Caregiving

Walt Disney: A Legacy of More than Animation (12.5.1901-12.15.1966)

Walt Disney, Walt Disney World

Walt Disney’s legacy lives on so vibrantly and timelessly in so many ways that it’s hard to believe that today, December 15, 2018 marks 53 years since he left this earth. He’s been a part of my life for as long as I can remember. I have such vivid memories of my mom talking about her favorite Disney movies and how she loved Mickey Mouse from the time she was a child. Mary Poppins was the first movie I ever saw in a theater. It just amazes me how Mickey and his friends touch the hearts of generation after generation. Now, I love to read about him and get a glimpse into his artistic vision and the building of his business enterprises. His belief in himself and commitment to his art are things that we can all learn from. I believe that Walt Disney’s words of wisdom and legacy will live on, as Buzz Lightyear would say, “to infinity and beyond.”

My blog was inspired by the way that I was affected by Disney films, characters and lyrics in light of caregiving and loss. As much as I love to be in NYC during the holiday season, I do have a sense of melancholy. So many of my more recent holiday memories have sadness. My dad was in the hospital and then a hospice during the holiday season of 2013 and the lights I saw were from the windows of a car that took me home from visiting him or the train to and from Long Island. When Ben was ill we couldn’t go together to see the holiday displays and I rarely had the time to go on my own. When I did have a little time, I either felt guilty or couldn’t really enjoy anything. It took a couple of years before I could bring myself to visit the tree at Rockefeller Center and look at the beautiful store displays.  I guess these memories loom, although just today I went to Rockefeller Center to admire the tree and other holiday treats.

Today seems a perfect day to honor Walt’s memory by reflecting on some of his words of wisdom.  They help me to look to the future with optimism, and I think that’s especially significant as we approach a new year. Also, they make me think about the concept of a legacy. My parents left me with a legacy of kindness, loyalty and compassion and always having a sense of humor and whimsy. I hope that I will always honor them and leave a similar legacy.

“That’s the real trouble with the world. Too many people grow up. They forget.”

ALS, Walt Disney World, Lilo and Stitch

The very first time we met Stitch, October 2006!

As someone who still has a lot of my childhood dolls and can’t resist adding new ones to my collection, it is obvious to everyone who knows me that I completely embrace the idea that you need to hold on to your inner child.  As I’ve said, my inner child is very much at the forefront of who I am. For me, watching a Disney film, and imagining a fairy or fairy godmother at my side, also allowed me to escape the realities of caregiving and loss. Ben always said that he loved Walt Disney World because you simply forgot your problems. With a diagnosis of ALS, his problems were huge, but immersed in that fantasy land, he was a big kid having a wonderful time, even despite his challenges. For him to be able to feel that sense of joy and excitement was a gift. Walt Disney envisioned and provided that magical setting. I never want to lose the attitude that allows me to step right into the fantasy the way I did with Ben. I never want to stop wishing on stars or forget the wonder and delight that I had as a child.

“Why worry? If you’ve done the very best you can, worrying won’t make it any better.”

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!

This is absolutely true. Alas, I am a worrier, and I have to work on this, but Walt was right. I can’t say that any of my worrying helped, although perhaps thinking through worst case scenarios may have helped me prepare for a variety of situations. I’ve heard that worrying burns calories, but I’ve seen no indication that this works! I worry now about my future, particularly without much family. I worry that I will never find love again and I will be alone. But, the worrying isn’t going to affect any change, so it’s time to proceed in the best way I can, and make decisions I feel will help me to create a new life, or, rather, enhance my current one with new love, laughter, joy and peace.  I’m going to try harder to listen to Walt on this piece of advice!

“Life is composed of lights and shadows, and we would be untruthful, insincere and saccharine if we tried to pretend there were no shadows.”

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

2010- First use of the scooter to go to Epcot.

There is more light in my life now, and less guilt about feeling happiness, and I know that the people who love and care for me are glad to see me enjoying life again. But there are also the shadows, and I am not someone who likes to, or can, put on a show of emotions. The good and bad moments are all okay. They make me human.

“I always like to look on the optimistic side of life, but I am realistic enough to know that life is a complex matter.”

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

2011- A visit to the Wishing Well at Cinderella’s Castle to wish for a cure for ALS.

