Thoughtfulness.

There are no words to thank everyone who has reached out, sent messages, sent cards, sent flowers and gifts and held space for us. I can only say, it means everything to me.

Several of you have made donations in Jake’s name.  I am so thankful for each and every one. Love lives on through your kind and generous gestures.

I wanted to share some of the gifts I have received…

My friend Virginia had pencil sketchings of Melvin and Jake done.  The detail is incredible.  I got Melvin’s shortly after he left me and she gave me Jake’s while he was still here but nearing the end.  I have them hanging in my kitchen, a reminder of where my heart is.

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A few days after Jake died, I received a package from a reader (Michelle) that I have never met, although we have a mutual friend in common. She made this. She made this for us. Our motto, hand-done by her with love.  I sat on the floor sobbing when I got it, because I was reminded that we are so blessed to have you all.

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I received this from our dear family friend, Mary. It arrived the exact moment I needed a pick-me-up.  And it lifted my heart and brought me so much joy.

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My sister-in-love got me these. When I wear them, they loop together just like the boys did when there were snuggling.  The pendents rest close to my heart, right where the boys are now. IMG_9952

 

Jen over at Sirius Republic had a print made that has a photo of the boys  and across it is printed ‘love lives on’.  She also handmade this heart for me, it’s a visual of my heart. I squeezed it so hard, I’m shocked I didn’t damage it or myself. IMG_0004

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Emily, over at Our Waldo Bungie, had this drawing done of the boys.  The first thing I thought when I saw it was -‘my superheroes’! I am going to have it framed with their Super Melvin and Super Jake collars.

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I got these from my friends Tayler and Melissa.  The rainbow bracelet represents my life and love with Jake and that fact that he is waiting for me, with a piece of my heart,  at the rainbow bridge.  The white bracelet represents Jake’s life and the mark our love left on my heart. The 22 white beads represent 22 dogs who were fed a meal in Jake’s memory. IMG_9987

This community and blog, this space heals me. You bring me joy. Thank you.  Yes, you, thank all of you for everything.

OK.

I’ve been honest with you. Losing Jake has been heavy and complicated. I thought I was ready to face it and I thought my grief journey with Jake would more closely align with my grief journey with Melvin.

I was wrong. It happens.

At some point last week, after a really sad night, I sat down and thought about all the parts that are harder, all the part that are holding me down, all the parts that make me unable to breathe. And so much of this, and grief in general, is about what I can’t control. In short, I can’t control that Jake is gone. I can’t control that he has been gone for one month and that this past month feels like a hurtful forever. Even before he died, I couldn’t control so much about his health. So I guess I’ve been out of control (but not in a Girls Gone Wild way), for a while. I thought about how I could get back on track.  Instead of thinking of all the things I was crying about, all the things that were out of my control, I instead made a list of the things I can affect. A list of all the things I can champion. It is exactly how I lived life with Melvin and Jake, not focusing on the things that we couldn’t fix, but focusing on all the ways we could shine. It is exactly how I need to continue to be, even in their absence.

No one said seeking joy is easy.

I tried to focus on, not on what is different about losing Jake and Melvin, but instead, what is the same. I tried to focus on the successes, on the things that could lift me up and remind me that it was OK and will be OK. And I thought for a long time and I came up with three things that were then and that are still now.

  1. “Love lives on” for me, was born the moment Melvin died. I honestly believe that it was my purpose last year to make sure that Melvin-love lived on and it’s my life’s work now to add Jake-love to that mix.
  2. Love and joy, are who I am. What guides me has not changed.  Part of it is perhaps lost in the grief shuffle right now, but it was the whole of me before and I still feel it at my core now. I just have to get out of my own way.
  3. Most importantly, the common denominator between last year and this year, is me. Sure, I could argue that is the hard part, but I survived losing Melvin. I went on to see Jake through last year, the worst health year of his life. I did that. I’ve been selling myself pretty short by focussing on all the things I can’t handle this past month. I got through last year. I’ll get through this year too.

So I added a new mantra to my day. Love lives on. Check. Go find your joy. Check, check. And now, I have to ‘make the not OK, OK‘. Part of that means that not everything will be OK…and that’s just how it is, but I don’t have to let those moments own me. I can acknowledge them and let them be for now. There are things I can make OK.  A new OK. A different OK.  OK is a town you pass through on the way to New Normal.

My GPS may be working again. I’ll keep you posted. Until then, here are a few things that brought me joy this past week…

My view into the washing machine last night. It was OK to wash them, they needed cleaned. IMG_0011

 

Jake is ‘Dog of the Month’ at our local and most favorite pet supply store, Happy Hound! IMG_0002

 

And this.  These two are sorta the whole of everything.  #lovelivesonIMG_9970

 

MY GPS is off.

The only thing I know for certain right now, is that losing Jake is not at all like losing Melvin. The difference is not about emotions, those are exactly the same, but my navigation through the loss and the day is completely different.

Sadness and missing them aside, when I lost Melvin, I had a strange sense of hope. I felt a lot of purpose. I felt him guide me. Jake was here when I lost Melvin.  We survived it together. With the loss of Jake, I am trying all the things I tried last year, they are not as successful this go around. I am paying things forward (his things) and while it makes me so, so happy to do it, it makes me miss him so much more.  Probably because I’m donating his things and wishing they were still needed by us.

You can donate my things, but not to other dogs. You know how I feel about other dogs. IMG_5971

I know that having no dogs in the house is a 25-foot wall roadblock to my grieving process; it gets in my way every time. I’ll have moments, normal grieving moments, when I’ll think about Jake and tears come and then a funny memory will pop into my head and I’ll start to laugh. If only I could have that little moment. Instead, right as I’m having my teary-laugh, this loud, scary, bully of a voice screams –  THERE ARE NO DOGS HERE,  YOUR LITTLE FAMILY IS GONE. That voice is ruining my life. I know in my heart that it is way too soon to think about getting another dog but I also know that trying could alleviate the empty house issue and that even if it’s hard, it might make grieving easier. I’d be rescuing someone who also lost their family.

So, I went to an adoption event this past weekend. Let me explain me and adoption events to you…it’s not my thing. I don’t make life decisions that quickly. I need to meet a dog then go home and think, and think some more and plan and make some checklists. So I knew it would not be a fit for that very reason. That’s mostly why I went, to just get out there and test the meeting waters.

I cried after leaving the event. For two impossible and opposing reasons. It was way too soon to be looking for a dog and it feels way to long since a dog has been here. I cried because no matter what I try, nothing feels right. Jake not being here breaks me and there being no dogs here takes a lot of the air away. Grieving Jake and dealing with the empty house has been… a bit complicated.

I will find my way.

