Jeanine Taylor, Riverside, NJ Community Mourns Beloved Member and Supports SPS Research

Jeanine Taylor, Riverside, NJ — The Riverside community is mourning the loss of Jeanine Taylor, who passed away on July 15, 2024. Jeanine was diagnosed with Stiff Person Syndrome (SPS), a rare autoimmune neurological movement disorder that affects 4-5 people per million. She bravely fought against this debilitating condition until her passing.

In honor of Jeanine’s memory, Chandler Kirby has organized a fundraiser to benefit The Stiff Person Syndrome Research Foundation. The goal of the fundraiser is to raise $6,000, which will support ongoing research at the Johns Hopkins Stiff Person Syndrome Center, led by Dr. Scott Newsome. The funds will also aid efforts to establish The SPS Global Registry and Natural History, aiming to enhance understanding of SPS, develop better treatments, and move closer to finding a cure.

Despite the immense challenges posed by SPS, Jeanine’s resilience and courage were an inspiration to all who knew her. Her family and friends are now channeling their grief into supporting this vital cause, hoping to make a difference in the lives of others affected by this rare condition.

Chandler Kirby, the organizer of the fundraiser, expressed his deep commitment to ensuring that Jeanine’s legacy contributes to advancements in SPS research. As of now, the fundraiser has not yet received any donations, but the community’s support and early contributions are highly encouraged to inspire others to donate.

The Riverside community stands united in their efforts to honor Jeanine Taylor and support research that could bring hope to many suffering from SPS.

Short Summary of Jeanine Taylor

Note:This post was written and edited by Zoey White, based on their expertise and research. It is intended for informational purposes only. It does not constitute legal advice. We welcome your feedback and questions on this content. Please feel free to contact us.