Too bad you are not Daddy

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As we brought out the pieces of the “Marker maker” one of the additions to the girls collection for art and craft, I looked a bit overwhelming.  My older daughter looked at me and she knew exactly what was on my mind and said “we have to build it, too bad you are not Daddy”. She was right.  There were so many pieces, where do I start? David will have figured it out immediately. Thanks to youtube, I watched a video and voilà we were making makers.

It breaks my heart knowing I can never fill that void for my children. My daughter now attributes most things that upset her to the absence of her Dad.  She cries every night, she is sensitive about most things, runs to her room at the smallest things and cries passionately for Daddy, she says she wants her old life back, I do too.

Shopping as a distraction

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In an attempt to distract myself from the gloominess in my life after David went into hospice care, I shopped, shopped and shopped.  The shopping was done almost exclusively online. Once I clicked send, I started looking forward to the arrival of the items. Unfortunately, as each package arrived once I looked through the items there was always a sense of disappointment, I wondered why I even ordered the items or what made me eagerly await its arrival. It brought no relief in fact, I felt more emptiness and sadness plus I was overwhelmed with the thoughts of processing the returns or flattening the boxes for recycling.

As I think back, I am reminded that I went through a similar process after my Dad passed away, I will go to the mall and shop around hoping that a new item will help bring a little bit of cheer.

I am relieved to say that I was quick to curb this habit, it simply is not easing the pain from my grief.

UPDATE: so maybe shopping can bring a little bit of cheer.

The joy in art

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It is no surprise that my daughters are missing their Dad, in fact they miss him more and more each day.  I am in frequent communication with my daughter’s school teacher and school counselor. I am also trying to be more present in her school activities. I joined her for lunch on Friday afternoon and this really brightened her day.

In order to try to provide the best support at home, I asked my older daughter what helps her feel better when she is sad and she said she likes drawing.  This is no surprise, they both like drawing or scribbling. Following a play date, the older one tends to draw something for her friends as a parting gift. In fact, she did the same for me after I met her for lunch at school.

I asked what products she wanted to further enable her interest and drawing and thanks to Crayola and Amazon they were ordered.  We spent a good bit of the weekend drawing and painting. My daughter even said it was better than watching TV or the iPad.

I recall when David started chemo the first time, walking down the hallways of the chemo suite, I noticed lots of drawings on display, it was there because it was perceived as therapeutic.  At that stage in our lives, I did not even want to look at them, not because I did not appreciate art but because I was afraid that people were drawing to remember a loved one, something I feared dearly.

I can say drawing with the girls this weekend was fun and hopefully therapeutic for all of us.

Breaking the silence – Hospice care

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The transition to hospice care changed everything since hospice care is essentially aimed at providing comfort and support until the imminent death NOT providing treatment to prevent death. It was the beginning of the end.

The day David began hospice care was the first time we talked about dying and it was the last time. We cried a lot and abruptly ended the conversation. David’s desire was to stay home and this was my desire as well. My Mom staying with us also made this possible, knowing that he was getting the best care and love. I continued to work, continued to maintain a normal routine for the girls. Unless you were in our house, nobody knew the extent of what we were dealing with.

The move to hospice made me angrier. The grieving began, I cried often when I thought I could not be seen or heard.  I became more open with my daughter letting her know Daddy was not going to get better as we were all hoping.

I found it hard to be grateful to any of the staff from the hospice care team.  The end goal of hospice was contrary to my heart’s desire. I was angry each time I saw them for sure they have the wrong house.  In my view, they brought their dirty feet into our home, I wondered what house they were coming from, bringing the germs and illness of a truly sick person’s house into our home.  They just did not belong in our house.  I tried to ensure that I was out of the house before they arrived and returned after the left.

My emotions in no way reflect the good work of hospice staff. They were understanding, did everything to ensure David was comfortable, responded to any need with prompt attention. At the end, they were there with sincere sympathy and support to try to ease the pain of dealing with David’s passing.

This is one of several posts that details our experience with bladder cancer. A concise summary of the overall experience can be found in the blog post titled “breaking the silence”.

Seriously….jury duty

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Could they have picked a worse time?  As much as this is our duty to country, part of how we preserve the integrity of the legal system in America, this is NOT the time for me to serve this civic duty.

I know for certain that my decisions will be based on emotions which have been erratic lately rather than facts, evidence, or the pursuit for justice. Depending on the case, I think I will either be unreasonably merciful or unbelievable brutal in serving what is my irrational perspective of justice.

So, in the need to protect the integrity of the legal system, I will complete the form and hope to have provided a good enough reason to be excluded from the invitation to jury duty.

UPDATE: I was excused from jury duty, they responded almost immediately.

Good days, bad days

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There is no logic to predicting which days will be bad or good for me. Some mornings, I wake up just knowing it is a crappy day. However, most days, I wake up with no clue how the day will turn out.

Yesterday, I woke up indifferent, got ready for worked, dropped my daughter at school and when I was less than a minute from work, the uncontrollable tears began. I continued to cry in parking lot then took time to recompose myself.  Once I thought I was ok, I proceeded to the office, suddenly, the tears started streaming down my face. Imagine the horror when I ran into a co-worker…oh no….no one is suppose to see me crying definitely not at work and there I was still crying uncontrollably. Eventually, I made it to my office and finally the tears stop and I proceeded my work day.

