GINA Webinar Announcement
Special Webinar on GINA this Wednesday 7/13
The Huntington’s Disease Society of America invites you to attend special webinar this Wednesday, July 13 2011 at noon EDT. Watch this webinar to learn how GINA protects YOU.
Our webinar will feature Peggy Tighe, JD, from Strategic Healthcare, who will discuss GINA, the Genetic Information Nondiscrimination Act. Peggy is a partner at Strategic Healthcare, and recently presented at the HDSA 26th Annual Convention. Peggy will be discussing a brief history of GINA, as well as how GINA protects individuals from discrimination by health insurers and employers.
The webinar will last one hour, with time at the end for questions.
Participating in a webinar is very easy. All you will have to do is go to the link you receive after you register. If this is your first Webinar, we recommend that you log on five minutes before the start of the Webinar as it may take a few minutes for the process to complete. After registering, you will receive a confirmation email containing information about joining the Webinar.
To register to attend, please follow the link below and fill in all fields:
After registering, you will receive a confirmation email containing information about joining the Webinar. If you cannot attend on Wednesday, the webinar will be available online about one week after broadcast.
If you have any questions, please contact Jane Kogan at firstname.lastname@example.org