Warrior & Contributing Writer, Author at MdDS Foundation

Raising Awareness, Faces of MdDS 11.25.2020

Life Rocks with Rocking Candles

I’m Kate and I Rock… Literally. In 2018, I developed a neurological disorder Mal de Débarquement. It left me with the constant feeling of rocking and swaying, like I’m on a boat. Basically I never got my land legs back and I live in constant motion. I started making candles and launched Rocking Candles this year to help in some way. The sale of each of my candles, over 700 so far, raises awareness of MdDS and 10% of the proceeds from rockingcandles.com will go the MdDS Foundation!

Faces of MdDS 1.24.2020

Russ’ Busy Day at the Lake

I had just spent the 2016 Memorial Day weekend on my parent’s boat and dock. After leaving the lake, we stopped at a favorite eatery. I finally sat down for the first time and felt “it.” I looked at my wife and asked, “Does the floor feel like it’s moving?”

Faces of MdDS 6.28.2019

The Perfect Storm

Young #MdDSwarrior, Ruthanne survived the Perfect Storm. With the support of Friends and family, she is ready for the next step in her #MdDS journey. Read her story and share to #shinealightonMdDS!

#facesofMdDS #newontheblog #sharingiscaring #mddsJAM

Faces of MdDS 6.7.2019

One day I hope to return from the sea.

Diane says she is ‘still on the ocean waiting to be rescued’ but has hope of coming home from the sea with the support of MdDS Friends.

Faces of MdDS 5.30.2019

You’re not in the boat alone.

With her first grandchild on the way, Nancy refuses to let MdDS rule her life.

Raising Awareness, Faces of MdDS 9.22.2018

Picture Perfect

After a day of flying and going up 107 stories to a restaurant in the sky, I felt a panic I had never felt before. It felt like I was walking on a bouncing floor.

Faces of MdDS 9.10.2018

I Look Normal, by Tami G.

I wrote this poem a number of years ago (maybe 5 years ago) and I sometimes post it as a status update. My daughter is no longer a toddler but the rest holds true. ~ Tami Grosset I look normal. I sit in my chair and chat. I giggle and gossip just like I’ve always […]

Guide for Caregivers 6.3.2018

A Guide for Our Caregivers

Mike Nelson, full-time caregiver to his wife and also a person with MdDS, shared this helpful guide to help you navigate life with MdDS.

Author: Warrior & Contributing Writer