So after months of waiting, we are finally getting home health services starting this coming Thursday. The nurse will be coming to change the port needle and dressing so that we don’t have to go to the clinic and face never ending fatigue. We are also in the process of trying to get a custom wheelchair for our postural orthostatic tachycardia syndrome and Ehlers-Danlos syndrome. I am also in the process of trying to discuss with my dysautonomia specialist the benefits of IV hydration and why it needs to continue and possibly be increased. We cannot get enough fluids through the feeding tube alone let alone sodium as well. Hoping all is well with everyone else, and have a great day. Always remember live to inspire.
I am not disabled, I am differently abled,