10.12.2010

diary...

I realized this is my diary. I never really kept a diary when I was young…not even a journal. I would always start one, keep it for a few weeks and put it down to never write in it again. Anything that I did write would be forgotten or would remain a distant memory. I wish I would have started a blog about my life…from the beginning…to look back on every day with fond and loving recollections….especially the life I shared with John. What this man has brought to me is nothing short of amazing seconds, minutes, hours and days. Since meeting one Thanksgiving almost seven years ago, he has been in my heart every day since then. No matter when the thoughts started coming through my fingers into words, the years prior I filed in my mind. I am glad I started this blog….I am glad we have amazing people to read along with us….I am even more humbled by those who have been touched in some way…but more than anything, I am beyond happy that John is a part of my life. I will never say “was” no matter when I speak my profound happiness with him or of him. To me, it will always be “is” because I know he will never leave…any of us really. When you have a spirit like his, those “-isms”, smiles, jokes, thoughtful sayings and sweet baby blues…they are all carried on…just like many others we have all loved in the past, but to me…this will be different. He is my one true love…my soul mate…my sweet angel.

He lies here next to me…having a hard time sleeping too. His noises, movements, night sweats, dreams and coughing all keep him from really delivering his body the sleep it needs at night. He finds himself sleeping most of the day and barely keeping his eyes open. Sleep is a large part and a majority of his life now. When he is awake for brief moments, he says hi to visitors or plays a quick game but then drifts back out. Many times, we continue to stand or sit around him…talking about the amazing man lying before us, as he drifts in and out of his own consciousness. It is amazing how his mind keeps fighting and his loving voice staggers into conversations midstream. His body is weaker and his breath is wheezy…it is hard to listen to because he never smoked a day in his life and was an active twenty seven year old man. I know this will never be easy…ever. There is nothing easy about what he has gone through these past eight months either. I will see him again…I know I will, but for now…I keep these thoughts flowing and keep loving this perfect creature.

My thoughts are all over the place…can you feel it? I am just writing…anything that comes to mind, I just wanted to let out. Thank you everyone…it feels good to know we have so much love, prayers and support flooding our way….keep them coming my dear friends…we continue to fight with that, no matter what the suggested outcome.

10.10.2010

fatigue...

I am not sleeping…period. I cannot seem to find my mind, control it long enough, and go to sleep without having to think about all the things happening in this moment. I am constantly making sure John is okay and every little movement he makes…I am awake. His convulsions and active dreams are becoming more and more frequent and longer throughout the night. It is hard to say at this point whether it is the mix of medications he is taking or cancer continuing to conquer his beaten body. This is something we are going to discuss with his nurses and doctors here first thing tomorrow morning. There is no reason he should have to feel anything but euphoric these final steps of his journey and I know his care takers will make sure of this….as it is a trial and error process with any medications one takes.

So, the short of it is…I am worn down. BUT…so is he and he rages on in his fight…and so will I. We are very fortunate to have so many who love our bubble we have formed around us and who will protect us whole heartedly. There are those same people who love us individually as well. They know what each one of us need in a given moment and who hold our hands through times when we need to talk and cry. I have many of these people in my corner…and I know many others in John’s.  We have had many visitors every day in this home and we are so thankful for every one of them. My brother and sister in law were here this weekend and even more love was stuffed into this house if you can imagine that. It feels good to have my family around with John’s…my mom and my dad included…it feels good to know all of these people adore John just as much as I do and who are also here for me too. Love, prayers, laughter and why not, a little more love. We feel it all.

This week we will continue to check his hemoglobin which has held strong since we left Florida and make sure his comfort is at the forefront of our daily concerns. Cancer is taking a toll on John just as it would anyone with the amount he has to endure. His appetite is not as high and his nausea is a continuous battle…have I mentioned the draining? He has several more swollen lymph nodes popping up on his body and each one is the reminder of what he is experiencing. We know what is happening but it does not make it any easier to see it take a charge on the love of your life. It is hard to stand by and watch with helpless eyes….I love him…more than anything in this world, I love him.

10.08.2010

my heart...

