Eight minutes of "Faces of Gastroparesis", and that is just a fraction of the amount of people affected by this. Barely anyone has ever heard of this. I hadn't before I was diagnosed. We need to get the word out, so there will be more funding by the National Institute of Health (NIH), to try to develop a cure for this. Please help us get awareness by voting and commenting on our gp admissions.
#ellendancewithraven #curegp #gpawareness

People who suffer with gastroparesis (gp) are hoping to get Raven Walton on the show with Ellen in hopes of bringing national attention to this dreadful (sh--ty, pukey) disease. Some feel like we're starving to death. Sadly, some of our fellow gp warriors have actually done that. None of us want to be the next one, though at times this disease feels like it's winning our losing battle. I have read posts from several members of our support group who are so close to giving up. Gastroparesis (gp) takes its toll on our body, mind and often our relationships with family or friends who just do not understand. Doctors often do not know the scope of what we go through, nor will they admit that it is the problem we say it is. Do you know what it's like to be told you're not that sick when your body tells you that you are? This invisible illness takes its toll on us, and we're sick of it. Please help get Ellen to invite Raven to her show so we can get national awareness for all gp sufferers. We also hope that by bringing national attention we will encourage the medical community to dedicate more of their research funds to gp, and eventually find a cure. Won't you help us please?
#gastroparesis #gpawareness #curegp #ellendancewithraven

#ellendancewithraven #dancedare

#ellendancewithraven #ellendegeneres #dancedare