Tag Archives: motherhood

Stable, Year 7

31 Aug

A couple of weeks ago I had my scans to check on the multiple cancer nodules housed in my lungs. It has been almost exactly 7 years since I was diagnosed with Stage 4 metastatic cancer and I’ve had scans every 3-6 months for SEVEN YEARS. STABLE. I usually greet the news with overwhelming relief and crazy joy but this time was different; still relief but with maybe more contemplation? I’m still processing the news and why the ‘celebration’ felt different. I’m thinking about what it has meant to be stable all these years and how it’s changed me and my perspective, how I’m living, and maybe how I want to live going forward. I cry thinking about how the word cancer first changed MY LIFE 16 years ago and how the words ‘Stage 4’ changed ME 7 years ago after wrestling with cancer two other times in between. 

We talk about gratitude a lot and I want to say I’m more grateful, but am I? I don’t want to have to think about cancer anymore. I don’t want to wonder if my next scan will still be stable or if I feel ‘off’ one day that my cancer is spreading, or if it’s humid and the air is heavy and I have a harder time breathing if it’s more or growing nodules in my lungs. I don’t want to wonder if I will make it to a child’s wedding or meet my first grandchild. I also don’t want to grieve what might be and miss what is. I know none of this is in my control and that there may be other factors that take me out, but cancer is what’s in front of me or should I say inside of me. I’m tired of the cancer dance. I’m tired. But yes, I’m still beyond grateful because without the weight of it, I would maybe miss the magic around me or waste even more time and air stressing about stupid stuff. I’m still tired.

The concept of impermanence is hard but living in duality may be even harder; making decisions can feel heavy, caught between I don’t care and I care too much. Talking and saving for retirement and but can’t focus on anything but today, planning for the future but wondering about the scan results six months from now, etc…it stinks. ‘I don’t care’ is my brain saying ‘I can’t process that right now’ or ‘does not compute’.

I’ve changed. Quality time has always been my top love language, but now it’s exaggerated. If I have a chance and the funds to see my kids, I will go. I want to surround myself with people whose joy is contagious. I crave community because the richest person in my book is one that’s filled with love, laughter, and time with family and friends. I will continue sharing my story and being vulnerable in hopes that it allows whoever else to be vulnerable with theirs. We learn from each others’ stories and vulnerability makes us more human. The perfection we see on Facebook and IG is mostly fake, fills us with fake longing, sometimes shame, envy and sadness that we don’t have what the picture shows us when truly the picture is just a picture. It’s flat and missing the three-dimensional parts of peoples lives. I’m softer, my heart feels like mush and I cry sometimes over the simplest of things. I’m also harder, I’ve learned to say no a little more without the guilt behind it. I don’t want to struggle or people please anymore to get attention or be included because time is too valuable and how exhausting is that?

The world feels like it’s on fire; people are more short tempered, judgmental, angry, self centered, and just ‘harder’ or hard hearted in general, unwilling or afraid to cross the lines or even share the lines of what they think how things ‘should be.’ Well, we all suck and I’m no better, but I don’t want to be one of those grouchy people, it’s such a waste of precious air.

I’m learning to embrace the impermanence of life even though it was by force (or I should say by diagnosis). No one gets to live forever. In a book I recently finished it said “That time always ends a second before you’re ready. That life is the minutes you want minus one. -The Invisible Life of Addie Larue, by VE Schwab. There’s no best time, no one’s ever ready. 

Hope. Hope to me shows up when an adult child texts me that they love or miss me (without my prompting), when someone shows kindness, when my dog looks at me and tilts his head like he’s paying attention and understands everything I say, etc. Hope is tangible, it’s simple and it’s always in your face when your heart is broken enough to let the light in. My heart is broken. It’s not a bad thing, it just means it’s tender and has lots of space for love, joy, hope, and empathy. Yes, grateful for that too.

Life is short. God loves me, Jesus carries me, that’s my solid. I’m reminded of His love and goodness constantly. My cancer is stable. 6 months from now it may not be, or maybe it will be for the next 20 years, who knows? Today I will breathe in life and take this word stable and add it to my bank of hope for however long it carries me.

Life is brutally hard & still holds holy beautiful holy moments & we are all standing on the edge of more joy, more wonder, more awe in God, who carries us through all the waves of heartache and heartawe, and into the expansive love of His heart.’~ Ann Voskamp

The Voice

26 Apr

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.

