This is me

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Then I got cancer.




One year after the cancer diagnosis that sent my life spinning into uncharted territories, my oncologist patted me on the back, told me he’d see me next year, and sent me on my way. I left his office, drove home, sat down on my couch, and sobbed for two hours. Ugly crying. Uncontrollable ugly crying. For two straight hours.

What the fuck had just happened to me?

From the outside, and certainly to my oncologist, it must have looked like I was in the home stretch of a scary chapter in my otherwise pretty good life. I had gone through surgeries and radiation treatments, facing my fears and medical challenges with the determined bravado I assumed was expected of anyone in my place. My four kids gave me a reason to look forward, my dear friends stepped up to help, and my dad and siblings lived close enough for regular visits. I had a roof over my head and decent health insurance. In the midst of everything, I had even managed to start up an advocacy organization to support other cancer patients and their families. Over the past twelve months, I had been called “brave,” “strong,” and “an inspiration,” but I felt like I was none of that. That morning, after receiving the news that I was cancer-free, I could have felt relieved, maybe even joyful. Instead, I felt mentally drained and emotionally untethered.

As I sat drenched in tears and snot, it occurred me that, through it all, not one person had asked me about my mental state. To be clear, I am not just a cancer survivor. I am a suicide attempt survivor. I am a rape survivor. I live with depression and anxiety. My mental illness “rap sheet” is diverse and lengthy. In fact, when I was diagnosed with cancer, I was barely a year into my recovery from a dangerous bout of post-partum depression that had wreaked havoc on my life. I had been perilously close to the edge of suicide. Despite outward appearances, the fight to reclaim my life wasn’t over.

A year earlier, in the weeks before my cancer diagnosis, I thought I was doing a fairly good job of putting my last breakdown behind me. Mentally, I was feeling okay. Physically, I felt good—I had gained weight; I felt strong. With the help of medication and lots of therapy, I had clawed my way back into a life and routine that was working for me. The diagnosis hit me like a friend’s betrayal. Suddenly, the body that I’d always turned to for sanctuary was no longer my ally. Once again, I felt like a failure.

I was no stranger to self-defeating thoughts, but now my body seemed to be confirming the worst of them: I got cancer because I didn’t breastfeed long enough. I had multiple pregnancies and multiple miscarriages. I smoked cigarettes. I ate too much sugar. I didn’t pray enough. I was a bitch. In other words, the disease was my fault. In hindsight, that kind of thinking seems ridiculous, but at the time it felt completely rational. Later, when I shared these feelings about my cancer with others, I discovered that it’s a common, even expected, response but at the time, I felt like I was completely alone.

As the youngest of three siblings in a family forever damaged by the violent murder of my mother when I was less than a year old, I grew up with an unspoken understanding that my role was to lift everyone else up. After her death, our family and friends sought consolation in my innocence and in my obliviousness to the tragedy that now encompassed us. “The baby will help us!” “Ann Marie is so funny; she’ll cheer us up!” I always sensed that I had a job to do, even though I was too young to know what had happened to my mother. I wasn’t told about the circumstances of her death until I was almost ten years old. No one talked about it; they had lived it. They didn’t want to talk about it. They still don’t.

Growing up without a mother defined me. To compensate, I surrounded myself with substitutes—my grandmother, my aunts, my godmother, my girlfriends’ mothers. When I was little, I made up scenarios about running into my mother. She isn’t dead, she just has amnesia. Maybe I’ll see her in the grocery store, and she will know me immediately. Her memory will come flooding back, and we will be reunited! I didn’t tell anyone about my fantasies, because I was just a baby when she died. I believed I wasn’t entitled to miss her, because I have no real memories of when she was alive—things like how she smiled, what she smelled like, or the sound of her voice—but the reality is; her sudden disappearance must have been devastating to me, to Baby Ann Marie who experienced a life-changing tragedy that no one talked about.

When I was a teenager, I tried to kill myself twice. No one ever talked about that either. They assumed I had just overdosed on drugs. They called me wild and said I was on the wrong path, but nobody ever thought to ask why. I was treated for addiction, but my depression was never acknowledged. I was depressed in part because everyone expected me to be happy. I had to live up to my pre-defined destiny. I couldn’t not be the life of the party. It was my job to make everyone laugh. To this day, I love that part of who I am. It makes me feel good to make other people feel good. That, in turn, helps my depression. But appearances can be deceiving—acting out and tearing it up doesn’t look like depression. Most people think depression means lying in bed for days, refusing to shower, sitting alone in a room with the shades drawn. That wasn’t me. I was lively, fun-loving Ann Marie, hiding the truth about how I felt from myself and from everybody else.

At sixteen years old, I was raped at a party. I had gotten drunk and was flirting with a guy that I knew was trouble because my soon-to-be ex-boyfriend hated him. It didn’t last long but, when it was over, my rapist looked down at me and said, “You’re not worth it.” Then he got up and walked away. I believed him. The incident left me with riddled with PTSD and anxiety. Shortly thereafter, I made my first suicide attempt. Years later, when my older sons hit their mid-teens, I had panic attacks inspired by an irrational fear that they would rape someone.

After I was married, my pursuit of my ideal motherhood was ferocious. Acutely aware of my own mother’s absence, I was determined to be the best mother, and my expectations of myself were impossibly high. Clinging to the tiny bits and pieces I knew about her—she was a go-getter who chaired committees; she was a fashionista who ran a hair salon in her basement; her nieces and nephews adored her; my father adored her—I did everything to live up to who I thought she had been.

I was a good mother, but beneath the surface, I felt like a failure. I nursed Ben for “too long” and put Sammy on a bottle “too soon.” After the first two kids, punctuated by multiple miscarriages (more failure!), I stopped making baby food from scratch and started using jarred food instead. Ben started showing signs of OCD at about 18 months; I blamed myself. My pregnancy with my third son, Anthony, was miserable and his delivery was traumatic. He was a happy baby, but he was always on the move. Unlike Ben and Sam, he didn’t go to bed without a fight, and wouldn’t sleep through the night. I assumed I was doing something wrong. As always, I felt my mother’s absence; she would have had the answers I needed. I ached to know if her experiences with motherhood were similar to mine or completely different.

My pregnancy with my fourth son, Julian, was a happy surprise, but, just before I gave birth, my grandmother, who had helped to raise me, had a heart attack and passed away. Because I was nine months pregnant and they didn’t want to upset me, my family delayed telling me that she was in the hospital. By the time I got there, she was gone. I never had a chance to say good-bye. I was hurt, angry, and devastated. When Julian arrived, he was extraordinarily clingy. He wouldn’t let me leave him, ever. Whether he was with his father, a babysitter, or the childcare at the Y, I would inevitably get a call: “He won’t stop crying. You have to come back.” I know now that this is part of the mental illness he lives with, but at the time I felt suffocated. I felt like I needed to free myself. I felt like a failure.

