Well, the IV is coming out soon.
No… Dad has not resolved any swallowing issues, but IV’s; although one of the fastest ways to deliver fluids and medications through the body; are not intended to be used for long periods of time.
Since Dad continues to have considerable difficulties swallowing, especially liquids, we’ve scheduled a Percutaneous Endoscopic Gastrostomy (aka PEG).
Sounds bad, but it’s not!
For those that don’t know, Percutaneous Endoscopic Gastrostomy is the procedure for placing a tube; in Dad’s case a gastric feeding tube, or 'G-Tube'; into the stomach through the abdominal wall. The procedure is primarily used as a long-term means of providing nutrition & fluids for patients who, due to poor control over the swallowing muscles, cannot obtain enough orally, and to avoid the risk of aspiration pneumonia.
Dad can & will continue to eat & drink as much as he wants, but with the PEG tube in place, will no longer be limited by either his ability swallow or his appetite. The nurses at the SNiF will instead be able to supplement any lack in calories or hydration, as well as any necessary medications directly into the stomach through the PEG tube.
At this time the scheduled date is Tuesday, the 12th. Dad will have to be transported offsite for the procedure. Dad will be sedated, with the insertion itself taking about 20 minutes, the tube kept within the stomach by a balloon on its tip.
Once out of recovery, Dad will be transported back to the SNiF. For about a week, the abdominal wound must be covered with sterile dressings until it's healed. The procedure is supposed to be a low risk, in & out kind of deal.
Please pray for continued comfort & strength for Dad as he forges on!
John
