Caregiving

Wisdom from Walt Disney on Moving Forward

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Walt Disney, Walt Disney World

“We keep moving forward, opening new doors, and doing new things, because we’re curious and curiosity keeps leading us down new paths.”- Walt Disney

I guess with December 5 marking Walt Disney’s birthday, and the anniversary of his death just a week away, his quotes have been on my mind. This quote seems to resonate a lot with me this holiday season. This is my fourth holiday season without Ben. During the first holiday season without him, his loss was very raw, and on top of feeling that devastation, I found myself caught up in the memories of the holiday season of 2013, right before my dad died. That year, I observed the holiday season from car and train windows on my way to and from the hospital and then the VA Hospice in Northport, NY. Though I did decorate the apartment for Ben and me, there was nothing festive about our lives. The truth was that I did not get to really grieve for my dad because I was preoccupied with caring for Ben. At the same time, Ben and I both felt the immense weight of my dad’s loss.

My first holiday season alone was painful. I had always made a silly holiday card starring my cat, Disney, but I wasn’t really in a festive frame of mind. I decided to make a card that was a tribute to Ben, using the lyrics to “Auld Lang Syne.” Since then, I have kind of gone through motions around the holidays. I always put up my tree. I continued to put the tree ornaments that Ben loved exactly where they were when he was here, placed where he could see them from his desk. I have gone to see a couple of the holiday store windows, which are usually such a treat in New York City. But, it left me feeling empty and alone. I walked through the holiday markets around the city but felt sad, remembering how I rushed through them looking for something to bring Ben but not wanting to waste time because I had to get home to him. I have not gone to see the Rockefeller Center tree in all this time. These things didn’t feel fun and happy to me. They were painful reminders of my caregiving days and how Ben could not get outside to enjoy things with me and how I did not have time to myself. Last year I simply could not muster the enthusiasm to make a holiday card. I did take a photo of Disney, as I frequently do, and I emailed it to a few people, but I could not put on a happy face and pretend that I was feeling the holiday spirit.

This year feels different. I had to get a new tree- it’s purple, but Ben’s favorite ornaments still have their places of respect in tribute to him. Last weekend, on my way to meet a friend, I walked through one of the holiday markets- I was not terribly enthusiastic, but I also did not dread it. Yesterday, on my way home from school, I decided to go to Macy’s to see the windows. I was keenly aware of this change in my mindset. I also made the usual mental note that I am now able to make spur of the moment decisions to do things that I’d like to do, and although it didn’t exactly feel good, I did not feel the guilt that used to surround me whenever I did something that I was not able to do when I was caregiving or that I enjoyed with Ben. I still feel the loneliness, but it’s a feeling that I’ve integrated into my life that no longer keeps me from pushing forward.

Today, I took an “ugly sweater” cookie decorating class. Baking and decorating cookies is one of my favorite things to do. It’s like my therapy- usually a three-day epic event which thoroughly engages my attention and sense of whimsy. I’m happy that my friends love them. Ben delighted in watching me because it made me so happy and because his daughter was thrilled to get them. We carefully counted the number of each design, remembering how my grandma always counted the matzah balls she made because my dad would sneak into the kitchen to eat them. As I was walking to the class, I thought about how my life has changed. I can freely take classes now. I can feel the excitement of the holidays. Tomorrow, I am going to try to make time to see the Rockefeller Center tree. I am used to missing Ben, at the same time knowing that he is with me. I am more purposeful in my planning and more energetic. There are times when I get overwhelmed and I allow myself those moments of tears and loneliness. But, I am also able to enjoy activities and occasions and I welcome and embrace that joy, too. It’s a kind of emotional juggling act that I seem to be mastering.

The paths won’t be the ones I planned. Right now, I don’t have the purpose that I had as a caregiver. I don’t really know what awaits me, though I know that I would like to find love again and I would like to pursue my blog and pet business ideas. I know there will be bumps, and since I am a klutz, I don’t know how well I will navigate them. I have learned, however, that I will be okay. The good thing is that, as Walt said, I keep moving forward and discovering new things about myself and life.

