The Nelson Family: Paving the Way for Schaaf-Yang Research

the-nelson-family-paving-the-way-for-schaaf-yang-research-01.jpgIn 2014, when Emma Nelson was born, NICU staff told her parents, Kim and Justin, to prepare for the worst.

But for the next two years, Emma had no diagnosis. Kim and Justin were directed from one specialist to the next trying to find answers to their daughter’s unique symptoms. 

In the fall of 2016, Emma underwent whole-exome sequencing, which revealed a single mutation in the MAGEL2 gene, a mutation that was too small to be detected on less-refined tests. Finally, the Nelsons had the diagnosis they had been searching for. Their daughter had an ultra-rare genetic disorder: Schaaf-Yang Syndrome (SYS). Emma was only the 28th patient to be diagnosed.

Over the past several years FPWR has became involved in SYS research because the MAGEL2 gene, which is implicated in SYS, is also missing in PWS. That provides an opportunity for research to benefit both rare syndromes. To date, FPWR has funded a number of studies to understand how MAGEL2 normally functions and how the loss of MAGEL2 function causes the symptoms associated with SYS and PWS.

the-nelson-family-paving-the-way-for-schaaf-yang-research-2.jpgMelting Hearts & Raising Funds

Within a week of receiving Emma's diagnosis, Kim Nelson called FPWR, and I spoke with her. She asked how she could help move Schaaf-Yang research forward. She was passionate and determined to help Emma. She wasn’t going to let this diagnosis define their daughter.

For eight years, Kim and her family had been hosting the annual "I Gotta Guy Sausage Festival" in Chicago, donating the proceeds to the Cystic Fibrosis Foundation. After they received Emma's diagnosis, they shifted the focus of the event to fundraise for the best Schaaf-Yang research in the world. Last month, they hosted the ninth annual event in downtown Chicago. More than 450 guests came to the event, raising $170,000.

“The support we received from our family and friends was truly remarkable,” said Kim. “The sausage festival is a well established event, but this year, in honor of Emma, we were able to raise more money than any previous year. Emma is loved by so many. Her personality just draws you in, and when she smiles at you, your heart melts. Most people knew they were coming out to support research on a rare disease, but some didn't know the extent of how rare. Now they do!”

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First Conference for SYS Families

With Kim’s involvement, FPWR was able to host the first conference for SYS families this fall. FPWR’s 2017 family conference, with the theme "Dream, Believe, Achieve," welcomed seven Schaaf-Yang families and their children from across the U.S. and Canada. Drs. Schaaf, Potts, and Wevrick gave informative presentations about SYS (you can watch them here). Families and researchers also participated in an important sharing session that will be used to prioritize further SYS research as we work to address the most pressing challenges of the disease.

“It was such an honor to meet everyone at the conference,” said Roya Malaekeh, who had traveled from San Jose, CA with her husband and 14-month-old daughter. “I feel so much more empowered, and I’m ready to help make a change.”

Kim and Justin aren’t going to stop their efforts to spread SYS awareness and raise funds for SYS research any time soon. With their Sausage Festival less than a month behind them, they are already preparing for next year’s event — scheduled for August 23, 2018 — and brainstorming about how they can make the event even better. 

 

 FPWR Enewsletter

Topics: Stories of Hope, News

Susan Hedstrom

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Susan Hedstrom is the Executive Director for the Foundation for Prader-Willi Research. Passionate about finding treatments for PWS, Susan joined FPWR in 2009 shortly after her son, Jayden, was diagnosed with Prader-Willi Syndrome. Rather than accepting PWS as it has been defined, Susan has chosen to work with a team of pro-active and tireless individuals to accelerate PWS research in order to change the natural history of PWS. Inspired by her first FPWR conference and the team of researchers that were working to find answers for the syndrome, she hosted her first One SMALL Step walk in 2010 and began the development of the One SMALL Step walk program which now raises over $1.5 million a year for PWS research.

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