CFI is a new foundation started by the Chicago CF Care specialist. This foundation is located in Hoffman Estates, Illinois. They will be having their first...
HI EVERYONE THIS IS DAVID WITH THE CYSITIC FIBROSIS PEN PAL CLUB AND SUPPORT GROUP I WANTED TO LET YOU KNWO THAT THERE IS GOING TO BE 2 WEEKENDS THAT WE ARE...
Hey I was wondering if any of you guys knew of some ways to stop coughing up blood. I due the IPV and still coughing up blood...my fev1 is 51% and it seems...
In loving memory of Jaycie Milner who passed away Feb 7th, 2004 from Cystic Fibrosis. She was seven years old and the apple of her mothers eye. She is so sadly...
Hey Doug, Coughing up blood can indicate infection and inflammation. If you are coughing a lot, and expelling blood, perhaps you are allergic to a mediciation...
This message is about Human beings, Democracy, UNHCR, Refugees, The Iraqis, Islam, Kurds, Human rights, Respect, Money, Donations, Angelina Jolie, Pavarotti,...
hyperi8@...
Feb 5, 2006 4:25 pm
1136
My heart goes out to you....the loss of a child is one of the hardest things a parent will ever have to go through. I would like to invite you to...
Hi, Doug. First of all, call you doctor. If you're doing more than streaking, your doctor needs to know. My husband used to bleed quite a bit. It occured...
who here spent last weekend alone? *raises hand*. pretty sad huh, anyway, who here has plans this weekend *raises hand* :) :). Who here, wants to know how...
thomasina-kirby883@...
Feb 16, 2006 3:39 pm
1139
Hi, everyone! Please do not click on the link posted here or any other type of messages like this, it lets the sender know that this is a good site to keep...
Thank you for that information, you learn a new thing everyday!! ... -- "It is never too late to be what you might have been" [Non-text portions of this...
hey ppls just wanted to give u a helping hand if ur bored this week and just feel like messing around and having a bit of fun online. this place here...
barbi-elizabeth783@...
Feb 21, 2006 1:01 pm
1142
who here spent last weekend alone? *raises hand*. pretty sad huh, anyway, who here has plans this weekend *raises hand* :) :). Who here, wants to know how...
barbi-elizabeth783@...
Feb 21, 2006 2:17 pm
1143
... My name is Debbie, and I just wanted to let you know that, your not alone in this. My husband and I found out that we were CF carriers 4 months into my...
I was wondering if there was anyone who is working full time to get there health insurance and is able to get bcmh? I want to make sure I dont make to much to...
This might be a stupid question, but what is BCMH ... __________________________________________________ Do You Yahoo!? Tired of spam? Yahoo! Mail has the...
Is it some type of Blue Cross? Love & Hugs Cloyce mom of Tara 23 w/cf, tx'd 5-27-99, diabetes author of:Inner Strength, One Family's Experience with Cystic...
Good morning everyone! First of all let me apologize to any of you whom belong to several lists on the cf subject and will have to see this messege a few...
Thank you for informing us about the book. :) ~ Rach. -- "It is never too late to be what you might have been" ... [Non-text portions of this message have been...
Thank- YOU! I got an email tonight that said the first printing of the book sold out, so they are into the second round. That's very exciting for us, and It...
Hey everyone!!! Gosh I have missed you guys!!!!! I am so sorry to have "disappeared" for a while but please know I have been thinking of you guys. It got...
hi this is david and i wanted to let you all know that im starting a talk group on the nextel network starting on april 4 06 if you would like to be included i...
Hi Sue, It's so good to see you and Valerie are back with us!!! Oh I do hope that your back pain has been cured. You sure have been missed! :-) Do you know...
Congratulations Carrie!!!! Such wonderful news! Wishing you the very best with your book! Love & Hugs Cloyce mom of Tara 23 w/cf, tx'd 5-27-99, diabetes author...
Hi there, Welcome! I don't have cf, my daughter does but I did want to say welcome :-) Isn't it something after all these years to finally have a name to what...
Cloyce You are so sweet. Thanks so much for the kind words and hugs. My son most likely will have mild sx's (genetic testing is so amazing) which we are going...
Allison, I have no clue to this day what our cf mutations are! I have known about cf for 30 yrs....my first son had cf as well. Then along comes Tara and she...
Cloyce, These days it really is not all that expensive to learn what mutations are present in CF. Well, that is sort of true anyhow. There is one commercial...
Having problems with message search?
Fill out this form to ensure your group is one of the first to be migrated to the new message search system.