It’s been three weeks. I miss him. After losing Melvin, Jake made me laugh every day. I miss my little comedian. Melvin traveled through life spreading love and joy; Jake scooted along spreading love and comic relief. If you are having visions of me sitting around crying all day, there is no need for worry. I go about my day, I’m keeping busy, I’m honoring Jake in as many ways as possible. When a sad moment hits, I close my eyes to calm down and I have a vision, pretty much the same vision every time. It’s of a line of dogs that have touched my life. Not just my dogs, but dogs that impacted my life in some way too — my heavenly dog army. They are all sitting in a straight line in a field of grass, facing me. In front of the line of them sits Melvin and Max. And in front of my first two angels sits Jake. And they sit, still as can be. I know they are coming together for me and Jake. Jake is so close in this vision, I can almost touch him. He can almost reach me. And almost, at this point, is everything.

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I know that everything will work out. I know that this home will not be empty forever and I know that the grieving process for Jake, while complicated is somehow just as it’s supposed to be. For all the beautiful love, I will carry all the heavy grief. I will continue paying love forward in Jake and Melvin’s memory and I will keep going to meet dogs that in no way could ever be Jake or Melvin.  One day, one of them will say to me, I am not them I’m just me. And that will be the one.

A look back to my little bug, using his good eye to conduct neighborhood watch. IMG_9817

 

 

Photo shoot.

We had a photo shoot a few weeks before Jake died.  I’ve shared a few of the photos with you already, here are a few more of my bug and our love.

Thank you so much to Bridgette E. Photography for capturing these moments.

#loveliveson

Meatballs from Heaven.

Losing Jake is hard in obvious ways and different in unexpected ways. It’s always different for each loss,  but as hard as it was to lose Melvin, losing Jake comes with a swell of other losses and disruptions.

There is the expected part where I am incredibly sad, I miss him so much and I still need to be taking care of him. This part…it’s the given. The price we pay for true love. I say ‘I love you, Jakey’ out loud, all day, because it’s everything that I feel.

Then there is this house. When I lost Max and Melvin, while taking up their things was hard, I still had water bowls and beds to leave out. Each time, there was still a dog. Jake has SO MUCH more stuff than just beds and bowls and toys. This home is set up for him. There are yoga mats running the width and length of this house. The mudroom is a makeshift vet treatment room. There are washable pee pads, diapers and diaper inserts, everywhere. And for one dog, there are more beds than I can count on two hands and just as many waterproof mattress covers.  I have slowly started gathering things up but with each thing I pick up there are emotions to work through. First, picking up the things that made his life easier feels like saying, ‘these things are in the way’. Jake was never in my way and those solutions brought us both so much joy. No one wants to have to clean-up joy! Secondly, picking up his things is a reminder that there are no dogs here.

There is no ‘our’ or ‘we’. It’s just me.

The moment Melvin died, I immediately felt him in a new way. I felt him become a part of me. I missed him and the ache was palpable but he wrapped himself around me and I carried him forward with me. I never I thought I’d say these words about anyone but…he imprinted on me.

I don’t feel Jake all that much (yet). I worry that his googly eyes got confused at the end and maybe he imprinted on the couch instead of me.

I think I know why Jake feels so far away.

While Jake most definitely knew I loved him and we felt love with no words…so much of Jake’s and my love was also through touch and action. He felt my love, literally by feeling me taking care of him. I channeled so much of my love through nurturing. My hands were on him caring for him. Love felt when lifting him, carrying him, holding him up. He’d look up at me with a single glance (and a single eye), and I’d reach down, knowing exactly what he needed, to help him maneuver. Now, my hands feel idle much of the day. I know that part of not feeling him is that, I literally can no longer reach out to help him. I don’t lean over or kneel down 50 times a day. My apple watch is probably worried I’m dead based on the drop in activity.

I never thought I’d miss meatballs.

The other thing is, and this one might not be one that everyone will understand and I may not do a great job of explaining it but even if you don’t get it, it’s the perfect example of how odd grief can be. When Max died, I could picture his old-dog body healed and him running again. I’d known Max his whole life.  When Melvin died (he’d only had cancer for 40 days), he looked exactly the same on earth as I thought of him at the Rainbow Bridge. The only difference was, he was cancer and allergy free, easy to see. Jake is different.  I was not Jake’s mom during his healthier years. The majority of time I knew Jake, he had progressive mobility issues.  I was wonky-legged-paralyzed-Jake’s mom. I saw those issues as challenges and together, we made a life where Jake lived his own version of normal and I thought we’d have many, many more years together so I had let go of ‘upright Jake’. I always wanted more for Jake, but I never wanted more than Jake. When someone says ‘Jake’s not suffering anymore’ or ‘Jake is running in heaven’…it is everything I always wanted for him, but I also feel…disconnected. I still see, my Jake. When I have visions of Jake now, he’s usually laying with Melvin or sitting next to him. Although he’s happy, I can’t (yet) bridge my mind to zooming Jake. I can easily see him with no diaper rash (yay), I can even see him with no hamburger eye (oh those gorgeous googly eyes).   I think this is just another reason why I don’t feel him as much yet (in the way I felt and saw Melvin). Grief has a way of making random shit more difficult than it needs to be and this is just a strange grief barrier I need to break through.

Maybe, maybe I’m just looking for him in the wrong places. I have faith it will work out.

This past week I have felt Melvin more than usual. I know he is letting me know he’s got our boy. It’s funny how roles can flip.  Now I’m the one who is somewhat paralyzed at moments. I’m the one with separation anxiety. I’m the one with wide-eyes, looking to be lifted up. The boys moved forward every day, no matter what.

That legacy will live on in me.

As for no dogs being here, well that will feel lame until there are dogs here again. I had to come to terms with Jake not wanting other dogs. I committed to that for him so it’s not easy to turn that switch and say ‘ok Jake’s gone, there can be other dogs now’. I am still the impassioned leader of Team Jake. This week, I’ve slowly started looking at rescue sites again. As always, there are dogs that make my heart thump. I know that rescue is my calling. I hear it.

I just wish Jake was still here. It’s only been two weeks.

There have been so many beautiful people; my family, my friends, you…who have been there, here, wherever you are…sharing stories of how Jake inspired you, that you miss him also, reminders that we made a difference. To say I am blessed, is to say love lives on.

