{"id":15494,"date":"2025-07-17T04:24:08","date_gmt":"2025-07-17T04:24:08","guid":{"rendered":"https:\/\/www.newsbeep.com\/us\/15494\/"},"modified":"2025-07-17T04:24:08","modified_gmt":"2025-07-17T04:24:08","slug":"hope-for-a-cure-hangs-on-research","status":"publish","type":"post","link":"https:\/\/www.newsbeep.com\/us\/15494\/","title":{"rendered":"Hope for a cure hangs on research"},"content":{"rendered":"

\u201cWait for science to catch up,\u201d a physician told Hailey Adkisson<\/a> after failing to diagnose or effectively treat Adkisson\u2019s daughter Juniper, who suffers from undiagnosed epilepsy. Statements like these are common in the rare disease world that Adkisson\u2019s family navigates.<\/p>\n

\"Hailey<\/p>\n

Hailey Adkisson<\/p>\n

Hailey Adkisson and daughter Juniper, age 4, pose with the book Adkisson wrote to explain epilepsy to children. Find her on Instagram: @growing_juniper.<\/p>\n

Adkisson’s reality has become a nightmare amidst the cuts and dismantling<\/a> of scientific research happening in the U.S. For example, the president\u2019s proposed budget<\/a> for fiscal year 2026 slashes NIH and National Science Foundation funding by 40% and 55%, respectively.<\/p>\n

\u201cIf rare disease research slows down or stops,\u201d Adkisson said, \u201cpeople \u2014 including children (my family) know(s) directly \u2014 will die. It\u2019s not a question of if; it\u2019s when. This includes Juniper. Her seizures are getting more severe as she gets older. Seizures lead to more seizures. We need treatment options before it is too late. We need people to care.\u201d<\/p>\n

In the U.S., a disease is considered rare if it affects fewer than 200,000 people<\/a>, but many impact far fewer. With over 10,000 rare diseases<\/a>, there are nearly 30 million Americans, mostly children, impacted. Most of these conditions are life-threatening, genetic and lack approved treatment.<\/p>\n

For families like Adkisson\u2019s, research is their only hope. Adkisson became part of the rare disease community after her daughter, Juniper, began having seizures at six months old. Until then, Adkisson said Juniper seemed healthy. But once the seizures began, they never stopped.<\/p>\n

Juniper\u2019s doctors have tried more than a dozen antiseizure medications, and she has undergone two brain surgeries. One was a hemispherectomy to remove one side of Juniper\u2019s brain in the hopes of stopping her seizures. It didn\u2019t work. She now lives with a device implanted in her chest to help regulate brain activity.<\/p>\n

In search of answers, Juniper and her family underwent genetic testing multiple times, which yielded no known deleterious mutations. Eventually, they reached out to the Undiagnosed Diseases Network<\/a>, or UDN, a federal research initiative that studies cases like Juniper\u2019s. They are currently conducting studies using some of her brain tissue. According to a UDN\u2019s 2024 report<\/a>, they have helped diagnose 750 patients and defined 75 new conditions.<\/p>\n

However, Juniper remains undiagnosed, making it difficult to find treatments or assess whether relatives are at risk of a similar disorder. Continued research through the UDN is their only path forward, but the federally funded<\/a> program could be affected by proposed budget cuts.<\/p>\n

Those who have rare and complex health conditions often feel alone, especially now. Adkisson has taken her family’s experience and launched an organization, Simply Complex Stories<\/a>. They publish illustrated books to teach children about complex medical conditions, like epilepsy.<\/p>\n

Life-saving power of newborn screening<\/p>\n

\"Lauren<\/p>\n

Lauren Hughes<\/p>\n

Lauren Hughes is a mother to a rare disease patient, a pediatrician and a social media educator. Find her on Instagram: @bloomdpc.<\/p>\n

Lauren Hughes<\/a>, a pediatrician and mother to a rare disease patient, said research saved her son\u2019s life.<\/p>\n

He lives with medium-chain acyl-CoA dehydrogenase deficiency<\/a>, or MCAD, a rare metabolic disorder that prevents the body from breaking down medium-chain fatty acids. MCAD affects about 1 in 20,000 children in the U.S.<\/p>\n

