My tiny dog, who has been my constant companion for 14 years is dying. I have been nursing her 24 hours every day for more than 3 weeks now and I believe today is the day that she will pass over. I’m holding her until she goes and therefore I will not be blogging until tomorrow. I apologize for all the unanswered comments. I just cannot cope with them right now.
Monthly Archives: May 2009
Relationships: Little things mean lots

Be sure that you appreciate
everything you’ve got
And be thankful for the
Little things in life
that mean a lot.
…Author Unknown
Notice: Readers and Subscribers
Please forgive me for being behind in publishing new posts, answering comments and leaving comments this week. I have spent most of my blogging time this week arguing with blog scraping content thieves (who have stolen entire posts from both of my blogs), and sending DMCA complaints to their web hosts to get my content removed from the splog sites. I have now set my RSS feeds to summary so I can get back to blogging. I apologize for the inconvenience but I can see no other alternative.
First Drug for Fibromyalgia pain in Canada
Relief in sight for Canadians suffering from a common chronic
widespread pain conditionKIRKLAND, QC, May 12 /CNW/ – Pfizer Canada Inc. announced today that LYRICA(R) (pregabalin) is now indicated for the management of pain associated with fibromyalgia, giving the approximately one million Canadians who suffer from this debilitating condition a key component towards managing their disease.
This new indication announcement, made on International Fibromyalgia Awareness Day, represents positive news for fibromyalgia sufferers since pain associated with the condition previously had no approved treatment options in Canada. Read full article
Coping with Fibromyalgia
You could say that I know quite a bit about this disease as it’s had me in it’s grips for 20 years. Simply put, fibromyalgia won’t kill you, but you will die with it. It doesn’t favor anyone … it affects men, women, and children of all ages and races. We live every day, hoping for a cure, praying our families can continue to cope with having to help us live with our invisible disabilities. There is really no definitive cause, and there’s no cure, so coping it what we focus on.
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