The story of Joseph

Our little boy was originally diagnosed with Global Developmental Delay as he wasn’t reaching his milestones.
In 2019 he was then diagnosed with Homocystinuria which is a metabolic condition that can have serious affects if not monitored and the correct medication and diet followed including blood clots and strokes.
Three years later he was also diagnosed with Nurofibromitosis (NF1) which is a condition that can create non-cancerous tumours (although there is a chance that these tumours can turn cancerous) one of these conditions are rare enough but our special little Pea has two.
Our little one now has a long list of conditions including SLD, ASD, lower limb spasticity but to us this just adds to how special he is and unique.