{"id":222,"date":"2026-10-20T22:46:40","date_gmt":"2026-10-20T22:46:40","guid":{"rendered":"https:\/\/rightstopbd.com\/gliomatosiscerebri\/?page_id=222"},"modified":"2026-10-21T18:49:33","modified_gmt":"2026-10-21T18:49:33","slug":"daryns-story","status":"publish","type":"page","link":"https:\/\/rightstopbd.com\/gliomatosiscerebri\/daryns-story\/","title":{"rendered":"Daryn\u2019s Story"},"content":{"rendered":"[vc_row type=&#8221;full_width_background&#8221; full_screen_row_position=&#8221;middle&#8221; column_margin=&#8221;default&#8221; column_direction=&#8221;default&#8221; column_direction_tablet=&#8221;default&#8221; column_direction_phone=&#8221;default&#8221; bg_color=&#8221;#595959&#8243; scene_position=&#8221;center&#8221; top_padding=&#8221;2%&#8221; constrain_group_1=&#8221;yes&#8221; bottom_padding=&#8221;2%&#8221; text_color=&#8221;light&#8221; text_align=&#8221;left&#8221; row_border_radius=&#8221;none&#8221; row_border_radius_applies=&#8221;bg&#8221; row_position_desktop=&#8221;default&#8221; 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column_position=&#8221;default&#8221; gradient_direction=&#8221;left_to_right&#8221; overlay_strength=&#8221;0.3&#8243; width=&#8221;1\/1&#8243; tablet_width_inherit=&#8221;default&#8221; animation_type=&#8221;default&#8221; bg_image_animation=&#8221;none&#8221; border_type=&#8221;simple&#8221; column_border_width=&#8221;none&#8221; column_border_style=&#8221;solid&#8221;][vc_column_text css=&#8221;&#8221; text_direction=&#8221;default&#8221;]\n<h2 style=\"text-align: center;\">Daryn\u2019s Story<\/h2>\n[\/vc_column_text][\/vc_column][\/vc_row][vc_row type=&#8221;in_container&#8221; full_screen_row_position=&#8221;middle&#8221; column_margin=&#8221;default&#8221; column_direction=&#8221;default&#8221; column_direction_tablet=&#8221;default&#8221; column_direction_phone=&#8221;default&#8221; scene_position=&#8221;center&#8221; top_padding=&#8221;2%&#8221; constrain_group_1=&#8221;yes&#8221; bottom_padding=&#8221;2%&#8221; text_color=&#8221;dark&#8221; text_align=&#8221;left&#8221; row_border_radius=&#8221;none&#8221; 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text_direction=&#8221;default&#8221;]\n<div class=\"et_pb_module et_pb_text et_pb_text_0 et_pb_text_align_left et_pb_bg_layout_light\">\n<div class=\"et_pb_text_inner\">\n<p><em>Daryn Clark of Homer, Louisiana, was 50 years old when he was diagnosed with gliomatosis cerebri \u2013 one of the few adults to develop this rare brain tumor, which is more common among children, adolescents and young adults. His story is told here by his daughter Kathleen Clark, who has become an outspoken advocate for brain tumor awareness and research.<\/em><\/p>\n<div class=\"caption caption-right panopoly-image-original panopoly-images-processed\">\n<div class=\"caption-width-container\">\n<div class=\"caption-inner\"><\/div>\n<\/div>\n<\/div>\n<p>My family was forever changed on June 15, 2012.\u00a0 My dad, a fifth-degree black belt, was waiting for his special Friday afternoon karate class to begin when he suddenly had a grand mal seizure. Dad was rushed to a small local hospital, where he had a CT scan and then was quickly transferred to larger hospital in Shreveport, an hour from our home. Thus began a two-week odyssey: He had multiple CT scans and MRI scans, a spinal tap, a PET scan and a brain biopsy, but doctors had no idea what was wrong with him. My dad was sent home the day before his 50th\u00a0birthday without a diagnosis, and told to come back in two weeks for another MRI.<\/p>\n<p>My mom immediately made an appointment with M.D. Anderson Cancer Center in Houston, Texas, because the neurologist in Shreveport thought that he might have primary central nervous lymphoma. And whatever was going on, something was terribly wrong: Dad\u2019s behavior and demeanor had undergone significant changes since his first seizure. This was not the same man who had left for his karate class two weeks earlier.