Travis Robinson, LPN
CEO/Founder

After my brother (Ti'Rell Robinson) passing from complications from Sickle Cell Disease in 2014. My mother and I (Julia Robinson) decided to fund The Robinson's Sickle Cell Foundation, so the foundation can help those in certain areas get the resources for their well-being. From their appointments, assist with medication regimens, and spread awareness of SCD and how important it is. Just to name a few. Not to mention, I am a Sickle Cell Warrior!

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Thank you for reaching out to Robinson's Sickle Cell Foundation: HOLD a HEART! If you or someone you know is living with SCD and could benefit from our services, or if you have any questions or comments, please don't hesitate to contact us using the form below. We will do our best to get back to you as soon as possible.