Stories Archives - Page 3 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=””] Bladen’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] When Bladen was eleven I decided to stop the meds and try Haleigh’s Hope, and it was the best decision I’ve ever made. Bladen was born with tuberous sclerosis, which led to infantile spasms by five months.  Fortunately, […]

[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=””] Peanut’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] Unable to speak since birth, Peanut called me “mama” after just six days on Haleigh’s Hope. Peanut is seventeen and has been afflicted with seizures since birth, diagnosed with both hydrocephalus and epilepsy shortly thereafter. Pharmaceuticals were ineffective […]

[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=””] Channing’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] What a gift to see Channing’s presence and personality emerge! Channing has a genetic disorder so rare (DENND5A) that only eleven other children in the world are known to have it.  He’s been on adult seizure medication since […]

[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=””] Jack’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] On Haleigh’s Hope Jack is alert, present, and collected –  and has had a massive reduction in seizure activity. Jack was starved of oxygen by negligent doctors at birth.  He developed multiple afflictions as a result of this […]

[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=””] Amber’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] On multiple pharmaceuticals, Amber had between thirty and fifty seizures a week.  Using Haleigh’s Hope alone cut that number to under ten. Now 15-years-old, Amber has gone from having thirty to fifty seizures per day (while on multiple […]

[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=””] Solice’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] This is my Solice. She smiles, she laughs, and I am her favorite person! A geneticist once told me “don’t expect too much from her.” I was told she would never smile, never laugh, never recognize ME, her […]

[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=””] Tegan’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] I started her on Haleigh’s Hope just after her 3rd birthday. By November she had 2-3 word sentences and by January she talked in paragraphs. By March, she could recount her day at school. I want to share […]

[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=””] August’s Story [/vc_column_text][vc_row_inner][vc_column_inner width=”2/3″][vc_column_text css=”” el_class=”hh-story-txt”] We started him on CBD and two weeks later, I woke up and said when did he start talking? My son, was diagnosed Apraxia of Speech and Autism in December 2020. He had limited words and spoke only […]

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