Rediscovering Myself Through- And After- Caregiving

ALS, Caregiving,Grief,Disney,Pixar,The incrediblesElastigirl.“Your identity is your most valuable possession. Protect it.”

Yesterday, I went to see New York City Ballet perform Jewels. It’s one of the first ballets I ever saw. I saw my first NYC Ballet, The Nutcracker, at age three and was enthralled by ballet from that young age. I read about Jewels and my mom took me to see it at Lincoln Center. How lucky was I? Going to the theater or ballet is my favorite activity and my most loved way to lose myself and feed my soul. As I walked to Lincoln Center, after making a last-minute decision to get a ticket, I thought about my caregiving days. As Ben’s ALS was progressing and he was nervous about being alone, I could not simply make a quick decision to go to the theater or ballet. It had to be planned in advance and Ben had to negotiate with his daughter to stay with him. I went from being someone who saw everything to someone who barely knew what was on Broadway. It was a choice I made with no regrets, and I can still look back and know that I did the right thing for Ben and for me and for us, but I also admit that I did not take care of myself, physically or emotionally.

As I watched the ballet, I thought about how I can now spend my time as I choose. Even after three years, I’m still not entirely comfortable saying that. I don’t want it to be construed as my having any sense of relief that I am free from a burden. It was hard work that was also loving and meaningful, and unquestionably the most important thing I have ever done, although I did lose a part of myself in the process. After I lost my dad and Ben, returning to the theater and ballet helped me distract myself from grief, sort through feelings, and rediscover myself. There were and there continue to be times when events are not as fulfilling and enjoyable as I wish they would be because I profoundly feel Ben’s absence. But, I have established new normals, new routines and an evolving sense of myself. The arts are the way I take care of myself- I can think, imagine, reflect and just enjoy the magic. I feel fortunate that my passion for the arts has always helped me to heal and grow.

When I think back on my caregiving days, I remember that I constantly struggled with feeling detached from life.  I tended to put caring for myself aside, always concerned that worrying about myself was being selfish. Of course, my indulging in arts events seemed so trivial compared to Ben’s battle with ALS. But, as Ben’s needs increased and his denial of that persisted while the devastation clearly affected both of us, I grew more isolated from people and things I loved and I became resentful, angry and frightened. Reconciling those negative feelings and the guilt for feeling them has not been easy.

Throughout my caregiving days, the people around me told me that I HAD TO take time for myself. It really irritated me, because it was stating the obvious but also felt impossible. I could not voice my need to take care of myself. In my mind, since my dad and Ben were ill, they were the ones who mattered. On the occasions that I was able to go out, those things didn’t offer the same satisfaction that they did before, because I never went with Ben, I felt guilty for going out and because I was worried about what was going on at home if I was not there, and lamenting what I missed:  the life we had, who we were before illness took over, the things that I, and we, couldn’t do.

It was through our love for Disney films that I discovered my greatest source of self care. Ben and I loved to watch Disney movies, and what I found was that the films were more than simply distracting and entertaining together time. I was seeing the films in a whole different way when I watched them through the eyes of a caregiver.  They were shedding light on my caregiving situation. Disney films let me feel understood because they tapped exactly what I was feeling and gave me perspective on a situation that was very daunting. They were simultaneously giving me a much needed break from reality and letting me think through my feelings about my reality. While having someone stay with my husband while I went out was sometimes possible, though less and less ideal, I realized that I was so busy thinking that taking care of myself meant planning a major outing, and dwelling on the negatives like the help that I didn’t have, that I didn’t see that taking time to watch a Disney film was also time to reflect and enjoy my own company right within our apartment!

What turned out to be the most valuable thing I did for myself was that I began keeping a journal of the Disney quotes, films and characters that made an impact on me and I wrote about how they related to my experiences in caregiving. Writing was always a passion of mine, but I stopped writing in my journal because I felt like I kept repeating the same issues without finding solutions. By creating this journal, I unexpectedly combined my love of Disney and writing with my caregiving, and held onto a vital part of myself without having to leave home.

