My husband had a Peg tube inserted 6 days ago, he is undergoing radiation and chemo, he had a laryngectomy last Dec. however the cancer progressed and now more treatment is necessary. He already speaks with a prosthetic TEP. Since he's had it put in he's been in pain with increased bloating and cannot use his prosthetic voice as that pushes more air down into the stomach. Has this been the problem with anyone else when they've had a Peg tube put in ?? if so how long until it becomes more comfortable? He is using Boost Plus, he can also drink and eat soup etc. but when/if the throat gets worse it's there for him.