I have been re-reading my post that talks about how ‘the one love’ should move forward (click here to read).  Trying to remind myself of who I am. Up until this moment right now, I have never lost a dog and not had a dog and faced how to go about moving forward with a new dog. I have always gotten a dog before losing a dog. There has always been a dog! So that post about ‘the one love’ was written by the old me. It’s still me, but since writing it there has been a lot of loss and there has been a wonky-legged-googly-eyed-I-hate-any-dogs-that-are-not-Melvin dog. So when I read that post now, I tend to laugh because up until Jake, all the dogs I have had wanted me to love again. Melvin and Max loved love. They wanted me to always be paying our love forward. Jake…well Jake loved being loved. But sharing was not his thing. Some with Melvin but definitely after Melvin, he did not share his neighborhood, his yard, his toys, his food, me or his Melvin’s our home. Something tells me Jake is in heaven being reminded that the F-word is absolutely not permitted…

‘Uh, F no mom. Step away from the rescue sites. We did fine without dogs when I was there and you can totally do this no dog thing without me. If you see someone with a F-ing dog, look away, you do not want what they have. We talked about this, NO DOGS IN MY HOUSE!                                That one-love crap, that ended with me!

Of course that is all said in his Barry White bark voice while he continues to flip and flail long after he’s done saying it and there are probably heavenly meatballs (made of glitter). Jake behaving exactly like he did every time I tried to bring a dog home to him. And in true form, Melvin is just laying next to him, calm as can be, rolling his eyes over the idea that Jake uses up so much energy on such silly things. And Max is thinking…there is no way we are related.

I sorta like the vision of spirited Heavenly Jake. It allows the hashtag #lifewithJake to live on, just like the love does.

I pity the fool that gets another dog. IMG_0835

What happened.

I’m not sure how it’s been one week already.

Let me start by saying, this post is sad. And it’s happy. But it’s sad. No matter how hard I try to inject joy or humor (I gave it my all!), the answer to the question that so many of you have reached out to ask, ends with some obvious heartbreak.

I thought Jake and I would have a little more time together. I had also hoped that I’d be able to share with you when his time had come, but as I realized what was before us, my mind and heart and existence only had space for Jake. In our last few days, I gave myself fully to my boy.

You knew Jake’s health plight, oh so well. He had a crappy spine that took his hind legs down. The mobility part, was a lot. But we worked towards solutions and he learned to move forward, literally and heroically.  When strangers would see Jake they would always say, ‘poor thing, he really struggles’ and I’d say, “he’s fine, he’s Jake”. And that was truth. But the secret life of a special-needs pet-parent is that you are constantly evaluating the current state of struggle and being. I was always tracking the balance of joy. Jake always just kept finding a way to move forward in his spunky little way. It was my honor to join him on his journey and share in such an incredible love.

He taught me so, so much.

Jake’s challenges did not end at his legs. If only they ended there. The universe seemed to single him out sometimes, with issues that we tried so hard to overcome and we could almost fix, but not really. He had a strain of MRSP with no compatible treatment. He developed not one, but two eye ulcers at the same time, one that formed a hole in his pupil and while emergency surgery helped keep the eye, his eyesight, his beautiful wall-eyed eyesight, suffered. So he had a hamburger eye. Yet, still he kept going.  He lost control of his pee and meatballs (to be fair, this did not bother Jake!).  Even though diapers helped, they also weighed him down and he battled many diaper rashes.

The spine and leg issues were enough. Add in all the other things and as his mom, I sometimes cursed the universe for unloading on my boy. But for every issue, we worked out a solution. For every single situation that made his eyes look at me with worry, I came back with something that helped it. My goal with Jake was that his balance always went towards joy. He returned my every gesture, with laughter and love.

Teamwork at it’s finest.

We even found our way after we lost Melvin. In the past year, we were each other’s everything. Our little family, was perfection.

Then came spinal cancer and the soft tissue cancer in his hind leg. The universe bearing down on him, again. A cancer that we couldn’t treat and one that would be painful. A battle we were not going to win or solve. My evaluation structure changed. I no longer had to balance the struggles, I just had to monitor the pain.

Or so I thought.

When Jake was diagnosed with cancer, he still had some upright moments in his hind legs. Not many, but he could wobbly stand to eat sometimes, or he’d do a walk-drag (a move that earned him a ‘drunk uncle’ nickname). But the cancer took his left leg down pretty quickly and then his right leg tried hard, but it too lost that fight. The odd part about this chapter was, the hind legs part was always going to happen to him. That was a plight we’d accepted after figuring out his wonky spine. So sometimes, I’d forget he had cancer or that it was actually the cancer doing the current damage. In a way, having had accepted his mobility plight before the cancer, helped us stay strong and closer to joy after he was diagnosed.

Yoga mat runways throughout the house helped a lot too.  He strutted his stuff like a boss.

Over his last few weeks, Jake became less active. Some days much less, but some days were better. When we’d go out back, I’d put him down to go potty and he’d just sit at the end of the ramp and pee there. I’d pick him up and put him in the yard and try to get him to move around but he’d just sit again, looking towards the door to go inside. I’d carry him inside. If it was a mealtime potty break, I’d go in and make his breakfast or dinner. Prior to this time, if I said ‘dinner‘ he’d come ‘running’. But now, Jake would still be sitting in the mudroom. So I’d go and get him and carry him to meals. His pain management was constantly reevaluated and he was, for all we could measure, comfortable. He just wasn’t moving around on his own very much.

He was still so happy though. His face was pure love.

There was also a  change in how he dragged his legs, going from dragging his legs to the side (normal and easier for him as he could use his bum to help push himself forward) to having his legs drag directly behind him (so much harder for him to pull his weight that way). He tired easily. I just loved on him harder.

Normally, through these changes, we’d be at the vet or have the vet to us. But I knew what the decline was about. And like so many things in Jake’s life, I couldn’t fix it. I could only try to make it easier on him. So I carried him a lot more, knowing him so very well and knowing where he liked to be at each hour of every day. When Jake was in my arms, he’d kiss me constantly, as if kisses were the gas pedal that kept me going. And they were.

I’d carry Jake to the end of eternity and back again.

Jake had also been having some very minor seizures. We were not sure why. Part of me thought maybe it was his medication. During his last two weeks he’d also started having little spasms when he was laying down. At first it was two to three a minute. Towards the end, it was 20-30. They were like these zingers, it almost seemed like he had the hiccups. But he didn’t have the hiccups. They seemed to bother me more than they bothered him.

Yet though it all, my bug still knew so much joy.

Then there was the terrible infection that stemmed from his most recent diaper rash. And all our usual tricks that battled diaper rash before, failed. Cancer was being a real jerk. The thought that a diaper area infection would take my ninja warrior down seemed so unacceptable so I fought that rash harder than I think I have ever fought anything. We battled it hours and hours a day. I set a time limit on the infection, if it continued to win, I could not let him continue battle it. It would have infected the joy.

