Help4Halle - Halle has 5q14.3 Deletion Syndrome
$19 raised
1 contributor
3 Years running
Baby Halle was born on the 6 March 2014 and a few months ago was diagnosed with a Rare Chromosome Symdrome known as 5q14.3 deletion syndrome. 5q14.3 deletion is a rare genetic condition in which a piece is missing from one of the body’s ...

Baby Halle was born on the 6 March 2014 and a few months ago was diagnosed with a Rare Chromosome Symdrome known as 5q14.3 deletion syndrome.

5q14.3 deletion is a rare genetic condition in which a piece is missing from one of the body’s 46 chromosomes. Most likely features early and severe hypotonia (low muscle tone), marked developmental delay, epilepsy, marked learning disability and need for special support, marked delay in learning to sit and move, marked language delay. Most children do not speak but communicate in other ways, delay in making eye contact, stereotypic or unusual movements, some unusual facial features, brain abnormalities on magnetic resonance imaging (MRI).

Halle's family needs your support to help them through their journey to provide Halle with the best care possible.

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