By the time Julian was around two-and-a-half, I felt myself breaking. I was exercising two to four hours a day and weighed 87 pounds. I ate bags of Skittles for breakfast, lunch, and dinner. My insomnia was through the roof. Alone with my kids during the day, I felt like the walls were closing in on me. When I tried to bring up my declining mental state to the people around me, they dismissed my growing panic. “Oh, you’re fine. You just need to get out and spend some time with your girlfriends.” So, I lurched back into my pre-motherhood comfort zone: out every weekend, life of the party, wild and ridiculous Ann Marie.

I started having suicidal thoughts again. I knew why I had to do it. I was exhausted and nobody was listening. No one saw my side. I looked around at my friends and they all seemed to be doing just fine. I felt like I was all alone. I felt like I was crumbling. I started formulating my escape; I made a step-by-step plan for taking my own life. I wanted the pain to end so desperately, looking back I know it was the pain I wanted to end not my life. But when you are struggling you can not see that.

When I finally admitted to myself that I needed professional intervention, my life broke wide open. I had decided to seek help at a professional treatment center in another part of the country, but my husband didn’t understand my urgency or welcome the expense. I got a friend to drive me to the airport. Baffled and perturbed, Tom phoned me while I was waiting for my flight to be called. He told me to come home, that he wanted a divorce. I didn’t get on the plane. 

When I got back to the house, we launched into a full-on argument. It was ugly, and I knew as it happened that I was going to complete my well-laid plan to kill myself. Despite the horrible moment we were having, I had the presence of mind to tell Tom what I was thinking. I asked him to drive me to the hospital immediately, and even though he didn’t understand what was going on in my head, he took me to my therapist. When I told her that I had a suicide plan and that I was ready to act on it, she checked me into the hospital for a mental health assessment.

After hours alone in a room with only a mattress, the clothes on my back, and the unyielding stare of the police officer assigned to watch over me, I got a bed in the psych ward at about two in the morning. Looking around me, I saw disheveled people talking to themselves, yelling, and very disoriented . There was a man running screaming down the hall, with several staff members chasing after him. Honestly it was something out of a really bad movie. I could not believe this is how we treated those living with a mental illness who needed help. Here I was; a soccer mom from a nice little suburb in Central New York, surrounded by mayhem, confined at my own request, because I was afraid I would harm myself. Yet again, I felt like a failure. Truth is I should have been proud that I was getting the help I needed, without that help I would not be here.

I did my time in the hospital, figured out my meds, made the most of group therapy, and came home. I worked hard to recover. I felt better. Thanks so some amazing friends who watched over me, kept me on track and let me be me. I needed to take my mask off and see who was really there. And then I got cancer.

I had a lumpectomy. 

I had a double mastectomy. 

I had radiation. 

I had reconstructive surgery, which failed, so I had to have it reversed. 

In the wake of my treatments for cancer, I developed lymphedema. By the time I found myself sitting in my oncologist’s office for the one-year follow-up, listening to him congratulate me on a job well done, I was experiencing a shit-storm of side effects. My whole right side was numb. I had pain that I couldn’t explain. When I tried to talk about it, I was told it was all in my head.“It’s stress.” “Take a muscle relaxer.”“You’ll be fine!” As a woman with paranoia and a lifetime of feeling unworthy, who lacks confidence and assumes that other people are all smarter than me, I believed them. I let it go. A year later, I would be diagnosed with multiple sclerosis.

I’d like to say that my two-hour torrent of tears had a healing effect on my spirit, if not my body, but I don’t think it did. Yes, it was a much-needed release, but as the wave of emotion faded, what I experienced felt more like resignation. I was still fighting for my life. Despite reassurances from all sides, I had work to do, and I had to do it myself. My kids need their mom. I needed to be heard. I had an organization to run, a network of people that relied on me, and dinner to cook. “I am enough,” I told myself and took one more deep breath. Then I stood up and began again the relentless uphill battle of convincing myself that it was true.

I started blogging to keep my family and friends informed about what I was going through and unintentionally discovered that my story matters to people that I don’t even know. I began to work as an on-call advocate for organizations that support cancer patients and their families. I started receiving invitations to speak about cancer and, later, about mental health issues, at conferences and seminars. All of it helped me to heal.

One friend, who has since passed away, encouraged me to continue speaking out. “Be my voice,” she urged. Today, whenever I Tweet, or post a new blog entry, or speak at an event, someone reaches out to tell me how deeply my words resonate. When I engage with people who are suffering, and when I can help someone feel less alone, I am filled with relief. My voice matters. What I have to say about my experience is vitally important. And speaking out for someone who can’t speak up is hands down the best therapy I’ve ever had.

When the depression set in again two years ago I saw it happening because I was actually aware of my triggers and signs. I needed to revamp my safety plan, add more tools and reach out to those I knew I could trust. I was talking to a friend who lost her son to suicide and I asked her “what do you miss?”, she told me everything. I asked again but wanted her to be specific. When I did that she could not stop talking about him. It made her feel good to think about him in that way. Later that day I was looking at the pills in the medicine cabinet thinking about how many I could take to just not feel and close my eyes. I was rattled by how quick I went there and started to think what I would miss. Instantly I thought about singing in the car, dancing, unicorns, cooking, coffee- the list was long.

I found myself crying and realized I would miss me! Yes my kids, family and friends would be missed but truth is when I thought about them it made me feel guilty for having these thoughts which then made me feel like a failure which then made me want to die. The things I would miss are what make me who I am and as small as they are I would miss them. I told a friend I would miss Bunco to which she replied “you would be missed at bunco”. And now I saw I would be missed, I felt seen.

I found myself sharing my story of depression and suicide right along side of my cancer story. This is where I see my legacy. This is who I want to be remembered. This is who I am. This is for all those who can not talk about it. I see you because I am you.



Posted on January 3, 2021 .

A little hope

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I guess part of why I have not written in so long is because there is too much in my head. Scary right? 2020 has been a royal pain in the ever loving ass. There are so many things we lost this year and I do not just mean the deaths we are grieving. The isolation, the fear, missing our family and friends are all giving us so much grief. Grief many do not know how to handle or what to do with that feeling. Let me be the first to tell you that it is ok to be pissed you can not do the things you normally do. To be angry you lost your job. You can be annoyed, you can not get your nails or hair done. For sure you can be sad that you can not have cousins night after Christmas like you normally do. It is ok to really miss those who are in the next town but you can not see. It is all ok to feel that way all while being Covid smart. This is not about me telling you to get tested or quarantine or wear your mask. I am reminding you that you can have feelings around all of this. I am reminding you because I have been a mess this year and I need the reminder too. I did not organize shit nor did I clean any closet out. My kids are struggling in school (not the college ones but they sure missed out on their running) but I have made a conscious decision to focus on what they need mentally. To be really honest we are closer than ever but that does not mean they have not suffered this year. 