Collecting and writing about Disney things gave me an opportunity to reflect on my experiences in a way that was honest about the not great people and things, but also reminded me of why I continued to be a caregiver: love, dedication, a personal desire and sense of responsibility to do the profoundly meaningful work on behalf of people I loved who needed me. As Cinderella said, “they can’t stop me from dreaming.” And, when I began to think that my quotes and experiences could at some point be a book or blog, I had something positive to think and fantasize about and plan for in my future.  It took a year, but I did eventually launch PixieDustForCaregivers.com. It has been an invaluable way to take care of myself, heal and connect with other caregivers.

Sometimes, even very small actions provided a huge dose of self care. For example, the thermos of tea that I drank on my daily 2.5 hour train ride back home after visiting with my dad in hospice became my precious “Abby time” to reflect, listen to meaningful music and read. Yes, my phone was in hand for texts and issues that might arise, but each sip of tea allowed me to take a deep breath and, as Frozen’s Elsa said, Let it Go!”

A requirement for earning my certification as a caregiving consultant was to create a webinar. Since a significant issue during my caregiving days was the concept of losing myself while caregiving and knowing that I was also going to lose Ben, and I have heard similar anecdotes among other caregivers, I decided to create a webinar exploring this theme. Finding Inspiration and Protecting Your Identity During Caregiving explores ways in which I maintained my identity and tapped important parts of myself, often right at home. There are ideas for finding inspiration, protecting your identity and how to make your plans happen. You can see the webinar by clicking here to view it on Caregiving.com.

Today, I will see the new Broadway show, Pretty Woman. A weekend of the arts always does wonders for my soul. And, as I discovered, so does caregiving. Now, I am so proud to have earned my certification as a caregiving consultant. I’m not exactly sure how I’m going to use it, though I know that I one thing I would like to do is work with children who have a parent or family member with ALS. The important thing to me is that I have learned from my experiences, I continue to learn about myself and I protecting my identity and honoring Ben and my dad.

What are you doing for yourself? Please leave comments with your questions, comments, revelations and/or struggles.

July 2014, Breakfast at the Polynesian Hotel.

 

 

Kindness- It’s Pixie Dust For Caregiving!

ALS,Caregiving,Epcot,Walt Disney World

July 2014

In Disney’s live action Cinderella (2015), Cinderella mother advised her to “have courage and be kind.” That phrase became the centerpiece for a lot of merchandise and marketing efforts. I believe it was so well embraced and successful because it was so true, so succinct and yet so wise. Examples of courage abound in their battles with cancer and ALS, and even, I’ve come to realize, in my work as their caregiver. The Mighty, a portal with information about a number of illnesses and personal experiences with these conditions, and for which I am a contributor, created a #KindnessChallenge this month, and it got me to thinking about how fortunate Ben, my dad and I were to have experienced much kindness.

After my dad went to the wonderful VA hospice, the simple acts of decorating his room with his favorite books and his favorite model of the fighter plane he flew when in the Marine Corps, and making a calendar of his favorite pictures, meant the world to him. Bringing a book or article and reading it aloud to him, and even sitting and holding his hand while we watched television were little, and yet big, acts of kindness. At this time, Ben’s ALS was progressing, and as the disease took away his abilities, he sometimes felt that he had little to give. However, he found movies and documentaries that he knew my dad would enjoy and he burned them onto DVDs for my dad to watch. These acts of kindness moved me as much as they did my dad, because we knew that nothing was easy for Ben, and because although Ben could not physically be there for my dad, or even communicate by phone with him, with this kindness Ben let my dad know that he was in his heart.

