Original on Transparent.png

To support Salla disease treatments, research, education, awareness, & family networks

Original on Transparent.png

To support Salla disease treatments, research, education, awareness, & family networks

Original on Transparent.png

To support Salla disease treatments, research, education, awareness, & family networks

Salla Treatment And Research

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To support Salla disease treatments, research, education, awareness, & family networks

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Jess and Michael Foglio

Oct 13, 2018
1 min

A wonderful meeting happened! Research is on the horizon.

Almost 2 weeks ago, families from around the world met for the first time! It was empowering to be together and give our support to the esteemed doctors who...

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Jess and Michael Foglio

Sep 1, 2018
1 min

A Party with a Purpose!

We are so excited to host doctors and families in Tarrytown, NY! September 27th and 28th will be the beginning of the research for the rare Salla Disease. D...

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Jess and Michael Foglio

Jul 23, 2018
1 min

A sip for you, a sip for me!

We have been working with a local wine distributor and sharing his product in our farmer's market! 10 percent of all wine sold goes toward Salla Treatment A...

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Jess and Michael Foglio

Jul 22, 2018
1 min

Videoconference with Dr. Walkley and Dr. Wasserstein

The Salla Treatment and Research Foundation (A STAR for Ben, Inc., a new tax-exempt status pending organization) will convene an unprecedented think tank and...

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Jess and Michael Foglio

Jul 22, 2018
1 min

Welcome!

We are excited to embark on this new, rare journey. Together with families and researchers from around the world, we are hopeful to find a viable treatment f...

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Jess and Michael Foglio

Jul 22, 2018
1 min

Salla Think Tank & Family Camp

We are really excited for the upcoming event. Check out how nice this hotel is -- fancy!

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