LUPUS

 

 

About Us

Welcome all! Our group is peer-led once a month by people living just like you. We are a group for ANYONE living with lupus. We have been through our own triumphs and failures and hope to give you a sense of hope as we all come together monthly.

There are no judgments, discrimination or any negativity in our group. We support all living with lupus. Danielle (aka, Keto Lupie and director
of Laxin’ for Lupus), Dion and Emmitt (co-founders of The Lupus Dream Team) each have their own journey and ways to live it. Where the 3 of them come together is in their positivity and encouragement to empower you. They want you to be the best you can be every single day and will be here supporting you every step of the way!

A few of the topics that may be discussed, but not limited to are:

  • Treatments
  • How lupus affects you personally
  • Friends and family reactions to you day to day
  • Coping mechanisms for stress, anger, depression, loss of hope, etc…
  • How lupus has changed you as a person
  • Intimacy and sexuality
  • Diet and lifestyle
  • How to become your best advocate

WE truly look forward to meeting you!

When and Where

Our video chat virtual group meets on the 3rd Tuesday of each month at 8 pm Eastern, 7 pm Central, 6 pm Mountain and 5 pm Pacific in the AnCan Schmier Room. You can join online or by phone at +1 646 749 3127 Access # 656-182-845. See the Joining Instructions Panel above right for more information and other Country Access codes.

Partners

 

AnCan Is proud to partner with Keto Lupie, Laxin’ For Lupus, and The Lupus Dream Team for this virtual support group. 

 

 

Upcoming Lupus Groups

 

There are no upcoming events.

Instructions for Joining a Group

 

Scroll Down to "HOW TO JOIN" on this page for link and other instructions.


Click HERE to sign up for email reminders for this, and other groups we offer.

All of our groups are FREE...

and you can drop in at any time!

Quick Links

 

 Click HERE for a complete list of resources

 

 

Meet our moderators

Related Blog posts

Art with Hannah Garrison, Summer Edition!

Art with Hannah Garrison, Summer Edition!

On July 22nd, we had so much fun once again with our very own Hannah Garrison (Artist, MS activist, and moderator for our MS virtual support group) lead our appropriately titled..."Art With Hannah Garrison"! It has a Saturday Night Live ring to it, don't you think?...

Our services are free, but if you benefit then please consider a tax deductible donation. You can also support us by signing up to Amazon Smile and nominating Answer Cancer Foundation at no cost to you.

AnCan does not provide medical advice – we do empower you to manage your own care.

Our calls are recorded and posted on this website for later listening; please note we are a peer-to-peer support group and not subject to HIPAA compliance.