What are your gifts, passions, and talents? I believe everyone has something they’re really good at whether it’s cooking, socializing, hospitality, a sport, etc. At the very least you have something you LOVE to do whether you’re good at it or not.
I used to sing. I LOVED to sing. Singing for me used to be like breathing (both of which are now difficult for me since cancer). Growing up, I had plenty of opportunities to sing. It was my special gift, my passion, and because I’m a melancholy introvert, it was how I expressed myself and my emotion I could be who I wanted to be. I could bare my soul through song better than through words, and dare I say, I was pretty good. I sang on a TV show, radio jingles, weddings, sporting events, and even auditioned for a Broadway musical, and made the final cut to play the lead. And then cancer. It was actually a change in my singing voice that told me something was wrong. My first surgery resulted in a paralyzed vocal cord and singing was done; in the blink of an eye, what I did so easily most of my life, and loved to do was gone.
I realized the other day while driving alone in the car, that over the past maybe 5-10 years, I had switched to only audiobooks and podcasts. That day, I switched my car bluetooth from podcast to Spotify and I got emotional. I missed music. I missed singing, and right there while I was humming along in the car, I felt the grief of that loss all over again. No, this was not the first time I’ve grieved about losing that part of me, but grief hits at weird times and can hurt just as deeply as when you first experienced the loss.
All this to say, ever since cancer took a vocal fold, I’ve tried to kind of ignore that singing part of me but there has been one event that reminds me that although my old voice is gone, what I do have left is a miracle. I have been part of a concert event that one of my doctors puts on annually in honor of World Voice Day. I think I’ve been part of it every year since maybe 2009 (minus pandemic shutdown and last year when I was out of town). I rarely tell people about it because I am no longer confident about my voice, and I am nervous and breathy and always wonder if I’ll pull it off. It’s emotional and overwhelming every single time, and I know it’s not perfect, but I still do it. All those in the concert have a story about some adversity with their voice and what a miracle it is to have it back (thanks to an expert medical team). I feel the grief of losing the one talent I thought I was blessed with, but also the gratitude of still being alive. Every year, as difficult as it is, I get to sing and while I do it, remember all that I’ve been through to still be able to get on that stage.
There were long stretches in my cancer walk that I completely lost my voice. Cancer hit my neck and took a vocal cord. Still now when I get sick it’s usually the first thing to go. If you still have full capacity of all 5 senses, consider it a blessing not to take for granted. The voice and the words you speak are powerful. If you still have yours, use it to tell people you love them, use it to stand up for what you believe in, use it to thank God you still have it, and use it to tell yourself that you are amazing no matter what.
This weekend I visited my youngest child for his family weekend at his university. I was super weepy most of the weekend, breaking down in tears at random times, and really, all of the time. I can’t really describe it as sadness, but more a combination of overwhelming joy at seeing him in his element and brokenhearted because I miss him. My other son flew into town too so both my boys were with me…oh my heart. Beautiful and brutal.
With my dad’s sudden passing earlier this year the reality that life is incredibly short is at the top of my mind, not to mention having Stage four cancer. I hate talking about it all of the time, but it informs pretty much my every thought. I think I have cried more this year than I can recall and not just because of the heart ache of losing my dad and my dog but the knowledge about the absolute brevity of life and the beauty in our days always in my face. So, every time I say goodbye to one of my babies, my heart breaks. Hence the tears. Tears from relishing the joy of each moment AND tears of heartache at how fast time ticks; the intermingling of grief and joy. This past weekend time felt like my enemy or maybe it’s that cancer is stealing it away. When will I see them again?
I was listening to a podcast and someone shared that having adult children was like sitting back and watching a show where we don’t have much of a role. I grew up in musical theater so that really resonated with me; earlier in kids’ lives we are producers and directors-overseeing everything, directing their paths, but as they grow into young adults, we become the audience with ‘guest appearances’. Only we hold the memories of their childhood because we were the adults. Think about it, most of the stories and knowledge from my own childhood came from my parents. Only I will remember reading I Love You Forever and Where The Wild Things Are and so on while they were babies sitting in my lap. Only I will remember sitting up many nights holding my son up and setting an alarm every few hours to give breathing treatments to my baby with asthma, the look on my daughters face at her first elementary school concert or when she got a part in the school play, their faces when they were excluded or didn’t make a team, when they were hurt by a friend, first day of school, last day of school, putting them on the schoolbus for the first time, seeing my son hooked up to machines in the ICU after his stroke, birthdays parties, the joy at Christmas opening presents…all the memories that only I have and cherish because they were too young to remember or their focus was a little different. So many memories overflowing with joy, love, and of course, heartache.
I will see my kids again around the holidays but then…? They are all adults now with jobs and college, complicated schedules.
I don’t know when my cancer will decide to progress.
