Spina bifida warrior Ellarae

Never have I met a more extraordinary baby girl than my goddaughter Ellarae.

Her mom was told during pregnancy that she had spina bifida, a neural tube defect where in which the baby’s spine and spinal cord does not develop properly in the womb. However, from the moment of her entering this world she has been nothing short of amazing, fighting odds proving highly educated doctors wrong, and enduring surgeries that 90% of adults would struggle with… recovering with the biggest sweetest smile still on her face

Ellarae is now four months old and her wonderful parents are constantly researching ways in which to help their beloved daughter, to improve the outcome of her movements as she grows and to make her stronger.

This go fund me page is for them to be able to take Ellarae to private physiotherapists. To undergo groundbreaking use of electrical stimulation therapy, which in pediatric patients with spina bifida has shown remarkable promise in increasing mobility! Let’s give little Ellarae the best chance in life by helping her parents afford the cost of these life changing medical bills: if you can give anything it will be appreciated more than you will ever know, thank you.