[vc_row full_width=”stretch_row” bg_type=”image” parallax_style=”vcpb-default” bg_image_new=”id^57503|url^https://jasoncranf3stg.wpenginepowered.com/wp-content/uploads/2020/04/blog-head-a-1.jpg|caption^null|alt^blog header|title^blog-head-a-1|description^null” bg_image_repeat=”no-repeat” css=”.vc_custom_1750817096851{padding-top: 80px !important;}”][vc_column][vc_column_text css=””]
[/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”]
At 20-years-old, Sean is the youngest of four children. He was diagnosed at birth with tuberous sclerosis, which caused the onset of seizures soon thereafter. His secondary diagnosis is Lennox Gasault syndrome. After 15 years of pharmaceutical medications and without relief from seizures, we turned to Haleigh’s Hope. Within days, Sean made eye contact. Now, four years later, Sean’s seizure control is the best it’s ever been. He goes days without a tonic clonic seizure, which is a particularly aggressive form. The best part is that his true personality has emerged. We are forever thankful to Jason and the Haleigh’s Hope family for the chance to know the real Sean.[/vc_column_text][/vc_column_inner][vc_column_inner width=”1/3″][vc_single_image img_size=”full” alignment=”center” css=””][/vc_column_inner][/vc_row_inner][/vc_column][/vc_row]