Sully lent a hand to help Ben out of his electric wheelchair! October 2012

A most gracious act of kindness towards Ben came from the palliative care team at Mount Sinai Medical Center. When Ben was in the hospital after a respiratory crisis, it took him a few weeks to decide to get a feeding tube and tracheostomy. During this time, we had visits from the palliative care team. I was happy to talk to anyone about anything they could possibly do to help Ben. The team asked about his interests and I shared that he loved music and anything to do with computers. Shortly after their visit, Ben had a complication that required that he be intubated, which landed him in the ICU. The ICU staff was wonderful, but there is understandably a lot of anxiety in that unit. Late one afternoon, a man named Todd showed up at Ben’s bedside with a guitar to play for Ben. Although musicians are not generally sent to the ICU, and teams are usually organized by floor within the hospital so Ben could have been discharged from the team on his original floor, the palliative care unit members knew that Ben loved music and they thought he would enjoy it and that it would be good for him. Ben expressed to Todd that he loved everything by the Beatles and any Disney songs and also relaxation music and Todd played several songs as Ben watched so intently- Ben loved to watch musicians. Ben was thrilled and moved to tears. I was, too. On the day that Ben separated from the vent, the team arranged for Todd to once again return and play the guitar, which was an overwhelmingly beautiful and peaceful way for Ben to leave this world. In a busy and huge hospital, people took the time to think of Ben as a person more than as a patient, and they extended a treasured act of kindness. I tried to repay that kindness by donating to the hospital the keyboard that I had given to Ben so that others who enjoy music can embrace it during difficult times.

I, too, received many acts of kindness through the years of caring for my dad and Ben, and after those days had ended. I think about how difficult it was to juggle full-time teaching with full-time caregiving. There were many instances of crisis when I had to rush either to the ER to meet my dad or home to help Ben. In one instance, Ben texted me that he had fallen (he wore his phone around his neck in case of such issues). I ran to my principal that I had to go home but that I would be back after I got Ben settled. When I got home and tried to lift Ben off the ground, I realized that Ben had lost so much strength in his legs that he could not help me in any way. At that time, he probably weighed about 190 pounds. More than two hours later, Ben was still on the floor and I was exhausted and in pain. This was the first such incident, and I did not even think about calling 911. I sent a text to my principal that Ben was still on the floor and it didn’t look like I would make it back to school. Even though it still would not have gotten me back to school in time, my principal offered to travel across the city to come to my apartment with our Assistant Principal to help me to lift Ben. I did not take him up on the offer- but I have never forgotten that kindness extended to Ben and me. In a school system that is increasingly anything but kind to teachers, I remain grateful that my principal was always understanding of my situation, despite many emergencies that required that I leave school early, arrive late, or be absent.

Two Goofy guys! July 2014

Ben showed me much kindness and love over the years. Yes, he gave me lovely gifts, but it was his gestures that truly touched my heart. I’ve written about one of my very favorite memories of kindness was something that Ben did for me during one of our visits to Walt Disney World after his ALS had progressed a bit. Click here for that post. But, he showed me kindness by his sense of humor as I experimented with different foods in the Vitamix, always encouraging and appreciating my efforts. He showed me kindness whenever he texted me that he had asked his private aide to stay an extra hour so that I could stay out- either by myself or with a friend- a little bit longer. He showed me kindness by asking his daughter to stay with him so that I could attend an event and by being happy for me that I enjoyed myself. And, mostly, he showed me kindness with his love and appreciation of me.

Here’s a conversation between Piglet and Pooh from Disney’s Christopher Robin that I believe sums up the role of kindness at its most simple and most complicated.

“I don’t feel very much like Pooh today,” said Pooh.

“There there,” said Piglet. “I’ll bring you tea and honey until you do.”

