Baby Lliam Epilepsy Superhero

On July 2, 2018, My grandson Lliam was born. He was 2 weeks early but a healthy beautiful baby boy. Approximately 2 weeks after Lliam came home, mom and dad started noticing some twitching in Lliam. They immediately called his pediatrician and took him in to have him evaluated. His pediatrician said it was normal and he would outgrow the twitching. The twitching got worse over the next few weeks and the pediatrician continued to say they were normal. On August 25th, at just 8 weeks old, they were much much worse so my son and daughter in law took him to Pittsburgh Children's hospital ER where Lliam has been since. They have ran many many tests. MRIs, CT scans, lumbar puncture, and genetic testing. All tests have come back clear so far except for his genetic testing. Lliam continued to have many seizures daily and medicines weren't controlling them. His pediatric neurology team has diagnosed him with Intractable Epilepsy and Infantile epileptic encephalopathy. Lliam is currently on 4 seizure medications and the ketogenic diet. They've seen a decrease in his seizures, but he has a long ways to go. When Lliam is released from Children's,there will be daily needs and medical treatment supplies that his insurance doesn't cover. We are asking for donations to help relieve some of the financial burden of his parent's. His mama is still in school full time and his daddy isn't working right now so that he can be with home with Lliam. Any amount helps and prayers are also appreciated! Thank you for taking the time to read Lliam's story and God bless you all! ❤