I don’t know how much time I have left, but who does?
Here’s what I do know:
I can call or FaceTime my kids anytime I want and if I’m desperate for a hug, I can book a flight to visit (it would be a really expensive hug but…)
I have today.
I have this moment.
It’s all about not letting moments pass me by, as I’m aware that my moments are fewer than in the past.
For now, I will linger in the joy of being able to see my boys this past weekend for just a little longer
I lost two greats within 6 weeks of each other, my dad who I wrote about in my last blog, and then my dog, Moose. Both were diagnosed with cancer out of nowhere and both passed away quickly after diagnosis; my dad 11 weeks after and my dog, 5 days after-just a little over a week ago. It has been a lot. There are moments the sadness overwhelms me, sometimes without warning. Losing Moose was the tip of the iceberg, and I honestly wasn’t sure I could bounce back from all the grief I’ve collected over the years. Moose was my comfort after my Stage 4 diagnosis, through Alex’s stroke, the global pandemic and lockdown, my sadness over being an empty nester and missing my kids who are all so so far away, my dad’s diagnosis and passing, and all the times in between. Moose was the loving, always present, positive thread throughout the most difficult times. His sudden illness and death was the pin prick that finally popped my already stretched balloon full of grief. 2023 has been rough but SLOWLY I’m feeling life come back without tears attached.
Two things happened this week that helped me a little, the first was a quote I read a few days ago and it impacted me so much that I wrote it on a sticky note and stuck it to my laptop, ‘We live daily and die once, so we must make the most of the time we have.’ ~Dr. Howard Tucker, the oldest practicing doctor alive at 100 years old (he’s in the Guinness Book of World Records). Take a pause right here and repeat, ‘We live daily and die once…’ One thing I remember my mom saying in her grief just moments after my dad passed, ‘We still had so many plans.’ As hard as it was to hear that, it was a reminder AGAIN that life is so brief and we need to steal those moments of joy, but not just that, we need to REMEMBER and make the most of them.
The second thing was an interview on Kelly Corrigan’s podcast with author and journalist, Michael Lewis whose high school daughter died suddenly in a car accident. I resonated so much with his insight as he processed through his grief. First he acknowledged that we all want easy stories, and of course, who wants a life complicated by grief and sadness? But spoiler alert, fairy tales don’t get a happy ending without all the crap in the middle. Next he used the phrase ‘radical gratitude.’ I have heard the phrase ‘radical love’ from therapists and I get it. Radical love to me is loving someone ‘despite’ or ‘even though we don’t agree’, or ‘even though I’d rather not be in the same room as you, I still care.’ I believe in Jesus and I believe his life and death were examples of radical love and I try, I really really try. I’ve never heard the phrase ‘radical gratitude.’
Radical gratitude (to me) means the act of taking all your circumstances, good or bad, and consciously choosing gratefulness. It is the exercise of being completely devastated but still actively searching for one thing, one tiny thing to be thankful for. It’s hard but it’s the magic sauce. In 2008 after years of singing at church, on tv, on the radio, at events, I got cancer in my neck that cut the nerve to my right vocal fold. What once was what I was known for, my identity, and also what I LOVED to do, was gone, but after that surgery and radiation, the cancer was gone too. I was grateful to be alive. In 2009 and 2010 when cancer came back again and again, they took it out without harming anything else even though both were high risk surgeries. And then in 2017 when the cancer traveled to my lungs, well, I’m still here. I have had LOTS of practice, too much practice in my opinion, being devastated and having to focus on things to be grateful for (and not just from having cancer). I’ve learned that grief over what’s lost never goes away, you just build your life around it. Life is NEVER what we expect and most things we can’t control. Grief transforms us and it’s radical gratitude that keeps us soft and hopeful for another day.
I came home tonight from a couple days of travel and broke down. It was the first time in 7 years that I’ve come home from being gone a couple days and my 90lb Moose was not bounding after me, happy and longing for pets and hugs from his human. Ugh, I was so sad..and then I saw a box. It was a care package a friend sent to let me know that she was thinking of me after the loss of my dad and Moose. I cried harder. It was my fairy tale happy ending to the day. That is life, brutal and beautiful. Sure, fairy tales are not real but happy endings happen all the time in the in between. We get to narrate our story, we get to react and grieve how we need to, but practicing radical gratitude is perspective changing. Grief can make us hard or soft and I choose soft because life is too short and too difficult to walk around with that heavy coat of armor. I’ve heard time and again that I don’t look sick. Not everyone who is sick or sad or struggling internally has that on their face, they just carry it in their bodies and hearts. EVERYONE carries some form of hurt and grief from an imperfect life, is it possible to start looking at people from that lens? Yes, and hopefully it changes you and allows for more grace, patience, and understanding. I will caveat this by saying there are still jerks, abusers, and those who cause harm or pain–try to understand where that came from for them and leave it at that; forgive, let go, and radical love them from afar. I’m no expert.
