Because We Are Strong

INTERVIEW: Orah Lasko & Hao Fountain Syndrome

November 20, 2020 Kristine Hoestermann / Guest: Orah Lasko Season 1 Episode 17
Because We Are Strong
INTERVIEW: Orah Lasko & Hao Fountain Syndrome
Chapters
Because We Are Strong
INTERVIEW: Orah Lasko & Hao Fountain Syndrome
Nov 20, 2020 Season 1 Episode 17
Kristine Hoestermann / Guest: Orah Lasko

Hey peeps! It was just Kristine this episode and I am back this week again hosting solo but we have another great episode for you today as I have the pleasure of sitting down with Orah Lasko who is the mother of Luke; Luke has a rare genetic disorder syndrome called Hao Fountain syndrome. As with to many of these rare genetic disorders Jake is among the ultra-rare with only 73 older cases known in the world. As you all know there is so much that goes into being a rare family so let's dive right in and hear from someone who knows best

I advocated for my son for over nine months before he finally got his rare disease diagnosis. I want to create awareness of his disease but also teach people how important it is to be your child’s advocate and always push for answers.

Connect With Orah:
@orahlasko and also the USP7

(Hao-Fountan Syndrome) foundation website usp7.org

Support the show (https://www.patron.com/findyourrare)

Show Notes

Hey peeps! It was just Kristine this episode and I am back this week again hosting solo but we have another great episode for you today as I have the pleasure of sitting down with Orah Lasko who is the mother of Luke; Luke has a rare genetic disorder syndrome called Hao Fountain syndrome. As with to many of these rare genetic disorders Jake is among the ultra-rare with only 73 older cases known in the world. As you all know there is so much that goes into being a rare family so let's dive right in and hear from someone who knows best

I advocated for my son for over nine months before he finally got his rare disease diagnosis. I want to create awareness of his disease but also teach people how important it is to be your child’s advocate and always push for answers.

Connect With Orah:
@orahlasko and also the USP7

(Hao-Fountan Syndrome) foundation website usp7.org

Support the show (https://www.patron.com/findyourrare)