Some people might think that my obsession with all things Disney and talk of pixie dust and wishing on stars is silly. Well, I think silly is just fine (okay, within reason.) I like to think that it is my inner child reminding me of possibilities and letting me believe in my own happy endings. But, just like Walt, I am realistic and I have experienced enough of life to know that things get complicated, and sometimes, downright ugly. In the face of life’s complexities, it helps me to stay positive if I escape for a while into a Disney frame of mind.

“In bad times and in good, I have never lost my sense of zest for life.”

ALS,Caregiving,Grief,Walt Disney World, Disney

This quote made me think of Ben and his determination to enjoy life despite ALS. He surrounded himself with music and technology, and he ventured into the world and enjoyed all that he could with a zest for life that, I believe, let him manage the disease well for about four years. It was certainly a good lesson for me.

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

Ben would not be at all surprised that this Eeyore came home with me.

This quote is my inspiration for the future. It’s allowed me to reach out to people, to travel to new places and make dreams come true- I even returned to Walt Disney World, paying tribute to Ben but also creating new memories with dear friends. Throughout these experiences, I did miss Ben. I also struggle with feeling lost and lonely. At the same time, I believe that my curiosity, desire to learn, love and compassion will keep carrying me forward to find new and more love, laughter, peace and joy. I feel cautiously optimistic about the exploration.

“All our dreams can come true, if we have the courage to pursue them.”

My buddy is Cruz. Summer 2019- finding happiness! Meeting otters- I made a dream come true!

I think that I finally have the strength to summon the courage to follow my dreams. It feels pretty great, and yet a bit scary, to say that. I do believe that pixie dust would help.

“Laughter is timeless, imagination has no age, dreams are forever.”

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

2011- This is one of my very favorite pictures of Ben because he was so full of happiness and laughter. Here, he was laughing at me when I met Tinker Bell.

This is one of my very favorite quotes. Laughter, imagination, dreams and, of course, love, were the key ingredients in surviving years of caregiving and loss. They have always been there when I needed them, even if, at times, they felt out of reach. This is something to remember always. Never lose hope. Never lose the spark of a dream.

“First, think. Second, believe. Third, dream. And finally, dare.”

ALS,Caregiver,Caregiving,Disney,Dumbo

Here I go!

That sounds like a good plan! I’m hitting bumps in the road and struggling with confidence, but I’m working on it. Thank you, Walt

 

Gratitude: A Super Power at Thanksgiving, but also In Caregiving, Grief and Always!

Today is Thanksgiving. Of course, I always take comfort in Disney, so I try to heed the advice of Walt Disney who said, “The more you are in a state of gratitude, the more you will attract things to be grateful for.” I have really tried to embrace that attitude and, for the most part, it helps me.

Thanksgiving has become a bittersweet event for me. It is a holiday that reinforces that I’ve lost the family to which I was so close. Last night, as I walked on Broadway and reveled in the tree stands filling with trees and the wonderful fragrance on the streets, I felt a mix of excitement and sadness. Ben and I loved this time of year and we always picked a tree from one of the stands near our apartment. Though I’ve learned to coexist with a constant feeling of missing Ben, last night I couldn’t fight the tears. I came home and talked out loud to him about how much I miss him and how hard it is at this time of year.

I’m not someone who attaches a lot of sentiment to food other than baking cookies and humentashen that my grandma taught me to make using my great-grandma’s recipe, but I realize that now, foods actually carry a lot of memories for me. I have flashbacks of my last Thanksgiving with my dad, spent in the hospital, where I schlepped a full turkey dinner that he ate, mostly, to make me feel better because I’d been crying and pleading with him to eat and get stronger. My last Thanksgiving with Ben was melancholy because he was understandably down about so many things regarding his ALS, including not wanting to eat pureed versions of traditional holiday dishes. Last week, seeing the turkey gravy display at Trader Joe’s was an unnerving reminder of the laughter and tears of my making all sorts of combinations of foods for Ben in the Vitamix as eating became increasingly difficult for him. I always had many boxes of Trader Joe’s turkey gravy because Ben liked it mixed with chicken and mashed potatoes, and I mixed it with all kinds of things to create a puree that he liked, including, if you can believe it, teriyaki chicken! Although it was easy to lose sight of it at the time, we did have things for which to be thankful. Being able to feel gratitude was indeed a super power, because it gave us perspective that allowed us to always see the love that was there, be present in the moment and have hope for the future. Now, at these more challenging times, reminding myself of the many things for which I’m grateful continues to warm my heart, even if those memories come with tears.

