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Military veteran embraces ‘new service’ of helping others after his Parkinson's diagnosis: ‘There is hope'

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Military veteran embraces ‘new service’ of helping others after his Parkinson's diagnosis: ‘There is hope'

After 17 years of serving his country, Mark Kelm is now providing a different type of service: He’s advocating for others who, like him, are living with Parkinson’s disease (PD).

Kelm, who lives in a small Minnesota town with his wife of 23 years and three children, was just 38 years old when he was diagnosed with PD, a nervous system disorder that causes tremors, stiffness, loss of balance and other movement issues.

He credits his military background for preparing him for this latest challenge.

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“I believe the times that I had in the military really prepared me to handle living with a disease like Parkinson’s — knowing how to adapt and overcome in any given circumstance,” he told Fox News Digital in an interview. 

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“And I think those life skills that I learned in the Army are still quite useful today.”

After 17 years of serving his country, Mark Kelm is now providing a different type of service: He’s advocating for others who, like him, are living with Parkinson’s disease. He’s shown in the family picture at left, center, plus on the right.  (Mark Kelm)

Surprise diagnosis

Raised by a police deputy and a nurse, Kelm said that for as long as he can remember, his life has been geared toward service.

Since enlisting in the Army Reserves in 1989, Kelp has served many years of active duty, spent time in the National Guard and held a role as a military chaplain.

In 2006, Kelm transitioned to a role as a chaplain for a federal law enforcement agency.

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Two years later, at just 38, he was alarmed when he started experiencing involuntary twitching. 

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“One muscle in my arm kept twitching, and it was causing my finger to twitch as well, and it just wouldn’t stop,” he recalled. 

That began Kelm’s journey toward a diagnosis of young-onset Parkinson’s, which he received at the Mayo Clinic’s neurology department in Minnesota.

“That was a pretty dark day — knowing that it’s a progressive, degenerative neurological disorder that currently does not have a cure or any disease-modifying drugs,” he said. 

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Mark Kelm, pictured at right, enlisted in the Army Reserves in 1989 and served for many years in active duty. (Mark Kelm)

“As a chaplain, I performed funerals for people who had died from complications of Parkinson’s. So I was very familiar with some of the end-stage aspects of the disease.”

Kelm started taking Levodopa, a central nervous system drug that helps to manage Parkinson’s motor symptoms.

“I believe the times that I had in the military really prepared me to handle living with a disease like Parkinson’s.”

For eight years, he “stayed quiet” on the disease. In 2016, he said, “It was affecting me enough that I no longer could hide it.”

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That’s when Kelm retired from full-time work — but his next chapter was just beginning.

New form of service

“After having my own little pity party after my diagnosis, I realized that wasn’t really helpful,” he said. 

Kelm’s older daughter, who was in high school at the time, immediately started researching his disease. She soon became involved with fundraising and awareness efforts through the Parkinson’s Foundation.

Kelm, at right, is pictured on a mission trip to Uganda in 1998 while he was serving as a military chaplain. (Mark Kelm)

He was so impressed by his daughter’s efforts that he decided it was time to “get off the bench and get back into the game.”

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Kelm has since “jumped in with both feet.”

He became the national chair of the Parkinson’s Foundation People with Parkinson’s Council, which ensures that the perspective of people living with PD is integrated into the foundation’s program development.

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In 2020, Kelm helped create an annual Parkinson’s Awareness Day at Target Field, in partnership with the Minnesota Twins.

He has also organized events to raise funds for the Minneapolis-based Struthers Parkinson’s Center, and volunteers on the U.S. Department of Defense’s medical research programs for Parkinson’s.

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“My service is connected to Parkinson’s now,” Kelm told Fox News Digital.

Kelm, at far right, is pictured with his family during a visit to the Grand Ole Opry in Nashville, Tennessee. (Mark Kelm)

“It has been an absolute blessing, because it’s allowed me to meet people from all around this great nation and even the world,” he went on. 

“It’s been very positive for me, and I’m very hopeful that there’s a lot of research being done right now.”