You’ve Got A Friend In Me- Friendships During Caregiving, Illness and Grief

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You’ve Got a Friend in Me
By Randy Newman

You’ve got a friend in me
You’ve got a friend in me
When the road looks rough ahead
And you’re miles and miles from your nice warm bed
You just remember what your old pal said
Boy, you’ve got a friend in me
Yeah, you’ve got a friend in me

You’ve got a friend in me
You’ve got a friend in me
You’ve got troubles, and I’ve got ’em too
There isn’t anything I wouldn’t do for you
We stick together and we see it through
‘Cause you’ve got a friend in me
You’ve got a friend in me

Some other folks might be a little bit smarter than I am
Bigger and stronger too, maybe
But none of them will ever love you the way I do
It’s me and you, boy

And as the years go by
Our friendship will never die
You’re gonna see, it’s our destiny
You’ve got a friend in me
You’ve got a friend in me
You’ve got a friend in me

Last week, November 23, marked the 23rd anniversary of the release of the original Toy Story. Ben absolutely loved Buzz Lightyear and we both loved this film and its sequels. In the context of Thanksgiving and the film’s anniversary, I’ve been thinking all week about the lyrics to the song You’ve Got A Friend In Me.

The song applies to so many aspects of my life. It is almost a caregiving anthem. I was there for Ben no matter what, seeing him through the darkest days. As the song says, there might have been stronger or smarter people, but the love we had was stronger than those qualities. As Ben was more vulnerable and more dependent on me for help, I know that he worried that I would say that I could or would no longer be able to take care of him. In his heart, though, when the road looked rough ahead, Ben knew that I would never leave him and that no one would ever love or care for him the way that I did. The unique bond we shared in our romance, despite the tragic circumstances, was a supreme kind of friendship.

Thanksgiving is a difficult time because it is a painful reminder of the family I no longer have. To be more positive, I try to put my energy into reflecting on how grateful I am to have friends who have become my family. There’s good reason this song comes to mind at this time.

Friendships can help to sustain us. I consider myself fortunate to have known my best friend for more than 50 years and to have had my closest friends for much of my life. We have been there for each other through the good and bad times. Sadly, over the past several years, I feel like I needed my friends often- as my dad became more ill and as Ben’s ALS progressed, and then, of course, as I grieved their loss. My patient and devoted friends listened to me repeat the same issues without any resolutions, and despite any opinions they held, they did not give up on me or Ben. They were also there to help Ben, being my backup if he needed assistance when I was with my dad. They voiced their concern for me. They asked what they could do for us. I knew that, as the song says, “there isn’t anything I wouldn’t do” was the way my friends felt about me, and it was and is mutual. I always placed a high priority on being there for my friends, but I still was not happy being on the receiving end of the giving during this time. At the same time, it was a huge comfort to know that I could depend on my friends, and it is beyond heartwarming to see them cheering for me as I have more steadily and confidently moved forward.

Sometimes friendships last forever, sometimes they are brief but deep. Sometimes we make connections that touch our lives although they are not even actual friendships. When I was the caregiver for my dad and Ben, I experienced all of these relationships. There were the people who unexpectedly reached out with a kind word or helpful gesture. There were people whom I did not know very well who had helpful insight, were there to talk at just the right moment, or were simply genuine in their expressions of concern. There were even people I did not know well who were kind enough to keep Ben in their hearts and do the Ice Bucket Challenge or contribute to ALS causes and our fundraisers with their families in Ben’s honor. I will forever be grateful for those moments and people. It’s an important reminder of optimism and faith in humanity.

Friendships also shift over time, even during good times, and that’s natural. People move, they get involved with different activities, have families. Terminal illness and my caregiving definitely caused a shift that forced me to evaluate what I considered good friendships. Some people whom I thought were good friends proved to be terribly disappointing. These are the people who said they never called because they knew I was busy, or who did not really ask much but were extremely judgmental. They were people who wrote lots of niceties on social media but never actually reached out or demonstrated friendship.

There were also people who, when we did communicate, would tell me that they knew they weren’t being good friends, seeming to want me to excuse them. At first, I did console them and say that I knew they were thinking of us and would have been there if I’d asked. Eventually though, I felt no sense of responsibility to make them feel that they were great friends because it simply wasn’t true. I felt abandoned when I needed to feel friendship. I suppose I could have reached out and asked for help or support or just a friendly conversation to help me feel like I was connected to my life and friends beyond my caregiving world. It’s hard to do that when you’re feeling overwhelmed by life. That would have been a way to care for myself but I was not up to it. I needed people to step up to me. When they didn’t, it was hard to accept that I simply didn’t fit into the lives of some friends the way I wished or expected. In many cases, I have remained friends with these people, but I do not feel the connection that I used to feel.

Ben also struggled with friendships as his ALS progressed. There were a handful of people who were loyal to him throughout his illness. ALS is known to be an isolating disease and, indeed, a person with ALS (pALS) loses the ability to easily communicate. Ben managed to text through his computer. His speech became impaired and if it was too difficult for him to be understood, he gave up trying. The number of people who reached out to him steadily dwindled. He felt unimportant and abandoned, which was heartbreaking.

