What is HOPE?

I was diagnosed with stage iv lung cancer in August 2015. I didn't register for the 2016 LUNGevity Hope Summit. At the time, I was just getting used to life with lung cancer. I followed the social media posts and photos. It looked like a good time was had by all. It gave me hope and inspiration. I got to attend and be in the photos this year.

Hope Summit features inspirational speakers, medical expert forums, lung cancer survivor-specific sessions, and opportunities for lung cancer survivors to connect with other survivors and share their stories. Their stories of hope. Hope Summit is appropriately named because that's what this last weekend delivered. I'm at a new step in my treatment plan. You would think being immersed in three full days of lung cancer talk would be depressing and make me worry about these next steps. It was just the opposite.

As a first time attendee, I applied for and was granted airfare and hotel stay to attend this year's Lungevity Hope Summit in Washington DC . Lungevity provides this so all lung cancer patients have an opportunity to participate in this event.

I also attended an advocate day, which was on the eve of the Hope Summit kick off. I was interested in finding out information on advocacy and how to be more involved, if possible.

On Thursday evening I went out to dinner with a fairly large group of lung cancer patients and survivors. This was one of my favorite moments of my trip. I find it interesting that 17 people, with 17 different backgrounds, 17 different lung cancer stories and probably 17 different combined lung cancer treatments and/or drugs and we instantly bond with one another. Some have had it rough and some have been to hell and back. Some have been dealing with this for months and others for 12+ years. But having lung cancer is our common ground. I heard a good comparison once. Someone was taking about skiing. He said the downhill skier going 70+mph has the same adrenaline rush as the beginning skier, even when they aren't going the same speeds. I'm guessing the 17 of us have the same hatred for lung cancer.

Having time with other lung cancer patients and survivors was my best part of going to Hope Summit. It gave me the opportunity to thank two of them, in particular, in person.

I was at the top of my physical fitness game when I was diagnosed. One of my first fears was the possibility of never running again or working out like I used to. But I watched videos of Juanita power lifting and doing what she loved and what she did before lung cancer. That gave me hope.

The other was Patty. I would see her online, participating in events with Team Draft. Her smile and attitude would shine in the photos and videos.

I knew I wanted to be a part of that. It gave me hope that one day I would. And I did! Down to the wire, Patty was my biggest competition during the Team Draft Lung Cancer Survivors Super Bowl Challenge. If anyone was going to raise more funds than me and knock me out of the running, I wanted it to be Patty.

Several weeks ago this question came up. What is hope? Without thinking too hard about it, this acronym came to mind.

Hope

is

Having Optimistic Perspectives Everyday.

Super Bowl Challenge

I kicked off my Cleveland Fans Against Lung Cancer fundraising campaign this month. This is part Team Draft's 2017 Lung Cancer Survivors Super Bowl Challenge. This is a friendly competition between lung cancer survivors to raise funds for lung cancer foundations and cancer centers of the survivor's choice. The survivor that raises the most funds will win a trip to the Super Bowl in Houston, TX. Second place is a trip to the Pro Bowl in Orlando, FL and third place gets to attend  26th Annual Taste of NFL.

I set my fundraising goal high. I know with your help I can reach that goal. Lung cancer research funds are critical to my future and my quality of life.

My funds will be donated to the International Association for the Study of Lung Cancer in Denver, CO. I attended my first lung cancer event in September 2015. It was just two weeks after my stage iv lung cancer diagnosis. That event was the Pancake Walk Kickoff Breakfast for the World Conference on Lung Cancer in Denver. That day I was introduced to a handful of peopleand survivors in the lung cancer community. They gave me information, hope and advice that I will always remember and hold near and dear to my heart.

In Week 10 of  NFL season, the Browns have an 0-10 record. The Cleveland Browns may not be going to the Super Bowl this year. I may never get to see the Browns at a Super Bowl in my lifetime. But you could help send this Cleveland fan to the big game this year.

Together we can #tacklelungcancer.

I challenge you to make a donation today and find one (or more) person to match your donation.

Click HERE to make a donation today.

How Not To Let Lung Cancer Win

I completed my Livestrong at the Y program. I tried not to miss any Livestrong days at the gym during the program. There was one particular day that I was feeling very down and tired. I just didn't have it in me that day. But my boyfriend gave me a pep talk. If you would put his pep talks in a book, the title would be, "How Not To Let Lung Cancer Win". Think in this instance he used my, no missed opportunities, motto to remind me that I should not stay at home on the couch that evening.

I went to class. It was yoga that day. Even when I was feeling some pain and I was run down from the day, I was there. I was able to fully participate. The instructor said some words that made quite an impression that day and impacted me for the rest of my life. We were holding a pose and she said something along the lines of, "this is how you are today. Recognize it. But it doesn't mean that's how you will be tomorrow."