(Catch the entire concert here: WVD)

Producer, Director, Audience

3 Oct

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

Hello 2022

19 Jan

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, ‘Kairos is 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.

Empty Nest (yes I’m crying)

18 Aug

By the end of this week I will be an empty nester. Who came up with that name? I don’t think I like it. Plus, if it’s being compared to a birds nest, that implies they never come back. Am I wrong? Also, don’t mama birds shove their babies off and force them to fly when they’re ready? Ok. There were/are definitely times I’d love to shove the kids into the world and force them to fly but there are times I equally if not more, want to hold on and squeeze them in a hug and force them to just stay near. ‘The greatest gifts you can give your children are the roots of responsibility and the wings of independence.’~ Denis Waitley. Yes, yes, sure. I am not afraid of being an empty nester, it’s actually exciting to think the house will be more quiet, the tv/kitchen/couch will be just ours, our grocery bill will be significantly less (and I won’t have to think too hard about pleasing everyone for dinner), we can be more spontaneous, whimsical, and maybe even walk around in our underwear in our middle aged bodies.

I have been swallowed up in mixed feelings since Alex’s graduation last June, knowing he chose a college 2000 miles away and that this day would be coming sooner than later. I want to say that Alex is my hardest goodbye but I can barely remember launching the others so I know I’ll be ok. Alex is the baby and that in and of itself makes it harder. I was first diagnosed with cancer just as Alex started kindergarten and am now in my 4th recurrence. I was diagnosed as Stage 4 cancer when Alex was about to start his freshman year and I remember praying to just be alive to see him graduate high school. He has pretty much only known his mom as a mom with cancer. I’m still here, cancer has been stable since then but life was not easy within that 4 year period. Two years ago this month, Alex had a stroke and was right side paralyzed. In fact, almost everyday this month a memory has popped up on FB or in my google photos and it is of Alex at the hospital. This was the week, 2 short years ago, that he started moving his right arm and right leg again. Pictures have come up from the prayer vigil at his high school, of friends sending me encouraging videos, and of the night his friends gathered outside the hospital with flashlights and banners for him to see from the windows from his hospital floor. I lived at the hospital for 6 weeks and it wasn’t for me, it was for the child who is now ‘flying away’ and who had to fight hard both physically and mentally. Every memory and picture brings a flood of emotion. This is a hard goodbye.

A few nights ago we took a packing break and he laid down facing me on his bed and said, ‘let’s just talk.’ As I lay there facing him, I burst into tears. At the hospital, I would be in the exact position, staring into his eyes and praying at first for him to survive, then that he would just get better. I bargained with God to take me instead, after all, I was the one with cancer; the one who should be in the hospital bed. I remember the very last night at the hospital, looking at each other and both weeping about all that had happened, and expressing fear over his future and what leaving the safety of the hospital meant. I could not hold back the tears being in the exact same position looking in his eyes, I guess I have PTSD. All he said was, ‘Don’t let my last moments home be sad, be happy for me.’ I am ecstatic for him…for real!

As I try to process the last one leaving the house, I know that it’s not the fact that we are becoming empty-nesters, it’s the fear of an unknown future for both of us because of our health ‘scares’. I am also filled with questions about whether I was a good mom or not, did I help guide them on the right path, will they be ok and if they’re not, are they strong enough to ask and seek help, so many questions but I know I did my best. It seems the most random things melt me into a puddle of tears like the face to face talk, bringing something to his room and realizing he won’t be in it anymore for a long while (and then less and less), seeing the bag of almost 200 notes and letters he got at the hospital, the stupid picture memories that keep popping up on my phone, and even the random food items that only he likes that are still in our pantry and fridge. I know that as time passes these feelings will soften, he’s not the first kid to leave. It’s just another reminder that time goes so fast and to make each moment count. ‘Making the decision to have a child is momentous. It is to decide forever to have your heart walking around outside your body’.~Elizabeth Stone.

I learned after the first one graduated high school and left that raising kids is a long series of goodbyes and as they learn to ‘adult’, we learn to let go. Now I prepare myself once again to have my house as a place he visits instead of a place he lives and to leave another piece of my heart someplace else.

