Leading the worldwide fight to treat and cure
Tay-Sachs, Canavan, GM1 and Sandhoff diseases

An evening with astronaut John Grunsfeld

An evening with astronaut John Grunsfeld

Please join us for an evening of inspiration, hope, and wonder with astronaut John Grunsfeld, the veteran of five Space Shuttle missions, including three to the Hubble Space Telescope!

The event will be held on Sunday, October 13 from 6:30-9:00 pm at the Denver Jewish Community Center, 350 S. Dahlia.

John Grunsfeld will join the Flamenbaum/Goldstein family to share his experiences, underscore the promise of hope and determination, and celebrate the brilliant memory of Russell Elliott Goldstein, who passed away in 2016 after a three and one half year struggle with Prader-Willi Syndrome and infantile Tay-Sachs disease.

The evening’s proceeds will directly benefit research and family services for children and families who face Tay-Sachs and related rare diseases by supporting National Tay-Sachs & Allied Diseases (NTSAD), a 501(c)3 non-profit organization. Our goal is to establish the Russell Elliott Goldstein Fund of NTSAD.

We welcome your interest, your support of rare disease research and family services, and your generosity on behalf of Russell and every family challenged by Tay-Sachs and related diseases.

Together with John Grunsfeld and our dear friends and colleagues, we can aim for the stars and advance real work toward treatments and potential cures—thank you!

Tickets for the event are $75 per person, $180 per family, $50 for seniors and $30 for college students ($50 and $30 payments can be made by going to the “other” payment amount). Once you make your contribution you are ticketed for the event.

To buy tickets, please follow this link.




Day of Hope in Memory of Abhinav


2015 Day of Hope


In memory of 



"He was a sweet boy!

We miss him a lot"

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Jase's Benefit for a Cure for Canavan Disease

Thank you to all of you who have helped to support Jase's Ride!


Jase was a beautiful 8 pound and 1 ounce bouncing baby boy when he was born on March 27th of 2011. He was everything we had hoped for; 10 fingers, 10 toes, a head full of hair, and healthy. So we thought! Soon after he was born he developed what we now know of as a nystagmus. Puzzled, our pediatrician sent us straight to Children’s Hospital the day of his 8 week check-up. They ran test after test with nothing to show. My motherly instinct kicked in knowing that something was wrong and I begged for more testing. Three days later we got a call from the neurologist telling us that he wanted to see us in his office the following morning. Our hearts sank! 

The next morning our family piled into that dreaded small white room where we received the unbearable news. Our son had Canavan disease. Prognosis, death. The next 2 months became a whirlwind of bad news, long hospital stays, trips to specialists around the country, fundraisers, tears, heartache, and prayers. 

We were soon connected with a Facebook page of families that had affected children. They became our friends and our support. They helped us with the hardest of questions; “How could this happen?” “We aren’t Jewish!” “Did we just get struck by lightning?” Our new Canavan family quickly welcomed us with open arms and shared with us a non-profit organization called the National Tay-Sachs and Allied Diseases Association (NTSAD). NTSAD gave us hope and direction, but with every effort, every drug, every doctor, every trial, the inevitable happened. On August 14th, that same year, our sweet baby boy passed in his sleep curled up between Mommy and Daddy. 

NTSAD immediately reached out to us with comforting words. They were God sent at such a tragic time in our lives. We stayed in contact with them over the next few months and decided to attend our first Annual NTSAD Family Conference. There we poured our hearts out to people we didn’t know, but would soon become our adopted family. Words cannot express the feeling of being surrounded by people that know exactly what you are going through. It felt safe, secure, and comfortable. There was no judgment, only hugs and words of encouragement. 

I quickly got involved with fundraising and family outreach committees as I was full of hope and determination to live out my little boy’s legacy.

Join us for our 9th annual Jase cure for Canavan event in September 14th. There will be a poker run, live and silent auction, music, and food. All proceeds go to the NTSAD to find a cure for this devastating disease. So far, we have raised over $100,000 and we are so excited to reach our goal of $15,000 this year! If you are unable to attend, but would like to donate please follow the link below. Thank you from the bottom of our hearts! - The Watson and Cornett family

Mommy and Daddy love and miss you so much, Sweet baby Jase!

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Our Lil’ Chunk


Celebrate our Sweet Baby Jase and Support Canavan Research!