Draft:Jill Viles

• Comment: 90% unreferenced content so little chance of acceptance. Theroadislong (talk) 07:10, 22 April 2024 (UTC)

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Jill Viles (born 1974) is an American writer recognized for her self-discovery of Emery-Dreifuss muscular dystrophy.

Early life and education

Jill Viles was born in Des Moines, Idaho, in 1974, the eldest of five children. Viles' mother was a stay-at-home parent, while her father worked as an assistant U.S. attorney. Up until the age of 4, Viles exhibited typical developmental milestones. However, at age 4 she began frequently tripping and falling, describing the sensation as "witches' fingers" pulling on her legs.

Her parents took her to the Mayo Clinic, where Viles was diagnosed with a mild form of muscular dystrophy, a group of genetic diseases characterized by progressive weakness and degeneration of muscle fibers. Despite her family members also exhibiting elevated creatine kinase levels, an enzyme that leaks out of damaged muscles, only Jill experienced such difficulty with walking.

Despite the diagnosis, Viles described her childhood as fun and playful.

By the age of 12, with the onset of puberty, Viles encountered further physical limitations, finding herself unable to ride a bike and noticing a significant thinning of her arms and legs.

After graduating from Roosevelt High School in Des Moines, she attended Iowa State University where she majored in genetics.

Muscular dystrophy research

While studying genetics at Iowa State University, Viles dedicated her free time to reading literature on muscular dystrophy. In addition to personal research, Viles secured an internship at the Human Gene Therapy Research Institute, affiliated with Iowa Methodist Medical Center. It was here that Viles supplemented her understanding of molecular biology.

Emery-Dreifuss muscular dystrophy

Following her sophomore year, Viles had an internship at the Whitney Research Laboratory in St. Augustine, Florida. While perusing a neurology textbook, she stumbled upon an article detailing Emery-Dreifuss muscular dystrophy. Struck by the resemblance of the symptoms and physical features described to those of her father, she realized the condition's association with cardiac issues—a health concern her father had been battling with.

Further investigation

Viles took this information to the Iowa Heart Center, where cardiologists implanted a pacemaker in her father to mitigate potential cardiac complications. Following unsuccessful attempts to engage neurologists in Iowa, Viles reached out to a research laboratory in Italy that was studying four families affected by Emery-Dreifuss muscular dystrophy. Impressed by her letter, the laboratory requested a blood sample from Viles for gene sequencing.

Four years later, in 1999, Viles received an email from the Italian laboratory confirming that her family, along with the four other families under study, had a mutation in the LMNA gene, specifically known as the lamin gene. The lamin gene is responsible for making nuclear lamina, and influences how genes in the nucleus regulate growth and development, specifically fat and muscle production. Viles in particular had a point mutation within the lamin gene, where a cytosine nucleotide was replaced with a guanine nucleotide. This specific mutation led to the difficulties in developing muscle and fat, especially in periods of rapid growth such as puberty. These results were confirmation that Viles and her family had Emery-Dreifuss muscular dystrophy.

Partial lipodystrophy

After news of her self-diagnosis spread, Viles was offered a summer internship at Johns Hopkins University at the age of 25. It was here that she read of another rare genetic disease, partial lipodystrophy. Partial lipodystrophy is a rare condition characterized by an abnormal distribution of fatty tissue.

Upon comparing pictures of partial lipodystrophy patients, Viles speculated that she might be affected by both partial lipodystrophy and Emery-Dreifuss muscular dystrophy. She attended a medical conference at Hopkins where she showed photos to doctors and informed them of her belief that she had not one, but two, rare genetic mutations. However, instead of support, she encountered skepticism from some medical professionals, who dismissed her concerns as manifestations of "intern syndrome." Viles continued her investigation; however, the stress of the research started to affect her mental health, and she abandoned her research.

Connection with Canadian Olympic athlete, Priscilla Lopes-Schliep

After seeing a photo of a Canadian Olympic athlete by the name of Priscilla Lopes-Schliep, Viles believed she and Lopes-Schliep were among the few who had partial lipodystrophy. Priscilla Lopes-Schliep was exceptionally muscular, so much so that she often faced accusations of steroid use due to her remarkable physique in track and field. In 2016, Viles reached out to David Epstein, journalist and author of "The Sports Gene: Inside the Science of Extraordinary Athletic Performance,"after his appearance on Good Morning America in 2016. Epstein became intrigued by Viles' research and agreed to help connect her with Lopes-Schliep.

Despite Lopes-Schliep boasting greater muscle mass, both exhibited comparable definition, owing to minimal body fat. Lopes-Schliep then enlisted the expertise of Dr. Abhimanyu Garg, an expert in lipodystrophy, who conducted comprehensive genetic testing and a thorough evaluation for lipodystrophy at the University of Texas Southwestern Medical Center.

The test results confirmed Viles' intuition. She and Lopes-Schliep shared a genetic link, both were diagnosed with the same subtype of partial lipodystrophy known as Dunnigan-type. Priscilla's nuclear membrane exhibited invagination and a non-circular shape, while Viles' variant in the lamin gene resulted in a rounded oval nucleus with highly disorganized genetic material in the cell cytoplasm.

Personal life

Viles married her husband in 2005. The couple shares a son, who, notably, does not inherit any of the gene mutations associated with Viles' medical conditions.. In addition to writing, Viles enjoys traveling and spending time with her husband and son.

Writing experience

Aside from her research in the science field, Jill Viles also spends time writing books and articles to raise awareness about her condition and share her journey.. Viles earned her master’s degree in creative writing from Iowa State University, her writing has appeared in Johns Hopkins Magazine, and her essay, “Loss of Control”, was recognized in the 88th Annual Writer’s Digest Writing Competition.

Viles has also spent several years working on her personal memoir and attending writing workshops.. Viles has described this book as one of the pieces she is most proud of, as she worked on it for more than 20 years.