‘If you would have your child to walk honorable through the world, you must not attempt to clear the stones from his path, but teach him to walk firmly over them-not to insist on leading him by the hand but let him learn to go alone.’~Anne Bronte

Caregivers

9 Feb

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I found out a little over a week ago that one of my caregivers has cancer. She was diagnosed a few years ago and it has returned with a vengeance. I met her when I first got cancer in 2008 and she was integral in my healing process both physically (helping me regain my voice) and mentally because she is one strong woman. She pushed me hard to help my healing and I am so grateful. A few days ago I found out another strong woman who has cared for me and my kids was just diagnosed with cancer as well. The news made me sad because you just never think the people who have made it their job to care for you and others would ever get sick themselves. Cancer is a bitch (excuse my language but it just sucks).

Over the past 11 years with cancer I have been a patient at a few different institutions and have had img_6957amazing doctors, nurses, and support staff. About 4 years ago one of my original doctors that helped navigate my cancer journey retired and I cried my eyes out.  He was the one who called me with the news that my cancer had returned the 2nd and 3rd time. He researched new therapies and called different surgeons and oncologists; this busy doctor made me feel like I was his only patient for the 6 years that I saw him. I love all of the people that cared/care for me. What a difficult job they have trying to comfort and encourage patients, while also doing their jobs and what’s medically necessary. The impact that caregivers have on our lives is pretty astounding. Having cancer comes with baggage; fear, sadness, uncertainty~ it’s a dark time and medical staff play an important part. No matter what is happening in their lives they are tasked to care and love hard. Dr. M and Dr. D, my prayers are with you and I love you both hard.

February also marks 6 months since Alex had the stroke. He is doing remarkably well! After having full right side paralysis, he’s now walking, driving, and back in school facetune_05-12-2019-17-31-34part time getting all A’s. He still gets a little tired writing but that is coming along. Here’s my mom struggle…before the stroke he was a normal teen boy doing the push and pull; the pushing of my nerves while trying to pull away into his own adulthood. I get it, I’ve had to let go of my other two and that’s how it goes. After the stroke, he became my baby again. It was an incredibly difficult time and sometimes when I close my eyes I can still see him lying in that bed in the ICU and it makes me cry. There are things I can’t even talk about without choking up including the last night we spent at the hospital together, praying, crying, and talking about all that had transpired, before img_6960being discharged to come home. Now that he’s about 95% back to being a normal teen boy, there’s that push and pull again, and I have to relearn it. As one radio DJ said, it’s like a hard break up. For me it’s like breaking up, getting back together, then going through an even harder break up again. Makes me sad but I know it’s necessary. Motherhood is hard and time flies. Besides Alex, my oldest is graduating college in a few months and planning grad school farther away, and Audrey is studying overseas this whole semester. It’s a mixed bag of sadness and joy.

I was a guest on another podcast last week and the topic was hope. She asked my definition of hope which I responded that it’s knowing your mission here on earth is not yet finished. It’s looking forward to another day with the expectation of something good despite your circumstances. Hope is the active response to gratefulness, recognizing the beauty of what, and who surrounds you.  The month of January my lipstick company, The Lipstick Journey, did a ‘buy one/give one’ to a cancer thriver and it was amazing. I got stories and emails and pictures of people across the country. I got to write notes of encouragement with every lipstick I sent. This is the mission that gives me hope and the motivation to keep my lipstick company alive. What else gives me hope? My faith in God knowing He’s ultimately in control, and people. Despite what we see on the news, the ugliness of politics, and people still judging others, there are kind people all around that want change and want to be helpful. I’ve seen it and felt it. When you’re sick or in need, people rise up. That’s hope. We are all caregivers. Be kind and love hard.

