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Toy Story 4: Caregiving Personalities Through a Pixar Lens

July 2014, Hollywood Studios.

Toy Story 4 was released on June 21, 2019. It received mixed reviews, but that never colors my desire to see a new Disney Pixar film. I also kept to the tradition that Ben and I had of seeing the film on opening weekend, going by myself to keep the experience sentimental and to feel that I am somehow with Ben. It may be no surprised, but I loved the film. I could relate to it on many levels, particularly as a caregiver who then transitioned to grief. Also, as a lover of toys, I simply have not been able to part with some from my childhood but have passed some of them on to others who needed and will love them. I did not write about it at the time, but it has stayed on my mind, and I watched it again yesterday, finally able to commit my thoughts to paper.

At the end of Toy Story 3, Andy brings his cherished toys to sweet young Bonnie as he goes to college and starts a new chapter in his life. It was heart-wrenching for all of us who have loved the Toy Story films and yet heartwarming that Andy gave such thought and love to his decision to give his toys to Bonnie. In Toy Story 4, the toys have settled in with Bonnie, but Bonnie has told her mom that it was okay to give away her Bo Peep lamp. Woody wants to rescue Bo Peep, but Bo Peep is okay with the letting go. She bravely accepts it as part of life. Letting go and adjusting to change is a big theme in the film. It is a big theme in the life of a caregiver, too. In the film, the toys are the friends and emotional support of their child. They all approach their role as caregiver with a different perspective.

Throughout the film, we see how the toys perceive their responsibilities as caregivers, much the same as people have varied ideas of their responsibilities. Woody is the take-charge caregiver, completely devoted to Bonnie, although he still has an attachment to Andy. Woody finds his self-fulfillment in the caregiver role. He is Bonnie’s advocate, even sneaking into a backpack to secretly accompany her to kindergarten and working behind the scenes to help her get comfortable. The other toys don’t agree with what Woody considers loyalty. I can relate to hearing much advice but having to go with my gut as Ben’s caregiver. Even in the hospital, there were times that I had conversations on Ben’s behalf, defying the advice of hospital staff because I knew what Ben wanted and sometimes, what he didn’t even know he needed.

Poor Forky, the new character, hand-crafted by Bonnie, never asked to be a caregiver. He didn’t want to be responsible for a child. Woody, who is proud of and dedicated to his role as Bonnie’s caregiver, constantly needs to teach and remind Forky of how much Bonnie depends on him. Forky is in some ways oblivious, but also reluctant and ambivalent about this new role. He was happy as trash. I’m pretty sure that many caregivers can relate to this feeling, or to family members who vaguely knew they had a responsibility, or even offered to take on responsibility, but were never reliable and did not want to be held accountable.

When Woody surprisingly discovers Bo Peep, he reverts to the memories of when they were all in Andy’s home. Bo Peep still has those memories, but she maintains that she is happy to be on her own, or what is termed a “lost toy.” Bo Peep explains to Woody that she’s moved on and enjoys her freedom. Over the years, I have met many people who did feel an immediate freedom from caregiving, also relieved to be free of the bad memories of illness. They are not involved in causes related to those illnesses. I was not one of those people. I got upset when people would tell me I was free or that I had my life back. I am not judging, because everyone has their own experiences and frames of mind with regard to caregiving. I do understand wanting distance from the pain. For me, it was all tied to my identity, so giving me freedom was also taking away all that I was, or all that I saw as myself and the reflection of the people I loved and lost.

Woody does judge Bo Peep, and when she presses him on why he clings to Bonnie, and to his attachment to the memories of Andy, he finally admits that, “It’s all I have left. I don’t have anything else.” Next month will be five years since Ben left this earth and I still struggle with that feeling. So much of my identity, and even my self-esteem, was entwined in caregiving. I transitioned from caring for my dad to caring for both of them, and after losing my dad, caring for Ben, for what amounted to more than twelve years. I related so much to the caregiving experience that part of my coping with grief was starting this blog and volunteering with ALS organizations to try to support others who were caregivers. It was a way to stay loyal to Ben and my dad and to hold onto the only Abby I had known for quite a while. I could not step forward into life without carrying that part of myself. Although there were a lot of unpleasant times, it was the loving, meaningful and important part of who I was and wanted to be.

