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Susan Cornett

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Blog Entries posted by Susan Cornett

  1. Susan Cornett

    cancerversary
    Today marks 6 years since my diagnosis. In 6 years, I've had surgery, chemo, more surgery, thyroid cancer, more chemo, radiation and SBRT. But I have survived and (mostly) thrived. The path hasn't been easy and I have a number of side effects that are trying, but I'm here. At the end of the day, that's all that matters. 
    Looking forward to next year's cancerversary!
  2. Susan Cornett

    cancerversary
    Today marks 5 years since my diagnosis. It seems like just yesterday but also a lifetime ago - at the same time. It brought me to the club I never wanted to join but introduced me to so many wonderful people. I am thankful for my medical team and all of the research and advancements that got me to this point. 
    Looking forward to marking next year's cancerversary with all of you.
  3. Susan Cornett
    I haven't been on here much in the last few months, maybe a year. Work kept me much busier than usual but I *think* that is going to finally level out now that we've hired a new director and a couple of additional consultants. I also find it more difficult to break away from my work when my daily commute is now just a walk down the hall. I'm fortunate - and I know it - because I've been able to continue working without interruption. My employer has offices in CA, FL, NJ, OH, and TX and all of our offices were closed through May. They continue to encourage us to stay home through June and to come back at our new pace. 
    Now I have to figure out what this new "new normal" looks like for me. When do I return to the office? Should I return? When can I go see my parents? I know that we don't have a crystal ball but I'd love to have an idea of what's next. I take an annual beach trip with my girlfriends in September but I'm beginning to think that won't happen this year. Two of my friends have jobs that require them to interact with people all day. Even if I drive to our destination, they will all be coming off an airplane and possibly exposing me. I know the beach will still be there next year but this is one of those trips that I look forward to all year.
    I see Super Doc in a couple of weeks and Super Pulmonologist in July. Hopefully they'll have some thoughts on all of this. Until then, I'll continue to stay at home. Ugh.
    Please stay well, friends.
  4. Susan Cornett
    Today marks 4 years of survival! By most standards, my path hasn't been as difficult as others. There have definitely been highs - when my hair grew back, my lashes grew in longer  - and lows - two recurrences and a secondary cancer diagnosis. But as I say often - I'M STILL HERE! I tell my story to anyone who will listen. People need to know that lung cancer doesn't have to be an automatic death sentence. Does it suck? Yes. Will it change your life? Definitely. But you move forward, one step at a time. Forward is forward ,no matter the speed.
    I am looking forward to the Breathe Deep Denton event in April. I enjoy visiting with the other survivors and bringing attention to this cause. I've also been asked to speak at a function in March so I'll be sharing my story again. The more the public understands lung cancer and all of its causes, the better our funding will be for research. 
    Most importantly, though, is this: I stumbled across this site one night when I was looking for answers. I have met wonderful friends - in person and online - here. Those friends have made this journey easier. Thank you, all. 
  5. Susan Cornett
    Most days, the cancer is buried somewhere in my thoughts, my work, my hobbies - not at the surface.  But there are days when it hits me right between the eyes.  Cancer.  How the hell did I get here? Is this really my life?  
    Wondering if anyone else has experienced this.
  6. Susan Cornett
    I've said it before and I'll say it again:  cancer can be as hard, if not harder, on the loved ones than the patients.  Our family is very close  - I don't have any siblings and my husband and I don't have children.  Our family unit is small.  After 2.5 years, my husband and I have a process.  He goes with me to all of my scan result appointments.  As soon as Super Doc gives us the results, Neal steps out and texts or calls my parents with the updates.  I always want to be with them if we have to give them bad news. My parents live 4 hours away; otherwise, I think they'd crowd into the exam room with us.
    Although we had to give them bad news a couple of weeks ago, we actually had something in our favor.  A lifelong friend of mine was visiting with them on the way to take her daughter to tour a college.  She was able to keep my parents somewhat balanced this time.  I'd been preparing them for the results - figured this was coming.  But no one wants to have to call their parents and tell them the cancer is back.  Stupid cancer.
  7. Susan Cornett
    Today, I happily paint two of my toes red, to celebrate two years of being a survivor.  Some days I ask myself it has really only been 2 years because it feels like I got the diagnosis so long ago.  Lots of scans and needles and chemo and radiation and....I'm still here!  
    I woke up this morning, very cheerful, almost like I was celebrating a birthday.  I realize that EVERY SINGLE DAY is a gift, whether we have lung cancer or not, but that cancer seems to make each day that much more important.  While I was thinking about everything today, I was overcome with emotion.  I know that I am blessed to have as much time as I've had.  I think about the friends I've made in this "club" that are no longer here.  For those friends, and for the rest of us, we continue to choose life.  

  8. Susan Cornett
    I'm in the middle of my quarterly scan appointments.  While I was waiting for my blood draw yesterday, I noticed a couple that was apparently new to the oncology clinic.  The wife is the patient and, when she was called into the lab, her husband got up to walk with her and she told him she was fine, just going for a blood draw.  I looked at his face and saw fear and I just wanted to give him a hug.  This is the part I hate the most - when we look into our loved ones' eyes and see their fear.  I just want to fix everything and I can't; we have so little control over this part of our lives.  I have no idea why she was there or what her diagnosis is, but I definitely said a prayer for them last night.  
     
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