I’m starting new treatment this week for my Crohn’s disease called Humira. Hopefully it will put my inflammation flares into remission so that I can stay off cortisone for longer than a few months! Busy looking at all the information about it and getting answers to all my questions from the nurse that assists with the injections.

Biologics like Humira is usually in injection form so I’ll have to inject myself every two weeks. Luckily it is in a pen type contraption which means i need to point, keep still and click a button to inject.  Hopefully it doesn’t burn too much and that I don’t have a weird reaction to it.  Said my prayers and holding thumbs…