MdDS after a Cruise in 2019. 🚢 It’s 2024.
When I found out I wasn’t alone in having MdDS, knowing many suffered and many had remissions or found ways to feel better, it helped me change my attitude. ~Kim
When I found out I wasn’t alone in having MdDS, knowing many suffered and many had remissions or found ways to feel better, it helped me change my attitude. ~Kim
Exciting news you can use! This edition is filled with important information that you definitely want to read.
“I hope to help people understand how debilitating MdDS is and how frustrating it is to look fine on the outside but silently suffer.” ~Dawn #thestruggleisreal
“This journey has given me a new perspective on life,… You are stronger than you think, and your story can inspire and help others.” Yoseim
“I saw every ENT doctor in my area. None of them had ever heard of MdDS.” Refusing to give up, Joan found an otolaryngologist who diagnosed her immediately. Read her story of encouragement. It’s on the blog today.
In spite of the variability, unpredictability and invisibility to others, Palm’s story contributes to the crucially important work of educating each other and the wider public about MdDS.
For some, MdDS is a cloak of darkness that settles over them. But Dawn McGhee is helping people who struggle like herself, to find light in the darkness.
For eight years, Rocking Candles has been explaining to others what daily life is like for MdDS sufferers. Kate, owner and MdDS warrior herself, has also been giving back through donations to support research so we can all “get off that boat.” Read to learn more about Kate and her custom candles.