But you know what, as of that last Saturday night, the infection turned a corner, and it was on the mend! And I high-fived the shit out of Jake and we did a ‘we won dance’  and it had been a long time since we got to do a ‘we won dance’ and we went to bed Saturday night renewed in our fight! The time I had given us to beat the infection had not run out.

Time is funny. It doesn’t care who you are or what you want or how hard you fought or how many things you faced down or how much you danced. It doesn’t care that your little guy worked harder to travel through life than most will ever have to.

Time didn’t care that Jake was only eight.

On Sunday morning, the day after our we beat the infection parade, Jake woke up, toppled over and had a seizure. This was not a minor seizure like the others, it was major and it was terrible. His body went so rigid that at first I thought he was having a heart attack. I held him in my arms and I told him that he was going to be ok and that if he saw Melvin he should run towards him with all that he had. I told him over and over and over that I loved him. During the seizure, he pooped (this is normal for a seizure but I think Jake was sending me a ‘I love you, too’). As his body started to relax, he stared up at me…with love and then kisses. And in that moment, in that tiny, giant moment with my little warrior, we were the only two living creatures on earth. In that moment, we won at love.

I called the vets. We briefly discussed the reasons it could have happened.  A conversation that didn’t really require words.

Jake was not himself on Sunday. I know some of that was the seizure. But as he and I traveled through the day, and as I started to paint the picture of our last few weeks and months…I knew.

I know Jake. I know his body better than anyone. I know the exact moment during that day that he let me know he was tired. Tired of challenges. Tired of having to overcome. Aware that his ability to travel though our life together, was becoming too much.

If Jake had a wonky spine and seizures, well I’d clear the calendar and we’d be a regular at the neurologist. If he had the worst diaper rash and wonky legs, we’d tackle it. If he had MRSP and a wonky spine and eye ulcer surgery with months of a cone, well we call that 2015.

Sometimes you can’t outrun reality. Even when you can’t really run at all and your mom is carrying you and she is running as fast as she can. Jake had cancer and all the other crap that the universe dumped on him and now seizures were invading our precious space and I knew, in a way that only I could know, that his joy would only be reigning supreme for a few more days.

I couldn’t let him go through anything more, except love.

The day I let Melvin go, he was not having a bleed. It was an ordinary day with my extraordinary boys, he woke up with joy in his heart. He ate, he walked out back on his own and he snuggled with me and Jake. His tumors hadn’t ruptured yet. There was no collapse. There was only joy.

I wanted the same for Jake.  His life had known such struggle, 100% more struggle than I ever wanted him to have known, and yet my little superman choose love and perseverance every single time. Jake’s end was coming and I would rather die myself than have him feel one more ounce of struggle or confusion as to what was happening now. So Jake had a beautiful Monday. His village came over and loved on him and he gave them the sweetest, gentlest kisses. He had the best meal he could have ever imagined. He and I went on a stroller walk, right down memory lane. To all the places he and Melvin used to walk, on all eight of their legs. We went out back and reminisced about all the things he ate in our yard. We did his last neighborhood watch at the front door.

Then he and I tuned out the entire world and we snuggled. We snuggled so hard and so perfectly. I breathed him in. He kissed away my tears. I told him all the things I wanted to tell him and he looked into my eyes and told me all the things he needed me to know.

We could not have loved each other more. We got each other through the roughest year of our two lives. We chased joy, and we caught it.

I let Jake go at home. In his favorite spot.

I know that as his vision of me faded, Melvin appeared. I know that Jake leapt into Melvin’s face with an unimaginable joy and I know Melvin shared gleefully in that glorious moment. Jake moved forward, cancer free and struggle free, eyes wide and his second leap was likely straight towards Melvin’s butt. There is a part of me that finds such peace in that even as the whole of me grieves. The heartache and sadness I feel, is worth every ounce to know that Jake and Melvin knew my love and that they are reunited in sweet, joyful, odd-couple joy. To know that they have each other, for forever this time.

#loveliveson #findyourjoy

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Heartbreak.

I miss Jake. That is my entire existence right now.

All of me, misses all of him.

I’m surprised to even be here on the blog.  When I learned of Jake’s cancer, the future of the blog loomed in the back of my mind. I thought that when I lost him, so many things would go silent, including this space. This is a blog about my little family. My little dog family. And that little family…is gone now.

It has only been two days. To say it’s been two days seems crazy because it feels like forty lifetimes since we parted. I’m not sure why he feels so far away from me, I’m sure it has something to do with my protective barrier. Losing Jake is familiar in some ways, Melvin has not been gone that long and I know how grief goes. I know that sadness will try to hold me down and that I have to move through it. But like any loss, losing Jake is also completely different. Jake is my baby. Jake and I got each other through the last year. I know, I will work through this. This part, I know is torture and heartbreak that will one day find its way into joy and love and memory. This part I know is the heavy debt of true love.  I know that wonky little monkey will light the way with his magical googly eyes for me. I will learn to persevere the same way he did, making every difficult step count.

I keep telling myself, it’s only been two days.

If it was just losing Jake, that would be enough, losing him is unbearable. While that part is ‘the given’ part of loss and grief, there is this new and complicated part of losing him that began to suffocate me an hour or two after Jake died and that has continued to spiral ever since.

I am overwhelmed to not be caring for Jake.

Not the normal things we all miss about caring for our pets, like meal time, or potty breaks or walks or training or treats or them just being there and needing us. I am overwhelmed by the things that fill up the day when you are taking care of someone with special needs. Like getting up several times a night to check to make sure Jake has not fallen out of his bed and to make sure he is not sleeping on or near poop. To carry him down and out in the morning, to clean his diaper area in case bugs got on him while he was outside. To change his diaper 25 times a day. To clean up all the accidents. To apply ointment after ointment after ointment to his infection. To care for his eyes, his MRSP, his mobility, his movement from room-to-room, to cook for him, to answer the ten alarms I had set throughout the day for all his treatments. To get him to the front door for neighborhood watch, to his stroller for walks, to his sunspots in the afternoon and to the couch for evening lounging. To carry him upstairs and help him get into his bed each night, tucking his legs in exactly the way he liked them. I do my laundry once a week.  I do Jake’s laundry daily. I don’t leave the house for more than 3-4 hours without making a plan to have Jake’s diaper changed or to go home and change it myself. Jake is gone and I have gone from providing 24/7 care to providing nothing. Every minute that goes by and he does not need me to help him anymore, breaks me. I get up at night and he’s not there. I stand up at 1pm and 2pm and 3pm to change his diaper. I had alarms set for the entire day so I would stay on track with his treatments and although I have silenced the alarms, I am unable to silence the ache that occurs each time I realize, he does not need my nurturing anymore. Additionally, with or without the alarms, my body still gets up to stay on track with our schedule.

