I’m sure by now you’ve seen me talk about the book that I’m putting together with the mom of a young girl with cystinosis. (Follow here blog here.) (Cystinosis is a rare, genetic, metabolic condition that I myself also have. All of the proceeds from this book will go to the Cystinosis Research Network.) Well, that book is going to go live VERY soon. We just have a few things to get ironed out first.
In the meantime, a friend put together this campaign on a website called ThunderClap. This how it works: You go to the site and you can support the campaign three different ways. Facebook, Twitter or Tumblr. You can do any or all of them. You click the option you want and then confirm. All you’re confirming is that ThunderClap can post a one time message to that social media platform on the date it lists. (In this case July 25th.) We need 100 supporters for the campaign to actually show up your social media platform (if you support it) on the 25th. We would LOVE your support!! Thank you SO much!! ❤ ❤
Support ThunderClap Campaign HERE.