Aloha all!

Our friend Angie has been struggling with being diagnosed with a disease known as Ehlers-Danlos Syndrome (EDS) within the last 2 years. It has been challenging for her as it has progressed in the last few months.

EDS is incurable and ranges within a group of 13 heritable connective tissue disorders. The conditions are caused by genetic changes that affect connective tissue. Each type of EDS has its own set of features with distinct diagnostic criteria. Some features are seen across all types of EDS, including joint hypermobility, skin hyperextensibility, and tissue fragility. In Angie's case, she is struggling to walk and function daily. She has been rendered to a wheelchair and has to use a walker. She is currently working on receiving in-home healthcare.

If you know Angie, you know she’s usually pretty private about her life and struggles, so this may come as a surprise to many. But she tries to battle in private, yet manages to smile through the pain.

She is asking for any support at this time, as you know, medical bills and expenses are becoming an issue, along with daily needs. She is unable to work any longer as this is affecting all the joints in her body along with crippling arthritis. She has raised her amazing, helpful daughter on her own and has always helped others when she can. It’s not easy for her to ask for help, so we’re doing it for her.

Anything helps, no matter how small. You can always just send her prayers and love, too.

She’s one of the strongest people I know, and she’s "in a bad way" with her health. So please consider and help where you can.

Thank you all so much!