We’ve heard the expression that to have a friend you have to be a friend. Friendship is a beautiful gift to give and receive. I do have to remind myself  that everyone has their own definitions of friendship and people form friendships for a variety of reasons with many different expectations of giving and receiving friendship. Some people need their friends during difficult times and others withdraw. It’s also important to see a big picture: as I needed more than I could give while my dad and Ben were ill, my friends might have those experiences as well. We cannot always be there for each other. What we can do is communicate openly, honestly, and compassionately.

It’s not always easy to know how to be the best friend you can be. Sometimes, in the case of someone who is caregiving or who is ill, it means asking how you can be a good friend, or just being genuinely present and available to listen, validate and comfort, or to let your friend know that you are giving them the space they seem to want but that you are there for them when and if they are ready for you.

Through our actions and expressions of love and support, I believe and am so very grateful that my dear friends and I agree that
And as the years go by
Our friendship will never die
You’re gonna see, it’s our destiny
You’ve got a friend in me.

 

Happy 90th Birthday, Mickey Mouse!

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Dear Mickey,

Happy 90th Birthday!

You may turn 90 today, but you are the eternal child who brings out the inner child in all of us. I know it’s Minnie’s birthday, too, and I also wish her a Happy Birthday! Walt Disney said to remember that it all started with a mouse, and what a special mouse you are!

In the pre-ALS days, 2006

I miss my mom and Ben today. They would surely have joined in the festivities. I must admit that I feel pretty lonely. But, I’m celebrating the long history that we have and remembering wonderful, whimsical times with and about you.

Though you’re a few years older than my mom would have been, she loved you from the time she was a child and she passed that love on to me. She was in her 50s when she and my dad went to Walt Disney World for the first and only time, and without me! I will never forget her phone call, giggling as she exclaimed, “Abby, I met Mickey!” This picture was taken on that day, and it is my favorite picture of my parents because, for me, it captures my mom at such a happy moment with her inner child aglow, and my dad was so amused. When I picked them up at the airport, my mom deplaned like the other children, unabashedly carrying a big Mickey Mouse and Epcot Figment in her arms. My mom was the consummate child at heart, and I get that from her!

Mickey Mouse, Walt Disney World, Disney

My parents with Mickey in 1987

When I first started dating Ben, he was not as obsessed with Disney as I was. That changed quickly, and our first dates often began with a stroll through the Disney Store that was near the office where we worked and met. We went to every new Disney film on opening day and we practically studied the Disney Catalogs, which, sadly, are no longer published. I found several copies that he kept because he loved the covers and I’ve kept those.

We always treasured our visits to Walt Disney World, but after Ben’s ALS diagnosis, we immediately booked a trip to Walt Disney World, and we were so fortunate to be able to go four more times. We didn’t know what we were dealing with, or how much time we had, and we wanted to go to the place that made all our worries disappear, at least temporarily.

Mickey Mouse, Minnie Mouse, ALS, Walt Disney World, Disney

Epcot, Walt Disney World, Halloween 2012

I admit that I was the one who had to greet all of my Disney friends. But, with you it was different. Ben always wanted to see you (and Minnie). And, after his ALS diagnosis, it was emotional and tear-filled. With an ALS diagnosis, we wanted and needed to feel the pixie dust, and more than once I asked you for some magic. I do remember that a sensitive cast member saw that Ben’s meeting with you was deeper than just seeing a favorite Disney friend. As we left, he quietly handed me a “ruby” that he told us was found by one of Snow White’s dwarfs in the mines, and he said he hoped it made our wishes come true. I still have it. It may not have fulfilled the wish that ALS would be cured, but I still believe that it helped us to create many wonderful memories. I thank you for that.

Mickey was always there to help Ben.

For as long as he could, Ben would insist on walking to stand in his pictures with you. It was truly touching when you spotted Ben in the electric wheelchair, helped him up and escorted him to the area where photos would be taken. He rode up to you when he lost the strength in his legs. It was then that I was hit with the reality of his situation. It might seem strange that this moment was a revelation, when I was living with his ALS. But, living with something didn’t mean I really reflected on the entire situation. We adapted to the issues as they arose without really looking at them as milestones in the progression of the disease. Deciding that he could no longer walk up to you was a sign that ALS was winning the battle. But, Ben also had an incredible attitude, never lost his smile and laughter, and he remained determined to engage in life, especially with you at Walt Disney World.