Doctors identified MCAD in Hughes\u2019 son via newborn screening, an optional medical initiative that tests newborns for about 38 genetic conditions<\/a>, enabling early detection and treatment. This program would not exist without federally funded science that helped identify the mutations responsible for these conditions.<\/p>\n

The Trump administration recently terminated<\/a> the advisory committee responsible for recommending updates to the newborn screening program, meaning rare genetic diseases discovered in the future could go undetected. Hughes said she finds this action greatly concerning.<\/p>\n

\u201cIf (my son) had been born even 25 years in the past, he wouldn\u2019t have survived,\u201d Hughes said. \u201cWithout newborn screening and the advisory committee that expanded the testing to include my son\u2019s condition, I wouldn\u2019t have a living and healthy five-year-old boy.\u201d<\/p>\n

\"Shown<\/p>\n

Battaile, K.P., Mohsen, A.-W., Vockley, J. via Protein Data Bank<\/p>\n

Shown is a crystal structure ribbon diagram medium-chain acyl-CoA dehydrogenase. Lauren Hughes\u2019 son suffers from a rare disease caused by a deficiency in this enzyme.<\/p>\n

Unlike many rare diseases, MCAD can be managed. However, early diagnosis is key to patient survival. Those with MCAD cannot go without food for long periods; if they do, they develop dangerously low blood sugar levels, causing them to become comatose and potentially die.<\/p>\n

According to Hughes, receiving her son\u2019s diagnosis early allowed her and her family to adapt and keep him alive.<\/p>\n

\u201cWhen he was a newborn, I had to wake and nurse him every two hours, around the clock,\u201d she said. \u201c(I)t was scary, stressful and exhausting, but it enabled him to survive.\u201d<\/p>\n

Hughes said she still lives with daily fear because each overnight requires careful planning, and even the common cold could become a health crisis for her son.<\/p>\n

\u201cEven if a rare disease isn\u2019t always fatal, it can still be life altering,\u201d Hughes said. \u201cThese kids matter. These families matter. Their lives can be improved by continued research.\u201d<\/p>\n

Rare disease research benefits all<\/p>\n

The Trump administration\u2019s proposed cuts<\/a> to biomedical and public health research<\/a> might seem like distant policy decisions to some and a professional crisis to scientists \u2014 but for families affected by rare disease, it could mean the difference between life and death.<\/p>\n

\"In<\/p>\n

Hailey Adkisson<\/p>\n

In a hospital room, Juniper Adkisson, age 4, smiles for a photo while hooked up to an electroencephalogram to monitor her brain waves for seizure activity. Despite trialing over a dozen medications and undergoing multiple surgeries, Juniper still experiences daily seizures due to an undiagnosed rare disease.<\/p>\n

\u201cOur daughter is in the rarest of rare categories,\u201d Adkisson said. \u201cThere is so little funding already for undiagnosed rare disease.\u201d<\/p>\n

Rare disease research benefits all of us, even if we aren\u2019t part of the rare disease community. It has led to breakthroughs<\/a> in our understanding<\/a> of genetics, cell biology, cancer and more.<\/p>\n

Despite this mutual benefit, many rare disease families feel invisible. Adkinsson said conditions like epilepsy receive less funding<\/a> than other neurological disorders. For example, in fiscal year 2023, the NIH budget totaled approximately $47.7 billion<\/a>. Of this, $245 million<\/a> funded epilepsy research, while Alzheimer\u2019s and dementia research received over $4 billion<\/a>.<\/p>\n

This is why parents like Adkisson and Hughes speak out on social media about the dismantling of scientific research happening in the U.S.<\/p>\n

From both stories we can learn an important lesson: Science isn’t just a job or new knowledge. It\u2019s a lifeline to patients who have little hope. When the government cuts rare disease research funding, it tells families across the country, like Adkisson and Hughes\u2019, that they don\u2019t matter. Science can\u2019t catch up to help these rare disease patients and families if we don\u2019t fund it.<\/p>\n

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