I have one tip: several years ago I read a series of articles about a
gadget that CF patients use to breathe in ordinary air. The device in
some manner caused the air to enter the lungs in a pattern or manner
that breaks up mucous.
I do not recall all the details, but a Google search might turn up this
information. The device was not expensive, simple to use, and
according to the claims, very effective. It saved parents from having
to pound on their childrens' backs to break up the mucous, and was much
more effective.
Hope this helps.
JBB
On Thursday, Oct 19, 2006, at 19:36 Asia/Tokyo, M. G. Devour wrote:
Mining my archive for some tips for you...
Mike D.
------- Forwarded message follows -------
Date forwarded: Fri, 9 Oct 1998 13:22:24 -0700
Date sent: Fri, 09 Oct 1998 13:23:20 -0700
From: Ni Orsi <[email protected]>
Send reply to: [email protected]
To: "[email protected]" <[email protected]>,
[email protected],
[email protected]
Forwarded by: [email protected]
Subject: CS>CF
Dameon, I have a grandchild with CF. He is now 3. At a very early age
fluid slowly started building in his lungs. We did and are still done
enzyme therapy. As of now he no longer has any fluid build-up. The
doctors have no answer other than he now has a mild case of CF.
Our explanation is a little different. When he was only 1-1/2 we
started feeding him a product called Ambrotose™, and a lot of it.
Within 3 months we notice that the fluid build-up had significantly
reduced. Today he no longer has any build-up. About 4 months we started
him on Immunocal for GSH production and weight gain. He is a twin and
is now equal to his twin sister is all respects. Recently we started
him on a "Chi" machine to increase the oxygen in his blood. The first
thing we have noticed is better sleep and more calm.
Best of Health, Ni.
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[Mike Devour, Citizen, Patriot, Libertarian]
[[email protected] ]
[Speaking only for myself... ]
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