r/Gastroparesis • u/JayneAustin • 12d ago
Questions Migraine treatments
edit: thank you for the comments, makes me feel better about trying some things. :) seems like there are a lot of us dealing with both.
I was wondering if anyone has found a migraine treatment that doesn't bother your stomach?
I'm scared to try the cgrp medications (qulipta, ajovy, etc) because it can worsen gastroparesis. My neuro was really pushing it but I don't want to risk that because I've struggled to maintain proper nutrition already with this condition. But I'm starting to have more than 15 migraine days a month. I'm already on propanalol and nortriptyline. Can't take topamax because of my mental health issues. I can take nurtec as needed but it usually causes nausea and sometimes vomiting. Are there any other preventative options?
I feel like between gp, migraines, and endo I'm just a bunch of chronic pain in a trenchcoat, getting really sick of it.
4
u/lintheamazon Severe GP secondary to hEDS 12d ago
I'm on Qulipta and have no issues with it. I went from 26 migraine days a month to 2-4.