August 20, 2026
September 19, 2026

Porch Nite: Johnson City, TX

When:
August 28, 2026 6:00PM

Porch Nite is Jett Foundation’s national support group that brings together mothers, grandmothers, aunts, and caregivers of children affected by Duchenne to bring love, support, and laughter across the United States. During the weekend of August 28-30, 2026, we will host an in-person Porch Nite in Johnson City, Texas. Come and hang out at this weekend retreat and enjoy days of connection, fun, and laughter! Even if you can only come for a day or a few hours, we would love to have you!

Porch Nite: Johnson City, TX
August 28-30, 2026 | In-Person

Agenda:

Host: Rae Lorance and TBD

Friday
6PM: Check-in and welcome bags

Saturday
TBD

Sunday
10AM: Checkout/Farewells


Accommodations are being covered by Jett Foundation, including light snacks on Friday night during arrival, as well as breakfast, lunch, and dinner items for the house on Saturday. Jett Foundation will also provide breakfast items for the house on Sunday. Any meals outside of what is provided above will be at the expense of each individual. More specific information will be provided two weeks prior to the event. If you have any questions to ask ahead of time, or any meal option suggestions, please email them to [email protected].

A $50 deposit is required to secure your spot. This deposit will be refunded when you attend Porch Nite, but will not be refunded if you do not attend. We recognize that unforeseen circumstances can occur, but please understand that a considerable amount of time and resources go into organizing each in-person Porch Nite, so proper planning is essential. Please register separately per person. If you have any questions, please reach out.

Experience the magic this summer!

How is the rare disease community accomplishing goals?

Tune in on February 29 to hear from our panel and moderators on how they are accomplishing goals and living life to the fullest!

Your gift helps Jett Foundation provide programming and opportunities, such as Camp Promise, to many families impacted by Duchenne muscular dystrophy each year.

Accessible Vehicle Fund Applications Open