As you can see, I have done a redesign of this website! Now with a homepage for easier navigation to articles (or so I hope). Check out my homepage here or by clicking ‘Home’ in the menu section or my name at the top. Have you seen the pages I created? One is for the … More Redesign
To commemorate ME/CFS Month and ME/CFS Week, which was last week, Open Medicine Foundation conducted an interview with me about living with the illness for two decades. You can find the full interview here on OMF’s website. I hope you check it out! Below you find a snippet. Love,Sandra
I want to shout a loud THANK YOU to all of you who so kindly donated some of your money to my fundraiser for research into myalgic encephalomyelitis/chronic fatigue syndrome. It has been one of the proudest achievements of my life. Not just because of the amount you all raised ($600!!!) for it, but also … More $600 Raised For OMF and ME/CFS Research!
Today is May 12 and that means it is ME/CFS Awareness Day! This also means it is the last day of my fundraiser to raise money for Open Medicine Foundation which funds research into this still so often misunderstood but so very debilitating condition. Want know more about ME/CFS? Check out my earlier blog on … More LAST CHANCE TO DONATE TO MY FUNDRAISER FOR ME/CFS RESEARCH
With one more week to go on my fundraiser to fund research into the condition myalgic encephalomyelitis (also ME or chronic fatigue symdrome), I wanted to share some other articles with you on the reality of this illness for others. People Magazine dedicated an article and video to the story of Whitney Dafoe, a once … More ONE MORE WEEK TO DONATE TO MY FUNDRAISER FOR ME/CFS RESEARCH