Kindness can be a matter of being present, sometimes it’s being a good listener, sometimes it’s ensuring that routines- including medications- are followed. Mostly, it’s about caring to figure out exactly what will soothe someone in the moment. For Pooh, honey was always a good solution. It’s not always that easy. But communicating the desire to be there, to help and support, can only strengthen a bond. Although we could lose patience with each other, and sometimes we needed our moments to feel down, Ben knew that I would always at least try to find the thing that would be his tea and honey.  Often, things like a smile, a thank you, a kiss, holding hands, remembering something special or an inside joke were the small yet huge gestures that lessened the tensions and brought us back to love. Those small kindnesses were priceless. The memories of those kindnesses and that love far outlast the disappointments, frustrations and devastations.

Who wouldn’t be happy with a big hug from Mickey!?!?! July 2014

What are acts of kindness you showed or that were shown to you that were especially memorable? Please share them here as part of the #KindnessChallenge.

2011- The first time we went to Fantasmic!

An Important Book for Caregivers: Home Hospice Navigation

In addition to sharing my Disney-ish reflections on caregiving, grief and beyond, I also want to share resources that can help with caregiving and grief. It will not come as a shock that I happen to agree with Walt that “There is more treasure in books than in all the pirate’s loot on Treasure Island.” I guess I was a little like Goldilocks when it came to reading books about caregiving, grief, and ALS—some were too clinical, some were too spiritual or faith-based, some were too heavy-handed, with so much detail that I ended up feeling confused or defeated. I wanted a concise and accessible how-to resource.  I recently discovered just that, an easy to read, informative, understandable  and engaging book called Home Hospice Navigation: The Caregiver’s Guide by Judith Sands, RN, MSL, BSN, CPHRM, CPHQ, CCM, LHRM, ARM who is a healthcare professional, nurse, recognized authority in the areas of care coordination, quality, risk management, and patient safety.

I read many caregiving books, and receive frequent comments from caregivers with questions, concerns and misconceptions of home hospice. I know that it’s difficult to research things when you’re caregiving, and when you do have the time you don’t always have the energy. However, if the notion of home hospice has crossed your mind, I strongly recommend that you take a look at this informative read and wonderful resource that does, indeed, help you to comfortably approach the navigation of home hospice options. Home Hospice Navigation is written for the caregiver in easy to read, well organized sections, with good advice that is offered as if Ms. Sands is standing next to you anticipating your questions.  First and foremost, it clears up the glaring misperception that home hospice is the equivalent of euthanasia and that someone needs to be close to death to receive home hospice services. Instead, Ms. Sands points out that “hospice should be thought of as living fully as long as possible and helping your loved one to die a peaceful and comfortable death.”  I have to admit, I found it confusing when Ben was put on home hospice. It was the physical therapist from our visiting nurse program who suggested it when Ben needed more help and was nervous about being alone but reluctant to accept that he needed to hire an aide. This woman set in motion a process that allowed Ben to receive helpful care, support and medical supplies. As caregivers, we often neglect our own physical and emotional needs and hospice care services also provided a lot of emotional support to me. Yes, there is a trade-off at times with what is covered by insurance, but home hospice is definitely an option worth exploring. This benefit is covered through Medicare, Medicaid and most commercial insurance policies.

Ms. Sands lets you know what information is applicable across the board and what may be specific to your state or insurance. Throughout the book you will find anecdotes about Ms. Sands’ experience with home hospice with her mom. These stories show the very personal inspiration for this book and make it very relatable for many caregivers. There are references to the important documents that everyone should complete, which are conveniently organized and available through her web site, www.JudithSands.com (the book can also be purchased through her site). Also, you will find suggestions of considerations, conversations that should take place, and a step-by-step, very accessible process for how to begin to engage hospice services and work with medical and related staff.

I wish I had this book when Ben and I were making decisions about his health care.  I highly recommend Home Hospice Navigation: The Caregiver’s Guide to those of you who are daunted by home hospice and do not know where, how or whether to consider it as an option. The book can be purchased in paperback or digital versions through JudithSands.com. Please feel free to contact me with any questions or comments.