‘Hope is like the sun, which, as we journey toward, casts the shadow of our burden behind us’~S Smiles

Weary

16 Sep

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Alex (and I) left the hospital a little over a week ago and it’s been so good to be home. He’s been getting better at hyper speed and it’s been amazing to watch and honestly, pretty miraculous. He still has some work to do but his recovery has been phenomenal and I am beyond grateful. The Monday after we came home I had my appointment with my oncologist and just like that, I was back into my ongoing cancer journey.hospital

This past weekend Alex spent some time at his dads and it was the first time since the stroke that I wasn’t around him. It made me a little anxious to be away from him but gave me time to sit and digest everything that had happened over the past month and a half. I’m tired, but more than that, I’m exhausted and soul-weary; physically, mentally, and spiritually. Over the past 10 years I have fought and beat cancer 3 times and am now fighting for the 4th time, Stage 4 metastatic…then Alex has a stroke. That doesn’t even include divorce from a (still) difficult ex, remarriage, step-kids, new jobs, moving, sending kids off to college and all the daily obstacles ‘normal’ life brings. I. Am. Tired. I picked up a couple of my old journals, one from almost 20 years ago and one just 5 years ago and both were filled with so many struggles but all my entries ended with ‘thank you for…’ I have never asked God why I got/have cancer, I did ask why Alex had a stroke, and I have asked why life just can’t be easy for awhile because there always seems to be something, and that something has felt enormous (cancer, stroke). God didn’t promise easy. If you’re familiar with the Bible at all, NONE of those stories point to easy. But still…

‘The world breaks everyone, and afterward, some are strong at the broken places.’~
– Ernest Hemingway

When I was first diagnosed with cancer 10 years ago, there was a time when my prognosis was not great, and while I was praying one night I audibly heard God say ‘trust.’ Maybe it was in my head, but it was an interrupted thought and just the word ‘trust.’ Since then, that has been my mantra, trust Him. I am not questioning my faith because man, without faith in these trials I would be flailing. In fact, I believe I can still stand strong because I am trusting God to hold me up. I am not alone in this crazy thing called life. I do feel at this moment like my soul needs refreshment. It feels heavy, sometimes sad, and honestly it feels harder right now to find a thank you because I’m just tired; tired for my child, tired of fighting cancer. Matthew 11:28-30 ‘Come to me all who are weary and burdened, and I will give you rest.’ I am craving that rest, not just sleep, soul rest and refreshment. Psalm 71:14 ‘But I will hope continually and will praise you yet more and more.’ Small steps, Big God.

alex homeIt was a tough 6 weeks. What sustained me and gave me energy? Love. Love is a superpower; love beyond any words, love that took action. My fierce momma bear love gave me the energy I needed to take care of Alex and to be there fully for him. The crazy love I received from my home team: my husband, kids, parents, friends, Alex’s friends and teachers, the parents of Alex’s friends, etc, helped sustained my spirit and kept me secure that yes, the world at home and around me were also taken cared of. The love Alex and I felt from the nurses, staff, work friends, acquaintances, and even wishes from social media strangers was incredible. Love does make the world go round and life always moves forward. ‘It is good to love many things, for therein lies the true strength, and whosoever loves much performs much, and can accomplish much, and what is done in love is well done.’~Vincent Van Gogh

 

Courage

28 Aug

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This has been one of the toughest weeks in the hospital with my son. As you know from my last blog, my 16 year old suffered a stroke on August 2nd. Since then he went from the ICU to a step down unit, to in patient rehab. He has made TONS of progress in terms of speech and his right side gaining movement, but all of this progress was leading up to 2 procedures to ‘fix’ the AVM in his brain; one to stop the blood flow in that area, followed by brain surgery to fix the actual malformation. What went from deepest sorrow, to joy from getting better, returned to grief and fear this past week for these next two steps. Everyday since last Friday, grief, fear, and joy lived simultaneously in his hospital room. During the day we would experience the joy of something gaining motion but at night, the fear of the upcoming procedures and what changes may happen would steal the joy. Then there were the questions amidst tears in the quiet before bed each night; Why did this happen to me? Why can’t I just be a normal teen? Why me? I didn’t know this momma’s heart could break even more, but watching your child in pain and struggling with these unanswerable questions broke the remainder of what I had left.

How do you answer these questions when you don’t have the answers? How do you remain courageous when you yourself have fear? All I could do was hug him, cry with him and tell him that it was ok to cry, be afraid, and ask questions but in the morning he needed to fight back and to push forward. I told him to ask God to strengthen and sustain him and to give him peace. For a kid (and even for an adult), that sounds so generic and blasé’, but it’s what I have to hang on to so I’m going to hang on to it. I also told him when he’s older, he can tell his kids and grandkids about the scar on his head and how he overcame the biggest challenge of his life when he was just a kid. Ann Voskamp speaks of grief and loss as a type of empty or negative space in our hearts which gives our lives definition; its constant presence in our thoughts and actions. She then says that God uses this space to give us permission to pause, help us reevaluate and draw our attention to what is positive-God Himself and the hope we have.

