All Boards >> The Living Room

Posts     Flat       Threaded

Pages: 1
just a question...cause i am a curious creature
      #229077 - 12/03/05 05:35 PM
tistenleigh

Reged: 10/16/05
Posts: 43
Loc: Edmonton, Alberta .Canada

I was just wondering why someone with Cystic Fibrosis would eat so much food? i volunteer at a hospital and just noticed the gigantic meals they get and i feel silly asking the patients and i was hoping someone on here might know

Print     Remind Me     Notify Moderator    

wow new
      #229084 - 12/03/05 06:25 PM
_Willow

Reged: 04/06/05
Posts: 2090
Loc: Canada.

amazing how they feel that crappy and CAN eat that much food! I am surprised, because when my asthma's severe, I hardly want to touch a morsel. Sadly, my asthma has been great for years, LOL!

--------------------
Keep on keepin' on...

Print     Remind Me     Notify Moderator    

I used to know this! new
      #229094 - 12/03/05 07:35 PM
Augie

Reged: 10/27/04
Posts: 5807
Loc: Illinois

I was on a hospital unit with CF kids and they ate trays (plural) of food for their meals. I just can't remember why the dietician told me they had to do this. I assume they metabolize it very quickly, but I can't remember the medical reason.

I think a google search would give us the answer. BTW, CF kids are awesome! So full of faith and gratitude despite their condition, and inevitable death. I was pretty good friends with a couple of them who died so young. Didn't even make it to their twenties.

--------------------
~ Beth
Constipation, pain prodominent,cramps, spasms and bloat!

Print     Remind Me     Notify Moderator    

Re: just a question...cause i am a curious creature new
      #229282 - 12/05/05 12:07 AM
thepurplelollie

Reged: 11/11/04
Posts: 374
Loc: Wellington, New Zealand

Here we go: they need extra energy, and they don't absorb nutrients as well as other people.

http://kidshealth.org/parent/medical/digestive/cf_nutrition.html

--------------------
*Emma*

Print     Remind Me     Notify Moderator    

my niece new
      #229314 - 12/05/05 07:54 AM
Portageegal

Reged: 06/28/05
Posts: 940
Loc: Massachusetts

My niece Lauren is 25 and has CF. It effects the mucus in your body and makes it very sticky and glue-like. It really does a number on the lungs. The sticky mucus clogs normal absorbtion of things and blocks certain things from getting into the system, like insulin from the pancreas, thus she is diabetic. She has to take digestive hormones with every meal because hers cannot get into her digestive tract. Stuff tends to "go right through" people with CF. Putting on weight is hard but very important. Unfortunatly she has come down with GERD and has a hard time eating now. She was down to 80 pounds a few weeks ago. It SUCKS !!!! She is a great kid, too.


--------------------
Carol

nós somos o que nós somos e o descanso é merda

Print     Remind Me     Notify Moderator    

re: Carol my heart goes out to your niece and you.. thank you for answering my question..=) new
      #229524 - 12/05/05 08:49 PM
tistenleigh

Reged: 10/16/05
Posts: 43
Loc: Edmonton, Alberta .Canada



Print     Remind Me     Notify Moderator    

Pages: 1

Extra information
0 registered and 1970 anonymous users are browsing this forum.

Moderator:  Heather 

Print Thread

Permissions
      You cannot post until you login
      You cannot reply until you login
      HTML is enabled
      UBBCode is enabled

Thread views: 869

Jump to

| Privacy statement Help for IBS Home

*
UBB.threads™ 6.2


HelpForIBS.com BBB Business Review