Please join us for Webinar- Participating in Turner Syndrome Research: TSRX PIN, to learn about an easy way that you can contribute to Turner Syndrome research! Brittany McLarney from Invitae will explain TSF’s TSRX Patient Insight Network (PIN) and how to participate. You will understand how to sign-up and how your participation will impact the advancement of research.

Brittany McLarney completed her genetic counseling degree in 2011, and since then has worked as a laboratory genetic counselor, a prenatal genetic counselor, a registry coordinator, and finally a program manager with Invitae. Her focus is working on and in registries to improve the research process for rare disease, including Turner Syndrome.

This webinar is free to attend, but donations make this program possible.

Register today for this webinar. You will need a computer with internet service and/or telephone to participate in this learning activity. Activity instructions will be emailed to registrants on a first come first serve basis.

The webinar will be recorded with English captions available, and the presentation slides will be made available afterwards as well, so sign-up even if you can’t attend to receive those materials in your inbox.

Webinar- TSRX PIN 3.9.21