My sister recently made the comment that nobody really discusses loss and grief on an everyday level.
(Don’t mind me over here, typing away about…loss…and grief…)
After I was finished feeling righteous and offended, I realized she’s right. Even those of us that write about it (and talk about it), still do so in mostly sweeping statements about waves and universal truths and fragmented stages in time. Usually, I’ll share a moment - a moment of struggle or a moment of joy, allowing you the reader to get a glimpse of myself in that particular place in time. But we don’t talk about the everyday grief. The part of grief that is small and constant. The part of grief that is so regular, it becomes a part of your days. It becomes part of yourself.
And I think it’s because dealing with grief and loss on an everyday level is, frankly, depressing. And talking about grief and loss on an everyday level is equally depressing.
So we avoid. We reference it - the sadness, the loneliness, the anger - but we don’t go deep on a linear level. Most of us are uncomfortable sitting in sadness and loneliness and anger for too long. We gloss over it in favor of positivity and hope. Everyone likes positivity and hope.
But today is 4 months since Brad died. So today I am skipping positivity and hope. Today I am going deep in loss and grief on the most basic, everyday level.
So 4 months in, this is what my everyday grief looks like:
I wake up. I am usually exhausted because sleep - like grief apparently - comes in waves. Maybe I got a solid 2 hours, maybe I got 6, broken up by bouts of restlessness. Whatever amount I got, I am sure it wasn’t 8 hours. I can’t remember the last night I had 8 full hours of sleep.
I lie in bed and have to convince myself to get up. Convince myself to not waste my life. Convince myself to be responsible. Convince myself to make Brad proud. Usually I settle for convincing myself to make it to the coffee maker.
Coffee in hand, I check Facebook and email. On some days someone has sent me a note or video or article. Sometimes from a stranger, sometimes from a friend. They are always appreciated, but I never know how to respond or am too exhausted to respond thoughtfully. So usually, I don’t. I add it to my mental to-do list for another day (“write thoughtful and appreciative response”). I look at my Facebook memory of the day - hoping Brad posted on this day and I get to remember another piece of him I normally wouldn’t have remembered. Usually they are all too serious articles from the New York Times. But sometimes, they are things like “Dana won the pool. I won at life with the best girl ever.” or a hilarious Instagram photo of Dune taking a shit next to the tacky “No Dog Pooping” sign outside the hotel next door. I love those moments. And hate those moments. I smile and cry at those moments. I screenshot them and put them in a folder for safe keeping in case Facebook decides to one day implode.
I debate doing normal adult human activities, like eating breakfast, showering, or getting dressed. On any given day, it’s questionable whether any these things will happen. On a day where all three occur, it feels like a fucking miracle.
I try and figure out my future. This has always been a struggle for me - the “future.” But now I attempt to do it alone. Without Brad whiteboarding ideas for me and asking me relevant (and seemingly irrelevant) questions. Now I have to accept the fact that I can’t rely on my business alone and need more income in order to maintain my life. That my little entrepreneur soul is probably going to have to get a 9-5. This thought, combined with the fact that most days I can barely eat breakfast, shower, and get dressed, depresses me. On a good day, I’ll avoid this by daydreaming about a future business idea that excites me. On most days, I just avoid altogether.
A familiar song comes on. It makes me think of Brad. Either I smile or cry (oftentimes both), but I lose my concentration, knowing whatever I was hoping to accomplish probably won’t get finished now. This happens about 20 times a day. I tell myself I should turn off the music, but then it’s quiet. Too quiet. And through all my grief and loss, music is still my one constant companion and I just can’t stand to lose that too.
I check the mail. I used to love checking the mail. I loved the possibility that on any given day, someone may have thought of me and sent me a letter. Now I dread the mail. It almost always involves communication from creditors, vultures trying to buy my home, hospice surveys, medical bills, student loan bills, attorney bills. I feel overwhelmed and angry. On days I feel strong, I tackle this mail. But usually I put it off for another day.