<\/p>\n<p>We went to Houston the following week for Dad\u2019s appointment with a lymphoma specialist, who scheduled Dad for yet another MRI. In the meantime, the biopsy slides were to be sent to M.D. Anderson for further review.<\/p>\n<p>Ten days later we drove back to Houston for the scheduled MRI.\u00a0 When we met with the neurosurgeon the next morning, he told us that the biopsy slides indicated that my dad had a late Grade III or IV gliomatosis cerebri. He couldn\u2019t be sure about the exact grade until another biopsy was performed. Our worst fears were confirmed shortly afterward, when we were told that my dad\u2019s tumor was a Grade IV gliomatosis cerebri.\u00a0 We were told in a very compassionate manner that there was no cure. The treatment available would prolong his life for 12 to 18 months so that we could get our affairs in order.<\/p>\n<p>My mom made the decision for Dad to undergo six weeks of full-brain radiation along with a concurrent low oral dose of Temodar.\u00a0 After those six weeks, there was a four-week break from everything. Treatment then resumed with a higher dose of Temodar along with Avastin infusions.\u00a0 These continued until about a month before my dad\u2019s death.<\/p>\n<div class=\"caption caption-right panopoly-image-original panopoly-images-processed\">\n<div class=\"caption-width-container\">\n<div class=\"caption-inner\"><\/div>\n<\/div>\n<\/div>\n<p>We will never know if my dad had noticed anything suspicious happening with his body before he had that seizure, as he never mentioned anything.\u00a0 In hindsight, my family had noticed my dad acting differently at times, but there was nothing to alarm us.\u00a0 We were completely blindsided by his seizure and subsequent diagnosis.<\/p>\n<p>My father was never the same after that first seizure on June 15. He became immediately dependent upon my mom for everything. Dad went from being an extremely successful business owner and karate black belt to someone incapable of making adult decisions. His ability to communicate was immediately affected, and we were robbed of having meaningful conversations with him.\u00a0 We used to playfully tell him that he was Daryn 2.0, but it was very difficult seeing someone so capable lose all of his independence.<\/p>\n<p>Dad lived almost exactly 12 months from the date of his diagnosis.\u00a0 We were very fortunate that he did not lose his mobility until about a month before his death, when he was placed under the care of hospice.<\/p>\n<p>I decided early on that I wanted to make a difference. This is a very rare and aggressive type of brain cancer. My web site What\u2019s YOUR Fight? is dedicated to raising funds and awareness for this little-known cancer.\u00a0 I have teamed up with\u00a0<em>Elizabeth\u2019s Hope<\/em>\u00a0and the Children\u2019s Brain Tumor Project with the intent of further advancing the medical community\u2019s knowledge of brain cancer.<\/p>\n<\/div>\n<\/div>\n[\/vc_column_text][\/vc_column][\/vc_row][vc_row type=&#8221;full_width_background&#8221; full_screen_row_position=&#8221;middle&#8221; column_margin=&#8221;default&#8221; column_direction=&#8221;default&#8221; column_direction_tablet=&#8221;default&#8221; column_direction_phone=&#8221;default&#8221; bg_color=&#8221;#6E6E6E&#8221; scene_position=&#8221;center&#8221; top_padding=&#8221;4%&#8221; constrain_group_1=&#8221;yes&#8221; bottom_padding=&#8221;4%&#8221; text_color=&#8221;dark&#8221; text_align=&#8221;left&#8221; row_border_radius=&#8221;none&#8221; row_border_radius_applies=&#8221;bg&#8221; row_position_desktop=&#8221;default&#8221; row_position_tablet=&#8221;inherit&#8221; 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