|
More site info...
|
|
Forum profile page for Families on http://www.cysticfibrosis.com.
This report page is the aggregated overview from a single forum: Families , located on the Message Board at http://www.cysticfibrosis.com.
This forum profile page summarizes the general forum statistics such as: Users Activity, Forum Activity, and Top Authors, which are reported in either a table or graph below for a given reporting time period.
Additional forum profile information for "Families " on the Message Board at http://www.cysticfibrosis.com is also shown in the following ways:
1) Latest Active Threads
2) Hot Threads for Last Week
Warning: These statistics are generated using 'best efforts' and can experience delays and reporting errors at times. Please note that such statistics do not constitute a forum's popularity and/or exact posting volumes at any given reporting period.
|
|
|
|
|
Posting activity on Families :
|
|
Week
|
Month
|
3 Months
|
|
Threads:
|
7
|
155
|
588
|
|
Post:
|
12
|
406
|
1,746
|
|
|
Families Posting activity graph:
|
Top authors during last week:
user's latest post:
Crazy doctor
Published (2009-01-09 03:10:00)
OMG Katie, I can't believe it was Cooks. I find it strange that you can't see the other docs. They are a clinic but don't work like every other CF clinic we've gone to, as a collective practice. You only see one doctor, exclusively, unless it's urgent or you are admitted and your doctor is "off" or on vacation. That is one thing I found strange about the clinic. I don't even remember the names of the...
user's latest post:
Crazy doctor
Published (2009-01-08 18:10:00)
Liza, unfortunately it is Cook's that has kicked us out. There were other doctors that I have met during our span of 4 yrs going there that seemed really great but thanks to Dr. X I can not even see them. Thanks anyways. Sara, yes I would like more info on your doctor. It is Medical city that I mentioned that is supposed to be awesome. They don't take Chips insurance though. I am trying to figure how to get something else. All this...
user's latest post:
CRIB RECALL
Published (2009-01-09 09:44:00)
can someone else post this on cysticfibrosis.com? for some reason it won't let me get on the website. i want everyone to be aware of this recall. FOR IMMEDIATE RELEASE January 6, 2009 Release #09-084 Firm's Recall Hotline: (800) 646-4106 CPSC Recall Hotline: (800) 638-2772 CPSC Media Contact: (301) 504-7908 Jardine Expands Recall of Cribs Sold by Babies"R"Us; Cribs Pose Entrapment and Strangulation Hazards WASHINGTON, D.C....
user's latest post:
HI everyone!! I am new here
Published (2009-01-09 09:15:00)
Hi there, my name is Jen - I live in St. Pete, FL. I just joined this forum last night, after recieving the results that my hubby is definitely a CF carrier, as am I. I found this out when I was preggo w/ my daughter, who does not have CF. We want to have one more child, but don't think we should just get pregnant knowing (tested 2x each)we both have the gene. Can you help me find more info about the IVF procedures and if there is any...
user's latest post:
Crazy doctor
Published (2009-01-08 21:43:00)
I pm'd you ------------------------- Sarah, mom to beautiful Ellie w/ CF (born 11/20/2007)DDF508
user's latest post:
Crazy doctor
Published (2009-01-08 23:13:00)
I was wondering the same thing as Sakem, why can't you see another doctor at the same clinic? And that other doc seems like a pretty suspicious character to me anyhow; paranoia is NOT a desirable characteristic in a doctor, trust, I work for one like that. ------------------------- Valerie, mother to Trystan, 11, w/o CF, and Noah, 8, w/ CF, Autism, ADHD, and GH deficiency, unknown mutations, pancreatic insufficient
user's latest post:
Crazy doctor
Published (2009-01-08 21:25:00)
WOW! I've heard of doctors firing patients for non payment or non compliance, but to refuse to treat a child is questionable. I don't understand why u can't see the other doctors at the hospital. Have u spoke to anyone in the hospital administration? What r u suppose to do? It's not like there is a CF doc on every corner in the city? I wonder if the CF Foundation would have any suggestions? If there is not more to this...
user's latest post:
Do you do anything special with...
