Oct 29, 2026
2 min read
Two-year-old Larissa Kissoon, who once had up to 100 seizures a day, is now seizure-free after starting treatment in India, her mother said, as the family appeals for financial help.
The family, however, is still struggling to cover the cost of her ongoing treatment and additional medical expenses.
Her mother, Juliann Pereira, said the family travelled to India on October 15, and Kissoon began treatment at Artemis Hospital. Since then, she has seen a significant reduction in the seizures that once affected her daughter throughout the day.
“Everybody feel happy that Larissa is finally not doing no seizure because she had a lot of pain,” Pereira said, describing the relief the family feels at the improvement.
While the treatment has brought encouraging changes, Kissoon continues to face developmental challenges. Pereira said doctors have identified developmental delays and brain damage, and have explained that they cannot predict how much progress she will make.
To support her development, Kissoon is expected to begin physiotherapy after completing a 15-day course of medication. Her mother said further care is needed to address her physical challenges.
Kissoon was diagnosed with West syndrome at two months old, after her parents rushed her to the Georgetown Public Hospital because she had cried uncontrollably through the night.
Pereira previously told Ignite News that the family was struggling to raise funds for specialised treatment abroad, estimated at US$10,000 excluding travel, accommodation, food and other expenses. At the time, the family had raised $1 million.
Despite the progress, the family continues to face financial pressure as it works to meet those costs. Pereira said a donation promised by an organisation has not yet been received.
Persons wishing to assist can send contributions through MMG to Juliann Pereira at 652-1067.
