Guest guest Posted November 3, 2003 Report Share Posted November 3, 2003 that is one of the tapes that I have a few of. It is very good It is titled : AUTOGENETIC DRAINAGE. (Known simply as AD...) I have several others as well titled;- PEP/FLUTTER techniques for those who use the flutter. It is of no use to anyone who isn't using FLUTTER tho. Another tape is one for adults only, titled: A CF LIFE-COLLEGE & CAREER CHOICES FOR CF ADULTS TAPE titled: :PROPER NUTRITION FOR ADULT CF PATIENTS I have only a few tapes of: LIVE STRONGER LONGER. ( PLEASE , IF YOU HAVE ALREADY RECEIVED ONE OF THESE IN THE PAST, LET OTHERS GET ONE. They are in great demand & I only got a few sent to me. Many went at the ED day, as you can imagine:) I also have the booklet : CF & ME This Is PAUL CYSTIC FIBROSIS RELATED DIABETES Another tape: LOVE, HOPE & HUGS O.K. -remember . Must have addy. I can not remind you . Sorry to be such a B--c-:) LOVE & HUGS, GRANDMOMBEV [CYSTIC-L] diaphram breathing About 15 years ago I attended the National CF Conference - back when they weren't mental about cf'ers going to the conference. There was a dr there from Swedin, who was teaching Autogenic Drainage. The first step to doing AD correctly was to learn good diaphram breathing. I had a hard time learning that, so he got a belt and put it around my chest. He'd have me take a breath in, and then he'd tighten the belt. Eventually the belt got so tight that my chest couldn't expand, but I was forced to breathe using my diaphram. Ever since then my health has improved and I think it's because I've learned a more efficiant way to breathe - it also helps me cough up deep down junk. Just wondering - what's up with the Foundation not allowing patients to attend the National Conference's now? I guess I'm just paranoid, but it makes me think they are keeping things from us. Cheers, Jeff 32 yr old mwcf *-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-* WARNING: Consult a trusted doctor before ANY change to your treatment. @}->- @}->- @}->- Visit us at Http://Cystic-L.org and see our extensive Handbook on-line (contains much CF information, and references to other CF resources), the Photo Archives (people with CF, parents with CF, subscribers to Cystic-L, and a memorial page), the CF Shop, the world's largest cystic fibrosis bookstore (in the CF Shop), and much more! @}->- @}->- @}->- KNOWLEDGE IS POWER! *-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-**-.,,.-* Quote Link to comment Share on other sites More sharing options...
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