Maybe I’ll leave my house. Either because I have to or because I am attempting to avoid being the isolated hermit I instinctively want to become. Either way, I will inevitably see someone I know. I will smile and say hello and they will smile back, the kind of half smile of pity. Well intentioned, they will ask, “how are you??” I will have a split second to decide. Do I answer honestly or do I say I’m doing "fine" and quickly move on. It usually depends on how much time I have and how exhausted I am and whether or not it is okay to cry in whatever public space I am in. Usually I lie. Then feel guilty. Then tell myself I am never leaving the house again.
My car is rattling. It needs an oil change and new break pads. I’m pissed I have to do this alone. Which is absurd because even when Brad was alive, I still took care of my car myself. But I’m looking for reasons to justify feeling angry (aside from the obvious). So I focus on the noises in my car and the fact that I don’t have a man to take care of that for me. My feminist self dies inside a little, but I don’t care. I just want to be angry, so I let myself pitifully go there.
I start thinking about dinner. I used to cook. I used to love to cook. But now cooking requires going to the grocery store. And seeing how Detroit is “the biggest small town in America” (as Brad used to say), I know there is a high probability I will run into someone I know at the grocery store. And wanting to avoid the half smiles of pity, I avoid the store completely. Plus I don’t know how to shop - or cook - for one person. So I buy too much and it goes bad. And Brad would be upset at the wastefulness. So I feel guilty. And I don’t shop. So dinner, which used to be a shared experience of love, is now one of guilt, dread, and loneliness.
Some days I’ll meet up with friends and watch a movie or grab a drink. I’ll probably drink too much because even with my closet friends, even through my smile, I feel alone and in a thick layer of grief. Usually I’ll bail and go home early. But sometimes, I’ll connect in an authentic way, where for a brief period of time, I don’t feel so alone. Sometimes I’ll have joyful experiences with people I love. We will laugh and talk and it will feel incredible. And then I feel guilty. Even though I know it’s bullshit and I deserve to have fun and Brad would want me to connect and blah blah blah. But I feel guilty, because I am human and miss my husband and can’t imagine being able to have a joyful moment with him being dead.
I think about Dune and how he will be factored into this new life of ours. Right now he is with my mom in Virginia. But soon I will have to figure out how to readjust my dog to life without his Papa. Readjust him to being left alone for extended periods of time or going to doggy day care most days of the week. I worry about his separation anxiety that was already present before Brad got sick. I worry how I am going to take care of both him and myself. I worry that I cannot provide enough love for the loss we both feel. I know this readjustment will not be easy. Dune - like most of us - does not like change. So I worry about this too.
I get ready for bed. This is the hardest part of my day. Even with music, there isn’t enough noise to drown out the deafening silence of Brad’s absence. I crawl into the king size bed we upgraded to a year ago. After 10 years, it was the only bed we ever picked out together. I loved this bed. Now I fucking hate this bed. I curl up in the corner where Brad used to sleep, taking up the tiniest fraction of my too big bed. Maybe I’ll fall asleep quickly. Usually, I’ll toss and turn for hours, get out of bed, and walk aimlessly around. Sometimes I’ll be fortunate enough to talk a friend or family member who is also still awake. Eventually I will sleep.
The next morning I wake up, exhausted, and do it all again.
And that’s my everyday grief.
Fucking depressing, right? I’m naturally inclined to want to immediately tell you that in between all of that grief is hope and laughter and love. And that’s true - there is. But I feel the need to say it because, like the rest of you, I am also uncomfortable just sitting in the openness of my grief. I still have the urge, even on paper, to want to rush through and gloss over it by yelling, “BUT DON’T WORRY, I’M OK!”
But I’m not OK. And that’s OK.
I don’t tell you all of this for pity - although that is naturally where most people will go, followed by the immediate and helpless desire to fix and solve my grief.
I tell you all of this because it’s real.
