alysonscfidsblog.blogspot.com
Alysons CFIDS Blog: The 2013 Roller Coaster and Hope for 2014
http://alysonscfidsblog.blogspot.com/2014/01/the-2013-roller-coaster-and-hope-for.html
My life with multiple chronic illnesses and my quest for answers. Saturday, January 4, 2014. The 2013 Roller Coaster and Hope for 2014. And went on another round of antibiotics. In case you weren't counting, I was on six different antibiotics from October through December. Was I doing too much and pushing my body too hard? Or is there something else going on that I need to be concerned about? I'll be making an appointment with my rheumatologist soon. I finished my last round of antibiotics a few days ago...
alysonscfidsblog.blogspot.com
Alysons CFIDS Blog: Part III: Almost Normal
http://alysonscfidsblog.blogspot.com/2013/10/part-iii-almost-normal.html
My life with multiple chronic illnesses and my quest for answers. Thursday, October 31, 2013. Part III: Almost Normal. I'm so sorry about my long absence. This time I've been away because I've been feeling good and have been out and about almost like a normal person. I suppose you can say I've been making up for lost time. I'm actually recovering from a nasty throat infection right now, but I'm otherwise doing well. Fast forward to today. I saw my neurologist this afternoon, and she confirmed my stre...
alysonscfidsblog.blogspot.com
Alysons CFIDS Blog: Part I: Um, So It Might Be Lupus...
http://alysonscfidsblog.blogspot.com/2013/05/part-i-um-so-it-might-be-lupus.html
My life with multiple chronic illnesses and my quest for answers. Tuesday, May 28, 2013. Part I: Um, So It Might Be Lupus. Wow This month has been full of medical drama with skin biopsies, ignorant nurses, and arrogant dermatologists with a couple of amazingly awesome doctors sprinkled in. Read my entry Not Mitochondrial Disease, Probably Not Lupus. The doctor backtracked a little and said she understood how frustrating it can be for patients trying to get answers. She also said it would be a good id...
alysonscfidsblog.blogspot.com
Alysons CFIDS Blog: April 2013
http://alysonscfidsblog.blogspot.com/2013_04_01_archive.html
My life with multiple chronic illnesses and my quest for answers. Sunday, April 28, 2013. If you're a regular reader, you'll know that I'm a generally positive, happy person. I know this might come as a shock to some, but I'm still human! I have my share of pity party days and days when I'm angry or frustrated. Well, today is one of those days. I feel hurt and frustrated when well-meaning friends and family tell me that, well, at least what I have isn't "more serious"/"fatal"/[insert something dismissive...
alysonscfidsblog.blogspot.com
Alysons CFIDS Blog: Three Things I'm Thankful For
http://alysonscfidsblog.blogspot.com/2013/11/three-things-im-thankful-for.html
My life with multiple chronic illnesses and my quest for answers. Thursday, November 28, 2013. Three Things I'm Thankful For. Image from http:/ savingmorethanme.com/2013/10/vintage-thanksgiving/. Improved health (and doctors who listen). Speaking of family and friends, I am thankful to have them! Simply put, they just make life better. There's plenty more that I'm thankful for, but I wanted to highlight my top three for 2013. Happy Thanksgiving to all who celebrate! Subscribe to: Post Comments (Atom).
arimayasheart.com
Useful Sites for Sickies – Life in the Autoimmune Lane
http://arimayasheart.com/useful-sites-for-sickies-2
Life in the Autoimmune Lane. Useful Sites for Sickies. Chronicles of a New Sick Chick: 2007. Life in the Autoimmune Lane. Move over, I wanna change lanes! Useful Sites for Sickies. Useful Sites for Sickies. John Hopkins Myositis Center. NIH Office of Rare Disease Research. American College of Rheumatology. American Autoimmune Related Disease Association. Center for Disease Control. Myasthenia Gravis Foundation of America. Sjögren’s Syndrome Foundation. National Institutes of Health. Show Us Your Hands.
alysonscfidsblog.blogspot.com
Alysons CFIDS Blog: May 2014
http://alysonscfidsblog.blogspot.com/2014_05_01_archive.html
My life with multiple chronic illnesses and my quest for answers. Monday, May 12, 2014. Subscribe to: Posts (Atom). Subscribe To My Blog. Follow My Blog by Email. View my complete profile. Volunteer for Research (in alpha order). Do Your Own Search. Blue Butterflies (social network). Co-Cure's Good Doctor List. Dr David S. Bell's Website. Heal Kick (social network for under 40). Int'l Association for CFS/ME. ME-CFS Community (social network). Learning to Live With CFS. Quixotic: My M.E. Blog. I may be Fa...
alysonscfidsblog.blogspot.com
Alysons CFIDS Blog: January 2014
http://alysonscfidsblog.blogspot.com/2014_01_01_archive.html
My life with multiple chronic illnesses and my quest for answers. Saturday, January 4, 2014. The 2013 Roller Coaster and Hope for 2014. And went on another round of antibiotics. In case you weren't counting, I was on six different antibiotics from October through December. Was I doing too much and pushing my body too hard? Or is there something else going on that I need to be concerned about? I'll be making an appointment with my rheumatologist soon. I finished my last round of antibiotics a few days ago...
alysonscfidsblog.blogspot.com
Alysons CFIDS Blog: ME/CFS Awareness Day
http://alysonscfidsblog.blogspot.com/2014/05/mecfs-awareness-day.html
My life with multiple chronic illnesses and my quest for answers. Monday, May 12, 2014. Cameron Von St James. My name is Cameron Von St. James and I had a quick question for you about raising awareness and was wondering if you could please email me when you have a free moment. Thanks! I really hope to hear from you soon and appreciate you taking the time. ☺ cvonstjames AT gmail DOT com. July 7, 2014 at 9:22 AM. Subscribe to: Post Comments (Atom). Subscribe To My Blog. Follow My Blog by Email. Sweet sleep...
agentforchange.blogspot.com
One Agent for Change: March 2012
http://agentforchange.blogspot.com/2012_03_01_archive.html
One Agent for Change. Well-Come to Agent for Change, a blog created by Marly Silverman, to serve as a catalyst for change that is much needed on the issues affecting millions of individuals stricken with neuroendocrineimmune disorders worldwide. Through this blog I want to share ideas, exchange, communicate and find solutions for everyday living. The goal is to pursue quality of life that will make a difference in the lives of individuals with neuroendocrineimmune disorders (NEIDs). That embraces and pro...