Penelope’s Story After using Haleigh’s Hope for only a short while, Penelope began hitting milestones that her seizures caused her to miss Penelope is 3-and-a-half years old and has down syndrome. Diagnosed at 7-months-old with infantile spasms, she was put on a high dose of prednisone and was able to gain moderate seizure control. When…
Casey’s Story Casey communicates more now and has fewer seizures- we were even able to reduce his behavioral medications! Casey has been using Haleigh’s Hope for over 3 years. He’s currently on the 20:1 ratio and the results have been remarkable. Casey has mitochondrial disease and autism in addition to a rare genetic disorder. Since…
Landon’s Story What a lifesaver! In just a week we started to notice a difference. In a couple weeks, Landon was a new child. Fast forward several months, and this school year has brought perfect behavioral reports and allowed us to begin general education classes. Landon is 8-years-old and has been diagnosed with autism, sensory…
Ava’s Story We are eternally grateful for Haleigh’s Hope and will be a customer for life. Finally… seizure freedom! At only 2-and-a-half months Ava began having seizures, and by 4 months of age she was given the devastating diagnosis of CDKL5 (cyclin-dependent kinase-like 5), a rare genetic disorder caused by mutations in the CDKL5 gene…
Kinsley’s Story Given a dose of Haleigh’s Hope before bed, Kinsley woke up seizure-free. Kinsley contracted bacterial meningitis at only 3-weeks-old, which led to a stroke that destroyed the entire right half of her brain. At 4-months-old she began having infantile spasms, a type of seizure disorder in babies. In addition to three rounds of…
Emma’s Story It’s incredible that Emma can now go almost three weeks without any seizures at all! Emma is 4-years-old and and has a rare brain disorder called lissencephaly (smooth brain), of which epileptic seizures are a symptom. At one point, Emma was up to between twenty and twenty-five seizures per day as a result…
Niklaus’s Story Haleigh’s Hope has drastically reduced both the frequency and severity of Niklaus’s seizures. Niklaus is 9-months-old and experiences seizures from two very rare brain diseases, lissencephaly (smooth brain) and microcephaly (small head), both diagnosed in utero. Niklaus suffered severe infantile spasms early on, consisting of around ten episodes per day, thirty minutes each…
Dylan’s Story Haleigh’s Hope has smoothed Dylan’s transition from special needs kid into a fully functioning adult: “I’m a huge fan!” Dylan is a 21-year-old medical refugee that has been using Haleigh’s Hope for more than three years and, in that time, he has become one of your company’s biggest fans. As a child Dylan…
Oscar-Ray’s Story Oscar-Ray has learned to focus. His eyes find yours and you can feel that he is truly listening. We call Oscar-Ray our epilepsy warrior because he fights every single day. And finally, after taking Haleigh’s Hope for the past six months, we’ve seen him start to get on top of that fight. He…