29/01/2025
All the time it was important for the parents to understand this weakness may progress and we have to monitor him. The fathers smile was gone. Next day the child also developed weakness of trunk muscles so he was unable to sit up independently. Further he was also unable to swallow and developed what we call as the bulbar palsy in medical language forcing us to put a feeding tube lest he may aspirate if fed orally. The mother and father both were looking desperate and it was difficult for them to understand that why the weakness was progressing.
Fortunately there was no further progression of weakness and over next week we could remove his feeding tube. Mast AP was looking happy to take food orally again. Daily exercises were started and child was sent home as it was his 4th birthday with a promise to do daily physiotherapy. 2 months later mast AP is standing and walking before me independently. The joy on his face and smile on the parents’ lips is the picture I want to remember lifelong.