Welcome to my blog. I have had ALS for 10 years now.


Since I started this blog in June 2008 I've had amazing feedback. Family, friends, people from all over North America, Australia, Scotland, England, and places I can't recall, have commented, encouraged and corresponded. I had no idea when Cynthia taught me how to set this up, how much I would love posting and how many people would read it. I want to say THANK YOU to everyone who has helped propel this therapeutic exercise into a daily routine. All of you, both friends and visitors, are now part of my blog family. Welcome.

From Go Pro

From Go Pro
View from my living room

Wednesday, December 17, 2008

What's a PEG?


PEG=Percutaneous Endoscopic Gastrostomy--a procedure for placing a tube into the stomach. It's used when swallowing is a problem and the patient needs nutrition. This is something I will get eventually if a bus doesn't get me first. I've often been asked to explain it so I thought a picture was best. It is a tiny button that you hook a tube to and pour down the beer--oops I mean liquid formula or pureed food or water or Starbucks latte. A direct buzz.
Just be thankful that I used a child's picture and not my own!

1 comment:

Alice said...

You are so funny, Karyn. I know this whole ALS matter isn't funny. I don't know that I would handle it with as much ease as you seem to. God bless ya!