cysticgal.blogspot.com
Cystic GalThe daily randomlings of women with Cystic Fibrosis, moderated by ME
http://cysticgal.blogspot.com/
The daily randomlings of women with Cystic Fibrosis, moderated by ME
http://cysticgal.blogspot.com/
TODAY'S RATING
>1,000,000
Date Range
HIGHEST TRAFFIC ON
Saturday
LOAD TIME
0.8 seconds
16x16
32x32
PAGES IN
THIS WEBSITE
19
SSL
EXTERNAL LINKS
287
SITE IP
172.217.11.33
LOAD TIME
0.783 sec
SCORE
6.2
Cystic Gal | cysticgal.blogspot.com Reviews
https://cysticgal.blogspot.com
The daily randomlings of women with Cystic Fibrosis, moderated by ME
cysticgal.blogspot.com
Cystic Gal: November 2011
http://cysticgal.blogspot.com/2011_11_01_archive.html
The daily randomlings of women with Cystic Fibrosis, moderated by ME. Wednesday, November 16, 2011. Hello, Springfield and also Connecticut! Hello to my new readers tonight from Springfield, Mass and also from Connecticut via Catie Talarski's wonderful blog about her docu-series! I had a great night at the Springfield CF Team event, and it is so wonderful to come home and see Catie's blog! The presentation at Bay State Health's CF clinic was broadcast online, but I can't find it - I will post it tomorrow.
Cystic Gal: June 2012
http://cysticgal.blogspot.com/2012_06_01_archive.html
The daily randomlings of women with Cystic Fibrosis, moderated by ME. Wednesday, June 6, 2012. International Readers, "Whaazzzuuupp? Some of you may not know that Cystic Gal enjoys a healthy international readership. Today, alone, I have readers from Vietnam, West Africa, Germany, Hong Kong, Canada, South Africa, the UK and. Australia. WOW. I wonder what I wrote about last time that drew so much attention! The international readers as listed above! Most readers come to my blog thru:. Most people leave my...
Cystic Gal
http://cysticgal.blogspot.com/2013/04/i-am-sad.html
The daily randomlings of women with Cystic Fibrosis, moderated by ME. Thursday, April 25, 2013. I am sad. I miss my cat. Moving is hard. I miss my family. 4/25/13, 9:04 AM. Your comment will be posted! Subscribe to: Post Comments (Atom). There was an error in this gadget. FEEDJIT: CGin' All Over the World! Feedjit: Who's Reading CG? 85,000 Unique Readers! View Stats at StatCounter. View Stat Summary by CG. Click on this picture to learn about the moderator of the blog and its original purpose. The World ...
Cystic Gal: December 2012
http://cysticgal.blogspot.com/2012_12_01_archive.html
The daily randomlings of women with Cystic Fibrosis, moderated by ME. Sunday, December 9, 2012. Wanted you to write warmly about. Better.” - Anne Lamott. Links to this post. Subscribe to: Posts (Atom). There was an error in this gadget. FEEDJIT: CGin' All Over the World! Feedjit: Who's Reading CG? 85,000 Unique Readers! View Stats at StatCounter. View Stat Summary by CG. Click on this picture to learn about the moderator of the blog and its original purpose. Blogs We Love to Love. New poem - ten thousand.
Cystic Gal: My Top Ten Causes of Stress
http://cysticgal.blogspot.com/2012/05/my-top-ten-causes-of-stress.html
The daily randomlings of women with Cystic Fibrosis, moderated by ME. Monday, May 14, 2012. My Top Ten Causes of Stress. Scary pictures of birds stress me out. My last post made me think about things in my day that acutely stress me out. Here is my list from today. Oh yeah, here's the list:. Top Ten Stresses for Me, Myself and more Me. 1 Waking up late. 3 People swearing for no good reason. See above. 5 People calling my on the phone who I don't know to talk about something I don't care about. 8 Pieces o...
