Matthew's LGS Journey: When Hugs Speak Louder Than Words 

My son is also an LGS hero. Prayers to your son and to your whole family. I’m very thankful for you sharing.

You guys are just lovely 🥰 I am a single mama with two kiddos, one with LGS, both disabled-doing it all on my own unfortunately. Thank you for your message 🤟🏼✊🏼🫶🏼

My son is also has LGS. He is 29 years old now.He was 2 years old when it is started . I wish you and your son the best❤From Hungary🇮🇳

My son is 7 and has this. Thanks for sharing

Thank you for sharing with us your family life story . For me is a great reminder of how strong we can be to give our children a life that’s worth. My daughter was recently diagnosed with lgs. We’ve been on this journey since she was 14 mo. Now she’s 5 yo.

My son, Zachary had a massive stroke at birth, due to med malpractice. Zachary only has the right hemisphere of his brain except for 5 percent of the left frontal lobe. We were told he wouldn’t make it to be a few months old due to his sever CP, blindness and seizures. When Zach was 2 he was properly diagnosed with LGS and again were again told that it would only be a few years. I raised him and three daughters as a single mom for many years. Zachary will be celebrating his 22 birthday Jan 30th. You are not alone and now I feel less alone. ❤ from NC

Thank you for sharing your story. You're such a strong and loving family- and Matthew is such a wonderful, happy guy! He's so blessed to have you as his parents.