Help Jeanna Achieve Her EDS Treatment Dream

Hi, my name is Olivia Simmons, and i’m making this GoFundMe for my sweet mama, Jeanna.

Since she was young, she has been suffering from a rare condition, called Ehlers-Danlos Syndrome.

About 4 or 5 years ago, she discovered a Doctor who specializes in treating those with EDS and all of the conditions that stem from it. It has been a huge dream and goal for her since, and now she finally has the chance.

Ehlers-Danlos Syndrome (EDS) is a group of hereditary connective tissue disorders that manifests clinically with skin hyperelasticity, hypermobility of joints, atrophic scarring, and fragility of blood vessels.

If my Mom goes to this Doctor, she has a chance to experience an individualized, 3-5 (or longer) day treatment plan several hours a day, an in depth education on how to manage EDS, and much more. She would finally, for the first time, receive treatment from someone who has full, in-depth knowledge of EDS. She has never experienced that before.

The full cost of this entire treatment plan comes to $5,000 (that our insurance will not cover), which is why we’re humbly asking for your support.

Every dollar, prayer, and every share helps tremendously. We GREATLY appreciate you for your generosity and support.