How to Pick a Plan – ASG Webinar: Section 2/4
Monica Fawzy Bryant, co-founder of Triage Cancer, provides a detailed overview and answers questions on health insurance considerations for patients with amyloidosis.
Monica Fawzy Bryant, co-founder of Triage Cancer, provides a detailed overview and answers questions on health insurance considerations for patients with amyloidosis.
Monica Fawzy Bryant, co-founder of Triage Cancer, provides a detailed overview and answers questions on health insurance considerations for patients with amyloidosis.
Monica Fawzy Bryant, co-founder of Triage Cancer, provides a detailed overview and answers questions on health insurance considerations for patients with amyloidosis.
NORD is pleased to announce a collaboration with the Rare Disease Diversity Coalition (RDDC) on a three-part webinar series discussing the role that health care providers play in addressing health inequity in the rare disease community. The series will explore underlying issues that lead to inequities and encourage participants to evaluate their interactions with members …
Amyloidosis Support Groups’ webinar for light chain (AL) amyloidosis was hosted on January 15, 2022. Led by ASG President Muriel Finkel, this webinar discusses the current treatments for light chain amyloidosis and features amyloidosis expert: Michael Spector, Executive, Alexion, Astra Zeneca Rare Disease, Boston, MA
The Foundation for Peripheral Neuropathy (FPN) invites you to join us for a discussion on Hereditary Neuropathy and Genetic Testing. Brett McCray, M.D., PhD, will join us to share his insights into hereditary neuropathy, as well as current advances in the space which may be of interest to patients with hereditary neuropathy as well as …
FPN Webinar: Hereditary Neuropathy and Genetic Testing Read More »
Amyloidosis Support Groups’ webinar for light chain (AL) amyloidosis was hosted on January 15, 2022. Led by ASG President Muriel Finkel, this webinar discusses the current treatments for light chain amyloidosis and features amyloidosis expert: Paula Schmitt, Executive Director, Amyloidosis Support Groups
This webinar is hosted by Amyloidosis Support Group. In this chapter of the webinar Paula Schmitt, Executive Director, Amyloidosis Support Groups explains about the financial assistance that are provided to ATTR patients during the course of their treatment
Amyloidosis Support Groups’ webinar for light chain (AL) amyloidosis patients and caregivers in the Northeast region on September 18, 2021. Led by ASG President Muriel Finkel, this webinar discusses the current treatments for light chain amyloidosis. Paula Schmitt, ASG Executive Director, gives an update on financial assistance for AL patients.