Flare Day Plan
Morgan Siebs | OCT 27, 2025
When symptoms spike, it can be hard to think about what might help in the moment.
A Flare Day Plan is a ready-to-go guide you can follow without decision fatigue.
This template gives you ideas for rest, comfort, and basic needs — so you can adapt it to fit your body, your home, and your preferences.
Change into soft, non-restrictive clothes.
Adjust lighting (dim lights or close curtains if needed).
Reduce noise — use earplugs, noise-canceling headphones, or white noise.
Find your comfort spot (bed, recliner, “nest” corner, or couch).
Gather cozy items: blanket, heating pad, favorite pillow, stuffed animal.
Take prescribed or recommended medications (as directed by your provider).
Sip water or electrolyte drink throughout the day.
Choose easy-to-digest snacks/meals — pre-prepped or no-cook if possible.
Use mobility aids, braces, or supports as needed — even if you don’t usually.
Adjust posture with pillows or rolled towels for extra support.
Cancel or reschedule non-urgent tasks.
Set a “do not disturb” on your phone (or selective notifications).
Use short activity bursts (5–10 minutes) followed by rest.
Give yourself permission to do less and move slower.
Listen to calming music, nature sounds, or a favorite audiobook.
Watch something light and comforting (short episodes are best).
Do something hands-on but low-energy (coloring, knitting, fidgeting).
Use sensory comfort (warm tea, cool washcloth, scented lotion).
Use a quick body scan: “What feels okay right now? What needs adjusting?”
Keep a short log if helpful (symptoms, meds, hydration, food).
Notice any signs that you need to reach out for help.
Have a “flare buddy” or friend you can text just to say, “I’m having a flare day.”
Contact your provider if symptoms worsen unexpectedly.
If you feel unsafe physically or emotionally, use your safety plan or call a crisis resource (list in Hard Day Support section).
💡 Pro Tip:
Print or save your Flare Day Plan where you can find it easily — in your phone notes, taped to the fridge, or next to your bed. That way, you don’t have to think about what to do when your energy is low.
Writing takes a lot of energy — especially with a brain injury — so I sometimes use ChatGPT to help me put my thoughts into words. I still guide the content, tone, and message, but using this tool lets me share more reflections and resources with you without draining my limited spoons.
Morgan Siebs | OCT 27, 2025
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