As you know, 2019 has been a big year for the CMD community. As 2019 SciFam recedes from view, we’re gathering the lessons we’ve learned and, coupled with your feedback, are continuing to make Cure CMD the place where you are represented, you are advocated for, and where you feel at home.
To that end, we’re launching the Community Blog Initiative to shine a spotlight on the CMD community - a place for sharing thoughts and issues you care about and sparking both awareness and conversations. Beginning in 2020 and led by Editor-in-Chief, community member Luke Hoban, we’re offering $50 per blog post of approximately 350-500 words, for up to 50 (approved) posts throughout the year. Your posts will be featured on the Cure CMD website, Facebook, and shared on other news outlets to grow awareness of CMD.
Blog posts don’t have to specifically be about CMD, but should relate, at least indirectly, to living a life with this ultra rare condition.
Rather vlog than blog? There’s also plenty of room for community created video content on our YouTube Channel. Get in touch with us to share your ideas.
To apply, please send the following information to firstname.lastname@example.org:
Your blog/vlog post idea(s) in fewer than 50 words
Info about past writing experience, if any (previous experience not required!)
Your/your child’s CMD subtype
A short bio and headshot that will be shared on the Cure CMD website and social media pages
We look forward to hearing from you and highlighting your voice!