didn’t make it any easier. 
Very early on, my husband Rob and I made the decision to be open and honest with Madison. We kept it as age-appropriate as possible, but we never told her that something wouldn’t hurt if it would. We were honest, for example, about the blood draws stinging for a bit, but we also made sure that she knew it was temporary, and that at least one of us would be there for her. 
As our journey progressed, so did the questions. Explaining that she would need to be on IV therapy, for example, and that she would have a tube permanently extending from her chest.
The “Why me?” question. It’s okay to honestly say, “I don’t know.” Go ahead and acknowledge that it’s not fair, if this is a statement made by your child. It isn’t. It isn’t fair for any of us.
As Madison got older, the questions got harder: “What happens when people get buried? What do you think Heaven is like? What does ‘terminal’ mean?”
Many of these questions don’t have easy answers. As a parent, we inherently want to protect our children but, in this case, you can’t swoop in to save them. You can’t promise them that everything is going to be fine. What you can do is to listen, to ask them what they think, to validate their feelings—even the ugly ones—and reassure him or her that you will be there every step of the way. 
The Seven Stages of Grief
In speaking with my own therapist early on in this journey, she told me that we would likely experience the seven stages of grief and at first, I was confused. Isn’t that for after someone has died? And I learned that it isn’t, necessarily. You see, as parents, we are grieving. We are grieving what once was—our vision of a happy, healthy, “normal” family. We are grieving the loss of some of the dreams we had. We are grieving the fact that it is very possible that we will outlive our child. 
Many of you have likely experienced some of these stages. Shock and Denial generally come first. For Rob and I, the seriousness of what we were dealing with slowly unfolded over the course of several days. Reality began to set in. 
Next is often anger. The reality of the situation becomes apparent, and this hurts. If we’re not ready for this hurt, we may lash out. 
Bargaining? “The normal reaction to feelings of helplessness and vulnerability is often a need to regain control” (Axelrod). We might attempt to strike a deal with God or a higher power. Others go through a series of “If only” statements: If only we had seen a doctor sooner. If only we had gotten a second opinion. If only I had been a better person...
“Guilt often accompanies bargaining. We want to believe that there was something we could have done differently to have helped save our loved one” (Axelrod).
Then there is Depression, which can come in many forms—feeling sad, crying often, experiencing changes in your appetite or sleep patterns, or even having unexplained aches and pains. 
The Testing Stage is where you try to find realistic solutions for coping with the loss and the rebuilding of your life. 
The final stage is Acceptance—you understand what you lost and recognize how important it was to you. You no longer feel angry about it, and you’re finished with bargaining to get it back. However, not everyone is able to fully grasp this stage.
Just as PH is very individualized in its attack, so is grief. Everyone grieves differently. Many people do not experience each stage of grief, and oftentimes the stages that are experienced come in a different order. These stages are not a checklist, per se, but a guide to the grieving process. 
The Seven Stages of Grief in Children
Be aware that children, too, will be going through these stages. As they adjust to their own diagnosis or that of a sibling, they, too, will at some point feel sad, depressed, angry, or afraid. Open communication is key, and professional counseling can also be quite beneficial.
Our son was age three-and-a-half when Madison was diagnosed. We had left Michigan and everyone and everything that he’d ever known eleven months prior, and suddenly things were rapidly changing again. Neighbors helped to care for him those first fifteen days that Madison was in the hospital. When she did come home, she was on 24/7 oxygen. Later, there were late-night ER trips and canceled plans and clinic appointments and more hospital stays. He developed anxiety and depression. He became angry. At a young age he did not have the words to process his emotions, so he did so via his actions. This led to him being “asked to leave” several daycare facilities and, later, a Montessori school. He, too, sees a therapist, and she is convinced that for a time, soon after Madison’s diagnosis and the chaos that followed it, Matthew stopped growing emotionally. He experienced a PTSD-like reaction and to this day, at nearly ten years-old, he continues to work on managing his emotions. While we had recognized that Matthew worried about his sister, it wasn’t until this year—when the sister of one of his classmates died—that he was able to verbalize that he worries about Madison dying nearly every day. 
Logistically, you can help to combat behavioral issues by treating a sick child as normally as possible, sticking to normal routines, avoiding overindulgence, and setting limits and/or consequences for unacceptable behavior.
Strive to be flexible. You will likely create a “new normal” for yourself and your family. This is okay. 
Communicate, both with the members of your family unit and relevant people outside of it. For example, when something unusual is going on with Madison, I make sure that both her teachers and Matthew’s teachers know about it. 
If possible, consider reserving some one-on-one time with each child. It is common for siblings of an ill child to feel pushed aside by the medical demands of their brother or sister. 
On top of everything else, don’t forget to nourish both your relationship and yourself. 
Sound like a lot? It is—some days. Other days, not-so-much. You simply need to “keep it real.”
Another book, The Velveteen Principals (Toni Raiten-D’Antonia), addresses the very concept of “being real.”
Being Real is possible. While a PH diagnosis may change you—it certainly changed each member of my immediate family—it also provides a platform for you to clarify your own identify and self-worth. You really are stronger than you think. Remember that rabbit? In the book, as soon as the rabbit learns what real is and he believes that it is possible, he starts to show signs of being real. 
Being Real is a process, and being Real is emotional. 
Being real is empathetic, and being Real is courageous. It can also be painful, and it requires one to be flexible. Ultimately, real love endures. The Velveteen Rabbit becomes real due to the boy’s love and affection. You’ve already demonstrated your capability for being real simply by being here today. 
At my first conference, ironically enough, at this very same hotel, a veteran PH mom took my hands in hers, looked me in the eyes, and said, “You can do this.” In a way, she was my Skin Horse. Today, I hope that the three of us have offered you information that has you walking out that door knowing that you, too, can do this. You, too, can become real."

