Lupus Connect

Lupus Connect Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Lupus Connect, Nonprofit Organization, Oak Park, MI.

Our Health, Our Terms: Solving The Lupus And Multiple Sclerosis Mystery WebinarSee the link to Webinar Registration in t...
06/17/2026

Our Health, Our Terms: Solving The Lupus And Multiple Sclerosis Mystery Webinar

See the link to Webinar Registration in the comment section below.πŸ‘‡

You are not alone.Living with lupus can feel overwhelming at times, but support makes a difference. Whether you're newly...
06/17/2026

You are not alone.

Living with lupus can feel overwhelming at times, but support makes a difference. Whether you're newly diagnosed, caring for a loved one, or simply looking for understanding, there is a community here for you.

At Lupus Connect, we believe that no one should have to face lupus alone. Together, we can learn, encourage one another, and find strength through shared experiences.

Remember:
πŸ’œ Community matters.
πŸ’œ Support matters.
πŸ’œ You matter.

If Lupus Connect has encouraged you, please help us reach someone else who may need support. Follow our page, share this post, and invite others to join our community.

What has helped you feel supported on your lupus journey? Share below. We'd love to hear from you. πŸ’œ

06/17/2026

Upcoming Lupus Support Group Meeting

06/16/2026
Share your personal story and/or one thing you wish more people knew about lupus in the comments or send us a message.  ...
06/15/2026

Share your personal story and/or one thing you wish more people knew about lupus in the comments or send us a message. πŸ’œ

πŸ’œ Every Lupus Story Matters πŸ’œLupus looks different for every person.For some, it affects energy.For others, it affects p...
06/12/2026

πŸ’œ Every Lupus Story Matters πŸ’œ

Lupus looks different for every person.

For some, it affects energy.
For others, it affects pain, skin, joints, organs, emotions, or daily routines.

No two lupus journeys are exactly the same, and that's why sharing our experiences matters. When we listen to one another, we learn, support, and remind each other that no one has to face lupus alone.

✨ Question of the Day:

What is one thing you wish more people understood about lupus?

Whether you're living with lupus, caring for someone who is, or supporting a loved one, your voice can help increase awareness and understanding.

πŸ’œ Share your thoughts in the comments or send us a private message. Your story may be exactly what someone else needs to hear today.

πŸ’œ We Need Volunteers! πŸ’œLupus Connect is growing, and we're looking for caring individuals who want to make a difference....
06/11/2026

πŸ’œ We Need Volunteers! πŸ’œ

Lupus Connect is growing, and we're looking for caring individuals who want to make a difference.

Whether you enjoy planning events, helping behind the scenes, managing social media, community outreach, fundraising, or simply lending a helping hand, there's a place for you on our team.

Every volunteer helps us reach more individuals and families affected by lupus. Your time, talents, and passion can help bring awareness, support, education, and hope to our community.

Would you consider volunteering with us?

Tell us in the comments: What volunteer activity do you enjoy most, and why?

πŸ“© Interested in volunteering? Send us a message to learn how you can get involved.

β˜€οΈ Summer can be a wonderful time to enjoy the outdoors, but for many people living with lupus, the sun can bring additi...
06/09/2026

β˜€οΈ Summer can be a wonderful time to enjoy the outdoors, but for many people living with lupus, the sun can bring additional challenges.

A little extra planning can go a long way. Remember to protect your skin, stay hydrated, take breaks, and listen to what your body needs. Your health and well-being always come first.

What is one thing that helps you manage lupus during the summer months? Share your tips and experiences below. You never know who might benefit from your advice. πŸ’œ

Help us spread awareness and support by sharing this post with someone managing lupus this summer.

πŸ’™πŸ’œ June is Men’s Health Month β€” Let’s Talk About Lupus in Men πŸ’œπŸ’™When people think of lupus, they often think of women. B...
06/09/2026

πŸ’™πŸ’œ June is Men’s Health Month β€” Let’s Talk About Lupus in Men πŸ’œπŸ’™

When people think of lupus, they often think of women. But men can live with lupus, too.

Men living with lupus may experience delayed diagnoses, face stigma, or feel pressure to ignore symptoms and "push through" their health challenges. These barriers can make an already difficult journey even harder.

This Men’s Health Month, Lupus Connect is helping raise awareness for the fathers, brothers, sons, husbands, friends, and caregivers whose lupus stories are often overlooked.

Every voice matters.
Every story matters.
Every person deserves to be heard and supported.

By talking openly about lupus and men’s health, we can help break down misconceptions, encourage earlier diagnoses, and create stronger support systems for those affected.

πŸ’œ Share this post to help expand the conversation around lupus and men’s health.

Have you or someone you know been affected by lupus? Share your experience in the comments and help raise awareness.

πŸ’œ What does support really look like? πŸ’œWhen someone is living with lupus, support isn't always about grand gestures.Some...
06/05/2026

πŸ’œ What does support really look like? πŸ’œ

When someone is living with lupus, support isn't always about grand gestures.

Sometimes it's believing them when they say they're exhausted.
Sometimes it's checking in, even if they don't respond right away.
Sometimes it's being patient when plans change unexpectedly.

The smallest acts of understanding can make the biggest difference.

If you have a lupus warrior in your life, what is one thing you've done or wish others would do to show support?

Share your thoughts below and help us build a community rooted in compassion, understanding, and encouragement.

πŸ“£ Share this post with someone who wants to support a lupus warrior better.

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Address

Oak Park, MI
48237

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