TOTAL PAGES IN THIS WEBSITE
19
Tim Williams | On The Road Less Traveled: Lungs-Liver Transplant
https://garyrobertson68.wordpress.com/author/nukejuice
On The Road Less Traveled: Lungs-Liver Transplant. My struggle with cystic fibrosis and the journey down the lungs-liver transplant path. Only 41 lungs-liver transplants have been performed in the United States. Who is Gary Robertson? Author Archives: Tim Williams. April 21, 2011. April 21, 2011. April 20, 2011. From his sister: “It has been almost 24 hours(12:00 AM) since my brother Gary has gotten out of his surgery and you would never know he had a double lung and liver transplant! April 19, 2011.
Gary Robertson | On The Road Less Traveled: Lungs-Liver Transplant
https://garyrobertson68.wordpress.com/author/garyrobertson68
On The Road Less Traveled: Lungs-Liver Transplant. My struggle with cystic fibrosis and the journey down the lungs-liver transplant path. Only 41 lungs-liver transplants have been performed in the United States. Who is Gary Robertson? Author Archives: Gary Robertson. 5th Year Transplant Anniversary. April 20, 2016. Today I celebrate my 5th double lung and liver transplant anniversary! Donate Life Transplant Games 2014. July 18, 2014. 2014 Dallas Great Strides. May 31, 2014. Had a wonderful Great Strides ...
Great News at Lung Clinic | On The Road Less Traveled: Lungs-Liver Transplant
https://garyrobertson68.wordpress.com/2014/04/21/great-news-at-lung-clinic
On The Road Less Traveled: Lungs-Liver Transplant. My struggle with cystic fibrosis and the journey down the lungs-liver transplant path. Only 41 lungs-liver transplants have been performed in the United States. Who is Gary Robertson? 3 Year Transplant Anniversary. Lungs and Liver 3 Year Check-Ups →. Great News at Lung Clinic. April 21, 2014. I went to lung transplant clinic @ Baylor Hospital today with my mother. They had me do extensive pulmonary function tests. It took almost an hour. Wow! Dr Huang is...
July | 2014 | On The Road Less Traveled: Lungs-Liver Transplant
https://garyrobertson68.wordpress.com/2014/07
On The Road Less Traveled: Lungs-Liver Transplant. My struggle with cystic fibrosis and the journey down the lungs-liver transplant path. Only 41 lungs-liver transplants have been performed in the United States. Who is Gary Robertson? Monthly Archives: July 2014. Donate Life Transplant Games 2014. July 18, 2014. Enter your email address to subscribe to my blog and receive notification of new posts by email. Join 70 other followers. Great Strides – Please Watch. Houston, TX 77030-2707.
Sandy's CF Life: Time Flies!
http://sandyscflife.blogspot.com/2011/02/time-flies.html
Sunday, February 13. I think I'm due for a bit of an update. The last few weeks have gone well in terms of my health. I had a run-in with CMV, but after a couple of weeks of oral anti-virals, it's gone again. Otherwise, I'm keeping up with my workouts, meds, sleep, and I'm even eating better. I have probably eaten more vegetable this year than I did all. I have also officially read my first novel in over a year. It's an awesome feeling to get back to the things I enjoy! I am making all sorts of goals and...
Sandy's CF Life: Merry Christmas
http://sandyscflife.blogspot.com/2010/12/merry-christmas.html
Saturday, December 25. It's been a while since I posted, but things have been going so well and I've been busy with other stuff! To be honest, I have a harder time sitting at the computer and focusing, so I haven't been on it nearly as much. So many people complain about hitting the big 3-0, but I see it as an accomplishment. Sure, we're all getting older but it's an achievement to pass a milestone. I have gotten back into one of my hobbies- scrapbooking. I am about two and a half years behind, but t...
unleashyourstory.wordpress.com
Racing for the finish line | Unleash Your Story: Make a Difference
https://unleashyourstory.wordpress.com/2009/09/29/racing-for-the-finish-line
Unleash Your Story: Make a Difference. Racing for the finish line. September 29, 2009 at 5:09 pm. Tomorrow is the last official day of the event. As of yesterday we were at $6451. There’s still time to add to that total! Entry filed under: Announcement. Support for your fellow readers and writers while you help fight cystic fibrosis. It's easy to donate online. Thanks in advance for your support! How we’re doing…. What is Unleash Your Story? Check out our FAQs. Uarr; Grab this Headline Animator. Her goal...
