Hello, I am Christina Hall. My son Liam is 11. He has Cerebral Palsy Spastic Quadriplegia, Epilepsy, Dysautonomia , global delays, g tube continuous drain and j tube continuous feed, non verbal, non ambulatory but completely cognitively aware. He communicates through facial and verbal cues, as well as by eye gaze communication device.

Back in January Liam’s stomach stopped working. It no longer absorbed medications or tube feeds. He required immediate surgery to do a J tube to get his feeds by intestines (bypassing the stomach).

Liams dysautonomia has been a real struggle for us these past couple of years. It has slowed down all of his internal motility. There is no cure for neuro divergent cases of dysautonomia.

Our handicap accessible vehicle is about to say goodbye to us and we could really use some help to purchase a new vehicle that can transport his wheelchair, and possibly even be a big enough vehicle to add a changing table etc .

The last hospital stay was 15 days and we almost lost our home. My income is based on my son’s care needs. Unfortunately I am not able to claim hours while he is under hospitals care (even if I do most of the work). I feel very blessed to have my Liam. He is the sweetest most gentle soul. He has a typical little boys sense of humor and sometimes even an adult sense humor. His laugh is infectious. He almost never cries! He is such a happy boy. He is super tall and is getting so much bigger so much faster now that he has the J tube.

I am a single mom and could really use the help. Anything helps! I just need to be able to get him around everywhere he needs and WANTS to go like Disneyland, Oregon, school and to family events etc.

Thank you so much and please come to our lemonade stand hosted by Dining For Hope

at Velvet Grill And Creamery on Mchenry Ave in Modesto California on May 3, 2025 from 11am-2pm