I am still sad, I will be for a long time and it’s ok. I have carried grief around like a siamese twin for years and it has continually broken my heart but I refuse to let it harden my heart. There is still magic. There is still love. God has been so good to me.
I was told that when my dad left for the United States when I was 2 that I stopped talking for a long time. My parents finally got the visa to immigrate to the United States from the Philippines. The plan was for my dad to go first, find a job and apartment and then my mom and I follow. I’m not sure how long afterwards we came (maybe a few months) but I know from my mom that I stopped speaking because I missed him so much. My mom was so worried that she took me to a doctor who found nothing wrong with me.
I’ve been processing my feelings since his passing on February 28th. It was a whirlwind of busy and emotions since taking him to the hospital December 12 for what we thought was a stroke but ended up being brain cancer. Everyday for those 11 weeks brought different challenges and my life revolved around being there for his and my mom’s needs whether it be for appointments, discussions with medical personnel at the hospital, or picking up groceries or my dad’s favorite foods; extreme grief and sadness living alongside beauty and joy. After dropping my sons off at the airport the day after the funeral I wept uncontrollably for a long time, a floodgate of tears held back that started at the funeral.
My dad was a man of few words but his eyes and his ‘look’ told stories; you always knew if he was mad or content, or filled with joy based on his eyes. Although the first thing he lost early on was his speech which became mostly babbling, we could see the frustration, fear, and any other expression just by looking into his eyes. What I will remember most were the quiet conversations he and I had about the kids, what they were up to, the joy in his eyes when I would talk about them and show him pictures. The day we watched AJs graduation from grad school live streaming and his joy while watching but also the pain in his eyes looking at me knowing I missed the event to stay with him. I will remember the miraculous time he called me late at night from the hospital because he didn’t know how to turn the tv off in his hospital room; miraculous because at a time he couldn’t speak, and was confused, but he somehow grabbed his phone, dialed my number, and spoke clearly saying ‘can’t turn off tv’. I was able to call the nurses station and get someone in there to help him. I will remember his giant smile when Roxy the therapy dog came into his room. Roxy was the name of his dog who passed away almost a year ago and by the way, Roxy came at the beginning (December), and happened to show up again his last week at the hospital before going to home hospice. I will remember his giant smile as all the grandkids showed up at the hospital at Christmas time and then his tears of sorrow when he realized it was Christmas and we were all celebrating at the hospital because he couldn’t get home. I will remember singing Nat King Cole to him and him humming along and smiling just a few days before home hospice (and yes, I have that last precious video saved). And I will also remember that last week when it was just the two of us in his hospital room a few days before going home for hospice care and the short conversation: him pointing to his head then pointing to himself and saying ‘better?’ ‘Are you asking me if you’re going to get better?’ ‘yeah.’ ‘Dad, we’re doing all we can so you just keep fighting and getting stronger.’ ‘I hope so.’ I cry thinking about it.
I’ve been searching lately for something that reminds me of my dad, a symbol that when I see it, I know he’s still here. My friend’s mom loved ladybugs so when she sees a ladybug she’s reminded of her mom and feels her close, while another friend has the same thing with cardinals. I started thinking about this days before his death asking, ‘what is it, one symbolic thing that would remind me of him?’ He loved clothes, playing golf, baseball hats but none of these gave me the warm ‘this is my dad’ feeling. Then it hit me. As I was driving home after taking my sons to the airport, I turned on Spotify to the same station I played for my dad in the hospital filled with his favorite artists from the past and I realized my dad gave me music. Growing up there was not a single day that passed that he wasn’t playing records on our stereo; Johnny Mathis, Nat King Cole, Perry Como, etc. On Sunday mornings before and after church he would play classical music like Beethoven and Mozart and he’d pretend to be conducting the orchestra. He played the trombone and harmonica, sang in his church choir, and he took us to DSO (Detroit Symphony Orchestra) at the park. He brought me to my first Broadway touring show, Annie, which started my love for musicals and musical theater. I cannot hear music without thinking about my dad and I am so grateful.
His funeral was beautiful and packed with hundreds of friends and family, he and our family have been so loved. People spoke of his warm smile and how he was most proud of his kids and grandkids. Many of the church choir members outside of the small funeral choir, came to sing at his funeral and I know my dad would’ve been so proud. I can still see his face proudly singing and grinning with joy. What will I miss most? Seeing his smile, laughing with him through his jokes, and his laughter and joy when I’d speak about the kids. Also, ever since I learned how to drive until even just a month or two ago, whenever I would leave our house and then their house he’d stand at the storm door and watch me pull out of the driveway. Every. single. time. A man of few words, that’s my dad, expressive eyes, a big smile, funny joke, laughter, and always always a song.
