PLA2G6 -associated neurodegeneration is an extremely rare, inherited degenerative disorder of the nervous system characterized by abnormalities of nerve endings within the brain, spinal cord and peripheral nerves. Also characterized by psychomotor delay and regression, increasing neurological involvement with symmetrical pyramidal tract signs and spastic tetraplegia.
The prevalence for PLA2G6-associated neurodegeneration as a group is estimated to be about 1 in 1,000,000 in the general population.
aNAD The symptoms of aNAD are more variable than those of INAD with symptoms developing usually by 4 years of age. Delayed speech and autistic features may be the first evidence of disease with regression or slowed development of milestones. Common muscle symptoms: -Involuntary muscle contractions (dystonia) -Poor articulation and speech (dysarthria) -Muscle tightness and weakness in both arms and legs -Reduced joint mobility due to muscle tightness -Overactive reflexes developing early disease -Absent reflexes developing late in disease Common neuropsychiatric symptoms: -Poor attention span -Impulsivity -Hyperactivity -Emotional lability aNAD shares common eye symptoms with INAD. Despite this diagnosis we are so optimistic and hopeful that Jade would defy the odds and that her story will be a testimony of God's faithfulness and healing power. Our focus is to keep Jade active, engaged, happy and living life to the fullest. To follow more of Jade's journey please follow us on Instagram @jadekennedifoundation. Also follow us on Facebook at The Jadekennedi Foundation. We are looking forward to sharing more of Jade's journey with you.
If you would like to donate please donate below, anything helps. The funds will be used to pay for medical visits not covered by insurance, mobility equipment, and any other associated expense regarding future medical visits and expenses.
Thank you so much for all your donations and prayers throughout this journey.
- Troylyn & Alfred family Jefferson
- ERIKA ALLEN
- Terry Perkins
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