My dad and I

When things are not going well, it helps to think of even the tiniest thing for which to be grateful- be it a favorite song or snack. I do validate the need to have a pity party from time to time, but said that once you begin to think of those little things for which you’re thankful, you may very well find that there are many of them.

Indeed, feeling and expressing gratitude has been a super power that’s helped me throughout caregiving and grief and emotions that have turned me Inside Out. What more appropriate time to summon gratitude than Thanksgiving?!

  • At the top of my list is gratitude to have been the caregiver for two supremely important people in my life. Caregiving surely was not easy, and I don’t think I was always good at it, but it was the most important, valuable, loving and rewarding thing I have ever done. I could not save them, but they knew that I was completely devoted to them, and that I would love them, care for them and provide a sense of security to them until they left this world. I treasure the knowledge that they loved me.
  • I have said it before, but can never say enough, that I am grateful for my friends, who have shown me such kindness, generosity, compassion and encouragement, while I was caregiving and then, in grief. Their spirit extended to Ben as well. When family didn’t step in or made empty promises to him-and there were indeed disappointments and dramas-Ben and I could always count on friends. I consider it a precious gift to have these wonderful people in my life and to know that I am loved and that Ben is in their hearts. To be able to return to Walt Disney World a couple of months ago with Monica and her daughters (click here for that post) and pay tribute to Ben and my sweet Disney, while creating new memories with most special friends was an unforgettable and heartwarming experience and celebration of friendship.

  • It is always hard to lose a pet because they are family, and it was particularly hard for me to lose Disney. She was there for me in good and bad times and she was there for Ben, too. Disney was my closest remaining connection to Ben, since she was home with him every day and she witnessed his ALS progression. I became her caregiver, as she had many medical issues, but she brought so much to my life and it was my privilege to take care of her.

    Brave Disney during her hospital stay.

Now, I am grateful for my cat, Tinker Bell. She is young- not yet three years old- and has kitten energy that I have never experienced, and which keeps me on my toes, and makes me laugh and smile. Disney and my previous cat, Tiffany, were senior cats when they came into my life. Tinker Bell has helped me through my sadness over losing Disney. She has a lot to say, loves to be next to me at all times and she listens to all of my stories about Disney. She reminds me that there will always be good things to welcome into my life.

On Disney’s “Gotcha Day,” February 18, 2019 at NYC’s Meow Parlour

  • I’m grateful for my love of animals, as they are often more intuitive, honest and more humane than humans. And, they completely delight me! Discovering the Georgia Aquarium has brought so much joy to me as I have reshaped my life. After losing Ben, it was hard to find my own way and to feel like I was trying to find ways to enjoy our favorite things without him. Planning my first trip to the Georgia Aquarium to meet otters, dolphins and penguins was fun and yet awkward, but I realized that being close to the animals and doing the encounter programs has been a most wonderful opportunity, not only to greet, touch and feed them, but to have discovered a joy that is all mine, though I know that Ben is with me because we did love aquariums. I went back last summer, which was otterly amazing (click here to read about it) and I plan to return this summer, too.

My buddy is Cruz. Summer 2019- finding happiness!

  • I am grateful to be teaching in a wonderful public high school. Not only is it a healthier environment than my prior school, but it allowed me to start fresh, away from my old school and the memories it held of the crises, illnesses and, ultimately, the losses of my dad and Ben. Those memories certainly follow me, but it’s good to see that I can move beyond being seen only as Abby, the person everyone marveled at and felt bad for because I spun in circles juggling caregiving and teaching; Abby the caregiver and the Daddy’s girl who lost her dad and then her husband, even though those experiences are an integral part of me. My stories sometimes help my students share their own stories, and we build a strong sense of community and compassion.
  • As I’ve said, I lost myself in caregiving but I also found myself. I discovered that I am a caregiver to my core. I still have not quite figured out how to use my certificate as a caregiving consultant. However, I have enjoyed doing volunteer work and I am grateful to have met some terrific people who, tragically, are experiencing, ALS as patients or caregivers. This year, I began a club in my school that I intended for students who are caregivers for ill family members or even just for siblings. It is shaping up to be a club of caring, and somewhat shy, kids who need to find themselves and are interested in volunteering. So, in a sense, I am their caregiver! In all of these situations, sharing our experiences is emotional and powerful.
  • I am grateful to find comfort in the arts and in my creative endeavors.  Blogging has been tremendously helpful, and I am grateful to know that readers find comfort in my words and I am thankful to have connected with many people.
  • I’m grateful to have settled into my life, enjoying many of the things I always loved, like going to the theater and spending time with old and new friends. Yes, there is still loneliness and aloneness, but I never lose sight of how fortunate I am to be surrounded by wonderful people, a lot of love, and to carry with me in my heart very beautiful memories.
  • I’m certainly not grateful to have had a romance cut short by ALS and to have to try to date and look for love again. However, I’m grateful to have met some nice people who give me hope that someone may very well be out there for me! And, it’s nice to feel the excitement of a little crush or at least the possibility of romance from time to time!
  • I am grateful to Walt Disney and all he created for providing me with entertainment, inspiration, motivation, joy and opportunities to reflect and sort through my feelings. I’m grateful to believe that wishes can come true and that there will one day be a cure for ALS and all devastating and terminal diseases. I’m grateful for my sense of whimsy and belief that if you wish and dream enough, your wish will come true. It lets me know that I will have even more to be grateful for next year!

