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!
Wednesday, July 14, 2010
Day 8: Leaving home again!
Wow, I have more energy and balance; the few hints of spasms haven't materialized; my swallowing continues to be better, dare I say "normal." That said, I have less energy today than yesterday because of another bladder infection (or the same one as before treatment back again??), which normally knocks me onto the couch for a few days (ask Wayne!). Despite this, I'm headed to a conference in Vancouver on my own for 3 days then some visits with friends and family! ~Sandra
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