Kelm’s advocacy could also indirectly benefit his health, according to Dr. James Beck, PhD, chief scientific officer for the Parkinson’s Foundation in New York City.

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“My service is connected to Parkinson’s now.”

“The symptoms of PD – slowness of movement, difficulty in movement, etc. – can shrink a person’s world,” Beck told Fox News Digital. 

“Mark’s effort to be involved and make a difference has helped him learn more about his own disease and to be a model advocate for his own care and health.”

What to know about early-onset Parkinson’s

People who are diagnosed with Parkinson’s before age 50 are considered early-onset patients.

Just 4% of people are diagnosed before the age of 50 — and Kelm was one.

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Early-onset patients are three times as likely to have a genetic form of the disease, according to Beck.

In 2020, Kelm helped to create an annual Parkinson’s Awareness Day at Target Field, in partnership with the Minnesota Twins. (Mark Kelm)

“People with EOPD typically have a much slower rate of progression of their disease than those diagnosed at an older age,” Beck noted.

Younger patients, however, are more likely to notice stiffness earlier in the course of the disease.

“They will often experience dystonia (e.g., cramping of a hand or toes) as an early symptom,” Beck said. 

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Patients with early-onset disease will also often experience levodopa-induced dyskinesia (involuntary movements of body parts) more frequently than those diagnosed after the age of 50, according to Beck.

Kelm said he does experience dyskinesia from time to time.

“At first, I thought, ‘I’m going to beat this,’” he said. “And after a few years, I started having some swallowing issues, which led to choking while eating.”

Kelm is pictured with his wife of 23 years, Beth Kelm. “She is the rock of the family. She does 99% of the work, and I go in for the 1% of glory.” (Mark Kelm)

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“It was a wake-up call, and an awareness that I needed to do more to manage the disease.”

Coming to terms with his mortality was tough, Kelm acknowledged — but he found some comfort in knowing.

“I found peace in knowing that everything is going to be OK.”

“You don’t die from Parkinson’s — you die with Parkinson’s,” he said. “You die from complications of the disease, especially if you’re younger. And I found peace in knowing that everything is going to be OK.”

He added, “All of us are going to leave this earth one way or another. Some of us are given knowledge beforehand, while others are not.”

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The military-Parkinson’s link

There are currently more than 110,000 veterans with Parkinson’s disease who receive care through the U.S. Department of Veterans Affairs (VA), according to the Parkinson’s Foundation.

In 2009, the Health and Medicine Division of the National Academy of Sciences, Engineering, and Medicine released a report stating that there is “suggestive but limited evidence that exposure to Agent Orange and other herbicides used during the Vietnam War is associated with an increased chance of developing Parkinson’s disease.”

Second from right, Kelm is pictured delivering tailgate Communion while serving as a military chaplain. (Mark Kelm)

As the Parkinson’s Foundation stated, PD is a “presumptive condition for veterans who were exposed to Agent Orange and certain other toxins during military service.”

Due to this designation, veterans with Parkinson’s who were exposed to these toxins are automatically eligible to receive health care and disability benefits from the VA.

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Beck of the Parkinson’s Foundation said it makes sense that there could be a link between PD and military service.

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“Although I have not seen a report of a direct increase in PD after military service, given the environmental exposures of many of our service members – head trauma, solvent exposure, etc. – it would not surprise me to see a higher prevalence of PD among veterans,” he told Fox News Digital.

Kelm noted that although the U.S. veteran population is getting smaller, the Parkinson’s rate within the community is “increasing significantly.”

Kelm and his family are pictured at the Minnesota Twins game on Parkinson’s Awareness Day at Target Field. (Mark Kelm)

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He told Fox News Digital, “I suffered two TBIs (traumatic brain injuries) in service, which the VA believes likely contributed to my Parkinson’s, along with chemical exposure.” 

The Parkinson’s Foundation partnered with the VA in 2020 in an effort to improve the health, well-being and quality of life for veterans with PD and their loved ones.