Mickey Mouse, Minnie Mouse, ALS, Walt Disney World, Disney

Mickey’s Not So Scary Halloween Party 2012

ALS,Caregiver,ALS Awareness Month,Walt Disney World, Mickey Mouse

2012- A subtle but significant change: Ben stayed in the scooter when he met Mickey Mouse.

You and your friends brought us a lot of joy at very trying times. You welcomed us into your kingdom and gave us fantastic memories. Since he has been gone, you have continued to entertain, console and inspire me. I have to admit that this very auspicious occasion has made me a little sad because my mom and Ben aren’t here to help me celebrate, but my memories of our times with you keep me smiling, even though there are also tears.

ALS,Caregiver,ALS Awareness Month,Walt Disney World, Mickey Mouse

2011- Mickey’s Not So Scary Halloween Party. I held Ben on one arm and Minnie held him on the other!

Happy Birthday, Mickey. May you always continue to be the spark of hope, inspiration and happiness for children of all ages.

I will always love and thank you,

Abby

 

Veteran’s Day and What My Dad and Walt Disney Had In Common

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Today is Veteran’s Day, and yesterday was the 243rd birthday of the United States Marine Corps. I’ve written about how the USMC was so important to my dad (click here for more). He was a patriot through and through. My dad was not a huge Disney fan, though he had a healthy respect for Mickey Mouse (he really had no choice in our house!) Truth be told, he and Walt Disney had something important in common: patriotism.

My dad was in the USMC during the Korean War but he had a tremendous fascination with World War II, during which he was a child. He and I were so close and spent a lot of time together, but when he was ill, I cooked and ran errands for him every weekend, and Ben and I found lots of documentaries about WWII for him to watch that Daddy liked to watch with me. I still miss the days of going to bookstores and finding the new World War II titles, calling him and reading the jacket descriptions to see if they piqued his interest and buying the ones that intrigued him, despite his protests of his (not really)  impending death and that he “won’t need them where I’m going.” Daddy and Ben actually enjoyed discussing the war when Ben was well and we visited him together. Sometimes, Ben would ask me a history question and we would call Daddy and get a very detailed history lesson by phone. My dad loved that Ben knew all the important USMC and war event anniversary dates. Ben and Daddy bonded over their shared love of history, but they felt particularly close when they were both ill with terminal illnesses. The other thing they had in common was needing me as their caregiver.

Ben and I found this book at a used/rare bookstore in Nyack, NY. Without even knowing that, the rabbi at the VA hospice told me that my dad treasured and was so proud of it, which touched my heart.

In his last years, my dad was concerned about the young men serving in the military. He took such interest in the guys in our neighborhood who were returning after various deployments and were struggling to adjust to civilian life. I met some of these young men when I visited my dad and was amazed at how well my dad knew their stories. He genuinely cared about these “kids,” as he called them. He felt they were the disenfranchised, abandoned by the government and that the general public did not relate to them. Daddy found reasons to tip the kids, give them things he knew they needed, and probably most importantly, listen to them.

Ultimately, Daddy ended up at the VA hospital out in Northport, Long Island, in the palliative care/hospice unit. We were both grateful for the amazing care he received. It certainly is not the case at all VA Hospitals around the country. I was grateful to have had the experience of meeting many veterans in that palliative care unit, hearing their stories and feeling their dedication to this country. It fueled my own pride in this country and my devotion to the men and women who have fought and continue to fight to keep us safe. I proudly display his beloved model F7- the plane he flew and one of his USMC caps, and I keep his dress blues jacket safe and sound in my closet.

Not many F7 planes were made during the Korean War- he studied aviation and this was the plane he trained on- so it was hard for my dad to find a model of it and this was treasured.

My dad’s dress blues jacket. I loved to try it on when I was young. He didn’t keep his cap, but this was dear to him and it carries loving memories for me.

It pains me to think of how distraught my dad would be over what’s happening in the country now. Growing up, I dismissed his warnings that history was important because history repeats itself. I think about that so often now as I read the news. It scares me, and I fluctuate between wishing so much that I could talk to him about it and being relieved that he is not eating his heart out.

Regardless of our individual opinions on America, today is a day to honor the veterans who have served this country. Their patriotism runs deep beyond politics that often puts their lives on the line. Daddy always wore a USMC cap and he loved when people thanked him for his service. When he saw other veterans with caps, he thanked them for their service. They would sometimes chat and reminisce. I think they liked to revisit the times when they felt strong and active.