My Aunt died in May not from Covid but in a way Covid because we could not go see her as she declined. We got on Facetime while we said goodbye to her in her room and sang her song to her. How is this a way to send someone so amazing off? It is not! I was so angry when she died because I needed my family to grieve with, actually we were all angry. We all needed each other. We sat in our cars in the parking lot of the church as my 8 cousins went in to say goodbye because that was all that was allowed. Sat in that car and sobbed with my other cousins in cars with me in a row. Our hearts crushed as our beautiful Mimi was gone and we were not together. We sat, cried and sang her song “You are my sunshine” and prayed hard for some sun on such a gloomy year. Sure enough a week later a fantastic baby was born. Only to have us not be able to celebrate him the way we all wanted to. Talk about bittersweet. Talk about grief. 



I got great news in the beginning of the year before the shit storm, I was NED- no evidence of disease. It was so great to have some light in the darkness. My doctor let me come off some meds and my MS was really under control. My personal life was changing (another post another time) which was both good for me and difficult all rolled into one. There was grief beyond words but luckily I am blessed with such amazing family and friends it was something I could get through. I was learning about myself more than I ever did in my life. I was facing some real hard emotions and using the word accept more and more. 

My cousins are my best friends. They have been there for me at all hours with cheese, cards and a lot of sarcasm. My friends are really my family-those are just the facts. They reminded me to lean on them and they will support me no matter what. They opened their doors to take care of me, to let me cry and to tell me to shut my mouth. Everything I needed. My people reminded me of who I am and I remembered I actually like her. What would you miss was really becoming something bigger than I ever thought and in all fairness I needed it the most. I started paying attention more to my own triggers and how I could cope with them. Just what I needed as I went for tests at the end of this year and was smacked with some crappy news (another post for another time). Throw in a few cousins- one of which my godmother, being diagnosed with cancer and I really want to kiss 2020 goodbye! And to be real and authentically me, I wanted many times to give up. Depression, anxiety and a lot of PTSD was in overdrive. Many times I was very scared yet at the same time thankful I was reaching out. I found many things I would miss and a lot of the time it was just that feeling of knowing I got through the hardest of my days because of me. 

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I could throw a bunch of quotes here and what they mean to me but I am sick of all those. I don't really want to read another “it's ok to not be ok” post, I need more than that. I need to see something I can hold onto. I needed something to really ground me. So it is a story I will leave you with. I was sent a picture on Christmas morning from my best friend’s kids. This beautiful bright eyed baby of 13 months named Charlotte with no cares and no worries in pure bliss. She was simply unwrapping some very small gifts. A toy or two, an outfit, a box with tissue in it, maybe some onesies but not much. Her parents commented “Charlotte is having the time of her life”. She is loved not just by her parents but aunt, uncle, grandparents, great-aunt and uncles, friends and me. This child is proof that with the smallest things we can find some sort of happiness. There is beauty and peace in something so small we just forget to look. It does not matter what is going on in the world when you close the door, your heart can be right in that room. This small little human is showing us that we need very few things, we just need to be safe and loved. Her name means free, ironic? I do not think so. I think she is the true symbol that you can be free to find happiness, free to find peace, free to let love in you just have to accept that it may come in a tissue box. These were the images I needed because I have had a hard time being free to let all those in my life. Charlotte reminded me to accept that small box, find the beauty in it, let myself love it and give myself some peace in what could be filled in it. I do not think Charlotte’s parents understood what I saw in those pictures or how I needed them. I got those pictures when I was really having a very hard morning but she reminded me it is not about the big things it is the smallest things that give us hope. She found all she needed Christmas morning and it was not the presents that gave her the time of her life, it was the love she has. A few of those gifts were from me, what that baby gave me without knowing it was a little hope. The best gift I could ask for right now. 

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Now I just need to get her a tiara because I know she is royalty.






Posted on December 27, 2020 and filed under cancer, mental health.

And then I got cancer

One year after the cancer diagnosis that sent my life spinning into uncharted territories, my oncologist patted me on the back, told me he’d see me next year, and sent me on my way. I left his office, drove home, sat down on my couch, and sobbed for two hours. Ugly crying. Uncontrollable ugly crying. For two straight hours.

What the fuck had just happened to me?

From the outside, and certainly to my oncologist, it must have looked like I was in the home stretch of a scary chapter in my otherwise pretty good life. I had gone through surgeries and radiation treatments, facing my fears and medical challenges with the determined bravado I assumed was expected of anyone in my place. My four kids gave me a reason to look forward, my dear friends stepped up to help, and my dad and siblings lived close enough for regular visits. I had a roof over my head and decent health insurance. In the midst of my battles I had even managed to start up an advocacy organization to support other cancer patients and their families. Over the past twelve months, I had been called “brave,” “strong,” and “an inspiration,” but I felt like I was none of that. That morning, after receiving the news that I was cancer-free, I could have felt relieved, maybe even joyful. Instead, I felt mentally drained and emotionally untethered.

As I sat drenched in tears and snot, it occurred to me that, through it all, not one person had asked me about my mental state. To be clear, I am not just a cancer survivor. I am a suicide attempt survivor. I am a rape survivor. I live with depression and anxiety . My mental illness “rap sheet” is diverse and lengthy. In fact, when I was diagnosed with cancer, I was barely a year into my recovery from a dangerous bout of post-partum depression that had wreaked havoc on my marriage and my family life. I had been perilously close to the edge of suicide. Despite outward appearances, the fight to reclaim my life wasn’t over.

A year earlier, in the weeks before my cancer diagnosis, I thought I was doing a fairly good job of putting my last breakdown behind me. Mentally, I was feeling okay. Physically, I felt good—I had gained weight; I felt strong. With the help of medications and lots of therapy, I had clawed my way back into a life and routine that was working for me. The diagnosis hit me like a friend’s betrayal. Suddenly, the body that I’d always turned to for sanctuary was no longer my ally. Once again, I felt like a failure.

I was no stranger to self-defeating thoughts, but now my body seemed to be confirming the worst of them: I got cancer because I didn’t breastfeed long enough. I had multiple pregnancies and multiple miscarriages. I smoked cigarettes. I ate too much sugar. I didn’t pray enough. I was a bitch. In other words, the disease was my fault. In hindsight, that kind of thinking seems ridiculous, but at the time it felt completely rational. Later, when I shared these feelings about my cancer with others, I discovered that it’s a common, even expected, response but at the time, I felt like I was completely alone.

As the youngest of three siblings in a family forever damaged by the violent murder of my mother when I was less than a year old, I grew up with an unspoken understanding that my role was to lift everyone else up. After her death, our family and friends sought consolation in my innocence and in my obliviousness to the tragedy that now encompassed us. “The baby will help us!” “AnnMarie is so funny; she’ll cheer us up!” I always sensed that I had a job to do, even though I was too young to know what had happened to my mother. I wasn’t told about the circumstances of her death until I was almost ten years old. No one talked about it; they had lived it. They didn’t want to talk about it. They still don’t.

Growing up without a mother defined me. To compensate, I surrounded myself with substitutes—my grandmother, my aunts, my godmothers, my girlfriends’ mothers. When I was little, I made up scenarios about running into my mother. She isn’t dead, she just has amnesia. Maybe I’ll see her in the grocery store, and she will know me immediately. Her memory will come flooding back, and we will be reunited! I didn’t tell anyone about my fantasies, because I was just a baby when she died. I believed I wasn’t entitled to miss her, because I have no real memories of when she was alive—things like how she smiled, what she smelled like, or the sound of her voice—but the reality is; her sudden disappearance must have been devastating to me, to Baby AnnMarie who experienced a life-changing tragedy that no one talked about.