Wishing well at Walt Disney World
July 2014

At this time of year in particular, I think about Pollyana, her wonderful world view and the “Glad Game” in the 1960 Walt Disney Productions film of the same name, and based on the novel by Eleanor Porter. (click to read my original post about that). This was a game that Pollyana’s father taught her to deal with disappointment, in which you turn every bad situation around and think about something you’re glad about regarding that situation. As time has passed, I’ve learned that being “in a state of gratitude” is not to naively play the Glad Game. It is not to ignore the bad experiences or diminish their impact, but, instead, to draw upon the very important power of perspective. I have a good cry when I need to, or when something triggers it, but I can also shift my focus to aspects of these experiences that compel gratitude. That said, I don’t like when people tell me that things happen for a reason with regard to my Dad and Ben and their experiences- there is no reason for those kinds of illnesses. The lessons could have been learned without that kind of suffering and loss.

Film clip: Pollyana, 1960, Copyright © Walt Disney Productions  For those of you who remember the TV series Bewitched, the woman in this clip, Agnes Moorehead, was Endora!

There are and there will be setbacks and I am consumed with feelings of wanting to be respectful to Ben’s memory and to make my dad proud. My memories will accompany and guide me on my journey and will always be a part of me, and that gives me great comfort and peace. And, I keep reminding myself of what Christopher Robin said to Pooh: “You are braver than you believe, stronger than you seem and smarter than you think.” I know I’ll be okay because I have the super power of gratitude that gives me a positive perspective.

Thank you for indulging this reflection and for sharing in my experiences in caregiving and grief. Please feel free to use the comment space to share your own expressions of gratitude. You will likely find it comforting and encouraging.

Happy Thanksgiving.

With all good wishes,

Abby

 

Happy 52nd Anniversary to The Jungle Book- With Thanks for Its Lessons on Caregiving and Fighting the Shere Khans

Disney’s Animal Kingdom- 2001, pre-ALS. Ben was psyched to meet Baloo!

Today marks the 52nd anniversary of Disney’s The Jungle Book. I love this classic tale of Mowgli, a man-cub who is raised in the jungle, nurtured by some animals and hated by Shere Khan, the tiger who hates man and is determined to kill Mowgli. I even enjoyed the live action remake. I am moved by the sweet tale of Mowgli’s relationship with Bagheera, the wise panther who teaches and watches over him, and Baloo, the big goofy bear who is a great and caring friend. I always smile when I watch this film, because Ben loved Baloo and fancied himself a big,cuddly bear- a description with which I must agree! When I watch the film, I cannot help but reflect upon how much The Jungle Book has to say about a caregiving relationship and how Ben and I confronted ALS.

