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In 2019, Cami and Jake Bartel, married for just five months, faced a life-altering event in their Chicago home. Jake, then 27, mentioned having a headache before bed, a symptom which Cami, 23 at the time, considered minor. At 4 a.m. on October 1, Cami woke to find Jake having a seizure. She called 911 immediately, and Jake was rushed to the hospital.
Doctors discovered brain swelling along with the seizure, initially suspecting a severe viral or bacterial infection, such as meningitis or West Nile virus. Tests for these conditions returned negative, leaving the medical team without answers. They informed Cami that Jake had a five percent chance of survival, assuming an unidentified virus was to blame.
Despite the grim prognosis, Jake stabilized and was discharged after two weeks, still without a clear diagnosis. One resident doctor had suggested MELAS, a rare mitochondrial disorder typically seen in children, though Jake’s age made it seem unlikely.
The couple pursued genetic testing, and by late 2019, results confirmed Jake had MELAS—Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes. This genetic condition impairs mitochondria, the cell’s energy producers, causing Jake’s body to struggle with energy production.
The diagnosis reshaped their lives. Jake left his position as an attorney, adopted a low-stress lifestyle, started new medications, and followed a specialized diet to manage the condition. In early 2020, he experienced stroke-like episodes, requiring further hospitalizations.
Despite these challenges, Jake returned to university in 2021, earning a master’s degree in education, and the couple relocated to Arizona, where he began teaching. In October 2022, after purchasing their first home, Jake suffered a major stroke that impaired his speech. He underwent two years of rehabilitation to recover his speech and strength.
Today, Jake works again as an attorney, and the couple shares their story on TikTok to raise awareness about MELAS syndrome. They clarify that the condition, maternally inherited, will not affect any future children.
Cami and Jake emphasize the importance of partnership through chronic illness, offering support to others facing similar challenges. Their journey highlights the difficulties of diagnosing rare conditions like MELAS, often overlooked in adults, and underscores their commitment to living fully despite ongoing health struggles.
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