livingwithcertainty.com
Executive Search Consultant | Professional Development Consulting Services | Kristi LeBlanc
Is a spiritual, self-help philosophy and lifestyle that gives you a fresh, practical, and prescriptive formula for. And discovering the life the universe always intended for you to live. Is it Time to Change Your Life? Are you grappling with a lack of fulfillment or purpose, career difficulties, unemployment, financial problems, bankruptcy, divorce, relationship problems, poor health, or a poor body image? Do you generally just want a better, more joyous life? Living with Certainty Can Change Your Life.
livingwithcf.com
Living with Cystic Fibrosis - Landing
After a fantastic three years of documenting my life with Cystic Fibrosis I feel this. Website has, for now at least, served it's purpose. Having received thousands of. Visitors and hundreds of messages of support, www.livingwithcf.com. Is no longer being maintained. A huge thank you to everyone who has supported me through my illness. And followed my progress. During the time I have been documenting my life with CF,. University and am now finally pursuing my passion. Here's to finding a cure.
livingwithcf.wordpress.com
Living with Cystic Fibrosis | Hmong, Torah, Cystic Fibrosis
Living with Cystic Fibrosis. Hmong, Torah, Cystic Fibrosis. My Passage to Yexus (Yeshua)…. January 31, 2010. Here we are again…. Well, I’m starting to get tired so I’ll go and see if I can get some sleep…. Posted in Cystic Fibrosis. January 17, 2010. Shortness of breath…. Posted in Cystic Fibrosis. December 30, 2009. How I’ve been feeling…. Got the tune up I’ve been dreading for in the back burner for a while and I’m ready to take on the cold weather of MN winter. Or so I thought. November 30, 2009.
livingwithcfs-amanda.blogspot.com
Living with Chronic Fatigue Syndrome
Living with Chronic Fatigue Syndrome. Thursday, 21 August 2014. Shingles Bites Me On The Bum! Friday, 20 June 2014. Wow Four months since the last post. Where does the time go? Tuesday, 11 February 2014. New Year New Challenge. Well, since November (can you believe that was my last post? Where does the time go? Life is good. I am socialising, I have a wonderfully supportive partner, I have a good support work of friends, family and last but by no means least parents and step-parents.Work continue...I can...
livingwithcfs.blogspot.com
livingwithme
This blog describes my experiences of living and coping with ME / CFS. Chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis (ME), post-viral fatigue syndrome (PVFS), and various other names, is a syndrome (or group of syndromes) of unknown and possibly multiple etiologies, affecting the central nervous system (CNS), immune, and many other systems and organs. Saturday, 22 March 2008. Preparing for the nipper. I'll keep you posted on my progress. Labels: sugar-free yeast-free diet. This ...
livingwithcfs.com
Home - Living With CFS & Fibromyalgia
Living With CFS and Fibromyalgia. Information, inspiration, and insight about living with CFS/FM. Things I Wish I Wrote. Live Well with CFS/FM. Chronic Fatigue Syndrome (CFS) and Fibromyalgia (FM) have a way of turning life upside down and inside out. But living with chronic illness can bring new life lessons and even plant seeds of growth. Learn to thrive and bloom. Be Sociable, Share! A Catalyst for Hope. CFS and Fibromyalgia: The Meaning of Recovery. Resilience: Bouncing Back in The Face of Adversity.
livingwithcfs.wordpress.com
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livingwithcfsblog.wordpress.com
Wherearemymarbles – Living With CFS/ME
Life has become a roller coaster with no off switch. This afternoon I was over tired aching and cold yet positive a glimmer of light. My gp had got my back and is trying to help me get back to work. It’s what I really want. This evening for no real reason it has all come crashing down. I’m feeling stressed, anxious and tearful. How this will affect my future and how I’ll cope? I’d like a few weeks of normal is that possible please? November 24, 2015. Remember remember the 5th of November. Yet for some re...
livingwithcgd.org
Living with CGD - The Immune Deficiency Foundation Resource for the CGD Community
Emotional, Social & Family Life. Coordinating Your Child’s Healthcare. Family & Friends. CGD and Attending School. Passing CGD on to Your Children. For Parents of Young Adults with CGD. IDF Young Adult Program. IDF Reel Stories of CGD. IDF ePHR & PI CONNECT. How You Can Help. About Living with CGD. Living with CGD – The IDF Resource for the Chronic Granulomatous Disease Community. The Immune Deficiency Foundation (IDF). Successful CGD Symposium at the IDF 2015 National Conference. July 17, 2015. Today CG...