saysomethingsister.blogspot.com
Say Something, Sister: Jan 13, 2013
http://saysomethingsister.blogspot.com/2013_01_13_archive.html
Say Something, Sister. Sunday, January 13, 2013. Good Days, Hard Days. Feeling a vague sense of what might be desperation, anticipating the inevitable moment of the next bad day. Links to this post. Subscribe to: Posts (Atom). Good Days, Hard Days. Subscribe Feed For You. Say Something, Sister. CUSS and Other Rants. Fetch Me My Axe. I Need More Cowbell. It's All About Balance.
About My CF – From A to Pink | A Blog by Katharine Scrivener
https://fromatopink.wordpress.com/about-my-cf
From A to Pink A Blog by Katharine Scrivener. The life of a 30-something writer, cystic fibrosis patient advocate, with a penchant for hoarding books. Each CF patient’s story is a little different; here’s my version. I was diagnosed late, at 16. After being sick with a cough and numerous bouts of pneumonia for almost three years, my doctors were ready to throw up their hands. Asthma? Not that, either. It was then that I was taken to Johns Hopkins, as a sort of last resort, for a sweat test. The hardest p...
saysomethingsister.blogspot.com
Say Something, Sister: Jun 21, 2009
http://saysomethingsister.blogspot.com/2009_06_21_archive.html
Say Something, Sister. Sunday, June 21, 2009. Vegetables Are Not Funny. I said feelings, and then I looked at some chicken, or watched a dumb commercial, and I thought that looks disgusting and I don't wanna eat it. Maybe I will miss sushi and star. T eating fish again or maybe one day I will want meat but I don't right now. So for awhile Ball and Chain kept putting big hunks o' meat or fish in front of me as if I'd change my mind instantaneously or maybe just to see what I'd do? Won't I miss it? Say Som...
TOTAL LINKS TO THIS WEBSITE
287
cysticfibrosisuf.wordpress.com
cysticfibrosisuf
What is Cystic Fibrosis? Common treatment/therapies for CF. October 12, 2015. Cystic Fibrosis (CF) has no cure but treatment is available. There are many treatment and therapy regiments for people with CF. How much and how many depends on your severity and symptoms. Engaging in regular physical activity for people with CF is encouraged. It helps improve lung function and overall body condition. It also helps with managing diabetes and heart disease. Picture provided by: Julie Quintrall, RRT. Then with th...
cysticfibrosisutah.wordpress.com
Cystic Fibrosis, 65 Roses | Cystic Fibrosis, looking forward to a future with a cure.
Cystic Fibrosis, 65 Roses. March 20, 2011 · 6:52 pm. Life Expectancy is Rising! In 1955 the majority of children with Cystic Fibrosis didn’t live long enough to attend grade school, making the average life expectancy. Just under five. In 2000 it was up to 32, and in 2008 it rose to 37.4 years. Hearing things like this gives me hope for Jameson. Here’s an article. That was on ABC.com about a man who is now 30 years old, when he was told he’d never make it to 18. 3 Regular exercise and a healthy diet. ...
Victoria BC chapter of Cystic Fibrosis Canada
Victoria BC chapter of Cystic Fibrosis Canada. Cystic Fibrosis Canada – BC Region Staff. Victoria Chapter Board Members. Chapter and Event Sponsors. BC Travel and Medical Grant. Current Chapter Positions Available. Give Us Your Ideas. What is Cystic Fibrosis? Feel Good Yoga and Pilates has offered Cystic Fibrosis Victoria their May 2014 Karma classes. The Hatha Yoga classes will be at 5:15-6:30pm on May 4, 11th & 25th. Please mark your calendar and come out to support us! Feel Good Yoga and Pilates.
