SABRIL is indicated as monotherapy for pediatric patients 1 month to 2 years of age with infantile spasms (IS) for whom the potential benefits outweigh the potential risk of vision loss. Please see Important Safety Information and full Prescribing Informa
Infantile Spasms (IS) are an uncommon form of epilepsy that typically begins in infancy. Early diagnosis and treatment is critical to improve the child's long-term development. At infantilespasmsinfo.org, our goal is to increase awareness and understandi
SABRIL is indicated as monotherapy for pediatric patients 1 month to 2 years of age with infantile spasms (IS) for whom the potential benefits outweigh the potential risk of vision loss. Please see Important Safety Information and full Prescribing Informa
Find out about a prescription medicine used in babies, 1 month to 2 years old, with infantile spasms, if the possible benefits outweigh the possible risk of vision loss. Please see Important Safety Information and full Prescribing Information, including b
Melissa Kerkhove was born on July 28th 2004. The first six months of her life she had very little development. She had trouble doing the simplest of things like holding up her head and supporting her body. She smiled only occasionally. At six months old s
Discover seizure causes, spot epileptic seizures in infants, understand the symptoms of epilepsy in children. Take a seizure symptoms quiz, call our pediatric neurology expert with your questions here.
Elena was diagnosed with Infantile spasms--a damaging form of epilepsy. We did several tests, genetics, spinal tab, MRI, labs and everything came back normal. Yet no matter what treatment we tried Elena's seizures continued. She sometimes had over 100 a d
Research and information to improve the quality of life of children and their families living with rare and life-threatening genetic disorder CDKL5. Organized
Research and information to improve the quality of life of children and their families living with rare and life-threatening genetic disorder CDKL5. Organized
Research and information to improve the quality of life of children and their families living with rare and life-threatening genetic disorder CDKL5. Organized
Research and information to improve the quality of life of children and their families living with rare and life-threatening genetic disorder CDKL5. Organized