When I was a teenager, I tried to kill myself twice. No one ever talked about that either. They assumed I had just overdosed on drugs. They called me wild and said I was on the wrong path, but nobody ever thought to ask why. I was treated for addiction , but my depression was never acknowledged. I was depressed in part because everyone expected me to be happy. I had to live up to my pre-defined destiny. I couldn’t notbe the life of the party. It was my job to make everyone laugh. 

To this day, I love that part of who I am. It makes me feel good to make other people feel good. That, in turn, helps my depression. But appearances can be deceiving—acting out and yucking it up doesn’t look like depression. Most people think depression means lying in bed for days, refusing to shower, sitting alone in a room with the shades drawn. That wasn’t me. I was lively, fun-loving AnnMarie, hiding the truth about how I felt from myself and from everybody else.
At fifteen years old, I was raped at a party. I had gotten drunk and was flirting with a guy that I knew was trouble because my soon-to-be ex-boyfriend hated him. It didn’t last long, but when it was over, my rapist looked down at me and said, “You’re not worth it.” Then he got up and walked away. I believed him. The incident left me with riddled with Ptsd and anxiety. Shortly thereafter, I made my first suicide attempt. Years later, when my older sons hit their mid-teens, I had panic attacks inspired by an irrational fear that they would rape someone.

After I was married, my pursuit of my ideal motherhood was ferocious. Acutely aware of my own mother’s absence, I was determined to be the best mother, and my expectations of myself were impossibly high. Clinging to the tiny bits and pieces I knew about her—she was a go-getter who chaired committees; she was a fashionista who ran a hair salon in her basement; her nieces and nephews adored her; my father adored her—I did everything to live up to who I thought she had been.

I was a good mother, but beneath the surface, I felt like a failure. I nursed Ben for “too long” and put Sammy on a bottle “too soon.” After the first two kids, punctuated by multiple miscarriages (more failure!), I stopped making baby food from scratch and started using jarred food instead. Ben started showing signs of OCD at about 18 months; I blamed myself. My pregnancy with my third son, Anthony, was miserable and his delivery was traumatic. He was a happy baby, but he was always on the move. Unlike Ben and Sam, he didn’t go to bed without a fight, and wouldn’t sleep through the night. I assumed I was doing something wrong. As always, I felt my mother’s absence; she would have had the answers I needed. I ached to know if her experiences with motherhood were similar to mine or completely different.

My pregnancy with my fourth son, Julian, was a happy surprise, but, just before I gave birth, my grandmother, who had helped to raise me, had a heart attack and passed away. Because I was nine months pregnant and they didn’t want to upset me, my family delayed telling me that she was in the hospital. By the time I got there, she was gone. I never had a chance to say good-bye. I was hurt, angry, and devastated. When Julian arrived, he was extraordinarily clingy. He wouldn’t let me leave him, ever. Whether he was with my husband, a babysitter, or the childcare at the Y, I would inevitably get a call: “He won’t stop crying. You have to come back.”I know now that this is part of the mental illness he suffers, but at the time I felt suffocated. I felt like I needed to free myself. I felt like a failure.

By the time Julian was around two-and-a-half, I felt myself breaking. I was exercising two to four hours a day and weighed 87 pounds. I ate bags of Skittles for breakfast, lunch, and dinner. My insomnia was through the roof. Alone with my kids during the day, I felt like the walls were closing in on me. When I tried to bring up my declining mental state to the people around me, they dismissed my growing panic. “Oh, you’re fine. You just need to get out and spend some time with your girlfriends.” So, I lurched back into my pre-motherhood comfort zone: out every weekend, life of the party, wild and crazy AnnMarie.

I started having suicidal thoughts again. I knew why I had to do it. I was exhausted and nobody was listening. No one saw my side. I looked around at my friends and they all seemed to be doing just fine. I felt like I was all alone. I felt like I was crumbling. I started formulating my escape; I made a step-by-step plan for taking my own life.

When I finally admitted to myself that I needed professional intervention, my life broke wide open. I had decided to seek help at a professional treatment center in another part of the country, but my husband didn’t understand my urgency or welcome the expense. I got a friend to drive me to the airport. Baffled and perturbed, Tom phoned me while I was waiting for my flight to be called. He told me to come home, that he might want a divorce. I didn’t get on the plane. 

When I got back to the house, we launched into a full-on argument. It was ugly, and I knew as it happened that I was going to complete my well-laid plan to kill myself. Despite the horrible moment we were having, I had the presence of mind to tell Tom what I was thinking. I asked him to drive me to my therapist immediately, and even though he didn’t understand what was going on in my head, he drove me there. When I told her that I had a suicide plan and that I was ready to act on it, she checked me into the hospital for a mental health assessment.

After hours alone in a room with only a mattress, the clothes on my back, and the unyielding stare of the police officer assigned to watch over me, I got a bed in the psych ward at about two in the morning. Looking around me, I saw disheveled people talking to themselves. There was a man running screaming down the hall, with several staff members chasing after him. Here I was; a soccer mom from a nice little suburb in Central New York, surrounded by mayhem, confined at my own request, because I was afraid I would harm myself. Yet again, I felt like a failure.

I did my time in the hospital, figured out my meds, made the most of group therapy, and came home. I worked hard to recover. I felt better. And then I got cancer.

I had a lumpectomy. 

I had a double mastectomy. 

I had radiation. 

I had reconstructive surgery, which failed, so I had to have it reversed. 

In the wake of my treatments for cancer, I developed lymphedema. By the time I found myself sitting in my oncologist’s office for the one-year follow-up, listening to him congratulate me on a job well done, I was experiencing a shit-storm of side effects. My whole right side was numb. I had pain that I couldn’t explain. When I tried to talk about it, I was told it was all in my head. “It’s stress.” “Take a muscle relaxer.”“You’ll be fine!” As a woman with paranoia and a lifetime of feeling unworthy, who lacks confidence and assumes that other people are all smarter than me, I believed them. I let it go. A year later, I would be diagnosed with multiple sclerosis.

I’d like to say that my two-hour torrent of tears had a healing effect on my spirit, if not my body, but I don’t think it did. Yes, it was a much-needed release, but as the wave of emotion faded, what I experienced felt more like resignation. I was still fighting for my life. Despite glib reassurances from all sides, I had work to do, and I had to do it myself. My kids need their mom. I had an organization to run, a network of people that relied on me, and dinner to cook. “I am worthy,” I told myself and took one more deep breath. Then I stood up and began again the relentless uphill battle of convincing myself that it was true.

I started blogging to keep my family and friends informed about what I was going through and unintentionally discovered that my story matters to people that I don’t even know. I began to work as an on-call advocate for organizations that support cancer patients and their families. I started receiving invitations to speak about cancer and, later, about mental health issues, at conferences and seminars. All of it helped me to heal. But was it ever enough?

