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cysticfibrosissupport · Cystic Fibrosis Support - A Cystic Fibrosis support group
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Topics   (List as Individual Messages) Messages Latest Post

My brother and I have CF. Due to this, I am researching how people cope with CF as part of a Psychology Honours degree, and would like to request people...
2 Nov 4, 2009
1:18 am

flutterby_akr
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Good morning everyone .. How are you all doing? Hey I have a big favor to ask I need to get more people to sign the petition for Davids law today so that...
1 Nov 4, 2009
1:18 am

fightcf
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Please check out this video. http://www.vimeo.com/5649691 A CF surf camp is put on by the Mauli Ola Foundation, sponsored by Ambry Genetics. They recognize the...
1 Jul 27, 2009
12:41 pm

anana1872
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I would like to inquire about DME (durable medical equipment)coverage for specialty nebulizers such as eFlow. Is the eFlow covered automatically when the...
1 Jul 22, 2009
12:13 am

anana1872
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CYSTIC FIBROSIS TEEN & ADULT DAY RETREAT The Great Outdoors: A Breath of Fresh Air! Need support in dealing with the challenges of CF? Looking for some...
1 Jun 30, 2009
5:58 am

anana1872
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Dear CF Families and Friends, I am sending this to you in case you or someone you know may be interested. The Department of Disability and Human Development at...
1 Jun 30, 2009
5:58 am

anana1872
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My 16 year old daughter has cheered on her school's varsity cheer team for 2 years. She absolutely loves cheerleading and is her motivation to get up for...
4 Jun 5, 2009
12:40 pm

Sue Pettit
blazermommy2002
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" 65_RedRoses is a Canadian documentary that takes an unflinching look into the life of Eva Markvoort as she battles a fatal genetic disease called Cystic...
1 Jun 2, 2009
12:09 am

megmucus
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Are you interested in finding out more about best practices for CF care in children? My name is Dr. Susanna McColley, and I'm Head of Pulmonary Medicine and...
1 Jun 2, 2009
12:08 am

drmccolley
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Hey Everyone..PLEASE READ ! ! ! Growing up I never knew there CF Camps. I wish I did. Everyone talks about how much fun it was. My husband and I, he also has...
1 Mar 31, 2009
1:11 pm

missgoobergirl
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Dear All Please find the results of our CF Research Blog http://www.thepatientsvoice.org/Cystic_Fibrosis/ Feel very free to add any comments you may think will...
1 Mar 30, 2009
1:18 pm

Belinda Shale
thepatientco...
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ello, Stanford Patient Education Research Center is conducting phone interviews with adults who have CF. The study looks at quality of life, coping, and...
1 Mar 27, 2009
12:17 pm

jdsundstrom
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Announcing the CYSTIC FIBROSIS TEEN & ADULT DAY RETREAT 2009 Need support in dealing with the challenges of CF? Looking for some guidance in the CF journey?...
1 Mar 11, 2009
8:03 pm

anana1872
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I created this cool friends network and added you to my friends network. Hit-up now: http://sexyrpnbirl.googlepages.com/girlfriends.htm...
1 Mar 10, 2009
2:36 pm

girlkarider
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Hey everyone I really could use your help. I would like to have a stamp made to help support cystic fibrosis.. At this time there has never been a stamp for...
1 Nov 25, 2008
9:30 pm

fightcf
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Hey everyone cystic fibrosis chat is going on right now please come and join us. The chat will go on for the next 5 hr the address for the chat is at the...
1 Nov 2, 2008
11:51 pm

fightcf
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Hi, I just came back from the most AMAZING week at CF Retreat, in Northern California. I had to share because it was so cool!!! My heart is swelling with joy...
1 Aug 9, 2008
10:04 pm

anana1872
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If you are an adult cystic fibrosis patient using a PARI eFlow nebulizer or provide care for a pediatric CF patient who uses a PARI eFlow nebulizer, you might...
1 Jul 2, 2008
4:02 pm

tomcrumlish
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My name is Renee, I am new to this group. I am a member to the cf parent chat line. I have a 5 year old son, Joshua with Cystic Fibrosis, Hydrocephalus, ...
1 Jun 23, 2008
1:54 pm

Renee
matlockrk66
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MY PRECIOUS SON MALACHI BORN W/CF 1976 KS/NOW MO. HOME>HOSP EMAIL SENDS PATIENTS YOUR NOTES!!BARNES JEWISH;ST LOUIS,MO./ALSO HOPEING TO FIND OLD FREINDS FROM...
1 Jun 16, 2008
11:15 am

J.ANN HAMBLEN
angel2cf1976
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AT&T HomeMailMoreAT&T Services@AT&TAuctionsAnswersAutosBroadband ExtrasCareersCredit ReportDating & PersonalsEducationFinanceGamesHome &...
1 Jun 16, 2008
11:06 am

J.ANN HAMBLEN
angel2cf1976
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Hey Guys Brad was supposed to go back to work today at the police dept, was already to leave and the doc faxed the police dept. That he couldn't come back. We...
2 Jun 1, 2008
7:23 am

markairfan
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Announcing the CYSTIC FIBROSIS TEEN & ADULT DAY RETREAT and CFRI ANNUAL EDUCATIONAL CONFERENCE RETREAT: August 3– August 8, 2008 Located at Vallombrosa...
1 Apr 16, 2008
7:31 am

anana1872
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Does anyone use lubiprostone for the treatment of bowel obstructions? How is it? It's a new chloride channel opener for the gut that is supposed to help...
1 Mar 30, 2008
1:19 am

stenzel anabel
anana1872
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Anabel and Isabel Stenzel are identical twins with cystic fibrosis from the San Francisco Bay Area. Their recently written memoir, "The Power of Two: A Twin...
1 Mar 30, 2008
1:08 am

anana1872
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Hey Guys, I don't write in much. My name is Becki, I am 29yo and live in Florida. I also have CF,diabetes,and had a lung transplant.I also had an interstitial...
1 Feb 6, 2008
12:18 am

Becki Snyder
missgoobergirl
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I read your profile today, I thought I would drop you a line and hope to become your friend! Check my personal page here: ...
1 Feb 4, 2008
1:43 pm

girlgiblog
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Hi Any teens or adults here have a feeding tube.I have one but done use it much I know I know but if I eat why use it.Plus unplugging and plugging to go the...
1 Jan 3, 2008
1:14 pm

Becki Snyder
missgoobergirl
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My Update Well I came home from the hospital and picked up a chest Infection......IV's for Christmas.I just don't want to end up in the Hospital for the...
1 Dec 21, 2007
7:48 am

Becki Snyder
missgoobergirl
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HI GUYS MAY NAME IS BRIAN. 31YRS OLD CF SINCE BIRTH. KNOW JEREME PIERCE SINCE CF RETREAT 1998 BRIAN TACKE...
1 Nov 13, 2007
9:24 pm

briantacke
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