Talking about loss and grief on an everyday level is depressing as hell. But grief in itself is depressing as hell. And sometimes acknowledging that grief on the most basic level makes it easier to “move through,” instead of being “stuck in.” It means I have to take off my warrior mask and be vulnerable. It means I have to acknowledge a reality that I don’t want to admit is mine. It means I have to own up to feeling…everything.
And sharing this, as hard and depressing as it is, gives me the opportunity to connect with others sharing similar pain. Sharing my grief hopefully allows others to feel less alone in theirs. Otherwise we all sit alone in our everyday grief feeling like no one in this entire universe "gets it." So we share. And we connect. And isn’t that what this is all about? Connection?
So tomorrow we’ll go back to positivity and hope (maybe). But for now, let’s just sit in our everyday grief a little longer. And be OK there. Together.
I’m on my final leg of this journey. I’m dirty. I’m exhausted. I’m sore. I feel beat up and raw. I also feel powerful and proud. I found a strength and openness I didn’t acknowledge before that I will carry with gratitude as I head towards home. Tomorrow.
Tomorrow I will be home.
I’ve spent 10,000 miles lost in my thoughts and emotions. I’ve been pushed and challenged. I’ve relied on myself and on others. I’ve felt connected and I’ve felt lost. I’ve searched for everything and searched for nothing. I’ve experienced weakness and I’ve experienced incredible strength.
My life is a pendulum of conflicting emotions. Most days, all at once.
Now, I both yearn for and dread going home. I crave comfort, but also know the only comfort I really want is no longer there. My bed and clean clothes will only provide me temporary relief for my tired and hurting body. I worry the strength I found on the road will disappear the second I walk through my door. I worry I will stop connecting. I worry I will hide in my grief and loneliness.
I am filled with anxiety and uncertainty. Uncertainty about myself, about my future, about my relationships. About it all. Everything I left behind still remains, waiting for me, unchanged. But I’ve changed. I am no longer the person I used to be. That person disappeared on January 22nd. I still don’t know who this new person is. I still don’t recognize her.
But tomorrow - tomorrow I head home. Tomorrow I will begin to find out...
6 months ago, my life - my happy, perfect life - changed forever. 6 months ago today, Brad and I walked into the Saint Joseph Mercy emergency room, hoping and expecting for an infection and instead getting a stage 4 cancer diagnosis.
It was a day filled with fear, anger, sorrow and pain, but also one of hope, love, and determination. It is a day I will remember for the rest of my life. The anxiety I felt as we squeezed into the small hospital bed, holding each other while we waited for results. The gut wrenching fear I felt as our friend and doctor, Josh - off duty for the night - walked in after midnight to deliver us the news. The numbness and shock I felt hearing “stage 4.” The compassion I felt being told by a trusted friend instead of the random on-call doctor. The unstoppable love I felt from Brad as he held me and let me cry in his arms, assuring me that we were going to be okay.
6 months later, I am not okay.
Three days before that day in October, Brad and I were blissfully unaware, on vacation in the Upper Peninsula. We were celebrating my 4 years of being in remission, wrongly believing that we had already gotten through the worst part of our lives. We spent hours talking about our future - and not just the near future, our whole future. We talked about retirement and the kind of life we wanted as we grew old together. We talked about our lifetime together.
My life is now divided into two completely separate lives. The life that I wanted - the life that I chose - and the life I was recently given. The life I want more than anything to fucking give back.
I would give anything to go back to 6 months and 1 day ago. To go back and have Brad’s pain be an infection. To go back and hold on for dear life to everything I had.
I just want to go back.
Instead I am sitting in Arizona, unintentionally and regretfully staying miles away from where I spent several months for my own cancer treatment, being reminded of what now feels like a faded memory of a trauma I experienced a lifetime ago. In a way it was.
I feel tired, I feel broken, I feel lost. I am at the point where I don’t really want to go forward, but what is there to go back to? If home is where your heart is, how do you go back to a home without your heart? I want to go back to before 6 months ago. Back to that life. My real life.