Sunday, December 17, 2017

Katy's Passing

With the deepest sadness, I regret to tell you that Katy had severe lung complications with her bone marrow transplant.

Two weeks ago, Katy's oxygen needs increased so drastically she was moved to the ICU at Huntsman Cancer Institute.  Two days later she had to be placed on a ventilator.  The doctors believe that she had Graft vs. Host Disease (or some other kind of rejection) in her lungs.  Or it could have been damage from the ablative chemotherapy.  Or a mixture of both.  The doctors tried to treat her with high dose steroids, but nothing could reverse the damage that was done.

Katy died yesterday afternoon, December 16, with Jim, Emily and I by her side, as well as her grandmother, Susan, and our very close friends, Bethany and her parents, Nancy and Phillip.

She will be so deeply missed by countless family, friends, medical personnel, teachers and others.  She was a ray of sunshine in our world for 18 years, and our lives will have an everlasting shadow with her gone.

I will post more information about the memorial service, etc. when it is finalized.  But know we are shooting for the end of this week.

Thank you for all your love and support.

Christina



Thursday, November 9, 2017

Stem Cell Transplant Day!

Happy Day To Everyone!

Obviously, Katy has made it to Stem Cell Transplant (aka Bone Marrow Transplant).  After 3 rounds of Vidaza, Katy's leukemia cells fell to 1%, which is the best her doctors felt they were going to get.  She was strong and healthy overall, so the transplant team gave the green light for the transplant.

Last Friday, November 3, Katy had a triple lumen central line placed, got admitted to the hospital, and started an ablative chemo regimen (to kill off as much leukemia as possible, and her immune system as well).  She has received 6 days of chemo and today was the infusion of Emily's stem cells.  I'll post some pictures in the photo albums.

So it is a wait and see time.  Katy has been receiving IV tacrolimus and steroids for over a day now (an anti-rejection regimen).  It will take about 2 weeks for the stem cells to start building a new immune system, and even when that starts happening, it is an immature system.  It will be like a new born baby's immune system.  She is watched extremely closely for 100 days post transplant with 2-3 days a week appointments after discharge.  She cannot ever be left alone during that time, as fevers and infections can come on quickly.  Rejection in stem cell transplantation is called Graft vs. Host Disease (GVHD for short).  Katy's lungs will also need to be watched closely as the new immune system could reject her lungs as well.  These are the 3 biggest risks for Katy at the moment.

Before transplant, we were able to take a short trip to Zion National Park, Antelope Canyon, and the Grand Canyon during Emily's fall break.  We had a great 4 day weekend until the last evening.  We went to a lookout to see the sun setting over the Grand Canyon.  I stopped looking at the rocky steps I was going down, rolled my ankle, landed on it, and broke my fibula.  Needless to say, I had to slow down for a good week.  I'm almost 3 weeks out and am getting around much better now.  Luckily, it was my left foot so I can drive, and I can also weight bear.

I'll post some pictures of our Grand Canyon trip as well.

Thank you to everyone for your support of Light the Night fundraiser for Leukemia and Lymphoma.  And many thanks to those who are providing us meals and other support.  We could not do it without you.

