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Our goal is to be a soft landing for families affected by this mutation, by connecting families to each other and appropriate resources. We are rare and few but together we are strong.
Through our grassroots effort we are fundraising to support research efforts for better understanding of this mutation and effective treatments.
Raising awareness of TBC1D24 and it's symptoms helps educate families and caregivers. We aim to have quicker diagnosis and improve the quality of life for all affected.
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