How do you move forward when all you want to do is go back?
I’m trying to slow down. To embrace this journey. To embrace the fact that this isn’t a trip for me to see the country and tour the sites. It’s a trip for me to be alone with my thoughts and emotions. To be alone with my grief.
It’s strange showing up in a new place and not having a plan. To not have already mapped out every single thing I wanted to do and see, fearful to miss out because of lack of research.
My researching drove Brad crazy. For months before a trip, I would spend countless hours in books and on the internet, mapping out the perfect vacation: a balanced mix of “must sees,” off the beaten path finds, and down time for relaxing and spontaneous exploration. Hours planning the kind of trip that felt magically unplanned. Planning brought me joy. The excitement and build up leading up to the trip were almost as much fun as the trip itself. Brad wanted me to be more “go with the flow” and just show up. To let our trip unfold naturally. I used to swear that our vacations were always so wonderful because I planned. And I knew Brad enough to know how to plan for him too: the perfect outdoor cafe that’s not overrun by tourists; the main attraction’s less visited and often forgotten sister site; sex breaks.
I’m actually doing this road trip how Brad would have wanted - unplanned. Not as a way to honor Brad (although I wish I could say that were the case). But because I was too busy with my grief and sorrow to plan. Because I just didn’t care to plan. Because some mornings telling myself to get up and put one foot in front of the other, to walk out the door, is exhausting enough.
As I am sitting here at 9:15 in the morning, my hair wet from my shower, sipping coffee on a patio, and writing, I realize this is exactly the type of slow morning Brad would have craved. I would have been eager to get out the door by 8 - to check out the perfectly adorable coffee shop around the corner before a full day of exploration. I would have been antsy and eager, fearful we were wasting the day. Fearful of missing out.
I am trying to embrace this new me. Or at least this temporary me. Eventually I’ll get dressed and head out, unsure of where I’m headed. I will try and ignore the pit in my stomach that regularly inhabits my body these days. Try and ignore the fear of exploring a new place without a plan. I will try and find joy in my day.
But for now, I am going to sit here a little longer, sip my coffee, and watch the day unfold around me. Not just for Brad, but for me.
What if you only had 100 days to live? What would you do? Quit your job? Travel the world? Start living? Start loving? Start making your moments count?
What if, of those 100 days, 90 of them you felt sick, in pain, or fatigued? That simple tasks like showering or getting dressed required help? That riding in the car was difficult because of the discomfort it caused? That staying awake for several hours in a row felt like a phenomenal feat? And what if the last 10 of those days you were drugged out on morphine, toeing the line between living and dying? Aware for some moments? Confused and out of it for others?
What if you only had 100 days to live? What would you do? How would you live? Would it be too late?
You don't get to choose your last 100 days. And you definitely don't get to choose the condition you will be in during those days. On December 8th, Brad started to plan his life in 100 day increments - never imagining he might not make it through the first 100. He was going to write his memoir. We were going to buy an RV and travel the country and visit the life he lived. The life that we lived. We were going to connect with friends and family. We were going to have adventures.
Today would have been Brad’s 100th day. 100 days after his “Day Zero” blog post. 100 days after starting to take Cabozantinib. 100 days to see how he was responding, to see how the disease was being managed.
Brad died on his Day 46.
What if you only had 100 days to live?
Of Brad's last 100 days, most were spent in bed. Most of them he was too tired to write. Too tired to talk. Sometimes too confused to get his thoughts in order. Brad spent his last 100 day frustrated that the physical state of his body was preventing him from achieving the goals he set for himself. Always hoping that tomorrow would be a better day. That tomorrow he would write more than a paragraph at a time. That tomorrow the meds, the supplements, the diet, the meditation, would all kick in. That tomorrow never came.
What if you only had 100 days to live?
