LUPUS FOG | Stay RADD

LUPUS LIFE

I’m in the process of launching a new Lupus focused project that prioritizes creating a brutally honest space for people living with Lupus to answer, ask, and share.

All answers are subject to being reposted on a blog, website, or Instagram post in the future.

All personal information, screennames, etc. will NOT be included and will be displayed as an anonymous quote within a collection of responses from others.

The goal here? To build a relatable, raw, and sometimes dark-humored collection of what it’s really like to live with lupus—
so no one has to feel alone in this mess ever again <3

What can we call you?

Whereabouts do you live?

How old were you when you first started experiencing Lupus symptoms, and what were they?

How old were you when you were diagnosed, and how old are you now?

How do you answer when casually asked by someone unfamiliar "What is Lupus?" and "What does Lupus feel like?"

Lupus often displays itself differently for each person, some symptoms and manifestations weirder than others. What are some of your strange, or hard to explain symptoms?

A lot of us experience brain fog/Lupus fog (forgetfulness, confusion, difficulty with concentrating, expressing yourself). Any funny/cringy/memorable moments come to mind where your brain fog played a key part in a misunderstanding or awkward moment?

Any developed food allergies post Lupus diagnosis?

Have you found any specific things that cause your body to react so negatively , you had to cut it out of your life completely? If so - what are they?

What are some of your swear by, go-to items/products when it comes to over the counter, trying to make yourself feel better, self-care?

What is your brutally honest advice and insight to someone with a fresh Lupus diagnosis who is having trouble accepting/understanding it?

RADD

Co.

LUPUS LIFE

STAY RADD