My son "Junie" (currently 6 months) was diagnosed with a rare disability known as Pan Plexus Palsy, due to a preventable birth injury (brachial plexus nerve stretch/tear). This resulted in no movement in his left arm when he was born.

He had an MRI at 4 months old, and now has surgery next month. It will consist of multiple nerve grafts or a nerve transfer that will hopefully allow full function of his left arm in years to follow. 

He will require Occupational Therapy for at least a year and based on what is found during surgery, possible further surgeries in his life. Worst case scenario, he has 0-5% chance of finger and hand motion for the remainder of his life.

I never imagined this would be our journey or my son's, but this has become a last resort.

Any help or even sharing would be appreciated.