Answers, plainly.

Consistent steroid timing, visible sick-day rules, symptom notes, and emergency information kept easy to reach. Our guides cover practical routines.

Personal instructions from your endocrine team on extra hydrocortisone during illness, fever, vomiting or procedures. Your own plan always comes first.

Yes, with planning: spare medication, a travel letter, your injection kit if prescribed, and dose timing across time zones agreed with your team.

A simple way to count your energy. You start each day with a number of spoons. Things you do use some up; rest gives some back.

No. MyAddi reminds and records. Only your prescriber or endocrine team changes doses.

Follow your steroid card or clinic letter. If you’re vomiting, confused or collapsing, treat it as an emergency.

Yes. Pharmacy collections, blood tests, clinic calls and appointments, kept separate from your dose schedule.

Step-by-step guidance through an adrenal crisis. You hold to start it, it walks you or someone nearby through five steps, and it tells your care circle.

If someone is collapsing, severely confused, vomiting and can’t keep medication down, or otherwise very unwell. Apps guide; emergency services treat.

Yes. Paramedics often look for physical ID first. MyAddi sits alongside it.

Yes, while it’s in beta. Join on the beta page and choose iPhone or Android.

People with Addison’s disease, adrenal insufficiency and other chronic illness, and the parents and carers who support them.

No. It’s a supportive app for reminders, tracking, your care circle and emergency guidance. It doesn’t diagnose or prescribe.

Use the contact page for beta help, partnerships or anything else.