I was diagnosed with RED/CRPS in the fall of 2012. Within a year I was wheelchair bound as it became excruciatingly painful to be weight baring at all. Then my blood pressure started flipping all over the place, in the space of an hour it can go from 90/60 to 225/115. Now it has spread to my right arm-so apparently I will be one of the cases that is going full body. My question is this … Why is no research being done? Why are we being left to basically a situation of ‘let’s try this, no-let’s try that’. The treatment of patients suffering with RSD/CRPS is archaic.