Hydrocephalus Association to host International Spina Bifida & Hydrocephalus day

Chidochashe Kossam, kossamchido@gmail.com

The Hydrocephalus Association is set to mark International Spina Bifida and Hydrocephalus Day on 26 October. 

The aim of the event is to raise awareness about hydrocephalus, an incurable disease that affects many individuals worldwide. 

Pastor Lynn Ndlovu, the director of the Hydrocephalus Association, believes that it is crucial to educate the public about this condition as most people were unaware of its existence.

In an interview, Pastor Ndlovu emphasised the importance of providing support and hope to those living with hydrocephalus.

“Hydrocephalus is an incurable disease, so there’s a need to commemorate this day with them while they’re still alive,” she shared. By organising the event, the Hydrocephalus Association aims to give individuals with hydrocephalus a reason to live and find the closure they need. 

The Hydrocephalus Association has partnered Nust Medical School, where Professor Mavondo and his medical team are conducting research to find a cure for hydrocephalus. 

This collaboration demonstrates the commitment of both organisations to improving the lives of those affected by this condition. Additionally, the Hydrocephalus Association has adopted one of the wards at Mpilo, where they provide care for patients living with hydrocephalus.

This initiative showcases their dedication to supporting individuals with the disease and ensuring they receive the necessary medical attention.

The upcoming International Spina Bifida and Hydrocephalus Day is expected to raise awareness about hydrocephalus and its impact on individuals’ lives. By shedding light on this often overlooked condition, the Hydrocephalus Association hopes to foster understanding and empathy among the general public.

Furthermore, the event aims to provide a platform for those living with hydrocephalus to share their experiences and find solace in a supportive community.

Pastor Ndlovu expressed her optimism that the event would bring about positive change. “We hope this event will raise awareness about this disease, and those living with it will find the closure they need,” she shared.