Jessica Jean Wilson

Jessica has been diagnosed with Infantile Spasms, a rare genetic abnormality (chromosome 14q12 duplication) and hypermobility 
since March 2014. She receives High level care DLA. 
Her development is sitting around the nine month mark (eight month delay), with exception to her communication which
 has recently been scored at four months. She has low muscle tone and cannot sit unaided for long periods of time.