So happy to finally have found a medical charity that, unfortunately, isn't government-funded but that is adding biomedical research to something nobody really cares about: LEAKY GUT and Chronic Fatigue Syndrome. With celiac disease, IBS, Chron's and Fibromyalgia having gotten in fashion lately as to be given funding and benefits almost worldwide, leaky gut is still thought to be "alchemy" and "fake". I have been suffering from leaky gut syndrome for 16 years and like me so many people in the world, disregarded by conventional medicine and laughed at my many people around us. New research is showing that leaky gut is the systemic cause to all the abovementioned diseases. Yet,there is no recognition whatsoever for leaky gut/CFS sufferers. That's why I'm supporting this charity whole-heartedly!  

Invest in ME Research is an independent UK charity finding, funding and facilitating a strategy of biomedical research into Myalgic Encephalomyelitis (ME or ME/CFS).The charity is run by volunteers - patients or parents of children with ME - with no paid staff.Overheads are kept to a minimum and all funds raised to go to promoting education of, and funding for biomedical research into, ME.Our efforts are focused on setting up a UK Centre of Excellence for ME which will provide proper examinations, diagnosis and in time treatment(s)/cure(s).

Happy holidays!