The annual Walk for Waldenstrom’s fundraiser will be taking place across the globe throughout the month of September. Please join us in raising Waldenstrom Macroglobulinemia awareness and support for the International Waldenstrom’s Macroglobulinemia Foundation (IWMF).
If you would like more information on arranging an in-person walk in your community, or if you need assistance setting up a Mightycause fundraising page to share on social media, please reach out to Annette Preston at [email protected] or 317-919-8238.
Scheduled Walks
September 16
Eunice Quast, Kate Beverley, & the Minnesota/W. Wisconsin
Support Group
Shelly Postek, Sharon Piotrowski & The Sarasota, FL Area
Support Group
September 24
Marcia Klepac – Western Pennsylvania, Eastern Ohio and
West Virginia Support Groups
September 30
September
Don & Mary Brown – Chicago Area & SE Wisconsin Support Group
Paul Kitchen, Rothesay, New Brunswick, Canada
Featured Walks
Walk for WM with Eunice Quast, Kate Beverley, & the Minnesota & W. Wisconsin Support Group
Sunday, September 16th, 2023 from 10:30AM Walk for Waldenstrom’s followed by a picnic on Saturday, September 16th. The event will take place at Autumn Hills Park in Oak Park Heights, MN.
Questions? Eunice at [email protected]
Sarasota Walk for Waldenstrom's with Sarasota Co-Leaders, Shelly Postek, Sharon Piotrowski, & the IWMF Home Office Staff
Saturday, September 16th, 2023 at 8:30AM! Ashton Park Legacy Trailhead in Sarasota, Florida, located at 4301 Ashton Road Sarasota, FL 34233. There is a playground and it is a dog friendly, paved trail. We will plan to walk one mile on the trail, and we will have some drinks and breakfast snacks to share.
PLEASE RSVP: [email protected] if you plan to attend.
HOW CAN THE IWMF HELP?
Newly Diagnosed?
Getting a diagnosis of WM can feel overwhelming. You have questions, we have answers! Tap in to our comprehensive resources about this rare disease.
Get Support
We are here to support you throughout your journey living with Waldenstrom macroglobulinemia. Remember, with the IWMF, you are never alone.
Join Us
When you join the IWMF, you become a member of an international community of people affected by Waldenstrom macroglobulinemia.
This is a paid clinical trial advertisement.
Stories of Hope
People with Waldenstrom macroglobulinemia and their caregivers share how they have coped living with this rare disease. Learn from these inspirational stories.
CALENDAR OF EVENTS
How Can We Help You?