Cystic Fibrosis WA Inc
Self Care Circle Line. Under construction. Please come back! Under construction. Please come back! Health Care Card Health Care Card. Disability Support Disability Support. Australian Taxation Office (equipment/medications). Taking Charge: Chapter 7 Further study and CF. Information for schools and the community. Kidshealth website for kids. Cystic Fibrosis and You: A guide for young people with CF aged 8-12. Ronald McDonald Learning Program. What is Cystic Fibrosis? Have you washed your hands? Health Ex...
cysticfybrosis.com -
Cystic Gal
The daily randomlings of women with Cystic Fibrosis, moderated by ME. Thursday, April 25, 2013. I am sad. I miss my cat. Moving is hard. I miss my family. Links to this post. Sunday, April 21, 2013. So, I chose last week to proactively address my high stress level, which pretty much landed me in the ER last Monday afternoon, just before the bombs went of in Boston. Suffice to say that I have not lowered my stress level at all this week. We can also choose positive energies, positive thoughts, positive wo...
Cystic Hygroma - Experiences, treatments and effects of this congenital defect also know as lymphangioma
Experiences, treatments and effects of this congenital defect also know as lymphangioma. Cystic Hygroma Prognosis What To Expect From It. August 6, 2015. Fetal Cystic Hygroma – Is Ultrasonography a Successful Diagnosis. October 6, 2011. Filed Under: Cystic Hygroma. Tagged With: Cystic Hygroma. Curing Cystic Hygroma Some Treatment Options. September 30, 2011. Cystic Hygroma is a congenital defect mostly affecting the head and neck portion in fetus or any other patient. This disease involves surgical i...
cystichygromaandhydrops.blogspot.com
Virginia's Story
Not in our arms but in our hearts. Two servants and a king. Dancing with the Angels. Now I Lay Me Down To Sleep. Burial and memorial service. Friday, May 3, 2013. When daddy came home from work we enjoyed some Panda Express, went outside and took pictures and let go of three balloons and came back inside and sang Happy Birthday to you! Tomorrow is your big brother, Josiah's first t-ball game and then we are looking forward to going away for a night. Thursday, May 3, 2012. To our Virginia,. We were also s...
Cystic Hygroma Pictures
Photos Of Cystic Hygroma. Cystic Hygroma Picture Cystic Hygroma Image Cystic Hygroma Photographs Photos Of Cystic Hygroma. Picture Of Cystic Hygroma. Photos Of Cystic Hygroma. Photographs Of Cystic Hygroma. Be the first to post a comment! If you can read this, don't touch the following text fields. Comments on cystichygromapictures.com. Http:/ cystichygromapictures.com/index.php. Place send social about cystichygroma because my 1and haf month baby is cystichygroma pesiatian.
Cystická fibróza - Zdravě.cz
Cystická fibróza - mukoviscidóza. Je geneticky podmíněné a smrtelné onemocnění postihující dýchací a trávící soustavu. Ovlivňuje také reprodukci a růst jedince. Nemoc způsobuje chybný přenos iontů a solí přes buněčnou membránu. Nositelem je člověk, který nemusí být sám nemocný, ale má zmutované geny, které mají na starosti přenašeče. Má nejvážnější dopady na dýchací systém. Nemocný má v plicních sklípcích - alveolech hustší hlen (surfaktant), který znesnadňuje dýchání a odkašlávání. Cystická fibróza je j...
Cystická fibróza - úvod - Cystická fibróza - portál o CF
Příběhy rodičů a jejich dětí s CF. Odborné články - rodiče dítěte s CF. Odborné články - CF a rodičovství. Transplantace plic u CF. CF a škola, práce. Psychologická problematika u CF. Hygienický režim u CF. Žít život beze strachu a naplno, jak jen to půjde. Bylo mně 4,5 roku, když mně diagnostikovali cystickou fibrózu a to je fakt příliš nízký věk na porozumění této nemoci. Bez transplantace bych nepřežil. Během puberty jsem měl plno momentů, kdy jsem byl na dně, plněj nenávisti a s depresema. Léčba Kaly...