Christina

Thursday, September 21, 2017

Life's Been a Whirlwind... 09/21/17

Happy Autumn!

I thought my last entry was long overdue!  I can't believe it has been 5 months since I have written anything on this blog.

A lot has happened in those 5 months.  I don't want to overwhelm with too many details.  I think I will take it month by month and summarize the events that way.

In late April, we took our trip to Hawaii.  It was a great vacation that we ALL enjoyed immensely.  We swam, snorkeled, ate, drove, shopped, and generally relaxed.  The only downfall was the 4 trips we took to the hospital for Katy's platelet and blood transfusions.  The highlights of our trip included our hotel, snorkeling with wild dolphins, motorized hanggliding (Emily and Katy), and seeking out the best shrimp trucks.  It was a vacation we will not soon forget.  I will post a photo album of our trip on the blog.

We came home and I got busy with end of school stuff, Emily's physical therapy, and Katy's many appointments.  I also planned a surprise party for Katy (in lieu of a graduation party).  I compiled a book of letters from friends, family, teachers, medical personnel and others so Katy would have a better idea of how she has affected the world around her, and the impression she makes on so many people.  We continued going to see Katy's doctors and getting infusions 2-3 days a week.  During this time, Katy only received supportive care with no treatment.  However, we did tell Dr. Afify that Katy was interested in talking to doctors at Huntsman Cancer Institute about adult medical trials.  Like Primary Children's Hospital, Huntsman Cancer Institute (HCI) is on the University of Utah Campus.

The surprise party was a success.  Katy was genuinely surprised and appreciated all the effort put into the book.  Again, I will post an album of pictures here.

In June, we got news that Katy's AML was beginning to grow a bit faster.  It was still low, but we decided to meet with Dr. Shami at HCI.  We were surprised to learn that the bone marrow team at Huntsman was willing to consider a bone marrow transplant for Katy if we could lessen her leukemia with another round of chemo.  After spending 3 months recovering from her last hospital stay, which had many complications, and was her 3rd chemo round for AML, Katy decided to go for it.  She was admitted to HCI for 5 days to undergo this chemo (her 4th round).

Also, in June, I got word from my family that I might want to fly to California to visit my step-father, Brent.  He was also battling a different kind of cancer, and his health was becoming more fragile.  I decided to fly Emily and I out, on very short notice, over Father's Day weekend.  It was so nice to see Brent, my Mom, Deb, Amanda, etc.  We had a nice, albeit quick, trip.  Katy, due to her low blood counts could not travel.  The following week, Brent chose to stop treatment because his chest tumor was beginning to grow again.

In late June/July, we received news that Katy did not make it to bone marrow transplant.  They called off the transplant, but the team recommended, and Emily agreed, to harvest Emily's stem cells regardless, in order to freeze them, and hasten the transplant process in case Katy makes it to transplant in the future.  Katy decided to try an antibody therapy that the FDA only approves in last resort AML cases, called Mylotarg.  She started this treatment in July.  On July 17, I had Katy up at Huntsman receiving the all day treatment, while Emily was in the same infusion room having her bone marrow harvested.  Craziness to say the least.

Around July 24-25 Katy started getting a cold.  The night of July 27, Katy spiked a fever and we spent the night in the ER getting her admitted to Huntsman.  She received a bone marrow aspirate on Friday, July 28, as planned.  Katy got diagnosed with pneumonia which they started treating with antibiotics.  On Sunday morning, July 30, Brent died at home in California.  We also received the news that Katy's leukemia was up to 40% as calculated by the Minimal Residual Disease (MRD) test of her bone marrow.  The Mylotarg had done nothing.  Saying it was a rough day is an understatement.

Katy got released from the hospital, and we met with her medical team multiple times over the next week.  Katy decided to start a treatment called Vidaza.  Vidaza is used in older AML patients that cannot sustain the more difficult chemotherapies.  It is considered a maintenance drug to extend life, and improve quality of life, as it helps to sustain patients' blood counts, resulting in fewer transfusions.  It does work through a different mechanism than other AML chemotherapies, and we were told that there is an extremely small chance it could get Katy to transplant, but it is very unlikely at this point.  Also, Vidaza takes 2-4 monthly rounds to see the full effects from the treatment.