ALS,Caregiving,Grief,Walt Disney World, Disney

My silly Ben with his buddy, Buzz.

For Woody, everything comes down to the issue of loyalty to Andy and to Bonnie. However, his friends feel left behind. He felt they should understand his loyalty. I understand that feeling. We all define and express loyalty differently. That’s why communication is important. (click here to read my post on communication). When Ben and my dad were alive, I certainly saw my friends  less and often ignored advice to do what I felt was right, even if I, myself, was not happy with the effects those choices had on me. That was how I defined loyalty. I was rarely loyal to myself, although I felt that I was simply trying to be a devoted caregiver. If you’ve read my blog, you know that sometimes it took an unnecessary toll on me. Loyalty to oneself is important, though difficult to achieve as a caregiver.

Since I lost my dad and Ben, it has been very important to maintain a feeling of loyalty to them. I still have a difficult time balancing my connection to memories with what is now a desire to embrace my life. There can still be the nagging feeling of disloyalty, even when I go to the new Disney films, because I am enjoying them without Ben. My way of coping is to give him a big presence in all that I do, but, to be honest, I know that it is self-deceptive. It sometimes keeps me in a relationship that no longer exists, despite the fact that it will always stay in my heart. For a while, I did not like to attend holiday gatherings, because I did flounder. I didn’t really want to be by myself, but it was too hard to be around others and try to look happy. And, it was hard to return home alone. Woody tells Bo Peep that she is a “lost toy” because she does not have a child, but she says that he is the one who is lost. She’s right. Bo Peep is not as happy to be free from connection as she professes, but she has at least carved out a life for herself. However, Woody is lost because his entire identity is grounded in children who grow up and pass him along (unless, of course, he ends up with someone like me!).

Buzz Lightyear has a very special place in my heart because he was always Ben’s favorite superhero and I always remember how Ben had a hard time greeting Buzz after his ALS diagnosis because Buzz was strong and Ben felt weak. Buzz made a big fuss over Ben, which always warmed my heart. In Toy Story 4, Buzz turns out to be the character who provides the voice of reason. After all, he does have the “inner voice button.” I laughed at how he kept pushing that button till he got an answer he liked. I can relate to that idea! Buzz lets Woody know that Bonnie will be fine on her own and that it’s okay for Woody to let go of her and have an identity apart from those for whom he cared. As Buzz advises, “Listen to your inner voice.” It’s not easily done. I surely pushed that button repeatedly when it came to my caregiving responsibilities. It’s taken all this time, but I am now, finally, more at ease with letting my inner voice matter. I am finally acknowledging that loyalty to their memory does not have to keep me in the throes of grief anymore. However, although I feel it less, I still grapple with the guilt of living my life. It’s an adjustment to life and how it flows. I had to be ready to rediscover myself and I had to do it in my own timeframe. I can say that once I was ready to hear my inner voice, like Woody, I let it speak more loudly, and it has guided me to a place where I can happily and wholeheartedly engage with life. I no longer feel quite as lost, though I am not exactly where I want to be. Though I’m still very tied and loyal to my memories, I also love and seek out opportunities to create new ones, and I feel proud of myself for doing so, while also keeping Ben and my dad close in my heart. I just wish I had a cool inner voice button like Buzz Lightyear’s.

Just Buzz and me in 2019- my first time back at WDW without Ben, but I know he was with us.

A Birthday Tribute To My Mom

Today, July 8, would be my mom’s birthday. Although, I have written quite a bit about my mom and how close we are, I like to write an annual birthday tribute to her.

It was nearly five years ago that I spent her birthday in the hospital with Ben, lamenting the overwhelming and inescapable feeling of alone-ness, not knowing what was going to happen with Ben but acknowledging that ultimately, he was going to join my mom as one the beloved people in my life that I would lose. I do feel so fortunate to have known and shown so much love in my life. And, I still feel much love. But, my life has changed dramatically in many ways, and sometimes it can feel terribly lonely and ungrounded. I guess I miss the sense of belonging. I miss my mom and the closeness that we shared. I even miss what could easily be ten phone calls a day about everything and nothing. Sometimes, it is exhausting to miss so much.

We were always Mickey Mouse fans!

