I had my shoulder replaced two days ago and am still in hospital waiting to be discharged to a rehab facility. That has landed me in Medicare purgatory because Medicare considers the K as a chronic condition and even though I can't intubate it on my own, specifically because of the shoulder surgery, they say that I am only being treated for the shoulder surgery and that covers one day in hospital. Most of the staff has been very helpful and has arrange for me to continue to stay here until at least Monday. Subsequently I am stuck in the hospital, which at this moment is better than going home, as I live by myself.
The surgery replaced a failed artificial shoulder with a reverse shoulder – – the ball of the joint is on the body side and the cup is affixed to the humerus– – and the humerus fractured doing the surgery. At this point it will be another 12 days before I can remove my arm from the brace/sling and move my left arm either to the right or left, i.e. my left hand is used only if the elbow is right next to my body and the lower arm is sticking straight out as if holding a gun.
In the meantime a nurse helps me with evacuating. A couple of problems about which I would like some advice. When normally inserting the catheter I use both hands and primarily use the right fingers to slobber on the lubricant inevitably drips off the catheter . Is there a good way to guide the catheter in with only one hand? My concern, of course, is to make sure the catheter goes in straight and doesn't mess with the valve alignment .
I may have come up with a solution for irrigating, but if somebody has a better one please suggest it. I am thinking of hanging an IV bag, with water in it, and controlling the flow of water into the catheter with an on/off, in-line switch. Currently the nurse inserts a syringe into the catheter. If my solution works it would make me more independent.
My stoma looks like a little volcano as it protrudes from my abdomen. Usually I think the pouch is full when this happens, but in this case I evacuate and it comes down a small bit, but is not the normal flattish against my stomach. Also, the stoma is bleeding and it looks like it has tiny cuts in it. This hasn't happened before. Maybe the paper towels here are too rough?
Ideally I would like to figure out a way to manage the pouch on my own. Then I can go home and have a home healthcare aides come to the house. They will only come in once a day, although I could pay somebody to come in additional time. It just seems difficult to coordinate their time with my pouch activity. Thanks so much I know I will get some good ideas from you folks. Janet