Love, Laughter, and Hope

The Isaac Foundation’s mission is to fund innovative research projects that aim to find a cure for MPS, a rare, debilitating, and devastating disease.

We provide support for families of individuals suffering from MPS and advocate on their behalf to ensure government funding for expensive, life-sustaining treatments are covered by the health care system.

Since 2007, we have provided over $1 million to research grants for projects around the world that seek to cure and improve current treatments for MPS diseases. We will continue to work tirelessly to raise awareness of this disease and provide support for families dealing with this devastating diagnosis until a cure is found.

Dr. Isaac Bogoch joined The Isaac Foundation at our 12th Annual Rare Disease Symposium to discuss COVID-19, the Omicron variant, rapid testing, and the impact the pandemic has had on our rare disease patients and families. He also provided some tips to help keep our kids and families safe over the holidays.

Please take some time to watch, share, and send us any questions you might have.

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Together, We CAN Make a Difference!

The Isaac Foundation’s mission is to fund innovative research projects that aim to find a cure for MPS, a rare, debilitating, and devastating disease.

To do this, we host many fundraising events throughout the year and accept donations online and through the mail. We are very proud of the fact that 99% of all donations go directly toward our charitable activities and mission to support research aiming to find a cure. All donations receive a charitable tax receipt, delivered through email.

Thank you for your tireless support!