Colors of Lupus NV

06/18/2026

☀️🦋 SUMMER SUN & LUPUS: PROTECT YOURSELF! 🦋☀️

Summer is here, and while many people are enjoying vacations, pool days, BBQs, and outdoor activities, those of us living with Lupus have an extra reason to be cautious.

Did you know that exposure to ultraviolet (UV) rays from the sun can trigger Lupus symptoms and even cause a flare? For many Lupus warriors, too much sun exposure can lead to increased fatigue, joint pain, skin rashes, headaches, brain fog, and inflammation throughout the body.

💜 This doesn’t mean you can’t enjoy summer—it simply means you need to take extra precautions to protect your health.

✅ Wear broad-spectrum sunscreen (SPF 50+)
✅ Reapply sunscreen every 2 hours
✅ Wear hats, sunglasses, and UV-protective clothing
✅ Stay hydrated
✅ Seek shade whenever possible
✅ Avoid peak sun hours (10 AM – 4 PM)
✅ Listen to your body and rest when needed

Remember: Photosensitivity is one of the most common Lupus symptoms, and sometimes the effects of sun exposure aren’t immediately visible. Protecting yourself today may help prevent a flare tomorrow.

🦋 Your health comes first.
☀️ Your summer can still shine—just do it safely.

Tag a fellow Lupus Warrior and share this important reminder!

🦋💜☀️

06/15/2026

💜 IN THE LOOP – Lupus Support Group 💜

You don’t have to navigate Lupus alone.

Join Colors of Lupus for our upcoming In the Loop Lupus Support Group meetings, where Lupus Warriors, caregivers, family members, and supporters come together to connect, share experiences, learn, and encourage one another in a safe and supportive environment.

📅 Upcoming Meetings
• June 20, 2026
• July 18, 2026
• August 15, 2026

⏰ 11:30 AM – 1:00 PM

📍 In-Person Location
Colors of Lupus
Inside RB Wellness Clinic
2801 W. Charleston Blvd., Suite 200
Las Vegas, NV 89102

💻 Join Virtually via Zoom
Meeting ID: 826 0281 3415
Passcode: 183020

Whether you’re newly diagnosed, a longtime warrior, a caregiver, or simply looking for community, we invite you to join us. Together we learn, grow, support, and empower one another. 💜🦋

💜 Educate. Advocate. Empower.

🌐 www.colorsoflupusnv.com

📱 Follow us on all social platforms:
Facebook • Instagram • TikTok • LinkedIn


.o.l.n.

06/07/2026

💜🦋 JUNE IS MALE HEALTH AWARENESS MONTH 🦋💜

When most people think about Lupus, they think of women—and while it is true that Lupus affects women more often, men can and do develop Lupus too.

This June, during Male Health Awareness Month, we’re shining a light on the often-overlooked experiences of men living with Lupus and other autoimmune diseases.

Many men face:
💜 Delayed diagnosis because Lupus is often considered a “women’s disease”
💜 More severe organ involvement, including kidney and heart complications
💜 Misunderstanding and stigma surrounding chronic illness
💜 Challenges discussing physical and emotional health concerns

The truth is that Lupus does not discriminate.

Men living with Lupus deserve the same awareness, support, research, and understanding as anyone else affected by this complex autoimmune disease.

🔹 Know your body.
🔹 Pay attention to symptoms.
🔹 Don’t ignore fatigue, joint pain, swelling, rashes, or unexplained health changes.
🔹 Schedule regular checkups.
🔹 Advocate for yourself and your health.

To every man living with Lupus: You are not alone. Your story matters. Your health matters.

Together, let’s continue to educate, advocate, and empower while breaking the silence surrounding men’s health and Lupus.

💜 Because Men with Lupus Matter. 💜

💜🦋

06/07/2026

💜 LIKE • FOLLOW • SHARE • SUPPORT 💜

Help us continue spreading lupus awareness, empowering lupus warriors, and creating change throughout our community by connecting with Colors of Lupus Nevada on ALL social media platforms! 🦋

Every like helps raise awareness.
Every follow helps grow our community.
Every share helps us reach someone who may need support, hope, or resources. 💜

📱 Follow us everywhere:
Facebook:
Instagram:
TikTok:
X (Twitter):
YouTube:
Threads:
LinkedIn: Colors of Lupus Nevada

Together, we are stronger. Together, we can end lupus. 💜

🦋 JOIN. CONNECT. SUPPORT. ADVOCATE. 🦋

💜

06/05/2026

🦋💜 A New Chapter for Colors of Lupus 💜🦋

For nearly two decades, our organization has proudly served the Lupus community as Colors of Lupus Nevada. Today, we are excited to share a meaningful change that reflects our vision for the future.

As we continue to grow, expand our programs, and reach more individuals and families affected by Lupus, we are removing “Nevada” from our name and moving forward simply as Colors of Lupus.

While Nevada will always be our home, our mission has never been limited by state lines. This change allows us to broaden our impact and bring our support, education, advocacy, awareness campaigns, events, scholarships, and resources to communities in other cities, states, and regions.

Our commitment remains the same:
💜 Educate.
💜 Advocate.
💜 Empower.

Whether you have been with us from the beginning or are just joining our journey, we thank you for your continued support. Together, we will continue raising Lupus awareness, supporting Butterfly Warriors and their families, and fighting for a future where no one faces Lupus alone.

This is more than a name change—it is a reflection of our growth, our purpose, and our promise to serve wherever the need exists.

🦋 Same Heart. Same Mission. Bigger Reach.

💜🦋

06/05/2026

💜 June is Antiphospholipid Antibody Syndrome (APS) Awareness Month 💜

COLORS OF LUPUS

EDUCATE. ADVOCATE. EMPOWER.

⸻

What is Antiphospholipid Antibody Syndrome (APS)?

Antiphospholipid Antibody Syndrome (APS) is an autoimmune disorder that causes the immune system to mistakenly create antibodies that increase the risk of abnormal blood clotting.

APS can affect:
🩸 Veins and arteries
🫀 The heart and circulatory system
🧠 The brain and nervous system
🤰 Pregnancy and fertility outcomes

⸻

How Does APS Relate to Lupus?

Many people living with Lupus also test positive for antiphospholipid antibodies.

Did You Know?

🔹 Approximately 30–40% of people with Lupus have antiphospholipid antibodies.

🔹 Not everyone with these antibodies develops APS, but they may still be at increased risk for complications.

🔹 APS is considered one of the most common autoimmune conditions associated with Lupus.

⸻

Common Signs & Symptoms

⚠️ Blood clots in the legs, lungs, or other areas

⚠️ Recurrent miscarriages or pregnancy complications

⚠️ Stroke or transient ischemic attacks (TIAs)

⚠️ Migraines or severe headaches

⚠️ Livedo reticularis (lace-like purple skin pattern)

⚠️ Low platelet counts

⸻

Why Awareness Matters

Early diagnosis and treatment can help reduce the risk of serious complications.

If you have Lupus, talk with your healthcare provider about APS testing if you have:
✔ A history of blood clots
✔ Pregnancy complications
✔ Unexplained neurological symptoms
✔ Positive autoimmune laboratory findings

⸻

Together We Raise Awareness

Because understanding APS can help save lives and improve outcomes for people living with Lupus.

💜 June is APS Awareness Month
💜 Knowledge is Power
💜 Advocate for Your Health

Colors of Lupus
Educate. Advocate. Empower.

BloodClotAwareness LupusWarrior ColorsOfLupus EducateAdvocateEmpower LupusEducation ChronicIllnessAwareness 💜

06/03/2026