Monica Fawzy Bryant, co-founder of Triage Cancer, provides a detailed overview and answers questions on health insurance considerations for patients with amyloidosis.
How to Pick a Plan – ASG Webinar: Section 2/4 Read More »
Monica Fawzy Bryant, co-founder of Triage Cancer, provides a detailed overview and answers questions on health insurance considerations for patients with amyloidosis.
How to Be an Effective Advocate – ASG Webinar: Section 4/4 Read More »
Monica Fawzy Bryant, co-founder of Triage Cancer, provides a detailed overview and answers questions on health insurance considerations for patients with amyloidosis.
Health Insurance Basics, Terms, Options – ASG Webinar: Section 1/4 Read More »
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
Health Equity and Rare Disorders 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: Michael Spector, Executive, Alexion, Astra Zeneca Rare Disease, Boston, MA
Followup Questions on CAEL101: Michael Spector – ASG Webinar 8/13 Read More »
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
Financial Assistance Update: Paula Schmitt – ASG Webinar 5/13 Read More »
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
Financial Assistance Update by Paula Schmitt – ASG Webinar – 12/12 Read More »
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.
Financial Assistance for AL Patients – ASG Webinar 5/13 Read More »