Colors of Lupus NV

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Colors of Lupus NV

Non-profit organization dedicated to improving the quality of life for individuals affected w/ Lupus

09/05/2026

🏡 Now That You Own It—Protect It!

Homeownership is a major accomplishment, but protecting your home, loved ones, and legacy is just as important. Join us for a FREE practical estate-planning seminar for current and future homeowners.

Learn—in plain English—what you need to know about:

🔑 Wills and trusts
🔑 Probate
🔑 Nevada homestead protection
🔑 Steps you can take now to protect your legacy

📅 Thursday, September 10, 2026
⏰ 5:30 PM–7:00 PM
📍 KW Las Vegas
9420 W. Sahara Avenue, Suite 100
Las Vegas, NV 89117

Hosted by Dawn W. Barlow, REALTOR®, CPRES®, MPA, with special guest speaker Mary Ann Andrews-Merrett, MBA, Estate Planning Facilitator.

Admission is FREE, but registration is required and seating is limited. Snacks, refreshments, giveaways, helpful resources, coupons, and discounts will be available!

🎟️ Reserve your seat today:
https://www.eventbrite.com/e/1998495222007?aff=oddtdtcreator

📞 (702) 970-0555
🌐 dawnbarlowsells.com

Plan today. Protect tomorrow. Create peace of mind for yourself and the people you love.

08/30/2026

💜 CALL FOR SPEAKERS & VENDORS! 💜

Colors of Lupus is excited to host our First Annual Lupus Conference, and we’re looking for healthcare professionals, organizations, and businesses to join us!

📅 Saturday, February 6, 2027
⏰ 10 AM – 2 PM
📍 Pearson Community Center
1625 W. Carey Avenue, North Las Vegas

🎤 Speaker topics include:
Clinical Trials & New Treatments • Nutrition • Lupus, Hormones & Menopause • Mental Health • Physical Therapy & Exercise

🛍️ Vendors: If you provide healthcare services, resources, products, or support that can benefit the Lupus community, we’d love to have you participate in our Healthcare & Community Resource Expo!

💜 Be a Voice. Share Knowledge. Change Lives.

Interested in being a speaker, vendor, or both?
📧 [email protected]
📱 (702) 722-8553

🦋 Colors of Lupus — Educate. Advocate. Empower.

08/25/2026

💜 Tuesday Check-In, Lupus Warriors! 💜

How are you feeling today—physically, mentally, and emotionally?

❤️ I’m great
💜 I’m okay
💚 I’m “meh”
💛 I’m struggling
🩵 I’m having a tough time and wouldn’t mind a check-in
💙 I’m not doing great

Drop the heart that matches your mood in the comments. No explanations are required—just know that you are seen, supported, and never alone in this journey.

If you notice someone could use a little extra love today, take a moment to check on them. Sometimes a simple message can make all the difference. 🦋

EducateAdvocateEmpower

08/17/2026

💜 Lupus does not have a face until it’s yours—or someone you know.

Lupus can affect anyone, and many people living with it are fighting battles others cannot see. Behind every diagnosis is a real person navigating pain, fatigue, uncertainty, treatments, and life-changing challenges.

Let’s continue to educate, advocate, and empower while reminding every Lupus Warrior that they are seen, supported, and never alone. 🦋

SomeoneYouKnowHasLupus LupusSupport

08/15/2026

🚨💜 CANCELLATION NOTICE — IN THE LOOP SUPPORT GROUP 💜🚨

Please be advised that our “In the Loop” Lupus Support Group Meeting scheduled for Saturday, August 15, 2026 has been CANCELLED.

There will be NO in-person or virtual Zoom meeting this month.

We apologize for any inconvenience and appreciate everyone’s understanding. Most importantly, we want to make sure our Lupus Warriors, caregivers, family members, and supporters see this update before making plans to attend.

💜 Please SHARE this post with anyone you know who may have planned to join us.

Although we won’t be gathering this month, remember that you are still part of a community that understands, supports, and stands with you.

You are not alone. 💜🦋

Stay connected with Colors of Lupus for information about our next “In the Loop” Support Group Meeting and other upcoming programs and events.

🌐 www.colorsoflupusnv.com
📱 Facebook • Instagram • TikTok • LinkedIn

Educate. Advocate. Empower.

08/14/2026

💜 AUGUST IS NATIONAL HAIR LOSS AWARENESS MONTH 💜

This post is a little different for me because it requires me to be transparent, vulnerable, and real.

Living with Lupus has changed many things about my body over the years—including my hair.

I’ve experienced bald spots. Losing my edges. Thinning. Breakage. I’ve looked in the mirror frustrated, embarrassed, angry, and sometimes heartbroken as I watched my hair change right before my eyes.

Eventually, I made the decision to cut it short. ✂️💜

For many people living with Lupus, hair loss isn’t “just hair.” It can affect our confidence, our identity, and how we see ourselves. Lupus-related inflammation, medications, stress, hormonal changes, and different forms of alopecia can all contribute to hair loss.

But here’s something I’ve had to learn along my journey:

💜 My hair may have changed, but my strength hasn’t.
💜 I am still beautiful.
💜 I am still worthy.
💜 I am still ME.
💜 And whether my crown is long, short, thin, growing back—or gone completely—I will wear it with PRIDE.

I’m sharing these pictures because sometimes advocacy means allowing people to see the parts of the journey we would rather hide.

To every Lupus Warrior struggling with hair loss: you are not alone. Give yourself permission to grieve the changes, ask for help, try something new, cut it off if YOU choose, wear the wig, rock the scarf, embrace the bald spot, or simply take it one day at a time.

At Colors of Lupus, we believe awareness also means talking about the things that affect us emotionally—not just medically.

Let’s break the silence, normalize the conversation, and continue supporting one another one spoon at a time. 🥄💜🦋

Educate. Advocate. Empower.

08/11/2026

💙 LUPUS BELLY IS REAL 💙

Lupus can affect much more than your joints, skin, and energy levels—it can affect your digestive system too.

Many people living with lupus experience digestive symptoms such as nausea, bloating, acid reflux, abdominal pain, diarrhea, and constipation. These symptoms can sometimes be related to lupus itself, medications, inflammation, or other gastrointestinal conditions.

If stomach issues have become part of your lupus journey, don’t ignore them or simply assume you have to live with them. Talk with your healthcare provider about persistent or worsening symptoms so the cause can be evaluated and the right treatment plan can be developed.

💙 You are not alone.
Living with lupus means learning to listen to your body—even when the symptoms aren’t always visible.

At Colors of Lupus, we’re committed to helping our community better understand the many ways lupus can affect the body.

🦋 EDUCATE. ADVOCATE. EMPOWER.

Address

2801 W. Charleston Avenue Ste. 200
Las Vegas, NV
89102

Website

http://www.colorsoflupusnv.com/

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