Stories Archives - Page 2 of 3 - Haleigh's Hope

[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=””] Kiaryn’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] Kiaryn is so alive and happy!  His seizures have dropped in number and severity, and his overall cognitive function has improved. Born nine years ago with cerebral palsy, Haleigh’s Hope allowed Kiaryn to wean off three different pharmaceutical […]

[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=””] Billy’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] We spent every holiday in the hospital for the first six years of Billy’s life. This year will mark our fourth consecutive Thanksgiving at home. We’ve been totally blessed by Haleigh’s Hope. Billy is a ten-year-old-twin with tuberous […]

[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=””] Emily’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] We’re so grateful to have discontinued Emily’s Botox! Emily was born at twenty-six weeks with cerebral palsy and epilepsy.  When she started on Haleigh’s Hope in August of 2017, Emily was up to 1,800 mg of seizure medication […]

[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=””] Quintin’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] Quintin’s depression lifted and he was finally able to sleep. Quintin’s diagnoses are epilepsy and Tourette syndrome.  His tics disappeared in the first three weeks on Haleigh’s Hope, and we saw improved withing three months. More importantly, it […]

[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=””] Ryan’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] Ryan will never be seizure-free, but he does have his quality of life back thanks to Haleigh’s Hope. Ryan has Dravet syndrome, a severe form of epilepsy. After seventeen years of searching, we still couldn’t find anything that […]

[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=””] Scout’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] Haleigh’s Hope has been the only treatment to get Scout’s seizures under control. Suffering from seizure disorder from eleven months on, Scout had a brain tumor removed at age three and was subsequently diagnosed with cortical dysplasia.  After […]

[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=””] Hiro’s Story’s [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] Hiro hardly has any seizures anymore! Hiro’s intractable epilepsy had caused him to have hundreds of seizures a day… now, he only has a few seizures in a week! We believe largely as a result of Haileigh’s Hope, […]

[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=””] Sean’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] After 15 years of pharmaceutical medications and without relief from seizures, we turned to Haleigh’s Hope. Within days, we made our first real eye contact with Sean. At 20-years-old, Sean is the youngest of four children. He was […]

[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=””] Hardy’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] For Hardy, Hope is literally in a bottle of Haleigh’s Hope. Hardy, only 8-years-old, has come a long way in his short life.  In October of 2015 he was being pumped full of pharmaceuticals, all while continuing to […]

[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=””] Emily’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] Since starting Haleigh’s Hope Emily is so relaxed that we no longer need Botox. This is my daughter Emily. She was born at 26 weeks. She has CP and Epilepsy. We started Haleigh’s Hope in August 2017. At […]