I know I’ve been slack in posting posts, but in this case anyway, no news is good news. I’ll have a more in-depth report in a few days when I go back to Bethesda.. But for now, I stopped in at the new offices of my very good friends at Growing Bolder, and we made some television. It’s a message I’ve delivered consistently through the years, but I figure nearly five years after my original Thymic Carcinoma diagnosis is a good time to show you that I’m still shouting YES. No excuses. #DEFY
Wendy,
You are a true inspiration to me and so many others. Thank you for fearlessly making every day count.
Your fearless courage brings out the tenacity in me to fight off the progression of Parkinson’s and to raise awareness in finding a cure.
Your fearless courage brings out a bolder voice in me to wipe out “hate” replaced with respect for each other
Your fearless courage has inspired me to continue my blog encouraging people with and without Parkinson’s to keep moving. I also have not posted in awhile. Foxyladyversuskilimanjaro.com. .
I look forward to your posts and keep moving. I would love to team up with your on one of your adventures…seriously, I’m all in!!!!!
Margaret
Hi Wendy
I can so relate to your story….I live in Ottawa ON,Canadawas just diagnosed with another rare cancer 5 months ago, had my first 3 month Follow up Cat scan in late Feb and all is well for now. The cancer is a GIST, gastrointestinal stromal tumour…is treatable , but not cureable.
I am feeling well, so we r planning a trip to San Diego for April, as have to still live our lives for sure.
We had our first Grandchild last year, so she is a great motivation and the love of my husband and my life.
All the best to you, as you continue your personal journey….!
Will add you to my prayers …..
LaVon