Sign up documents are coming soon.  In the meantime, contact

Your Story

We are running a campaign, inviting you to share YOUR STORY.

This is about you.  Let’s get personal.  The only way to learn, share and thrive is through learning from others.  So please, send us an article, or your story, or even if you just want to talk, please REACH OUT to us.  You are strong, you are a warrior, and you are worth it.  We WANT TO HEAR from you.
Whether you are a lupus patient, caregiver, or friend, please share with us your story.  If you want, we will publish it.  It is by awareness and sharing that we can help eradicate this disease.  Speak up, and lend your voice.
Do you want to share what it’s like for you to have lupus?  Or how you have coped?  Perhaps you can share what is going on in your illness.  Any and all ways you want to tell your story are welcome.

Thank you for sharing!  IT’S YOUR TIME!  

Throw Your Own Fundraiser

This is where it gets fun.  

Did you know that all this came about because of ONE fundraiser?  One tiny action can cause a huge reaction.  We’d loved you to be involved.  Let us know how you’d like to raise money for a cause that matters to YOU.  And let us help!  

To get in touch, email or call 720 470 8049.

Thank you!   

And why contribute to our organization?  

We can host and be part of the biggest events of their kind in the world.  So you are not only raising money for research but you are promoting lupus awareness world-wide.

If you believe in our mandate, then you should join us.

Examples of fundraisers:

  • Throw a dinner party
  • Create a wine event
  • Run a walk/run
  • Create an event of your choosing

Have fun!

Join “Team Lupus” for Lupus Spiel USA!

Team Lupus is responsible for the success of the Lupus Spiel.  We have a group of about 20 people working together, brainstorming, laughing, getting creative, and HAVING FUN to make this spiel the largest of its kind in the U.S., and soon to be North America!

Join us!

  • You might be asked to:
  • Share your ideas
  • Speak up
  • Recruit friends
  • Find silent auction items or live auction items
  • Be at the spiel as a Team Lupus member ready to answer questions
  • Spend time with us
  • Laugh with us
  • Share with us and eat with us
  • Meet famous curlers!
  • Chaperone famous curlers
  • Chauffeur famous curlers
  • Curl
  • Tell people about the event and the foundation
  • Plan more ideas
  • And more!

When you’re ready to jump in, and ANY level of participation is welcome, reach out!  NO level of participation is too small.  And none too big.  Make this what you want.  Family members and care givers are welcome!

Become a Curler

Do you want to learn how to play this awesome sport?

Regan and Todd will teach any person wanting to learn the sport for free.  That’s right, especially lupus, arthritis, and fibromyalgia patients – this is a sport you can do – reach out to us!  

This can be your first step into getting involved with the Lupus Spiel!  Or joining a community that cares!  Let’s curl!

Become a Curling Partner

Curling Clubs and organizations across the country are partnering with the Lupus Research Foundation to help find a cure!  

There are all sorts of ways to partner, and for the basic gist, here’s how it works:
We will partner with you to bring in a new group of people for Learn-to-Curls, lupus groups, which will raise awareness of your club, and advance the cause of raising funds for research and raising awareness.
Other ways to partner can include exchanges.  For example, for a portion of your  club’s memberships or registrations, we can provide a discount to the Lupus Spiel for your members!  Don’t forget we’re home to the LARGEST PRO-AM FOR CURLING IN THE UNITED STATES (soon to be North America).  We will also include your club on our signage, and promote your club on facebook, twitter, and instragram. As you may know, the Lupus Spiel has incredible viewership on facebook.
We are open to all ideas by way of partnership.

When you think curling and caring, think lupus!

Partner your curling club with us.  Give us a call, at 720 470 8049.  Thanks and GOOD CURLING!


Become a Community Partner

The Lupus Research Foundation partners with businesses and organizations to elevate one another within the local community and beyond.  We appreciate our Community Partners and thank them for helping us meet our mandate of finding a cure.  

To learn more about this program, please contact us. 

We are proud to partner with:

Wagamon Brothers Auto & Marine Service Center, and Wagamon’s Ogilvie Raceway

Pat Wagamon, his wife, Cathy, and the entire Wagamon family and crew have been amazingly supportive of the Lupus Spiel for all the years of its existence.  We thank Pat and Cathy and the Wagamon family, and encourage everyone to take part in what their businesses have to offer.  You couldn’t ask for a nicer group of people or for better quality of service.  And, the racetrack is a heck of a good time!  Plan your social event with them!

Minnesota Moose Junior A Hockey Team

Jon Jonasson, head coach, GM
Minnesota Moose USPHL Premier
T: 952 457 0525 E:

More opportunities are available; please contact us.

Join the Team

Is there a special skill you would like to share with us?  Are you interested in contributing to our mission of raising funds for research and raising awareness?  We need you!  Call us at 720 470 8049 or email, and share what you’d like to do.  

Let’s do this!