Friday, July 24, 2015. Tecfidera; Notes From The Lobster Pot. I feel like I can think clearly again. I was going to let the temporary nausea win - it usually only lasts about six weeks.

whatever I find of interest to share. Tuesday, September 29, 2009. Happiness is not a matter of intensity but of balance, order, rhythm and harmony. I took quite a few pictures of the sunset on the Pamlico River while on vacation but none as amazing as this one taken by my Daughter In law. I enjoyed our family reunion. We had a wonderful time.

Bugs, bikes, brains, and buffalo. Thoughts of a myelin challenged woman now living in Fort McMurray. Wednesday, January 8, 2014. The holidays were a mixed bag of tricks and emotions. Sad to be away from family and happy to be making new friends, but the roller coaster of emotions takes its toll. However, it is new year. Speaking of years, it was 16 years ago this week that I was diagnosed with MS.

Wednesday, 22 August 2012. Well, this serves me right.

Friday, June 17, 2011. Come join me over here so I can quit posting in 2 spots. Since Novartis decided to change the name of the drug from Fingolimod to Gilenya, I redid my blog and have a new home for it. Friday, June 17, 2011. Tuesday, May 24, 2011.

WOW how time has changed. I just realized that the last post I made for nearly 2 years ago was posted on now what is my due date . how things have changed in 2 years! I can tell you on that day in Colorado, this was not even on my radar. Colorado Military Spartan Sprint Race - May 5, 2012. Picked up the rental car, had some lunch and drove to Colorado Springs.

Did you know Montel Willams has that? The continuing adventures of Bald Ben, his loving family and his battle with Multiple Sclerosis. Thursday, August 13, 2009. Is this thing on? Testing, testing 1,2,3. Yes this bemused bastion of bald fancy is still alive and kicking. Hmm, did I just hear more applause? What did the last MRI say? .

Sunday, October 12, 2014. The loss of a good woman. On the evening of September 1st Janine passed away at home in my arms. Her breathing was labored and her limbs were cold, and I told her everyone here would be okay and that she could go. Fifteen minutes later she was gone. He curled his fingers a little as a gentle embrace. His cell phone glowed with its promise of immediacy and he squinted at the icons then punched his thi.

Hot enough for ya? On the lookout for anything that might help me walk better. Because I have a disease for which there is no cure, I tend to take a second look at just about any product that might help ease my MS symptoms and my make day-to-day life more bearable. If you follow my blog, you may know MS has affected my ability to walk. For some years now, I have been using a cane to help me walk better. Having worn them for a month, I feel that they help impr.