My mom is the person who introduced me to Mickey Mouse and instilled in me an eternally child-like wonder. When we were in London together, I remembered how excited my mom was to go to Paddington Station and the Paddington store in Paddington. The woman in the shop was so taken by my mom’s exuberance over the little bear and being in the shop- it was hard not to get caught up in my mom’s child-like delight- that she excitedly handed my mom a Paddington Bear doll to hold while I took her picture. Each year I put the little Paddington ornament she got there on my Christmas tree so that she is a part of the tree. I’ve always returned from visits to London with something Paddington to remind me of her. So, it wasn’t all Disney, but Mommy’s first true love was Mickey.

London 1987. My mom could not wait to visit the Paddington store!

I look at our old photographs and remember the laughter. I am proud to have inherited her ability to celebrate her inner child, her youthful demeanor and her joyful spirit. I still miss our shopping and theater excursions in the city. Sometimes people are surprised that she passed away more than 25 years ago, because I talk about her so frequently and vividly. She is always dear to my heart and so much a part of who I am, but also, of the person I aspire to be.

My mom visited my great-aunt, Tanta Rosie, with our Standard Schnauzer, Dulcie, almost every day.

My mom was my example of the consummate caregiver, perhaps being too selfless. She was so generous and kind, always smiling as she balanced the needs of everyone around her. She tended to my grandmother, who lived with us, and also took care of my great-aunt in the nearby nursing home, and my great-uncle who insisted on living alone but needed much assistance. After she passed away, I followed her lead and although I did not realize it at the time, I was stepping into the role of caregiver, tending to and trying to bring cheer to my dad and my grandma, and always visiting my great-aunt and great-uncle.

On her birthday, I will continue my tradition of watching The Little Mermaid, because it was one of the last films we watched together. I love to remember how much we laughed when we watched it together, particularly when we looked at my grandma, who just did not understand our amusement. I wish that I had gotten a chance to visit Walt Disney World with my mom, but she has always been present when I have been there. It always touched my heart that Ben was so aware and acknowledging of her when we were there. I know she would have loved Disney+!

I proudly say like mother, like daughter!

Happy Birthday, Mommy! I love and miss you every single day.

 

ALS And International Kissing Day Without Kisses

ALS,Walt Disney World

A PhotoPass photographer caught this moment in front of the Castle at Walt Disney World. It was actually the first time we returned after Ben’s ALS diagnosis in 2010

Today, July 6, marks the fifth anniversary of the day that Ben had a respiratory crisis and we ended up in the Emergency Room at Mount Sinai Medical Center.  For me, this will always be thought of as the date when everything changed. Over the years, I have learned to go with the flow on milestone dates, but this particular day has remained a terrible and vivid memory filled with tears. How ironic it is that today is International Kissing Day, because on this date Ben was connected to a ventilator and his mouth was covered with a Bipap mask. For the next few weeks, before he agreed to a tracheostomy, our way of kissing was to blink our eyes tight and then I would smile and throw him a kiss- he couldn’t use his arms or hands to throw one back. In these days of COVID19, I relate to people lamenting not being able to hug because I missed Ben’s hugs so much as his ALS progressed.

It’s still morning and I have been replaying that day five years ago, when we woke up and Ben said he could not breathe. He was always nervous about breathing, so I stayed calm even as he followed my direction and blinked to indicate that he wanted me to call 911. I think of how time stood still as we waited for the ambulance, not knowing what would happen. I called and emailed his doctor and remembered that he had once told us that if we had to call for am ambulance, they would take us to whichever hospital they thought closer. Fortunately, EMS agreed to take us to Mount Sinai so we could be close to his doctor, who met us at the ER and, always kind and comforting, stayed with us till Ben was situated, emailing me throughout the day and coordinating with Ben’s ALS team. I remember that in the midst of the frenzy of an Emergency Room, it did not even occur to me that I could lose Ben at that time. I was kept very busy as the health care proxy and the only family member present. I didn’t have time to think. I didn’t even have time to be in denial. I just went through motions. I emailed and texted his family and our friends and answered a lot of questions. I tried to stifle resentments towards his family, a couple of whom had lots of questions, absurd suggestions and judgments but had never been there for him as his ALS was progressing. I was surrounded by people but felt very alone. I talked to Ben but had difficulty reading his lips through the mask. We ended up in the ER for at least 36 hours waiting for a room, meeting with specialists, and in contact with his ALS team, all of which was overwhelming and exhausting. Ben slept a lot, and during that time I struggled with my emotions and guilt about the frustration that I had been feeling because I was so angry that, without discussing it with me, he let go his paid part-time caregiver and insisted that I be his 24/7 caregiver since I am a teacher and it was summer vacation. Now, summer had barely begun and here we were in a hospital. I shared all of this in a previous year’s post.