There is not a countdown here…we have to enjoy the time we have left with him. If there was an expiration date, it would take away from the fact that he is still here. There is always going to be the natural wonder of when, how, and what it will look like…but why is no longer a part of the questions I ask. I know where I will be too…that is definitely a given. If the consumption of the previous when, how and what were entertained in the least bit, John’s spirit would be robbed of its giving energy and he deserves more than that from me…from his wife. How much longer do we have with John? I do not know…nor do I care. I will make every minute of every day seem like an eternity in my thoughts and he will never leave me….he will never be a brief thought in the daily grind when I get back to what will seem to be a life after him…he will forever be etched in my heart and on my mind. He deserves this from me. There will always be a familiarity of his smell, of his touch, of his voice, of his face, of his love…running rampant inside of my soul. He still, to this day, thanks me for taking care of him…I have always replied back in greater thanks. “Thank you for taking care of my heart,” I say every time. Just because he cannot do the physical things he would do in the past that he considered taking care of his little family, he has always and has continued to take care of my heart….and he has done an incredible job of doing so.

10.07.2010

our second home...

It has taken me a while to write this post. I started it on the plane ride to Indianapolis and have been working on it every night since then. As you can see….we have made it home. Indiana will always have a sense of home to the two of us. This is where he grew up, where his entire family resides, where my parents moved to when I went off to college and where we met. We agreed since the day he was diagnosed that we would end up here if there were no other options in his treatment…and here we are, resting in the Kennemore household. We were welcomed with open arms by his sister, Megan, and her husband, Chad, to stay as long as we needed and to make their home our home. For this, we will forever be grateful. There is a tremendous sense of comfort being here…in this home…with our family.

Leaving Florida was impossible to say the least. Since John’s release from the hospital late Friday night, we said our goodbyes to our friends in Florida the entire weekend. It was a revolving door of friends, food, love, family, strength, tears and laughter. Laughter is something we needed most that weekend because the realization that many might not see him again was too hard to bare. Hour after hour was met with a trip up the stairs to go see John in bed, say their few words and moments later, the descent back down the stairs to meet others also in shambles. One by one, every person got their moment with John. We never could have imagined how difficult this weekend could have been….and we are about to do it again in Indiana. With each visit, we realized the trip was getting closer and the moments with friends in Florida were drawing to a close. It was like a ripple effect. I have never heard so many, “I am so sorry” avowals whispered in my ear as I did this weekend. The harsh reality of his weakening was becoming more and more evident. The fleeting thoughts of flight and transport in the moment were consumed with what was to happen in the coming days.

Monday morning came in a hurry…we stepped onto the plane and John was incredibly strong throughout the ride. We thankfully arrived to family and friends with the same open arms we left in our home in Florida. Since our arrival, we have been draining the bloody fluid from his chest every day and without fail, there is more and its consistency is even thicker. We had a scheduled blood transfusion Tuesday morning and found out his hemoglobin was holding strong. All of this despite the amount of fluid we are getting from his body. It fared well. Hospice was also waiting for us to arrive and pain management is an important part of this leg of the journey.

He has been under the stress of knowing what is happening and faithfully, he does not waiver. His head is held as high as he can in a moment like this and his love still permeates the room. I do not know how he does it. I really do not know how he can know how the chips are falling and yet, he tries so hard to be the best companion he can be. I have thanked him for fighting and for being the bravest person I have ever met every chance I get….and I will do the same unto you. I have always said it and I will say it again…thank you. Thank you to those who have supported us throughout this journey. The selflessness and love shown by all of you has been amazing and we honestly could not have done it without all of you. Even just reading this shows a great deal of care even though many have no idea who we are…that is a gift. It takes a village….and with his caring sister and loving mother in tow….we arrived in Indianapolis with the utmost power and fight we can unearth within ourselves. It is not over. He is still here. He is still who we all want to save right now. Though we can try and pretend it does not hurt. We can pretend it is not happening. We can say how much we all just want this to stop and go away. We can yell and scream with tears flooding our eyes. We can do all of these things, but the reality of it is….this is what we are going through. Though rough and completely overwhelming, we still have each other for these moments along with the power of our family and friends backing us every step of the way.

10.02.2010

our song...

Sail away with me honey
I put my heart in your hands
Sail away with me honey now, now, now
Sail away with me
What will be will be
I wanna hold you now

Crazy skies all wild above me now
Winter howling at my face
And everything I held so dear
Disappeared without a trace
Oh all the times I've tasted love
Never knew quite what I had
Little Darling if you hear me now
Never needed you so bad
Spinning round inside my head

Sail away with me honey
I put my heart in your hands
Sail away with me honey now, now, now
Sail away with me
What will be will be
I wanna hold you now

I've been talking drunken gibberish
Falling in and out of bars
Trying to get some explanation here
For the way some people are
How did it ever come so far

Sail away with me honey
I put my heart in your hands
Sail away with me honey now, now, now
Sail away with me
What will be will be
I wanna hold you now
Sail away with me honey
I put my heart in your hands
Sail away with me honey now, now, now
Sail away with me
What will be will be
I wanna hold you now

9.30.2010

dear John...

