Ep. #762 SLC6A1 Connect - SLC6A1 Research & Support - aWayforWill.org

The story of young Will Feldman and his fight against a rare genetic disorder has been one of inspirational determination for many across Story County. The disease, currently identified by its affected gene, SLC6A1, is being researched, but more funds and outreach are needed to help the process along.

Just last month, Will's father Nate sat down with StoryCounty.News to talk about his family's story, as well as to put a plug in for donating towards a noble cause.

For more information on the Feldman family, SLC6A1, and how to make a contribution towards research, visit www.aWayforWill.org.

Be sure to subscribe to our YouTube channel and stay tuned to www.StoryCounty.News for the latest Story County, Iowa news coverage!
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What is SLC6A1
as quoted from: https://rarediseases.org/rare-diseases/slc6a1-epileptic-encephalopathy/

"SLC6A1 epileptic encephalopathy is an autosomal dominant genetic disorder characterized by the loss-of-function of one copy of the human SLC6A1 gene. Clinical manifestation of SLC6A1 epileptic encephalopathy is characterized by early onset seizures (mean onset 3.7 years) and mild to severe intellectual disability. Seizure types include absences, myoclonic and atonic seizures. Language impairment and behavioral problems have also been observed. Some patients have shown intellectual disability without seizures or associated with focal epilepsy."

For more information, visit https://slc6a1connect.org/ and https://awayforwill.org/

https://charity.gofundme.com/o/en/campaign/awayforwill
Be sure to subscribe to our YouTube channel and stay tuned to www.StoryCounty.News for the latest Story County, Iowa news coverage!

For more information on The Cornucopia in west Ames, visit www.TheCornucopia.com.

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Видео Ep. #762 SLC6A1 Connect - SLC6A1 Research & Support - aWayforWill.org канала The Johnny O Show