Five year increments always seem to be distinctive markers of time, so I can’t help but reflect on that. I wonder if five years should feel like more time has passed. This is my fifth time feeling the pain of this day and it is still debilitating. My only plan for the day is to await a delivery of shelving items to help me in my ongoing effort to organize my apartment. It’s already been a morning of tears, so it’s all for the best that I’m here and writing about my thoughts. Even organizing my apartment brings back memories of the chaos of this place when it was an obstacle course of clutter and medical supplies. I’ve significantly improved it- painted, re-carpeted, and added some new furniture, but the memories remain. I still think of my new dining table as the table that replaced Ben’s desk. I am listening to Ben’s favorite relaxation/new age music on his computer- something I could and will not replace because it was his lifeline. Today is not a day that I want to hear that I should make plans to distract myself, or should be proud of myself for carving out a new life for myself, or that Ben would want me to be happy. Sure, it’s all true, but it doesn’t matter. Today, my heart is stuck in that day. Unfortunately, COVID19 has unearthed a lot of those difficult caregiving memories and has added another layer of sadness to this time.

Summer has never been my favorite season because I dislike warm weather, and now summer is filled largely with the memories of Ben’s last summer. It’s an odd contrast to my being a teacher and eagerly awaiting summer break. I have, however, come to cherish my frequent summer walks in Central Park. I do look for signs that Ben is with me, and finding turtles there is an important sign that he is present and watching over me. I always bring some coins to toss into the fountain and make wishes (see my post on wishes), often shedding a few tears. Last week there was even a little turtle scampering through the fountain and I believe it was Ben sending a message that those wishes will come true! I must remind myself that summer memories also include the summer before his last one, when we had a most magical time at Walt Disney World. I try my Disney best to be optimistic even when I’m sad.

In my mind, July 6 may be International Kissing Day, but for me, it was the first day that I couldn’t kiss Ben. It was the beginning of the end. It’s an odd feeling that nobody else would even remember this date, and I wouldn’t expect them to. That does, however, underscore that when this crisis hit, it was just Ben and me. I was there for Ben, he knew he could rely on me, and there was profound love and trust.

I find myself wondering if I will always struggle on this day. I have learned that today’s fog will lift. I do and will continue to have many days where I remember recall the days in the hospital that, despite the devastation and horrible decisions, were filled with love, music and even laughter. Today is just not one of those days.

Walt Disney World, 2002
The pre-ALS days.

Happy Anniversary to Lady and the Tramp and the Hunchback of Notre Dame: Thanks for Perspective on Memories and Living

Today is the 65rd anniversary of the release of Disney’s Lady and the Tramp. It was always a favorite of Ben’s and mine. We actually loved to sing the “Siamese Cat Song”; in fact, I used to sing it to my first cat, Tiffany (but she preferred “Born Free,” to which she actually meowed along!)

A poignant quote came from Tramp to Lady, when he told her, “Aw, come on, kid. Start building some memories.” I am always drawn to quotes about memories because memories played such an important part of our lives when Ben was fighting his battle against ALS. Memories became increasingly significant to Ben, particularly as he became more homebound. He loved to look at our photos and videos from Walt Disney World and to listen to the theme park music soundtracks. We could do that for hours. It was my motivation for designing the photo calendars, throw, shower curtain and towel (click here to read more about them)– Ben was surrounded by our photos everywhere in our home. It’s nearly three years since he’s left and I remain surrounded by those things. They are a comfort for the memories the photos hold and for my memory of the happiness that I gave to Ben with those gifts.

Dessert at Tony’s Town Square Restaurant- The Lady and the Tramp-themed restaurant at Walt Disney World. The Lady and the Tramp drawings were done with caramel- pretty fabulous!