I have no idea how to transition from caretaker to just me. Not on top of dealing with the loss of Jake. As Jake’s mother, there is nothing more I want for him than to be running and jumping and leaping in heaven. To be able see all the loveliness and all the joy with both eyes. To be struggle free, infection free and most importantly, enveloped in Melvin’s embrace and love. Soul mates, reunited eternally. Being together, is where they belong. But there is still a part of me, a raw part of me, that also wants Jake here.

In addition to the loss, and the disruption to the beautiful cadence of my day with Jake, I am also now a mom, with no dogs. The boys are both gone. If I thought coming home to Melvin not greeting me at the door was hard, coming home to no Melvin and no Jake and no need for a noise machine and radio is a most deafening silence. This one, this one is just going to have to suck until I get used to it. It’s more just a reality that will have to sink in.

When Max died, I got up because Melvin needed me and he kept me going. When Melvin died, I got up for Jake. Jake needed me and we moved forward together. In this now dog-less house, I get up because I know  they would want me to. I try to remember who we are, even if we, is just me now. And there are parts of me that know I’m capable even though I feel incredibly weak.

It’s only the start of day three. I’m trying to be kind to myself.

I will find my way. The boys will guide me and love will continue to live on.

Thank you for your messages, your comments, your thoughts, your prayers and your general awesomeness. Thank you, for you. I do plan on sharing with you what happened with Jake, probably next week. Until then, here is a photo of my little angel from our recent photo shoot.

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Run free, my love.

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Jake Holupka

September 27, 2007 – July 18, 2016

“I know you haven’t made your mind up yet, but I would never do you wrong. I knew it from the moment that we met, no doubt in my mind where you belong…

…no there’s nothing that I wouldn’t do, go to the end of the earth for you, to make you feel my love.”

I love you, bug. Forever. xoxoBT4A9988

The infection.

Jake still has an infection.  He has had it for a few weeks. Other times battling his diaper area infections have turned out fine. Those other times however, we were not also battling cancer.

This infection has consumed me. It owns my mind and all my time and energy goes into battling it or worrying about it. This is one of those times when you start to understand what they mean when the cause of death is something other than the disease at hand.  Like…he died of complications from cancer. This infection, is most certainly a complication.

There have been a lot of vet visits, countless efforts to fix it, so many creams that I had to make room in the garage. There have also been some tough conversations in the case we can’t get it under control. Luckily, his pain meds seem to be protecting him from feeling much of it at all.  And his wonky spine takes care of diminishing the rest of the sensation, so for that I’m thankful. He is for the most part, still Jake.

Since returning from my trip, I have not really left Jake’s side. I lay with him so he can have the infected area uncovered and untouched. I put different medications on him. I have to use surgical gloves which makes sense but feels strange.  I do homeopathic treatments (made for us by our amazing holistic vet), making a paste out of herbs and honey and I put that on the area for 15 minutes.  Then I meticulously clean it off and start back on the medications. I have everything on a timer and the timer is almost always going off.

I’m desperate for more time with him.

But more so, he still feels joy.

I had the worst migraine of my life this past weekend and every time that alarm went off, I somehow got up. He is my purpose right now. He is my goal.

There is a part of me that knows that this infection might be the sign that it’s time. To let him go before the cancer takes him. I know that his time is coming. But there is also still this light in him that ignites a light in me and it makes me wants to solve just one of his problems before I say goodbye. I’m not sure that light ever goes out. But I have started adjusting the glow. Instead of always saying ‘you’ll be fine bud’, I have started saying ‘if it’s time to go to Melvin, I understand.  I’ll carry all the sadness bud, you need only travel with joy’.

I had a conversation with someone recently. I was working through a let down, trying to focus on forgiveness so I could move on. Forgiveness is way better than bad mojo. I learned that from Melvin.  During the conversation, came some great advice.  He said… ‘never set yourself on fire to keep someone else warm’.

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And I thought a long time about that and it hit home in ways that were probably way outside of the scope of his meaning for it (although it made sense that way too).  I decided I was going to cut back on everyone else’s needs for a bit and only focus on Jake and me. I had been spreading myself too thin. I recall feeling this way last year with Melvin. When my capacity was focused on him.  And now it’s the same with Jake.

Right now, my plan is Jakey. His time is short and my time is his.

It’s funny, during this past week with Jake, I realized that the fire advice has some parameters — if setting myself on fire would help Jake, I’d be ablaze right now.

Love is so infinitely wonderful and so incredibly hard sometimes. What love looks like can change in an instant. We work so hard to make the end lovely but the reality is that it’s also impossible and messy and it always feels like yours is the very first end ever and no matter how many people surround you or call you or show up, you are still…alone. The end is lonely. So my advice is…don’t feel bad for needing ‘me/us’ time. Remember that being human has its limitations. For cripes sake, do not set yourself on fire! Most importantly, try to forgive the end (even more importantly, always try to forgive yourself).

But don’t forgive infections, they suck.

 

Side note:we had the infection cultured and it’s not an easy one to treat but there are medications we can try so we are going try that route, for now.

I promise you that suffering is not in Jake’s future. I’m still hopeful this infection won’t be the end.

Don’t forget to feed me woman. IMG_9625

 

Leaving.

I had to leave Jake for a few days.  Leaving anyone towards the end of their life feels impossible and complicated and emotionally painful but sometimes other loved ones in your life need you also and you make compromises.

The only saving grace was that if Jake were able to make his own bucket list, the first nine out of ten items would be to have his dog sitter, Tayler (and her mom), come stay with him.  He may love her more than me.  And I’m fine with that. For the record, Jake’s tenth item on the bucket list would be for us to go live wherever Melvin went and for me to pack really good snacks for the journey.

Tayler has watched him many times before,the last time this past winter.  That did not stop me from channeling my inner insanity detailing every step of Jake’s day in notes. Here is a look at the note, the highlighted areas are items that are new/different since the last time she watched him.

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Crazy, party of one.

The original plan was to take Jake on the trip. But sometimes life puts cancer in your day and you cannot add to your baby’s struggle anymore than it already does.

Jake’s bucket list: own a harem. Check.IMG_9599IMG_9600

 

Most of you don’t know this but I had to leave Melvin for a few days, just after we found out he was dying.  There was a very special and important family trip and although I could have canceled, there was the potential for regret no matter what choice I made. As it turned out, Melvin was just fine without me and he too got to spend a special last visit with his love, Vasha.

Even in dying and death, we have to live. It’s not always easy (I cried so much when I left Melvin for that trip but I also had some wonderful people around me, giving me strength to go back and face the hardest phase of my life).