One friend, who has since passed away, encouraged me to continue speaking out. “Be my voice,” she urged. Today, whenever I Tweet, or post a new blog entry, or speak at an event, someone reaches out to tell me how deeply my words resonate. When I engage with people who are suffering, and when I can help someone feel less alone, I am filled with relief. My voice matters. What I have to say about my experience is vitally important. And speaking out for someone who can’t speak up is hands down the best therapy I’ve ever had. I would miss that feeling so incredibly much. I would miss the part of me that some may not understand the part that makes me who I am. I would miss knowing I am worthy.

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Posted on October 5, 2020 .

Perspective

It's been forever since I've written and I'm not really sure why I guess I am busy, covid, kids-ya know life. I've been dancing with NED for  a month now and it's been truly surreal. I do feel as though so I got a bit of my life back almost like I feel alive again. Does that mean I don't think about cancer and what it's done to me the past 8 years absofuckinglutly not. The reality is it still looming in the background. Through this ridiculous pandemic that's going on, no hate I know it's a thing it just took it in a different way because ya know-Cancer is still part of my life. I found myself like “screw you covid- I had cancer I sure as fuck am not going to let covid kill me”. I think a lot of us in the cancer world found ourselves saying that. But I started to think what the hell has happened these past 8 years. So much has happened and truthfully it is all on cancer. 

It all hit me last night when I had a headache. I've always had headaches. I haven't had a brain MRI in a long time and it doesn't usually stress me out but for some reason last night it did. What people don't realize is when you have a PET scan it is from your neck to about your upper thigh -does not hit your brain.  So I started to freak out if they missed my brain and it's headache is really brain METS. Now two things here first of all I know that many people find their brain METS this way. I totally get it, that's not what this blog post is about though. This is about the fact that every ache or pain will always be “could it be cancer coming back”. Like I'm serious every pain I don't care if it's a hangnail or you stub your toe and all the sudden you have extreme pain in your foot after having a cancer diagnosis the fear of it coming back never goes away. 

Maybe I'm feeling this way because my 8-year anniversary is coming up. Next week will be 8 years that I had my lumpectomy and they told me “it's nothing, don't stress about it”. So I went to that doctor's appointment by myself to get the results. I remember it like it was yesterday seeing my doctor walking in the door and saying I wish you weren't my first appointment. I knew right away what was going to happen so I looked at her and said “why because it's cancer?”. Funny cause we all sort of have that feeling whether we have a biopsy or testing that it could be cancer but no matter what you think just maybe it is nothing. But deep down you know. After hearing those words the rest is like a dream big nasty fucking dream.  You hope you're going to wake up from that nasty dream but then you realise, nope here to stay. I remember having the attitude that I will just get this shit over with and I can get on with my life. How freaking naive I was. I now know that cancer does not leave you but you can learn to live with the stupid dumb fool.  My perspective changed so much. 

My very close friends now I'm a worrier it's just how I am. The funny thing is I worry more about other people.  I can make a whole story in my head about how someone simply going to work, a drive they do everyday; hit a bump, car flipped, went into a ravine, they can't get to their phone and they're going to die because no one knows where they are-in a heartbeat. I just worry about others, it's truly who I am. I don't necessarily worry about myself. Part of that is because I have faced death so many times I just don't think about it. Living with depression and suicidal thoughts I had many a moment where I just was like ok cancer just kill me and let’s be done. That way people would not worry about me. I had a hard time letting my friends and family worried about me during my diagnosis. I was the worrier who took care of them. I didn't like it being flipped onto me. It was very hard for me to let them take care of me. After all, how many times did they all tell me how strong I was? This isn't a dig it is just hard to be taken care of when you are “strong”.  I realize that being strong is about getting help. Again my perspective changed. 

Cancer affects you physically there is no doubt there we can see it. They forgot to send the memo about cancer and the mind fuck it does to you. Self body image is screwed up, depression/anxiety is peaked, PTSD is no joke, anger mixed with happiness is confusing- just to name a few. Cancer is scary as hell and there is no rule book about it. I learned that every emotion is valid and ok for you to have. I went and got therapy, support groups and kept SDBC going for me. SDBC is just as much my therapy as it is for those asking questions. I started to see those “cancer free” moments and I held them. The times when I am laughing, singing, cooking and there is not one single cancer thought in my head. I had to change my perspective and embrace these moments. 

Now one thing remained the same. This tiara has never left me. Maybe it needed polishing or to be straightened but it remains. I am not any stronger or braver than anyone else going through this. I am just a North Side, Italian girl who has changed her perspective but is bringing herself back-tiara, stilettos and all.

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If I could….

I don’t really talk about my mom’s death very much. I guess mostly because my family still has so much grief around it. There was no real processing of it back then or learning how to handle your grief. It was all about making it through the day and survival but not what you were really feeling. For me it’s so intense sometimes I can’t contain my tears. What the reality of her death has meant to me and how real my grief is on a day-to-day basis is something I struggle with. If I could get over it I would. 

 It’s funny because recently I was with a friend and somebody asked about my family. I think they were referring to my mother and father but I was trying to divert the conversation. Nothing like a buzzkill when you say your mother was raped and murdered. People don’t know how to react they really. They think I am going to say Cancer of course then when they hear it out loud it’s a shock. For me I felt like I watched a movie but do not remember. You know the one you swear you know it and you watch it and at the end you say “ oh my God I remember this movie”.  I have felt like that about my mother's death like I know what happened as I’ve read about it, people told me but I never actually lived it. I guess I’m sort of glad I haven’t. I see what it’s done to my family from them seeing it. It doesn’t lessen my darkness just is different. When you have grief and tragedy start your life at one years old is incredibly impactful. It shaped and defined me-it’s made me who I am. I have before how I was that person that the family turn to because hell they needed something to laugh at. And that became my role my job and my family to comfort everybody. Don’t think they meant to do it it’s just what happened. Man that’s some pressure that I don’t think I can ever really explain. So I buried my grief for years so that I could comfort them. I needed to mourn my loss too though. If I could just be that girl I would. 

As hard as it is to understand my birthday is the hardest day for me. You see she was taken just days after. So here my family had this party to celebrate their baby’s first birthday with food and laughing but I have no memory of it. They all can think even a little about it something so small and remember that day. I have nothing. It’s supposed to me joyous but it’s surrounded by pain. Don’t get me wrong they all do an amazing job of trying to make my birthday grand but the truth is I see what’s going through their eyes. The dread of the days to come. Trying to enjoy something to only be followed by pain is exhausting. Dates have a way of setting off your emotions. If I could just snap out of it I would. 

I think about my birthday starting January 1st. I try to say “this one will be different “ but my tears take over. I never got to see how my mother would have done my party. Ribbons in my hair and party dresses were stolen from me. Maybe that’s why I make such a big deal of the kids birthdays. It’s not that I want to forget my birthday I just want to not feel such pain. I am not sure how to do that. Trust me neither does my therapist. Hard when your trigger is your birthday. If I could forget I would. 

