My Personal Fundraising Page
Raising money and awareness on Smith Magenis Syndrome
Please help us support SMS Research foundation. The SMS Research Foundation knows that increased funding for research is the only way to improve the lives of children born throughout the world with this complex, congenital disorder. We hope and pray that one day we will be able to have a better understanding of Smith Magenis Syndrome.
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My Supporters
- Ana Ramos Love you, Lily Alonso! November 2018
- Eva Romero September 2018 $75.00
- Eva Romero September 2018 $75.00
My Teammates
- Eva Romero Team Captain $136.20
- RR Rebecca Romero $40.00
- MA Mayra Alonso $40.00
- AA Antonio Alonso $40.00
- TA Teresa Alonso $40.00
- JA Joey Alonso $30.00
- DL Danielle Lozano $30.00
- JA Javier Alonso $30.00
- MA Martha Alonso $30.00
- JA Jose Alonso $30.00
- JA Joel Alonso $30.00
- LA Lucia Alonso $30.00
- AR Amelia Romero $30.00
- AR Antonio Romero $30.00
- JA Joseph Alonso $10.00
- LA Lily Alonso $10.00
- DR Denise Romero $10.00
- JA Joel Alonso $10.00
- LA Lauren Alonso $10.00
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