These Disney Quotes and Lyrics Sprinkle Pixie Dust On The Pain of Loss and Grief

Walt Disney World, Halloween

Ben and I at Walt Disney World, Halloween 2011. Good memories are always a comfort.

 

Last week was the three-year anniversary of the day that Ben left this world. Holiday weekends also add to the loneliness and feeling of floundering, as does the anxiety of a new school year. I got to thinking about the many Disney quotes that have helped me deal with loss and grief. I am aware that loss and grief did not begin with death. As soon as there was a diagnosis, and throughout the progression of ALS (and my dad’s cancer), I grieved the loss of the relationship that we knew and enjoyed, the loss of Ben’s abilities and how he mourned them, and the loss of dreams of our future together. Here are some favorite quotes and songs that remind us that as hard as it is to lose those we love, they do remain with us in our hearts.  That’s not always enough, and sometimes it isn’t even close, but it is a lot. There are times when we miss them so much that we ache and there are times that we recall memories that make us smile and laugh. We hear their voices and their guidance in our heads, we are comforted by some memories and haunted by others, but, in my mind, we were fortunate to have that kind of love in our lives.

I am including links to posts in which I refer to these quotes and songs, but I don’t think they need explanation. They are offered here to give perspective and comfort during difficult times. Please feel free to share your reactions. Or, share your own favorite inspirations.

“Love is a song that never ends”From Bambi (1942)

From Bambi. (1942), Walt Disney Pictures

Here is the music clip to accompany the lyrics to this beautiful song.

Music by Frank Churchill
Lyrics by Larry Morey

Love is a song that never ends
Life may be swift and fleeting
Hope may die yet love’s beautiful music
Comes each day like the dawn.

Love is a song that never ends
One simple theme repeating
Like the voice of a heavenly choir
Love’s sweet music flows on.

Click here for the post.

 

“Look at the stars, the kings of the past look down at us from those stars. Whenever you feel alone, just remember that those kings will always be there to guide you and so will I.” – Mufasa to Simba, The Lion King, Walt Disney Pictures 1994

Click here for the post.

 

Evermore
Written by Alan Menken and Tim Rice
Performed by Josh Groban, from the Beauty and the Beast (2017) soundtrack.

Now I know she’ll never leave me
Even as she fades from view
She will still inspire me
Be a part of everything I do
Wasting in my lonely tower
Waiting by an open door
I’ll fool myself, she’ll walk right in
And as the long, long nights begin
I’ll think of all that might have been
Waiting here for evermore

Click here for the post.

 

How Does a Moment Last Forever
Written by Alan Menken and Tim Rice, Disney’s Live Action Beauty and the Beast, 2017.

How does a moment last forever?
How can a story never die?
It is love we must hold onto
Never easy, but we try
Sometimes our happiness is captured
Somehow, a time and place stand still
Love lives on inside our hearts and always will

Click here for the post.

 

There’s nowhere you could go that I won’t be with you.Gramma Tala, Moana, Walt Disney Pictures 2016

Grief,Grandmother,Moana,Gramma Tala,Walt Disney Pictures
Click here for the post.

 

Remember Me
Lyrics from Coco,
Disney Pixar 2017

Written by Kristen Anderson-Lopez and Robert Lopez
Performed by Miguel, featuring Natalia Lafourcade

Remember me
Though I have to say goodbye
Remember me
Don’t let it make you cry
For even if I’m far away I hold you in my heart
I sing a secret song to you each night we are apart

Remember me
Though I have to travel far
Remember me
Each time you hear a sad guitar
Know that I’m with you the only way that I can be
Until you’re in my arms again
Remember me

Click here for the post.

 

When you lose someone  you love, they never really leave you. They move into a special place in your heart. – Mrs. Frankenstein, Frankenweenie, Walt Disney Pictures 2012

Click here for the post.