I once gave my dad a 2-disc DVD set called Walt Disney Treasures: On the Front Lines, which highlights Disney’s contribution to American military participation in World War II. My dad was amused by my ability to find this connection between my love for Disney and his love for WW2!  In 2014, shortly after my dad passed away, Disney During World War II: How the Walt Disney Studio Contributed to Victory in the War,  a fascinating coffee table book, was published. I bought the book because it reminded me of my dad and how much we embraced each other’s lives. John Baxter, the author, pointed out that during the war, Walt Disney’s studio primarily did military contract work- morale-boosting war dramas, troop entertainment and training films for the military and, unlike big companies like US Steel and the Ford Motor Company, Walt Disney insisted that the studio did not profit from this work. Walt Disney said, “Actually, if you could see close in my eyes, the American flag is waving in both of them and up my spine is growing this red, white and blue stripe.” I think my dad could relate to that comment.

I had to have Stitch as a Marine! The USMC would never be the same!

Today, and always, I honor my dad and all veterans on this day, with an extra special shout out to the USMC! Semper Fi! Thank you for your service! And, because he found his way to use his unique and brilliant talents to show his patriotism, thank you, Walt Disney!

Daddy at Mitchel Field and the Cradle of Aviation Museum out on Long Island. He loved to go there.

Halloween- Disney Magic and Memories

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It’s here- Happy Halloween!

I dutifully counted down the days on my Halloween calendar figurine and here we are- today is Halloween. My fourth without Ben.  Being home with bronchitis is adding to my melancholy. I did find comfort and joy in using that figurine. It made me smile to think about how Ben loved it and it felt good to honor that tradition. Stuck inside, I won’t see kids dressed up or give my students candy, though that will happen when I return. I will look at our photos and videos, listen to my Walt Disney World Halloween music, and reminisce about how much fun we had at Walt Disney World on Halloween. Halloween was truly magical there- after all, Ben proposed to me on Halloween at Walt Disney World.  It was perfect!

I did bake Halloween cookies and make Halloween cards with a photo of Disney. As I’ve said before, baking and decorating cookies is like my therapy. I am able to relax and get lost in the whimsy. I tried hard to embrace my decorations (click here for that post), acknowledging that I was able to begin to embrace the Halloween spirit that, until this year, had left me along with Ben. Now, I’m more of a participant in the holiday, but I don’t feel the gleeful whimsy that I felt with him. I look at footage from Walt Disney World’s Mickey’s Not So Scary Halloween Party and although part of me would love to experience it again, I wonder if I will ever again be able to attend that celebration.

   

Without distractions at school, I’m surrounded by only memories, albeit good ones. Every year, I’ve made a calendar that is a collage of favorite photos from Walt Disney World. It was a very positive process to make these calendars. I made them for Ben when he was here, too, since he loved to be surrounded by our photos. As you can see, October is filled with Halloween memories. I rejoice in them because Halloween is a treasured part of our relationship. At the same time, I grieve for Halloweens and other events, and even non-events, that we won’t have. And, over the past several months, I’ve struggled with anger that he was cheated out of so much life.

The October collage on my calendar.

Understandably, the most poignant memories were during our visits after Ben’s ALS diagnosis.  I think about how Ben was embarrassed to meet Buzz Lightyear when he was in the scooter. Ben loved Buzz, but after ALS began to weaken him, he said he didn’t want to meet Buzz because Buzz was a strong super hero. I think he agreed to meet him more for me than for himself, though he thoroughly enjoyed watching Buzz interact with the kids on line and he had a child’s excitement. He was able to walk a bit with his cane at this point, and he wanted to stand with Buzz. We were never much for dressing up for the holiday, but Ben loved the Buzz shirt we found and I wore Minnie Halloween ears. Buzz made such a fuss over Ben’s shirt and he made Ben laugh, which made me so happy. Those are the important and beautiful memories. Ben truly did embrace life while facing death. Yes, some of that was denial, but much of it was inner strength and determination, and I believe it helped him to navigate life with ALS in a positive way.

I’m still proudest of our summertime Halloween- our last but most magical visit to Walt Disney World. Here’s a link to that post. I hope that it offers some inspiration to anyone struggling.

Ben did say that when the time came, he was going to be a grim grinning ghost at the Haunted Mansion. I hope he is and that he is having a ghostly good time.

I wish everyone a Happy, Not So Scary, and Healthy Halloween!

Mickey Mouse, Minnie Mouse, ALS, Walt Disney World, Disney

Mickey’s Not So Scary Halloween Party 2012

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