There are no pictures to “remember” the party I go by hearsay. I have conjured up the day in my head but I don’t feel anything. Like a story I have written but the characters are made up. Your mother is supposed to be there for all those birthdays and celebrations it makes me so angry it was stolen from me. Mothers are irreplaceable the hole in your heart can’t be filled. If I could fill that hole I would. 

 I bought my best friend a picture of his mom holding him. He loved it which made me so happy. Then the reactions his siblings had to it made it clear how much a photo can mean. Especially one of your mom when she is gone. The feelings, the smells, what the room was like are all embraced in a photo. How I wish I had more than two pictures of her with me. I am jealous of those who have them with her, I can’t even look at them. When was the last time you took a pic with your kid? Or your mom? If I could I would. 

Since grief has no timeline, it doesn’t have rules either. This is how I try to cope with all the thoughts in my head. I started this blog post because I wanted to explain why I grieve so deeply at my birthday. I realize it’s not about that it’s really just about missing my mother. At 48 I just miss her. If I could just straighten my tiara and embrace the day I would. 

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Posted on January 31, 2020 .

What would you miss?

Filming has wrapped for a 60-second PSA, which is onschedule for release at the end of November. To request a copy, to schedule an interview, or for more details, contact AnnMarie Giannino-Otis via email at wwym19@gmail.com.

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"What WouldYou Miss?"WWYM is catapulting forward with a PSA, a new website, a sweeping social media presence, and coming soon, a TV talk show and podcast.   Fayetteville,New York:  With Last month’s launch of What Would You Miss? AnnMarie Giannino-Otis has inspired a new kind of conversation about depression and suicide, and the response thus far has been nothing less than astonishing.  “The central idea is to start a conversation that inspires hope and reminds us about things in life we may be taking for granted,”says AnnMarie. “Knowing that others find you worthy opens the door to hope. And It’s already saving lives.”   Both a simple question and, perhaps, the seeds of a movement, What Would You Miss? creates a dialogue between people who struggle with mental illness, and those whose lives they touch.  Respondents have offered answer like “I would miss the way my dog wakes me up in the morning by gently tapping my face with his paw,” “I would miss Christmas time,” and “I would miss seeing how compassionate and caring my kids are.” Whole Depression and suicide are no longer as shrouded in secrecy and shame as they were even a few years ago, the topic can feel like a minefield, especially to someone who is not formally trained to handle it. When someone you love is suffering, the prospect of approaching that person and saying the “wrong” thing can be terrifying. And, if you’re immersed in the struggle yourself, the mere act of reaching out may seem like an imposition that will only drive loved ones away.  Simply asking or answering the question, “What would you miss?”connects people on both sides of the dilemma, giving them a softer way to have a difficult conversation.  After Wrapping up filming this week, AnnMarie and her team will soon release the60-second PSA that shares just a few of the sometimes funny, sometimes sad, but always deeply poignant responses she’s gotten from a range of people—mothers who have lost a child to suicide, teens and adults with chronic depression,suicide survivors, mental health professionals, and crisis counselors. “It’s Clear that the little things matter, a lot,” says AnnMarie, who is a suicide survivor herself. “In just over a month, the Facebook page [https://www.facebook.com/whatwouldyoumiss/]and Instagram account [https://www.instagram.com/what_would_you_miss/]” have attracted visitors and responses from around the country. It’s been amazing and a little overwhelming.”  With a growing number of organizations buying into the concept, including NAMI(National Alliance on Mental Illness) Syracuse, the Newhouse School of Public Communications at Syracuse University, the American Foundation for Suicide Prevention, and local school systems, What Would You Miss? is quickly gaining momentum in the community, as more people ask, answer, share their responses, and begin an important dialogue that can open the door to greater understanding and empathy, and give hope to someone who may feel worthless.  

To Encourage widespread participation and communication among people from all walks of life, the What Would You Miss? Facebook page and an Instagram Account provide platforms for anyone to submit an answer or read through the very personal responses that others have posted.  As part of the initiative, AnnMarie urges those in crisis, or those who just need someone to listen, to text the word “TALK” to 741741, the Crisis Text Line, where trained crisis care professional will respond immediately. The Evolution of a big idea about small moments AnnMarie,the founder of Stupid Dumb Breast Cancer who has also built a reputation for relentless advocacy in the mental health space, has struggled with depression and suicidal thoughts since she was a teenager. Known for being outspoken and irrepressible,with strong opinions and an edgy sense of humor, AnnMarie comes from atight-knit family with deep roots in Central New York. “When I tell people thatI have depression, that I have tried to kill myself more than once, they are shocked,” she says.  “They point to my family and friends, to all the good things in my life, and say, ‘Look at everything you have! Look at all the people who care about you!’ What they don’t realize is that I feel unworthy of those good parts my life. Especially when I’m in that dark place, I truly believe that the world would be better off without me.” Through lots of therapy, the right medication, and no small amount of faith in the assurances of those around her, AnnMarie has over time learned to believe tentatively in her own worthiness, but she worries that others in the grips of this mental illness will not get the message in time.  One day recently,after someone suggested that she consider how much she would be missed,AnnMarie turned the lens on herself and started thinking about what she would miss, or miss out on, if she were gone.  “I made it very specific,” sherecalls.  “I would miss singing at the top of my lungs as I drove in the car. I would miss telling my friends cheesy jokes at our monthly Bunco Game.”  Then she took the idea a step further. “I asked myself what the people in my life might miss about me in my absence. And when I brought it down to the particulars—my oldest son wouldn’t be able to call home and tell mom about his latest cross-country wins; my family’s traditional Sunday dinner would be permanently cancelled—my perception changed completely. It hit me at avery deep level that my impact on the lives of the people around me is both positive and very real. I want to give others that same sense of worth, and with it, hope.” AnnMarie immediately started reaching out to others about her revelation. She asked people who had lost children, siblings, or friends to suicide what they missed about their loved one. She asked people still struggling to hold on and others with loved ones who were struggling, “What would you miss?” if they were gone.The feedback was overwhelming. “People jump at the opportunity to speak what’s in their hearts, and to be heard by the person who desperately needs some hope to cling to. These insights open the door to a bigger discussion, the kind of dialog that could help change a mindset and save a life.” Inspired by the response, AnnMarie has established What Would You Miss? so that people impacted by depression and suicide can speak their truths around a mental health epidemic and a leading cause of unnecessary death in the United States.

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Posted on December 10, 2019 .

“You don’t get IT”, but it’s not your fault!


Th following is a guest blog post from an amazing friend.

I am one of the many faces of Metastatic Breast Cancer

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In a culture focused on survivorship, those with metastatic breast cancer who will be in treatment for the rest of their lives can feel isolated and misunderstood

Let me educate you on what this means:

  • Metastatic breast cancer, stage 4 breast cancer, is a stage of breast cancer where the disease has spread to distant sites beyond the axillary lymph nodes.