So I left Jake for a few days, and there were tears (mine, not his!). I worried way too much, but I did relax some. I overthought everything and yet still found some clarity. I checked-in like a crazy person and even had the vet come by to check on him and of course, he did fine.

I would care for Jake until the end of time. I would change his diapers, care for his infections, carry him…forever. But it’s always nice to get a little break.  I came back rejuvenated and when Jake pooped on me as I was giving him my snuggly hello, I laughed so hard. That is what our love looks like and I wouldn’t have it any other way.

 

 

Formal wear.

I pride myself on finding solutions for Jake. There have certainly been times when those efforts have failed to produce options, but usually just for the minor stuff.

Jake drags his hind legs around now, which means his diaper gives me a big F-you every time I put it on him.  I readjust his diaper, true story, 100 times a day. Ask all the carpets we have waved goodbye too, the system was not working great. I had tried suspenders but Jake is pretty small and since he is on his stomach a lot, having the underside suspender part was not ideal because it would cut into him.  I also tried wrapping a scarf around the diaper (tighter), the scarf also gave me the big F-you. I even tried that mesh wrap the vet uses but I’d have to get a 2nd and 3rd job to afford that for every friggen diaper change.

So  I did what Elsa suggested and I let it go, and I just became the re-adjuster. Then Amazon, who serves up ideas based on my previous searches (guys, my searches would make you full on pee your pants — and we would have a diaper for you!), put the solution in front of me. Sheet binders. The straps you put on your fitted sheet to keep it in place.  They were 8 inches, the EXACT length Jake is from collar to diaper. Same day delivery? Yes, please!

We are only on day two, but my back is already hollering hallelujah! And Jake looks like he just came from a wedding reception. Pretty much the ONLY time you’d see white suspenders.

I mean, try not to laugh!IMG_9448IMG_9441

It took a while to get the sizing right so he was not choking.  Choking is bad. IMG_9425

For the record, dude had just pee’d in this bed and I was taking it up to wash.  He has no shame. He is more like a wedding crasher. IMG_9437

 

Opposite.

Melvin and Jake’s cancers are completely different and my handling of them are also, almost opposite.

Melvin was, except for the cancer, very healthy at his end.  We’d beat and cured all his issues.  The one thing we struggled with was weight loss.  He lost 10 pounds his last month despite him eating a ton. His cancer type must have been hungry.  Jake on the other hand has a ton of problems to go along with his cancer. A cancer leg that refuses to move (and is changing color) and a TERRIBLE diaper rash, to name a few. He however, is one of the very few cancer dogs that gains weight — he gained one pound last week.  Woohooo!

Then there is me.

With Melvin’s cancer, writing about it kept me grounded. It gave me strength. With Jake’s cancer, I don’t always feel compelled to put the words to web. That might just be a round two issue.

When Melvin got diagnosed I was devastated (that is no different for Jake), but after seeing two radiologists, the oncologist, our regular vet and our holistic vet (all within one week), I knew he was terminal and I knew our time was going to be very short. I went from living mode to survival mode and everyday I focused on getting Melvin to his end with all his joy intact. I have zero doubt or guilt that letting him go when we did, was absolutely the right thing to do.  It was the worst day of my life, but it was one of the most right things I ever did for him.

With Jake, sometimes in my head I operate like his decline is just the normal progression of his spine. It is a plight we’d already begrudgingly accepted so my brain thinks it’s normal. And sure, you can argue that some denial is good, but I need to start being truer to Jake’s end. His decline, is due to cancer. My inability to cure this round of diaper rash, is due to his cancer.  When strangers see him and say ‘poor little guy’ my response can’t be ‘oh, he’s fine’ all the time. He is not fine. I can say he’s happy, he’s loved, and he has the best care imaginable but truth is, Jake is struggling. I need to become less ‘ok’ with what is happening to him in the sense that this is not our original diagnosis of spinal issues and become more ‘ok’ about the fact that he has spinal cancer.  I’m still so desperate to fix him. I still think that this is our normal progression and I still google solutions for everything. Which is the opposite of how I was with Melvin.  And that is not to say I give up or I gave up. It’s just a matter of learning where to put your energy. I wanted to save Melvin every minute that he was on this earth but when he got cancer, I understood (not accepted) the end was near.  He and I cured his life and although getting a terminal cancer with no options went against everything we were and had been through, it was what it was. With Jake, he has struggled so much these past few years that we now are used to it. We have really, solved nothing with him. We ‘saved’ his eye. We have products that help. But everything he has faced, we just sorta had to seek solutions to make it ok to live with. So when he got cancer, I probably thought the opposites would continue, that with him, we’d have options and maybe for once a cure for him. I have to accept some hard truths. It’s complicated to have a special needs dog and then have them get cancer and have that cancer affect the areas they were already special in. For Jake, It’s almost like I don’t comprehend.

So our vet(s) have suggested switching to a ‘hospice’ mentality.  It’s not Jake’s time yet, but the term hospice can sometimes help the human move into the necessary mindset. It helps me process things like ‘the radiation didn’t work as well as we hoped’.  My normal response to that is ‘what do we try next’ and I am fairly unable to process the words ‘nothing’.

Thankfully there are still some things we can try to ease the diaper rash. We may not cure it (but watch me try!).

I’ve been laughing about the differences between the boys situations (ahhhh, the ability to find humor in strange places),  and I know that most of the reasons there are differences is that they are not the same and neither are/were their cancers.  I’m grateful for the most remarkable ‘Team Jake’ vets and I’m grateful for all of you who read these posts and who understand why there might be fewer posts right now.

To conclude, there is always joy to be found.  The recipient of Jake’s wheelchair (Oliver) is going on tons of adventures in his new ride and he has gone from uncertain of how to get around to owning that cart like a boss!  Heart happy.  Heart full. Love lives on, even in wheelchairs!

Whatcha doing woman? When you gonna unroll that new carpet? IMG_9353

Oncology check-up.

Jake got diagnosed with spinal cancer and a nerve sheath tumor four months ago. I cannot decide if it feels like four-months, if it feels longer or if time is flying by.  I guess mostly, it feels like four months.

We had an oncology appointment this week. For the most part, Jake is doing great! He has maintained his weight (thank you home cooked diet and peanut butter!).  His mobility has declined (terminal spinal cancer will do that) but his decline has been slow and steady so he has been able to acclimate. He’s comfortable, our pain management approach is working. That last one, is everything.

Jake was always going to be paralyzed in the back, so that part was already (for lack of any control on our part) accepted. Of course it got accelerated by the cancer, but we had already made peace with his mobility plight. And he’s still perplexing the medical community, which I love doing, as his cancer leg is changing color and no one knows why!