Bagheera has all the qualities of a good caregiver: patience, the ability to listen and reason, understanding of Mowgli as a man-cub within the jungle environment, willingness to let Mowgli test himself, reliability, intelligence, common sense and loyalty. Who could ask for more in a caregiver? Baloo is a great buddy, and he and Mowgli have a deep friendship and love, but Baloo also needs the guidance of Bagheera. When Baloo resists the reality that Mowgli needs to return to the “man village” and be around people like himself, Bagheera needs to remind Baloo that although he loves his little buddy and thinks of him as a son, he has to see the big picture in caring for Mowgli and that he has to think about what was best for Mowgli and not just for himself. Those are tough choices and I remember them well. Caring for Ben meant never losing sight of what our priorities were. Like Baloo, there were many times when I felt Ben deserved to indulge in any of his whims because I did not know how long he would have that luxury. And, we knew that time was not on his side. Taking him to Walt Disney World for one last visit was a very joyful indulgence. There were also the gut wrenching realities. I remember that after Ben repeatedly said that he wanted to go home from the hospital, I just wanted to honor his wishes and I asked his doctor if it would be possible to bring him home. His doctor, who proved to be my Bagheera, provided the wisdom and the reasoning, and then I had to have those heartbreaking conversations with Ben. There were stressful times when, just like Baloo and Mowgli, we argued and sulked. But, the caring in caregiving never went away and neither did the love.

I suppose that ALS was our Shere Khan. The wolves who raised Mowgli from the time Bagheera found him knew that they could not stand up to Shere Khan. They did not stop loving Mowgli, but they knew that he could not continue to live with them or Shere Khan likely would have killed all of them. Caregiving also comes with these difficult decisions. Sometimes it’s a matter of caregiving becoming so difficult that it poses physical and emotional risks to a caregiver. In Ben’s case, had he not chosen to go to the hospital’s hospice unit and separate from the vent, he would have had to go to a facility because he could not have lived in our apartment with a tracheostomy and needing 24/7 nursing care. This was not an option we liked but it was one we had to accept.

I could also relate to the battle in which Shere Khan seriously wounds Baloo- the fight to protect and care for Ben did take a toll on me in many ways that have still left scars, but love and devotion kept me at his side and I have no regrets about that. Just like Shere Khan, ALS was a deadly force, but, unfortunately, in our true story, it was one that we could not outwit or defeat.

I don’t know that I would run to Baloo for help in a crisis, though he might be great comic relief! Still, Baloo was protective of Mowgli and he has a good message. As caregivers, we don’t often get to “forget about your worries and your strife” and life seems much more complicated than “the bare necessities.” However, it is so important to take the time to cherish and remember the simple and wonderful aspects of our relationships and life prior to caregiving. These are the things that let you remember who you were before you were in a caregiving relationship.

As for me, I think I was a combination of Bagheera and Baloo- a dedicated, thoughtful caregiver, acquiring skills and perspective during on the job training, with a sense of humor and incredible klutziness. Importantly, Ben always felt safe and secure with me. How about you? What do you consider the important skills of caregiving? Are you more Bagheera or Baloo?

 

What Alice Knew About Caregiving, Grief and My Identity

I saw this quote with an image from the Walt Disney Productions animated film, as I’ve shown here. In fact, it is from the book by Lewis Carroll.

 

School started last week. Two days of just the teachers and administrators and two days with the students. Of course, no teacher sprints back to school, but when my dad and Ben were ill, I especially  dreaded that day. In those days, some teachers knew not to even ask me how my summer was. They knew not to ask me how my weekends were! I would sit and observe everyone sharing their fun summer stories and just hope that I didn’t get asked questions so I didn’t have to shrug and get those sympathetic or pitying looks.  After I lost Ben, when I started in a new school, where only a couple of people knew me, I could just give a generic reply to strangers rather than reveal how difficult summers were. I’m not a terribly superficial person, so it felt like I was not really being myself, yet I was grateful to shed the image of the caregiver running in circles to tend to her dying dad and husband, or the woman grieving her losses. Last week, when asked how my summer was, it was a strange feeling to be able to respond with complete honesty and enthusiasm that it was great. I was keenly aware of feeling good and yet awkward about that answer.

Summer remains a time that is shadowed by the sad memories of Ben’s departure. As this summer approached, I braced myself for those memories but still made plans that I would enjoy. I am pleased, relieved and even proud that I truly had a delightful summer. It feels like an accomplishment. Still, it comes with a bit of guilt and confusion.

I sometimes wonder if my ability to fully immerse myself in life and joy means that I am distancing myself from the loss of Ben. Is it a lack of respect for Ben? Does it appear that way to others? If being Ben’s caregiver and grieving widow have been the ways I have defined myself for such a long time, who am I without those most important aspects of myself? Who do I even want to be?

