Waldenstrom’s macroglobulinemia (WM) is a rare, slow-growing cancer of the lymphatic system. Cancers of the lymphatic system are called lymphomas. WM is a type of lymphoma called non-Hodgkin lymphoma. Non-Hodgkin lymphoma is not a single disease; it refers to a group of different lymphomas that start in the lymphocytes (white blood cells). WM affects a specific type of white blood cell, called a B-lymphocyte or B-cell for short.

We’re happy that you’ve found us. After you’ve registered for this site which provides live and recorded virtual events, please visit our main website for more information and additional resources. https://iwmf.com/newly-diagnosed/

Yes! The IWMF Support Groups are the perfect place to talk with other people affected by WM, including patients, family members and caregivers. The groups provide mutual support and offer the opportunity to discuss concerns with others who share experiences with each other. This sharing strengthens the family bond and enhances everyone’s ability to cope with WM. Not only are Support Groups a good source of information about WM from others who are living with the disease…but you’ll make new friends! More information about support groups can be found here. https://iwmf.com/us-and-international-support-groups/

As part of our continued commitment to ensure that WM patients are never alone, we’ve launched this virtual platform to ensure all patients and caregivers can access our resources in real time with no cost to them.

This platform with all of its resources is open 24-7. Additional information and resources can be accessed on the IWMF home page iwmf.com

We’ve partnered with GRYT Health to build and host this platform. For any questions specific to this site navigation please email contact@grythealth.com

We’ve created an easy-to-use message system. Please go to this link to fill out some basic information and an IWMF staff member will contact you. https://iwmf.com/contact-us/