Cancer and I met almost 15 years ago; a youngish mom, 3 young kids.
She (cancer) came back to visit again and again until finally she came to live; she decided my body, my home was also home for her and she decided to take up more space..different ‘rooms.’
Now we live together. I know she wants to fully take over all my living space, but every few months I get confirmation that she is still sleeping in the different rooms she came to stay in 5 years ago. An unwelcome visitor to my home, my family, my body, my mind. Time marches on. The young kids are now young adults and a mom with cancer is all they’ve known.
6 weeks ago cancer came to visit my dad; a bigger, badder relative of my cancer. It’s been hard. The chemo regimen is rough. I now live with cancer and am caregiver/helper to my dad…and my mom who’s tired both mentally and physically.
Cancer is that unwelcome visitor that wants to stay. It’s rude and inconsiderate of peoples time and feelings. It has a ripple effect beyond the singular person; the reach is wide affecting family and friends.
But why? But also, why not? All of it can be maddening. I get sad then angry then tired, but now playing all the roles of cancer fighter and caregiver, I’m mostly tired.
I used to view hope as the long game , the ‘hope for a better future’ kind of deal, but now I know hope lives very much in the present moments. It’s in the friends that reach out, the ones who leave a small gift on your porch, the nurse that brings that extra cup of ice water, the PA who calls you on a weekend to see how you are, the stranger at the hospital that sees you crying so they sit with you a minute and offer a prayer, and even the dog who puts their face in your lap wanting pets. Yes, hope is present.
Cancer or any long term medical diagnosis puts mortality at the forefront; reminds you that your time on earth is finite so what do you do with your time? It has changed my life. Some of the things I thought were big deals are not so big and actually some of the smaller things, small moments, matter the most. Time is our greatest commodity. The words faith, hope, and love are always thrown around and sometimes flippantly but when you live devastated, hopeful, and grateful simultaneously, those three words are fully alive and pretty much carry you day to day.
This World Cancer Day, be kind, practice love, say a prayer of gratitude for being alive, and hug your loved ones extra ❤️
It’s a New Year and the past month has not been an easy one. My December story was going to be one filled with joy and reunion. Literally a month ago we were putting up our Christmas tree and decorations, my excitement for my three kids to come home was building since I hadn’t seen two of the three since August and none of them could be home for Thanksgiving. Also, we had a quick trip planned to Florida because my firstborn son was graduating with his doctorate two weeks before Christmas. My December was going to be amazing, but the story changed. The morning of December 12 we brought my dad to the hospital because we thought he was showing signs of a stroke and a few days later we found out it was brain cancer. In a few short days and the day before my son’s graduation, my dad’s health took a major turn for the worse and I had to make the difficult decision to not attend. My heart broke in a thousand pieces both for my dad and for missing a major milestone of my son.
On Faith. I had a friend ask the other day, ‘With everything you’ve been through, how can you not be mad at God? or do you ask God why?’ My answer? ‘I don’t get mad at God, I get mad at people saying dumb things. Making assumptions about what God’s intentions are or what His thoughts may be, making Him actually smaller.’ The God I follow would not create a story of hardship to teach you a lesson or to increase your faith the hard way. Does God give His strongest soldiers the hardest battles? I sure hope not because what does that even mean? No. The God I love and follow holds our hand through hardships because life is hard sometimes. God to me looks like kindness, generosity, laughter, that phone call, God is all around. The Jesus I follow is one of love, compassion, and mercy no matter who or what. The Jesus I pray to brings me peace and comfort because I believe He hears me. I read somewhere that the opposite of faith is certainty. I don’t need to have all the answers, I don’t want them, but I will continue to listen, question, read, and learn. I love my kids so much that I would do anything for them, does God love you less? I will not give up on God or my faith but there are ‘whys’ we will never be able to answer and me personally…I’m ok with that.
On Joy. Fr. Ken Tanner said this in his sermon last weekend (I’m probably paraphrasing), ‘Joy–in the midst of life you see something that reminds you existence is good, God is good. Despite the circumstances life is good and experiences are worthwhile. Happiness is fleeting and circumstantial.’ Despite the circumstances of the last month, there were MANY moments of joy and that is where I want to live. Although we weren’t able to go to AJs graduation, we were able to watch virtually and when my dad watched him cross the stage he pointed in recognition and cried. Christmas was spent in the hospital but having everyone there was again such a joyful moment. There was the day when my dad was finding his words again and when the PA asked him how old he was he said ’25’ followed by him chuckling and saying ‘kidding’. Then twice, the therapy dog that walked into the room was named Roxy, the name of my dad’s dog that passed away over the summer. The first time Roxy came in there was a parade of dogs in the hall that my brother and I were watching but she was the one that turned toward the room. Many have chosen a word of the year and I usually have a word or two but this year I have more of an intention: seek tiny joys. So many joy moments reminding me that simply existing was good and that God is still so good.
