I was diagnosed with gastroparesis about 8 years ago. There has been little help offered from various doctors at various hospitals. There is not enough education on this disease and not a lot of professionals looking for answers. I get almost all of my support from others with the disease. Doctors have offered little as far as information and education on the disease. Any medications have offered little or no relief from the daily symptoms and most medications have horrific side effects. The disease causing constant nausea, daily vomiting and pain. I stay in a state of fatigue due to the lack of nutrition. I am asking for support on bill HR3396. Just knowing that someone will have the ability to look for remedies or a cure because of this bill helps light up a dark existence. We just need to know someone hears us and wants to help.