CGRPS and Raynaud's

I posted this comment on Facebook and am looking for others with possibly the same experience and how long symptoms lasted and what you tried next:

Nothing has worked to stop my daily migraines including the CGRP's that my migraine doctor has tried. I had the first two injections of Emgality in March and after a week I noticed an increase in my Raynaud's symptoms. Upon research we saw that it can cause "auto amputation of digits" for people with Raynaud's who take these types of drugs. My specialist said to stop the injections, but I am still having very bad symptoms of numbness and tingling and pain that is extending into other parts of my body which hasn't happened before. She now wants me to try Botox but I had a previous doctor tell e that wouldn't be safe for me and am unsure what to do. I am worried that something even more serious could happen and feel like I may just have to live with the daily migraines. I do take amitriptyline which helps some but doesn't stop the daily pain. Has anyone else had issues with CGRP's and Raynaud's and how long did it take for the side effects to stop? Thank you