 

“Goodbye may seem forever, farewell is like the end, but in my heart is a memory and there you’ll always be.”Widow Tweed to Tod
The Fox and the Hound, Walt Disney Productions 1981

Click here for the post.

 

But if you want to leave, you can. I’ll remember you though. [looking at her picture of her dead parents] I remember everyone that leaves.Lilo, Lilo and Stitch, Walt Disney Pictures 2002

ALS,Caregiving,Grief,Walt Disney World, Disney

They aren’t always together, so May 2010 was a big deal! Well, it was for me!

July 2014, Breakfast at the Polynesian Hotel.

Click here for a post on family and click here for a post on the significance of Lilo and Stitch in our experience.

 

If ever there’s a tomorrow when we’re not together, there’s something you must remember…You are braver than you believe and stronger than you seem and smarter than you think…. But the most important thing is, even if we’re apart, I’ll always be with you. -Christopher Robin to Winnie the Pooh, 

This clip has the whole sweet conversation between Christopher Robin and Pooh, from Pooh’s Grand Adventure: The Search for Christopher Robin (1977), Walt Disney Television Animation

Click here for the post.

What Simba and I Know About Grief, Disappointment and Loneliness

On the heels of the third anniversary of the loss of Ben, I got medical test results that indicated that further testing is needed. My doctor is not concerned and believes I’m fine, but says it should be addressed. I am a terrible patient, which any of my doctors will attest. Just going for a check-up comes with a lot of anxiety. Ben was much braver than I am. My cat, Disney, is much braver than I am. Now, I have to go to a different doctor, which causes a lot more stress. And, this doctor is away for the week. Normally, I email or call a couple of friends to vent and get suggestions. This time, I chose not to. I don’t want to be the bearer of more sad news in my life, especially when I’ve been doing better. I guess this post will put it out there, but it is not something I want to discuss.

When my dad and Ben were ill, I was the dutiful and loving caregiver who accompanied them to every medical appointment. They were never alone. Likewise, when Ben was well, if I was nervous about an appointment, he accompanied me without my asking. Ben was frustrated that he could not join me when I called him from the emergency room that I had broken my shoulder, but he was still at home to comfort me. Things have changed. Two years ago, I had to have a pretty standard out-patient procedure. I had arranged, per protocol, to have a friend meet me afterwards, but I went to the hospital by myself. I didn’t think it would be so much like going into surgery, so I was overwhelmed by the situation. My doctor is pretty good at anticipating and handling what a nervous wreck I am, but I was not dealing well with all of the strangers.  I don’t think I ever felt so alone. It was then that I realized that I might carry Ben in my heart, but at times like this, the truth is that I am by myself. I am probably most comfortable as the caregiver rather than the caree, but this circumstance made me see that there are times I want to be cared for. I have wonderful friends who would be there if I ask them, but I no longer have that person who would be there without my asking. Thankfully, everything was fine. But, if there had been complications, or if there are any complications this time around, I am pretty much on my own to tackle them. Hopefully, my doctor is correct and I am fine. Right now, I’m having a little pity party and feeling like Simba- “You said you’d always be there for me, but you’re not.” Ben may be watching over me, but at times like this, it’s not enough.

Life happens, healing happens, and setbacks happen. Disney always helps me deal with my feelings. The Lion King is just one of the films that’s helped me deal with loss and grief (see that post by clicking here). Writing is another way that I cope with the setbacks. It helps me to channel my sadness and frustration. Writing sometimes takes the issue and breaks it down. It won’t change my reality, but it does relieve some of my near hysteria. It was a good way to start this period of waiting to see this new doctor. I hope that anyone who reads this has strategies to help cope with sadness and grief. Feel free to share your own strategies in the comments, as they may inspire others.

I like to put a positive spin on things, so maybe I have to say to myself that this will be one more way that I learn that I am braver than I believe and stronger than I seem. I will remind myself that I am fortunate to be able to function independently and at least fairly wisely. For now, I just wish they were here.