Breaking the stigma

Many military veterans with Parkinson’s find it difficult to bring themselves to ask for help after so many years of supporting others. This was the case for Kelm after his diagnosis.

“As a chaplain, my job was for people to come to me — not for me to seek them out.”

“I was in a pretty dark place at first,” he recalled. “As a chaplain, my job was for people to come to me — not for me to seek them out.”

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A doctor at Struthers Parkinson’s Center in Minnesota recognized that Kelm needed help and physically walked him to a psychologist’s office.

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“I sat down and started talking, and it really was my awakening — an awareness of how much I needed to listen to another person and have them sort through things.”

The psychologist helped Kelm realize that he could continue to serve others while also allowing others to serve him.

Second from right, Kelm is pictured during a mission trip to Uganda, during which the group helped to build a school for women. (Mark Kelm)

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Over time, people in the Parkinson’s community began calling on Kelm to help others with young-onset PD who had recently been diagnosed.

“I want to reach out to as many people as possible and get them the help they need to live the best quality of life that they can,” he said.

“I want to let them know that there is hope. It’s not all darkness — there is light. They still have a lot of life to live.”

Guided by hope and faith

During the harder days, Kelm finds encouragement and comfort in his faith.

“It’s the belief that no matter what happens, I don’t have to fear, because I know God is is with me,” he said. 

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“I have hope that as my body becomes weaker, God’s strength will become more and more evident.”

“I have hope that as my body becomes weaker, God’s strength will become more and more evident.”

Kelm said he is also optimistic that headway is being made toward improved Parkinson’s treatments and a future cure.

He is optimistic, said Kelm, that headway is being made toward improved Parkinson’s treatments and a future cure. “The needle’s moving in the right direction,” he said. (Mark Kelm)

He is encouraged by the increases in fundraising and research.

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“I’m hoping that I get to live until I’m 80 and chase grandkids around. But for that to happen, we’re going to have to do the research, so that science can point us in the right direction.”

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For others who are newly diagnosed, Kelm urges them to seek help and build a network — which may include a counselor or therapist, religious leaders, doctors, physical therapists or a speech therapist.

“Allow others to help you,” he encouraged. “It’s hard at first. You might think you can fight the disease and manage the struggle on your own. But even Jesus had help carrying the cross.”

For veterans with Parkinson’s, Kelm urges them to seek support from the VA.

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“I’m hoping that I get to live until I’m 80 and chase grandkids around,” said Kelm, who is pictured with his family. “But for that to happen, we’re going to have to do the research, so that science can point us in the right direction.” (Mark Kelm)

“Look around, ask and talk to others, and you will find dedicated people who will allow you to flourish as you live with your Parkinson’s disease.”

Beck echoed the importance of being open about a diagnosis to “help bring Parkinson’s out of the shadows … It can be a difficult first step, but is worth it in the end,” he said. 

“Loved ones will often already know something is amiss. Sharing your PD diagnosis with them will often result in relief at knowing what is wrong, and the opening of tremendous support.”

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People can call the Parkinson’s Foundation’s free helpline at 1-800-473-4636, or can visit parkinson.org or parkinson.org/veterans for information about where to get support. 

Fox News Digital reached out to the U.S. Department of Veterans Affairs requesting additional comment.

For more Health articles, visit www.foxnews.com/health.

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America’s national parks could add years to your life — here’s how they boost health

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America’s national parks could add years to your life — here’s how they boost health

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As the United States celebrates its 250th anniversary, many Americans are taking extra notice of all the things the country has to offer.

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One such case is our access to vast wilderness. Today, the nation’s national parks are bustling tourist attractions, but they may also serve as vital resources for public health, experts say.

The most immediate health boost comes from physical movement.

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Guidelines from the Centers for Disease Control and Prevention show that regular physical activity is crucial for reducing obesity, improving sleep quality and lowering the risk of chronic illnesses.

The nation’s public lands include parks, trails and open spaces that encourage outdoor recreation and physical activity.

