PEG in action

BobbyB · 10-18-2006, 10:55 AM

PEG in action at http://brainhell.blogspot.com/

A video of me using my feeding tube. Just remember that the camera adds 10 pounds:

brainhell
Location:United States
I am a husband and father of two young children. On January 13, 2004, at 41 years old, I was diagnosed with a 100-percent fatal, presently incurable disorder called ALS. If you know me in real life, and I didn't personally invite you to read this blog, please send me an email about reading this blog.

View my complete profile
http://brainhell.blogspot.com/

DaveWv · 10-18-2006, 11:02 AM

I know brainhell won't see this but life itself is 100% fatal.

Jeannie · 10-19-2006, 07:10 AM

Brain hell did reply to your comment on PLM "good for you" or something along those lines, Davey.

BobbyB · 10-26-2006, 04:36 PM

Feed your Body
Although it is initially difficult for many patients to realize, feeding tubes are not a stage of disease, they are a convenience item. Why take two hours to get a meal in when you can get your calories and energy in within 20 minutes? Then you can do what you want to do and get on with your life – go to the store, work, etc. Having a feeding tube doesn’t prevent you from still appreciating the tastes you enjoy. Feeding Tubes (PEG) will enabling you to keep weight on and frees up time spent on trying to eat. PEG tubes actually enhance your life rather than limit it. If only I had a dollar for every time I heard a patient say, "It wasn't that bad to get a tube - wish I had done it soon".

Keep Good Records As you may well know, ALS is a complicated disease that takes a lot of time and energy to keep track of. Developing a filing and recording system that is easy and works for you is a good way to make your daily life simpler and reduce your stress level when it comes to remembering what happened when. At first, it may be easier for a caregiver or patient to start this journal of information. Later someone else can take over if necessary. This is the place to record when you order drugs. When you talk to your insurance company, record who you talk to and what they agree to do for you. Record data when you interact with your different doctors. At your doctor’s visits, record measurements and conversations. Having all this information in one place will empower you to follow up effectively and to focus your mental energy in other areas.

Sleep Well
Be sure to get a good night’s sleep. This helps you have the energy to do what you want to do. With ALS, if you have low energy, you have to prioritize what you can do in a day. Sleeping well at night prevents you from missing out on things you want to do. A few routines can help you sleep better. Drinking a sleepytime tea with your medications about an hour before going to bed is one of them. Also, having someone help you do stretches in bed before going to sleep can help you relax. If you wake up regularly in the middle of the night, soothing music to relax your mind or stretching out your arms and legs helps. If you are sleeping with your spouse and have to wake them up during the night to turn you, it’s helpful to have satin sheets and wear satin or nylon clothing so that
you can roll over more easily.

Mary Beth Parks, R.N.
mbparks@als.net
Patient Resource Specialist
617-441-7250
FOR MORE INFORMATION contact me directly.

http://www.als.net/forum/topic.asp?TOPIC_ID=540

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