Hi baby. I love you….I know you know how much I love you because I tell you at least 100 times a day. Do you really know how much other people love you? I don’t think you do my sweet angel. It is evident in the outpouring of love, affectionate words, and compassionate action from everyone who has ever come in contact with you, even if it were for a brief second. I know you want to thank so many for what they have done and are doing for you in this time. You are adored by so many and an inspiration to everyone…especially to me, your wife.

When we got the news seven months ago I knew every ounce of our beings, together, were going to fight. I repeated those words to you as we sat on the living room floor…in tears…the day you told me the results…we are going to fight. Fight is exactly what you did. You knew how hard this was going to be….you knew it was going to try and break your spirit….you knew cancer was going to try and take you away from me, your family, your friends, and your life too early and you were not going to let that happen were you? You did it. You fought…you loved….you cried…you felt….everything. Every single thing that happened along the way you were in control of…except the cancer. That beast was relentless baby. It wanted to take over you sooner but again, you did not let it. You made it so much further than the expiration date you were given in the beginning and I am so proud of you. I am so amazingly proud of you and to have been through every part of it with you….right next to you. There was not a moment I felt as if I should be somewhere else. I knew this journey was going to be hard but your bravery, strength and love was all I needed to be right there with you.

I hate cancer baby love. I know you do too....and I know you hate it most of all because it cut our lives together short. Six years was not enough time to soak you in….I want more. How can I not? The light that radiates through you to me is intoxicating. You are a man of few sentences and you are never careless with your words, but when you do speak it seems so profound…even hilarious at times. Cancer also took our future together….especially having our own little ones to pour our immense love on one day. Even though we cannot have those beautiful, blonde haired, blue eyed little angels anymore…I will always have them in my heart….along with you. You are nowhere near being gone, so this is not a letter of goodbye…this is a letter of appreciation and love. We begin this new journey now together to spend every second we can showing our love to one another. I am so lucky I found you….I am so lucky to have loved and will always love you….I am so lucky you wanted to spend the rest of your life with a woman like me. Don’t worry….this is just the first of many letters I will write you as there is so much more to say to your beautiful face for the remainder of your time here with me. I adore you….I just simply adore every ounce of you. Thank you for loving me….

Your Wife

9.28.2010

my angel...

My sweet, amazing angel. What can I do or say to make this all better? There is nothing left…and it hurts. Everyone who has ever met John will say the same thing, “I wish I could take this away.” I do too. Since the last blog entry, we got the news we never wanted to hear. Let me walk you through the past few days.

Friday evening, John’s mom arrived in town and was put into this whirlwind with us. She is really a strong and amazing mother and I am thankful for her presence this week. She walked right into the mess by getting taken in the hospital hallway by the surgeon who put his larger chest tube in place. He took it upon himself to tell her…rather than the 27 year old man who has been going through all this for the past seven months…that things are a lot worse than they seem and we were not being told the entire truth about his diagnosis and life expectancy. With those few words, he stole the optimism and positivity we had been fighting so hard to keep through this full journey. Saturday and Sunday were spent in a fog with the anxiety of wanting to discuss his options with his oncologist. Soon came Monday and we hurriedly called him to ask of his schedule the following days. He let us know he was to arrive first thing Tuesday morning to look over his chart and discuss treatment options. All the while, John had been draining more, darker, bloodier fluid on top of countless transfusions and xrays to continue tracking his drainage and hemoglobin. Monday did seem to get better and the previously higher blood pressure John was battling, was decreasing hour by hour.

