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
“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.
“I suffered with this many times but I finally found someone who listened and something that worked for me and got my life back.” Laura’s story on the blog today. Read & Share!
Did you know? MdDS can be triggered by an event that doesn’t involve travel. Here is an unusual case, in a word: jishin-yoi Read & Learn!