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Beyond physical fitness, national parks contribute to documented mental health benefits. (iStock)

A review by the Community Preventive Services Task Force (CPSTF) found that implementing park, trail and greenway infrastructure directly increases physical activity across communities.

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When people walk, hike or bike through national parks, they are actively lowering their blood pressure, boosting immune function and reducing overall mortality, data shows.

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Beyond physical fitness, national parks may contribute to documented mental health benefits.

Previous research has demonstrated that direct exposure to nature significantly reduces physiological stress, lowers heart rates and decreases levels of stress hormones, like cortisol.

Engaging in educational activities and lifelong learning preserves brain function, improves memory and helps stave off age-related cognitive decline, research shows. (iStock)

This research also shows that natural environments boost attention span, combat mental fatigue and improve cognitive performance.

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Parks also act as natural venues for mindfulness and social connection.

Research shows that practicing mindfulness in quiet outdoor spaces lowers stress and mitigates feelings of loneliness and social isolation.

Research highlights that practicing mindfulness in quiet outdoor spaces lowers stress and mitigates feelings of loneliness and social isolation. (iStock)

Additionally, because parks protect cultural and historical resources, they can inspire lifelong learning.

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According to the data, engaging in educational activities and lifelong learning preserves brain function, improves memory and helps stave off age-related cognitive decline.

The National Park Service was established in 1916 to conserve the nation’s natural and historic resources for future generations, according to the organization.

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Today, that mission has expanded, as parks are recognized not only for their scenic and cultural value, but also the opportunities they provide for recreation and physical activity.

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Doctors thought man had brain cancer — they found live tapeworms instead

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Doctors thought man had brain cancer — they found live tapeworms instead

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Doctors thought a 60-year-old man had metastatic brain cancer after scans revealed multiple tumors – but further testing revealed a shocking diagnosis.

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The Spanish man, who was not named, was found to have a parasitic tapeworm larvae lodged in his brain — a case of neurocysticercosis, a parasitic infection of the central nervous system caused by the pork tapeworm (Taenia solium).

The patient, a lifelong resident of Castellón, Spain, had not traveled to any regions where the disease is endemic, according to the case report published in the CDC journal Emerging Infectious Diseases.

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The man had initially come to the hospital after suffering two weeks of progressive headaches and mild behavioral changes.

Radiologic findings from a study of autochthonous neurocysticercosis brain lesions mimicking metastatic disease. (Emerging Infectious Diseases)

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CT scans showed multiple abnormal spots that looked like tumors that had spread from cancer elsewhere in the body, leading doctors to suspect advanced brain cancer.

However, whole-body scans, a colonoscopy and specialized imaging failed to identify cancer anywhere in the patient’s body, the case report stated.

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When doctors performed a more detailed MRI, they discovered several fluid-filled cysts in the brain, some of which contained the head of a tapeworm. A blood test confirmed the diagnosis of neurocysticercosis.

The man was treated with a combination of albendazole and praziquantel (two antiparasitic medications), as well as corticosteroids to reduce inflammation. He successfully recovered with no complications, according to the case report.

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CT scans (not pictured) showed multiple abnormal spots that looked like tumors that had spread from cancer elsewhere in the body, leading doctors to suspect advanced brain cancer. (iStock)

The authors suggested that the patient may have gotten the infection after accidentally ingesting microscopic tapeworm eggs years earlier.

The exposure may have occurred while working a construction job with migrant coworkers from regions where neurocysticercosis is endemic.

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People can catch the pork tapeworm in two different ways. Eating undercooked infected pork usually leads to an intestinal tapeworm, but accidentally swallowing the parasite’s eggs — typically through food or water contaminated with feces — can send the larvae into the bloodstream, where they may form cysts in the brain and other organs. This can cause the disease the patient in the case report acquired.

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A photomicrograph shows histopathologic features in a brain tissue specimen from a case of neurocysticercosis caused by the pork tapeworm Taenia solium. The image documents pathological changes associated with this parasitic infection. (Smith Collection/Gado/Getty Images)

As this was just a single case, the source of transmission could not be proven, the researchers acknowledged, and the findings cannot be generalized to a wider population. The report shows that there is a possibility of local transmission in non-endemic settings, but cannot establish how often this occurs.

