Lupus Has No Face

10/14/2026

Great morning, Lupus Has No Face family!

WHEN A COMMUNITY STANDS TOGETHER, ANYTHING IS POSSIBLE!

We’ve already shown what the power of community can do and now we’re asking you to help us do it AGAIN!

Our founder is competing for TOP HOST 2026, and we want to KEEP HER who is I IN 1ST PLACE!

This is bigger than a competition. It’s about representation, advocacy, education and creating opportunities for voices that deserve to be heard.

Every vote helps bring more visibility to the work, the mission and the communities we serve.

💜 VOTE!
💜 SHARE!
💜 TAG A FRIEND!
💜 KEEP THE MOMENTUM GOING!

🔗 https://tophost.org/2026/savannah-burks

We did it before and together we can do it again!

Will Savannah Burks be a guest on an episode of On Air with Ryan Seacrest, win $25,000, and lead a podcast produced by iHeartRadio?

10/11/2026

OUR VOICE IS IN FIRST PLACE IN OUR GROUP!

Thank you for voting for me in the Top Host competition! Let’s keep going every vote helps us move closer to an opportunity to bring our conversations to a bigger audience.

As someone living with lupus and leading Lupus Has No Face, I know how much it matters to feel heard. This opportunity could help me bring more visibility to the stories, support and education our community deserves.

Please vote, return when you’re eligible to vote again and invite someone else to support! Sharing the link helps, too. 💜

First cut: Thursday, October 15, at 9 PM Central.

https://tophost.org/2026/savannah-burks

Drop a 💜 if you’re standing with us. Thank you for helping carry this voice forward!

Will Savannah Burks be a guest on an episode of On Air with Ryan Seacrest, win $25,000, and lead a podcast produced by iHeartRadio?

10/11/2026

YOUR PEACE IS PART OF YOUR WELLNESS. PROTECT IT!

Let’s have a conversation about something that doesn’t get discussed enough.

How allowing people to take us out of character can affect our emotional and physical well-being.

When you’re living with lupus or another chronic illness, managing stress is important.

Stress can affect sleep, fatigue, pain and overall well-being. For some individuals with lupus, stress may also contribute to symptom flare-ups.

So why are we allowing people, situations, and unnecessary conflict to consume the energy we need to take care of ourselves?

Here’s your reminder:

You can disagree without disrespecting.

You can establish boundaries without feeling guilty.

You can walk away without explaining yourself repeatedly.

You can advocate for yourself without allowing anger to control your response.

Protecting your peace doesn’t mean you’re weak. It means you understand the value of your health.

At Lupus Has No Face, we believe living well is about more than managing a diagnosis. It’s about learning how to protect your mind, body and emotional wellness.

💬 LET’S TALK: Have you noticed your body responding differently when you’re under emotional stress?

10/10/2026

“You look good!”

Thank you, but can we also ask, “How do you FEEL?”

The outfit, the smile and the accomplishments don’t tell the whole story. Someone can enjoy a beautiful moment and still be managing pain, fatigue, or a difficult day.

You shouldn’t have to look like you’re struggling to be taken seriously and you deserve support before you reach your limit.

What’s one question you wish people would ask instead of assuming you’re okay?

Remember to keep voting to keep us in place 1st place https://tophost.org/2026/savannah-burks

Will Savannah Burks be a guest on an episode of On Air with Ryan Seacrest, win $25,000, and lead a podcast produced by iHeartRadio?

10/09/2026

Who are you trying to convince, you or the world? 💜

When you live with lupus, you may feel pressure to prove you’re sick enough to need support or strong enough to keep going.

But how are YOU really feeling beneath the “I’m okay”?

You deserve space to answer honestly. You can be hopeful and exhausted. You can love your life and still need help navigating it. Your symptoms deserve attention, even when other people can’t see them.

I challenge you today, check in with yourself “What do I need and have I given myself permission to ask for it?”

What do you wish people understood without you having to explain it again?

Oh yeah, we are still holding the number one spot as of 10:20am this morning. Please continue to vote. Vote vote and share. 

10/09/2026

Great morning my lovely family. We have held number one spot down, so let’s continue to do that by voting every single day 

Will Savannah Burks be a guest on an episode of On Air with Ryan Seacrest, win $25,000, and lead a podcast produced by iHeartRadio?

10/09/2026

GREAT EVENING, LUPUS WARRIORS, SURVIVORS & SUPPORTERS!

AWARENESS IS POWERFUL BUT EDUCATION AND ACTION CHANGE LIVES!

Here at Lupus Has No Face, we understand that behind every diagnosis is a REAL person, a REAL family and a REAL story that deserves to be heard.

Some days, living with lupus means showing up with strength. Other days, it means giving yourself permission to REST.

And BOTH deserve to be respected. 💜

As we continue growing our community, expanding our conversations and connecting with medical professionals, advocates and organizations, our mission remains the same:

💜 EDUCATE the community.
💜 ADVOCATE for those living with lupus.
💜 SUPPORT patients and families.
💜 BUILD meaningful partnerships.
💜 CREATE spaces where every voice matters.

We are not just building followers. WE ARE BUILDING A COMMUNITY THAT MAKES A DIFFERENCE!

Continue supporting the Lupus Has No Face Podcast, the nonprofit organization and the book which can be purchased on Amazon and www.lupushasnoface.com ( Lupus has no face- living well with lupus) where we turn real-life experiences into meaningful conversations.

LET’S TALK:

What is ONE thing you wish people understood about living with lupus or another invisible illness?

👇🏽 Drop your answer below. Your story may help someone feel less alone.

LUPUS HAS NO FACE, BUT EVERY STORY HAS A VOICE! 💜🦋

Lupus Has No Face host a series of events such as our Annual Informational Summit. These events help raise funds for Lupus Awareness and a cure for this ugly disease. We strive to make a difference in the lives of our fellow lupus warriors and our community by educating, supporting and serving.

10/08/2026

What living well with lupus actually requires

10/08/2026

Have the uncomfortable conversations so others can help

10/08/2026

Living well with lupus: looks can be deceiving