    • Liver, Bones, Lung, Brain

  • Between 20 and 30 percent of women with early stage breast cancer go on to develop metastatic disease. While treatable, metastatic breast cancer (MBC) cannot be cured. The five-year survival rate for stage 4 breast cancer is 22 percent; median survival is three years. Annually, the disease takes 40,000 lives…I’ll let that sink in for a minute..tick tick tick. 

  • We will endure CT Scans every 3 months for the rest of our lives

  • Every 3 months, we have anxiety and anxiety that you can’t imagine

    • The results – we hold our breath and pray that cancer is at bay, not growing, not showing up in other areas

  • We will have some sort of therapy for the rest of our lives. 

    • Infusions every 3 weeks

    • Extra drugs to combat hormones

    • Most of us will endure Chemotherapy again, which means here we go again with:

  • Nausea

  • Gaining weight

  • Losing weight

  • Countless needed pokes at our portal

  • Mouth Sores

  • Rashes

  • Diarrhea

  • Loss of hair, including eyelashes and eyebrows 

  • Mood Swings – that we can’t apologize enough for

Think of it this way, we mentally live in a square with different levels of stairs.

We all come in on the first floor – this is where they give you the news of your port, how much chemo you will have and for how long. You may get a brief out lookout of your future treatment plans.
Then we must get the port put in. Read about how goes…it might scare you, I know I was 

2nd Floor leads to your first chemotherapy where we will be spending the next 3 to 6 months juggling doctors vs Chemo infusions every week for hours, sometimes 7 to 8 hours a day with our shortestest day 4 hours.

3rd Floor leads us to maintenance which may mean infusions every 3 weeks, extra drugs like Letrozole which have side effects of: think about that one for a minute…tick tick tick

Some people I have talked to have had to stop this drug and try another one.

  hot flashes

 hair loss, 

 joint/bon/muscle pains 

 tiredness – LOL that stays with you for a while

 unusual night swats – invest in a couple of extra sheets

 nausea, 

 diarrhea, 

 dizziness, 

 trouble sleeping, 

 drowsiness, 

 weight gain, - I say HA bring in on, 2oz at a time would be good 

 weakness

 flushing (warmth, redness, or tingly feeling), 

 headache, 

 constipation, 

 numbness/tingling/weakness/stiffness in your hand or fingers, or 

 pain in your hand that spreads to your arm, NEVER be CURED writs, forearm, or shoulder

4th Floor the floor we hope to never reach.   4th floor may mean surgery, radical drugs or the worst hospice-another friend is gone.

However, we can bounce to floor to floor at any time.  So, we may sit on 1 or 2 for years hopefully we can get a reprieve. 

We know that we will fight to keep the cancer at bay, if that’s what the cancer wants to do. 

  • Thinking of the future can scare the hell out of us – I hope I live to see my grandchildren
    can you imagine that thought running through your mind every time you see your grown children?

  • Angry, Stress, Outraged, Depressed, Scared are many of the feelings that we have

    • 5% this is where we could be at any time 

    • 95% of the time we are positive and as a matter of fact – can’t change what I have

How can you help? Please reread what you are sending us! We know that you are saying things with the BEST intentions. 

Things I’ve heard: 

  • Your just not being positive – read above

  • Your giving up – really you can say that to me? 

  • I’m Sorry – for what you didn’t do this? I heard a good response for this “Don’t be sorry, donate” 

  • When I look at my life, its not so bad compared to yours – sorry but WTF 

  • My favorite – What can I do for you? I don’t know, just do whatever you feel is good to do

    • I’ll never say no to a home cooked meal 

  • Not that I hear this per say, but I see it your eyes when you give me the pity look. I’m just out doing my thing shopping and have a great time and your look is just a reminder to me of what I have. 

When we post how we are feeling, it’s just that! We love your best intentions to respond. But the best response could be, hang in there, you’re doing great, I’m proud of far you have come, when’s a good time for a visit, let me help you with etc. Say things like this let’s us know that YOU GET IT. 

I know that you will not truly understand what we go through because, you can’t unless you’re in the same boat (I would never want that). 

To tidy this up, we love you and we so appreciate all the support you give to us.  We just want you to have a better picture of what our life is like. Plus we are trying to educate the public! 



Tell It Like It Is… Telling My Kids I Had Cancer

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The day I was diagnosed is a day I will never forget. Countless things were running through my mind and on the list was how was I going to tell my family -- especially my children. When I first became a mom, I knew I had to learn how to get through the diaper rashes, the terrible twos, potty training and the teenage years. Never did I think I would have to learn how to tell my kids I had cancer.

I came home after my appointment to my father watching my then 4 year old son. I revealed to my dad that I had cancer and he started to cry. I asked him to please stop, that this was my cancer and I was not ready to cry so he needed to stop. He mumbled that he needed to meet someone (which I knew was a lie), but I was relieved he was leaving. I was too scared I was going to break down. When he left, I’m sure he cried in his car after hearing his baby daughter had cancer. Throughout my process, he was the strongest I had ever seen him. When I needed him, he was strong.

The day went on like I was living it but not there. Telling your child you have cancer is the scariest thing to do because there is no definite that you are going to be ok. You instantly rip their childhood away, you strip them of innocence and enter them into a world of fear. How would I find the words and what should I say? Having four children, you learn that each one handles things differently, so I knew I needed to be generic in my words yet at the same time my reactions needed to be individualized so each child knew I was always going to be there for them. I knew my then 14 year old was going to handle it very differently than my 4 year old. Going into the conversation I felt like a liar because I told them it was nothing when I went into the lumpectomy. I wanted to tell them the news in a way that they understood I was telling them what the doctors told us. 

I was not going to wait to tell the kids. I wanted to be up front and just let it out. That night after dinner we sat all four down and told them. There were tears, anger, fear and some naughty words said -- “stupid dumb breast cancer” from the 4 year old -- but we talked. The tears came from the child who was 6 and unsure what cancer meant. The anger from the 13 year old who yelled that we told him I was ok. Why us? Was I going to die and how can he ever eat this meal again without thinking of this moment? The fear from the 11 year old worries what will happen to his mommy. Can he get breast cancer cause he breastfeed? We answered the questions and explained that we do not have all the answers because this is all new to us, but as we know they will know. That we will not lie, you can not get breast cancer from breast feeding and that we were scared too. 

Saying you have cancer out loud made it more real every time I told someone it felt like a punch in the gut. Keeping it simple and understanding that it is ok to be scared and angry even when you tell people makes it easier. Embraced the fact that like my emotions changed, others reactions will too. They could not understand what I was going through yet they were hurt and scared in their own way. But with my diagnosis came an entire new world-- the cancer world. I looked to them for support, education and advice. They gave me tips on how to tell my work or the school. Together they explained how they told their family. I gathered all the info they had and took a little of everyone’s to find mine. The best way to do handle this is your way. There is no right or wrong way to tell your family. Find your own way and don’t be pressured by how other have told their families-- this is your cancer no one else’s.  Not everyone has a shiny tiara to keep straight.