I asked the Oncologist point-blank (as I do each month)…”You said he’d have three to six months, do you still feel that is the case?”. She said…”I think so”.

It’s odd, but I left that appointment happy.  Sure, Jake has a cancer we can’t treat (the reality) but his slow, steady decline has given him a chance to keep his chin up (the blessing). We are controlling the parts that we can. We are doing it all as right as possible.

Focus on the joy.

A lot of loveliness can occur in a few months. Sure it will feel short when the end comes, but that is the case with all ends, there is just never enough time.

A few human months is about one to two dog years — Jake is going to have an AWESOME dog year or two!!

More peanut butter, please! IMG_9184

Rugs, they come and go.

Dogs have accidents.  You clean up and move on. Jake is a master of escaping his diaper or the diaper fails or meatballs pop out of his butt.  All of these things happen several times a day. I clean up and move on.

Despite having a 14-point clean-up process for every accident, sometimes it comes time to let rugs go. In three years, I’ve lost count of the number of rugs that Jake has killed ruined sent packing. Recently, it was one of our favorites. A high pile, thick shag carpet that was really never supposed to be ‘for Jake’ but in a pinch, I had to relocate Shaggy to an area so that Jake could move from kitchen to couch. As it turns out, Shaggy was ‘let go’ not due to accidents (although there were a few), but because Jake realized Shaggy was REALLY good at holding his peanut butter Kongs steady while he licked the good stuff out and she went from being white to being sticky and orange.

Note to all: peanut butter in a high-pile shag rug does not come out, regardless of how many cleaning products you use.

So we said goodbye.  Jake was pretty upset.  He spent two days sitting by her side before she finally made it to the curb.

Farewell, Shaggy.  And like all the others that came before you…I’m sorry.

Why are you doing this to us?IMG_9039

Try to unfold yourself, Shaggy. I need your softness on my body. IMG_9033

I don’t know why she keeps saying ‘this is a first world problem Jake’. Just ignore her.IMG_9037

UPS.

When the decision was made that Jake could no longer use his wheelchair, I had the normal reaction, put it in the corner and suppress the disappointment.

But that wheelchair kept calling out ‘someone needs me, do the right thing’.  So I reached out to Jake’s rescue and I asked if there were any alumni they knew of that REALLY needed a cart.  They had someone in mind and I reached to that little-big cow dog’s mom.  When she asked me how much I wanted for the cart, I explained that we really wanted to her guy to have it. The only thing we asked in return is that they pay it forward one day.

So last week I loaded it up with instruction (when that cart came I had zero idea how to get Jake in it so that instruction step was crucial) and I carried it out the door and put it in my car.  I stopped at UPS, grabbed the cart and walked in.

That is the exact moment that all the oxygen left the world. I was standing in UPS, there was no oxygen and I started hyperventilating, bawling and then out of nowhere came a honking sound from my body. I panicked (or perhaps terrified myself), turned to run out, ran into the man standing behind me (the wheelchair rammed into him) and somehow made it out the door with a bunch of voices yelling behind me ‘ma’am, are you ok?’

Oh sure, I always honk like a donkey, things are great.  Instead I yelled back, ‘I have nothing to mail’.  (HAHAHAHAH, I have nothing to mail, classic response. That totally makes the situation more normal.)

I got into my car, drove to a side street and parked. What the hell had just happened? I made a few calls to people who could talk me back into some realm of sanity.

I looked over at the wheelchair.

Sending the cart made Jake’s cancer too real for a moment. 

It’s OK to be human. Just breathe.

I did a few other errands. At one point I realized that UPS probably had security cameras so I just prayed that I was not currently trending on You Tube. I eventually went back and mailed the wheelchair. The people at UPS could not have been nicer, they took one look at the notes and said ‘seems like this cart is being sent with a lot of love’. It most certainly is. Love will live on in that cart.

The wheelchair is on its way to Oliver and he is going to rock the hell out of that cart and his mom will hopefully breathe some relief when she sees him take off in it. There is something really special that happens when your mobility challenged dog gets his wheels and is suddenly no longer hindered at all.  Jake and Oliver have similar spinal issues and they just happen to be the two biggest Frenchies in the world so the size should be perfect.

We had a great weekend, Jake is snoring in the next room and luckily for him he has a great replacement wheelchair, her name is Tracey. All is good here.

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Why did you honk like a donkey at UPS? I’m embarrassed. IMG_9050

Everything.

When it comes to Jake, most days  I don’t know what I’m doing.  I’ve pretty much felt this way for three and half years.

It started off because he does not react to anything I do. He has no tail to wag, he has wiggled his body maybe ten times since I’ve met him and all of those times were for Melvin. When I dance or sing for him, he sits like a statue, almost pretending like it’s not happening.  When I come home, Jake does not even get up, he looks to see what the noise is about then puts his head back down. I have no gauge of if he likes something or not. Except food, he will 100% eat anything and everything.

I know what to do for Jake, if something happens I take care of it, and there is nothing I won’t do to make his life be the best that it can be. But when it comes to most things about him, and his spine and his paralysis and now the cancer, there are a lot of grey areas and most days I just wing it.  I guess it was the same with Melvin’s allergies but I think it’s different when you are solving problems versus dealing with issues there are no solutions for. (I guess even then, love is a pretty good solution).

I have to carry Jake a lot now. I am never sure I am picking him up correctly.  I’ve read articles, watched videos and asked the vet(s) but there is no set way for every single thing that Jake goes through in a day that would suggest one way is the best way. Wing it.

I cook for him now, a cancer diet.  There are so many theories about what they should eat when they have cancer. Then there is balancing that food brings Jake joy. The nutritionist said ‘no dog treats’, only give him fruit or veggies.  I heard, give him peanut butter.  But to compromise I have his peanut butter freshly ground so that he doesn’t get added sugar.  Winging it.

I am a confident person. When someone compliments me, I almost always agree. If you ask me if I’m confident in my ability to care for Jake I would tell you without pause or thought, I am the best person for this job.  I can know this is my purpose, and still not know what the hell I am doing.

It’s called, hoping for the best.

Although I have complete faith I can and will make Jake’s life decisions, I have no clue what spinal cancer looks like at the end. Every day is different and while I do worry and I am sad, most days we just coast. Sometimes you have to provide the light for the dark corners, even when you have no idea where the flashlight is and you are pretty sure the batteries are dead.

Even when I am hoping for the best, it is impossible to avoid thoughts about all the loss that losing Jake will bring. I’ll lose him and that heartache alone is too much to consider. I’ll lose a connection to Melvin. There will be no dogs in the house, in fact I don’t recall the last time I didn’t have a dog.  I will go from taking care of a special needs dog, which takes up quite a bit of the day, to the dreaded void.  I worry about how I will get through. Not that I don’t have support and love and family and friends. But more about where I will derive strength if I don’t have Melvin or Jake to care for. But those moments are short lived, becasue the moneky is still here wtih me, and our life is beautiful.

