← Return to Advice for Amyloidosis with Waldenstrom's macroglobulinemia

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@colleenyoung

Hi @patio29dadio, welcome. You're facing some big decisions. Allow me to bring in fellow members who have experience with Amyloidosis, Waldenstrom's macroglobulinemia and bone marrow transplant (BMT) like @loribmt @gaetanche @irishk @jam5 @puffwithfluff @ejrquast to share their experience and advice.

While we wait for others to chime in, you may also be interested in reading about others in this related discussion:
- Waldenstroms and amyloidosis: https://connect.mayoclinic.org/discussion/waldenstroms-and-amyloidosis/

It sounds like you are also looking for an expert consultation to discuss your next steps for treatment and possible BMT. I might suggest reaching out for Mayo Clinic. Here's the contact information and how to request an appointment or a physician referral http://mayocl.in/1mtmR63

Is going to Mayo Clinic an option for you?

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Replies to "Hi @patio29dadio, welcome. You're facing some big decisions. Allow me to bring in fellow members who..."

Being a WM patient and knowing other WM and Amyloidosis patients, I concur with Colleen that consulting with a Mayo specialist who specializes in both WM and Amyloidosis is greatly advised before proceeding. I am aware that Dr. Morie Gertz, Mayo Clinic, specializes in both WM and Amyloidosis.

Thank you for recommending a consult with a a Mayo doctor specializing in both WM and Amyloidosis. Your continued support is greatly appreciated.