Although I felt relieved to be able to smile and say that I had a great summer, there was so much emotion and history behind that seemingly simple response. People who have known me through all the difficult years know that it is a big step to be able to experience joy again beyond just having some good times. I am so grateful and appreciative that they are happy for me. For those who don’t know me, it is just casual conversation among acquaintances. Part of me is happy to be a new Abby without that sad history. Part of me feels that those are such vital pieces of who I am that to be unaware of them is not to really know me. Also, it feels strangely disrespectful if Ben is not somehow a vibrant part of the new Abby. It’s hard for me that I’m no longer part of Abby and Ben. By saying I had a great summer, it feels that I am not acknowledging the pain that did exist and continues to haunt me. It dismisses my ongoing struggle to achieve a balance between living in the here and now and taking Ben, and essentially, my past, everywhere in my heart.

Alice was right. I can’t go back to the person I was before the caregiving days and grief. Those experiences did change and shape me. People will not necessarily know my experiences. If they get to know me, it’s likely they will because Ben, and our journey with ALS are vital parts of the person I have become. This blog, my volunteering and my goals to work with other caregivers evolved from those experiences. All these things keep me heading towards the future but also keep Ben with me as I venture forward.

Who am I? In some ways, am still floundering to define myself. I hope that in time I will become more comfortable with myself without so much self-assessment and self-criticism. I knew myself best as a caregiver and person in grief, and the transition to a life without those prominent roles has been difficult.  Of course, grief does not really go away, though it shifts. The Abby from before my days of caregiving and loss has always lived within me during those rough years, but I am just not exactly sure who I am at this point in time. Maybe this is simply who I am, realizing that as we go through life, it’s okay that people will enter and exit and not necessarily know my history. I have yet to be comfortable with who I am in the present and as I look to the future. Maybe I need a looking glass.

 

How Walt Disney Helped Me Understand Grief, Happiness and Optimism

Happy memories from Walt Disney World.

I have been hearing and reading so much about how we “have to” choose to be happy. Maybe it’s because last week was the fourth anniversary of the day that Ben left this world, but I have been thinking about the many pieces of advice I have received about dealing with grief. I have been thinking about my own happiness and attitude and how they continue to shift over time. Walt Disney has been an inspiration to me in so many ways. He said two things that make a lot of sense to me when it comes to grief and how we look at life. It seems to me that we tend to equate happiness and optimism, and while there may be a connection, we must draw a distinction between happiness and positivity or optimism.

 “I always like to look on the optimistic side of life, but I am realistic enough to know that life is a complex matter.”

Walt Disney, Walt Disney World

 “Life is composed of lights and shadows, and we would be untruthful, insincere and saccharine if we tried to pretend there were no shadows.”

From the time that Ben left this world, I received the rallying cheers about the good news: I had my life back, it was time for me, it was time to move on, time to close the book and start a new chapter. Sometimes, I felt like people said these things to make themselves feel better, or because they felt uneasy with my grief. Some people were simply judgmental and felt that I had exceeded their idea of an appropriate time to feel grief. Superficial clichés are easy to spout when you just don’t want to invest in conversation. Yes, I knew that Ben would want me to be happy, but what I realized is that if I wasn’t acting happy, certain people were uncomfortable. They wanted to advise but not to listen, but I was not happy and did not want to act. I learned when to be very superficial and when I could truly be myself. I am very fortunate to have been surrounded by a lot of genuinely caring and loving friends/family. They have been there for me throughout my experiences in caregiving and grief, and while I’m sure it was difficult for them to listen to and see my pain and stagnation, they let me express myself, validated my feelings and gently shared their thoughts. Those who were more adamant about what they felt I “should” or “had to” do definitely felt more tension when I asserted myself and my right to feel the way I did. Many times, the best support I got was a compassionate ear, and at times, a shoulder. Sometimes, the best help you can offer is your presence. Telling someone who is grieving to simply choose to be happy and do things to make themselves happy is dismissive and tone deaf.

The notion of happiness is not easy in grief. I may have found a lot of happiness-or maybe more comfort- in the memories, but the sadness was also palpable. Sometimes there were brief moments of happiness that snuck into my overall feeling of devastation, but I still did not feel happy in my life. It was often suggested that I do things that made me happy, but I did not know how to begin to identify those things, and frankly, I did not want to feel happy. Sometimes the grief was overwhelming and paralyzing, and at those times it took too much energy to be optimistic or positive enough to look for happiness. A happy event was frequently followed by confusion, frustration and amplified sadness when I realized that it was nothing more than a fleeting distraction and I was still arriving home to be alone without Ben. I was not quite sure how to define happiness- for a time it was just a moment of not feeling the pain of grief. Having experienced the loss of my parents, grandma and other loved ones, I did, however, know that there would be shifts and I chose to be optimistic that happiness was attainable- at some future and unpredictable date.

