07/22/2024
Hi 👋🏻 it’s Lisa posting today. This past weekend attending the ALK+ Summit in Nashville was amazing. I’ll share more about what we learned and the exciting advancements happening in the world of lung cancer soon, but first and foremost I want to tell you that in that conference of 350 people, I felt like the luckiest person alive. More than once I was struck by how incredible my support system is - from my husband Mark and our kids Peter, Hannah and Seanie to all of YOU in the Lisa’s Lads and Lasses community 🥰. The kindness my family and I have been shown these last few years has blown me away.
Betsy and Jackie giving up a summer weekend to come to Nashville and deep dive into things like nuclear protein, mRNA, mutations, tyrosine kinase inhibitors, next generation sequencing, biomarkers, blood brain barrier, MET, SHP2, PDL1, EML4, mechanisms of resistance and so on and so on……😳🤯🤪…..while also representing Lisa’s Lads & Lasses and sharing our mission AND making friends with other ALK+ patients and their families….that is true friendship and I am so grateful for their love and dedication to me!!!
I know so many more of you would have dropped whatever you had and done the same thing had I asked, and I am truly and deeply grateful just to know you care that much too. My heart is so full thinking about all of you. 💗
I wouldn’t wish living with this stupid, horrible disease and a ticking clock on anyone, but through it all you have shown me how vital it is to show up for and take care of each other in this life. It’s truly all that matters. I appreciate every one of you in this community and thank you for supporting me and helping the ALK+ world find answers that are desperately needed. You are making a difference to me and to others with this disease. To each of you I send love, and I hope your day and week is filled with peace, laughter and good health! 😘💗😍💕☀️