The International Waldenstroms Macroglobulinemia Foundation Inc

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Info, support, research grants, and more for lymphoplasmacytic lymphoma/Waldenstrom’s patients, caregivers and specialists. office@iwmf.com | 941.927.4963 Patient volunteer-run organization established to provide educational information and caring support to Waldenstrom's macroglobulinemia (WM) patients and caregivers, and to fund research that will lead to better treatment therapies, and eventually a cure Support and educate everyone affected by Waldenstroms macroglobulinemia (WM) to improve patient outcomes while advancing the search for a cure.

Founded

1998

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4100

X (Twitter)

529

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2802187

Address: 6144 Clark Center Avenue, SarasotaWeb: Sign in to see organisation websiteFacebook: waldenstroms.supportX (Twitter): WMIWMFEmployees: 10Volunteers: 217Revenue: 3292131ICO: 541784426

International Waldenstrom’s Macroglobulinemia Foundation What is WM. Treatment Resources Living Well With WM Support News Events Researchers Healthcare Professionals Donate Fundraise Participate About Us Contact International Waldenstroms Macroglobulinemia Foundation ACCELERATE THE CURE Wednesday May 212025 Chantilly France NEWLY DIAGNOSED. How Can We Help. Newly Diagnosed.

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David

❤️ Thank you, IWMF, for all the incredible support and resources you provide to patients and caregivers facing Waldenstrom's macroglobulinemia. Together, we will find a cure! 💪

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Rachel

Just registered for the upcoming webinar on fitness essentials for WM! So grateful for organizations like IWMF that empower us to live well while fighting this disease. 🌟 #HopeForCure

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Peter

1. What innovative fundraising strategies have proven effective for patient-run organizations like the IWMF in supporting research for Waldenstrom's macroglobulinemia?

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Louis

2. How can technology be leveraged to enhance the educational resources and support systems available to Waldenstrom's macroglobulinemia patients and their caregivers?

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