Today, was different, it was a better day, in fact I refer to it as a good day. Like yesterday, I woke up indifferent but managed to drive to work without crying, sang along to some songs on the radio, and maintained a decent demeanor for the rest of the day.

What makes some days better than others remains unclear. I wish I knew what sets me off some days and what keeps me calmer on other days. I am just relieved that today was better than yesterday.

Breaking the silence – dealing with end stage of cancer

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After the cancer reoccurred less than 6 months after completing intense chemotherapy treatment, David and I knew the odds were against us but this made us more determined to fight harder. David put up a great fight for his life. We were so caught up in the fight and finding the right treatment that I refused to be distracted by thinking that this ugly disease will lead to the end.

I could not accept David’s death as an option, I was not interested in discussing it. This was my coping mechanism since I could only function by believing David would live. Resiliently, we kept fighting for victory over cancer.

This changed in November 2013, it was not because I decided to listen to another Doctor of gloom, or over analyze yet another CT scan result.  It was because despite the treatments, the disease continued to take a toll on David’s health. His energy level was depleting, his pain progressed, fatigue increased, and he was less ambulatory.  It became very clear that the progression was irreversible, the treatments were ineffective and causing additional anguish to David.

For the first time, I allowed my self to start coming to terms with the inevitable, the unthinkable. I tried to numb my emotions. I became a different person, a person I that I did not know and one that I am quite sure I did not like. I asked the Lord to spare David from his pain and suffering to preserve his dignity and in David’s words “make it a quick death”. I felt guilty, like I was giving up on David, I became distant from the world.

I recall going on a business trip, it was an escape from my reality – interacting with colleagues like my life was normal. I felt like an impostor. I came back home to my reality, a sad one as I watched my husband deteriorate further. Later that week, I had to take David to the emergency room. Upon his discharge, I knew it was time to change from visiting nurse to in-home hospice care.

I felt defeated because the cancer seemed to be winning.  We are a winning family, we were suppose to win this battle, our biggest battle. How could we go from fighting so hard to accepting the end was near? My goal changed to ensuring that David was comfortable until the end.

David fought hard and was in hospice care at home for almost 2 months before he took his last breath. Those two months as the end approached were undoubtedly one of the worst phases of our life.

This is one of several posts that details our experience with bladder cancer. A concise summary of the overall experience can be found in the blog post titled “breaking the silence”.

Left work a married woman…..

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The last time I left my office I was a married woman, today, I returned with the most unwanted status, a word I despise. I struggle to even type it..WIDOWED. The word makes me feel handicapped. While I can understand that David is gone, this is one status I am not embracing.

Some have asked why am I going back to work already. For me it is simple, why not. What will I do at home? It does not take away the pain. In fact the longer I stay home the more difficult it may be to re-adjust to the routine of work.

I dressed for work making sure I did not look like a hot mess. I tried to keep my head up like it was a normal day at work. This was short lived, as I started driving to work, I was reminded that I did not see David in this morning:

  • He did not insist on ironing an outfit that looked perfectly fine to me
  • He did not give me a thumbs up or thumbs down on my outfit
  • He did not keep informing me of the time to ensure that I wasn’t running late for work (this used to annoy me)
  • He did not say “I love you”
  • He will not be calling to find out how my day is going
  • I will not hear him say “Happy Monday” or “it is almost Friday” (even on Monday)
  • He will not be leaving any messages for me or sending me any emails
  • He will no longer drive me to work or pick the kids from school

All I have now are the memories and that just does not seem sufficient. I managed ok at work today, thanks to a pep talk from my dear friend and thanks to David who always told me “you can do anything”. I am also thankful to my co-workers for being so supportive.

Thank you, thank you

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Where do I begin?

Thank you for everything. Your love and support has been extensive.

The cards, the groceries, the flowers, fruit baskets, cookies, cupcakes, more sweet treats, stuffed animals, monetary gifts . The gift of time – visits, phone calls, text messages, emails, homemade meals, plowing snow to name a few.

Reading the cards brought hope to me and feeling of gratitude that people were thinking about us and sympathetic to our grief. The flowers and the plants brighten the house. The fruit baskets, brownies, chocolate, cookies, cupcakes and other sweet treat became a balanced diet for us – one note stated “lets sugar up the kids” it worked, they ran around the house filled with energy. The homemade meals warmed my heart and provided much needed nutritious calories.

For those that attended the funeral, thank you for making the trip. Many traveled hundreds of miles, others thousands of miles, left your young children at home, found tickets at the last minute and in many cases paid exorbitantly. We were surrounded by your love and this made the day easier.

Thank you to everyone that is reading the blog, this is my therapy. It is my outlet, it allows me to feel connected with David.

Below is a picture of a dear friend of the family, Richard who flew in to offer condolences plowing snow in his suit and dress pants.

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How can you be gone?

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Seriously, how am I suppose to live without you? How can I really live without you? You were everything for me. You balanced me, you were my go to person, bad day – David will fix it, silly question – David will answer it, frustrated – David will bear the brunt of it.

When you went on business trips, we used to joke about how I barely managed to hold things down for a few days without falling apart. Now how am I suppose to hold things together for years, decades?  It has been a month since you have been gone,  it has been horrid. How can I manage for a year?

Seriously, how do I live without you? I do not know how, I have spent ALL my adult life with you. Where do I go now? How do I move on?  How can you be gone forever? NO

This is not fair…..i feel broken. I am broken. I miss you. I need you.