We were so fortunate to be able to visit Walt Disney World four times after Ben’s ALS diagnosis. Each time, we tried to recreate our favorite memories, attending our favorite shows and visiting our favorite attractions. We did, at times, lament the attractions that Ben could no longer ride. But, we laughed that we could take the “It’s a Small World” boat repeatedly because there was never a long line and we got a boat to ourselves. Ben’s attitude was amazing. He focused on what he COULD do and, thanks to the amazing Disney cast members, we could do almost everything.

Recreating memories was, however, a tricky endeavor. Given Ben’s physical changes, it had the potential to be incredibly fun or incredibly sad. However, we were so grateful to be able to return to a place that was so important and filled with joyful memories. At Walt Disney World, we were distracted by the excitement and caught up in the fantasy. Ben loved and frequently commented about that. Once home, when Ben looked at photos, he scrutinized how he looked and how his abilities had diminished from visit to visit. For me, looking at photos is sometimes filled with splitting my world into pre-ALS and post-ALS distinctions and observations. Still, more than the physical changes, I see the joy on his face.

Our final visit to Walt Disney World in 2014 was uniquely memorable, not only because we were not sure that we would ever get there again, but also because it was filled with the creation of new memories. Frankly, I was worried that Ben would be disheartened at not being able to do a lot of the things that we used to do. Also, he could not eat many foods, so going to the restaurants that we always loved might have been an upsetting experience. So, I organized several surprises- new and different  events that gave us the opportunity to create new memories. My plan was a resounding success, which makes me so proud and grateful. I wrote about our visit in a prior post, which you can see by clicking here.

Walt Disney World 2002, the pre-ALS days. We didn’t kiss over spaghetti, but we did kiss Eeyore!

Ben and I had 16 years and a dozen visits to Walt Disney World, all filled with wonderful memories. When I was the caregiver of my dad and Ben, those memories sustained me and took me from one Walt Disney World visit to the hope of another, and I lived vicariously through my friends, reading about their adventures on Facebook and occasionally, and proudly, posting photos of Ben and me at Walt Disney World or out in our neighborhood when he was still able to ride his scooter. Our friends did like to see him out in the world. I immersed myself in those memories for some time after Ben died. I know that some people think that this blog is a way to stay hidden in those memories and in the past, but the perspective I gain and thoughts shared with other caregivers in this writing process lead me forward.

Coincidentally, as I reflect on the importance of my memories, I realize that today is also the 24rd anniversary of the release of Disney’s The Hunchback of Notre Dame. I think about what the gargoyle, Laverne, told Quasimodo: “Life is not a spectator sport. If watching is all you’re gonna do, you’re gonna watch your life go by without ya’.” This quote holds an important message for me. I think that one of the most difficult things for me was when people told me it was time for me or time to take care of myself.  I don’t really like to put the spotlight on myself. It was particularly difficult to go out and be distracted and even somewhat happy, just to return to an empty apartment and reminded of the loss and alone-ness, as well as guilt for even trying to enjoy myself. I preferred to put my energy into helping Ben relive and create new memories and, after he left this world, I took pride and comfort in thinking about those memories. The truth is that I will always love to visit with my memories of Ben, the good and bad times. But, my memories don’t have to end there. I can delve into new adventures that will become a part of my treasure trove of beautiful memories. I do not have to live vicariously through other people.

The Hunchback of Notre Dame
1996 Walt Disney Pictures

A sadness looms over my summers because they represent the most difficult times in Ben’s battle, and ultimately when he succumbed to ALS. However, I suppose I have come to accept Laverne’s advice, proactively making plans to do things I love: travel to see my friends, take part in some animal adventures, do some volunteer work, and continue to work on my blog while formulating new ways to reach out to caregivers. This summer, due to COVID19, is a particularly odd one because I can’t help but dwell on what life would have been like if Ben was here. Being home so much of the time reminds me of the time that I was home with Ben and how I would have been even more reluctant to go outside now, for fear of bringing home any germs.

Although sometimes I do feel like more of a spectator in life and I get caught in fantasies of what I think I would like my life to look like without knowing how to proceed, I don’t want my life to go by without me. I don’t think that would even do justice to the love and belief in me that Ben and my dad had. I probably spend too much time with my memories. But, I do have those fantasies and dreams, which is a good indicator that I am invested in my future. I just have to find my way. I’d prefer not to be alone but maybe it won’t always be that way. It helps me to  find peace in the knowledge that Ben’s spirit will always accompany me as I follow my life’s paths, make some dreams come true and make new memories.