Brad didn’t get to spend his final 100 days chasing dreams and big ambitions. He didn’t get to write his memoir or take our cross country road trip. But he did spend those days doing what was most important: connecting with the people he loved.
In the end, Brad didn’t make any drastic life changes. He didn’t learn he was dying and start making amends (he didn’t need to) or start suddenly living and loving (he already was). Although we hoped for more - more time to write, more time to live - he was already living the life he wanted. He was already the man he wanted to be. He was connecting. He was contributing.
Over and over he would tell me, “Connect and Contribute.” Those were his priorities, above all else. And he honored his commitments to live and love presently - to connect and contribute - until the very end.
It is devastating to think of the impact Brad would have had if he was given more days. How he would have continued to contribute. But I am grateful he got the days that he did. Because he lived more in his 35 years (that’s roughly 12775 days) than most will live in a lifetime. And that impact will continue far beyond our days.
What if you only had 100 days to live? What would you do?
Don't wait until you are given 100 days to live your life. Because you don't get to pick what those days look like. How your body will or will not fail you. How the reality of everyday life will get in the way of the life you planned.
When Brad and I walked into the ER in October and found out he had stage 4 cancer, we never could have known that that day was Brad’s real “Day 0” - that he would only get 100 more days after that. That January 22nd would be his final day - his day 100.
You don’t get to choose your last 100 days.
So what if you only had 100 days to live? What if today is your Day Zero? What will you do tomorrow? What will you do today?
If you’ve been following along here or listening to the podcast, you know that Brad and I planned to go on an epic cross country trip together. Before we could leave, we were waiting for the scan that showed his treatment was working. That showed stability. The scan that said he would live a little longer. The scan that never came.
We thought we could make it. Thought he would make it. We put a deposit down on an RV, aptly named “The Gemini.” We talked about painting it and adding the Defending Your Life logo on the side. We planned our route. We would circle the country and visit places he’s lived. Converse with old friends. Make new friends. We wanted to podcast and document the journey. Show us living courageously while talking with other people on how they, too, live courageously. I would drive and he would write. We would listen to music and have adventures and live our life as fully as possible. We had a plan.
I now have to make new plans. The reality is, this road trip was just one of many plans we counted on that will never come to life. One of thousands of dreams and ideas and ambitions we discussed. It is part of a future that no longer exists. My future now looks wildly different. My future is unrecognizable.
After Brad passed away, I knew I still had to take this road trip. Not the exact trip we planned (buying an RV now seems outrageously irresponsible), but something that could partially mimic it. I’m not entirely sure why I feel the need to embark on this solo journey. Maybe because I just want to escape and run away. Maybe because I feel I owe it to Brad. Maybe because I just can’t accept the fact that I am supposed to make new plans and instead would rather cling to my old plans, our plans. Maybe I just need to share - and write - our story. Maybe I just need to honor Brad. I don’t know. Maybe it’s all of these reasons and a 100 others I don’t fully realize.
But in 10 days I am getting on the road. Leaving on the first day of spring.
Brad loved significant dates. He loved the equinox. The idea of a refresh. A new season. He proposed to me on the first day of fall. We got married a year later on that same date. Our anniversary date was rotating with the fall equinox, changing slightly each year, depending on the sun. “It’s gross how romantic it is,” Brad used to tell people.
So now on the spring equinox, I’ll be embarking on this new season of my life (it's gross how cliche it is). Generally, I feel lost in my life. Lost at home. Unsure of what to do and where to go. I’m hoping escaping for a bit will give some clarity, some sense of my next steps. If nothing else, it will give me an adventure. If there is one thing Brad and I loved together, it was an adventure.
And because you can’t just have a soul searching road trip without some bigger purpose (thank you Brad for your influence to always go beyond yourself and think bigger), in addition to writing, I am hoping to continue podcasting for Defending Your Life in a variety of ways.