“You can’t choose the length of your life, but you can do something about the width and the depth.” (saw this on FB this week).

Melvin reminds me to seek out the joy. Find the joy in the little moments. Be a joy seeker.

In being open to joy, one day, I’m at a party and I spot my dad (who I knew would be at the party) and I go up to say hi and he says ‘wait here, I have something for you’. He returns with an article cut out of the Washington Post about a woman who makes dog diapers for her paralyzed dog.  He is a not a dog person but he is a dog person for me and my boys and this non-dog person regularly cuts articles out about dogs and saves them for me. Upon delivering it to me, he tells the people around us that I am ‘a great dog mom’. He says it so proudly, so truly. And I of course think I am, I know I am, but in that moment with him and hearing him say it, it feels like everything.  Everything. Like someone just served up the whole world to me. I didn’t know that I needed to hear HIM say that at that exact point-in-time but in that joy moment, Jake and I won at this life. I realized that Jake I and have already won at what’s to come.  Little moments, are sometimes, the everything.

In life, it doesn’t matter if you know what you are doing.  It only matters that you keep showing up to try.

#findyourjoy #loveliveson

 

 

Memorial Day Weekend.

On Sunday, Jake and I went over to my parents house for a day of relaxation and pool.  I put Jake into the car at 10:15 and he was up ALL DAY. All day.  Jake is never up all day! But this is how it is at my parents house.  They don’t have a dog so there is food that falls on the floor that no one notices and Jake  swims on the hardwood floors to find it ALL (Melvin taught him well). Add to it that my niece Maddy was there also, and well all these things make my parents house Jake’s favorite place on earth.

While we were at the pool, Jake stayed inside the temperature controlled pool house (such a rough and tortured life). Maddy caught a frog and recalled that Jake loves hunting frogs so we let him hunt it (through the glass) (He was not fooled by the glass but he did try to take one bite!).  I immediately added this to his bucket list and then immediately checked it off. Photo and video below:

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Instead of frogs, he ate a kong full of hot dog (his eyes rolled back into his head). Then it was time to go, I put Jake in the car to go home, and he was passed out before we even got out of the neighborhood.  And on Monday, he got up to eat breakfast and then slept all day.

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Jake having a great weekend – check, check!

 

Rules are boring.

After Melvin died and Jake’s gang violence escalated territorial monitoring and prey drive increased, we called our dear friend and trainer Nancy to work with him (and me). I explained to her that his favorite thing to do was sit at the door but with every passerby, especially that of the dog variety, Jake would flip and flail and foam at the mouth.

Her advice, shut the blinds and work with him under controlled open-blind circumstances until we could give him the skills to handle the activity of outside.  It was brilliant and we set off on our positive reinforcement clicker training with fake and real dogs (Yes, our trainer would walk down our sidewalk in front of our house with a fake dog on a leash and I would click from inside with Jake the moment he saw them).  It was awesome! I believe in positive reinforcement training – not just for the dog, but for the human too. It’s not ‘all my rules all the time’, it’s ‘how can we both be the best that we can be together’.

Jake didn’t exactly ‘graduate’. We worked real hard but since he was diagnosed with cancer, the clicker got put in the drawer and the peanut butter came out.

There are so few activities that give Jake joy. Partly because there are so few activities that don’t require struggle. But staring out the front door, has always been at the top of his joy list. After his legs started failing even more and we found out about the cancer, he would drag himself to the front door several times a day to see if the blinds had miraculously opened again.  Sort of like in Willy Wonka where the candy factory has been closed but then one day, boom it’s wonkafied and back open!

So I ompa-lumpa’d and opened that blind and let him be the jerk he has always wanted to be! Even on the rainiest day when there is no activity, he watches the world. He naps and gets up to make sure the outside is still out there, then he goes back to napping. When he kids walk by from the bus, he makes sure they pass by our house safely.  If one of them stops to tie their shoe, he barks at them to keep moving. When the brown truck man drops off a package and gently door taps to say ‘hi’ to Jake,  Jake Barry-White-voice barks at him and tells him to scram. When a dog walks by, he flips the F out.

There are moments I think ‘you should be training him’. Then I think ‘just let him have the one activity he can do no matter how many legs work’. I don’t give in or up a lot so there is definitely an internal struggle.

Sometimes, cancer comes a-knocking and you have to lessen your grip. That said, Jake was an ankle biter and now is not an ankle biter and to his last breath, he is not permitted to be an ankle biter again.  I mean it’s not a totally rule-less society over here! And if Jake didn’t have cancer, we’d be clicker training every day.  I’m not giving up on Jake, I’m just giving up on some rules that don’t fully embrace ‘joy now’.

 

Happy weekend!  Go find your joy!

Ordinary.

Our life right now is fairly, ordinary. I love ordinary. We made some changes to Jake’s pain management and so far, he’s doing really great. We are in that phase where living in denial is not really possible anymore but we are also not in the phase of ‘this is the end’.

We’ve made it three months since diagnosis. Instead of thinking he has a certain amount of time left, we instead like to rest on our achievements. We made it three months!

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Jake is still eating. Peanut butter is a part of his every day. The pain meds help him sleep super soundly (so soundly that I have to set my alarm to check for meatballs because homeboy now does not wake up if he has gone in the middle of the night) but they don’t keep him sedated all day.  He is more limited than six months ago, heck he’s more limited than one month ago, but he in fact is, just Jake. He does the ramp to out back as if he has done it his whole life. He is clearly still CEO of the meatball factory. He still takes his Neighborhood Watch shift very seriously.

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Not every day is all lollipops and rainbows. Life is just not like that. I will admit, I do get a tad upset at Jake’s circumstance. Not that he has cancer, I mean geeze, I think it’s a given that I don’t want him to have cancer.  But cancer is out of my control. My angst is more centered around the added struggle for Jake. Why does his cancer have to limit his mobility even further? I mean this one is just hurtful. Why does he have an ear AND eye infection AND a diaper rash flair-up on top of it all? No seriously on that last one, WHYYYYYYY?  But all in all, I find my moments of frustration are brief and short-lived and we instead focus on the gratitude and joy. And peanut butter, Jake said not to forget to give another shout out to the glorious peanut butter.

AT the start and end of every day, I’m thankful. If cancer was going to be, I’m grateful that this time we get a slow decline, that he gets a chance to acclimate. I’m glad we got three months and I’ll be grateful for each and every day we have together.

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Wishing you joy and gratitude on this lovely Tuesday!