As most of you know, last
November was a crazy month with surgeries and hospital visits with Carson and Kaylee. And now it is Nick's turn to get surgery. Let me tell you the story...
When Nick was a little boy, about 10 or so, he swallowed 2 nickels...and got stuck in is throat...he was still able to breath, but got stuck in his
esophagus. His parents took him to the ER and they removed them. Since then, they always assumed he just had a small
esophagus. When he was 17, he was on a date, and got turkey stuck in his throat AGAIN! SO again, a trip to the ER, and it was removed. A month after we were married, he got POT roast stuck in his throat and we went to the ER to get it out. He is always getting things stuck in is throat..(technically
esophagus, but throat is easier to spell). But he can usually get it out after 10 or 20 minutes of physical pain and a puking technique he has figured out...I won't elaborate on that part too much. So, after this happened twice last November 2008, I finally made him an
appt to go and see a GI Specialist the first part of December. They did an endoscopy on him to look at his throat, esophagus, and stomach. They noticed a huge growth/lump in the lower 3rd of his esophagus, and recommended a CT scan to determine what it was. So more $$ and a week later, a CT scan was done at
Lakeview, and it didn't really determine anything, other than it WASN'T a vascular issue. They thought maybe it was a blood
vessel or something that was pushing in on the esophagus and creating the lump. So, they suggested an
EUS,
Esophagus Ultra Sound. So on January 2, we headed up to
Huntsmans Cancer Hospital for an
EUS. We were there all day waiting, since the Dr. had 3 emergency's that came up before he could see Nick. So our 11:00
appt, ended up getting done at 5 PM that night, and only lasted 20 Minutes. Poor Nick, he was in a hospital gown, hooked up to an IV for almost 5 1/2 hours waiting! The results from the
EUS showed that it was an
Esophageal Duplication Cyst. It is like a water balloon, outside of his esophagus, pushing in on his esophagus, creating a road bump or pinched water hose, making it difficult for him to eat food sometimes. They don't think it is likely cancerous or anything, which is a relief, but it still needs to come out. So today we met with T
horasic Surgeon, Dr. Glasgow, the Chief Surgeon at the U of U hospital. He is amazing, and we feel so lucky to have been referred to such a great doctor. Most surgeons who need to remove a duplication cyst, will open the chest and remove it, making it a 6-8 week recovery. But Dr. Glasgow will actually do it making small incisions on the side of his chest, deflate his lung, and then remove the cyst. Very high tech if you ask me!! There are always risks involved with surgery, but we are confident that Dr. Glasgow will be able to remove it with little problem. Nick will be in the hospital for a few days to recover, and then will take it easy at home for at least a week or so. I think we were both relived today to find out they wouldn't have to split his chest and that we can get this taken care of finally. This will make Nick's life so much better and easier, without having to worry about food getting stuck in his throat! I would have posted something about this earlier, but since we weren't 100% sure what it was and how we needed to deal with it, I didn't know what to explain. So there it is....our medical issues continue!! Again, thank goodness for insurance!!
If you are wondering what the cyst looks like...here is a picture from the first endoscopy. You can see that the cyst is pushing into his esophagus quite a bit. It should look like an empty tunnel...or garden hose...crazy, huh!?!?!