On Hope. Anne Lamott says, ‘Hope springs from that which is right in front of us, which surprises us, and seems to work.’ What does that even mean? To me it means I woke up to another day of life. It looks like a hot cup of coffee, an unexpected gift, a word of encouragement. Hope looks a lot like love. Anne Lamott’s words once again, ‘Against all odds, no matter what we’ve lost, no matter what messes we’ve made over time, no matter how dark the night, we offer and are offered kindness, soul, light, and food, which create breath and spaciousness, which create hope, sufficient unto the day.’
Enough of my babbling. I’m grateful for life, for having my kids home even though it wasn’t exactly the way we had planned. I’m grateful to be married to someone who has been by my side and helping me navigate through the most horrendous things (my Stage 4 cancer diagnosis, my son’s stroke, and now my dad’s health crisis all in the short time we’ve been married). I’m grateful that I’ve had a job that helps me understand medical language and my own diagnosis to help me advocate better for myself and my dad; for a great boss, great friends, the Instagram friends that emailed me Starbucks gift cards, notes, and even small care packages. Tomorrow I have my 6 month PET scan because I still have cancer. The good part is that because of what happened with my dad I forgot all about it and did not have to suffer from my regular two weeks of scanxiety, the bad part is that from now until I get the results on Friday I will have scanxiety. This is my story, This is life.
I had to look back to see the last time I wrote a blog, and it was July, just after I got the results telling me that my cancer was still stable after 5 years; those dumb nodules on my lungs are not really growing or at least not growing very quickly. I’ll take it. Writing has always been a release for me and a way to process my feelings, but this year it’s been tough to write, and I think maybe it’s because I have too many feelings to process. Before, it was just having cancer 4 times, motherhood, divorce, a child with a life changing health event (which was already a lot), but then the pandemic started and kept going, and I became an empty nester and then menopause, all the things politics, shootings, and absolute craziness. I have relegated myself to 3 bullet points in a journal highlighting 3 specific things I am thankful for each given day and sometimes that’s even hard. I recently read a book by Susan Cain called Bittersweet and boy did that speak to me. It’s a book about people with a more melancholic personality, ‘a tendency to states of longing, poignancy, and sorrow; an acute awareness of passing time; and a curiously piercing joy at the beauty of the world.’…Bitter and sweet are forever paired. Remember my word for this year was ‘AND’ because life was beautiful AND brutal, light AND dark? This book was validating and so me.
What does it look like as a Stage 4 cancer fighter on her 4th recurrence in 14 years to have an acute awareness of passing time? Pretty shitty, and yet…And yet there is so much beauty. And yet there is so much love from friends and family members and sometimes even strangers. And yet the time we do get to spend with family and those closest to us seem even sweeter, so although we don’t necessarily like ‘just be grateful and move on’, we can be grateful for another breath to keep moving forward. Moving on is different than moving forward. It also helps to seek out those things of beauty and be purposeful when it comes to finding joy.
I miss my kids. Being an empty nester is bittersweet to me, it’s great until it’s not. I’m happy they are all thriving and growing to be amazing adults, but there are days when the ache in my heart to see them, hug them and be around them is so overwhelming I can’t catch my breath. It doesn’t help that seeing them requires at least a 3-hour airplane ride and 2 of them are currently in two different time zones. And yet, they are thriving. And then, I remember my mom having to let go of me and my brother as we grew up and moved away; and her mother saying goodbye to her as she and my dad moved to the US, a different country; those who’ve had to send their kids off to war, and of course those who’ve lost a child, so many goodbyes and yet…
Tomorrow will be my first Thanksgiving EVER not having at least one of my kids here and not gonna lie, I’m pretty sad (although I got to see and spend time with my oldest last weekend). It’s the ‘take my breath away if I think too much about it’ sad but it’s just a day and I’ll see them soon. Also, that acute awareness of time plus having cancer is not cool. So tomorrow I may still cry, but it will be that perfect mix of sadness they’re not here and gratitude for life and living.
I’ve had lots of conversations about faith over the past few months and it’s been quite the journey. Here’s what I know, because of the pandemic, all the things happening in the world (including our own backyard), all the divisiveness, cancel culture, etc., people are asking questions. People are searching for truth but not pat phrases, bible verse responses, religious lingo, Christian-ese, etc…Truth in ACTION. Love in ACTION. Kindness in ACTION. Is that a tall order? I hope not. I will never abandon my faith, but I will continue to question rules that are manmade, those whose actions don’t match the love they speak about, and words and stories taken out of context to ‘win’ something when there are no winners and losers, just people trying to feel like they matter and that are loved. How do we love like Jesus? I’ll stick with that.