Katy started the treatment immediately.  She flew to California with me for Brent's Memorial.  We also went to see "The Book of Mormon" here in SLC.  Emily performed in her musical "Once on This Island", and all four of us went to Wyoming to see the eclipse.  Jim's brother, KC, and our sister-in-law Trudy, were our wonderful hosts in their beautiful home, which was in the totality zone.  (I'll post pictures of this as well).  Emily started her freshman year in high school.

After the first treatment of Vidaza, Katy went 6 days without a platelet transfusion, which hadn't happened in months.  She went through her second round of treatment with fewer side effects.  And her leukemia counts may be going down.

There are 4 ways to measure her leukemia load.  It includes 2 different counting tests, using 2 different samples, either blood or her bone marrow.  In one test the doctor counts the percentage of leukemia cells he/she can see under a microscope.  The second test is called Minimal Residual Disease (MRD) and uses a machine to count the percentage of leukemia  found in 10,000 cells.

Last Thursday, Dr. Shami told us he counted only 2% of blasts, under the microscope, from a blood sample of Katy's.  This was down from 11% the week before, and 15% the week before that.  This has given us a cautionary hope, that perhaps, Katy may still make it to bone marrow transplant.  We can never count Katy out.  She will have another bone marrow aspirate done at the end of next week, and we will receive the MRD results the first week of October.

Meanwhile, Katy has been feeling better, and more energetic, than I have seen her in a while.  She is pursuing her GED, working on art, seeing more of friends, and socializing with us more.  So for now, things are looking up and life is getting a somewhat normal rhythm to it again.  How long it lasts is anyone's guess.  But I will take it for now.

Last Saturday night, the 4 of us went to a lantern festival.  We had a nice time and made wishes as we let the lanterns go.  I'll post pictures of that as well.  Also, Jim's coworker, started a Pacificorp team for the fundraising event, Light the Night.  This event supports the Leukemia and Lymphoma Society.  We are participating and fundraising for the team. Follow the link to our fundraising page:
http://pages.lightthenight.org/ut/saltlake17/JDoak
Any donation amount will be appreciated!

Thank you to everyone for your continued support.  Thank you so much to our neighbors, for the continued support in meals, every other Monday.  It always seems to come on the most needed day.

Love to you all,
Christina




Thursday, April 13, 2017

A long overdue update... 04/13/17

It has been a long time since I posted.  And a lot has happened.  So here goes....

Katy got discharged from the hospital on March 2, which was also her 18th Birthday.  It was a crazy day!  There is always a lot of activity on discharge day, plus,  I was trying to have a little party at the hospital, as a surprise to Katy.  Also, Emily had seriously injured her knee at dance class the night before.  So we were also juggling an ER visit and MRI.  (I'll explain more about all that later in this update).  But we finally got it all done and Katy came home by dinner.  We ate and opened gifts and it was time for bed.

The bone marrow aspirate Katy received the day before discharge came back as 0.09% leukemia.  This may seem like very little, but it was not enough to get her to bone marrow transplant.  The plan became one of maintaining her blood infusion needs with the hope that she could start maintenance chemotherapy to prolong her life.  We hoped that we could check off some things on Katy's bucket list, including going to Europe.  But as life has unfolded in the past 5 weeks, things have changed.

As we approached the time Katy might start maintenance chemo, Katy requested she get her double lumen broviac changed to a port.  Dr. Afify decided to have another aspirate, as well as a bone marrow biopsy, to see where things stand with the leukemia, so we would have a starting number.  After two canceled tries to get the aspirate, it was finally performed on April 3.  We finally got the full scope of results last Friday.

Katy's levels of leukemia in her bone marrow are 0.28%.  Dr. Afify is not really concerned with this increase due to several complicated factors.  What is more concerning is the low cellularity counts in Katy's bone marrow.  This number measures the percentage of blood her bone marrow is producing.  The normal range varies with age, but Katy's should be at least 70%.  It was 20%.  Which explains why Katy has continued to be platelet and blood dependent.  She has even been on Neupogen, which stimulates her bone marrow to grow white blood cells.  Due to this low cellularity, Katy is not a candidate for maintenance chemo, as it will cause further suppression of her bone marrow production.

So what have we been doing with our time?  When Katy first got discharged, she had to come up to the hospital every day for platelets.   Then every other day, and now every 3-4 days.  However, we often seem to have other reasons for coming.  So, most weeks, I am at Primary Children's 3-4 times a week.  Emily also tore her Medial Patella Femoral Ligament, and took of a bone fragment and cartilage from the back of her Patella.  So Emily had surgery on March 17 for that.  She was on crutches for about 4 weeks.  Now she is receiving Physical Therapy 2 times a week.  Mostly, my time is spent as chauffeur to appointments.

