Lupus in the City

Lupus in the City Hi! I’m Angie, a 36 year old lupus warrior who's been battling Systemic Lupus Erythematosus since the young age of 15.

I've been in remission for 7 years now due to my mostly holistic lifestyle focusing on diet, nutrition, exercise & my mental health.

Happy International Day of Women and Girls in Science 🧪 🧬👩🏽‍🔬In honor of Black History Month I wanted to pay homage to t...
02/11/2026

Happy International Day of Women and Girls in Science 🧪 🧬👩🏽‍🔬

In honor of Black History Month I wanted to pay homage to the women that paved the way for women like myself to pursue a degree in Science and Healthcare.

The future of science doesn’t just need more voices, it needs HERS. 🧑🏾‍🔬👩🏾‍🔬👩🏾‍💻👩🏽‍🏭👩🏽‍⚕️👩🏿‍🚀

Today we celebrate the International Day of Women and Girls in Science. From uncovering DNA to launching rockets, women have always been at the forefront, even when the history books forgot to mention them!

Let’s break the bias and keep the curiosity alive.

Share, repost and save!

02/11/2026

I’m practicing my free will this year and doing whatever I want! 👏🏽

Calling all vendors/businesses that would like to collab for the 2nd Annual World Lupus Day celebration this May! 💜

Let’s give back to the community and show up for one another, the world needs it.✨

Check out my full yap on YouTube and make sure to subscribe so you don’t miss anything!

womenshealth

02/10/2026

You feel me? 🙄

02/09/2026

Head over to my YouTube to hear me yap more about cannabis and all the new changes to come with my content.

I’m also gearing up for the 2nd annual WORLD LUPUS DAY CELEBRATION in Los Angeles on Saturday May 9th!!! 🎉🙌🏽

Follow to learn more and keep up with the latest details. 💜

01/23/2026

Lupus in a nutshell! 😅

lupusawareness

01/18/2026

If I had a dollar for every time I heard this I’d be rich!!😅

If people could only understand the silent battles we fight everyday!

The fatigue getting out of bed, the body aches, the random tight chest, the mouth ulcers, rashes, thinning hair, the anxiety and itchy skin!!

I could go on and on but it doesn’t show, so people don’t know or really understand my everyday battle unless I actually explain what lupus is and how it affects me.

Lupus has so many faces, and various symptoms.

My 16 year battle with lupus (SLE) has shown me that no 2 cases are the same, so what works for one person may not work for the other.

It took me so many years of hard word and sacrifices to get to this point or remission.

Some days are better than others, but the fight for a long healthy life is always worth the battle!

Keep fighting warriors, you’re not alone in your battle against this cruel mystery disease.💜

01/17/2026

Literally my face every time someone tries to compare alcohol to cannabis. 🙃

I’ve been off medication for lupus (SLE) for 6 years and don’t plan on going back anytime soon. 🌱

So more research needs to be done on medical cannabis.

Follow along for more to come! 💚💜

01/15/2026

I’m so ready for this next chapter! 💜💚

Cannabis is such a powerful plant medicine that when used properly it can really change your life. 🌱

I’m looking forward to finally speaking more on cannabis and how it’s helped me remain in remission from lupus (SLE) for almost 7 years. 🙌🏽

I truly appreciate creators like that are putting in the work with research on cannabis. You have inspired me so much and I really hope to connect one day soon! 💚

Follow for more medical cannabis content and how it can help suppress lupus symptoms when used properly! ☺️

01/13/2026

Day 2 of operation get fit for my wedding! 🏃🏽‍♀️

I forgot to tell y’all I signed up for a 5K marathon on March 1st! 😅

Never minimize the impact you have on others, they see you always.💜

01/13/2026

So happy to have you all on this journey with me!💜

Operation get fit for my wedding is in full effect!💪🏽

12/30/2025

New year, new chapter! Let’s go 2026! 🎊

Living with lupus has taught me that healing isn’t linear, and that rest is productive. 🙌🏽

My New Year’s resolution with lupus isn’t about doing more, it’s about honoring myself more! 💜

I’m resolving to rest when I need to, fight when I can, and never measure my worth by productivity.

Lupus may be apart of my story, but it does not define my limits or hope!

Here’s to resilience, boundaries, and choosing health first in the new year! 👏🏽

My New Year’s resolution for 2026 is to do more:
-listening to my body
-resting without guilt
-protecting my peace
-celebrating small wins
-giving myself more compassion
-honoring my limits

And less:
-hustling over my health
-guilting myself
-chasing perfection
-people-pleasing
-pushing through
-stressing over things I cannot control

To my fellow warriors, you are doing enough, even on the hard days. Here’s to a year of compassion, strength, and self-love. Happy new year to you all! 💜

#2026

12/03/2025

I’ve been doing a lot of thinking and tons of research.👩🏽‍🔬

I will be shifting gears on here and educating more on holistic measuring for living with lupus, specifically cannabis, diet and other lifestyle changes.

With now 6 years of remission from systemic lupus erythematosus (SLE) thanks to this powerful plant and lifestyle choices, I feel ready to talk more about my journey with cannabis and lupus. 🙏🏽

I have so much knowledge to share, and the credentials to back it up. 🎓🎓

And with everything going on right now in our country it’s important to take your health into your own hands because “they” really do not care!

Our healthcare system has become such a commodity instead of an essential service for everyone.

Please let me know your thoughts. I’m really interested in feedback and want to provide the best FREE information for all you chronic illness warriors.

Stay safe and healthy!💜

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