Our Story

Molly Ouimet (born in 2003) and Matthew Ouimet (born in 2011) were both born with a rare genetic disease called Primary Hyperoxaluria Type 1. There is currently no treatment or cure. Matthew went into end stage renal failure when he was 5 months old. He needed hemodialysis 6 days a week and peritoneal dialysis 7 days a week for 2 years before he received a liver and kidney transplant when...

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Updates

Ouimet family blog, the journey with PH1 begins

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My husband Kelly and I have three children together:  Molly, Patrick and Matthew   Molly and Matthew Ouimet were born with a rare genetic disease called Primary Hyperoxaluria... Continue Reading »

The journey with PH1 begins Part 2

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A few years passed and I discovered I was pregnant with my third child, Matthew. I had an amniocentesis test done when I was 18 weeks pregnant and... Continue Reading »

Molly & Matthew

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