My photo collage calendar filled with wonderful memories and new events that will bring new memories. where Ben will be present in my heart

This Daddy’s Girl’s Father’s Day Is All About Memories

I’ve written in prior posts that my dad did not like attention on holidays like his birthday or Father’s Day. He preferred to do things for other people, and not necessarily on holidays.  For this reason, other than feeling a little displaced and lonely without a plan to spend time with my dad, the holiday did not really bring me down. After all, I already miss him. This year, without much distraction, seeing all of the holiday posts makes me a little more sad. Once again, I am hit with the reality that the people I was closest to are not here anymore (click here to see that post).  I do believe that they are always with me, and watching over me, and that is a comfort. But, there are those times that I just want to pick up the phone, or feel a touch. I don’t fight the moments of sadness, but today I want to summon the loving and good memories, because I never lose sight of how fortunate I am to have them. Believe it or not, he was not a huge fan of Disney or animation, but when I showed him videos of my Walt Disney visits with Ben, he beamed because he said he loved to hear me laugh and happy.

My dad, in one of his favorite photos, with our Miniature Schnauzer, Windy, at my Cornell graduation. Daddy liked to look serious, but he was quite the joker.

My dad and I spoke several times a day. He even called my cats! He was a very good Grampa to my first cat, Tiffany, and then, to Disney, and he spoiled them just as he spoiled our dogs. I knew that when I went out, I would come home to a message on my answering machine with him calling my cat to say that it was a grave injustice that Mommy left her alone. They even got packages of treats and toys, addressed just to them! Even six years later, I miss that. I tell Tinker Bell about her Grampa and that he loves her from heaven. With all of the chaos in the world, I miss getting his perspective, particularly given his extensive knowledge of history and the military. When my aunt, his sister, asks me what Daddy would say about the state of the world, we agree that there would have been many phone calls and there would have been a lot of yelling. I know that what is happening would have devastated him- he was a proud Marine and a patriot through and through- so I’m grateful that he’s not dealing with it, but I miss the comfort of his explanations. I did trust his judgment on world events. I certainly can’t trust our current administration. I think back to the days of Dan Quayle, when Daddy and I would rush to the phone to call each other as soon as we heard one of his mistakes. I even got him a subscription to the “Dan Quayle Quarterly.” Now, in light of what he and I would definitely consider damage to the country, Dan Quayle’s errors would be a welcome bit of relatively harmless comic relief!

I’ve been looking through old photographs because they do bring me joy despite some tears. It’s hard to find photos of my dad and me together because he was usually the one taking the photos. He loved capturing silly and sweet moments, often with our dogs. When I look at some of photos that he took, I know exactly what he was thinking, or what joke or prank he had in mind, and that, in itself, makes me smile. Daddy had the best giggle, which was kind of funny for a USMC!

You could take the man out of the USMC but you couldn’t take the USMC (or the camouflage) out of the man!

Today, I will try to remember that Daddy never wanted me to be sad. I cannot count the number of people who stopped me to tell me that I was my dad’s world. He was the consummate pessimist, except when it came to me and my potential and I was his consummate cheerleader. Since he was quite a character, a lot of nurses blessed me for my patience, which always made me laugh. I can’t even imagine his frenzy over the coronavirus. I still can’t shake the thoughts of how I would have managed caring for him and for Ben if they were here.

Camera on his shoulder, Daddy always wanted to be the photographer, not the photographed!

When Ben was ill, despite fighting cancer, my dad never failed to think of how he could help Ben. I think that on a certain level, he felt connected to Ben because they were both facing death. But, the gadgets that my dad found to make help Ben with dexterity were so genuinely appreciated. I was always surprised to find that Ben called my dad to check on him and to chat, but my dad became Ben’s dad, too, and that, in itself, is a special memory. Daddy called Ben a gentle soul- I think they were both gentle souls. I wish I had a photo of the three of us.

Daddy would be humbled that I remember him, which is so odd to me, because he is always with me and is so much of who I am. Thank you, Daddy, for the lessons you taught me, the laughs and sense of humor you shared, the moral compass and patriotism you instilled in me, and the unconditional love and generosity you showed me.

I love you and miss you, on Father’s Day and every day!