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The AnCan MS Support Group is a peer-led virtual monthly support group for people living with Multiple Sclerosis.

 

Our platform offers live interactive audio and optional video chat that you can join online or by phone. The group is for men and women living with the challenges that come with any form of MS.

 

We appreciate MS can change the challenges of even the simplest daily tasks … and we understand how it makes you feel  – physically and emotionally. Why? Because we are peers … we too live with MS and we understand it at the most basic level, Share your insight and commiserate with others who know.

 

To learn more about MS and meet two of our moderators, Dan & Jennifer Digmann, visit “A Couple Takes on MS” and read their blog.

 

The virtual group meets on the 2nd Tuesday of the month at 8.30 pm Eastern, and the 4th Tuesday at 1:30 pm ET in the AnCan Barniskis Room; participation is free and no registration is required. Joining instructions can be found here.

 

Our sessions may be recorded and posted to AnCan’s YouTube Channel, shared on social media and elsewhere.

Instructions for Joining a Group

 

Click HERE to learn how to connect with your computer or phone. No downloads required.


Click HERE to sign up for email reminders on virtual groups that interest you.

All of our groups are FREE...

and you can drop in at any time!

Quick Links

 

 Click HERE for a complete list of resources

Our Partners

National MS Society
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Multiple Sclerosis | Virtual Support Calls for Patients

Upcoming Multiple Sclerosis Groups

Multiple Sclerosis

This MS support group is a twice-monthly, peer-led group for men and women living with MS. This platform offers live interactive audio and optional video chat online or by phone to share stories of hope and support for the MS community.

Apr
23
May
14
May
28
Jun
11

Meet our moderators

Jennifer and Dan Digmann headshot
Multiple Sclerosis Patients
Dan and Jennifer share their perspectives on life from a husband and wife who each have Multiple Sclerosis.
Moderator
A Dx of PPMS, and the various symptoms that PPMS involves, has led Carmen to modify her guiding motto from “Go hard or go home” to “Go hard, then get home!”
Frank Austin headshot
Moderator
MS colors your life; but you choose the color!
Kim Stroeh headshot
Moderator
"Every day is an adventure and a surprise! 🤪 "
MS Moderator
Amanda R. Grego was diagnosed with Relapsing-Remitting Multiple Sclerosis in 2019 after a six month journey to a diagnosis.
Art Director and Instructor, MS Moderator
Hannah Garrison has been diagnosed with multiple sclerosis since June of 2017.

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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.