I am exhausted, mentally and physically. On top of this, we had 3 kids recently go off to college and another is starting her senior year of high school. Life moves forward. I thought that a Stage 4 diagnosis would do me in, but watching and caring for your child through such a major health crisis goes beyond human capability. I understand the being strong and fighting part when it comes to me and my fight, but for my child? It’s the next level. Children believe you when they see in your eyes that you believe, and it has taken every inch of my being, with HEAVY reliance on my faith to be strong and courageous for both of us. Love gives courage. We talk about life in seasons, ‘this is just a good or bad season,’ etc, but I heard Shauna Niequist on a podcast and she referred to life as more of a railroad track, the good and bad happen simultaneously side by side. I agree because I’ve seen it every day we’ve been here and even through my own cancer journey. In this hell, there has been light. On the worst of days, there have been glimmers of hope. There may have been tears but there has been laughter as well; always good and bad side by side.

The love we have experienced from friends, family, nurses, even strangers have meant so much and has lifted us up. I cannot thank you all enough for all the cards, texts, gifts, and prayers. As a Christian, I have always known the story of God and Jesus but now I understand even more the incredible sacrifice; a Father watching his son suffer real human suffering to give us all hope. That is love. Love gives courage.

Do not fear for I am with you; do not anxiously look about you, for I am your God. I will strengthen you…I will uphold you.’~Isaiah 41:10

 

Strength and Story

23 Mar

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Yesterday I had the chance to tell my story for a podcast that will be broadcast in a few weeks. I have to admit I was nervous for a few reasons; I didn’t know what to expect, I didn’t receive any questions ahead of time to prepare answers for, and I’m a little insecure about my voice because it is weak and ‘breath-y’ and a podcast is all voice. When Lauryn first called to get ready to record I asked what part of my story she wanted to hear, the cancer part, the lipstick part, how the cancer opened up the lipstick business, etc. She said, ‘Your whole story, beginning to end, everything you want to tell me, just keep talking.’ Woah. That’s a lot. I started with, ‘ I was born…’ I’m sure that freaked her out a little but I quickly jumped to my passions growing up then to the first time I had cancer. I described everything from finding out, to the procedures, work, kids, people, emotions, home life, etc. I described those things for every single time I was diagnosed until now. I spoke about being a mother to young kids the first time I was diagnosed and what that meant, then now being a mom to older teens/young adults and what being diagnosed with Stage 4 means to me and to them. And of course, I spoke about lipstick and the part it has played in my messy journey.

I talked for over an hour without interruption describing every nuance. I realized that this was the first time, if ever, I have shared all of those details out loud. Not just all of the times I was diagnosed, the when, and what happened, but all the emotions and most of my thoughts surrounding those times. Yes my voice shook, yes we both cried at times, but there was also laughter. I was literally exhausted for the rest of the day. The thing is, I let myself be super vulnerable and was able to open up, and after hearing myself speak about all that I had gone through up to this point, I felt strong. I have always thought that throughout my journey I did what I had to do to just keep going for me and my family and that was not strength, it was just will, and just because. After the interview I felt REALLY strong and realized that ‘the story’ was not really the big moments, it was every piece, fragment, emotion, in between. It was the filler in the pages between chapters and that is where the strength was really necessary. ‘You gain strength, courage, and confidence by every experience in which you really look fear in the face. You are able to say to yourself, ‘I lived through this horror, I can take the next thing that comes along.’~Eleanor Roosevelt.

At the end of my hour of babbling on the podcast, Lauryn had one question, ‘After everything, has your belief or faith in God changed?’ Good question. I have to say after the first 3 times with cancer I never asked God why. I just figured God had a plan and was generally at peace with whatever outcome. Total trust. This last diagnosis of metastatic cancer I finally asked God the why question. Not, ‘why me’, but more ‘why can’t my life just be good for awhile. Why can’t I just rest?’ I don’t know the answers but I still have peace with whatever. I absolutely still believe in God and if anything my faith has gotten even stronger. I told her that in the darkest of moments for me and with all the unknown, God was/is my only solid and that’s enough. ‘Never be afraid to trust an unknown future to a known God.’ -Corrie ten Boom 

I started my day yesterday seeing this quote on Lauryn’s Instagram and it was perfect,’Tell the story of the mountain you climbed. Your words could become a page in someone else’s survival guide.’~Morgan Harper Nichols. Amen and amen.

