Zig2017 wrote:Ok back to BRAF.... Mr Ziggy’s CEA was 1,807.7 and it’s now .... wait for it..... 207!!!!!! These biologicals are kicking butt. We have a CT scan January 2 so I’m expecting regression. I’ll let you all know what transpires! Happy New Year all!!
Zig2017 wrote:NHMike you were right about second opinions and going to a cancer center. If he had stayed at his local hospital I shudder to think... this is absolutely unreal! Dare I hope?!? Yes! We are so excited! And the poor man was crying yesterday. What a difference a day makes. Someday we won’t be doing chemo anymore this is my hope. Immunotherapy and or biologics are really practice changing for these patients. No hair loss, but has a rash and throwing up sometimes. Also constipated. We are working on that. He is MSS not MSI but, this is giving him response were there was none to be had. I’m wondering Mike how they sustain this, or if he has a complete response maybe just monitoring? God this is such a rollercoaster at times, but we are riding high right now! Love to all, Mrs Ziggy
Zig2017 wrote:Ok back to BRAF.... Mr Ziggy’s CEA was 1,807.7 and it’s now .... wait for it..... 207!!!!!! These biologicals are kicking butt. We have a CT scan January 2 so I’m expecting regression. I’ll let you all know what transpires! Happy New Year all!!
Zig2017 wrote:Celecoxib... is that a rheumatoid arthritis drug? Also Mr Ziggy is believe it or not allergic to vitamin c. He breaks out in rashes from eating oranges or lemons especially. Would the IV vitamin c be ok for him to take? Just wondering because I’ve heard good things about vitamin c infusions. I’m guessing eating the fruit and the pulp etc would be different and hopefully the infusion (different delivery) might not give him a reaction?
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