Five years ago this month I got the devastating news that my cancer was back for the fourth time, but it had spread to my lungs putting me in the category of Stage 4, Metastatic thyroid cancer with distant metastasis. This is rare, occurring in less than 10% of thyroid cancer patients. The statistics are not great; 50% gone in 5 years, 90% gone in 10. I did molecular testing on my tumors and they showed the BRAF v600 mutation (lots of science) but basically, cancers with this mutation tend to be more aggressive. For the first 2 years post diagnosis, I got scans every 3 months, and since scan after scan showed stable disease (tumors still there but not really growing), my scans were spread out to every 6 months alternating between CT and PET scans.
What. A. Ride.
Last Saturday I had my 6-month scan which was delayed from June because of a nationwide CT contrast shortage (yes, there’s even a supply chain shortage on that). Monday, my oncologist sent me a text that everything STILL looks good!! STABLE! I made it into the 50% of patients STILL HERE after FIVE YEARS (Although I know there have been major strides in cancer care in the last 5 years so hopefully the stats are much better now). 5 years ago my youngest son was going into the 9th grade and all I longed for was to be alive at his high school graduation and here he is about to start his sophomore year in college. Now the longing extends to weddings, and dare I say grand babies?
How has my life/perspective changed in the past 5 years? That’s a tough question because my cancer journey started 14 years ago. I feel like cancer has been riding my shoulders forever but the last 5 have been the hardest. Not only the statistic constantly looming in the back of my mind, but that youngest child of mine had a stroke 2 years after that diagnosis, then the year after that we headed straight into this worldwide pandemic. Moving into 2022, I’ve really struggled. The whole ‘being brave and strong and keep pushing forward’ seemed too much and all the stored grief upon grief punched me straight between the eyes. I learned that the research done by Elisabeth Kubler Ross on the stages of grief were mainly on dying people and that we could not apply those same stages to the living. The living has to LIVE with that grief because it is entwined in our bodies, hearts, minds, etc. There is no ‘check the box and be done’ checkmark for denial, anger, etc leading to acceptance, while we’re alive we just weave in and out of those in no particular order. So, some of the lessons?
Grief lives with us always, but it teaches us about ourselves, as well as our capacity to love
My faith has become so simple; I believe, and love God and I want to love how Jesus loved. That’s it. Faith is not a building, denomination, or ‘being religious’. (I have lots of thoughts about faith and maybe I’ll write more in a later blog)
Love lives in the small things, the in between moments of eye contact, lunch dates with friends, a hug, an encouraging text, etc
Life can change in a blink of an eye
You can’t stop time so make the most of those minutes. Stay present and notice.
Those are just a few things that come to mind. This year in particular I’ve been the angriest, and the saddest more than I’ve ever been. On a recent podcast, the speaker compared life these days to a tsunami. After the big earthquake a tsunami happens, then it’s waves and waves of aftershocks and destruction, but over time, the waves die down, then things slowly heal and become normal again. We just went through and are going through a global pandemic with the first hit in 2020. The aftershocks and waves are still happening giving us no time to heal; not just waves of Covid surges, we’ve had a war start in Ukraine, civil unrest, mass shootings, so so much. My ‘earthquake’ happened in 2017 with my Stage 4 diagnosis. We have had no time to heal.
Look up
I don’t mean to be trite but one day I was driving in my car, crying (which has been my norm over past months), and completely overwhelmed. After stopping at a stop light, I looked up. The sky was so blue and vast, and I was reminded of how small I was, literally just a speck in comparison. If you haven’t seen the latest images from the James Webb Space Telescope look them up. The universe is SO BIG. Looking up helped me feel better. Looking up reminded me that the God I believe in is SO BIG and that I am so small. That there are numerous unanswerable things in this world and it’s all a hodge podge of joys and sorrows but ultimately, I am so small in this ginormous universe and have very little control if any, of much of anything.
I listen to a podcast hosted by Kelly Corrigan called ‘Kelly Corrigan Wonders’. Every week she does an interview one day, reads an essay she wrote another day, then reads someone’s obituary on yet another day. All of her podcasts are great but the 5-10 minutes reading of someone’s obituary has had the most impact on me. Every week I get to hear a summary of someone’s life written by someone who loved them. All of them speak of the type of person their loved one was along with a smattering of examples like ‘he/she was the life of the party’ or ‘they would literally give the shirt off their back to a stranger,’ but what makes me catch my breath are the simple memories and the small moments like, ‘she made pancakes every Sunday’ or ‘I always came home to a hug no matter what.’ None of the memories spoke of grandiose events or big family trips. Love is in the small moments. What would you like a loved one to write in your obituary about you? I think about that all the time now and try to be that person while I’m living.
