Jenny Slatten, a familiar face to millions from the hit reality series 90 Day Fiancé, has revealed a deeply personal and challenging chapter in her life: a diagnosis of amyotrophic lateral sclerosis (ALS). The announcement, made in an exclusive interview with People and confirmed across several outlets on May 19, 2026, comes just as she and her husband, Sumit Singh, prepare to return to television for the third season of 90 Day: The Last Resort, premiering June 1 on TLC.
Jenny, now 68, and Sumit, 38, have been fan favorites since their first appearance on 90 Day Fiancé: The Other Way in 2019. Their cross-continental romance—a love story that saw Jenny leave her California home for India—captured the hearts of viewers worldwide. But behind the scenes, the couple has been navigating a much more daunting journey.
The first signs of trouble appeared in December 2024, when Jenny choked badly while drinking water. "We're doing what we can," she told People, reflecting on that moment as the start of a year-long search for answers. Soon after, she began experiencing migraines and difficulty swallowing pills. Initially, Jenny and Sumit believed these symptoms were due to “some kind of infection,” and medication offered her brief relief. But as her speech began to slow—a change so noticeable she started avoiding conversations altogether—both knew something more serious was at play. "That's when we knew something was wrong," Jenny recalled in her interview.
In December 2025, Jenny’s condition became a topic of public concern. At a 90 Day Fiancé holiday party in New York City, fans noticed her speech was markedly slower. Sumit initially chalked it up to exhaustion, but a comment from a concerned viewer struck a chord. “And then I find out that these symptoms she was having—this is what it looks like,” Sumit said, describing his reaction after researching ALS, which is also known as Lou Gehrig’s disease. The realization was especially jarring given that Jenny’s father had died from ALS more than a decade ago.
Upon returning to India, Jenny and Sumit sought medical advice from several neurologists. The first diagnosis suggested a minor brain clot, but a second opinion confirmed their fears: Jenny had ALS. The news, delivered after months of uncertainty, was devastating. “We cried and held each other,” Jenny shared. “It’s been very emotional and overwhelming for us. We were hoping to find some kind of solution before speaking publicly.”
ALS is a fatal, progressive neurodegenerative disease that attacks nerve cells in the brain and spinal cord, leading to muscle weakness, loss of mobility, and, eventually, loss of speech and independence. According to the Mayo Clinic and the U.S. National Institute of Neurological Disorders and Stroke, early symptoms can include muscle twitches, cramps, stiffness, slurred or nasal speech, and difficulty chewing or swallowing. There is currently no cure, making each diagnosis particularly heavy for patients and their families.
For Jenny and Sumit, the journey since the diagnosis has been one of both fear and hope. Doctors have described the progression of Jenny’s ALS as “slow,” giving the couple some breathing room to explore treatment options and plan for the future. Jenny is currently looking into genetic testing, which could determine if she carries the ALS gene and potentially qualify her for medications that might slow the disease’s advance. She has also joined online communities to learn about new and existing treatments, hoping that sharing her story might connect her with others who can help. “Right now we're just looking and searching,” she said. “Maybe somebody will come forward with something that could help.”
Initially, the couple tried to keep the diagnosis private, hoping to find a solution before going public. But as rumors swirled—including speculation that Jenny had suffered a stroke—they decided it was time to share the truth. In a statement posted to Instagram, Jenny wrote, “There was a rumor that I had a stroke, but it turned out to be ALS. At first, we tried to keep it private because it’s been very emotional and overwhelming for us. But after trying for some time, we feel like it’s time to reach out. Thank you so much for all the love and support. Right now, we are open to any kind of help—treatments, clinical trials, lifestyle changes, or anything that could help treat this disease or slow down its progression.”
Jenny’s openness comes at a time when ALS has been in the public eye. In April 2025, Grey’s Anatomy star Eric Dane revealed his own ALS diagnosis, and his subsequent passing in February 2026 brought renewed attention to the disease. Actor Russell Andrews, also known for roles in Grey’s Anatomy and Better Call Saul, disclosed his diagnosis last year, sharing his own struggles with early symptoms and the emotional toll of the disease.
Despite the uncertainty, Jenny and Sumit are determined to embrace life as fully as possible. “I don't want to be treated any different,” Jenny insists. “Let's just live our life as we have been while we can.” The couple has chosen to remain in India, where they continue to support each other through every challenge. Their bond, forged through years of overcoming obstacles both cultural and personal, has only deepened in the face of this new adversity. “Honestly, I never felt this much love, or I can love anyone this much,” Sumit told People. “I used to … live for myself. But from [the] last so many years, I feel like doing [things] for someone who you love gives you happiness, I think that's what love is. And that's why we do things for each other, and that's what make each other happy.” Jenny echoed his sentiment: “And we're happy that we're together.”
Jenny’s story is a reminder of the unpredictable turns life can take and the resilience required to face them. As she and Sumit look ahead to the June premiere of 90 Day: The Last Resort, they do so with a renewed sense of purpose and a message of hope for others facing similar battles. For now, they are taking things one day at a time—living, loving, and searching for answers, together.