Lupus Has No Face

05/11/2026

It was such a pleasure attending the 16th Annual Mother’s Day Show!

I want to personally thank for taking the time to show Lupus Has No Face so much love and support while helping bring awareness and attention to the importance of registering for the 6th Annual Lupus Has No Face Walk. 💜

Your kindness, your platform, and your willingness to support a cause that impacts so many people does not go unnoticed. This is what real community looks like people coming together, supporting one another, uplifting important causes, and creating impact bigger than themselves.

Thank you again for your kind heart, your support and for helping us continue spreading lupus awareness throughout our community. 💜

If you have not registered for the walk yet, make sure you do today! www.lupushasnoface.com
StrongerTogether

05/10/2026

Big love to Kelly Kellz for showing love and highlighting the 6th Annual Lupus Has No Face Lupus Walk! 💜

When people use their platforms to spread awareness, it means more than words can explain. Lupus warriors fight battles every single day that many people never see, so every repost, every mention, every ticket, every registration, and every conversation helps us continue pushing the mission forward.

Community support matters. Collaboration matters. Awareness matters and seeing powerful women like Kelly Kellz stand beside causes that impact real families and real lives is truly appreciated. 💜

Thank you for helping us bring visibility to a disease that has “no face” but affects so many. We appreciate you supporting the movement and helping us make an impact bigger than ourselves.

Now Milwaukee… are YOU registered yet?! 👟💜
Join us for the 6th Annual Lupus Has No Face Walk as we walk for awareness, strength, education, and community.

📍 Kletzsch Park (Picnic Area 😎
📅 Saturday, May 23rd
⏰ 1PM – 5PM

Register today and come walk with us!

www.lupushasnoface.com

05/10/2026

Big love to Kelly Kellz for showing love and highlighting the 6th Annual Lupus Has No Face Lupus Walk! 💜

When people use their platforms to spread awareness, it means more than words can explain. Lupus warriors fight battles every single day that many people never see, so every repost, every mention, every ticket, every registration, and every conversation helps us continue pushing the mission forward.

Community support matters. Collaboration matters. Awareness matters and seeing powerful women like Kelly Kellz stand beside causes that impact real families and real lives is truly appreciated. 💜

Thank you for helping us bring visibility to a disease that has “no face” but affects so many. We appreciate you supporting the movement and helping us make an impact bigger than ourselves.

Now Milwaukee… are YOU registered yet?! 👟💜
Join us for the 6th Annual Lupus Has No Face Walk as we walk for awareness, strength, education, and community.

📍 Kletzsch Park (Picnic Area 😎
📅 Saturday, May 23rd
⏰ 1PM – 5PM

Register today and come walk with us!

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.

05/07/2026

CALLING ALL VOICES FOR OUR LUPUS AWARENESS MONTH PANEL

This month, is looking to bring together powerful voices, real stories, education, healing, and representation for an impactful Lupus Awareness Month Panel discussion.

We are currently seeking individuals who would be interested in being featured panelists, including:

Lupus Warriors / Patients
Medical Professionals
(Doctors, Nurses, Nurse Practitioners, Therapists, Specialists)
Mental Health Advocates
Caregivers & Family Members
Entrepreneurs / Public Figures living with Lupus
Community Resource Representatives
Faith Leaders & Motivational Speakers

This conversation is about REAL LIFE. REAL STORIES. REAL IMPACT.

We want to educate, empower, inspire, and create safe conversations surrounding lupus, invisible illness, mental health, relationships, advocacy, self-care, and overcoming adversity.

If you or someone you know would be a great fit, please inbox us directly or email us. Tag someone below who needs to be part of this powerful discussion!

Together we continue proving that lupus has NO face, NO color, and NO limits.

05/02/2026

This was a successful 6th annual Lupus Has No Face information!!!


04/19/2026

EDUCATIONAL MOMENT: WHY LUPUS HAS NO FACE IS DIFFERENT AND WHY STARTING FROM THE BOTTOM MATTERS

Let’s be clear first there is room for ALL of us in this fight.
Organizations like the Lupus Foundation of America and the Lupus Research Alliance provide incredible, structured, and factual resources that are NECESSARY.