Published (2009-01-08 21:12:00)
If I take the whole day off we go to lunch and sometimes a movie. We usually giver her a video or new crayons and coloring book as well. Going every two months now makes this hard because I can't always take a whole day off sometimes it is just a half day so we rush to get her dropped off and me back to work. ------------------------- Lynsey mom to Avery 5yrs. old w/CF and Rhett 3yrs. old CF Carrier
user's latest post:
Do you do anything special with...
Published (2009-01-09 06:46:00)
We always go somewhere fun afterwards even if it's just to lunch. We used to go to the zoo or a park when they were younger. I think it helps them to have something fun to look forward to afterwards. It can be really hard being in clinic for 2-3 hours seeing all those specialists. (Especially for mom!) I also used to bring a new coloring book or a new small toy (so they wouldn't be tempted to touch the yucky ones there at the...
user's latest post:
Do you do anything special with...
Published (2009-01-09 06:53:00)
I responded in the adults thread but here it is again here: Garran has Pulmonary Rehab three times a week and for a treat for doing well at rehab (cause sometimes he can be a pill for the PT, because sometimes he is just not in the mood to exercise) we go to Starbucks afterwords. He always gets a Short Mocha Latte with extra whipped creme and extra chocolate, and I get a Tall of the same On Tx clinic days we usually go to Target or Walgreens...
|
|
|
|
Latest active threads on Families ::
Started 1 day, 6 hours ago (2009-01-08 21:12:00)
by flatfordl
If I take the whole day off we go to lunch and sometimes a movie. We usually giver her a video or new crayons and coloring book as well. Going every two months now makes this hard because I can't always take a whole day off sometimes it is just a half day so we rush to get her dropped off and me back to work. ------------------------- Lynsey mom to Avery 5yrs. ...
Started 18 hours, 23 minutes ago (2009-01-09 09:44:00)
by JazzysMom
can someone else post this on cysticfibrosis.com? for some reason it won't let me get on the website. i want everyone to be aware of this recall. FOR IMMEDIATE RELEASE January 6, 2009 Release #09-084 Firm's Recall Hotline: (800) 646-4106 CPSC Recall Hotline: (800) 638-2772 CPSC Media Contact: (301) 504-7908 Jardine Expands Recall of Cribs Sold by Babies"R"Us; Cribs Pose Entrapment ...
Started 18 hours, 52 minutes ago (2009-01-09 09:15:00)
by jbmagik2
Hi there, my name is Jen - I live in St. Pete, FL. I just joined this forum last night, after recieving the results that my hubby is definitely a CF carrier, as am I. I found this out when I was preggo w/ my daughter, who does not have CF. We want to have one more child, but don't think we should just get pregnant knowing (tested 2x each)we both have the gene. Can you help me find more ...
Started 19 hours, 10 minutes ago (2009-01-09 08:57:00)
by TeamColinD
Hi there. I am soooo glad I found this website and you all!! These last two days mine & my husbands heads have been whirling from the confirmed diagnosis of our littlest guy, Colin, born last August. So far he has no symptoms (Thank God!) but during his newborn screening, F508 was identified. The results from the newborn screening were sent to the wrong pediatrician's office for over a month ...
Started 1 day, 9 hours ago (2009-01-08 18:10:00)
by kate620
Liza, unfortunately it is Cook's that has kicked us out. There were other doctors that I have met during our span of 4 yrs going there that seemed really great but thanks to Dr. X I can not even see them. Thanks anyways. Sara, yes I would like more info on your doctor. It is Medical city that I mentioned that is supposed to be awesome. They don't take Chips insurance though. I am ...
Started 1 week, 4 days ago (2008-12-29 15:41:00)
by SARAHSARAH253
Hi there, Well, we survived Christmas. It was a tough holiday, since we decided it was not best to visit my side of the family. Due to my sisters 3 kids being sick with what turned out to be bronchitis. Sadly, this was a reminder that my mother really doesn't get any of this. As my mother and I battled it out on the phone on X'mas eve...very sad. Well, fast forward to yesterday and I found ...
