This past Wednesday, April 3rd, I participated in Advocacy Day sponsored by Solve ME/CFS and MEAction. I joined over 234 other advocates who spread out over Capitol Hill to more than 224 Senate and House offices to change minds through personal stories, education and facts. Advocacy is empowering. Not everyone is able to channel their anger at the injustice into advocacy and certainly the sickest in our society are often TOO sick to fight for justice.Read More
Yesterday I did something that has been on my “bucket list” for years. And I am so excited to share the experience with you. Read to the bottom to sign up and get a special coupon code if you want to experience what I did too! First some background —Read More
This past Saturday, on May 12th, Washington DC joined over 100 cities worldwide to call on governments and health officials to take critical action for people living with Myalgic Encephalomyelitis, commonly known as Chronic Fatigue Syndrome.
I spearheaded the DC Millions Missing event, sponsored by MEAction, which was held at the Freedom Plaza at 13th and Pennsylvania, between the White House and the U.S. Capitol.Read More