Philip Waisonovitz Posted November 23, 2019 Share Posted November 23, 2019 Hi everyone Recently diagnosed with non small cell stage 4 .Started targeted therapy 3 weeks ago .Tagrisso is the medication .anyone else getting the same treatment? Link to comment Share on other sites More sharing options...
Curt Posted November 24, 2019 Share Posted November 24, 2019 Hi @Philip Waisonovitz. Welcome to the forum. I’m sorry about your diagnosis. I don’t have any experience with Tagrisso but I’m sure others do and will be along to comment. Good luck with your treatments. Link to comment Share on other sites More sharing options...
Philip Waisonovitz Posted November 25, 2019 Author Share Posted November 25, 2019 Thanks Curt for responding best of luck to you also Link to comment Share on other sites More sharing options...
Rower Michelle Posted November 25, 2019 Share Posted November 25, 2019 Hi Philip, It's nice to meet you. I have the ALK mutation and take a medication similar to Tagrisso. I've met a number of "EGFR Mutants" in the last year since my diagnosis. Everyone is doing very well on Tagrisso. Some folks have been on an EGFR inhibitor going on ten years now. Another resource is Facebook, there is a vibrant EGFR community on line. You will find very knowledgeable and supportive people here. Let us know how we can help. Michelle Link to comment Share on other sites More sharing options...
Philip Waisonovitz Posted November 25, 2019 Author Share Posted November 25, 2019 Good Morning Thank you so much for the encouraging news and support .I will check out facebook the EGFR community that you mentioned. Link to comment Share on other sites More sharing options...
LUNGevityKristin Posted November 25, 2019 Share Posted November 25, 2019 44 minutes ago, Rower Michelle said: Hi Philip, It's nice to meet you. I have the ALK mutation and take a medication similar to Tagrisso. I've met a number of "EGFR Mutants" in the last year since my diagnosis. Everyone is doing very well on Tagrisso. Some folks have been on an EGFR inhibitor going on ten years now. Another resource is Facebook, there is a vibrant EGFR community on line. You will find very knowledgeable and supportive people here. Let us know how we can help. Michelle Hi Phillip! Here is a link to the EGFR Facebook Group. https://www.facebook.com/groups/EGFRlung/ You are always welcome to post here as well! Link to comment Share on other sites More sharing options...
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