I live with Stage 4 cancer as a chronic condition, much like someone who has diabetes or Crohn’s disease. It feels like a double life or split personality most of the time. Acting normal, working out, going out with friends, enjoying life, but every farther future decision is tinged with the question ‘but will I still be here?’ While every daily decision as tinged with ‘is that how I want to spend my minutes?’ or ‘Does that buy me more time with people I love?’ For now, I don’t get to say that I fought cancer and won, the before/after narrative for me is before/during. But gratefully saying I’m stable and ALIVE after 5 years is more than enough 🙂
We just moved. It’s been a lot and I didn’t think it would be, but so many changes have happened over the 2+ years of pandemic. I can’t seem to push past some of the sad days but there have been so many good ones. Warning, this may be a super rambling blog, so sorry not sorry. I’ve had lots of thoughts swirling in my mind so I’m writing to actually clear it up and put it out there. First, it’s Lent. Last year I did some amazing Lenten devotionals (from Kate Bowler and Erin Moon), and they were so helpful in quieting my mind and keeping my heart in focus of the season. I grew up Catholic and was ‘taught’ to give something up during Lent; a fast to remind you of the 40 days Jesus spent in the desert leading up to His death.’ Last year, I decided to partake in this ritual of fasting and give something up. This year, as I was prepping for lent, I downloaded and joined a few Lenten devotionals from people I love following, Kate, Erin, Sarah Bessey and had full intention of following and partaking in a sort of fast again. DID NOT HAPPEN. I read a beautiful article right before Lent (thanks Erin) that really resonated with me. The author spoke about her difficulty finding something to ‘give up’ this year and she asked, ‘over the last 2+ years of pandemic, haven’t we given up so much already?’ We’ve given up the false security that we are invincible (maybe that’s a good thing). We lost time with friends and loved ones, and many people even lost loved one and weren’t able to have a proper goodbye. We’ve lost jobs and safety, trust and confidence and to some extent, joy and maybe a little sanity. It seemed irrelevant to give up social media, chocolate, or whatever, when we’ve gone a strong 2 years giving up one thing after another. However, it is Lent, and I love Jesus. In Barbara Brown Taylor’s book An Altar in the World, she talks about altars everywhere we go and in everything we do, so to live with purpose, slow down, pay attention; to be in constant prayer, not just ‘making time’ in your day to sit, read, and pray. What does that look like for me? Waking up and walking to the coffee maker in the silent, dark of morning and praying, being aware of the sun and rain and grass and flowers of spring, and praying, being in conversation with a friend or a child and praying for them while in conversation. Lent for me this year has been living in prayer and remembering God is always there (and also, on occasion reading one of those devotionals).
Second topic, we moved. I don’t usually get attached to homes or physical objects and I’ve never been emotional over a sale of a house, even my childhood home. I have always loved the idea of a different place, reinvention, scaling back, etc, but this one hit me hard. It didn’t happen right away. In fact, I was excited to downsize, save money, and move onward as empty nesters. Most of the kids had taken much of their things to their college/grad school apartments, in fact, AJ, the oldest literally only had his winter boots and coat left at the house. Then came the youngest, Alex’s room. His room was the same as when he left for college. The posters were up, the desk still had pens on top and notecards in the drawers, his closet had clothes, shoes, and a couple backpacks in their regular stack; it felt like another day and that he would just walk in after school and plop onto his bed. Then, still in the plastic hospital bag from when we left the hospital after his stroke in 2019, were the hundreds of notes and letters from his friends and well-wishers; reminders of that dark time that transitioned into a time of strength and healing. Packing up his room was the first ‘break of the dam.’ So many struggles, so many memories.
The piano. As discussions were had about what we would move or not move walking around the house, the piano came up. At first it was a non-negotiable even though, as Jim reminded me, I haven’t touched it in a long time. It was coming with us, and we would find a space. I have not been without a piano since I was 7 years old and maybe it had become a source of comfort and my link to my musical past. When Alex was in elementary, he even wrote a short assignment for school and talked about how my playing and singing would bring him joy and comfort so yes, it was coming. The weekend before the move Jim headed up north to bring some tools to the cottage and I sat at the piano to try to play. Cancer took my singing voice, but I had the piano. Over the years after all the surgeries and radiation, I’ve developed neuropathy in my left hand and arm to the point that I can’t really feel my fingertips. Sometimes it’s manageable and at times, it’s not. As I sat at the piano and tried to play that particular day, my fingers would not cooperate and actually sent more numbness and a little pain up my arm. This was the second ‘breaking of the dam’. I was heartbroken, hated cancer, and was now willing to NOT move the piano. It was Jim who said, ‘don’t give up on it yet’, so the piano moved and sits in a small corner of our even smaller home.
