Join us for an amazing Ginny & Georgia livestream reunion event on Wednesday, May 26th at 6:30 PM (PT) / 9:30 PM (ET) in support of Huntington’s Disease Awareness Month (May) and our quest to raise $50,000 for the Huntington’s Disease Society of America.

The stars and creative forces behind the hit show will all be in one (virtual) place for one night only. Brianne Howey (Georgia), Antonia Gentry (Ginny), Felix Mallard (Marcus), Sara Waisglass (Max), Diesel La Torraca (Austin), Jennifer Robertson (Ellen), and Raymond Ablack (Joe), as well as creator Sarah Lampert and showrunner Debra Fisher will gather for a fun evening where we take a journey through the making of this fan-favorite show and what everyone has been up to since finishing Season 1. Moderated, fittingly, by Scott Porter (Paul) the Mayor himself, this portion of the evening is free and no fan will want to miss it.

In lieu of tickets, please consider making donation to HDSA.


Immediately following the reunion on May 26th, starting at 7:15 PM (PT) / 10:15 PM (ET) will be an exclusive Fan Q&A where you could have your own question answered* by the cast and creative forces behind Ginny & Georgia. Think of it like your own private G&G Convention. There may even be some surprise goodies available for auction as well.

When you donate $20 or more, you will receive an exclusive email invite to the Fan Q&A.

*Fan questions will be chosen from those submitted on social media before the event and from the live chat during the event. Please note, due to time constraints, fans are not guaranteed to have their question asked during the Q&A.

Every cent of every ticket sold for this portion of the night goes directly to support HDSA’s mission to improve the lives of everyone affected by Huntington’s disease and their families. 


Can’t attend the Fan Q&A but you still want to donate? The Huntington’s Disease Society of America (HDSA) is the premiere non-profit organization dedicated to improving the lives of everyone affected by Huntington’s disease. From community services and education to advocacy and research, HDSA is the world’s leader in providing help for today, hope for tomorrow for people with HD and their families. With your support, HDSA is able to provide the resources that HD families need. Every dollar helps, so give if you can.


Huntington’s disease (HD) is a fatal genetic disorder that causes the progressive breakdown of nerve cells in the brain. It deteriorates a person’s physical and mental abilities usually during their prime working years and has no cure. HD is known as the quintessential family disease because every child of a parent with HD has a 50/50 chance of inheriting the faulty gene. Today, there are approximately 41,000 symptomatic Americans and more than 200,000 at-risk of inheriting the disease.

The symptoms of HD are described as having ALS, Parkinson’s and Alzheimer’s – simultaneously.

To learn more about Huntington’s disease please visit


Wellsbury’s own Mayor Paul Randolph, Scott Porter, has Huntington’s disease in his family. Both his Wife and Mother-In-Law have the Huntington gene. The Porter family has made raising awareness of Huntington’s disease and raising funds for the HDSA a focal point of their lives, and luckily the Ginny & Georgia family has bravely taken up the call to join them on this journey.

Click here to watch a powerful HD story on ABC News.

Click here to learn more about The Porter Family story.


Thank you so much and we hope to see you for this amazing event on May 26th!