Bags of Inspiration

Donate a "Bag of Inspiration" In Honor of Your Loved One

For $35 you can donate a Bag of Inspiration to a cancer patient receiving treatments at Upstate Cancer Research Center. Each bag contains:

Warm Blanket
Acrylic Tumbler with lid and straw
Knit Hat
Bandana
Buddha Board
Aveeno
Candy
Chapstick
Queasy Drops
Activity Book
Markers

Faceplants warm Cozy Mermaid Slippers

When you donate a bag, your loved one’s name will go on the top of an inspiration letter that will go in each bag.  Or if you wish you can email your own letter to be included in the bag. 

Please inbox us for instructions on how to donate a bag to honor your loved one.

Sometimes when you are needing a little help it pops into your life. Laurie and I grew up in the same community only years later to connect cause of stupid dumb breast cancer. Then again when she was slammed with a Stage 4 diagnosis. I missed doing my bravery bags but no time. BAM Laurie has the drive, passion and reason to start this up. It is now called “Bags of Inspiration” and we are ready for action! Please read Laurie’s story…

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Hello, My name is Laurie Sutherland and I’d like to tell you a little bit about myself.  I am 52 years old and I have been married to my wonderful husband Jim for 32 years. We have 3 incredible kids (adults) that we are very proud of.  In 2009 our lives were interrupted when I was diagnosed with Breast Cancer. I went through several major surgeries and although my body was drastically changed, my outlook was positive.  

At the time my friend introduced me to her wonderful friend Ann Marie.  Ann Marie is the founder of Stupid Dumb Breast Cancer and like most breast cancer fighters/survivors there was an immediate connection, sort of like a sisterhood. I watched Ann Marie build Stupid Dumb Breast Cancer into a place where everyone regardless of what type of cancer could read, learn, voice their opinion, ask for advice etc. She amazed me, her strength was superwoman like! Ann Marie helped me recover in so many ways, but first and foremost she was a friend that I could count on. 

Now I’ll take you to this year!  In May I had a routine CT Scan as Pancreatic Cancer runs ramped in my family.  I was expecting the results to be negative as I wasn’t experiencing any symptoms.  Much to my surprise I received a call from my Dr. advising me that my results showed some spots on my liver. I had a biopsy and 3 days later I got the devasting news that I had Stage IV Metastatic Breast Cancer in my liver. WHAT??? How could this be?? I have been cancer free for 10 years!  Well it is what is, I can’t change it, so I put my BIG girl pants on and decided to FIGHT this BEAST! After the dust somewhat settled (it never will completely settle) I reached out to Ann Marie and as always, she was right there for me for whatever I needed.

My first day of Chemotherapy was scary (I didn’t have chemo the first time), but I was met with an incredible team at Upstate Cancer Center. When I checked in for treatment, I was given a beautiful basket with items that I would use throughout my fight.  I was so INSPIRED by this! After a couple of weeks, I reached out to Ann Marie and told her that I had been up all night thinking about ways that I could give back to other cancer patients. I came up with an idea of “Bags of Inspiration”, and Ann Marie’s response was “We are cut from the same cloth”, I too used to do bags.  Her bags were called “Bravery Bags”. And so, “Bags of Inspiration/Bravery Bags” were back in full force! 

If someone was to ask me why I do these bags, I would have to tell you that it gives me a sense of peace, satisfaction that we are helping other cancer patients, pride in knowing that we are making a difference. One of the most amazing things I have found throughout this process is how generous people and companies truly are.  Ann Marie and I are receiving boxes daily (we know the delivery drivers by name – lol).  

I would like to take a moment to THANK, not only everyone who has purchased items through our Amazon Wish List but to the list of our ever-growing companies listed below who have generously donated items to fill our bags. 




Faceplant Dreams –donated 200 of their warmest bedroom booties
Visit them at www.faceplantdreams.com

PJ Harlow – donated 10 of their softest silk pillowcases
Visit them at www.pjharlow.com

Buddha Board – donated 210 Mini Buddha Boards
Visit them at www.buddhaboard.com

MJD Associates
www.mjdcorp.com 




Mesothelioma & Breast Cancer


This article was written by a friend, hope it sheds some light on a very real issue.

Is there a link between breast cancer and mesothelioma? One is a common cancer in women, and the other is rare and caused by asbestos exposure, usually in men. Researchers are finding similarities between the two, and further studies are underway.  The connection between asbestos and mesothelioma is already clear, but scientists say asbestos might contribute to cancer of the breast, digestive system, reproductive, and lymph systems.

What is mesothelioma?

Mesothelioma is an incurable cancer that starts in the mesothelium, the tissue that covers internal organs. There are four kinds of mesothelioma: 

  • pleural which affects the lining of the lungs

  • peritoneal which affects the lining of the abdomen

  • pericardial which affects the heart 

  • testicular


Pleural mesothelioma, the most common form, causes breathing problems, chest pain, coughing, and unexplained weight loss. Symptoms may take from 20 to 50 years to develop, and the risk after exposure never goes away. 

How is breast cancer linked to mesothelioma?

Studies done on breast cancer and asbestos have been inconclusive, but a few suggest a link. In one United Kingdom study, women who lived near an asbestos manufacturing plant had a slightly higher chance of getting breast cancer.  Other research in Great Britain also found that women who had asbestos fibers in their lungs from past exposure were more likely to develop breast cancer. In 2009, however, an Australian study looked at over 3,000 women who lived in a town that had an asbestos plant until 1966. Compared to the general population, the women were more likely to get ovarian or cervical cancer, but their rate of breast cancer didn't go up.

Researches know asbestos enters the lungs when people inhale the fibers, but they don’t know if the fibers can spread to the chest cavity and breast through the lymphatic system. They are also uncertain if shards of asbestos can travel to the wall of the chest through the pleural tissue or lungs and cause cancer. 

What do researchers know about mesothelioma and breast cancer?

One factor that makes mesothelioma hard to diagnose is its similarity to other kinds of cancer. Although rare, at least one case of metastatic mesothelioma was mistaken for breast cancer. Symptoms of breast cancer may result from cancer in the mesothelium. Because markers, structure, and cell growth can be similar in both diseases, the origin of the cancer can be hard to establish.

Although rare, there have been incidents where high-energy radiation used to shrink tumors in breast tissue led to mesothelioma. Radiation used to treat breast cancer passes through the skin and pleural cavity, and it can occasionally cause changes that lead to cancer. 

Researchers who discovered that mesothelioma could be mistaken for breast cancer wondered if breast cancer treatment would also help mesothelioma. Treatment with a drug called aromasin reduces estrogen and slows the growth of tumors in breast cancer. When given to mice with mesothelioma, it slowed the spread of cancer cells and reduced the size of tumors. This could be because cells in the two diseases are similar. 

Pliny the Elder wrote about the dangers of asbestos in ancient Rome, but the toxin's link to mesothelioma was unknown until the 20th century. Although the government has taken steps to limit the use of asbestos since the 1970s, the Trump administration is trying to ease those restrictions. Americans need to stand up for environmental safety and medical research if diseases like breast cancer and mesothelioma are to be eliminated.



Posted on September 16, 2019 .