We gave up the keys to our house less than a week ago and over the weekend I flew to see Alex in Arizona for his mom’s weekend. I’m so grateful I got to spend time with him, and I decided, with the kids gone and mostly farther away, when they ask, I want to be there. The move was hard not because I loved the house or the ‘things’ inside of it, but because of all the memories. It was a house of safety, love, joy, and new beginnings for me; a place where I could mostly be myself and breathe. No, it was not all roses. We raised 5 teens in a blended family, Alex had his stroke, I got my fourth cancer diagnosis and Stage 4 on top of that: so many challenges but also so much love and support.
As far as the empty nest thing, what’s made it so hard for me is time and cancer. My same story. What actually helped me came from the show ‘This Is Us’ (spoiler ahead if you haven’t caught up to the current season). In a recent episode, Rebecca (the mom) who has early onset Alzheimer’s sits her adult kids down at a table and gives them a speech. I’m paraphrasing but basically she says, ‘Don’t let my illness make your world smaller. Take risks and live your dreams.’ It was a HUGE mindshift for me and I come back to that phrase when I get sad missing my kids. I will confess that I’ve used the phrase ‘don’t be mean to me, I have cancer and you don’t want that to be your last phrase/feeling/sentiment to me.’ Awful I know but sometimes I just want to hold them so tight. But, I too don’t want their worlds to become smaller because of me so here I am. This morning I did a meditation from Sarah Blondin and she talked about the constant tension of life between resistance and letting go. She said,’ Why hold on to the stones at the bottom of the river when you just want to be the water that flows freely?’ I want my kids to think of me and smile, feel loved, seen, and safe because they feel free and not burdened by my own expectations, sadness, disappointments, or my own pain. Heck, I want to be free of that too. How? Remembering that tension will always be there and that life is never perfect but is always beautiful. Thank you Jesus.
I feel better, not sure if you do. When is life not changing? Just like a river, it’s not always flowing peacefully, sometimes there’s rapids. Life is full of OMGs and WTFs but also full of love, joy, and moments of peace. I am so grateful I get to feel the gamut of emotions because that is living and that is growing and that is what it means to just be present. I am grateful for all of it.
It has been a LONG time since I’ve written a blog post and honestly, I wasn’t sure if I would ever write another, but here I am. The last blog I wrote was right around the time Alex left for school making us empty nesters. Since then, I’d like to say that I’ve enjoyed all this ‘independent time’ not having to think about meals, sporting events, clothes for homecoming or prom, etc., but I haven’t. For the last 6 months I’ve been mostly sad. Not only are we in what seems like an endless global pandemic, but I also have cancer; both pointing toward a daily life of uncertainty. Time is my love language so having the youngest leave the house meant that that phase of motherhood and seeing them more often than not, was gone. Cancer already opens your eyes to your mortality so any less time with those you love is exactly that, less time. HOWEVER, I do realize that our job as parents is to grow independent kids and cheer them on as they learn to fly, so I guess I’m sad AND happy.
In the past 3 months I have been to 2 funerals; one a friend from church and the other, wife of a childhood friend that I grew up with. Both women younger than me, both moms, and both passing away from cancer. A friend of my husband’s passed away suddenly, another friend’s dad passed from cancer, and another friend’s young (younger than me), healthy boyfriend passed away just last week. All within the past 3 months. Time is our most precious commodity. Faith in a big God is still my peace.
What now? The pandemic is still raging. I still have cancer. People are struggling. All people are struggling. I am still mostly sad but getting better. All of the kids were home for the holidays which brought me so much joy and watching them come and go and ‘do their thing’ helped me be grateful for where they are AND where I am in life. We can start there, gratitude.
I don’t do New Year’s Resolutions but for the past few years I have picked a word of the year. Last year I chose the word ‘simple’ and it was so helpful. It became a mantra and reminder for me to keep things simple and to really focus on simpler solutions. I had it on a bracelet, and I printed it on the opening page of my planner and journal. This year I have chosen 2 words and they’ve already been SO helpful. My first word is Kairos. There is linear, chronos or chronological time and then there’s Kairos, or my definition of those magical moments not necessarily confined within those minutes. Glennon Doyle has written, ‘Kairosis God’s time. It’s time outside of time. It’s metaphysical time. Kairos is those magical moments when time stands still.‘ Since cancer I have always sought after those magical moments and now more than ever, we need the magic.
My second word is ‘AND’. I chose this word because with most things in life, two things can be true at once. Life can be beautiful AND brutal (an amazing full life AND cancer). I can be both sad that my kids are gone AND happy that they’re becoming these healthy independent adults. We can be grieving lives we thought would be different AND still find joy and laughter. We can be disappointed AND still hopeful. We can be scared AND still be brave enough to take that next step forward. For me, focusing on this simple word has been so powerful. If we can remember that there is an ‘and’, it makes lots of things feel more ok…well at least it does for me.
Have you chosen a word? An intention? We have one life.
Anna's Lipstick Journey 