All Things Amyloid
Hi everyone! My name is Mackenzie and I was diagnosed with AL amyloidosis at age 23. We don’t know the cause of this disease, but we do know that it can lead to serious and potentially life-threatening issues. This disease has changed me and my life in so many ways, and as a result, I founded Mackenzie’s Mission to join the fight against this disease.
Part of our effort is to raise awareness which, we believe, will accelerate diagnosis, enable earlier treatment, and improve patient lives. We do this in several ways, including our “All Things Amyloid” podcast. In our episodes, we will speak with patients and caregivers about their journey on a wide array of topics. We will also hear from amyloidosis experts about the medical side of this disease.
There is more hope for patients than ever before, and raising awareness around the globe is critical to improving patient lives. If you want to learn more about the work we’re doing at Mackenzie’s Mission, please visit mm713.org. Thanks for listening!
All Things Amyloid
Empowering Patients via the Amyloidosis Support Groups
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For over two decades, Muriel Finkel has been running the Amyloidosis Support Groups (ASG). She’s a pillar in the industry and everyone knows her name. Her rolodex of physicians is unparalleled, and they all love her. The ASG is an extremely valuable resource for patients and caregivers, providing far more than just knowledge. Learning about current and potential treatments, advancements in the disease, and connecting with other patients and caregivers are just a few of the benefits. Hear from Muriel directly, who will share what she thinks is the #1 benefit the ASG offers. For an overview of amyloidosis, please see episode 2 (for clinicians) or episode 3 (for patients).