First, I want to have conversations with other people like me. Conversations with both cancer survivors and other widows (I have the unfortunate distinction of being a member of both clubs). The topic of each conversation will be how you live courageously in the face of cancer and/or loss and how do you find joy during your darkest moments. Two concepts I am currently struggling with. How do you go through this and make it out on the other side??
I’d also love to keep podcasting about Brad, his influence, and his life. Talk to friends and family (both those I know and others I don’t). I want all the Brad stories. Even better if those stories come with a couch I can crash on.
And finally there will probably be some “I’m all alone in the desert, what the fuck was I thinking?” solo podcasts. Because let’s face it, I am utterly unprepared (both emotionally and physically) to go on the road for the next two months and the combination of insanity, unpreparedness, and grief has got to lead to some stellar podcast content.
At the end of the day, I really see this trip as a search for joy and meaning - two things Brad and I proudly lived our lives by. And ever since Brad died, I feel like I’ve lost both. I'm hoping to stumble upon them somewhere along the way.
The rough route. Who has an extra place for me to stay?
I’ve been putting this off for sometime, but the most recent podcast episodes of Defending Your Life are up, including Brad’s last episodes and life after his death. Listening to these episodes was not easy for me, but this podcast was one of the most important projects in the last several months of Brad’s life, and it’s important to honor his passion and contribution.
The reality is, the last 10 days of Brad’s life was tough. After we learned of his pulmonary embolism and the progression of his disease, Brad declined rapidly. His body was already failing him, but it was watching his mind slip away that was the most difficult. In the end stage of life (that’s what everyone calls it), it is not uncommon for confusion, fogginess, and hallucinations. As Brad’s organs began to fail, so to did his mental capabilities. He was still mostly his witty, hilarious, intelligent self, but this side effect was something I was unprepared for and was the most difficult to accept. Brad’s mind - his words, his thoughts - are a gift to the world and acknowledging that I would never get another conversation with Brad being fully Brad was one of the most devastating losses before his death.
After Brad’s passing, the people in his life struggled on how to connect and move forward without him. Brad was our bridge and everyday we continue to make the effort to communicate and support each other. Jeremy and I are lucky enough to be in the same city and can podcast a bit of our process, but through texts, calls, emails, and visits, we regularly stay connected with Brad’s family and friends. I am incredible thankful for that.
Many have asked if we plan to continue Defending Your Life. The answer is yes, but as of now, we don’t know exactly what that means. We are still trying to figure out the best way to use this platform to honor Brad, his desire to connect, and passion for contribution. Until then, here are the newest episodes of 2017:
Season 2, Episode 1: PE & Progression
Summary: It's a new year and a new season of Defending Your Life. In this first episode of the year, Brad and Dana are given some bad news after the discovery of a pulmonary embolism.
Season 2, Episode 2: Love Story (Sort of) - Part 1
Summary: In this episode, Brad and Dana attempt to discuss their love story with Jeremy, Dave, Lindsey, and Margo. But with Brad on a cocktail of pain meds and others just on cocktails, what was supposed to be a love story, ends up being a hilarious, juvenile, laugh fest about sex, love, and relationships. Moms, Dads, and Grandparents, you may want to skip this one.
Season 2, Episode 3: Love Story (Sort of) - Part 2
Summary: Part 2 of the “love story” continues with Brad, Dana, Jeremy, Dave, Lindsey, and Margo.
Season 2, Episode 4: Post Brad
Summary: On the day of Brad’s passing, Dana, Jeremy, Dave, Lindsey, and Margo sit down and talk about their thoughts and feelings.
Season 2, Episode 5: No, But Yes
Summary: Jeremy and Dana - a little hesitantly - sit down for their first podcast together after Brad’s memorial service and reflect on life after Brad.
Season 2, Episode 6: Valentine's Day Solo
Summary: Dana talks about being alone on Valentine’s Day.
Season 2, Episode 7: Guilt and Shame
Summary: Suneil, a great friend of Dana and Brad, joins Jeremy and Dana to talk about the struggle to move forward without Brad and ways to cope throughout that process.
