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cysticfibrosissupport · Cystic Fibrosis Support - A Cystic Fibrosis support group
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Messages 454 - 483 of 1698   Oldest  |  < Older  |  Newer >  |  Newest
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454
Hi, we are looking all over for alternative ways to get enzymens in. We were recently diagnosed with CF, well our 19 month old was. The apple Sauce method is a...
trentcat2000
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Jul 3, 2003
9:11 pm
455
Hello trentcat2000: I am a 34yr. old woman with C.F. My mom used to give me cranberry sauce as well as apple sauce to mix it up so I wouldn't get sick of just...
tikkie1
Offline
Jul 4, 2003
4:19 am
456
Hi to all. please help us ... Do you Yahoo!? SBC Yahoo! DSL - Now only $29.95 per month! [Non-text portions of this message have been removed]...
parivash yeganegi
pyeganegi
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Jul 5, 2003
6:35 am
457
Hi, we always used plain water or herbal tea to flush the enzymes down. Many children with CF don't like the texture of enzyme beads in apple sauce and any...
Torsten Krafft
torstenkrafft
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Jul 5, 2003
10:06 am
458
Thank You Tiki, we will try it. Right now we are using fat free mash potatoes and having no problem getting them in, but we are worried she will chew them, but...
theemeraldwar@...
trentcat2000
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Jul 5, 2003
4:21 pm
459
Thanks for getting back to me. I will join that other group. Right now we are using fat free potatoes to get them in and they are working. But we will try your...
theemeraldwar@...
trentcat2000
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Jul 5, 2003
4:23 pm
460
can anyone provide me information on bringing a laptop into the hospital. I have CF and I am again.. going to be admitted in a week and I was wondering if I...
D
velveteen000
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Jul 5, 2003
11:58 pm
461
If you have a local number to dial into your server you will be able to connect. However, you may have to re-enter the dial up number in your computer with the...
tooshort41099
Offline
Jul 9, 2003
3:07 am
462
Cool. Yes it does. Thanks for your help! Do you use one when you go in the hospital? I just use the phone jack for my phone? Thats really neat. ... Do you...
Dawn Brotz
velveteen000
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Jul 9, 2003
10:47 am
463
I am new with your group and with Cystic Fibrosis. My grandson who is 7 has this disease. What can a grandparent do to find out what can be done for my...
irishdancer_57
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Jul 24, 2003
9:43 pm
464
My name is Angie K, my god sister has Cystic Fibrosis. While doing research, my mother found an article about Valerie Hudson. She has three sons that were...
djbookingsonline
djbookingson...
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Jul 26, 2003
5:56 pm
465
I haven't heard anything about that treatment, but she doesn't sound very healthy. If she is coughing up blood, she is scarring her lungs which leads to...
Peter Taylor
cephast
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Jul 27, 2003
5:10 am
466
Hello! I'm usually silent but I wanted to mention that my husband just bought me a laptop to use when I go into the hospital. I haven't been in since...
Jessica
nashville911...
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Aug 1, 2003
6:33 pm
467
Does your Grandson have a CF doctor that is a specialist, or just a primary care doc? Usually CF specialist docs are more than happy to let you borrow...
Jessica
nashville911...
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Aug 1, 2003
6:40 pm
468
cool... I am in the hospital right now with my new laptop! lol Also can watch DVD;s I got it all hooked up . Just have to dial a local number to your...
Dawn Brotz
velveteen000
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Aug 1, 2003
8:27 pm
469
Dear Jessica, I am interested in your e-mail address. Are you a 911 dispatcher? If so, can you tell me what type of training was necessary to obtain this...
Mary Holt
maryholt73
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Aug 1, 2003
9:19 pm
470
I hope you get out of the hospital soon!! It sucks, but I'm sure being able to chat outside of those walls makes it a lot easier. Best wishes to you! ...
Jessica
nashville911...
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Aug 2, 2003
1:49 am
471
hiya, my friends and i are setting up a website similiar to www.hugsandhope.com but in the UK. The basic idea is it will feature 5 pals a month (aged between 2...
vikki
vikki_louise...
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Aug 7, 2003
1:48 am
472
Dear Viki, This is a lovely idea. How did you start this group? Congratulations on your group's hard work. I know that you will help many wonderful children....
Mary Holt
maryholt73
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Aug 7, 2003
10:15 pm
473
Hi, I am replying because my fiancee and i were kinda thrown into the same deal. I am curious to know what your symptoms are. Normally if one has the 5T...
runthefox65
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Aug 9, 2003
2:14 am
474
Hi, I am replying because my fiancee and i were kinda thrown into the same deal. I am curious to know what your symptoms are. Normally if one has the 5T...
runthefox65
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Aug 9, 2003
2:14 am
475
Here are thoughts on the 5T allele, The 5T allele has had a lot of press recently (and rightly so) and it’s important to know what all the fuss is about....
Terry Geiger
tegeiger
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Aug 11, 2003
1:41 pm
476
It should be known this information was provided from a researcher in the field of cystic fibrosis. ... __________________________________ Do you Yahoo!? ...
Terry Geiger
tegeiger
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Aug 11, 2003
2:53 pm
477
Thanks for the info but I am already headed down that path. I was just asking to see if there were any chronic pancreatitis symptoms by chance. You see I am...
runthefox65
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Aug 11, 2003
3:21 pm
478
Luckily we had good news. Hubby tested Negative for any mutations!! We have changed Dr's!! Anyway, as far as me having any symptoms or problems...I'm...
Nicole Poole
txvettech
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Aug 11, 2003
3:31 pm
479
Hi Everyone, (From a note sent to another list …just an update – sorry it’s long. Hope this list becomes even more active. This is a great list, have had...
Mary Holt
maryholt73
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Aug 16, 2003
2:15 am
480
Hi Everyone, This is beautiful. I hope everyone enjoys the lovely pictures and encouraging words. It all helps in dealing with chronic illness. ...
Mary Holt
maryholt73
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Aug 16, 2003
3:11 am
481
Well after everything I read and all the research I have done for the last six months, I have decided to try the oral gsh from theranaturals. I will keep...
runthefox65
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Aug 16, 2003
9:59 pm
482
I am looking forward to what you say. Good Luck with everything. Len Paige diagnosed at 19 months, Irish, a fighter, this disease has never seen anything like...
theemeraldwar@...
trentcat2000
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Aug 16, 2003
10:02 pm
483
Thanks and if anyone is interested in reading up on this, if you go to yahoo groups home and type in cystic fibrosis, a group called wlgroup2 is where I found...
runthefox65
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Aug 17, 2003
12:36 am
Messages 454 - 483 of 1698   Oldest  |  < Older  |  Newer >  |  Newest
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