We've been able to have some fun too.  Katy wanted to go to La Caille for her 18th birthday, so we dressed up one night and had a fancy dinner.  We've seen some movies, gone to an art show, and visited the Leonardo (a museum here in Utah) briefly.  Katy has renewed her painting lessons.  We've spent time with friends, and as a family.  And Katy has crossed off one bucket list item by getting a tattoo.  Her long time friend Bethany got the same tattoo, of two birds flying together.  Finally, we have planned a last minute, 10 day trip to Hawaii.  We are going to Oahu, as Katy needs to be near medical facilities for her transfusions.  But the resort looks amazing and we are excited.  Katy wanted to go to Paris, but her oncology team highly recommended that we not travel to Europe.  So, second best is Hawaii!

I'll be honest, it has been a really emotional 5 weeks at home.  And the 7 week hospitalization before that was incredibly difficult.  We do not know how much time Katy has.  As usual she is a medical mystery.  Dr. Afify would have expected the leukemia to have returned by now, without treatment.  So it's hard to say how long Katy will ward off the inevitable.  Katy has decided against getting a second opinion in regards to a bone marrow transplant.  However, since she is 18, she can be considered at the Huntsman Cancer Institute for adult medication trials, once her leukemia begins to return more aggressively.  This is an option she most likely will consider.

Meanwhile, we will continue to enjoy all the time we can together, and with family and friends.  Katy may start to study for her GED.  And, as always, life will continue its rhythm until another event changes it.  It is like waves in an ocean, ups and downs, with the occasional rogue wave taking you off course.

I will post some photos of the last few weeks in a day or two.  Look for an album along the side bar on the right.

Love to you all,

Christina







Friday, February 24, 2017

Update 02/12/17

Hi Everyone,

I am happy to report that Katy has not used up all her 9 lives yet.  Per Katy's standard of defying odds, she has improved drastically from a pulmonary standpoint.  There is question now as to whether Katy ever had an infection or whether her lungs had were overloaded with fluid.  It may never be clear.  As of today, Katy is on 1-3 liters of oxygen, and that may be only because she is still bedridden and not up moving to improve those lungs.

As Katy was significantly improving from a pulmonary standpoint, she has had some setbacks in other areas.  She has something called the BK Virus in her urinary tract as well as her blood.  The doctors have known that Katy has this virus for weeks now, but did not treat it at first, as Katy had no concerning symptoms.  The treatment for this virus is very hard on the kidneys.  So they take a watch and wait approach to treatment.  Unfortunately, as Katy was recovering from the lung problems, this virus reared its ugly head.  She started to severely bleed in her urinary tract.  For Katy's sake, I will not go into great details of the treatment protocol, but lets just say it has been miserable.  We have been treating it for at least 12 days now.

Yesterday and today, we are finally beginning to see some improvement.  I believe it will still be at least a week before we can get Katy out of this hospital, but we are hoping we are beginning to turn a corner.

At this point, the doctors have not performed a bone marrow aspirate on Katy.  We need to get her recovered from this BK Virus.  I do not know the fate of a potential bone marrow transplant at this point.  I can tell you that all the hardships that Katy has had this round of chemotherapy gives both her doctors, and us, pause in thinking of putting her through these, or potentially other medical hardships in the future.  It is a fine line that one walks in dealing with quantity versus quality of life.  Many potentially hard decisions will lay before us in the coming weeks.

A day or two before Valentine's Day, a friend from our PH community sent Katy a care package.  It was a surprise to us.  There were Valentine's Day decorations included so we got to further decorate Katy's room.  Many thanks to Tiffani Frandsen and her family!  Our neighbor, Ali Thackeray, and her cute girls, gave our door a heart attack before Valentine's Day, as well.  (See all the pics below).  Also, a big shoutout to Deb and Amanda, who fly out to help us on a regular basis.  We couldn't do it without you!  Finally, continued thank you's to our friend's, neighbors and family.  It was overwhelming to have the love and support of everyone as Katy was on the brink.  We appreciate all of you.

Katy's 18th Birthday is March 2.  Please send Katy a shoutout on here, Facebook, Instagram, text or card.  This special day may be spent in the hospital, or at home, but in no shape for a large celebration.  Let's give her a big shoutout for reaching such a significant milestone.  We love our Katy!

Christina