Cure SZT2

Cure SZT2 Cure SZT2 is a non-profit organization dedicated to families affected by the genetic mutation SZT2.

Our mission is to improve the lives of those affected by SZT2, and to raise funds for scientific researches related to SZT2.

Dear Parents and Supporters,We are reaching out to you with a heartfelt request to join us in supporting a groundbreakin...
01/14/2025

Dear Parents and Supporters,

We are reaching out to you with a heartfelt request to join us in supporting a groundbreaking research initiative at the Biomedicine Institute in Italy. As parents of children affected by the rare genetic disorder SZT2, we understand the urgency and importance of finding effective treatments and interventions.

This research is unique and promising, as it utilizes a human skin cell model, avoiding animal testing, and aims to identify potential therapeutic options and interventional strategies. By supporting this research, we are taking a significant step towards improving the lives of our children and others affected by SZT2.

We believe that together, we can make a difference. Your support, whether through donations or by spreading the word to your friends, family, and community, will bring us closer to finding a cure for this devastating disorder.

Please help us reaching our goal and donate in this link: https://www.paypal.com/donate/?campaign_id=XESDSVDLL7SDS

Let's unite in this cause and give our children the hope and future they deserve. Thank you for your kindness and generosity.

With gratitude and hope,
Cure SZT2 Family

Help Cure SZT2 reach their goal by donating or sharing with your friends.

Help us meet our goal so we can fund our research and help our kids!Our kids need YOUR help! Please help us raise funds ...
11/23/2024

Help us meet our goal so we can fund our research and help our kids!

Our kids need YOUR help!

Please help us raise funds for our ongoing research of the Early Infantile Epileptic disease!

SZT2 disease, also known as Early Infantile Epileptic Encephalopathy, is a very rare genetic condition that occurs when a child carries two bad copies of the SZT2 gene. The common clinical features include intractable seizures (epilepsy) low muscle tone, loss of milestones, and severe neuroradiological anomalies affecting and risking the kids lives from a very young age (normally 3 to 5 months).

A current project suggests emerging ideas about SZT2 normal function and provide us hope that effective therapies will be developed.

PLEASE HELP us raise funds and support this research that is so much needed for this very rare disease.

Every donation makes a difference.

Click below to contribute and benefit from tax savings from your donation.

Help Cure SZT2 reach their goal by donating or sharing with your friends.

04/10/2020

Cure SZT2 is a non-profit organization dedicated solely to patients and families affected by the ultra-rare genetic mutation SZT2. Our mission is to improve the lives of children and families affected by SZT2. The “cure SZT2” group focuses mainly on raising and directing funds to scientific research with the goal of finding better, more effective treatments and, ultimately, a cure.

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Los Angeles, CA

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