In my day planner, in July 2016, there is one day marked with several stars. That was one of the very few days I had no pain, no fatigue, and I almost made it through the whole day without thinking or talking about my lung cancer. Those days are very rare. It's only happened a couple times since starting my treatment in September 2015.

I don't post too much about the bad days. My symptoms and side effects are intermittent. If I do complain, in the next few days things are different. My approach is the "life must go on" method. Almost like, putting the negatives in words will give them strength.

I had goals set for this fall that I've had to change or postpone to next year. Remember how excited I was about running again? I was only able to run a couple of times. At the same time as I started running again my side effects started kicking in. I was getting tired more easily. Stomach and digestive issues that I've been lucky enough to mostly avoid were happening often. I was experiencing new types of pain.  I was training to run the Run the Rocks 5k in October. If mental preparedness was all it took, I would have climbed the incline already. But the downside of feeling so well and living a half way normal life is feeling not so well at the same time.

The body and the mind are strange. Does the comfort of friends and family or the excitement of an opportunity/event overpower the negative effects and feelings caused by my lung cancer and treatment? The answer must be, yes.

Surrounded by my dearest friends and with the support of my family, I was able to complete and even run a good portion of the Run the Rocks 5k last month.

This is what Stage iv lung cancer looks like on a good day....and sometimes on a bad day too.

The Ones That Give Me Hope

Earlier this month I attended the GRACE Targeted Therapies in Lung Cancer Patients Forum in Denver, CO. It was a one day conference focusing on lung cancer treatments for patients with genetic mutations, like me.

Lisa Moran at GRACE Targeted Therapies
in Lung Cancer Patients Forum, August 20, 2016

While learning a few new things, I realized I already know a lot there is to know about my disease. Early on I found out that I must be my own patient advocate. The conference was full of other self educated, lung cancer patient advocates.

I was lucky enough to spend some time outside of the forum with these lung cancer patients. I said before that lung cancer was like a sorority that I didn't ask to be a member of. But this lung cancer community is more like a supportive family that I wouldn't want to be without. I learned just as much as about my disease at dinner than at the forum.

Lung cancer patients and family members at dinner

Holding up fingers for number of years we've been surviving lung cancer.
Bottom left: Linnea Olson had to borrow a finger from her son for 11 yrs.

When I first spoke to my lung cancer friend, Mara, on the phone, it was like we were old friends catching up. We had never met. But we had this common ground, kinship, and bond already.

I felt the same way when I met Linnea Olson at dinner after the forum. I was familiar with her. I had seen her profile photos and read about her online.

Linnea Olson, diagnosed with lung cancer 11 years ago

I now know what her profile photos sound like. Her laughter and zest for life are contagious. We shared the biggest, (maybe) too loud for a hotel restaurant, belly laugh at my expense. It was our own "Who's On First?" moment. I was racking my brain trying to remember a session from earlier in the day. Linnea said, "Chemo brain." I agreed and added something about how frustrating it is to have moments when I can't remember things. Turns out the session I couldn't recall was called 'Combating Chemo Brain'.

Linnea Olson and Lisa Moran, August 20, 2016

I wondered what the female version of The Godfather was. I almost felt like I should kiss Linnea's ring. I guess she's the Matriarch of lung cancer? But seriously, she is a remarkable woman, a pioneer in lung cancer research and a true inspiration to me and many others.

Recently the ASCO Post (American Society of  Oncology) published an article featuring Linnea Olson, her lung cancer story and her outlook on the future.

http://www.ascopost.com/issues/august-25-2016/my-oncologists-make-me-feel-safe-even-while-living-with-terminal-cancer/

Countdown to August 1, 2016

I will be released for all physical activities as of August 1. It just so happens to also be World Lung Cancer Day.

I am currently able to participate in low impact activities. After August 1 I'll be allowed to run again. I plan on running at least 1 mile symbolic run on August 1.

This was Week One of my Livestrong at the Y sessions. I'm so excited to get back to working out again. With the program my boyfriend/caregiver and I get free YMCA memberships to use anytime during the 12 week program.

Lisa Moran ready for Livestrong at the Y, June 11, 2016

I went to my first spinning class in a year. It was actually my first fitness class in a year. I have to admit, I got very emotional during the class. I was there, working out, just like before I got sick. I was there, working out! It was just like old times. I even had one of my dearest gym friends by my side. My friend, John, works out at the Y. We used to work out together in group fitness classes at Bally's and have known each other for over 10 years. 

During my spin class I got emotional thinking about being able to do the things I love again. I also thought of an online lung cancer connection, Don Stranathan. He is a seven year stage iv lung cancer survivor.  For several months I've followed his posts about going to his spin classes. His posts have been so inspirational and motivational. Thank you, Don.