Guest guest Posted August 9, 2003 Report Share Posted August 9, 2003 , Is this supposed to help with what part of cf. Aerosol or oral? I hope they do more study with it and perhaps it will benefit our kids well if it is not already with those who are trying. Thanks for the info. I will have to look into it more. I am so retarded sometimes those scientific research papers make no sense to me at all. I know one thing I find myself actually using parts of my brain that I didn't even know that I had trying to figure out all of this stuff for my family. Just kidding !!!!!!! kind of!!!!!! Ashauna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 10, 2003 Report Share Posted August 10, 2003 Ashauna, Believe me you are not retarded, I have to read this papers 6 and 7 times and still nothing :-)!! mom of a 10 wcf, Venanzio 7 nocf, Pepe 3 nocf > , > Is this supposed to help with what part of cf. Aerosol or oral? I > hope they do more study with it and perhaps it will benefit our kids > well if it is not already with those who are trying. > > Thanks for the info. I will have to look into it more. I am so > retarded sometimes those scientific research papers make no sense to me > at all. > > I know one thing I find myself actually using parts of my brain that I > didn't even know that I had trying to figure out all of this stuff for > my family. Just kidding !!!!!!! kind of!!!!!! > Ashauna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 10, 2003 Report Share Posted August 10, 2003 , If only they made a book ( medical papers for dummies ) I would do well with them then. I do not know if you have ever read a book Cystic Fibrosis ( A guide for patient and family second edition ) Written by M. Orenstein. I read the entire thing and you know I understood all of it. I think somewhere in there he even says it will give you " clear explanations " It really did I was surprised. If you have not read it really has a ton of info in it. your friend, Ashauna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 10, 2003 Report Share Posted August 10, 2003 Ashauna, I did, actually, when a was diagnosed, May 2002, our doctor recommended Dr. Orenstein's book. We found it to be very informative, and easy to comprehend. You are right, the dummy series, needs to get the medical one out, I would be one that would buy it, :-). Actually, I am very lucky, in my circle of very close girlfriends 5 are doctors, one my children's ped, so whenever I read one of those medical papers and I land in Jupiter, one of them usually helps me make my way to earth, lol! Love to you and your little angels, mom of a 10 wcf, Venanzio 7 nocf, Pepe 3 nocf > , > If only they made a book ( medical papers for dummies ) I would > do well with them then. I do not know if you have ever read a book > > Cystic Fibrosis ( A guide for patient and family second edition ) > Written by M. Orenstein. I read the entire thing and you know I > understood all of it. I think somewhere in there he even says it will > give you " clear explanations " It really did I was surprised. If you > have not read it really has a ton of info in it. > > your friend, > Ashauna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 10, 2003 Report Share Posted August 10, 2003 , How lucky you are. The only doc that I have that seems some what interested in personal relationships is my sons pediatrition. He has a huge crush and always makes little remarks about if I ever need anything just call him ( not his office HIM. ) It just makes me laugh though because he knows that I am happily married. I can't complain about it though because he is the only one who is willing to help me with my son. We are military and have had so many issues with doctors. Actually he is not a ped doc. I miss spoke. He is my doctor. When he found out about all of the crap that the pediatric clinc was putting me through he was completely discusted and offered his service to my son. At one point I thought that I was at a breaking point but with his help and advice I made it through those times for now anyways. I am sure that I will get there again. Although I hope not for my families sake. BOY WAS I A MESS!!!!!!! Anyways, i think more that anything we just have a great relationship going. He just thinks I'm cute. Oh well. who doesn't like the compliment. I am so limited with my choices on base as far as who I can see this doctor does not know anything about cf, but has taken it upon himself to have regular conferences with my clinic doc. How dedicated is that. I take the good with the bad. Ashauna I hope your little Louisa is great. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 11, 2003 Report Share Posted August 11, 2003 You did really well. I had to read the first few chapters several times. Gale > , > If only they made a book ( medical papers for dummies ) I would > do well with them then. I do not know if you have ever read a book > > Cystic Fibrosis ( A guide for patient and family second edition ) > Written by M. Orenstein. I read the entire thing and you know I > understood all of it. I think somewhere in there he even says it will > give you " clear explanations " It really did I was surprised. If you > have not read it really has a ton of info in it. > > your friend, > Ashauna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 11, 2003 Report Share Posted August 11, 2003 Gale, I find myself having to read it over again at times. A topic will come up that Colgan is going through so I will pick it up and read all that I can about it. I hope you had a great day. Ashauna Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.