Kate Bradford's Fundraiser
Help make a difference for a real life superhero!
Join me and help make a difference, please give today.
Currently SKS patients and their families face overwhelming day to day challenges as the overactive MTOR gene wreaks havoc on the body, including disrupting sleep and causing seizures. Imagine living with an unpredictable colicky newborn for years. Or feeling jetlagged every day. This is what life is like for SKS patients and their caregivers. The seizures and lack of sleep have negative impacts on cognition, health, and overall quality of life for people living with SKS.
Smith-Kingsmore Syndrome Foundation is working to change all of this.
Our dear friends have a son with SKS and he is a real-life superhero, fighting hard every day to live his best life as his family uplifts him through it all. This little man has a special place in my heart as he was born within days of our sweet Hailey Grace. I remember high fiving my friend as she was discharged with her son as I was going into labor to deliver my daughter. If you supported our journey with Hailey, I’d humbly ask you to consider also supporting this young man.
Your contribution today will help the Smith-Kingsmore Syndrome Foundation drive science further towards treatments and a cure. I’m fundraising for the Sunniest Day of Hope Campaign so that SKSF can assist each patient and their family with sleep, seizures and many other debilitating life factors by supporting research that will lead to targeted treatments.
Your donation to the Smith-Kingsmore Syndrome Foundation is fully tax deductible and not only brings help toward a disease but provides overall support to this worldwide community.