I'm Reema and we'd like to introduce you to our Son Kavish, He is a 11 months old now. He is little Boy with a terrible medical diagnosis, He has a rare genetic neurodegenerative mitochondrial disease called Leigh's Syndrome that has no known cure. What this means is that the disease is caused by a defect in his genes, affects all his major organs - especially the brain and nervous system and gets progressively worst with time. Doctors try to treat the symptoms rather than the disease itself.
For a child who met all his milestones and seemed to have a typical first year, Kavish at presents a completely different picture today. Crawl. Sit-up. Stand / walk with support. These are all things he could once do with ease. These are all things he can no longer do. And these are all things we hope he will one day be able to do again.
Currently Kavish going for physiotherapy and Medicines to manage the symptoms. Need help from all the save Kavish.