Finally, this morning came. We were woken up by the portable xray team, coming in to do their morning routine of John’s chest and stomach. As I was stumbling in the hallway, still half asleep, I realized….it was Tuesday. Tuesday was the morning we had been waiting for since the dreadful news on Friday. My hair disheveled and my eyes full of morning crust, I made my way back into the hospital room we have now called home for over a week. I plopped down on the couch and could not help but look at my feet and then over to the drainage kit lying beside John’s bed on the floor. I had noticed he was on his fourth kit, each one holding over 2,000 CC’s. The uneasiness and nervousness I felt in that moment was unbearable. Susie walked in the door around 8 that morning, handed me the ritual cup of coffee she stopped to get the two of us and sat down next to me. This wait for the oncologist took me back to the wait we experienced the very first time we sat in the cancer center waiting to hear the results of the first set of scans when John was originally diagnosed. I looked down, realized I was still in my sleeping clothes and proceeded to the bathroom to change into jeans. Just then…I heard the door open. I could not get my pants up fast enough and rushed out the door to find John’s oncologist sitting on the couch. Before I tell you what he said…I want everyone to know, we have been incredibly lucky to have the support of our family and friends, but equally, our amazing doctors and nurses. If we did not have the support and fight our doctors had along the way, we would not have been so optimistic. I sat right next to the oncologist and he began to talk to the room. In this small, cold hospital room sat John, Susie, the Nurse Practitioner from the surgical team and me…all hanging on what he had to say next…“John, treatment is just not an option anymore.” As the words rang through my ears like an ambulance siren, I got up and walked to John’s bedside to hold his hand. The doctor continued to talk about the amount of tumors in his chest, the progression, the quality of life he wanted for John for the remainder of time, how chemotherapy was too much for his low hemoglobin, and how the fluid was coming out pure blood and was preventing further treatment. He was getting transfusions every other day but it was literally coming out the other end of his chest the same way it went in. With those statements, it was like someone ripped my heart out of my chest and stomped on it. It continued when he said, “The tumors were responding but finally outsmarted the treatment and is back with a vengeance.” I squeezed John’s hand and watched him slowly break down. He hung his head and could not believe the news either. We always kept hope that one day he would beat this and now we were told there was no way. It was like a tidal wave…the entire room felt it and we all were sobbing uncontrollably. Hospice was mentioned…pain management…at home care…making John comfortable…and finally, sending him away for yet another surgery this week to put back the at home drainage tube in his chest so we can take him out of the hospital.

Susie and I followed the hospital bed as he was carted down to another floor for this surgery with a new surgeon. We requested a new one after the incident on Friday. It was over in less than an hour and we were met at the door by the surgeon as John was whisked back by on his way to his room. “Everything went as planned and I found another pocket of fluid the previous drain did not access,” he said. The thoughtfulness in his eyes and the way he held my arm showed me how much he really cared for his young patient. I asked if he retrieved a lot from his chest…even with all the draining John had done throughout the week. “Yes,” he nodded, “…a lot more actually.” Where and how was John carrying all this? It boggles my mind. We hurried up the elevators and met John in the room, where he was still coming out of anesthesia. He opened his eyes, saw his mom and me standing before him, and smiled. My angel smiled…then said the funniest thing I have ever heard. “Baby, I dreamed about giant green beans…they were the size of my arm.” We giggled together and it seemed to make every ounce of sadness vanish for a few moments.

After hours of recovery and coming out of the medicines they gave him from surgery….here we are…a mess. We are a freaking mess. These past seven months have been such an uphill battle with the hope of beating this horrendous leach growing inside of him. Our gastro doctor said it best weeks before, “We all want John to prove us wrong. We want him to make us all look like jackasses and beat this thing.” More than anything, we wanted and believed this too. He was going to be that rare case that won…the one who made it in the medical and record books as being the youngest case ever diagnosed with esophageal cancer and on top of all that, beating the bleak prognosis and living years beyond what anyone expected. We wanted this so bad. Today, we realized this was not going to happen. We have all fallen apart several times today and I am sure, as word spread of the results, others did too as if they were right next to us. I cannot blame anyone for feeling this pain because of the love you have for John. I am so lucky and thankful to have this man in my life and I know you all feel the same. We do not know how much time we have left with him, but I am going to be sure to spend every last second I can letting him know how much I love him. So…with that….we are headed back to Indianapolis on Monday after getting things together here in Orlando this week. His beautiful sister will be here on Friday and all four of us (John, myself, Susie and Meg) will fly all together to stay at her house as the cancer continues to run its course. I never thought I would say that…let the cancer run its course. I find myself looking down at my wedding rings, starring at John, or looking at the floor and completely zoning out. I think of all the beautiful memories we have shared and the amazing love we have for each other. It is like I am not even in my own body anymore. Today, a social worker came in the room to check on us and one of the last questions she asked was if we had kids. I told her no….but that we always wanted children. I sobbed and realized this would never happen with John and could not control my tears. One of the many things I wanted to have with this beautiful person is now gone….and I cannot stand it. My world is in shambles and the one person to make it all better, every single time…is leaving. We do have the most amazing support system…we really do…I know that….but selfishly, I only want one person here with me, and that is John. A part of me does not even think this is happening right now. I'm sorry...I know my thoughts are all over the place right now. Please…I beg of all of you…please, send your sweet love, prayers, thoughts, and compassionate words to my husband. This is what we need and this is what I ask of all of you. I just love him so much…