Today I’m wearing The Lipstick Journey lipstick in Playful which is a bright plum/berry. It’s the brightest color I created and it’s actually not super bright (meaning still wearable every day, not neon). I chose Playful because it’s spring and I’m feeling funky. Cheers!

 

Motherhood And Cancer

26 Sep

facetune_22-09-2018-17-18-00Last weekend my son went to his first official high school homecoming dance. He didn’t have a date but neither did most of his friends. Interesting times but I guess less pressure if you just decide to go with a bunch of friends. When I first found out cancer was back a little over a year ago my primary thoughts were of the kids not having a mom around to see them graduate, get married, have kids of their own, etc. Since I’ve been stable over a year some of those thoughts have faded (a little) but every time something significant happens like graduation, off to college, or this homecoming dance, my heart swells and I feel so grateful to still be here.img_4293

What can I say about being a mom with cancer? Many of my emotions I can’t even iterate on paper. This may be the hardest part. When I first got cancer the kids were 5, 7, and 10 and my thoughts were consumed with being able to raise the kids to at least adulthood when maybe they wouldn’t need a mom as much, but now that my kids are there or close to that ‘adulthood’ age I realize they still need a mom and maybe even more. Watching them grow up and being there for these moments is both heartbreaking and beautiful. I guess the best description of being a mom with cancer is ‘overwhelmed’; every event, every moment, every time they lay their head on my shoulder, every great conversation, every text or call just to say hello, and every ‘I love you’ is overwhelming, like my heart may burst into a thousand pieces with joy and love. On the other side, every harsh word or rude comment, every ‘you’re so annoying’, every time they make a bad decision, it is absolutely piercing heartbreak. Thankfully the negative is not often but it still happens and it’s hard. Having cancer has magnified every single emotion for me and as a mom, sometimes the emotions feel unbearable, both the good and the bad.

As it stands, motherhood is a sort of wilderness through which each woman hacks her way, part martyr, part pioneer; a turn of events from which some women derive feelings of heroism, while others experience a sense of exile from the world they knew.~Rachel Cusk

Metastatic cancer generally has no cure, it’s all about time. Being stable means more time. Being stable over a year? Slow growing…more time. I don’t want to miss anything. When they were young, I wanted to see them through to adulthood. Now that they’re older teens/young adults I want to see the rest of their stories and how it all shakes out so I’m kind of mad about it. There is no good time to have cancer. The teen/young adult years, I have decided, are the hardest years to parent. This is the time when kids push boundaries, try to bend the rules, and try to shove their way into adulthood and oh yeah, they can drive away. Why am I mad? Because at a time when I want to hold them tight and spend every possible moment I can with them,  they are trying to push off into the world. It stinks. It’s hard in general to parent during teen years but even harder with cancer because again, it’s about time. So. Incredibly. Frustrating.

You gain strength, courage, and confidence by every experience in which you really stop to look fear in the face. You must do the thing which you think you cannot do.’ – Eleanor Roosevelt.

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How has cancer changed my mothering? I stare at the kids longer when I see them trying to memorize every feature. I move heaven and earth to be available for the times that they want to see me. I cry a lot more and not just when I’m sad, but when I’m ecstatic as well. I cry so.much. I hug them until they have to push me away and I pray for them and their future without ceasing. Motherhood stretches our hearts bigger and wider than we could have ever imagined and when you add cancer or any illness for that matter, your heart  stretches to the point of breaking. I read somewhere that cancer is not just a disease of the body but of the mind, body, and soul. So true. I will not let cancer break my spirit. I will take ‘stable’ as long as possible. I am a mom. I am strong.

Today I wear one of my favorite lips products of all time, Dior Lip Glow in Berry. I have this in 3 different ‘colors’. Essentially these are lip balms but each brings out a natural hue from your lips. I love these because they’re moisturizing and give your lips enough color to feel ‘finished’. Cheers!