This morning Dune and I sat in your chair. The leather chair I promised you on our third anniversary in 2011, when we lived among cheap Ikea furniture and hand-me-downs and were too broke to invest in something so luxurious. The chair we finally splurged on 5 years later, after you got sick and needed a better place to read and write. We sat in your chair and looked out as the sun rose above the water. We sat in your chair, with the window open, feeling the cool breeze and the warm sun. We sat in your chair and experienced the morning exactly how you would have done. Quietly, thoughtfully, reflectively. We sat in your chair and wept.
It’s been 4 weeks.
I still keep waiting for you to walk in the door. Still reflexively grabbing for my phone to call you. Still reaching my hand over to hold you in bed. I still refer to myself as a “we” even though I am now just a “me.” We have been a unit, a team. We have been an unstoppable force. We have been a family. How do I go back to being just me?
But, because of you, I am not alone. The people closest to you - your family, your best friends, your core - have become my greatest sources of strength. I can’t possibly understand the cruelty of you being taken from me, from all of us, but I will forever be grateful for both the relationships you encouraged me to form when you were here and also the ones you left behind when you were taken from us. I am not okay. But because of your depth and nurturing of relationships, because of your connection, I have an army that looks out for me. One that allows me to laugh and cry and get really, really angry. One that allows me to just be.
That’s because of you.
A couple weeks before you passed away, you told us that the meaning of your name is a bridge: “Bradford literally means bridge!” You have no idea the bridge you are. Your work in the city, your passion for inclusive growth, your thesis on the divide at Alter Road, your relationships, your friends and family, your presence. You were a bridge, connecting us all in unimaginable ways. You are my bridge.
It’s been 4 weeks and even though I feel pain and loss in ways I didn’t know existed, I also know that my life is more connected, more meaningful, and more full of joy because of you. Because of you, I will spend my days trying to live more courageously.
Thank you for the greatest love story I’ll ever know.
Today my worst nightmare happened. We lost my love, my best friend, my heart, Bradford. He passed away in our bed, holding my hand, just like he wanted. I don’t think there is a person in this world that would disagree that we lost him far before his time. He had so much more to give in this life and was robbed of his full potential. But for the amount of time he did have with us, he lived more, loved more, and accomplished more than most do in 100 years. Brad affected the lives of everyone around him. Real connection was his top priority and I don’t think he fully realized how many people he truly reached - through his passion, drive, and search for deeper meaning.
Brad was the light of my life and always pushed me to be the best version of myself. He challenged me and questioned me. But most of all, he loved me. Fiercely. And Unequivocally. Our love was loud and obvious for the world to see. Our love was fearless.
Brad, the idea of living a life without you is more than unbearable. It’s impossible. You were my always. My forever. Already my life feels so quiet without you. I don’t know how to go on without you, how to be my best self without you by my side, but I will try. Because that’s what you wanted and that’s what you deserve. And I will figure out how to honor your life, every single day of mine. And I know I am not alone in that.
Love, I will miss everything about you. Every single day. I am so proud of the life you lived and the man you were - not just in the face of this terrible diagnosis - but every day I knew you.
You are my hero and no one lived their life more courageously than you. Sweet dreams my love - I love you more than the sun and the moon.
We wanted to provide a quick update. Last Thursday after finding a blood clot in his lungs, Brad's doctors found significant progression of the disease. The news was difficult for everyone. Brad declined rapidly over the weekend and his family has gathered in Detroit over the last week or so. During that time, Brad & Dana have been visited by immediate family, cousins, aunts & uncles, and close friends. Brad is in hospice care and surrounded by his favorite music, stories and poems. He is as comfortable as possible and spending as much time as he can with everyone. Unfortunately we cannot accept or respond to the calls, visits and texts at this time, so let this update be our way of sending our love back to you. We will continue to update each of you as best we can throughout this coming weekend. Much love and continue to live courageously. -Jeremy Potter