Hi, I'm Sandra's left jugular vein and, along with her right jugular and azygous veins, this is our story about Sandra's life now that we are fixed. Sandra's interest in us began in November 2009. She wanted to know what other patients knew about CCSVI. So, she started a Facebook page called "CCSVI at UBC MS clinic." People who share Sandra's thirst for information now go there to collect, share, and discuss developments in CCSVI. As veins, we love being the centre of all this attention!
Thursday, July 15, 2010
Day 9: Finding the new me
I'm at a conference still, but I am having zero problems swallowing fancy food every day, I shock myself with my good balance (but I'm still hitting walls from time to time!), and I don't run out of energy mid-step, mid-day or even at the end of the day (MOST unusual). I had glimmers of spasms yesterday, but they went quickly. So ~31years of MS vs. 9 days of seeing every change be a positive one, no matter how small. ~Sandra
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