Golfers tee off for cystinosis research
![](https://web.archive.org/web/20170805005541/http://www.theequity.ca/wp-content/uploads/2017/06/06.28cyst_golf-300x200.jpg)
Donald Teuma-Castelletti
PONTEFRACT June 24, 2017
Every time an eight-year-old Mansfield girl steps outside, she must put on her sunglasses. She could start puking at anytime, she’s constantly in and out of the hospital and requires a mix of medications all the time.
For MaryLynn Lepack, this is her reality everyday. Suffering from cystinosis, a genetic, metabolic disease, her body has an excessive build-up of the amino acid cystine in her cells. This disease negatively affects and destroys all major organs in the body and doesn’t have a cure.
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