That’s my lead. I’m more of an instant gratification girl, so I like to use benchmarks for longterm projects, of which I am one. I also count songs when I run or take a punishing gym class (every song brings me an average of four minutes closer to the end). And when I used to run long races, I would count down (from mile 1) like this: 1 down, 12 to go. 2 down, 11 to go. You get the idea. What the headline means is that my CT scan was good and that I’m in the CRLX101 trial for another 8 weeks.
Dr Thomas says there is no disease progression and MAYBE even some tumor shrinkage around my heart. We have also found a good balance of blood transfusions and Neulasta (to make my White Blood Cells hang around longer. I think it’s like $4 beer for WBCs), so I hit my blood value requirements comfortably again. AND, eight weeks of the blood thinner have worked on that pesky blood clot in my port line. The CT scan shows that it is gone. That means I can stop taking the blood thinner in one more month, which is great news. The two-a-day shots hurt, and my whole midsection is bruised and swollen (a different way to get a muffin top). Want to see something gross?
And there was one more bit of good news, in a perverse cancer way. Last time I was here, they did a test to see if I had a cold or allergies or was all the especially annoying coughing/wheezing/short of breathless (?) because of the drugs. I DID have rhino-itis (I swear that’s what they called it.. Not really, but it was close) and still do. That’s good news because it means I will feel better than I did then and do now. So bike training for Pelotonia should (should) get easier.
Here are the signs I found that made me believe this scan was going to be a good one:
1. I got this in the mail last week. It’s from Georgetown University’s Lombardi Center, where you may remember I was in a trial for 2 1/2 years. It’s a thank you card for folks who’ve supported their clinical trials program and a reminder that June 3 is National Cancer Survivors Day. We had this photo shoot almost a year ago. And it appeared in my PO box now. I’ll be making another donation to Lombardi at http://giving.georgetown.edu/lombardi
2. In the last yoga class (6 am) that I took in Park City before getting on my flight to Maryland, we were lying on our mats in savasana, and the sun came up out of the clouds, from behind the mountains and just was…. WARM. It’s hard to describe how amazing it was to be still and have sunbeams falling all over me. Now I am much more appreciative of what makes Linus and Lucy chase the sun all over the house.
3. And on the night before I went in for the CT scan (during a great Stanley Cup game that had the wrong ending), Patrick texted me this:
My brother looked at the picture and asked, “Is he actually smiling?” Why yes, yes he is. Linus knows all.
So I can look forward to at least another four 5-hour infusions and 40+ days of taking Olaparib that will make me cough. But this complicated, elaborate combination drug trial seems to be doing what it’s supposed to. I don’t even try to understand parts of the protocol anymore (Cycle 7, day 15? Or is it 1?); it doesn’t matter. I just feel blessed and lucky I was among the last couple of solid tumor patients to get into this trial as it changed from Phase I to Phase II. It’s now only for some lung cancer patients, and I wouldn’t have been able to participate.
And I can look forward to Delta Upgrades in 2019 already. Next benchmark: Delta Diamond. #defy #clinicaltrials #relentlessforwardprogress #complimentaryupgrades
**I reached Delta gold status without realizing it this week. One more sign!
Hello, Wendy! Fonda Ryan Cerenzio here (formally of SeaWorld) and forever CCI Volunteer and donor! I continue to be amazed at your incredible spirit and Love of Life! You continue to give hundreds/thousands of folks hope and I just wanted to send my Love and heartfelt thanks for all you do … every day! I recently shared the story of when you & me tag-teamed Harris Rosen at lunch in the hopes of gaining his support… and boy did we?! Rosen Hotels has remained a HUGE supporter of CCI and it all started that one day at lunch with me and you (mainly you) and that support has continued to thrive! Me and my husband, Don have a table at this year’s Gala on Saturday, 10/6/18 at Rosen Shingle Creek and we would love to have you join us?! Nancy, Trish and so many you know will be there and it would be great to have you join us?! Sending all my Love and sincere thanks for your commitment to CCI and SO many others here in Central Florida! Love and healing prayers! Fonda❤️🐾🐾❤️🌈🌹☀️🌻
Hi Fonda! I may be in LA that weekend, but will try to see if I can work it out. I still love CCI! I volunteer at the National Ability Center in Park City and I always stop those cute dogs in the yellow and blue capes to say hello and tell them that I love their work!! I’ll be in touch. Thanks! W
Great news! Keep your face turned toward the sun!
Wendy: Your blog is fabulous as are you. It’s been a very long time since we ran together and yet I remember it fondly like it was yesterday. I see you continue to fight the good fight and to find time to train and lived life fully amidst all of it. I am grateful to be able to reconnect with you through your blog and to read your notes and hear your continuous words of inspiration.
I stopped running for a long time in 2007. My last half marathon was the inaugural zing in AtlNta. I took up cycling and doing CrossFit. I met a man in Jacksonville and after we opened the hospital in 2012 I moved to Jacksonville. To be with him. We’ve been happily married for 6 years. I’ve just started back running with the Galloway program up here and while older and slower am grateful to be out there and couldn’t help but think of you. Hugs and continues good news and light to you. In friendship, Karen (Breakell) Bower—aka 1/3 of the brain
Wendy, I also had thymic cancer. Email me if you want…..