Started 3 weeks ago (2008-12-19 22:37:00)
by Aricia
Hi guys, I am new here and this looks like a great place for information and support regarding CF. Basically, my 6 week old is awaiting the results of his blood test to determine the CF mutation(s) that he carries. He was screened positive for CF following the Newborn Screening here in Ontario. He came back with one mutation (not sure which) and we were called in to do a sweat test. The ...
Started 1 week, 3 days ago (2008-12-30 11:25:00)
by Ratatosk
I'm blaming my germy MIL, who hadn't seen DS for several weeks and invited us over for dinner last week and told me once we got there that she had a little cough, but only at night and she thought it was her sinuses draining. She coughed the entire time we were there and I could hear that it was a productive, throaty cough. Grr! DH thought I was overreacting and besides -- "next year he'll ...
Started 2 weeks, 5 days ago (2008-12-21 19:15:00)
by Rebjane
We traveled yesterday to visit family, we are staying at a hotel. Today, at my sister's Maggie kept saying her stomache was upset, which is not unusual for her after traveling. So I wasn't too concerned. UNTIL she sat on my sister's couch and started turning green. I looked at my sis and said you better get a bucket. Sure enough she has the pukes...no fever but she feels awful. Must've ...
Started 1 month, 3 weeks ago (2008-11-18 20:04:00)
by JazzysMom
Now in Session ------------------------- Melissa ~ 40 Year Young Gal; Mom & Wife at 30; Daughter, Sis, Cousin, Aunt, Niece, Friend & Awesome Person at Birth; CF Dx @ 7; CFRD; PA & MRSA; DDF508
|
|
Hot threads for last week on Families ::
Started 1 day, 9 hours ago (2009-01-08 18:10:00)
by kate620
Liza, unfortunately it is Cook's that has kicked us out. There were other doctors that I have met during our span of 4 yrs going there that seemed really great but thanks to Dr. X I can not even see them. Thanks anyways. Sara, yes I would like more info on your doctor. It is Medical city that I mentioned that is supposed to be awesome. They don't take Chips insurance though. I am ...
Started 1 day, 6 hours ago (2009-01-08 21:12:00)
by flatfordl
If I take the whole day off we go to lunch and sometimes a movie. We usually giver her a video or new crayons and coloring book as well. Going every two months now makes this hard because I can't always take a whole day off sometimes it is just a half day so we rush to get her dropped off and me back to work. ------------------------- Lynsey mom to Avery 5yrs. ...
Started 18 hours, 23 minutes ago (2009-01-09 09:44:00)
by JazzysMom
can someone else post this on cysticfibrosis.com? for some reason it won't let me get on the website. i want everyone to be aware of this recall. FOR IMMEDIATE RELEASE January 6, 2009 Release #09-084 Firm's Recall Hotline: (800) 646-4106 CPSC Recall Hotline: (800) 638-2772 CPSC Media Contact: (301) 504-7908 Jardine Expands Recall of Cribs Sold by Babies"R"Us; Cribs Pose Entrapment ...
Started 18 hours, 52 minutes ago (2009-01-09 09:15:00)
by jbmagik2
Hi there, my name is Jen - I live in St. Pete, FL. I just joined this forum last night, after recieving the results that my hubby is definitely a CF carrier, as am I. I found this out when I was preggo w/ my daughter, who does not have CF. We want to have one more child, but don't think we should just get pregnant knowing (tested 2x each)we both have the gene. Can you help me find more ...
Started 19 hours, 10 minutes ago (2009-01-09 08:57:00)
by TeamColinD
Hi there. I am soooo glad I found this website and you all!! These last two days mine & my husbands heads have been whirling from the confirmed diagnosis of our littlest guy, Colin, born last August. So far he has no symptoms (Thank God!) but during his newborn screening, F508 was identified. The results from the newborn screening were sent to the wrong pediatrician's office for over a month ...
|
|