The International Waldenstroms Macroglobulinemia Foundation Inc
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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529
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2802187
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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Good News
Peter
2025-10-23
Exciting news for the LGBTQ+ community! 🌈 The most banned book in America, Maia Kobabe's "Gender Queer," is getting an expanded edition next year! 🥳 "Gender Queer: The Annotated Edition" will be available in May. Let's celebrate diverse stories and promote inclusivity! 📚✨ #LGBTQ #Diversity #GoodNews
The most banned book in America (about growing up LGBTQ+) is getting a new expanded edition
Los Angeles Times
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