Migraine tracking is a valuable tool that we can all use to communicate with our medial team. Details like what symptoms we have, how long the symptoms last, and potential triggers can all be documented.
Do you personally track your migraines? If so, what have you found the most helpful?
Do you feel like your healthcare team takes into consideration your migraine log when discussing treatment?
Where do you keep your notes? Is it in an app, on pen and paper, or somewhere else?
Please feel free to share any and all experiences related to this topic.
I know for me, I did a lot of migraine tracking before my diagnosis. Each time I started to feel migraine symptoms start, I wrote down the time, where I was, what I was doing, and the potential triggers. For example, one entry might read " 3pm, filling up my car with gas, potential triggers: bright light, smell of gas, head pain on left temple". I also remember feeling a bit disappointed that my neurologist didn't take my migraine log very seriously. I took a lot of time and effort to notice what may be impacting my migraines, but it didn't seem too important to him. As with anything, your mileage may vary!