Help Me Present HADDTS Research in D.C.

Research on rare HADDTS to fund conference travel, lodging, and fees

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$1,385 raised of 

Help Me Present HADDTS Research in D.C.

Family and friends,

Many of you know that over the past 6+ months, I’ve been deeply involved in a neuroscience research project studying the brain in a diseased state. My work focuses on Hypotonia, Ataxia, Developmental Delay, and Tooth Enamel Defect Syndrome (HADDTS)—an extremely rare neurological condition that has been identified in only about 14 individuals worldwide. My research examines neuronal development, meaning how brain cells grow and function, in order to better understand how this disease impacts the nervous system.

I’m incredibly honored to share that my abstract was selected for presentation at a national scientific conference this coming March in the Washington, D.C. area. This is a meaningful opportunity to contribute to the scientific community, raise awareness of a rare disorder, and represent months of hard work and dedication.

Unfortunately, as a non-traditional student, a mom of three, and a parent to a medically complex child, the costs associated with travel, lodging, and conference fees are difficult to manage on my own. I am hoping to raise funds to make attending and presenting at this conference possible.

If you’re able to donate, share, or help spread the word, I would be deeply grateful. Every bit truly helps, and your support means more than I can express.

Thank you so much for believing in me and in the importance of this work.

Organizer

Rebecca Carter
Organizer
Affton, MO
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