They offer:
Financial & prescription assistance, Insurance & mobility resources, Healthcare advocates you can speak with, Virtual & in-person support groups nationwide and Educational webinars, seminars, and lupus walks

These organizations are powerful pillars in the lupus community and we respect that.

So what makes Lupus Has No Face different?

We are grassroots. We are personal. We are lived experience in real time.

Lupus Has No Face was built from the ground up not from systems, but from survival.

We are:
The voice for those who feel unseen
The raw, unfiltered conversations people are afraid to have
The bridge between education and REAL LIFE
The community touch—events, walks, diaper drives, podcasts, outreach

We don’t just talk about lupus we live it, we show it, and we stand in it.

Why starting from the bottom matters

Because when you start from the bottom:
You understand the struggle firsthand
You build with purpose, not just position
You connect with people on a human level—not just informational
You create something that people can feel, not just read about

There’s a difference between:
Information… and IMPACT.
Resources… and REAL RELATIONSHIPS.

And both are needed.

Click the link to register for the lupus walk

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.

04/14/2026

Happy 414 Day 💜

Milwaukee… this one is for you.

A city full of strength, resilience, real stories
and today, we celebrate what we stand for.

At Lupus Has No Face, we’re raising awareness,
building community, and giving a voice to those
who are often unseen but deeply fighting every day.

Lupus Has No Face …but the strength behind it
You see it right here in our city, from our walks…
to our podcast… to every event where we show up with purpose….. this is bigger than awareness.

This is love, support, and community in motion.

Milwaukee, thank you for embracing the mission. Thank you for standing with us and thank you for continuing to show up.

💜 Register for the walk
💜 Tune into the podcast
💜 Be a part of the movement

www.lupushasnoface.com

InvisibleIllness SoftStrength 💜

04/14/2026

You can’t want more for someone than they want for themselves and that’s a hard truth a lot of people don’t want to accept.

People will keep repeating the same behaviors, making the same mistakes, and then turn around and get upset with you for having boundaries. Not because you’re wrong… but because your boundaries force them to face what they’ve been avoiding.

Accountability requires maturity. Growth requires honesty and healing requires looking in the mirror and owning the damage you’ve caused.

Some people aren’t ready for that.

So instead, they deflect. They blame. They project and when you stop allowing it… you become the problem in their story.

But let me be clear having boundaries doesn’t make you difficult. It makes you disciplined.
It makes you self-aware. It makes you healed enough to not tolerate what once broke you.

It takes a grown individual to say:
“I hurt you.” “I was wrong.” “I need to do better.”

Until someone can do that… they will keep repeating cycles.

You are not responsible for fixing what someone refuses to face.

Have you registered for the walk yet? Click the link below 👇

www.lupushasnoface.com

04/13/2026

BUILDING FOR THE FUTURE:

This is bigger than a walk… this is a movement.

At Lupus Has No Face, we are standing up for the warriors who fight battles you can’t always see. We are building support, visibility, and real resources for those living with lupus and we can’t do it alone.

Join us for the 6th Annual Lupus Walk
May 23, 2026
1 PM-5PM
Kletzsch Park

This is your chance to:
✔️ Stand for awareness
✔️ Support a powerful cause
✔️ Be part of something that truly changes lives

Ways YOU can show up:
Sponsor a family-friendly experience (Bounce House for the kids!)
Help us secure the space (Park Partner)
Boost our visibility (Banners, signage, branding)
Donate essentials (shirts, snacks, water, giveaways)

Every share. Every donation. Every step.
Matters.

We are the voice. We are the strength.
We are the change we’ve been waiting for.

Register NOW + Support the mission:
www.lupushasnoface.com

COMMENT “WALK” if you’re pulling up
TAG someone who should stand with us

Let’s show the world…
Lupus Has No Face, but WE DO.

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.