As Joy learned in Inside Out, in life, happiness and sadness are not mutually exclusive, and anger, disgust and fear also have their roles. When I have tried to process my caregiving days and the losses, the idea of happiness seemed way too elusive and simplistic an option and those happy moments that I experienced were only a superficial illusion. There was also a lot of anger at and disgust with ALS, some people around us, even Ben and myself, and that’s hard to think about, although I have gained some perspective with time. Fear has also been prevalent- first, it was the fear of impending loss and potential crises, then fear of the future and fear of being alone. I desperately wanted to be happy, despite not really knowing what would make that happen or how it would feel, but I also wanted to feel that I was reaching to be positive and optimistic.

For a long time, the idea of happiness came with a lot of guilt, because Ben could not share that happiness and so much opportunity was taken from him because his life was cut short. Was it appropriate to be feeling happy or enjoying my time? Did it mean that I didn’t miss Ben anymore? Did it mean that I was happy to have been absolved of my caregiving responsibilities? I judged myself as much as, or more than, I felt judged by others.

Grief comes with ebbs and flows, and good and bad days and moments. I have a lot more good days after four years, or five and a half if I count the loss of my dad. There is more light in my life now, and less guilt, and I know that the people who love and care for me are glad to see me taking positive steps and genuinely enjoying life again. But there are also the shadows, and I am not someone who likes to, or can, put on a show of emotions. The good and bad moments are all okay. They make me human.

Walt Disney also said, “In bad times and in good, I have never lost my sense of zest for life.”  For me, that is the distinction between being positive or optimistic and being happy. Some people might think that my obsession with all things Disney and talk of pixie dust and wishing on stars is silly. Well, I think silly is just fine (okay, within reason.) I like to think that it is my inner child reminding me of possibilities and letting me believe in my own happy endings. But, just like Walt, I am realistic and I have experienced enough of life to know that things get complicated, and sometimes, downright ugly. In the face of life’s complexities, escaping for a while into a Disney frame of mind helps me to be positive. Trying to stay positive is my choice, but it doesn’t mean that I am always happy. I wonder if being optimistic in our nature, but for me, it’s always worth the effort to be optimistic. Still, I accept all the emotions and phases of grief and of life.

I think about Ben and his determination to enjoy life despite ALS. He surrounded himself with music and technology, and he ventured into the world and enjoyed all that he could with a zest for life that, I believe, let him manage the disease well for about four years. There was happiness and certainly sadness, fear and anger, but he always did try to be positive. It was an important lesson for me.

I do want to add that social workers and other mental health professionals were also available to Ben and to me. I was more willing than Ben to discuss my feelings, but when I did feel overwhelmed, I did see a therapist and speak to some of the people from Ben’s team, even after he was gone. It is always a good option if you are struggling with your emotions or need an objective listener.

Being positive allows me to follow this advice from Walt: “First, think. Second, believe. Third, dream. And finally, dare.”

Am I happy now? Well, I’m happier. I am pleased and even proud of myself for creating a truly wonderful summer for myself, where I felt more joy and fulfillment than I have since I lost Ben. While the anniversary of Ben’s passing on August 26 was still a very difficult day, the sadness is something I accept and embrace because it is all part of my life experience. This summer, I realized that I have found ways to do things that bring me joy while keeping Ben close, in my heart, and that feels right and gives me balance. I think this gives me more moments of complete happiness rather than brief happy distractions from going through motions in my life. These moments are the ones that keep me optimistic and propel me forward and allow me to keep dreaming and believe that I can make my dreams come true. I know that happiness is not everything, particularly when it is fleeting and superficial- I am not that much of a Pollyanna. I do aim for contentment and trying to maintain an optimistic outlook that I will achieve it. I’m floundering and anxious about my next steps in life, and I am shaken when something triggers a setback in grief, but even when I’m getting caught in the undertow of emotions, I think positively like Dory and dare to just keep swimming.

My buddy is Cruz. Summer 2019- finding happiness!