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In the United States, less than 2% of neurocysticercosis cases are considered domestically acquired, according to the case report.

A prior systematic review identified only 18 confirmed locally acquired cases in Western Europe between 1990 and 2011.

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The authors suggested that the patient may have gotten the infection after accidentally ingesting microscopic tapeworm eggs years earlier. (Associated Press)

In some cases, NCC can cause serious symptoms, including seizures, stroke, neurological deficits and cognitive decline.

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“Our case emphasizes that the absence of travel history should not preclude NCC from the differential diagnosis of multiple ring-enhancing brain lesions, even in regions where metastatic cancer is statistically much more likely,” the researchers concluded in the case study.

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Detecting the worms earlier could have prevented “unnecessary invasive oncologic procedures and led to prompt, targeted antiparasitic therapy,” they added.

Fox News Digital reached out to the researchers for comment.

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Rare tick-borne virus turns deadly fast as US cases reach record high, experts warn

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Rare tick-borne virus turns deadly fast as US cases reach record high, experts warn

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A rare and potentially fatal tick-borne illness currently spreading across the United States can be traced back to a 1958 case involving a young boy on a farm.

The disease, known as Powassan virus, was named for the Ontario town near where it was first discovered.

At the time of his death, Lincoln Byers, a 4-year-old living in Canada, had a condition that medical professionals could not explain, the Boston Globe reported.

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Years later, researchers discovered a tick harboring the same virus on a dead squirrel, finally providing an answer to the tragedy, but foreshadowing a growing public health challenge.

While once considered an obscure medical anomaly, Powassan virus cases have reached historic highs in the U.S., data show.

Powassan is most prevalent from late spring through mid-fall, when tick populations peak and outdoor activity increases. (iStock)

According to the Centers for Disease Control and Prevention, 76 Americans were diagnosed with the virus in 2025, the highest annual total on record. Previously, the U.S. averaged just seven to eight diagnoses each year.

The virus is primarily transmitted to humans through the bite of an infected woodchuck tick or deer tick. Like other tick-borne illnesses, Powassan is most prevalent from late spring through mid-fall, when tick populations peak and outdoor activity increases.

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Public health experts warn that the virus’s transmission speed makes it uniquely dangerous.

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“One of the most dangerous aspects is its rapid transmission,” Dr. Jorge P. Parada, a medical advisor at the National Pest Management Association in Chicago, told Fox News Digital.

“Powassan can be transmitted in as little as 15 minutes after the infected tick bites, while Lyme disease usually requires a 36- to 48-hour attachment time for transmission.”

Powassan carries an incubation period of one to four weeks before symptoms manifest. (iStock)

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Parada noted that while Powassan remains rare compared to Lyme disease, it poses clinical concern.

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Dr. Marc Siegel, senior medical analyst for Fox News, confirmed that the virus transmits significantly faster than Lyme disease. He noted that Powassan carries an incubation period of one to four weeks before symptoms manifest.

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Initial symptoms include fever, headache, vomiting and weakness, though some infected individuals remain asymptomatic, according to the CDC.

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There are currently no specific medications or vaccines to treat or prevent Powassan virus. (iStock)

The virus can progress to severe neurological complications, including encephalitis (inflammation of the brain) and meningitis (inflammation of the spinal cord membranes).

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In severe cases, patients may experience confusion, loss of coordination, difficulty speaking and seizures, per the CDC.

“One of the most dangerous aspects of it is its rapid transmission.”

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Approximately 10% of Powassan cases involving severe neurological disease are fatal, and many survivors experience long-term neurological issues.

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There are currently no specific medications or vaccines to treat or prevent Powassan virus; clinical care is limited to supportive therapy, such as intravenous fluids and respiratory support.

While anyone can develop severe illness, those at the highest risk include children, older adults and immunocompromised individuals, experts caution.

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